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M Berant

Showing results (171-180 of 181) with videos related to

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The New England Journal of Medicine|March 21, 1996
Coexistence of hereditary homocystinuria and factor V Leiden--effect on thrombosisH Mandel, B Brenner, M Berant, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Zellweger-like phenotype in two siblings: a defect in peroxisomal beta-oxidation with elevated very long-chain fatty acids but normal bile acidsH Mandel, M Berant, A Aizin, et al.
Catheterization and Cardiovascular Diagnosis|September 15, 1998
Interventional catheterization decreases plasma levels of atrial natriuretic peptide (ANP) in children with congenital heart defectsB Zeevi, I Gil-Ad, R Zabreski, et al.
Harefuah|November 15, 1972
[Antibodies to streptozyme and antistreptolysin O in acute glomerulonephritis following streptococcal skin infection]I Ofek, S Bergner-Rabinowitz, A Brand-Auraban, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Further studies on erythrocyte thiamin transport and phosphorylation in seven patients with thiamin-responsive megaloblastic anaemiaG Rindi, C Patrini, U Laforenza, et al.
Paediatric Anaesthesia|November 7, 2001
A novel thermoregulatory system maintains perioperative normothermia in children undergoing elective surgeryN Nesher, T Wolf, G Uretzky, et al.
Prenatal Diagnosis|December 13, 2000
Prolidase deficiency among an Israeli population: prenatal diagnosis in a genetic disorder with uncertain prognosisH Mandel, N Abeling, A Gutman, et al.
The Israel Medical Association Journal : IMAJ|May 11, 2000
Anomalous origin of the left coronary artery from the pulmonary artery: diagnosis and postoperative follow upE Birk, A Stamler, J Katz, et al.
The Journal of Pediatrics|October 1, 1994
A new type of peroxisomal disorder with variable expression in liver and fibroblastsH Mandel, M Espeel, F Roels, et al.
Journal of Inherited Metabolic Disease|July 15, 2000
Transferrin protein variant mimicking carbohydrate-deficient glycoprotein syndrome in trisomy 7 mosaicismC Knopf, R Rod, J Jaeken, et al.
Pageof 19

Showing results (171-180 of 181) with videos related to

Sort By:
Pageof 19
The New England Journal of Medicine|March 21, 1996
Coexistence of hereditary homocystinuria and factor V Leiden--effect on thrombosisH Mandel, B Brenner, M Berant, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Zellweger-like phenotype in two siblings: a defect in peroxisomal beta-oxidation with elevated very long-chain fatty acids but normal bile acidsH Mandel, M Berant, A Aizin, et al.
Catheterization and Cardiovascular Diagnosis|September 15, 1998
Interventional catheterization decreases plasma levels of atrial natriuretic peptide (ANP) in children with congenital heart defectsB Zeevi, I Gil-Ad, R Zabreski, et al.
Harefuah|November 15, 1972
[Antibodies to streptozyme and antistreptolysin O in acute glomerulonephritis following streptococcal skin infection]I Ofek, S Bergner-Rabinowitz, A Brand-Auraban, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Further studies on erythrocyte thiamin transport and phosphorylation in seven patients with thiamin-responsive megaloblastic anaemiaG Rindi, C Patrini, U Laforenza, et al.
Paediatric Anaesthesia|November 7, 2001
A novel thermoregulatory system maintains perioperative normothermia in children undergoing elective surgeryN Nesher, T Wolf, G Uretzky, et al.
Prenatal Diagnosis|December 13, 2000
Prolidase deficiency among an Israeli population: prenatal diagnosis in a genetic disorder with uncertain prognosisH Mandel, N Abeling, A Gutman, et al.
The Israel Medical Association Journal : IMAJ|May 11, 2000
Anomalous origin of the left coronary artery from the pulmonary artery: diagnosis and postoperative follow upE Birk, A Stamler, J Katz, et al.
The Journal of Pediatrics|October 1, 1994
A new type of peroxisomal disorder with variable expression in liver and fibroblastsH Mandel, M Espeel, F Roels, et al.
Journal of Inherited Metabolic Disease|July 15, 2000
Transferrin protein variant mimicking carbohydrate-deficient glycoprotein syndrome in trisomy 7 mosaicismC Knopf, R Rod, J Jaeken, et al.
Pageof 19