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Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
August 24, 2007
Genomic analysis of Brazilian patients with Fabry disease
F S Pereira, L B Jardim, C B Netto, et al.
Clinical Genetics
|
August 17, 2000
Aspartame loading test in PKU heterozygous individuals bearing severe and moderate mutations
L C da Silva, T S Carvalho, F B da Silva, et al.
American Journal of Medical Genetics
|
December 26, 2001
Molecular analysis of the Pi*Z allele in patients with liver disease
L C Lima, U Matte, S Leistner, et al.
Neuropediatrics
|
October 1, 1994
Pyridoxine-dependent seizures associated with white matter abnormalities
L B Jardim, R F Pires, C E Martins, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
November 28, 2008
The polymorphism of the serotonin-2A receptor T102C is associated with age
P F C Jobim, P A S Prado-Lima, C H A Schwanke, et al.
Journal of Inherited Metabolic Disease
|
January 26, 2006
Nonviral in vivo gene transfer in the mucopolysaccharidosis I murine model
M Camassola, L M Braga, A Delgado-Cañedo, et al.
British Journal of Haematology
|
July 10, 2001
Effects of imilglucerase withdrawal on an adult with Gaucher disease
I V Schwartz, S Karam, P Ashton-Prolla, et al.
Arquivos De Neuro-Psiquiatria
|
September 1, 1986
[Börjeson-Forssman-Lehmann syndrome: report of a case]
M Wojciechowski, C S Dutra-Filho, A C Da Costa, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health
|
June 13, 2001
A comprehensive screening program in South Brazil
E C Neto, J Schulte, E Anele, et al.
Clinical and Experimental Dermatology
|
October 22, 2009
Angiokeratoma: a cutaneous marker of Fabry's disease
L M J Albano, C Rivitti, D R Bertola, et al.
Page
of 17
Search research articles
Search
Showing results (91-100 of 164) with videos related to
Sort By:
Page
of 17
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
August 24, 2007
Genomic analysis of Brazilian patients with Fabry disease
F S Pereira, L B Jardim, C B Netto, et al.
Clinical Genetics
|
August 17, 2000
Aspartame loading test in PKU heterozygous individuals bearing severe and moderate mutations
L C da Silva, T S Carvalho, F B da Silva, et al.
American Journal of Medical Genetics
|
December 26, 2001
Molecular analysis of the Pi*Z allele in patients with liver disease
L C Lima, U Matte, S Leistner, et al.
Neuropediatrics
|
October 1, 1994
Pyridoxine-dependent seizures associated with white matter abnormalities
L B Jardim, R F Pires, C E Martins, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
November 28, 2008
The polymorphism of the serotonin-2A receptor T102C is associated with age
P F C Jobim, P A S Prado-Lima, C H A Schwanke, et al.
Journal of Inherited Metabolic Disease
|
January 26, 2006
Nonviral in vivo gene transfer in the mucopolysaccharidosis I murine model
M Camassola, L M Braga, A Delgado-Cañedo, et al.
British Journal of Haematology
|
July 10, 2001
Effects of imilglucerase withdrawal on an adult with Gaucher disease
I V Schwartz, S Karam, P Ashton-Prolla, et al.
Arquivos De Neuro-Psiquiatria
|
September 1, 1986
[Börjeson-Forssman-Lehmann syndrome: report of a case]
M Wojciechowski, C S Dutra-Filho, A C Da Costa, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health
|
June 13, 2001
A comprehensive screening program in South Brazil
E C Neto, J Schulte, E Anele, et al.
Clinical and Experimental Dermatology
|
October 22, 2009
Angiokeratoma: a cutaneous marker of Fabry's disease
L M J Albano, C Rivitti, D R Bertola, et al.
Page
of 17