Eds
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Molecular Genetics And Pathogenesis Of Ehlers Danlos Syndrome And Related Connective Tissue Disorders
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Author : Marina Colombi
language : en
Publisher: MDPI
Release Date : 2020-12-14
Molecular Genetics And Pathogenesis Of Ehlers Danlos Syndrome And Related Connective Tissue Disorders written by Marina Colombi and has been published by MDPI this book supported file pdf, txt, epub, kindle and other format this book has been release on 2020-12-14 with Science categories.
Ehlers–Danlos syndromes (EDS) are a group of heritable connective tissue disorders (HCTDs) characterized by a variable degree of skin hyperextensibility, joint hypermobility and tissue fragility. The current EDS classification distinguishes 13 subtypes and 19 different causal genes mainly involved in collagen and extracellular matrix synthesis and maintenance. EDS need to be differentiated from other HCTDs with a variable clinical overlap, including Marfan syndrome and related disorders, some types of skeletal dysplasia and cutis laxa. The clinical recognition of EDS is not always straightforward, and, for a definite diagnosis, molecular testing can be of great assistance, especially in patients with an uncertain phenotype. Currently, the major challenging task in EDS is to unravel the molecular basis of the hypermobile EDS that is the most frequent form, and for which the diagnosis is only clinical in the absence of any definite laboratory test. This EDS subtype, as well as other EDS-reminiscent phenotypes, are currently investigated worldwide to unravel the primary genetic defect and related pathomechanisms. The research articles, case report, and reviews published in the Special Issue entitled “Molecular Genetics and Pathogenesis of Ehlers–Danlos Syndrome and Related Connective Tissue Disorders” focus on different clinical, genetic and molecular aspects of several EDS subtypes and some related disorders, offering novel findings and future research and nosological perspectives.
Our Stories Of Strength
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Author : Kendra Neilsen Myles
language : en
Publisher:
Release Date : 2015-05-05
Our Stories Of Strength written by Kendra Neilsen Myles and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 2015-05-05 with categories.
This listing is for the 6x9 black and white paperback version of the book. An inspirational collection of stories, filled with devastation, heartbreak, triumph, and strength as written by those affected by different types of Ehlers-Danlos syndrome."These are stories of hope and resilience, of strength under adversity, of self-reliance and new-found sources of support. They offer one core message to all who suffer from the diverse and difficult manifestations of EDS: You are not alone." - Dr. Clair Francomano, MD"Ehlers-Danlos Syndrome is another form of the human body. Just as there are tall people, short people, dark skin colored people, and light skin colored people, each with their own set of medical issues - similarly there are hypermobile people and not so hypermobile individuals who have different medical issues. Our understanding of EDS has improved, but we still have a lot of work to do. While the medical world works on understanding Ehlers-Danlos Syndrome, people with EDS have provided us with stories of courage and ingenuity. These stories give others and doctors the strength to find solutions." - PRADEEP CHOPRA, MD"As a physical therapist who works with many patients suffering from EDS, I've seen firsthand how isolating and frustrating EDS can be. Along with a more knowledgeable medical field, what these patients need most is an understanding that they are not alone and to be given hope. 'Our Stories of Strength' provides both community and hope and will be just as effective as any medication or exercise." - - CHRISTOPHER GNIP, PT, DPTEDS is a group of heritable connective tissue disorders that can cause a wide variety of symptoms throughout different body systems; each unique in presentation to the individual. The variety of symptoms and presentations proves challenging to the medical community in diagnosing and treating patients; many of whom are misdiagnosed and suffer as a result. EDS has been commonly viewed as just Benign Joint Hypermobility Syndrome (BJHS/JHS) or Hypermobility Syndrome (HMS). Based on recent research, the prevalence of EDS exceeds current estimates.Kendra Neilsen Myles founded Sisters Media, LLC with core values of giving back and providing an outlet to those willing to share their stories through submissions in the Our Stories of Strength(tm) anthology series. Sisters Media recognizes that it is through opening doors to needed conversations and sharing stories of strength, determination, and perseverance that we can facilitate positive changes in the way we live and help shape perceptions of those around us, as well as in the medical community. We are #Stronger2Gether.
Eds Survival Guide
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Author : Sonya Zappone
language : en
Publisher:
Release Date : 2021-11-04
Eds Survival Guide written by Sonya Zappone and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 2021-11-04 with categories.
