Nobel Prize Nominee Plastic Surgeon Joins Patients Medical’s Stem Cell Research Team

Dr. Paul A. Dreschnack Offers New Options for Those With Hair Loss.

New York City, NY (PRWEB) November 29, 2012

Baldness can cause social anxiety, depression and many other emotional and psychological conditions. The solutions currently being offered such as transplants and pharmaceuticals can be uncomfortable or may compromise other aspects of the patients health, explains Dr. Dreschnack. In my work around the world, I strive to find ways for people to look good and feel well so that they are able to enjoy their lives fully. Stem Cell Therapy seems to be a new frontier that may be a way for patients to improve their quality of life.

Dr. Dreschnack is a four-time Nobel Prize Nominee for his work with The India Project. He has traveled internationally, helping patients who need plastic, cosmetic and reconstructive surgery. He is now working with Dr. Kamau Kokayi, Medical Director of the New York Stem Cell Treatment Center (NYSCTC) at Patients Medical.

We are excited that Dr. Dreschnack is joining our Stem Cell Research Team, says Dr. Kokayi.

Dr. Dreschnack has been the recipient of numerous awards including the Distinguished Surgeon Award from the Association of Operating Room Nurses, a 2002 Rose Model Award from the Young Leadership Council. He has been nominated for the The Raoul Wallenberg Medal, celebrating people who embody humanitarian ideals. He has also established himself as an academician, reviewing articles for the American Journal of Cosmetic Surgery, serving as Clinical Instructor at LSU School of Medicine/Department of Surgery and SUNY Health Science Center in Brooklyn. Dr. Dreschnack has also given presentations for the American Society for Surgery of the Hand and has been published in Medforum.com, Plastic and Reconstructive Surgery and the Proceedings of the American Association for Hand Surgery.

People interested in receiving plastic, cosmetic and reconstructive surgery at Patients Medical with Dr. Paul A. Dreschnack can inquire directly with Patients Medical for rates, a complete list of services and fees. Those interested in participating in the Stem Cell Therapy Clinical Trial may apply online at http://www.patientsmedical.com/stem-cell-therapy/registration-form.aspx

About Patients Medical

Patients Medical (http://www.patientsmedical.com) is a unique integrative medicine center in Manhattan that combines the best of traditional and holistic medicine with modern technology to provide comprehensive care. Established in 1974, the center employs a multi-specialty staff using leading-edge treatment protocols such as Stem Cell Therapy, Ultraviolet Blood Irradiation, Nutrient IV Therapy, Hyperbaric Oxygen Therapy and more. The practice specializes in diagnosing the root cause of an ailment, then healing the whole person with personalized protocols that draw upon both Eastern and Western medicine.

Megan Franzen Patients Medical 212-679-9667 111 Email Information

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Nobel Prize Nominee Plastic Surgeon Joins Patients Medical’s Stem Cell Research Team

Professors Critique Stem Cell Medical Tourism

A panel at the Harvard Law School Wednesday discussed the ethical debate over the use of embryonic stem cells in the United States, focusing on the burgeoning controversy surrounding the role of stem cell therapy in medical tourism.

Medical tourism, in which patients travel internationally to gain access to specific health care services, has become increasingly common, panelists said. They said that reasons for medical tourism range from basic hip replacement surgery to black market organ sales. As most stem cell therapies are not approved in the United States, numerous patients are going abroad to countries like China and Russia where treatment is legal.

Panelist I. Glenn Cohen, an assistant professor at the Law School, said that it was probable that a Chinese stem cell facility performs several hundred thousand of these treatments yearly. He said that numerous celebrities, including football quarterback Peyton Manning, have reportedly traveled abroad to receive stem cell treatment not approved by the FDA.

A number of facilities claim to use stem cells to cure a wide array of diseases. University of Alberta law professor Timothy Caulfield, another panelist, pointed out that a simple Google search leads potential patients to a plethora of websites which claim that diseases such as autism and cancer can be cured through stem cell therapy.

Its being offered as routine, its being offered as safe, its being offered as effective, Caulfield said, citing his own 2008 study on the subject, Of course, none of them being offered matched what the scientific literature said.

According to American history professor Jill Lepore, the hyper-acceleration of enthusiasm for stem cell therapy is reminiscent of a century ago when science journalism and government funding for science research began to blossom. Lepore pointed out how public excitement over scientific procedures has affected society in the past, popularizing cryonics research and the work of Eugene Steinach, who claimed his vasectomy operation reversed the aging process.

