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G Chazot

Showing results (111-120 of 147) with videos related to

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Journal of the Neurological Sciences|December 1, 1996
Slowly progressive anarthria with late anterior opercular syndrome: a variant form of frontal cortical atrophy syndromesE Broussolle, S Bakchine, M Tommasi, et al.
La Nouvelle Presse Medicale|May 25, 1974
[Peripheral neuropathy in malignant dysglobulinemias. Immunopathological aspects]G Chazot, G Berger, B Bady, et al.
Revue D'Electroencephalographie Et De Neurophysiologie Clinique|February 1, 1986
[Clinical amyotrophic lateral sclerosis syndromes in gammapathies: clinical, electrophysiologic and histoimmunologic aspects]F Brudon, B Bady, G Chauplannaz, et al.
Clinical Genetics|November 1, 1994
New allele of probe D17S61 present in the Charcot-Marie-Tooth 1A duplicationM Bost, C Bonnebouche, P M Gonnaud, et al.
Life Sciences|March 31, 1980
Cerebrospinal fluid homocarnosine in Huntington's diseaseP Böhlen, G Tell, P J Schechter, et al.
Acta Neuropathologica|January 5, 2002
This is really a case of new variant Creutzfeldt-Jakob. Response to C.J.G. Lang et al. concerning our article Acta Neuropathol (2000) 99:704-708N Streichenberger, A G Biacabe, A Perret-Liaudet, et al.
Revue Neurologique|July 13, 2000
[Non-familial Creutzfeldt-Jakob disease: a study of 53 cases]P Giraud, A Perret-Liaudet, A G Biacabe, et al.
Journal of Neurology|May 22, 2002
Subthalamic nucleus stimulation in Parkinson's disease: clinical evaluation of 18 patientsS Thobois, P Mertens, M Guenot, et al.
Clinical Chemistry|April 28, 2001
Polymorphic short tandem repeats for diagnosis of the Charcot-Marie-Tooth 1A duplicationP Latour, L Boutrand, N Levy, et al.
Clinical Genetics|December 1, 1995
Charcot-Marie-Tooth type 1B neuropathy: third mutation of serine 63 codon in the major peripheral myelin glycoprotein PO geneF Blanquet-Grossard, D Pham-Dinh, A Dautigny, et al.
Pageof 15

Showing results (111-120 of 147) with videos related to

Sort By:
Pageof 15
Journal of the Neurological Sciences|December 1, 1996
Slowly progressive anarthria with late anterior opercular syndrome: a variant form of frontal cortical atrophy syndromesE Broussolle, S Bakchine, M Tommasi, et al.
La Nouvelle Presse Medicale|May 25, 1974
[Peripheral neuropathy in malignant dysglobulinemias. Immunopathological aspects]G Chazot, G Berger, B Bady, et al.
Revue D'Electroencephalographie Et De Neurophysiologie Clinique|February 1, 1986
[Clinical amyotrophic lateral sclerosis syndromes in gammapathies: clinical, electrophysiologic and histoimmunologic aspects]F Brudon, B Bady, G Chauplannaz, et al.
Clinical Genetics|November 1, 1994
New allele of probe D17S61 present in the Charcot-Marie-Tooth 1A duplicationM Bost, C Bonnebouche, P M Gonnaud, et al.
Life Sciences|March 31, 1980
Cerebrospinal fluid homocarnosine in Huntington's diseaseP Böhlen, G Tell, P J Schechter, et al.
Acta Neuropathologica|January 5, 2002
This is really a case of new variant Creutzfeldt-Jakob. Response to C.J.G. Lang et al. concerning our article Acta Neuropathol (2000) 99:704-708N Streichenberger, A G Biacabe, A Perret-Liaudet, et al.
Revue Neurologique|July 13, 2000
[Non-familial Creutzfeldt-Jakob disease: a study of 53 cases]P Giraud, A Perret-Liaudet, A G Biacabe, et al.
Journal of Neurology|May 22, 2002
Subthalamic nucleus stimulation in Parkinson's disease: clinical evaluation of 18 patientsS Thobois, P Mertens, M Guenot, et al.
Clinical Chemistry|April 28, 2001
Polymorphic short tandem repeats for diagnosis of the Charcot-Marie-Tooth 1A duplicationP Latour, L Boutrand, N Levy, et al.
Clinical Genetics|December 1, 1995
Charcot-Marie-Tooth type 1B neuropathy: third mutation of serine 63 codon in the major peripheral myelin glycoprotein PO geneF Blanquet-Grossard, D Pham-Dinh, A Dautigny, et al.
Pageof 15