الرئيسية › دليل الباحثين › Stéphane Mathis

Stéphane Mathis

الانتماء : Université de Bordeaux · Centre Hospitalier Universitaire de Bordeaux · Hôpital Pellegrin

• 13منشورات (انتماء فرنسي)
• 177مجموع المنشورات
• 3345الاستشهادات
• 29مؤشر h

ORCIDOpenAlex

مجالات البحث

• Peripheral Neuropathies and Disorders
• Hereditary Neurological Disorders
• Peripheral Nerve Disorders
• Neurology and Historical Studies
• Autoimmune Neurological Disorders and Treatments

المنشورات (13)

• Updating the classification of inherited neuropathies
  2018 · Neurology · استُشهد به 68 مرة
• The classification of Charcot-Marie-Tooth diseases, a never-ending story: CMT4?
  2018 · Brain · استُشهد به 4 مرة
• Some new proposals for the classification of inherited myopathies
  2018 · Journal of the Neurological Sciences · استُشهد به 2 مرة
• Maladies de Charcot-Marie-Tooth : discussion des relations génotypes-lésions ultrastructurales du nerf périphérique
  2018 · Bulletin de l Académie Nationale de Médecine
• Nerve Biopsy Is Still Useful in Some Inherited Neuropathies
  2017 · Journal of Neuropathology & Experimental Neurology · استُشهد به 27 مرة
• History and current difficulties in classifying inherited myopathies and muscular dystrophies
  2017 · Journal of the Neurological Sciences · استُشهد به 22 مرة
• Classifications of neurogenetic diseases: An increasingly complex problem
  2016 · Revue Neurologique · استُشهد به 26 مرة
• Reasons Charcot–Marie–Tooth disease due to mutations in the MME gene should not be named AR‐CMT2T
  2016 · Annals of Neurology · استُشهد به 4 مرة
• Pourquoi et comment actualiser la classification des maladies neurogénétiques ?
  2016 · Revue Neurologique
• Charcot–Marie–Tooth diseases: an update and some new proposals for the classification
  2015 · Journal of Medical Genetics · استُشهد به 110 مرة
• Hereditary motor and sensory neuropathies or Charcot–Marie–Tooth diseases: An update
  2014 · Journal of the Neurological Sciences · استُشهد به 93 مرة
• Peripheral Myelin Protein 22 gene duplication with atypical presentations: A new example of the wide spectrum of Charcot-Marie-Tooth 1A disease
  2014 · Neuromuscular Disorders · استُشهد به 26 مرة
• Other hereditary neuropathies
  2014 · استُشهد به 3 مرة

مجلات النشر

• Journal of the Neurological Sciences × 3
• Revue Neurologique × 2
• Neurology × 1
• Brain × 1
• Bulletin de l Académie Nationale de Médecine × 1
• Journal of Neuropathology & Experimental Neurology × 1

المنشورات حسب السنة

• 20184
• 20172
• 20163
• 20151
• 20143

التعاون العلمي

المؤسسات الشريكة : Centre Hospitalier Universitaire de Limoges · Hôpital Universitaire Dupuytren · Hôpital Mustapha Pacha · Centre Hospitalier Universitaire de Tours · Maladies Rares: Génétique et Métabolisme

بلدان المؤلفين المشاركين : الجزائر

المؤلفون المشاركون

• Jean‐Michel Vallat
• Laurent Magy
• Cyril Goizet
• Corinne Magdelaine
• Gwendal Le Masson
• Jean‐Michel Vallat
• Mathilde Duchesne
• Laurence Richard
• Philippe Couratier
• Fanny Duval
• Idoia Lacoste
• Mériem Tazir

البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).