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C Cazeneuve

Showing results (31-40 of 41) with videos related to

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Journal of Hepatology|December 22, 1999
Liver iron accumulation in patients with chronic active hepatitis C: prevalence and role of hemochromatosis gene mutations and relationship with hepatic histological lesionsC Hézode, C Cazeneuve, O Coué, et al.
Human Mutation|September 12, 2000
NF1 gene analysis focused on CpG-rich exons in a cohort of 93 patients with neurofibromatosis type 1E Girodon-Boulandet, J Pantel, C Cazeneuve, et al.
American Journal of Human Genetics|June 12, 1999
MEFV-Gene analysis in armenian patients with Familial Mediterranean fever: diagnostic value and unfavorable renal prognosis of the M694V homozygous genotype-genetic and therapeutic implicationsC Cazeneuve, T Sarkisian, C Pêcheux, et al.
Journal of Medical Genetics|October 22, 2008
Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patientsC Depienne, O Trouillard, C Saint-Martin, et al.
Neurology|September 22, 2010
Low disease risk in relatives of north african lrrk2 Parkinson disease patientsA R Troiano, A Elbaz, E Lohmann, et al.
American Journal of Human Genetics|October 6, 2000
Identification of MEFV-independent modifying genetic factors for familial Mediterranean feverC Cazeneuve, H Ajrapetyan, S Papin, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Familial Mediterranean fever in Lebanon: mutation spectrum, evidence for cases in Maronites, Greek orthodoxes, Greek catholics, Syriacs and Chiites and for an association between amyloidosis and M694V and M694I mutationsI Mansour, V Delague, C Cazeneuve, et al.
Human Mutation|August 3, 2000
Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in FranceM Claustres, C Guittard, D Bozon, et al.
Journal of Neurology|July 23, 2022
Unravelling the etiology of sporadic late-onset cerebellar ataxia in a cohort of 205 patients: a prospective studyT Bogdan, T Wirth, A Iosif, et al.
European Journal of Neurology|June 20, 2020
Deciphering the natural history of SCA7 in childrenM G Bah, D Rodriguez, C Cazeneuve, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
Journal of Hepatology|December 22, 1999
Liver iron accumulation in patients with chronic active hepatitis C: prevalence and role of hemochromatosis gene mutations and relationship with hepatic histological lesionsC Hézode, C Cazeneuve, O Coué, et al.
Human Mutation|September 12, 2000
NF1 gene analysis focused on CpG-rich exons in a cohort of 93 patients with neurofibromatosis type 1E Girodon-Boulandet, J Pantel, C Cazeneuve, et al.
American Journal of Human Genetics|June 12, 1999
MEFV-Gene analysis in armenian patients with Familial Mediterranean fever: diagnostic value and unfavorable renal prognosis of the M694V homozygous genotype-genetic and therapeutic implicationsC Cazeneuve, T Sarkisian, C Pêcheux, et al.
Journal of Medical Genetics|October 22, 2008
Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patientsC Depienne, O Trouillard, C Saint-Martin, et al.
Neurology|September 22, 2010
Low disease risk in relatives of north african lrrk2 Parkinson disease patientsA R Troiano, A Elbaz, E Lohmann, et al.
American Journal of Human Genetics|October 6, 2000
Identification of MEFV-independent modifying genetic factors for familial Mediterranean feverC Cazeneuve, H Ajrapetyan, S Papin, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Familial Mediterranean fever in Lebanon: mutation spectrum, evidence for cases in Maronites, Greek orthodoxes, Greek catholics, Syriacs and Chiites and for an association between amyloidosis and M694V and M694I mutationsI Mansour, V Delague, C Cazeneuve, et al.
Human Mutation|August 3, 2000
Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in FranceM Claustres, C Guittard, D Bozon, et al.
Journal of Neurology|July 23, 2022
Unravelling the etiology of sporadic late-onset cerebellar ataxia in a cohort of 205 patients: a prospective studyT Bogdan, T Wirth, A Iosif, et al.
European Journal of Neurology|June 20, 2020
Deciphering the natural history of SCA7 in childrenM G Bah, D Rodriguez, C Cazeneuve, et al.
Pageof 5