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Archives of Neurology
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August 2, 2001
A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndrome
S Seneca, H Verhelst, L De Meirleir, et al.
American Journal of Medical Genetics. Part A
|
March 13, 2012
Acetazolamide for severe apnea in Pitt-Hopkins syndrome
Stijn L Verhulst, J De Dooy, J Ramet, et al.
The Veterinary Quarterly
|
November 4, 2014
Ultrastructural mitochondrial alterations in equine myopathies of unknown origin
K Van Driessche, R Ducatelle, K Chiers, et al.
Journal of Medical Genetics
|
February 6, 2004
Respiratory chain complex V deficiency due to a mutation in the assembly gene ATP12
L De Meirleir, S Seneca, W Lissens, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
April 13, 2004
Intractable ulcerative colitis of infancy in a child with mitochondrial respiratory chain disorder
M Vanderborght, M C Nassogne, D Hermans, et al.
Child: Care, Health and Development
|
October 5, 2006
Visual contribution to walking in children with Developmental Coordination Disorder
F J A Deconinck, D De Clercq, G J P Savelsbergh, et al.
Acta Gastro-Enterologica Belgica
|
November 12, 2009
Abdominal pain and vomiting as first sign of mitochondrial disease
S Van Biervliet, P Verloo, S Vande Veldel, et al.
Clinical Genetics
|
June 24, 2011
A novel NDUFV1 gene mutation in complex I deficiency in consanguineous siblings with brainstem lesions and Leigh syndrome
C Vilain, C Rens, A Aeby, et al.
Journal of Clinical Pathology
|
February 3, 2009
Immunohistochemical analysis of the oxidative phosphorylation complexes in skeletal muscle from patients with mitochondrial DNA encoded tRNA gene defects
B De Paepe, J Smet, M Lammens, et al.
Molecular Genetics and Metabolism
|
January 18, 2018
Dysregulated autophagy in restrictive cardiomyopathy due to Pro209Leu mutation in BAG3
A Schänzer, S Rupp, S Gräf, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 46) with videos related to
Sort By:
Page
of 5
Archives of Neurology
|
August 2, 2001
A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndrome
S Seneca, H Verhelst, L De Meirleir, et al.
American Journal of Medical Genetics. Part A
|
March 13, 2012
Acetazolamide for severe apnea in Pitt-Hopkins syndrome
Stijn L Verhulst, J De Dooy, J Ramet, et al.
The Veterinary Quarterly
|
November 4, 2014
Ultrastructural mitochondrial alterations in equine myopathies of unknown origin
K Van Driessche, R Ducatelle, K Chiers, et al.
Journal of Medical Genetics
|
February 6, 2004
Respiratory chain complex V deficiency due to a mutation in the assembly gene ATP12
L De Meirleir, S Seneca, W Lissens, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
April 13, 2004
Intractable ulcerative colitis of infancy in a child with mitochondrial respiratory chain disorder
M Vanderborght, M C Nassogne, D Hermans, et al.
Child: Care, Health and Development
|
October 5, 2006
Visual contribution to walking in children with Developmental Coordination Disorder
F J A Deconinck, D De Clercq, G J P Savelsbergh, et al.
Acta Gastro-Enterologica Belgica
|
November 12, 2009
Abdominal pain and vomiting as first sign of mitochondrial disease
S Van Biervliet, P Verloo, S Vande Veldel, et al.
Clinical Genetics
|
June 24, 2011
A novel NDUFV1 gene mutation in complex I deficiency in consanguineous siblings with brainstem lesions and Leigh syndrome
C Vilain, C Rens, A Aeby, et al.
Journal of Clinical Pathology
|
February 3, 2009
Immunohistochemical analysis of the oxidative phosphorylation complexes in skeletal muscle from patients with mitochondrial DNA encoded tRNA gene defects
B De Paepe, J Smet, M Lammens, et al.
Molecular Genetics and Metabolism
|
January 18, 2018
Dysregulated autophagy in restrictive cardiomyopathy due to Pro209Leu mutation in BAG3
A Schänzer, S Rupp, S Gräf, et al.
Page
of 5