Do you have Ehlers-Danlos Syndrome (EDS)? Do you need an emotional survival guide? Feeling stuck with a debilitating condition that no one truly understands? Are you tired of merely surviving... and want to start thriving? It's one thing to survive and quite another to thrive. Perhaps you struggle daily to stay alive, while the thought of thriving seems like an impossible goal. There can be very little help available for this connective tissue disorder. Many people don't even know the name of this rare genetic condition. And even those closest to sufferers don't fully realize what it means for them. The lack of information and support available (even from medical professionals) can leave you feeling frustrated, alone, and discouraged. This EDS Survival Guide will walk you through 5 KEYS towards acceptance, peace, and taking the right action. If you have pain and problems from living with EDS, this book can offer you a place to reflect and be validated and supported. When you find yourself feeling like no one understands the amount of pain and problems you are experiencing, open this book to explore the 5 Keys of Thriving with EDS. Begin to improve your life with her suggested 7 Day Self-Love Solutions Checklists. Experience how even small changes in habits add up to better health--taking breaths and taking it. . . one day at a time. Learn to change your thinking from going through this to growing through it. Let the principles guide you to live with it and through it--as gracefully as possible. The key is to create new a definition of success. Please visit: SonyaZappone.com for more books, coaching, and free EDS resources!
A Guide To Living With Ehlers Danlos Syndrome Hypermobility Type
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Author : Isobel Knight
language : en
Publisher: Singing Dragon
Release Date : 2014-12-21
A Guide To Living With Ehlers Danlos Syndrome Hypermobility Type written by Isobel Knight and has been published by Singing Dragon this book supported file pdf, txt, epub, kindle and other format this book has been release on 2014-12-21 with Health & Fitness categories.
Covering everything from recognising symptoms and obtaining initial diagnosis to living with the condition on a daily basis, this complete guide to living with and managing Ehlers-Danlos Syndrome (Hypermobility Type - formerly known as Type III) has been revised and fully-updated in this accessible new edition. The author, who has the condition, looks at how it affects children and adolescents and explores pain management, pregnancy, physical and psychological aspects, and how it widely affects dancers and other performance artists. New material includes: changes in terminology information on how osteopathy and nutrition can help psychological approaches beyond CBT how to deal with professionals what to expect from support groups and rehabilitation programmes This new edition will be a must for anybody who suffers, or suspects they might be suffering from, Ehlers-Danlos Syndrome (Hypermobility Type) and provides everything needed to enjoy a fulfilling life with this complex condition. It will also be of interest to their families and friends, and professionals working with Hypermobility Type EDS.
Molecular Genetics And Pathogenesis Of Ehlers Danlos Syndrome And Related Connective Tissue Disorders
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Author : Marina Colombi
language : en
Publisher:
Release Date : 2020
Molecular Genetics And Pathogenesis Of Ehlers Danlos Syndrome And Related Connective Tissue Disorders written by Marina Colombi and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 2020 with categories.
Ehlers-Danlos syndromes (EDS) are a group of heritable connective tissue disorders (HCTDs) characterized by a variable degree of skin hyperextensibility, joint hypermobility and tissue fragility. The current EDS classification distinguishes 13 subtypes and 19 different causal genes mainly involved in collagen and extracellular matrix synthesis and maintenance. EDS need to be differentiated from other HCTDs with a variable clinical overlap, including Marfan syndrome and related disorders, some types of skeletal dysplasia and cutis laxa. The clinical recognition of EDS is not always straightforward, and, for a definite diagnosis, molecular testing can be of great assistance, especially in patients with an uncertain phenotype. Currently, the major challenging task in EDS is to unravel the molecular basis of the hypermobile EDS that is the most frequent form, and for which the diagnosis is only clinical in the absence of any definite laboratory test. This EDS subtype, as well as other EDS-reminiscent phenotypes, are currently investigated worldwide to unravel the primary genetic defect and related pathomechanisms. The research articles, case report, and reviews published in the Special Issue entitled “Molecular Genetics and Pathogenesis of Ehlers-Danlos Syndrome and Related Connective Tissue Disorders” focus on different clinical, genetic and molecular aspects of several EDS subtypes and some related disorders, offering novel findings and future research and nosological perspectives.
Eds Chronic Pain Journal
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Author : A. D Awareness
language : en
Publisher:
Release Date : 2020-06-07
Eds Chronic Pain Journal written by A. D Awareness and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 2020-06-07 with categories.
Are you suffering from Ehlers Danlos Syndrome? Are you looking for a tool that can help you manage the treatments you're trying? Do you want to record your daily thoughts and feelings about your illness? This EDS Chronic Pain Journal is perfect to help you get a handle on things and bring your illness to the best possible conclusion and live your healthiest life possible. This book includes: FOOD DIARY (Breakfast, Lunch, Dinner and Snacks) MONITOR PAIN LOCATION DOCTORS APPOINTMENTS SLEEP TRACKER INSPIRATIONAL QUOTES SYMPTOM TRACKERS ANXIETY, PAIN, FATIGUE AND MOOD TRACKERS DAILY ACTIVITIES MEDICATIONS & SUPPLEMENTS TAKEN HYDRATION (Water consumption) AND MORE... You can use this book to share with your doctor or specialist to help aid treatment methods or monitor any side effects you are experiencing. Your greatest wealth is health, and this diary could help you keep your health organized. TRACK IT AND TREASURE IT We at Ansart Design hope this journal is a great help and brings to clarity and quality to your life and well-being. Specifications: Cover Finish: Matte Dimensions: 6" x 9" (15.24 x 22.86 cm) Pages: 120 Please Use The Look Inside Feature To View The Interior To Ensure That It Meets Your Needs. Also Feel Free To Look At Our Other Items Available In Our Amazon Store
Eds
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Author : Jennifer Risseno
language : en
Publisher:
Release Date : 2019-06-29
Eds written by Jennifer Risseno and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 2019-06-29 with categories.
