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Gut
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January 26, 2008
Waist circumference correlates with liver fibrosis in children with non-alcoholic steatohepatitis
M Manco, G Bedogni, M Marcellini, et al.
Neuromuscular Disorders : NMD
|
July 19, 2000
A novel SURF1 mutation results in Leigh syndrome with peripheral neuropathy caused by cytochrome c oxidase deficiency
L Santoro, R Carrozzo, A Malandrini, et al.
European Journal of Clinical Investigation
|
December 12, 2001
Glutathione in blood of patients with Friedreich's ataxia
F Piemonte, A Pastore, G Tozzi, et al.
American Journal of Medical Genetics
|
April 5, 2000
Novel 7-DHCR mutation in a child with Smith-Lemli-Opitz syndrome
C Patrono, C Rizzo, A Tessa, et al.
Neuromuscular Disorders : NMD
|
December 4, 2001
Hypertrophic cardiomyopathy and mtDNA depletion. Successful treatment with heart transplantation
F M Santorelli, M G Gagliardi, C Dionisi-Vici, et al.
Experientia
|
December 1, 1986
Enhancement of peritoneal macrophage activity by bovine gamma globulin in mice
P Di Nardo, G De Sanctis, P De Sole, et al.
Neurology
|
July 27, 2001
Fatal infantile leukodystrophy: a severe variant of CACH/VWM syndrome, allelic to chromosome 3q27
P Francalanci, E Eymard-Pierre, C Dionisi-Vici, et al.
Neurology
|
October 15, 2003
Atypical Leigh syndrome associated with the D393N mutation in the mitochondrial ND5 subunit
V Petruzzella, G Di Giacinto, S Scacco, et al.
Archives of Disease in Childhood
|
April 24, 2002
Antioxidant enzymes in blood of patients with Friedreich's ataxia
G Tozzi, M Nuccetelli, M Lo Bello, et al.
Clinical Genetics
|
November 29, 2016
Novel mutations in KARS cause hypertrophic cardiomyopathy and combined mitochondrial respiratory chain defect
D Verrigni, D Diodato, M Di Nottia, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 34) with videos related to
Sort By:
Page
of 4
Gut
|
January 26, 2008
Waist circumference correlates with liver fibrosis in children with non-alcoholic steatohepatitis
M Manco, G Bedogni, M Marcellini, et al.
Neuromuscular Disorders : NMD
|
July 19, 2000
A novel SURF1 mutation results in Leigh syndrome with peripheral neuropathy caused by cytochrome c oxidase deficiency
L Santoro, R Carrozzo, A Malandrini, et al.
European Journal of Clinical Investigation
|
December 12, 2001
Glutathione in blood of patients with Friedreich's ataxia
F Piemonte, A Pastore, G Tozzi, et al.
American Journal of Medical Genetics
|
April 5, 2000
Novel 7-DHCR mutation in a child with Smith-Lemli-Opitz syndrome
C Patrono, C Rizzo, A Tessa, et al.
Neuromuscular Disorders : NMD
|
December 4, 2001
Hypertrophic cardiomyopathy and mtDNA depletion. Successful treatment with heart transplantation
F M Santorelli, M G Gagliardi, C Dionisi-Vici, et al.
Experientia
|
December 1, 1986
Enhancement of peritoneal macrophage activity by bovine gamma globulin in mice
P Di Nardo, G De Sanctis, P De Sole, et al.
Neurology
|
July 27, 2001
Fatal infantile leukodystrophy: a severe variant of CACH/VWM syndrome, allelic to chromosome 3q27
P Francalanci, E Eymard-Pierre, C Dionisi-Vici, et al.
Neurology
|
October 15, 2003
Atypical Leigh syndrome associated with the D393N mutation in the mitochondrial ND5 subunit
V Petruzzella, G Di Giacinto, S Scacco, et al.
Archives of Disease in Childhood
|
April 24, 2002
Antioxidant enzymes in blood of patients with Friedreich's ataxia
G Tozzi, M Nuccetelli, M Lo Bello, et al.
Clinical Genetics
|
November 29, 2016
Novel mutations in KARS cause hypertrophic cardiomyopathy and combined mitochondrial respiratory chain defect
D Verrigni, D Diodato, M Di Nottia, et al.
Page
of 4