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Orphanet Journal of Rare Diseases|March 15, 2024
Patient interest in the development of a center for Ehlers-Danlos syndrome/hypermobility spectrum disorder in the Chicagoland regionWendy Wagner, Tom A Doyle, Clair A Francomano, et al.
Prenatal Diagnosis|October 16, 2002
Issues surrounding prenatal genetic testing for achondroplasiaHolly C Gooding, Karina Boehm, Richard E Thompson, et al.
World Neurosurgery|February 4, 2021
Refractory Syncope and Presyncope Associated with Atlantoaxial Instability: Preliminary Evidence of Improvement Following Surgical StabilizationFraser C Henderson, Peter C Rowe, Malini Narayanan, et al.
American Journal of Medical Genetics. Part A|February 2, 2019
Heritable disorders of connective tissue: Description of a data repository and initial cohort characterizationRebecca Bascom, Jane R Schubart, Susan Mills, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 3, 2004
Klotho gene variation and expression in 20 inbred mouse strainsArsun Bektas, Shepherd H Schurman, Alexei A Sharov, et al.
Mayo Clinic Proceedings. Innovations, Quality & Outcomes|January 10, 2025
The Financial Impact of Ehlers-Danlos Syndromes on Patients in the United States in 2022Jane R Schubart, Eric W Schaefer, Susan E Mills, et al.
Medrxiv : the Preprint Server for Health Sciences|April 10, 2026
Multimodal Wearable and Survey Data Reveal Distinct Physiologic Profiles in Hypermobile-Ehlers Danlos Syndrome for Screening AdvancementsDamen Wilson, Maureen Shilling, Thomas Nowak, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 14, 2017
Ehlers-Danlos syndrome, classical typeJessica M Bowen, Glenda J Sobey, Nigel P Burrows, et al.
Human Molecular Genetics|September 11, 2003
A central nervous system specific mouse model for thanatophoric dysplasia type IITi Lin, Stacey B Sandusky, Haipeng Xue, et al.
Autonomic Neuroscience : Basic & Clinical|January 19, 2020
Prevalence of hypermobile Ehlers-Danlos syndrome in postural orthostatic tachycardia syndromeAmanda J Miller, Lauren E Stiles, Timothy Sheehan, et al.
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