Ehlers Danlos Syndrome EDS Graphic Design. You're affected yourself by EDS or you know someone with Ehlers Danlos Syndrome? Then this EDS Ehlers Danlos notebook is just right for you! This EDS notebook 6x9 with 120 pages makes a great gift for birthday or Christmas for Ehlers Danlos Syndrome people and EDS affected family members.
Living Life To The Fullest With Ehlers Danlos Syndrome
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Author : Pt Kevin Muldowney
language : en
Publisher:
Release Date : 2015-07-17
Living Life To The Fullest With Ehlers Danlos Syndrome written by Pt Kevin Muldowney and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 2015-07-17 with Ehlers-Danlos syndrome categories.
"This book was written to teach people with Ehlers-Danlos Syndrome (EDS) how to systematically progress through an exercise program to allow their muscles to support many joint subluxations commonly associated with this genetic disorder. This will allow people living wih EDS to have less pain throughout their body."--Back cover.
Bending But Not Breaking
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Author : Mohammad Barbati
language : en
Publisher: Mohammad E. Barbati
Release Date :
Bending But Not Breaking written by Mohammad Barbati and has been published by Mohammad E. Barbati this book supported file pdf, txt, epub, kindle and other format this book has been release on with Medical categories.
Bending But Not Breaking: Living with Ehlers-Danlos Syndrome is a comprehensive guide to understanding and managing Ehlers-Danlos Syndrome (EDS) and related connective tissue disorders. Written by Dr. Mohammad E. Barbati, a consultant vascular and endovascular surgeon, this book offers professional medical insights alongside empathetic guidance for those living with these challenging conditions. The book opens with an introduction defining EDS, a group of inherited disorders affecting the connective tissues that provide structure and support throughout the body. It provides an overview of EDS symptoms such as joint hypermobility, fragile skin, and cardiovascular complications. The next section explores connective tissue disorders more broadly, distinguishing between inherited conditions like EDS and acquired disorders like lupus. Detailed chapters follow on the classification and subtypes of EDS, including the genetic basis and diagnostic criteria for categories like classical, hypermobile, vascular, and more. Symptoms and clinical features of each subtype are thoroughly explained, providing specificity to enhance diagnosis and management. Guidance is then provided on diagnosing EDS through clinical assessment, genetic testing, and using diagnostic criteria while avoiding false positives or negatives. Extensive coverage is dedicated to treatment and management strategies for EDS, including physical therapy, pain management, various surgical interventions, and psychological support. Examples include proprioceptive exercises, counseling, and procedures like spinal fusion or corneal transplantation. Emphasis is placed on a multidisciplinary approach to improve quality of life. Overall, Bending But Not Breaking serves as an excellent guidebook for understanding the complexities of living with EDS or related conditions. Dr. Barbati’s expertise combined with compassion makes this book an invaluable resource for patients, families, and healthcare professionals seeking to better comprehend and manage these disorders.
Ehlers Danlos Syndrome A Multidisciplinary Approach
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Author : J.W.G. Jacobs
language : en
Publisher: IOS Press
Release Date : 2018-08-14
Ehlers Danlos Syndrome A Multidisciplinary Approach written by J.W.G. Jacobs and has been published by IOS Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2018-08-14 with Medical categories.
Generalized hypermobility has been known since ancient times, and a clinical description of Ehlers-Danlos syndrome (EDS) is said to have first been recorded by Hippocrates in 400 BC. Hypermobility syndromes occur frequently, but the wide spectrum of possible symptoms, coupled with a relative lack of awareness and recognition, are the reason that they are frequently not recognized, or remain undiagnosed. This book is an international, multidisciplinary guide to hypermobility syndromes, and EDS in particular. It aims to create better awareness of hypermobility syndromes among health professionals, including medical specialists, and to be a guide to the management of such syndromes for patients and practitioners. It is intended for use in daily clinical practice rather than as a reference book for research or the latest developments, and has been written to be understandable for any healthcare worker or educated patient without compromise to the scientific content. The book is organized as follows: chapters on classifications and genetics are followed by chapters on individual types, organ (system) manifestations and complications, and finally ethics and therapeutic strategies, with an appendix on surgery and the precautions which should attend it. A special effort has been made to take account of the perspective of the patient; two of the editors have EDS. The book will be of interest to patients with hypermobility syndromes and their families, as well as to all those healthcare practitioners who may encounter such syndromes in the course of their work.