Panelists said that one issue with stem cell tourism is the number of health risks associated with such procedures, citing a number of instances where stem cell therapy caused serious harm.

They also noted that public discussion about stem cell therapy has been markedly positive, lending an air of legitimacy to stem cell therapy that hasnt been validated by research.

Articles criticizing stem cell tourism, on the other hand, have generally received a less favorable response. Caulfield told the audience that when he co-wrote an article in The Atlantic criticizing stem cell therapy, he was accused as being a nutball Canadian socialist bioethicist.

The panelists emphasized that more accurate information should be provided to the public regarding stem cell treatments.

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Professors Critique Stem Cell Medical Tourism

International Stem Cell Corporation Announces Significant Progress Towards Clinical Development

CARLSBAD, CA--(Marketwire - Nov 29, 2012) - International Stem Cell Corporation ( OTCQB : ISCO ) (www.internationalstemcell.com) ("ISCO" or "the Company"), a California-based biotechnology company focused on the development of therapeutic products, today announced the achievement of a critical milestone towards the clinical development of its stem cell therapy.

The Company's research and development team has created the world's first human clinical-grade stem cell lines with the ability to immune-match millions of individuals. ISCO's existing research-grade parthenogenetic stem cell lines, one of which contains the most common immune type in the Caucasian population and may be an immune-match to approximately 70 million people, are used in pre-clinical development. These new clinical-grade stem cell lines position ISCO to be able to conduct clinical trials in the United States.

Dr. Semechkin, CEO and Co-Chairman of the Board, comments, "We've been working diligently for three years to perfect this technology, which was first developed by our scientific founder, Dr. Elena Revazova in Moscow, and I'm excited to report that we have been able to derive new stem cell lines in the United States under the US and California regulatory frameworks. I'm optimistic that the new parthenogenetic stem cell lines, by providing a potentially unlimited supply of cells and tissue for transplantation, will be of great benefit to the medical community and patients world-wide."

The new stem cell lines, created using ISCO's proprietary technology, are the first of a new generation of clinical-grade human parthenogenetic stem cell (hpSC) lines created in the United States under US regulatory oversight and designed to meet FDA regulations. The US Food and Drug Administration developed Good Tissue Practice (GTP) and Good Manufacturing Practice (GMP) standards to ensure the safety of products developed for clinical use. Conforming to GMP is extremely important as it means that the cells can be used in clinical development programs.

The new lines have been confirmed by independent third-party testing to be "homozygous" in the HLA coding regions meaning that they have a simple genetic profile in the critical areas of the DNA that code for immune rejection. This feature is one of the most important differences of hpSC when compared with embryonic stem cells and a distinct clinical advantage because of their ability to be immune-matched to the patient. We expect the new lines to immune-match millions of individuals, and will be added to ISCO's existing bank providing a platform from which to develop cells and tissue for clinical use.

"The importance of this breakthrough cannot be overstated," commented Dr. Craw, Executive Vice President of ISCO. "Expanding our collection is not only important for our therapeutic programs, but also further establishes our leadership position in human stem cell technology. Achieving this critical milestone moves us along the path to make the transition into a clinical stage company."

About International Stem Cell Corporation

International Stem Cell Corporation is focused on the therapeutic applications of human parthenogenetic stem cells (hpSCs) and the development and commercialization of cell-based research and cosmetic products. ISCO's core technology, parthenogenesis, results in the creation of pluripotent human stem cells from unfertilized oocytes (eggs) hence avoiding ethical issues associated with the use or destruction of viable human embryos. ISCO scientists have created the first parthenogenetic, homozygous stem cell line that can be a source of therapeutic cells for hundreds of millions of individuals of differing genders, ages and racial background with minimal immune rejection after transplantation. hpSCs offer the potential to create the first true stem cell bank, UniStemCell. ISCO also produces and markets specialized cells and growth media for therapeutic research worldwide through its subsidiary Lifeline Cell Technology (www.lifelinecelltech.com), and stem cell-based skin care products through its subsidiary Lifeline Skin Care (www.lifelineskincare.com). More information is available at http://www.internationalstemcell.com.

