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T Gelbart

Showing results (61-70 of 81) with videos related to

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Medicine|November 1, 1992
Gaucher disease. Clinical, laboratory, radiologic, and genetic features of 53 patientsA Zimran, A Kay, T Gelbart, et al.
Blood|December 9, 2000
Molecular characterization of a case of atransferrinemiaE Beutler, T Gelbart, P Lee, et al.
Blood Cells, Molecules & Diseases|January 1, 1995
The clinical course of treated and untreated Gaucher disease. A study of 45 patientsE Beutler, A Demina, K Laubscher, et al.
Medicina|January 1, 1995
[Molecular diagnosis of Gaucher disease in Argentinian patients]C E Argaraña, I Givogri, R Dodelson de Kremer, et al.
Blood Cells, Molecules & Diseases|December 9, 2000
A new exon 9 glucose-6-phosphate dehydrogenase mutation (G6PD "Rehovot") in a Jewish Ethiopian family with variable phenotypesM Iancovici-Kidon, D Sthoeger, A Abrahamov, et al.
American Journal of Human Genetics|January 1, 1993
Gaucher disease: gene frequencies in the Ashkenazi Jewish populationE Beutler, N J Nguyen, M W Henneberger, et al.
Blood Cells, Molecules & Diseases|October 13, 2009
Polymorphisms and mutations of human TMPRSS6 in iron deficiency anemiaE Beutler, C Van Geet, D M W M te Loo, et al.
The New England Journal of Medicine|December 3, 1992
A less costly regimen of alglucerase to treat Gaucher's diseaseM L Figueroa, B E Rosenbloom, A C Kay, et al.
British Journal of Haematology|February 13, 2001
Hereditary non-spherocytic haemolytic anaemia due to red blood cell glutathione synthetase deficiency in four unrelated patients from Spain: clinical and molecular studiesJ L Corrons, R Alvarez, A Pujades, et al.
Blood|July 27, 2000
Triose phosphate isomerase deficiency in 3 French families: two novel null alleles, a frameshift mutation (TPI Alfortville) and an alteration in the initiation codon (TPI Paris)C Valentin, S Pissard, J Martin, et al.
Pageof 9

Showing results (61-70 of 81) with videos related to

Sort By:
Pageof 9
Medicine|November 1, 1992
Gaucher disease. Clinical, laboratory, radiologic, and genetic features of 53 patientsA Zimran, A Kay, T Gelbart, et al.
Blood|December 9, 2000
Molecular characterization of a case of atransferrinemiaE Beutler, T Gelbart, P Lee, et al.
Blood Cells, Molecules & Diseases|January 1, 1995
The clinical course of treated and untreated Gaucher disease. A study of 45 patientsE Beutler, A Demina, K Laubscher, et al.
Medicina|January 1, 1995
[Molecular diagnosis of Gaucher disease in Argentinian patients]C E Argaraña, I Givogri, R Dodelson de Kremer, et al.
Blood Cells, Molecules & Diseases|December 9, 2000
A new exon 9 glucose-6-phosphate dehydrogenase mutation (G6PD "Rehovot") in a Jewish Ethiopian family with variable phenotypesM Iancovici-Kidon, D Sthoeger, A Abrahamov, et al.
American Journal of Human Genetics|January 1, 1993
Gaucher disease: gene frequencies in the Ashkenazi Jewish populationE Beutler, N J Nguyen, M W Henneberger, et al.
Blood Cells, Molecules & Diseases|October 13, 2009
Polymorphisms and mutations of human TMPRSS6 in iron deficiency anemiaE Beutler, C Van Geet, D M W M te Loo, et al.
The New England Journal of Medicine|December 3, 1992
A less costly regimen of alglucerase to treat Gaucher's diseaseM L Figueroa, B E Rosenbloom, A C Kay, et al.
British Journal of Haematology|February 13, 2001
Hereditary non-spherocytic haemolytic anaemia due to red blood cell glutathione synthetase deficiency in four unrelated patients from Spain: clinical and molecular studiesJ L Corrons, R Alvarez, A Pujades, et al.
Blood|July 27, 2000
Triose phosphate isomerase deficiency in 3 French families: two novel null alleles, a frameshift mutation (TPI Alfortville) and an alteration in the initiation codon (TPI Paris)C Valentin, S Pissard, J Martin, et al.
Pageof 9