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F Invernizzi

Showing results (81-90 of 90) with videos related to

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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.
Biochimica Et Biophysica Acta|December 4, 2004
Clinical and molecular findings in children with complex I deficiencyM Bugiani, F Invernizzi, S Alberio, et al.
Alimentary Pharmacology & Therapeutics|July 2, 2016
Liver stiffness measurement reliability and main determinants of point shear-wave elastography in patients with chronic liver diseaseM Fraquelli, A Baccarin, G Casazza, et al.
Brain & Development|October 25, 2018
Restless Legs Syndrome in NKX2-1-related chorea: An expansion of the disease spectrumA Iodice, M Carecchio, G Zorzi, et al.
Brain & Development|May 5, 2019
Corrigendum to "Restless legs syndrome in NKX2-1-related chorea: An expansion of the disease spectrum" [Brain Dev. 41 (2019) 250-256]A Iodice, M Carecchio, G Zorzi, et al.
Journal of Medical Genetics|July 3, 2008
Identification of new mutations in the ETHE1 gene in a cohort of 14 patients presenting with ethylmalonic encephalopathyR Mineri, M Rimoldi, A B Burlina, et al.
Clinical and Experimental Rheumatology|November 2, 1999
Five-year follow-up of 165 Italian patients with undifferentiated connective tissue diseasesM G Danieli, P Fraticelli, F Franceschini, et al.
Mitochondrion|November 21, 2012
A multi-center comparison of diagnostic methods for the biochemical evaluation of suspected mitochondrial disordersR J T Rodenburg, G C Schoonderwoerd, V Tiranti, et al.
Frontiers in Public Health|March 5, 2021
ARC: An Open Web-Platform for Request/Supply Matching for a Prioritized and Controlled COVID-19 ResponseJean-Denis Courcol, Cédric F Invernizzi, Zachary C Landry, et al.
Pageof 9

Showing results (81-90 of 90) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 90 results.
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.
Biochimica Et Biophysica Acta|December 4, 2004
Clinical and molecular findings in children with complex I deficiencyM Bugiani, F Invernizzi, S Alberio, et al.
Alimentary Pharmacology & Therapeutics|July 2, 2016
Liver stiffness measurement reliability and main determinants of point shear-wave elastography in patients with chronic liver diseaseM Fraquelli, A Baccarin, G Casazza, et al.
Brain & Development|October 25, 2018
Restless Legs Syndrome in NKX2-1-related chorea: An expansion of the disease spectrumA Iodice, M Carecchio, G Zorzi, et al.
Brain & Development|May 5, 2019
Corrigendum to "Restless legs syndrome in NKX2-1-related chorea: An expansion of the disease spectrum" [Brain Dev. 41 (2019) 250-256]A Iodice, M Carecchio, G Zorzi, et al.
Journal of Medical Genetics|July 3, 2008
Identification of new mutations in the ETHE1 gene in a cohort of 14 patients presenting with ethylmalonic encephalopathyR Mineri, M Rimoldi, A B Burlina, et al.
Clinical and Experimental Rheumatology|November 2, 1999
Five-year follow-up of 165 Italian patients with undifferentiated connective tissue diseasesM G Danieli, P Fraticelli, F Franceschini, et al.
Mitochondrion|November 21, 2012
A multi-center comparison of diagnostic methods for the biochemical evaluation of suspected mitochondrial disordersR J T Rodenburg, G C Schoonderwoerd, V Tiranti, et al.
Frontiers in Public Health|March 5, 2021
ARC: An Open Web-Platform for Request/Supply Matching for a Prioritized and Controlled COVID-19 ResponseJean-Denis Courcol, Cédric F Invernizzi, Zachary C Landry, et al.
Pageof 9