To receive ongoing corporate communications via email, visit: http://www.b2i.us/irpass.asp?BzID=1468&to=ea&s=0

To like our Facebook page or follow us on Twitter for company updates and industry related news, visit: http://www.facebook.com/InternationalStemCellCorporation and http://www.twitter.com/intlstemcell

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International Stem Cell Corporation Announces Significant Progress Towards Clinical Development

Stemlogix Reports Idaho Veterinarians Perform First in U.S. Combination Regenerative Medicine Treatment on Injured Horse

Procedure Combines Point-of-Care Stem Cell Therapy and Enriched Mesenchymal Stem Cell Injection

NAMPA, ID--(Marketwire - Nov 29, 2012) - Veterinarians from Idaho Equine Hospital, including Dr. William Maupin and Dr. Stuart Shoemaker, performed the first-ever combination regenerative medicine treatment on a six-year-old Quarter Reined Cow horse that suffered a significant injury to its distal straight sesamoidean ligament.

This injury can be challenging for veterinarians to successfully treat and return the horse to athletic competition.

The veterinary team and the scientific team at Stemlogix, LLC determined that the best treatment protocol would be to treat him with point-of-care stem cell therapy using the Stemlogix In-Clinic Regenerative Medicine System and then perform a follow up treatment a few weeks later using culture expanded mesenchymal stem cells. He received a dose of the point-of-care stem cell therapy three weeks ago and three weeks later received an injection of culture expanded mesenchymal stem cells.

Stemlogix, LLC pioneered the landmark stem cell therapy treatment regimen and this is the first time this combination stem cell therapy treatment has ever been performed on a horse. The team that treated the horse believes this revolutionary treatment protocol will give him the best chance for an improved quality of life and provides the best opportunity for restoring the injured tissue back to its normal structure instead of healing with scar tissue.

"Due to the severity of the injury and the poor circulation present in the sesamoidean ligament we elected to perform a two-step therapeutic approach," said Dr. Maupin. "We first injected adipose derived stem cell therapy produced patient-side to initiate an environment of healing.

"In addition, we injected culture expanded mesenchymal stem cells. This secondary expanded and enriched mesenchymal stem cell therapy treatment may further restore normal tissue structure or actual ligament tissue."

To provide him with this groundbreaking treatment, two small fat samples were taken from the base of his tail via a minimally invasive lipoaspirate procedure. Fat tissue is the richest source of stem cells for both human patients and animal patients. One of the tissue samples was processed on-site to provide a same-day, point-of-care stem cell treatment while the other tissue sample was sent to the Stemlogix state-of-the-art cGMP laboratory where the mesenchymal stem cells were isolated and expanded for three weeks. A portion of his stem cells were also cryopreserved for future use.

The Stemlogix In-Clinic Regenerative Medicine System rapidly produces a composition of stem cells at the point-of-care containing an abundance of mesenchymal stem cells, endothelial progenitor cells, among other cell types. This assortment of stem cells provides additional growth factors and therapeutic proteins to stimulate healing. This system offers veterinarians an optimal treatment tool that is convenient and effective in treating debilitating equine diseases and injuries.

On the other hand, the culture expanded stem cell therapy contains a high number of purified mesenchymal stem cells which makes this therapy better suited for treating specific indications such as orthopedic injuries, autoimmune diseases and other degenerative diseases. Mesenchymal stem cells are multi-potent or have the ability to form into a variety of new tissues such as bone, cartilage, ligaments, and tendons.

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Stemlogix Reports Idaho Veterinarians Perform First in U.S. Combination Regenerative Medicine Treatment on Injured Horse

Stem Cell 101: Mayo Clinic Expert Answers Commonly Asked Questions

Released: 11/28/2012 3:45 PM EST Source: Mayo Clinic Expert Available

Newswise ROCHESTER, Minn. -- Next week, more than 1,200 people from 25 countries are expected to attend the 8th Annual World Stem Cell Summit in West Palm Beach, Fla., a gathering co-sponsored by Mayo Clinic. As those close to the science explore potential stem cell applications, many patients have questions about what stem cells are and how they are being used. Timothy Nelson, M.D., Ph.D., director of Mayo Clinics Regenerative Medicine Consult Service, answers some of the most commonly asked questions about stem cells:

MULTIMEDIA ALERT: Multimedia resources, including a Medical Edge package, are available for journalists to download on the Mayo Clinic News Network.

What are stem cells? Stem cells are the bodys raw materials. These cells have the ability to renew themselves or change to become specialized cells with a more specific function, such as blood cells, brain cells, heart muscle or bone.

