Zobrazeno 1 - 2
of 2
pro vyhledávání: '"J. P. Vreyling"'
Autor:
J. P. Vreyling, M. de Visser, W. H. J. P. Linssen, J.H.J. Wokke, Frank Baas, Pieter A. Bolhuis, P.A. van Doorn, Nicolette C. Notermans
Publikováno v:
Neuromuscular Disorders, 8, 317-320. Elsevier Ltd.
Neuromuscular disorders, 8(5), 317-320. Elsevier Limited
Neuromuscular disorders, 8(5), 317-320. Elsevier Limited
Miyoshi-type distal muscular dystrophy (MMD) is an autosomal recessively inherited progressive disorder. The putative locus of MMD is linked to the limb-girdle muscular dystrophy 2B locus on chromosome 2p12–14. In this study three of four MMD pedig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d26b340ff3299c7716a6e696522b830
https://pure.eur.nl/en/publications/4d022d4a-98ca-4868-a162-4905c206b4b9
https://pure.eur.nl/en/publications/4d022d4a-98ca-4868-a162-4905c206b4b9
Autor:
J. P. Vreyling, P.H.S. Meijerink, W.A. van Gool, G. H. Jansen, Frank Baas, M van Meegen, Saskia Bulk, Afina W. Lemstra
Publikováno v:
Scopus-Elsevier
Neurology, 55(4), 514-516. Lippincott Williams and Wilkins
Neurology, 55(4), 514-516. Lippincott Williams and Wilkins
Objective: To study the sensitivity and specificity of 14-3-3 testing in a prospective series of patients suspected of having Creutzfeldt-Jakob disease (CJD). Background: The 14-3-3 protein immunoassay on CSF has favorable test characteristics as a p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9af3e1b752a871f4f62572c71e66a244
http://www.scopus.com/inward/record.url?eid=2-s2.0-0033837134&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0033837134&partnerID=MN8TOARS