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S W Moses

Showing results (41-50 of 71) with videos related to

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Pediatric Neurology|December 18, 2001
Neurophysiologic studies in congenital insensitivity to pain with anhidrosisZ Shorer, S W Moses, E Hershkovitz, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
A method for the diagnosis of glycogen storage disease type Ib using polymorphonuclear leukocytesN Bashan, R Potashnik, M Phillip, et al.
Israel Journal of Medical Sciences|January 1, 1991
Fructose-1,6-diphosphatase deficiency in IsraelS W Moses, N Bashan, B F Flasterstein, et al.
Pediatric Research|September 1, 1984
The dietary treatment of children with type I glycogen storage disease with slow release carbohydrateG P Smit, R Berger, R Potasnick, et al.
Journal of Inherited Metabolic Disease|May 19, 1998
Two new mutations in the 3' coding region of the glycogen debranching enzyme in a glycogen storage disease type IIIa Ashkenazi Jewish patientR Parvari, J Shen, E Hershkovitz, et al.
Journal of Inherited Metabolic Disease|May 26, 2004
Carnitine-acylcarnitine translocase deficiency: identification of a novel molecular defect in a Bedouin patientD Galron, O S Birk, A Kazanovitz, et al.
The Journal of Pediatrics|February 1, 1970
A clinical entity simulating familial dysautonomia in a North African Jewish familyR Schmidt, W J Alkan, S W Moses, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiencyS W Moses, M Aviram, R Geiger, et al.
Metabolism: Clinical and Experimental|January 1, 1974
Plasma renin activity and aldosterone in familial dysautonomiaD Rabinowitz, H Landau, A Rosler, et al.
European Journal of Pediatrics|January 1, 1993
Deficient glucose phosphorylation as a possible common denominator and its relation to abnormal leucocyte function, in glycogen storage disease 1b patientsN Bashan, R Potashnik, A Peist, et al.
Pageof 8

Showing results (41-50 of 71) with videos related to

Sort By:
Pageof 8
Pediatric Neurology|December 18, 2001
Neurophysiologic studies in congenital insensitivity to pain with anhidrosisZ Shorer, S W Moses, E Hershkovitz, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
A method for the diagnosis of glycogen storage disease type Ib using polymorphonuclear leukocytesN Bashan, R Potashnik, M Phillip, et al.
Israel Journal of Medical Sciences|January 1, 1991
Fructose-1,6-diphosphatase deficiency in IsraelS W Moses, N Bashan, B F Flasterstein, et al.
Pediatric Research|September 1, 1984
The dietary treatment of children with type I glycogen storage disease with slow release carbohydrateG P Smit, R Berger, R Potasnick, et al.
Journal of Inherited Metabolic Disease|May 19, 1998
Two new mutations in the 3' coding region of the glycogen debranching enzyme in a glycogen storage disease type IIIa Ashkenazi Jewish patientR Parvari, J Shen, E Hershkovitz, et al.
Journal of Inherited Metabolic Disease|May 26, 2004
Carnitine-acylcarnitine translocase deficiency: identification of a novel molecular defect in a Bedouin patientD Galron, O S Birk, A Kazanovitz, et al.
The Journal of Pediatrics|February 1, 1970
A clinical entity simulating familial dysautonomia in a North African Jewish familyR Schmidt, W J Alkan, S W Moses, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiencyS W Moses, M Aviram, R Geiger, et al.
Metabolism: Clinical and Experimental|January 1, 1974
Plasma renin activity and aldosterone in familial dysautonomiaD Rabinowitz, H Landau, A Rosler, et al.
European Journal of Pediatrics|January 1, 1993
Deficient glucose phosphorylation as a possible common denominator and its relation to abnormal leucocyte function, in glycogen storage disease 1b patientsN Bashan, R Potashnik, A Peist, et al.
Pageof 8