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P Bouche

Showing results (131-140 of 158) with videos related to

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Clinical Chemistry|February 13, 2001
Quantitative determination of vapor-phase compound A in sevoflurane anesthesia using gas chromatography-mass spectrometryM P Bouche, J F Van Bocxlaer, G Rolly, et al.
Annals of the New York Academy of Sciences|July 21, 1998
Antiglycolipid antibodies in motor neuropathiesN Baumann, M L Harpin, Y Marie, et al.
Journal of Neurology|January 1, 1989
Peripheral neuropathies during treatment with almitrine: report of 46 casesP Bouche, L Lacomblez, J M Leger, et al.
Nature Genetics|November 5, 1997
Sex-dependent rearrangements resulting in CMT1A and HNPPJ Lopes, A Vandenberghe, S Tardieu, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 1, 1992
Frequency of central lesions in polyneuropathy associated with IgM monoclonal gammopathy: an MRI, neurophysiological and immunochemical studyJ M Léger, A B Younes-Chennoufi, M Zuber, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1996
Peripheral neuropathy associated with essential mixed cryoglobulinaemia: a role for hepatitis C virus infection?E Apartis, J M Léger, L Musset, et al.
Human Molecular Genetics|September 1, 1995
Constant rearrangement of the CMT1A-REP sequences in HNPP patients with a deletion in chromosome 17p11.2: a study of 30 unrelated cases. The French CMT Collaborative Research GroupE LeGuern, R Gouider, J Lopes, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP)E Le Guern, F Sturtz, M Gugenheim, et al.
Anesthesiology|September 29, 2001
Only carbon dioxide absorbents free of both NaOH and KOH do not generate compound A during in vitro closed-system sevoflurane: evaluation of five absorbentsL F Versichelen, M P Bouche, G Rolly, et al.
Brain : a Journal of Neurology|May 1, 1997
Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 casesN Birouk, R Gouider, E Le Guern, et al.
Pageof 16

Showing results (131-140 of 158) with videos related to

Sort By:
Pageof 16
Clinical Chemistry|February 13, 2001
Quantitative determination of vapor-phase compound A in sevoflurane anesthesia using gas chromatography-mass spectrometryM P Bouche, J F Van Bocxlaer, G Rolly, et al.
Annals of the New York Academy of Sciences|July 21, 1998
Antiglycolipid antibodies in motor neuropathiesN Baumann, M L Harpin, Y Marie, et al.
Journal of Neurology|January 1, 1989
Peripheral neuropathies during treatment with almitrine: report of 46 casesP Bouche, L Lacomblez, J M Leger, et al.
Nature Genetics|November 5, 1997
Sex-dependent rearrangements resulting in CMT1A and HNPPJ Lopes, A Vandenberghe, S Tardieu, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 1, 1992
Frequency of central lesions in polyneuropathy associated with IgM monoclonal gammopathy: an MRI, neurophysiological and immunochemical studyJ M Léger, A B Younes-Chennoufi, M Zuber, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1996
Peripheral neuropathy associated with essential mixed cryoglobulinaemia: a role for hepatitis C virus infection?E Apartis, J M Léger, L Musset, et al.
Human Molecular Genetics|September 1, 1995
Constant rearrangement of the CMT1A-REP sequences in HNPP patients with a deletion in chromosome 17p11.2: a study of 30 unrelated cases. The French CMT Collaborative Research GroupE LeGuern, R Gouider, J Lopes, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP)E Le Guern, F Sturtz, M Gugenheim, et al.
Anesthesiology|September 29, 2001
Only carbon dioxide absorbents free of both NaOH and KOH do not generate compound A during in vitro closed-system sevoflurane: evaluation of five absorbentsL F Versichelen, M P Bouche, G Rolly, et al.
Brain : a Journal of Neurology|May 1, 1997
Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 casesN Birouk, R Gouider, E Le Guern, et al.
Pageof 16