Where do stem cells come from? Adult stem cells are found in tissues of the body, such as bone marrow. Emerging evidence suggests that adult stem cells may be more versatile than previously thought and have the ability to create other types of cells. Amniotic fluid stem cells come from the liquid that surrounds a developing fetus in the amniotic sac. More study of amniotic fluid stem cells is needed to understand their potential. Embryonic stem cells are a general stem cell found in embryos. Use of this type of stem cell has significantly declined due to the discovery of induced pluripotent stem cells. Induced pluripotent stem cells, commonly known as iPS cells, are derived from an adult stem cell that behaves like an embryonic stem cell. This new technique may help researchers avoid the controversy that comes with embryonic stem cells and prevent immune system rejection of the new stem cells. Mesenchymal stem cells are adult stem cells found in tissues such as bone marrow, blood and the fallopian tube. They can become bone, cartilage, fat and possibly other cells.

How are stem cells being used to treat diseases? Stem cell transplants, also known as bone marrow transplants, have been performed in the United States since the late 1960s. These transplants use adult stem cells.

Thanks to new technology, researchers are exploring the use of stem cells to treat a range of conditions. For example, teams at Mayo Clinic are investigating the use of adult stem cells to delay or eliminate the need for some hip replacements.

Adult stem cells are being tested to treat degenerative diseases such as heart failure. Stem cells from umbilical cord blood have been successfully used in clinical trials to treat cancer and blood-related diseases.

What does the future hold for stem cell therapy? The use of adult stem cells continues to be refined and improved. Researchers are discovering that these cells may be more versatile than originally thought, which means they may be able to treat a wider variety of diseases, such as diabetes; heart, liver and lung diseases; neurological and bone disorders; hand, face and other injuries; and congenital anomalies.

Dr. Nelson and other Mayo Clinic experts are available to discuss current research and the development of new stem cell therapies.

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Stem Cell 101: Mayo Clinic Expert Answers Commonly Asked Questions

Nose Offers Safe, Effective Pathway for Delivering Stem Cell Therapy to Brain Tumors

A group of researchers has found a safe, simple and effective way to deliver stem cells to treat brain tumors literally, through the nose. The results are published in the December issue of STEM CELLS Translational Medicine.

Durham, NC (PRWEB) November 27, 2012

Treatment options for gliomas, the most common type of primary brain tumors, are very limited due to their diffuse invasive nature and their ability to evade conventional chemotherapy and radiation treatments. Stem cells have shown great promise as a therapy, but how best to deliver them to the tumor site has proven a challenge.

The most frequently used method, surgical implantation, has a low survival rate for the stem cells plus the procedure itself can lead to complications such as inflammation. Injecting the cells into the blood stream is another way, but it carries an increased risk of the cells accumulating in peripheral organs, which could cause side effects and also means that not enough of the stem cells are getting to the targeted tumor.

We investigated the feasibility of intranasal administration of neural stem/progenitor cells [NSPC] as an alternative, said principal investigator Nils Ole Schmidt, M.D., of the University Medical Center Hamburg-Eppendorf, Hamburg, Germany. He and UMCHE colleague Matthias Reitz, M.D., oversaw the study, which also involved researchers from the University of British Columbia Hospital in Vancouver, Canada, and Chung-Ang University College of Medicine in Seoul, Korea.

The scientists tested their idea on three different glioma cell lines in mice. The results showed that not only did the stem cells make it to the targeted tumor, but that they did it quickly and without settling in any peripheral areas. Six hours after initial delivery, the stem cells had enriched within the tumor area. Twenty-four hours later, the number of cells in the tumor had increased even further with up to 24 percent of stem cells that had been applied as nose drops.

The study also revealed two major migration routes the olfactory nerve pathways and the tiny blood vessels that make up the bodys microvasculature system and a potential signal that attracted the cells to the malignant tumor. It is likely that guidance signals such as chemotactic factors released by the tumor itself and the adjacent reactive brain parenchyma drew in the stem cells, Dr. Reitz said.

Our study provides proof-of-concept that the non-invasive intranasal passage of NSPC is a highly attractive and efficient alternative method of cell administration for stem cell-based therapies in brain tumors. This offers the possibility of multiple treatments, potentially with different therapeutic payloads during the disease course, Dr. Schmidt added.

