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Laurence Strompf

Showing results (1-10 of 7) with videos related to

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Presse Medicale (Paris, France : 1983)|November 13, 2002
[Concerning residency, will the entropy end?]Laurence Strompf, Morgan Rouprêt
Hormone Research|March 30, 2005
Hereditary paraganglioma/pheochromocytoma and inherited succinate dehydrogenase deficiencyJudith Favier, Jean-Jacques Brière, Laurence Strompf, et al.
Human Immunology|November 24, 2004
Optimization of an elispot assay to detect cytomegalovirus-specific CD8+ T lymphocytesBrigitte Godard, Agnès Gazagne, Alain Gey, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 13, 2008
Evaluating PVALB as a candidate gene for SLC12A3-negative cases of Gitelman's syndromeEva Riveira-Munoz, Olivier Devuyst, Hendrica Belge, et al.
Annales De Biologie Clinique|January 9, 2026
Clinical biology and artificial intelligence: Objectives of the SFBC WorkgroupWalid Sabeur, Pierre-Adrien Bihl, Bruno Gauthier, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|November 30, 2005
Genetic testing in pheochromocytoma or functional paragangliomaLaurence Amar, Jérôme Bertherat, Eric Baudin, 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.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Presse Medicale (Paris, France : 1983)|November 13, 2002
[Concerning residency, will the entropy end?]Laurence Strompf, Morgan Rouprêt
Hormone Research|March 30, 2005
Hereditary paraganglioma/pheochromocytoma and inherited succinate dehydrogenase deficiencyJudith Favier, Jean-Jacques Brière, Laurence Strompf, et al.
Human Immunology|November 24, 2004
Optimization of an elispot assay to detect cytomegalovirus-specific CD8+ T lymphocytesBrigitte Godard, Agnès Gazagne, Alain Gey, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 13, 2008
Evaluating PVALB as a candidate gene for SLC12A3-negative cases of Gitelman's syndromeEva Riveira-Munoz, Olivier Devuyst, Hendrica Belge, et al.
Annales De Biologie Clinique|January 9, 2026
Clinical biology and artificial intelligence: Objectives of the SFBC WorkgroupWalid Sabeur, Pierre-Adrien Bihl, Bruno Gauthier, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|November 30, 2005
Genetic testing in pheochromocytoma or functional paragangliomaLaurence Amar, Jérôme Bertherat, Eric Baudin, 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.
Pageof 1