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A E Slonim

Showing results (41-50 of 48) with videos related to

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Biochemical and Biophysical Research Communications|October 12, 2000
Correction of glycogen storage disease type II by enzyme replacement with a recombinant human acid maltase produced by over-expression in a CHO-DHFR(neg) cell lineF Martiniuk, A Chen, V Donnabella, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1995
Metabolic and clinical response to recombinant human insulin-like growth factor I in myotonic dystrophy--a clinical research center studyE Vlachopapadopoulou, J J Zachwieja, J M Gertner, et al.
The Journal of Pediatrics|October 1, 1981
Dietary-dependent carnitine deficiency as a cause of nonketotic hypoglycemia in an infantA E Slonim, P R Borum, K Tanaka, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 7, 1999
Early onset of diabetes mellitus associated with the mitochondrial DNA T14709C point mutation: patient report and literature reviewM E Damore, P W Speiser, A E Slonim, et al.
The Journal of Clinical Investigation|August 1, 1978
ATP depletion, a possible role in the pathogenesis of hyperuricemia in glycogen storage disease type IH L Greene, F A Wilson, P Hefferan, et al.
The Journal of Pharmacology and Experimental Therapeutics|November 1, 1980
Regulatory role of glutathione and soluble sulfhydryl groups in the toxicity of adriamycinR D Olson, J S MacDonald, C J vanBoxtel, et al.
Neurology|January 1, 1983
Improvement of muscle function in acid maltase deficiency by high-protein therapyA E Slonim, R A Coleman, M A McElligot, et al.
Neurology|April 11, 2001
Familial cerebellar ataxia with muscle coenzyme Q10 deficiencyO Musumeci, A Naini, A E Slonim, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
Biochemical and Biophysical Research Communications|October 12, 2000
Correction of glycogen storage disease type II by enzyme replacement with a recombinant human acid maltase produced by over-expression in a CHO-DHFR(neg) cell lineF Martiniuk, A Chen, V Donnabella, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1995
Metabolic and clinical response to recombinant human insulin-like growth factor I in myotonic dystrophy--a clinical research center studyE Vlachopapadopoulou, J J Zachwieja, J M Gertner, et al.
The Journal of Pediatrics|October 1, 1981
Dietary-dependent carnitine deficiency as a cause of nonketotic hypoglycemia in an infantA E Slonim, P R Borum, K Tanaka, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 7, 1999
Early onset of diabetes mellitus associated with the mitochondrial DNA T14709C point mutation: patient report and literature reviewM E Damore, P W Speiser, A E Slonim, et al.
The Journal of Clinical Investigation|August 1, 1978
ATP depletion, a possible role in the pathogenesis of hyperuricemia in glycogen storage disease type IH L Greene, F A Wilson, P Hefferan, et al.
The Journal of Pharmacology and Experimental Therapeutics|November 1, 1980
Regulatory role of glutathione and soluble sulfhydryl groups in the toxicity of adriamycinR D Olson, J S MacDonald, C J vanBoxtel, et al.
Neurology|January 1, 1983
Improvement of muscle function in acid maltase deficiency by high-protein therapyA E Slonim, R A Coleman, M A McElligot, et al.
Neurology|April 11, 2001
Familial cerebellar ataxia with muscle coenzyme Q10 deficiencyO Musumeci, A Naini, A E Slonim, et al.
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