The study addresses an important aspect of any stem cell treatment identification of a safe and effective delivery method as the treatment advances toward clinical trials, said Dr. Anthony Atala, Editor of STEM CELLS Translational Medicine and director of the Wake Forest Institute for Regenerative Medicine. These results point to the potential of intranasal delivery as a convenient and non-invasive option for delivery.

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Nose Offers Safe, Effective Pathway for Delivering Stem Cell Therapy to Brain Tumors

Fate Therapeutics Initiates Phase 2 Clinical Study of ProHema for the Treatment of Hematologic Malignancies

SAN DIEGO, Nov. 27, 2012 /PRNewswire/ -- Fate Therapeutics, Inc., a biopharmaceutical company engaged in the discovery and development of adult stem cell modulators, announced today the initiation of a randomized, controlled, Phase 2 multi-center study of its investigational hematopoietic stem cell therapy, ProHema, in adult patients undergoing double umbilical cord blood transplantation (dUCBT) for hematologic malignancy. The advancement of ProHema into later-stage development builds upon positive results from a Phase 1b single-center study, interactions with the U.S. Food and Drug Administration and refinements to the product manufacturing process. The previously completed Phase 1b study achieved its primary objective of demonstrating safety and tolerability. The study also established early clinical proof-of-concept trends of accelerated neutrophil recovery, improved 100-day survival and low rates of graft-versus-host disease were evident, and durable and preferential reconstitution with ProHema occurred in 10 of 12 evaluable patients. ProHema is produced through a proprietary, two-hour, ex vivo modulation process, which has been shown to significantly activate key biological pathways involved in hematopoietic stem cell homing, proliferation and survival in preclinical models.

"Allogeneic umbilical cord blood transplantation holds great promise as a potentially curative treatment for children and adults with hematologic malignancies and many other life-threatening, non-malignant disorders," said Christian Weyer, M.D., M.A.S., President and Chief Executive Officer of Fate Therapeutics. "ProHema is being developed with the intent to improve outcomes in patients undergoing cord blood transplantation by facilitating both accelerated engraftment and durable reconstitution using a simple, point-of-care, ex vivo modulation process. The initiation of Phase 2 marks an important milestone for the company and brings us one step closer towards achieving this objective."

The Phase 2 study is expected to enroll at least 45 adult patients undergoing dUCBT for the treatment of hematologic malignancies. Patients will be randomized, with a ratio of 2:1, to receive either ProHema plus an unmanipulated cord blood unit or two unmanipulated cord blood units. The study will evaluate time to neutrophil and platelet recovery, incidence of serious infections and graft-versus-host disease, 100-day mortality and relative dominance of ProHema over the unmanipulated cord in contributing to reconstitution. Results are expected in 2013.

"The preclinical and clinical data obtained to date suggest that ProHema may address several of the unmet medical needs in the evolving field of hematopoietic stem cell transplantation," said Steven Devine, M.D., Professor of Medicine and Program Director of the Blood and Marrow Transplant Program at the Ohio State University and a principal investigator of the Phase 2 clinical study. "While further investigation is required, an intervention that enables early and durable reconstitution of the best-HLA-matched cord blood unit has the potential to improve patient outcomes and substantially enhance the therapeutic value proposition of cord blood transplant."

About ProHema

ProHema is an innovative cord blood-derived cell therapy containing pharmacologically-modulated hematopoietic stem cells (HSCs). ProHema is produced through a proprietary, two-hour, ex vivo cell modulation process that results in rapid activation of key biological pathways involved in homing, proliferation and survival of HSCs. In preclinical testing, ProHema has demonstrated the potential to accelerate engraftment and to drive durable hematopoietic reconstitution, without the need for multi-week expansion protocols. In an initial Phase 1b study in adult patients with hematologic malignancies undergoing double umbilical cord blood transplant (dUCBT), the median time to neutrophil recovery (> 500 cells/microliter) with ProHema was 17.5 days, which compares favorably to historical norms for patients undergoing dUCBT. In that study, ProHema provided the dominant source of hematopoiesis in 10 of 12 evaluable subjects, suggesting that treatment with ProHema may accelerate engraftment and drive durable and preferential reconstitution.

About Fate Therapeutics, Inc.

