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Joint Hypermobility Handbook- A Guide for the Issues & Management of Ehlers-Danlos Syndrome Hypermobility Type and the Hypermobility Syndrome Paperback – 12 July 2010
| Brad T Tinkle (Author) See search results for this author |
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Enhance your purchase
- ISBN-10098257715X
- ISBN-13978-0982577158
- Edition1st
- PublisherLeft Paw Press, LLC
- Publication date12 July 2010
- LanguageEnglish
- Dimensions15.24 x 1.5 x 22.86 cm
- Print length260 pages
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Product details
- Publisher : Left Paw Press, LLC; 1st edition (12 July 2010)
- Language : English
- Paperback : 260 pages
- ISBN-10 : 098257715X
- ISBN-13 : 978-0982577158
- Dimensions : 15.24 x 1.5 x 22.86 cm
- Best Sellers Rank: 630,537 in Books (See Top 100 in Books)
- 118 in Orthopaedic & Fractures
- 175 in Medical Genetics
- 220 in Orthopedic Surgery
- Customer reviews:
About the author

Brad T Tinkle, M.D., Ph.D., is a clinical geneticist at Peyton Manning Children’s Hospital in Indianapolis, Indiana. Most recently, he was the Medical Director of Clinical Genetics at Advocate Children’s Hospital in Chicagoland. His clinics included Ehlers-Danlos (for adults, children, and families) and pediatric Down’s Syndrome.
Prior to Advocate, Dr. Tinkle was a clinical and clinical molecular geneticist at Cincinnati Children’s Hospital Medical Center (CCHMC). He specializes in caring for individuals with heritable connective tissue disorders such as Ehlers-Danlos syndromes, Marfan syndrome, osteogenesis imperfecta, and achondroplasia among the many. He served as director of the Skeletal Dysplasia Center (CCHMC), co-director of the Marfan/Ehlers-Danlos Syndrome Clinic, as well as director of the Connective Tissue Clinic.
In addition, he served as associate director in the Clinical Molecular Genetics Laboratory at CCHMC. He earned a bachelor’s in science for engineering (BSE) in genetic engineering from Purdue University in 1989. He received his Ph.D. in Human Genetics from the George Washington University in the District of Columbia in 1995.
He attended medical school at Indiana University and completed a pediatric/clinical genetics residency at CCHMC. He also finished a fellowship in clinical molecular genetics at CCHMC following residency.
He formerly served on the Board of Directors and on the Professional Advisory Network of the Ehlers-Danlos National Foundation.
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I was initially worried that this would be a tedious read, but the format turned out to be very easy to get through in just a few hours. The language is accessible without being condescending, and the entire book is thoroughly referenced at the end of each section.
A really great source for anyone with EDS/hypermobility!
One thing to point out: the book is American so some things that are written about benefits and entitlement to funding etc do not apply to us in the UK






