Search Results - "Ehlers–Danlos syndromes"

Musculocontractural Ehlers-Danlos syndrome and neurocristopathies: dermatan sulfate is required for Xenopus neural crest cells to migrate and adhere to fibronectin by Nadège Gouignard, Marco Maccarana, Ina Strate, Kristoffer von Stedingk, Anders Malmström, Edgar M. Pera

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The first case report of Kyphoscoliotic Ehlers-Danlos syndrome of chinese origin with a novel PLOD1 gene mutation by Xiaolin Ni, Chenxi Jin, Yan Jiang, Ou Wang, Mei Li, Xiaoping Xing, Weibo Xia

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New genetic mutations in a Chinese child with Ehlers-Danlos syndrome-like spondyloepimetaphyseal dysplasia: A case report by Shu Han, Xuan Xu, Jie Wen, Jianzhou Wang, Sheng Xiao, Li Pan, Jiang Wang

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Exploring Comorbidities in Adolescent and Young Adults with Hypermobile Ehlers-Danlos Syndrome with and without a Surgical History: A Preliminary Investigation by Haley Gagnon, Claire E. Lunde, Ziyan Wu, Eduardo N. Novais, David Borsook, Christine B. Sieberg

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Síndrome de Ehlers-Danlos e gravidez: relato de caso Ehlers-Danlos syndrome and pregnancy: a case report by Marcelo Luís Nomura, Fernanda Garanhani de Castro Surita, Mary Angela Parpinelli

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Clinician-associated traumatization from difficult medical encounters: Results from a qualitative interview study on the Ehlers-Danlos Syndromes by Colin M.E. Halverson, Heather L. Penwell, Clair A. Francomano

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Using social media listening to understand barriers to genomic medicine for those living with Ehlers-Danlos syndromes and hypermobility spectrum disorders by Erika Kline, Amanda Leigh Garrett, Catherine Brownstein, Sonja Ziniel, Erica Payton, Aleah Goldin, Kathleen Hoffman, Judy Chandler, Shani Weber

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Fetal Fractures in an Infant with Maternal Ehlers-Danlos Syndrome, CCDC134 Pathogenic Mutation and a Negative Genetic Test for Osteogenesis Imperfecta by Michael F. Holick, Arash Shirvani, Nipith Charoenngam

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Case Report: Identification and Functional Analysis of a Homozygous Synonymous Variant in the PLOD1 Gene in a Chinese Neonatal With the Ehlers-Danlos Syndrome by Xiaodan Yan, Xiaodan Yan, Jianbo Shu, Jianbo Shu, Yanyan Nie, Ying Zhang, Ying Zhang, Ping Wang, Ping Wang, Weiwei Zhou, Weiwei Zhou, Xiaoyu Cui, Xiaoyu Cui, Yang Liu

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Classical Ehlers-Danlos syndrome: clinical, Histological and ultrastructural aspects Síndrome de Ehlers-Danlos clássica: aspectos clínicos, histológicos e ultraestruturais by Eduardo de Barros Coelho Bicca, Fabiano Bonow de Almeida, Giselle Martins Pinto, Luis Antônio Suíta de Castro, Hiram Larangeira de Almeida Jr

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Reverse-namaskar: A new sign in <i><i><i>Ehlers-Danlos syndrome</i></i></i>: A family pedigree study of four generations by Premalatha S, Sarveswari K, Lahiri Koushik

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Evaluating the effects of two different kinesiology taping techniques on shoulder range of motion and proprioception in patients with hypermobile Ehlers-Danlos syndrome: a randomized controlled trial by Frank Tudini, Max Jordon, David Levine, Michael Healy, Sarah Cathey, Kevin Chui

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A Personalized Medicine Approach to the Diagnosis and Management of Autism Spectrum Disorder

Subjects: “…Ehlers-Danlos syndrome…”
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The differential diagnosis of children with joint hypermobility: a review of the literature by Elliott Elizabeth J, Tofts Louise J, Munns Craig, Pacey Verity, Sillence David O

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THE DIFFERENTIAL DIAGNOSIS OF CHILDREN WITH JOINT HYPERMOBILITY: A REVIEW OF THE LITERATURE by Louise J. Tofts, J. Elliott, Craig Munns, Verity Pacey, David O Sillence

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Classic Ehlers-Dalnos syndrome presenting as atypical chronic haematoma: a case report with novel frameshift mutation in COL5A1 by Wei-Ching Chiu, Shu-Huey Chen, Mei-Chen Lo, Yung-Ting Kuo

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BENEATH THE SURFACE: EXPLORING A CASE OF LEFT CIRCUMFLEX ARTERY DISSECTION by Menon Tushar, MD

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Physical activity and physical fitness in children with heritable connective tissue disorders by Lisanne de Koning, Lisanne de Koning, Jessica Warnink-Kavelaars, Jessica Warnink-Kavelaars, Marion van Rossum, Marion van Rossum, Selina Limmen, Ruth Van der Looven, Laura Muiño-Mosquera, Laura Muiño-Mosquera, Annelies van der Hulst, Jaap Oosterlaan, Jaap Oosterlaan, Lies Rombaut, Raoul Engelbert, Raoul Engelbert, Raoul Engelbert, on behalf of the Pediatric Heritable Connective Tissue Disorders Study Group

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The Style Evolution of Glasses: Acknowledging Well-being for Wearable Medical Device by Lydia Royeen

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Generalised joint hypermobility as a symptom of chosen diseases and syndromes by Aneta Przymuszała, Magdalena Roszak, Oksana Kulik, Artur Uździcki, Agnieszka Turon-Skrzypinska, Iwona Rotter, Magdalena Ptak

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