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Showing results (91-100 of 98) with videos related to

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Clinica Chimica Acta; International Journal of Clinical Chemistry|August 31, 1995
3-Hydroxyisovalerylcarnitine in patients with deficiency of 3-methylcrotonyl CoA carboxylaseW Röschinger, D S Millington, D A Gage, et al.
Archives of Biochemistry and Biophysics|March 1, 1993
Expression and accumulation of lysyl oxidase, elastin, and type I procollagen in human Menkes and mottled mouse fibroblastsS Gacheru, C McGee, J Y Uriu-Hare, et al.
Neurology|March 26, 2003
Periventricular heterotopia associated with chromosome 5p anomaliesV L Sheen, J W Wheless, A Bodell, et al.
Archives of Dermatology|January 8, 1998
Methylmalonic acidemia, cobalamin C type, presenting with cutaneous manifestationsR Howard, I J Frieden, D Crawford, et al.
Clinical Genetics|March 4, 2008
Improvement of bone disease by imiglucerase (Cerezyme) therapy in patients with skeletal manifestations of type 1 Gaucher disease: results of a 48-month longitudinal cohort studyK B Sims, G M Pastores, N J Weinreb, et al.
Molecular Genetics and Metabolism|July 17, 2017
Biochemical characteristics of newborns with carnitine transporter defect identified by newborn screening in CaliforniaN M Gallant, K Leydiker, Y Wilnai, et al.
Human Molecular Genetics|May 1, 1997
The molecular basis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in compound heterozygous patients: is there correlation between genotype and phenotype?B S Andresen, P Bross, S Udvari, et al.
Blood|June 1, 1996
Outcome of unrelated donor bone marrow transplantation in 40 children with Hurler syndromeC Peters, M Balthazor, E G Shapiro, et al.
Pageof 10

Showing results (91-100 of 98) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 98 results.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 31, 1995
3-Hydroxyisovalerylcarnitine in patients with deficiency of 3-methylcrotonyl CoA carboxylaseW Röschinger, D S Millington, D A Gage, et al.
Archives of Biochemistry and Biophysics|March 1, 1993
Expression and accumulation of lysyl oxidase, elastin, and type I procollagen in human Menkes and mottled mouse fibroblastsS Gacheru, C McGee, J Y Uriu-Hare, et al.
Neurology|March 26, 2003
Periventricular heterotopia associated with chromosome 5p anomaliesV L Sheen, J W Wheless, A Bodell, et al.
Archives of Dermatology|January 8, 1998
Methylmalonic acidemia, cobalamin C type, presenting with cutaneous manifestationsR Howard, I J Frieden, D Crawford, et al.
Clinical Genetics|March 4, 2008
Improvement of bone disease by imiglucerase (Cerezyme) therapy in patients with skeletal manifestations of type 1 Gaucher disease: results of a 48-month longitudinal cohort studyK B Sims, G M Pastores, N J Weinreb, et al.
Molecular Genetics and Metabolism|July 17, 2017
Biochemical characteristics of newborns with carnitine transporter defect identified by newborn screening in CaliforniaN M Gallant, K Leydiker, Y Wilnai, et al.
Human Molecular Genetics|May 1, 1997
The molecular basis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in compound heterozygous patients: is there correlation between genotype and phenotype?B S Andresen, P Bross, S Udvari, et al.
Blood|June 1, 1996
Outcome of unrelated donor bone marrow transplantation in 40 children with Hurler syndromeC Peters, M Balthazor, E G Shapiro, et al.
Pageof 10