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Cell Calcium
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March 22, 2016
Mitochondrial cytopathies
Ayman W El-Hattab, Fernando Scaglia
European Journal of Medical Genetics
|
May 3, 2012
Molecular bases and clinical spectrum of early infantile epileptic encephalopathies
Y Jane Tavyev Asher, Fernando Scaglia
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
February 7, 2013
Mitochondrial DNA depletion syndromes: review and updates of genetic basis, manifestations, and therapeutic options
Ayman W El-Hattab, Fernando Scaglia
Molecular Genetics and Metabolism
|
September 20, 2015
Disorders of carnitine biosynthesis and transport
Ayman W El-Hattab, Fernando Scaglia
Pediatrics in Review
|
May 31, 2026
Subacute Onset of Tremor, Ataxia, and Seizure-Like Episodes in a 7-Year-Old Boy
Steven H Lang, Ekta Bery, Fernando Scaglia
Journal of Inborn Errors of Metabolism and Screening
|
July 25, 2017
Arginine and citrulline for the treatment of MELAS syndrome
Ayman W El-Hattab, Mohammed Almannai, Fernando Scaglia
Essays in Biochemistry
|
June 29, 2018
Mitochondrial DNA replication: clinical syndromes
Mohammed Almannai, Ayman W El-Hattab, Fernando Scaglia
Molecular Genetics and Metabolism
|
March 31, 2004
Effect of alternative pathway therapy on branched chain amino acid metabolism in urea cycle disorder patients
Fernando Scaglia, Susan Carter, William E O'Brien, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
February 21, 2017
Mitochondrial DNA maintenance defects
Ayman W El-Hattab, William J Craigen, Fernando Scaglia
Molecular Genetics and Metabolism
|
October 27, 2018
Mitochondrial dynamics: Biological roles, molecular machinery, and related diseases
Ayman W El-Hattab, Jehan Suleiman, Mohammed Almannai, et al.
Page
of 19
Search research articles
Search
Showing results (11-20 of 190) with videos related to
Sort By:
Page
of 19
Cell Calcium
|
March 22, 2016
Mitochondrial cytopathies
Ayman W El-Hattab, Fernando Scaglia
European Journal of Medical Genetics
|
May 3, 2012
Molecular bases and clinical spectrum of early infantile epileptic encephalopathies
Y Jane Tavyev Asher, Fernando Scaglia
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
February 7, 2013
Mitochondrial DNA depletion syndromes: review and updates of genetic basis, manifestations, and therapeutic options
Ayman W El-Hattab, Fernando Scaglia
Molecular Genetics and Metabolism
|
September 20, 2015
Disorders of carnitine biosynthesis and transport
Ayman W El-Hattab, Fernando Scaglia
Pediatrics in Review
|
May 31, 2026
Subacute Onset of Tremor, Ataxia, and Seizure-Like Episodes in a 7-Year-Old Boy
Steven H Lang, Ekta Bery, Fernando Scaglia
Journal of Inborn Errors of Metabolism and Screening
|
July 25, 2017
Arginine and citrulline for the treatment of MELAS syndrome
Ayman W El-Hattab, Mohammed Almannai, Fernando Scaglia
Essays in Biochemistry
|
June 29, 2018
Mitochondrial DNA replication: clinical syndromes
Mohammed Almannai, Ayman W El-Hattab, Fernando Scaglia
Molecular Genetics and Metabolism
|
March 31, 2004
Effect of alternative pathway therapy on branched chain amino acid metabolism in urea cycle disorder patients
Fernando Scaglia, Susan Carter, William E O'Brien, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
February 21, 2017
Mitochondrial DNA maintenance defects
Ayman W El-Hattab, William J Craigen, Fernando Scaglia
Molecular Genetics and Metabolism
|
October 27, 2018
Mitochondrial dynamics: Biological roles, molecular machinery, and related diseases
Ayman W El-Hattab, Jehan Suleiman, Mohammed Almannai, et al.
Page
of 19