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I V Schwartz

Showing results (1-10 of 12) with videos related to

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American Journal of Medical Genetics|May 15, 1994
Jones-Waldman syndrome: another report?L Schuler, A C Puga, I V Schwartz, et al.
Arquivos De Neuro-Psiquiatria|May 29, 1999
Clinical and molecular studies in five Brazilian cases of Friedreich ataxiaI V Schwartz, L B Jardim, A C Puga, et al.
Journal of Inherited Metabolic Disease|October 22, 2008
A Brazilian galactosialidosis patient given renal transplantation: a case reportA Kiss, P R G Zen, V Bittencourt, et al.
British Journal of Haematology|July 10, 2001
Effects of imilglucerase withdrawal on an adult with Gaucher diseaseI V Schwartz, S Karam, P Ashton-Prolla, et al.
Journal of Human Genetics|April 20, 2001
Glycogen storage disease type Ia: molecular study in Brazilian patientsF de C Reis, H C Caldas, D Y Norato, et al.
Public Health Genomics|May 2, 2009
The management of Gaucher disease in developing countries: a successful experience in Southern BrazilB C Krug, I V Schwartz, F Lopes de Oliveira, et al.
Clinical Genetics|October 1, 2010
Origin and spread of a common deletion causing mucolipidosis type II: insights from patterns of haplotypic diversityM F Coutinho, M Encarnação, R Gomes, et al.
Pediatrics|November 11, 2009
Multidisciplinary management of Hunter syndromeJoseph Muenzer, M Beck, C M Eng, et al.
Journal of Inherited Metabolic Disease|June 7, 2012
Enzyme replacement therapy for mucopolysaccharidosis VI: long-term cardiac effects of galsulfase (Naglazyme®) therapyE Braunlin, H Rosenfeld, C Kampmann, et al.
Clinical Genetics|August 25, 2004
Clinical and biochemical study of 28 patients with mucopolysaccharidosis type VIA C M M Azevedo, I V Schwartz, L Kalakun, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
American Journal of Medical Genetics|May 15, 1994
Jones-Waldman syndrome: another report?L Schuler, A C Puga, I V Schwartz, et al.
Arquivos De Neuro-Psiquiatria|May 29, 1999
Clinical and molecular studies in five Brazilian cases of Friedreich ataxiaI V Schwartz, L B Jardim, A C Puga, et al.
Journal of Inherited Metabolic Disease|October 22, 2008
A Brazilian galactosialidosis patient given renal transplantation: a case reportA Kiss, P R G Zen, V Bittencourt, et al.
British Journal of Haematology|July 10, 2001
Effects of imilglucerase withdrawal on an adult with Gaucher diseaseI V Schwartz, S Karam, P Ashton-Prolla, et al.
Journal of Human Genetics|April 20, 2001
Glycogen storage disease type Ia: molecular study in Brazilian patientsF de C Reis, H C Caldas, D Y Norato, et al.
Public Health Genomics|May 2, 2009
The management of Gaucher disease in developing countries: a successful experience in Southern BrazilB C Krug, I V Schwartz, F Lopes de Oliveira, et al.
Clinical Genetics|October 1, 2010
Origin and spread of a common deletion causing mucolipidosis type II: insights from patterns of haplotypic diversityM F Coutinho, M Encarnação, R Gomes, et al.
Pediatrics|November 11, 2009
Multidisciplinary management of Hunter syndromeJoseph Muenzer, M Beck, C M Eng, et al.
Journal of Inherited Metabolic Disease|June 7, 2012
Enzyme replacement therapy for mucopolysaccharidosis VI: long-term cardiac effects of galsulfase (Naglazyme®) therapyE Braunlin, H Rosenfeld, C Kampmann, et al.
Clinical Genetics|August 25, 2004
Clinical and biochemical study of 28 patients with mucopolysaccharidosis type VIA C M M Azevedo, I V Schwartz, L Kalakun, et al.
Pageof 2