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N Setian

Showing results (1-10 of 25) with videos related to

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Jornal De Pediatria|July 1, 1997
[Childhood hypoglycemia - still a challenge]D Damiani, V Dichtchekenian, N Setian
Revista Do Hospital Das Clinicas|September 1, 1971
[Hypoglycemia induced by leucine. Study of a case]N Setian, G Quarentei, E Marcondes, et al.
AMB : Revista Da Associacao Medica Brasileira|November 1, 1975
[Metabolic adaptations in infant malnutrition]N Setian, A A Pupo, G Sperotto, et al.
Genetic Testing|February 24, 2001
Prader-Willi syndrome: genetic tests and clinical findingsC Fridman, M C Varela, F Kok, et al.
American Journal of Medical Genetics|June 15, 1993
Macrosomia, obesity, macrocephaly and ocular abnormalities (MOMO syndrome) in two unrelated patients: delineation of a newly recognized overgrowth syndromeD Moretti-Ferreira, C P Koiffmann, M Listik, et al.
Clinical Genetics|December 25, 2004
Impact of molecular mechanisms, including deletion size, on Prader-Willi syndrome phenotype: study of 75 patientsM C Varela, F Kok, N Setian, et al.
Revista Do Instituto De Medicina Tropical De Sao Paulo|January 1, 1971
[Complement of human serum in normal male and female children]C F Netto, T L Kipnis, A Manissadjian, et al.
Revista Do Instituto De Medicina Tropical De Sao Paulo|May 1, 1971
[Total human serum complement in acute diffuse glomerulonephritis, and in the nephrotic and Schönlein-Henoch syndromes]A Manissadjian, H A Penna, N Setian, et al.
Human Genetics|June 1, 1990
Investigation of the ZFY gene in XX true hermaphroditism and Swyer syndromeD Damiani, A E Billerbeck, A C Goldberg, et al.
Jornal De Pediatria|December 4, 2003
[Persistent hyperinsulinemic hypoglycemia of infancy: case report]D F Lazarine, M M Pahl, D Damiani, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Jornal De Pediatria|July 1, 1997
[Childhood hypoglycemia - still a challenge]D Damiani, V Dichtchekenian, N Setian
Revista Do Hospital Das Clinicas|September 1, 1971
[Hypoglycemia induced by leucine. Study of a case]N Setian, G Quarentei, E Marcondes, et al.
AMB : Revista Da Associacao Medica Brasileira|November 1, 1975
[Metabolic adaptations in infant malnutrition]N Setian, A A Pupo, G Sperotto, et al.
Genetic Testing|February 24, 2001
Prader-Willi syndrome: genetic tests and clinical findingsC Fridman, M C Varela, F Kok, et al.
American Journal of Medical Genetics|June 15, 1993
Macrosomia, obesity, macrocephaly and ocular abnormalities (MOMO syndrome) in two unrelated patients: delineation of a newly recognized overgrowth syndromeD Moretti-Ferreira, C P Koiffmann, M Listik, et al.
Clinical Genetics|December 25, 2004
Impact of molecular mechanisms, including deletion size, on Prader-Willi syndrome phenotype: study of 75 patientsM C Varela, F Kok, N Setian, et al.
Revista Do Instituto De Medicina Tropical De Sao Paulo|January 1, 1971
[Complement of human serum in normal male and female children]C F Netto, T L Kipnis, A Manissadjian, et al.
Revista Do Instituto De Medicina Tropical De Sao Paulo|May 1, 1971
[Total human serum complement in acute diffuse glomerulonephritis, and in the nephrotic and Schönlein-Henoch syndromes]A Manissadjian, H A Penna, N Setian, et al.
Human Genetics|June 1, 1990
Investigation of the ZFY gene in XX true hermaphroditism and Swyer syndromeD Damiani, A E Billerbeck, A C Goldberg, et al.
Jornal De Pediatria|December 4, 2003
[Persistent hyperinsulinemic hypoglycemia of infancy: case report]D F Lazarine, M M Pahl, D Damiani, et al.
Pageof 3