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Journal of the American Society of Nephrology : JASN|July 10, 2019
Resistance to Insulin in Patients with Gitelman Syndrome and a Subtle Intermediate Phenotype in Heterozygous Carriers: A Cross-Sectional StudyAnne Blanchard, Marion Vallet, Laurence Dubourg, et al.
Journal of the American Society of Nephrology : JASN|March 19, 2011
Spectrum of mutations in Gitelman syndromeRosa Vargas-Poussou, Karin Dahan, Diana Kahila, et al.
Journal of the American Society of Nephrology : JASN|April 14, 2006
Genetic investigation of autosomal recessive distal renal tubular acidosis: evidence for early sensorineural hearing loss associated with mutations in the ATP6V0A4 geneRosa Vargas-Poussou, Pascal Houillier, Nelly Le Pottier, et al.
The Journal of Clinical Investigation|August 14, 2020
Mutation affecting the conserved acidic WNK1 motif causes inherited hyperkalemic hyperchloremic acidosisHélène Louis-Dit-Picard, Ilektra Kouranti, Chloé Rafael, et al.
The Journal of Clinical Endocrinology and Metabolism|March 11, 2016
Familial Hypocalciuric Hypercalcemia Types 1 and 3 and Primary Hyperparathyroidism: Similarities and DifferencesRosa Vargas-Poussou, Lamisse Mansour-Hendili, Stéphanie Baron, et al.
Geriatrie Et Psychologie Neuropsychiatrie Du Vieillissement|November 8, 2016
French law: what about a reasoned reimbursement of serum vitamin D assays?Jean-Claude Souberbielle, Claude Laurent Benhamou, Bernard Cortet, et al.
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