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M. Gugenheim

24

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Polyneuropathy in autosomal dominant cerebellar ataxias: Phenotype–genotype correlation

1999 Muscle & Nerve
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X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: Clinical and electrophysiologic study

1998 Neurology
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Intrt de la stimulation magntique dans les paraplgies spastiques familiales (PSF)

1997 Neurophysiologie Clinique-clinical Neurophysiology
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Intérêt de la stimulation magnétique dans les paraplégies spastiques familiales (PSF)

1997 Neurophysiologie Clinique-clinical Neurophysiology
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Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 cases

1997 Brain
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Peripheral neuropathy associated with essential mixed cryoglobulinaemia: a role for hepatitis C virus infection?

1996 Journal of Neurology, Neurosurgery, and Psychiatry
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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 American Journal of Human Genetics
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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 Human Molecular Genetics
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M25 Intrafamilial variations of motor nerve conduction in CMT1A patients

1996 Electroencephalography and Clinical Neurophysiology
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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

1996 Cytogenetic and Genome Research
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Citations (13)