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R Cerone

Showing results (51-60 of 55) with videos related to

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American Journal of Human Genetics|January 1, 1985
The natural history of homocystinuria due to cystathionine beta-synthase deficiencyS H Mudd, F Skovby, H L Levy, et al.
Metabolism: Clinical and Experimental|September 1, 1992
The pathobiochemistry of uremia and hyperargininemia further demonstrates a metabolic relationship between urea and guanidinosuccinic acidB Marescau, P P De Deyn, I A Qureshi, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Respiratory-chain and pyruvate metabolism defects: Italian collaborative survey on 72 patientsU Caruso, A Adami, E Bertini, et al.
Clinical Genetics|January 12, 2010
Phenotypic variability, neurological outcome and genetics background of 6-pyruvoyl-tetrahydropterin synthase deficiencyV Leuzzi, C A Carducci, C L Carducci, et al.
Journal of Inherited Metabolic Disease|October 13, 2001
Glycine N-methyltransferase deficiency: a novel inborn error causing persistent isolated hypermethioninaemiaS H Mudd, R Cerone, M C Schiaffino, et al.
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Showing results (51-60 of 55) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 55 results.
American Journal of Human Genetics|January 1, 1985
The natural history of homocystinuria due to cystathionine beta-synthase deficiencyS H Mudd, F Skovby, H L Levy, et al.
Metabolism: Clinical and Experimental|September 1, 1992
The pathobiochemistry of uremia and hyperargininemia further demonstrates a metabolic relationship between urea and guanidinosuccinic acidB Marescau, P P De Deyn, I A Qureshi, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Respiratory-chain and pyruvate metabolism defects: Italian collaborative survey on 72 patientsU Caruso, A Adami, E Bertini, et al.
Clinical Genetics|January 12, 2010
Phenotypic variability, neurological outcome and genetics background of 6-pyruvoyl-tetrahydropterin synthase deficiencyV Leuzzi, C A Carducci, C L Carducci, et al.
Journal of Inherited Metabolic Disease|October 13, 2001
Glycine N-methyltransferase deficiency: a novel inborn error causing persistent isolated hypermethioninaemiaS H Mudd, R Cerone, M C Schiaffino, et al.
Pageof 6