Fleur S van Dijk (F S van Dijk)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 6

Top Topics

Electron Microscopy

Systematic Review

Bone Regeneration

Top Venues

Orphanet journal of rare diseases

American journal of medical genetics. Part A

Genetics in medicine : official journal of the American College of Medical Genetics

The British journal of dermatology

This page only lists publications with an associated author ORCID identifier.

Publications

Raymond Dalgleish, Dimitra Micha, Andrea Superti-Furga, Fleur S van Dijk, David Owen Sillence
Letter to the editor: Re: Pathogenic mechanisms of osteogenesis imperfecta, evidence for classification. Orphanet journal of rare diseases 19 (1) (2024)
Raymond Dalgleish, Dimitra Micha, Andrea Superti-Furga, Fleur S van Dijk, David Owen Sillence
Letter to the editor: Re: Pathogenic mechanisms of osteogenesis imperfecta, evidence for classification. Orphanet journal of rare diseases 19 (1) (2024)
Raymond Dalgleish, Dimitra Micha, Andrea Superti-Furga, Fleur S van Dijk, David Owen Sillence
Letter to the editor: Re: Pathogenic mechanisms of osteogenesis imperfecta, evidence for classification. Orphanet journal of rare diseases 19 (1) (2024)
Claire Green, Neeti Ghali, Rhoda Akilapa, Chloe Angwin, Duncan Baker, Marion Bartlett, Jessica Bowen, Angela F Brady, Joanna Brock, Erin Chamberlain, Harveer Cheema, Vivienne McConnell, Renarta Crookes, Hanadi Kazkaz, Diana Johnson, F Michael Pope, Anthony Vandersteen, Glenda Sobey, Fleur S van Dijk
Classical-like Ehlers-Danlos syndrome: a clinical description of 20 newly identified individuals with evidence of tissue fragility. Genetics in medicine : official journal of the American College of Medical Genetics 22 (10) (2020)
Sandy Ayoub, Neeti Ghali, Chloe Angwin, Duncan Baker, Stella Baffini, Angela F Brady, Maria Luisa Giovannucci Uzielli, Cecilia Giunta, Diana S Johnson, Tomoki Kosho, Katherine Neas, F Michael Pope, Frank Rutsch, Gloria Scarselli, Glenda Sobey, Anthony Vandersteen, Fleur S van Dijk
Clinical features, molecular results, and management of 12 individuals with the rare arthrochalasia Ehlers-Danlos syndrome. American journal of medical genetics. Part A 182 (5) (2020)
C Angwin, N Ghali, D Baker, A F Brady, F M Pope, A Vandersteen, B Wagner, D J P Ferguson, Fleur S van Dijk
Electron microscopy in the diagnosis of Ehlers-Danlos syndromes: correlation with clinical and genetic investigations. The British journal of dermatology 182 (3) (2019)