Fate Therapeutics is a biopharmaceutical company engaged in the discovery and development of adult stem cell modulators. The Company's first clinical program, ProHema, is an innovative cord blood-derived cell therapy containing ex vivo pharmacologically-modulated hematopoietic stem cells and is being developed to improve hematopoietic reconstitution in patients undergoing stem cell transplant. In addition, Fate Therapeutics has preclinical programs of novel in vivo stem cell modulators for skeletal muscle regeneration and hearing restoration. To advance its discovery and development efforts, the Company applies its award-winning, proprietary, induced pluripotent stem cell technology to generate rare cell populations and model disease. Fate Therapeutics is headquartered in San Diego, CA, with a subsidiary in Ottawa, Canada. For more information, please visit http://www.fatetherapeutics.com.

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Fate Therapeutics Initiates Phase 2 Clinical Study of ProHema for the Treatment of Hematologic Malignancies

Dramatic Rise in Stem Cell Therapy Use in 2012

PHILADELPHIA, Nov. 26, 2012 /PRNewswire/ --RRY Publications LLC today announced that the use of stem cell therapies in 2012 significantly exceeded forecasts which were originally presented at the February 2012 New York Stem Cell Summit. Said Robin Young, stem cell industry analyst and host of the New York meeting: "The range and scope of stem cell therapeutic use in the United States grew much faster than we'd forecasted earlier this year. Virtually all of the increases we're seeing are for adult stem cell therapies and, in particular, the use by physicians of both allograft and autologous stem cell products. It would not be an exaggeration to call this unexpected and remarkable growth."

Mr. Young's revised forecast of stem cell commercialization revenues for 2013-2020 will be presented at the February meeting in New York.

The companies, scientists and physicians that are at the forefront of this remarkable increase in stem cell therapeutic use will be presenting at the 8th Annual New York Stem Cell Summit. Listed below is the preliminary lineup of presenters for the 8th Annual Stem Cell Summit.

The Stem Cell Summit, an intensive one-day event, allows attendees to learn about the latest developments in the stem cell marketplace, evaluate the groundbreaking stem cell products physicians are using today, and discover the growing market potential in terms of revenues. For 2013, the Summit will feature 30+ presenters, a research review and debate session, and a special track on expanding the range of stem cell therapies.

The 8th Annual Stem Cell Summit will take place on Feb. 19, 2013, at Bridgewaters in the heart of New York City's historic South Street Seaport. The preliminary roster of companies featured will include representatives from 2012 presenters and new 2013 presenters.

Aastrom Biosciences, Inc.

Advanced Cell Technology

Aldagen, Inc.

AllCells, LLC.

Aruna Biomedical, Inc.

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Dramatic Rise in Stem Cell Therapy Use in 2012

Deftones’ Chi Cheng’s family consider stem cell therapy to aid recovery

November 25, 2012 12:54

Former bassist is said to be still in a "partially conscious state" four years on from car accident

Photo: Tom Oxley/NME

Former Deftones bassist Chi Cheng's family are considering stem cell therapy to aid his recovery from a car accident which put him in a coma in 2008.

Cheng is said to be in a "partially conscious state" and is unable to speak, although he can move his legs on command. The bassist has been in and out of hospitals over the past four years and only got home to recover in June this year.

Now, according to Revolver Magazine, the family is considering alternative therapy in order to speed up Cheng's recovery, as they say the last few months have been a struggle for him.

His brother, Ming Cheng, said: "Once his health gets a little better, we'll start looking into other options... but they don't even do it [stem cell therapy] in the US yet.

"It's a miracle he's still with us," he added. "He's alive and kicking and he's fighting, and I think there's a reason for it. I'm hoping there's a light at the end of the tunnel for Chi."

Deftones released their new album 'Koi No Yokan' on November 12. You can stream the new record, which features 'Entomb (Dazzle)', 'Swerve City', 'Graphic Nature', 'Goon Squad' and 'Leathers', below.

The band tour the UK in 2013. They will play five dates, kicking off at Glasgow's Barrowland on February 15, before heading to Nottingham, Manchester, Birmingham and finishing at London's 02 Brixton Academy (20).

