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Michel Gugenheim

Observed names: M Gugenheim, M. Gugenheim
OpenAlex ID: A5076428812
X-linked Charcot-Marie-Tooth disease with connexin 32 mutations
1998 · N. Birouk, E. LeGuern, et al. · Neurology · 170
Neurologic manifestations associated with COVID-19: a multicentre registry
2020 · Elodie Meppiel, Nathan Peiffer-Smadja, et al. · Clinical Microbiology and Infection · 157
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Clinical, electrophysiologic, and molecular correlations in 13 families with hereditary neuropathy with liability to pressure palsies and a chromosome 17p11.2 deletion
1995 · R. Gouider, E. LeGuern, et al. · Neurology · 109
Peripheral neuropathy associated with essential mixed cryoglobulinaemia: a role for hepatitis C virus infection?
1996 · E Apartis, J M Leger, et al. · Journal of Neurology Neurosurgery & Psychiatry · 101
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Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: Characterization of 14 C×32 mutations in 35 families
1997 · H Rouger, E LeGuern, et al. · Human Mutation · 64
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Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group.
1996 · J Lopes, E LeGuern, et al. · PubMed Central · 54
Polyneuropathy in autosomal dominant cerebellar ataxias: Phenotype-genotype correlation
1999 · Nathalie Kubis, Alexandra D�rr, et al. · Muscle & Nerve · 50
Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP)
2008 · E. Le Guern, F. Sturtz, et al. · Cytogenetics and Cell Genetics · 48
An amyotrophic lateral sclerosis-like syndrome revealing an amyloid polyneuropathy associated with a novel transthyretin mutation
2013 · Pierre Lozeron, Catherine Lacroix, et al. · Amyloid · 42
Duplication within chromosome 17p11.2 in 12 families of French ancestry with Charcot-Marie-Tooth disease type 1a. The French CMT Research Group.
1992 · A Brice, N Ravisé, et al. · Journal of Medical Genetics · 40
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A de Novo Case of Hereditary Neuropathy with Liability to Pressure Palsies (HNPP) of Maternal Origin: A New Mechanism for Deletion in 17p11.2?
1996 · E. LeGuern, R. Gouider, et al. · Human Molecular Genetics · 30
High frequency of mutations in codon 98 of the peripheral myelin protein P0 gene in 20 French CMT1 patients.
1996 · H Rouger, E LeGuern, et al. · PubMed Central · 23
Feasibility and benefits of home initiation of subcutaneous apomorphine infusion for patients with Parkinson’s disease: the APOKADO study
2023 · Fabien Zagnoli, Amélie Leblanc, et al. · Journal of Neural Transmission · 21
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Natalizumab treatment shows low cumulative probabilities of confirmed disability worsening to EDSS milestones in the long-term setting
2018 · Maria Trojano, Helmut Butzkueven, et al. · Multiple Sclerosis and Related Disorders · 19
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Constant rearrangement of the CMT1A-REP sequences in HNPP patients with a deletion in chromosome 17p11.2: a study of 30 unrelated cases
1995 · E. LeGuern, R. Gouider, et al. · Human Molecular Genetics · 19
Fourth meeting of the European Neurological Society 25–29 June 1994 Barcelona, Spain
1994 · The European Velnacrine Study Group, L. Harms, et al. · Journal of Neurology · 13
Microsatellite mapping of the deletion in patients with hereditary neuropathy with liability to pressure palsies (HNPP): new molecular tools for the study of the region 17p12→p11 and for diagnosis
2008 · E. LeGuern, R. Ravise, et al. · Cytogenetics and Cell Genetics · 12
Linkage analyses between dominant X-linked Charcot-Marie-Tooth disease, and 15 Xq11–Xq21 microsatellites in a new large family: Three new markers are closely linked to the gene
1994 · Eric Le Guern, Nicole Ravise, et al. · Neuromuscular Disorders · 12
Prevalence, characteristics and management of migraine patients with triptan failure in primary care: the EMR France-Mig study
2025 · M. Lanteri-Minet, C. Casarotto, et al. · The Journal of Headache and Pain · 10
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Migraine management in France: Practices of general practitioners and neurologists
2025 · C. Lucas, V. Raclot, et al. · Revue Neurologique · 6
Long-Term Effectiveness, Safety and Tolerability of Fingolimod in Patients with Multiple Sclerosis in Real-World Treatment Settings in France: The VIRGILE Study
2022 · Caroline Papeix, Giovanni Castelnovo, et al. · Neurology and Therapy · 6
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[Leptomeningeal gliomatosis. 2 clinicopathological cases].
1994 · G Fayet, C Bertout-Lemercier, et al. · PubMed · 5
[Pauci-symptomatic sensory polyneuropathy in Refsum's disease].
1996 · R Lévy, M Verny, et al. · PubMed · 2
Pratiques de prise en charge médicamenteuse des migraines par des médecins généralistes
2024 · Christian Lucas, Valentin Raclot, et al. · Revue Neurologique · 1
Pratiques de prise en charge médicamenteuse des migraines et perception des nouveaux traitements par des médecins neurologues
2024 · Anne Ducros, Michel Gugenheim, et al. · Revue Neurologique · 1
Works count: 32
Citation count: 1,029
H-index: 15
I10-index: 20
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