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Works (4)

Clinical diagnosis of the monogenic Ehlers-Danlos syndromes

Medizinische Genetik
2024-11-29 | Journal article
DOI: 10.1515/medgen-2024-2060
Contributors: Fleur S. van Dijk, MD, PhD; Chloe Angwin; Serwet Demirdas, MD, Ph.D.; Neeti Ghali, MBChB, MRC; Johannes Zschocke, Ph.D.
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Genetic diagnosis of the Ehlers-Danlos syndromes

Medizinische Genetik
2024-11-29 | Journal article
DOI: 10.1515/medgen-2024-2061
Contributors: Johannes Zschocke, Ph.D.; Serwet Demirdas, MD, Ph.D.; Fleur S. van Dijk, MD, PhD
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Vascular Ehlers-Danlos Syndrome: A Comprehensive Natural History Study in a Dutch National Cohort of 142 Patients

Circulation: Genomic and Precision Medicine
2024-06 | Journal article
DOI: 10.1161/CIRCGEN.122.003978
Contributors: Serwet Demirdas; Lisa M. van den Bersselaar; Rosan Lechner; Jessica Bos; Suzanne I.M. Alsters; Marieke J.H. Baars; Annette F. Baas; Özlem Baysal; Saskia N. van der Crabben; Eelco Dulfer et al.
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Management of childbearing with hypermobile Ehlers-Danlos syndrome and hypermobility spectrum disorders: A scoping review and expert co-creation of evidence-based clinical guidelines

PLOS ONE
2024-05-15 | Journal article
DOI: 10.1371/journal.pone.0302401
Contributors: Sally Pezaro; Martin E. Matsumura; Isabelle Brock; Maggie Buckley; Sarahann Callaway; Serwet Demirdas; Alan Hakim; Cheryl Harris; Carole High Gross; Megan Karanfil et al.
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Peer review (1 review for 1 publication/grant)

Review activity for European journal of human genetics (1)
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