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Head & Neck|October 16, 2010
Gene expression profiling in head and neck squamous cell carcinoma: Clinical perspectivesBenjamin Lallemant, Alexandre Evrard, Guillaume Chambon, et al.
European Journal of Endocrinology|January 2, 2008
Restoration of ovulation after unilateral ovariectomy in a woman with McCune-Albright syndrome: a case reportVincent Lavoué, Karine Morcel, Philippe Bouchard, et al.
The Journal of Urology|August 8, 2006
Activating mutations of Gsalpha in kidney cancerNicolas Kalfa, Serge Lumbroso, Nathalie Boulle, et al.
Maturitas|June 9, 2006
Association between androgen receptor gene polymorphism and bone density in older women using hormone replacement therapyFréderique Retornaz, Françoise Paris, Serge Lumbroso, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|November 9, 2019
Theme 4 In vivo experimental modelsAleksandra V Chudinova, Mireille Rossel, Annette Vergunst, et al.
Molecular and Cellular Endocrinology|July 4, 2012
Emerging roles for LXRs and LRH-1 in female reproductionKevin Mouzat, Silvère Baron, Geoffroy Marceau, et al.
International Journal of Molecular Sciences|September 19, 2020
Clinical and Molecular Landscape of ALS Patients with <i>SOD1</i> Mutations: Novel Pathogenic Variants and Novel Phenotypes. A Single ALS Center StudyEmilien Bernard, Antoine Pegat, Juliette Svahn, et al.
European Neurology|February 5, 2020
Electrophysiological Characterization of C9ORF72-Associated Amyotrophic Lateral Sclerosis: A Retrospective StudyAntoine Pegat, Françoise Bouhour, Kevin Mouzat, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|December 6, 2021
Amyotrophic lateral sclerosis associated with a pathological expansion in the <i>ATXN7</i> geneFlorent Cluse, Emilien Bernard, Isabelle Strubi-Vuillaume, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 20, 2021
Compound heterozygous P67S/D91A <i>SOD1</i> mutations in an ALS family with apparently sporadic caseElisa De La Cruz, Claire Guissart, Florence Esselin, et al.
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