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I Bergada

Showing results (1-10 of 8) with videos related to

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Diabetes Research (Edinburgh, Scotland)|June 1, 1989
The effect of islet-activating protein (IAP) of pertussis toxin on the spontaneous diabetic syndrome in the ratI Bergada, E Colle, T A Seemayer
Diabetes Care|April 1, 1989
Severe hypoglycemia in IDDM childrenI Bergada, S Suissa, J Dufresne, et al.
Archives of Disease in Childhood|April 8, 1999
Long-term follow up of persistent hyperinsulinaemic hypoglycaemia of infancyJ C Cresto, J P Abdenur, I Bergada, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 1, 1997
Mutations of the steroid 21-hydroxylase gene in an Argentinian population of 36 patients with classical congenital adrenal hyperplasiaA Dardis, I Bergada, C Bergada, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 26, 1998
Functional adrenal cortical tumors in childhood: a study of ploidy, p53-protein and nucleolar organizer regions (AgNORs) as prognostic markersM Venara, R Sanchez Marull, I Bergada, et al.
European Journal of Pediatrics|March 29, 2001
Intermittent hyperaldosteronism in a child due to an adrenal adenomaD Rogoff, I Bergada, M Venara, et al.
Human Genetics|September 1, 1988
Kenny syndrome: description of additional abnormalities and molecular studiesI Bergada, A Schiffrin, H Abu Srair, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|April 10, 2009
Glucokinase gene mutation screening in Argentinean clinically characterized MODY patientsA P Lopez, S A Foscaldi, M S Pérez, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Diabetes Research (Edinburgh, Scotland)|June 1, 1989
The effect of islet-activating protein (IAP) of pertussis toxin on the spontaneous diabetic syndrome in the ratI Bergada, E Colle, T A Seemayer
Diabetes Care|April 1, 1989
Severe hypoglycemia in IDDM childrenI Bergada, S Suissa, J Dufresne, et al.
Archives of Disease in Childhood|April 8, 1999
Long-term follow up of persistent hyperinsulinaemic hypoglycaemia of infancyJ C Cresto, J P Abdenur, I Bergada, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 1, 1997
Mutations of the steroid 21-hydroxylase gene in an Argentinian population of 36 patients with classical congenital adrenal hyperplasiaA Dardis, I Bergada, C Bergada, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 26, 1998
Functional adrenal cortical tumors in childhood: a study of ploidy, p53-protein and nucleolar organizer regions (AgNORs) as prognostic markersM Venara, R Sanchez Marull, I Bergada, et al.
European Journal of Pediatrics|March 29, 2001
Intermittent hyperaldosteronism in a child due to an adrenal adenomaD Rogoff, I Bergada, M Venara, et al.
Human Genetics|September 1, 1988
Kenny syndrome: description of additional abnormalities and molecular studiesI Bergada, A Schiffrin, H Abu Srair, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|April 10, 2009
Glucokinase gene mutation screening in Argentinean clinically characterized MODY patientsA P Lopez, S A Foscaldi, M S Pérez, et al.
Pageof 1