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A Zimran

Showing results (111-120 of 135) with videos related to

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QJM : Monthly Journal of the Association of Physicians|September 1, 1996
Occurrence of Parkinson's syndrome in type I Gaucher diseaseO Neudorfer, N Giladi, D Elstein, et al.
Acta Haematologica|January 1, 1997
Pulmonary hypertension in two patients with type I Gaucher disease while on alglucerase therapyD Harats, R Pauzner, D Elstein, et al.
Blood Cells, Molecules & Diseases|May 16, 1998
Geographic variance in the frequency of the t(14;18) translocation in follicular lymphoma: an Israeli series compared to the worldM J Segel, O Paltiel, A Zimran, et al.
Pediatric Research|March 1, 1990
Identification of the heterozygotes for deficiency of the beta-subunit of the eighth component of complement by reduced levels of C8 beta and increased amounts of free C8 alpha-gammaW Nürnberger, V Wahn, L Roncelli, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|July 6, 2016
Anthropometric adjustments are helpful in the interpretation of BMD and BMC Z-scores of pediatric patients with Prader-Willi syndromeT N Hangartner, D F Short, T Eldar-Geva, et al.
European Journal of Neurology|February 5, 2019
Prodromal substantia nigra sonography undermines suggested association between substrate accumulation and the risk for GBA-related Parkinson's diseaseD Arkadir, T Dinur, M Becker Cohen, et al.
Journal of Clinical Immunology|November 1, 1995
Natural autoantibodies in sera of patients with Gaucher's diseaseY Shoenfeld, A Beresovski, D Zharhary, et al.
The European Respiratory Journal|February 1, 1996
Pulmonary function abnormalities in type I Gaucher diseaseE Kerem, D Elstein, A Abrahamov, et al.
The American Journal of Medicine|July 1, 1994
Low-dose enzyme replacement therapy for Gaucher's disease: effects of age, sex, genotype, and clinical features on response to treatmentA Zimran, D Elstein, R Kannai, et al.
American Journal of Human Genetics|October 1, 1993
Prevalence of nine mutations among Jewish and non-Jewish Gaucher disease patientsM Horowitz, G Tzuri, N Eyal, et al.
Pageof 14

Showing results (111-120 of 135) with videos related to

Sort By:
Pageof 14
QJM : Monthly Journal of the Association of Physicians|September 1, 1996
Occurrence of Parkinson's syndrome in type I Gaucher diseaseO Neudorfer, N Giladi, D Elstein, et al.
Acta Haematologica|January 1, 1997
Pulmonary hypertension in two patients with type I Gaucher disease while on alglucerase therapyD Harats, R Pauzner, D Elstein, et al.
Blood Cells, Molecules & Diseases|May 16, 1998
Geographic variance in the frequency of the t(14;18) translocation in follicular lymphoma: an Israeli series compared to the worldM J Segel, O Paltiel, A Zimran, et al.
Pediatric Research|March 1, 1990
Identification of the heterozygotes for deficiency of the beta-subunit of the eighth component of complement by reduced levels of C8 beta and increased amounts of free C8 alpha-gammaW Nürnberger, V Wahn, L Roncelli, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|July 6, 2016
Anthropometric adjustments are helpful in the interpretation of BMD and BMC Z-scores of pediatric patients with Prader-Willi syndromeT N Hangartner, D F Short, T Eldar-Geva, et al.
European Journal of Neurology|February 5, 2019
Prodromal substantia nigra sonography undermines suggested association between substrate accumulation and the risk for GBA-related Parkinson's diseaseD Arkadir, T Dinur, M Becker Cohen, et al.
Journal of Clinical Immunology|November 1, 1995
Natural autoantibodies in sera of patients with Gaucher's diseaseY Shoenfeld, A Beresovski, D Zharhary, et al.
The European Respiratory Journal|February 1, 1996
Pulmonary function abnormalities in type I Gaucher diseaseE Kerem, D Elstein, A Abrahamov, et al.
The American Journal of Medicine|July 1, 1994
Low-dose enzyme replacement therapy for Gaucher's disease: effects of age, sex, genotype, and clinical features on response to treatmentA Zimran, D Elstein, R Kannai, et al.
American Journal of Human Genetics|October 1, 1993
Prevalence of nine mutations among Jewish and non-Jewish Gaucher disease patientsM Horowitz, G Tzuri, N Eyal, et al.
Pageof 14