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Deftones' Chi Cheng's family consider stem cell therapy to aid recovery

Stem Cell Therapy For Alzheimer’s Disease | Stem Cell Malaysia – Video


Stem Cell Therapy For Alzheimer #39;s Disease | Stem Cell Malaysia
stemcellmalaysia.com Stem cell therapy for Alzheimer #39;s Disease is currently in research and soon there may be a cure using stem cells treatment. Stem cell therapy through non-medical channel using a legal and licensed oral placenta product has produced amazing effects on an 81 years old, stage 7 Alzheimer #39;s sufferer. The effects were shockingly effective beyond words. For more information on stem cell therapy, please visit Stem Cell Malaysia at stemcellmalaysia.comFrom:stemcells2012Views:487 62ratingsTime:21:27More inScience Technology

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Stem Cell Therapy For Alzheimer's Disease | Stem Cell Malaysia - Video

Stem Cell Therapy Overview | Stem Cells Treatment | Stem Cell Malaysia – Video


Stem Cell Therapy Overview | Stem Cells Treatment | Stem Cell Malaysia
stemcellmalaysia.com Stem cell therapy is getting a lot of attention in the news and media these days. This video gives an overview of what stem cell therapy is all about. The content will help people without the scientific background to understand the important elements of stem cell therapy. For more information on stem cell therapy, please visit Stem Cell Malaysia at stemcellmalaysia.comFrom:stemcells2012Views:5 1ratingsTime:20:17More inScience Technology

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Stem Cell Therapy Overview | Stem Cells Treatment | Stem Cell Malaysia - Video

Introduction To Stem Cell Therapy For Parkinson’s And Alzheimer’s Diseases | Stem Cell Malaysia – Video


Introduction To Stem Cell Therapy For Parkinson #39;s And Alzheimer #39;s Diseases | Stem Cell Malaysia
stemcellmalaysia.com Stem cell therapy projects so much potential and hope for patients of different illnesses. This is due to the unique characteristics of stem cells. For more information on stem cell therapy, please visit Stem Cell Malaysia at stemcellmalaysia.comFrom:stemcells2012Views:17 1ratingsTime:03:51More inPeople Blogs

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Introduction To Stem Cell Therapy For Parkinson's And Alzheimer's Diseases | Stem Cell Malaysia - Video

Introducing Stem Cell Therapy Using Oral Placenta Stem Cells | Stem Cell Malaysia – Video


Introducing Stem Cell Therapy Using Oral Placenta Stem Cells | Stem Cell Malaysia
stemcellmalaysia.com Stem cell therapy can take on various forms and choices. Due to the advent of technology, stem cell therapy using oral placenta stem cells is now available. For more information on stem cell therapy, please visit Stem Cell Malaysia at stemcellmalaysia.comFrom:stemcells2012Views:3 1ratingsTime:05:23More inScience Technology

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Introducing Stem Cell Therapy Using Oral Placenta Stem Cells | Stem Cell Malaysia - Video

Official Presentation of Live Cell Therapy Using Purtier Placenta | Stem Cell Malaysia – Video


Official Presentation of Live Cell Therapy Using Purtier Placenta | Stem Cell Malaysia
stemcellmalaysia.com Live cell therapy is a very effective stem cell therapy for improving health and even disease treatment other than for beauty and anti-aging. Purtier Placenta is a live cell therapy using deer placenta stem cells from New Zealand. Watch this official presentation for a complete understanding of live cell therapy with Purtier Placenta. For more information on stem cell therapy, please visit Stem Cell Malaysia at stemcellmalaysia.comFrom:stemcells2012Views:9 0ratingsTime:08:59More inScience Technology

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Official Presentation of Live Cell Therapy Using Purtier Placenta | Stem Cell Malaysia - Video

Whatever happened to? Bonita stem cell doctor's case moves to decision stage

Photo by Allie Garza

Zannos Grekos

Editor's note: The Daily News takes an occasional look back at people and issues that have been in the local news, though not lately. Have an idea? Post it below this story at naplesnews.com or call (239) 435-3457 and leave a brief message.

NAPLES There's been more legal wrangling since a state hearing last month to address Dr. Zannos Grekos' stem cell practice and if he committed medical malpractice or not.

A few issues were left unresolved after the four-day hearing that was held in Naples, including whether videotaped testimony of a state Department of Health witness would be admitted for the administrative law judge to consider.

Grekos' attorney, Richard Ozelie, of Boca Raton, sought to have the testimony of the witness stricken based on issues of how he arrived at his medical opinion in the case and related matters. The witness is Dr. Thomas Freeman, a professor of neurosurgery, molecular pharmacology and physiology with the University of South Florida's College of Medicine in Tampa.

In a Nov. 15 order, Administrative Law Judge J. Lawrence Johnston ruled that the witness' testimony would be allowed.

