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Medicina|January 1, 1990

[Hepatic glycogen synthetase deficiency or glycogen storage disease-zero. Mild phenotype with partial enzymatic defect]R D de Kremer, A P de Capra, C D de Boldini, et al.

Medicina|January 1, 1992

[Phenotypic expression variation of isovaleric acidemia in Argentinian patients. A long term follow-up]R Dodelson de Kremer, C Depetris de Boldini, A Paschini de Capra, et al.

Scandinavian Journal of Rheumatology|March 18, 2000

Mesangial nephropathy in Sjögren's syndromeS Gamrón, G Barberis, C M Onetti, et al.

American Journal of Medical Genetics|September 15, 1992

Mucopolysaccharidosis type VII (beta-glucuronidase deficiency): a chronic variant with an oligosymptomatic severe skeletal dysplasiaR D de Kremer, I Givogri, C E Argaraña, et al.

American Journal of Medical Genetics|March 10, 2001

Barth's syndrome-like disorder: a new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation)R D De Kremer, A Paschini-Capra, S Bacman, et al.

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Search research articles

Showing results (11-20 of 15) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 15 results.

Medicina|January 1, 1990

[Hepatic glycogen synthetase deficiency or glycogen storage disease-zero. Mild phenotype with partial enzymatic defect]R D de Kremer, A P de Capra, C D de Boldini, et al.

Medicina|January 1, 1992

[Phenotypic expression variation of isovaleric acidemia in Argentinian patients. A long term follow-up]R Dodelson de Kremer, C Depetris de Boldini, A Paschini de Capra, et al.

Scandinavian Journal of Rheumatology|March 18, 2000

Mesangial nephropathy in Sjögren's syndromeS Gamrón, G Barberis, C M Onetti, et al.

American Journal of Medical Genetics|September 15, 1992

Mucopolysaccharidosis type VII (beta-glucuronidase deficiency): a chronic variant with an oligosymptomatic severe skeletal dysplasiaR D de Kremer, I Givogri, C E Argaraña, et al.

American Journal of Medical Genetics|March 10, 2001

Barth's syndrome-like disorder: a new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation)R D De Kremer, A Paschini-Capra, S Bacman, et al.

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