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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 line
F 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 study
E 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 infant
A 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 review
M 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 I
H 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 adriamycin
R 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 therapy
A E Slonim, R A Coleman, M A McElligot, et al.
Neurology
|
April 11, 2001
Familial cerebellar ataxia with muscle coenzyme Q10 deficiency
O Musumeci, A Naini, A E Slonim, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 48) with videos related to
Sort By:
Page
of 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 line
F 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 study
E 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 infant
A 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 review
M 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 I
H 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 adriamycin
R 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 therapy
A E Slonim, R A Coleman, M A McElligot, et al.
Neurology
|
April 11, 2001
Familial cerebellar ataxia with muscle coenzyme Q10 deficiency
O Musumeci, A Naini, A E Slonim, et al.
Page
of 5