State health regulators last year restricted Grekos' license and forbid him to do anything with stem cells after a 69-year-old patient, Domenica Fitzgerald, died in 2010 shortly after undergoing a stem cell therapy in his practice in Bonita Springs.

Grekos had extracted bone marrow from her and infused her unfiltered bone marrow into her circulatory system in hopes of alleviating nerve damage in her feet, which was limiting her mobility. The nerve damage was a side effect from chemotherapy for breast cancer treatment several years earlier. After the stem cell procedure, she suffered brain damage and was hospitalized. She later was taken off life support.

In February, the state fully suspended Grekos' license after he and another physician, Dr. Konstantine Yankopolus, performed a similar stem cell therapy on a 77-year-old man, Richard Poling, who went into cardiac arrest in Grekos' practice and later died at a local hospital. A joint administrative hearing for both doctors will be held in that case, tentatively in February, but a motion is pending for a continuation.

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Whatever happened to? Bonita stem cell doctor's case moves to decision stage

Deftones Bassist Still Struggling Four Years After Car Crash

The family of tragic Deftones rocker Chi Cheng are considering controversial stem cell therapy to speed up the bass player's recovery from a 2008 car accident, which left him in a coma.

The star's brother admits recent months have been challenging for the family as Cheng has been in and out of hospital in New Jersey and in his native California, but now he is back at home making slow progress.

Ming Cheng tells rock publication Revolver that his younger brother can now lift his legs but he still can't communicate or move other parts of his body. However, there is still hope.

He says, "Once his health gets a little better, we'll start looking into other options... but they don't even do it (stem cell therapy) in the U.S. yet.

"It's a miracle he's still with us. He's alive and kicking and he's fighting, and I think there's a reason for it. I'm hoping there's a light at the end of the tunnel for Chi."

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Deftones Bassist Still Struggling Four Years After Car Crash

The year (so far) in stem cells

Stem cell research took a few surprising twists during 2012, and California's $3 billion stem cell program completed its last building to support stem cell research.

Here are some of the highlights for this year.

-- People are composed of a genetic mosaic of cells, which slightly differ from each other.

-- The 12th and last stem cell facility funded by the California Institute for Regenerative Medicine, in Santa Barbara, has opened.

-- Geron's embryonic stem cell therapy for spinal cord damage, dropped in the middle of clinical trials, has been picked up by another biotech company, StemCells Inc.

You can find out much more about each finding from the three stem cell blogs I got them from. They are:

-- Knoepfler Lab Stem Cell Blog, run by prolific blogger and stem cell scientist Paul Knoepfler

-- California Stem Cell Report, by veteran journalist David Jensen

-- CIRM's official blog.

But if you would rather read the gist of these findings here, read on. Plus, you'll get a video of one of the top scientists in the field giving his vision of where stem cell science should go.

Original post:

The year (so far) in stem cells

Two Delhi centres ready to try stem cell therapy on paraplegics

Ahead of a planned five-centre nationwide trial, the Indian Council of Medical Research (ICMR) has approved a special project at the AIIMS Trauma Centre in New Delhi where stem cell therapy will be conducted on complete paraplegics and quadriplegics to try and revive limb function.

A similar trial will be conducted at the Indian Spinal Injuries Centre (ISIC) in Vasant Kunj, south-west Delhi where 21 patients have already been registered. This project too has been approved by the ICMR.

Senior ICMR scientists from the apex committee to monitor stem cell research said the five-centre trial will be coordinated from ISIC and is in the final stages of approval.

This will be the first national ICMR trial of autologous bone marrow stem cell transplant on complete quadriplegics and paraplegics. We are finalising the number of patients. The ISIC will be the coordinating centre. The next meeting has been scheduled for December 4, a senior scientist said.

An autologous stem cell transplantation is a procedure in which stem cells are removed, stored and returned to the same person.

For its project, the AIIMS Trauma Centre has registered eight patients. They will be injected with stem cells from their own bone marrow to see if the damaged neurological function can be regenerated. Doctors have cautioned that earlier trials on incomplete quadriplegics and paraplegics have not suggested significant clinical improvement.

Dr Deepak Aggarwal, associate professor of neurosurgery at the AIIMS Trauma Centre who is coordinating the study, said: We have necessary clearances from our internal ethics committee and the national apex committee for stem cell research and therapy which has members from the ICMR and Department of Biotechnology.

... contd.

Read more here:

Two Delhi centres ready to try stem cell therapy on paraplegics