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Orphanet Journal of Rare Diseases|June 9, 2007
Fibromuscular dysplasiaPierre-François Plouin, Jérôme Perdu, Agnès La Batide-Alanore, et al.
Clinical Endocrinology|November 24, 2006
Phaeochromocytoma, new genes and screening strategiesAnne-Paule Gimenez-Roqueplo, Hendrik Lehnert, Massimo Mannelli, et al.
Biochimica Et Biophysica Acta|April 5, 2014
Unsuspected task for an old team: succinate, fumarate and other Krebs cycle acids in metabolic remodelingPaule Bénit, Eric Letouzé, Malgorzata Rak, et al.
The Journal of Clinical Endocrinology and Metabolism|October 5, 2016
A SDHC Founder Mutation Causes Paragangliomas (PGLs) in the French Canadians: New Insights on the SDHC-Related PGLIsabelle Bourdeau, Solange Grunenwald, Nelly Burnichon, et al.
The Journal of Clinical Endocrinology and Metabolism|October 5, 2002
Functional consequences of a SDHB gene mutation in an apparently sporadic pheochromocytomaAnne-Paule Gimenez-Roqueplo, Judith Favier, Pierre Rustin, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|August 7, 2019
Carbonic anhydrase 9 immunohistochemistry as a tool to predict or validate germline and somatic VHL mutations in pheochromocytoma and paraganglioma-a retrospective and prospective studyJudith Favier, Tchao Meatchi, Estelle Robidel, et al.
Hormone Research|March 30, 2005
Hereditary paraganglioma/pheochromocytoma and inherited succinate dehydrogenase deficiencyJudith Favier, Jean-Jacques Brière, Laurence Strompf, et al.
Journal of Hypertension|December 5, 2003
Evidence for carotid and radial artery wall subclinical lesions in renal fibromuscular dysplasiaPierre Boutouyrie, Anne-Paule Gimenez-Roqueplo, Erika Fine, et al.
BMC Biochemistry|January 30, 2010
Rapid determination of tricarboxylic acid cycle enzyme activities in biological samplesSergio Goncalves, Vincent Paupe, Emmanuel P Dassa, et al.
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