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R Carrozzo

Showing results (21-30 of 76) with videos related to

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The Journal of Biological Chemistry|March 30, 2001
Cytochrome c oxidase-deficient patients have distinct subunit assembly profilesB J Hanson, R Carrozzo, F Piemonte, et al.
Circulation|October 1, 1991
Muscle carnitine deficiency in patients with severe peripheral vascular diseaseG Brevetti, C Angelini, M Rosa, et al.
American Journal of Medical Genetics|October 23, 1997
Multiple congenital anomalies, brain hypomyelination, and ocular albinism in a female with dup(X) (pter-->q24::q21.32-->qter) and random X inactivationR Carrozzo, G Arrigo, E Rossi, et al.
Molecular and Cellular Biochemistry|October 8, 1990
Liver fatty acid-binding protein in two cases of human lipid storageL Vergani, M Fanin, A Martinuzzi, et al.
Journal of Inherited Metabolic Disease|May 7, 2005
Increased NO production in lysinuric protein intoleranceL Mannucci, F Emma, M Markert, et al.
American Journal of Medical Genetics|November 1, 1991
Deletion of the distal short arm of the X chromosome (Xp) in a patient with short stature, chondrodysplasia punctata, and X-linked ichthyosis due to steroid sulfatase deficiencyA Ballabio, M Zollo, R Carrozzo, et al.
Muscle & Nerve|September 1, 1997
Changes in skeletal muscle histology and metabolism in patients undergoing exercise deconditioning: effect of propionyl-L-carnitineG Brevetti, M Fanin, V De Amicis, et al.
The Journal of Clinical Investigation|October 1, 1993
Expression of muscle-type phosphorylase in innervated and aneural cultured muscle of patients with myophosphorylase deficiencyA Martinuzzi, L Vergani, R Carrozzo, et al.
Human Molecular Genetics|February 1, 1997
Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndromeC Lo Nigro, C S Chong, A C Smith, et al.
Biochemical and Biophysical Research Communications|May 25, 1995
MtDNA mutations associated with Leber's hereditary optic neuropathy: studies on cytoplasmic hybrid (cybrid) cellsL Vergani, A Martinuzzi, V Carelli, et al.
Pageof 8

Showing results (21-30 of 76) with videos related to

Sort By:
Pageof 8
The Journal of Biological Chemistry|March 30, 2001
Cytochrome c oxidase-deficient patients have distinct subunit assembly profilesB J Hanson, R Carrozzo, F Piemonte, et al.
Circulation|October 1, 1991
Muscle carnitine deficiency in patients with severe peripheral vascular diseaseG Brevetti, C Angelini, M Rosa, et al.
American Journal of Medical Genetics|October 23, 1997
Multiple congenital anomalies, brain hypomyelination, and ocular albinism in a female with dup(X) (pter-->q24::q21.32-->qter) and random X inactivationR Carrozzo, G Arrigo, E Rossi, et al.
Molecular and Cellular Biochemistry|October 8, 1990
Liver fatty acid-binding protein in two cases of human lipid storageL Vergani, M Fanin, A Martinuzzi, et al.
Journal of Inherited Metabolic Disease|May 7, 2005
Increased NO production in lysinuric protein intoleranceL Mannucci, F Emma, M Markert, et al.
American Journal of Medical Genetics|November 1, 1991
Deletion of the distal short arm of the X chromosome (Xp) in a patient with short stature, chondrodysplasia punctata, and X-linked ichthyosis due to steroid sulfatase deficiencyA Ballabio, M Zollo, R Carrozzo, et al.
Muscle & Nerve|September 1, 1997
Changes in skeletal muscle histology and metabolism in patients undergoing exercise deconditioning: effect of propionyl-L-carnitineG Brevetti, M Fanin, V De Amicis, et al.
The Journal of Clinical Investigation|October 1, 1993
Expression of muscle-type phosphorylase in innervated and aneural cultured muscle of patients with myophosphorylase deficiencyA Martinuzzi, L Vergani, R Carrozzo, et al.
Human Molecular Genetics|February 1, 1997
Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndromeC Lo Nigro, C S Chong, A C Smith, et al.
Biochemical and Biophysical Research Communications|May 25, 1995
MtDNA mutations associated with Leber's hereditary optic neuropathy: studies on cytoplasmic hybrid (cybrid) cellsL Vergani, A Martinuzzi, V Carelli, et al.
Pageof 8