Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 3 (of 3 Records) |
Query Trace: Hypermobile Ehlers-danlos Syndrome[original query] |
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Hereditary alpha-tryptasemia modifies clinical phenotypes among individuals with congenital hypermobility disorders. HGG advances 2022 3 3 (2): 100094. Vazquez Maribel, Chovanec Jack, Kim Jiwon, DiMaggio Thomas, Milner Joshua D, Francomano Clair A, Gurnett Christina A, Ritelli Marco, Colombi Marina, Lyons Jonathan |
High overlap in patients diagnosed with hypermobile Ehlers-Danlos syndrome or hypermobile spectrum disorders with fibromyalgia and 40 self-reported symptoms and comorbidities. Frontiers in medicine 2023 5 10 1096180. DeLisa Fairweather, Katelyn A Bruno, Ashley A Darakjian, Barbara K Bruce, Jessica M Gehin, Archana Kotha, Angita Jain, Zhongwei Peng, David O Hodge, Todd D Rozen, Bala Munipalli, Fernando A Rivera, Pedro A Malavet, Dacre R T Knig |
Genetic complexity of diagnostically unresolved Ehlers-Danlos syndrome. Journal of medical genetics 2023 10 . Anthony M Vandersteen, Ruwan A Weerakkody, David A Parry, Christina Kanonidou, Daniel J Toddie-Moore, Jana Vandrovcova, Rebecca Darlay, Javier Santoyo-Lopez, Alison Meynert, , Hanadi Kazkaz, Rodney Grahame, Carole Cummings, Marion Bartlett, Neeti Ghali, Angela F Brady, F Michael Pope, Fleur S van Dijk, Heather J Cordell, Timothy J Aitm |
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- Page last updated:May 13, 2024
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