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Author/Creator Schouten, Meyke

1. Biallelic variants in LARS2 and KARS cause deafness and (ovario)leukodystrophy. (12th March 2019)

Authors:
van der Knaap, Marjo S.; Bugiani, Marianna; Mendes, Marisa I.; Riley, Lisa G.; Smith, Desiree E.C.; Rudinger-Thirion, Joëlle; Frugier, Magali; Breur, Marjolein; Crawford, Joanna; van Gaalen, Judith; Schouten, Meyke; Willems, Marjolaine; Waisfisz, Quinten; Mau-Them, Frederic Tran; Rodenburg, Richa...
Journal:
Neurology
Issue:
Volume 92:Number 11(2019)
Page Start:
Record Type:
Journal Article
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2. Clinical, genetic, and histological features of centronuclear myopathy in the Netherlands. Issue 6 (25th September 2021)

Authors:
Reumers, Stacha F. I.; Erasmus, Corrie E.; Bouman, Karlijn; Pennings, Maartje; Schouten, Meyke; Kusters, Benno; Duijkers, Floor A. M.; van der Kooi, Anneke; Jaeger, Bregje; Verschuuren‐Bemelmans, Corien C.; Faber, Catharina G.; van Engelen, Baziel G.; Kamsteeg, Erik‐Jan; Jungbluth, Heinz; Voerman...
Journal:
Clinical genetics
Issue:
Volume 100:Issue 6(2021)
Page Start:
692
Record Type:
Journal Article
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4. Spectrum of Clinical Features in X-Linked Myotubular Myopathy Carriers: An International Questionnaire Study. (3rd August 2021)

Authors:
Reumers, Stacha F.I.; Braun, Frederik; Spillane, Jennifer E.; Böhm, Johann; Pennings, Maartje; Schouten, Meyke; van der Kooi, Anneke J.; Foley, A. Reghan; Bönnemann, Carsten G.; Kamsteeg, Erik-jan; Erasmus, Corrie E.; Schara-Schmidt, Ulrike; Jungbluth, Heinz; Voermans, Nicol C.
Journal:
Neurology
Issue:
Volume 97:Number 5(2021)
Page Start:
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