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Christian Hamel

Showing results (21-30 of 74) with videos related to

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Medecine Sciences : M/S|October 9, 2010
[From yeast to neurodegenerative diseases: ten years of exploration of mitochondrial dynamic disorders]Guy Lenaers, Patrizia Amati-Bonneau, Cécile Delettre, et al.
Digestion|July 1, 2006
Glucagon-like peptide-1 is involved in sodium and water homeostasis in humansJean-Pierre Gutzwiller, Petr Hruz, Andreas R Huber, et al.
Neurology. Genetics|March 23, 2018
<i>ACO2</i> mutations: A novel phenotype associating severe optic atrophy and spastic paraplegiaCecilia Marelli, Christian Hamel, Melanie Quiles, et al.
Journal of Laparoendoscopic & Advanced Surgical Techniques. Part A|August 21, 2007
Assessment of construct validity of a virtual reality laparoscopy simulatorRachel Rosenthal, Walter A Gantert, Christian Hamel, et al.
Human Mutation|June 1, 2010
Nasal epithelial cells are a reliable source to study splicing variants in Usher syndromeChristel Vaché, Thomas Besnard, Catherine Blanchet, et al.
Molecular Vision|January 6, 2012
Mutational analysis of the RB1 gene in Moroccan patients with retinoblastomaOmar Abidi, Sara Knari, Hajar Sefri, et al.
Journal of Inherited Metabolic Disease|March 31, 2010
Should transcobalamin deficiency be treated aggressively?Manuel Schiff, Hélène Ogier de Baulny, Ghislaine Bard, et al.
American Journal of Human Genetics|August 24, 2004
Retinal dehydrogenase 12 (RDH12) mutations in leber congenital amaurosisIsabelle Perrault, Sylvain Hanein, Sylvie Gerber, et al.
Human Mutation|November 5, 2011
RP1 and autosomal dominant rod-cone dystrophy: novel mutations, a review of published variants, and genotype-phenotype correlationIsabelle Audo, Saddek Mohand-Saïd, Claire-Marie Dhaenens, et al.
American Journal of Human Genetics|January 8, 2003
The ABCA4 gene in autosomal recessive cone-rod dystrophiesDominique Ducroq, Jean-Michel Rozet, Sylvie Gerber, et al.
Pageof 8

Showing results (21-30 of 74) with videos related to

Sort By:
Pageof 8
Medecine Sciences : M/S|October 9, 2010
[From yeast to neurodegenerative diseases: ten years of exploration of mitochondrial dynamic disorders]Guy Lenaers, Patrizia Amati-Bonneau, Cécile Delettre, et al.
Digestion|July 1, 2006
Glucagon-like peptide-1 is involved in sodium and water homeostasis in humansJean-Pierre Gutzwiller, Petr Hruz, Andreas R Huber, et al.
Neurology. Genetics|March 23, 2018
<i>ACO2</i> mutations: A novel phenotype associating severe optic atrophy and spastic paraplegiaCecilia Marelli, Christian Hamel, Melanie Quiles, et al.
Journal of Laparoendoscopic & Advanced Surgical Techniques. Part A|August 21, 2007
Assessment of construct validity of a virtual reality laparoscopy simulatorRachel Rosenthal, Walter A Gantert, Christian Hamel, et al.
Human Mutation|June 1, 2010
Nasal epithelial cells are a reliable source to study splicing variants in Usher syndromeChristel Vaché, Thomas Besnard, Catherine Blanchet, et al.
Molecular Vision|January 6, 2012
Mutational analysis of the RB1 gene in Moroccan patients with retinoblastomaOmar Abidi, Sara Knari, Hajar Sefri, et al.
Journal of Inherited Metabolic Disease|March 31, 2010
Should transcobalamin deficiency be treated aggressively?Manuel Schiff, Hélène Ogier de Baulny, Ghislaine Bard, et al.
American Journal of Human Genetics|August 24, 2004
Retinal dehydrogenase 12 (RDH12) mutations in leber congenital amaurosisIsabelle Perrault, Sylvain Hanein, Sylvie Gerber, et al.
Human Mutation|November 5, 2011
RP1 and autosomal dominant rod-cone dystrophy: novel mutations, a review of published variants, and genotype-phenotype correlationIsabelle Audo, Saddek Mohand-Saïd, Claire-Marie Dhaenens, et al.
American Journal of Human Genetics|January 8, 2003
The ABCA4 gene in autosomal recessive cone-rod dystrophiesDominique Ducroq, Jean-Michel Rozet, Sylvie Gerber, et al.
Pageof 8