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Physiological Reports|August 13, 2015
Seasonal influence over serum and urine metabolic markers in submariners during prolonged patrolsXavier Holy, Laurent Bégot, Sylvie Renault, et al.Frontiers in Psychiatry|August 28, 2020
Neuropsychological and Psychiatric Features of Children and Adolescents Affected With Mitochondrial Diseases: A Systematic ReviewElise Riquin, Philippe Duverger, Cindy Cariou, et al.Orphanet Journal of Rare Diseases|July 11, 2012
Dominant optic atrophyGuy Lenaers, Christian Hamel, Cécile Delettre, et al.Journal of Gynecology Obstetrics and Human Reproduction|May 28, 2021
Fertility in McCune Albright syndrome female: A case study focusing on AMH as a marker of ovarian dysfunction and a literature reviewMikaël Agopiantz, Arthur Sorlin, Pierre Vabres, et al.Archives of Dermatology|March 19, 2008
Heterozygosity for a single mutation in the ABCC6 gene may closely mimic PXE: consequences of this phenotype overlap for the definition of PXELudovic Martin, Frédéric Maître, Pierre Bonicel, et al.American Journal of Medical Genetics. Part A|January 19, 2008
Carotid artery dissection in an adult with the Simpson-Golabi-Behmel syndromeIsabelle Pénisson-Besnier, Thibaud Lebouvier, Marie-Pierre Moizard, et al.Prenatal Diagnosis|April 21, 2012
Prenatal diagnosis of CHARGE syndrome by identification of a novel CHD7 mutation in a previously unaffected familyEstelle Colin, Dominique Bonneau, Francoise Boussion, et al.Clinical Genetics|May 28, 2026
Novel Postzygotic Variants Associated With Hypomelanosis of Ito Expand the ACTB-Related Neurocutaneous Disease SpectrumEstella Castillon, Paul Rollier, Didier Bessis, et al.Ultrasound in Medicine & Biology|July 2, 2015
Reliable protocol for shear wave elastography of lower limb muscles at rest and during passive stretchingGuillaume Dubois, Walid Kheireddine, Claudio Vergari, et al.BMC Research Notes|October 25, 2013
Is ABCC6 a genuine mitochondrial protein?Marc Ferré, Pascal Reynier, Arnaud Chevrollier, et al.Pageof 33