المؤلفون: Schreiber S; Department of Neurology, Otto-von-Guericke University, Leipziger Straße 44, 39120, Magdeburg, Germany.; German Center for Neurodegenerative Diseases (DZNE) within the Helmholtz Association, Magdeburg, Germany., Debska-Vielhaber G; Department of Neurology, Otto-von-Guericke University, Leipziger Straße 44, 39120, Magdeburg, Germany., Abdulla S; Department of Neurology, Otto-von-Guericke University, Leipziger Straße 44, 39120, Magdeburg, Germany.; German Center for Neurodegenerative Diseases (DZNE) within the Helmholtz Association, Magdeburg, Germany., Machts J; Department of Neurology, Otto-von-Guericke University, Leipziger Straße 44, 39120, Magdeburg, Germany.; German Center for Neurodegenerative Diseases (DZNE) within the Helmholtz Association, Magdeburg, Germany., Schreiber F; Department of Neurology, Otto-von-Guericke University, Leipziger Straße 44, 39120, Magdeburg, Germany.; German Center for Neurodegenerative Diseases (DZNE) within the Helmholtz Association, Magdeburg, Germany.; Institute of Control Engineering, Technische Universität Braunschweig, Braunschweig, Germany., Kropf S; Institute of Biometry and Medical Informatics, Otto-von-Guericke University, Magdeburg, Germany., KÖrtvelyessy P; Department of Neurology, Otto-von-Guericke University, Leipziger Straße 44, 39120, Magdeburg, Germany.; German Center for Neurodegenerative Diseases (DZNE) within the Helmholtz Association, Magdeburg, Germany., KÖrner S; Department of Neurology, Hannover Medical School, Hannover, Germany., Kollewe K; Department of Neurology, Hannover Medical School, Hannover, Germany., Petri S; Department of Neurology, Hannover Medical School, Hannover, Germany., Dengler R; Department of Neurology, Hannover Medical School, Hannover, Germany., Kunz WS; Division of Neurochemistry, Department of Epileptology, University Bonn Medical Center, Bonn, Germany., Nestor PJ; German Center for Neurodegenerative Diseases (DZNE) within the Helmholtz Association, Magdeburg, Germany., Vielhaber S; Department of Neurology, Otto-von-Guericke University, Leipziger Straße 44, 39120, Magdeburg, Germany.; German Center for Neurodegenerative Diseases (DZNE) within the Helmholtz Association, Magdeburg, Germany.

المصدر: Muscle & nerve [Muscle Nerve] 2018 Feb; Vol. 57 (2), pp. 273-278. Date of Electronic Publication: 2017 May 22.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 7803146 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-4598 (Electronic) Linking ISSN: 0148639X NLM ISO Abbreviation: Muscle Nerve Subsets: MEDLINE

مواضيع طبية MeSH: Amyotrophic Lateral Sclerosis/*cerebrospinal fluid , Amyotrophic Lateral Sclerosis/*diagnostic imaging , Axons/*ultrastructure , Peripheral Nervous System Diseases/*diagnostic imaging , Progranulins/*cerebrospinal fluid, Adult ; Aged ; Anatomy, Cross-Sectional ; Atrophy ; Biomarkers ; Cross-Sectional Studies ; Electrophysiological Phenomena ; Female ; Forearm/diagnostic imaging ; Forearm/innervation ; Humans ; Male ; Median Nerve/diagnostic imaging ; Middle Aged ; Prospective Studies ; Ulnar Nerve/diagnostic imaging ; Ultrasonography

المؤلفون: Schreiber S; Department of Neurology, Otto-von-Guericke University, Magdeburg, Germany. stefanie.schreiber@med.ovgu.de, Oldag A, Kornblum C, Kollewe K, Kropf S, Schoenfeld A, Feistner H, Jakubiczka S, Kunz WS, Scherlach C, Tempelmann C, Mawrin C, Dengler R, Schreiber F, Goertler M, Vielhaber S

المصدر: Muscle & nerve [Muscle Nerve] 2013 Mar; Vol. 47 (3), pp. 385-95. Date of Electronic Publication: 2013 Feb 04.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 7803146 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-4598 (Electronic) Linking ISSN: 0148639X NLM ISO Abbreviation: Muscle Nerve Subsets: MEDLINE

مواضيع طبية MeSH: Charcot-Marie-Tooth Disease/*diagnostic imaging , Hereditary Sensory and Motor Neuropathy/*diagnostic imaging , Median Nerve/*diagnostic imaging, Adolescent ; Adult ; Aged ; Charcot-Marie-Tooth Disease/genetics ; Connexins/genetics ; Electrodiagnosis ; Electrophysiological Phenomena ; Female ; Forearm/anatomy & histology ; Forearm/innervation ; GTP Phosphohydrolases/genetics ; Hereditary Sensory and Motor Neuropathy/genetics ; Humans ; International Classification of Diseases ; Male ; Middle Aged ; Mitochondrial Proteins/genetics ; Myelin Proteins/genetics ; Neural Conduction/physiology ; Phenotype ; Ultrasonography ; Wrist/anatomy & histology ; Wrist/innervation ; Young Adult ; Gap Junction beta-1 Protein

SCR Disease Name: Charcot-Marie-Tooth Disease, Axonal, Type 2a1; Charcot-Marie-Tooth disease, X-linked, 1