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A Zimran

Showing results (71-80 of 135) with videos related to

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Clinical Genetics|July 25, 2008
Attitudes of couples identified through screening as carriers of Gaucher disease type 1S Zuckerman, A Lahad, A Zimran, et al.
QJM : Monthly Journal of the Association of Physicians|November 3, 1998
Low-dose low-frequency imiglucerase as a starting regimen of enzyme replacement therapy for patients with type I Gaucher diseaseD Elstein, A Abrahamov, I Hadas-Halpern, et al.
Retina (Philadelphia, Pa.)|December 22, 1999
Preretinal white dots in adult-type Gaucher diseaseG Wollstein, D Elstein, I Strassman, et al.
Clinical and Laboratory Haematology|October 31, 2001
Effect of ozone on neutrophil function in vitroM Margalit, E Attias, D Attias, et al.
Harefuah|December 16, 1990
[Pneumatosis cystoides intestinalis of the splenic flexure]G A Morali, D Z Braverman, A Zimran, et al.
British Journal of Haematology|December 1, 1993
Low-dose high-frequency enzyme replacement therapy for very young children with severe Gaucher diseaseA Zimran, I Hadas-Halpern, S Zevin, et al.
Oral Diseases|January 19, 2012
Mandibular and dental manifestations of Gaucher diseaseH R Saranjam, E Sidransky, W Z Levine, et al.
The Journal of Clinical Investigation|January 1, 1990
A glucocerebrosidase fusion gene in Gaucher disease. Implications for the molecular anatomy, pathogenesis, and diagnosis of this disorderA Zimran, J Sorge, E Gross, et al.
Lancet (London, England)|August 12, 1989
Prediction of severity of Gaucher's disease by identification of mutations at DNA levelA Zimran, J Sorge, E Gross, et al.
British Journal of Haematology|September 1, 1999
Is there a correlation between degree of splenomegaly, symptoms and hypersplenism? A study of 218 patients with Gaucher diseaseY Gielchinsky, D Elstein, I Hadas-Halpern, et al.
Pageof 14

Showing results (71-80 of 135) with videos related to

Sort By:
Pageof 14
Clinical Genetics|July 25, 2008
Attitudes of couples identified through screening as carriers of Gaucher disease type 1S Zuckerman, A Lahad, A Zimran, et al.
QJM : Monthly Journal of the Association of Physicians|November 3, 1998
Low-dose low-frequency imiglucerase as a starting regimen of enzyme replacement therapy for patients with type I Gaucher diseaseD Elstein, A Abrahamov, I Hadas-Halpern, et al.
Retina (Philadelphia, Pa.)|December 22, 1999
Preretinal white dots in adult-type Gaucher diseaseG Wollstein, D Elstein, I Strassman, et al.
Clinical and Laboratory Haematology|October 31, 2001
Effect of ozone on neutrophil function in vitroM Margalit, E Attias, D Attias, et al.
Harefuah|December 16, 1990
[Pneumatosis cystoides intestinalis of the splenic flexure]G A Morali, D Z Braverman, A Zimran, et al.
British Journal of Haematology|December 1, 1993
Low-dose high-frequency enzyme replacement therapy for very young children with severe Gaucher diseaseA Zimran, I Hadas-Halpern, S Zevin, et al.
Oral Diseases|January 19, 2012
Mandibular and dental manifestations of Gaucher diseaseH R Saranjam, E Sidransky, W Z Levine, et al.
The Journal of Clinical Investigation|January 1, 1990
A glucocerebrosidase fusion gene in Gaucher disease. Implications for the molecular anatomy, pathogenesis, and diagnosis of this disorderA Zimran, J Sorge, E Gross, et al.
Lancet (London, England)|August 12, 1989
Prediction of severity of Gaucher's disease by identification of mutations at DNA levelA Zimran, J Sorge, E Gross, et al.
British Journal of Haematology|September 1, 1999
Is there a correlation between degree of splenomegaly, symptoms and hypersplenism? A study of 218 patients with Gaucher diseaseY Gielchinsky, D Elstein, I Hadas-Halpern, et al.
Pageof 14