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E Lamantea

Showing results (21-30 of 27) with videos related to

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European Journal of Pediatrics|January 7, 1999
Acute, severe cardiomyopathy as main symptom of late-onset very long-chain acyl-coenzyme A dehydrogenase deficiencyR Parini, F Menni, B Garavaglia, et al.
European Journal of Pediatrics|May 14, 1998
Mild or absent clinical signs in twin sisters with short-chain acyl-CoA dehydrogenase deficiencyA Ribes, E Riudor, B Garavaglia, et al.
Journal of Inherited Metabolic Disease|January 7, 2009
Clinical and molecular features of mitochondrial DNA depletion syndromesA Spinazzola, F Invernizzi, F Carrara, et al.
Neurology|May 29, 2001
Epileptic phenotypes associated with mitochondrial disordersL Canafoglia, S Franceschetti, C Antozzi, et al.
Biochimica Et Biophysica Acta|December 4, 2004
Clinical and molecular findings in children with complex I deficiencyM Bugiani, F Invernizzi, S Alberio, et al.
Journal of Inherited Metabolic Disease|April 5, 2001
Sequence variations in the NDUFA1 gene encoding a subunit of complex I of the respiratory chainI Wittig, P Augstein, G K Brown, et al.
Journal of Medical Genetics|September 27, 2005
ETHE1 mutations are specific to ethylmalonic encephalopathyV Tiranti, E Briem, E Lamantea, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
European Journal of Pediatrics|January 7, 1999
Acute, severe cardiomyopathy as main symptom of late-onset very long-chain acyl-coenzyme A dehydrogenase deficiencyR Parini, F Menni, B Garavaglia, et al.
European Journal of Pediatrics|May 14, 1998
Mild or absent clinical signs in twin sisters with short-chain acyl-CoA dehydrogenase deficiencyA Ribes, E Riudor, B Garavaglia, et al.
Journal of Inherited Metabolic Disease|January 7, 2009
Clinical and molecular features of mitochondrial DNA depletion syndromesA Spinazzola, F Invernizzi, F Carrara, et al.
Neurology|May 29, 2001
Epileptic phenotypes associated with mitochondrial disordersL Canafoglia, S Franceschetti, C Antozzi, et al.
Biochimica Et Biophysica Acta|December 4, 2004
Clinical and molecular findings in children with complex I deficiencyM Bugiani, F Invernizzi, S Alberio, et al.
Journal of Inherited Metabolic Disease|April 5, 2001
Sequence variations in the NDUFA1 gene encoding a subunit of complex I of the respiratory chainI Wittig, P Augstein, G K Brown, et al.
Journal of Medical Genetics|September 27, 2005
ETHE1 mutations are specific to ethylmalonic encephalopathyV Tiranti, E Briem, E Lamantea, et al.
Pageof 3