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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 deficiency
A Ribes, E Riudor, B Garavaglia, et al.
Journal of Inherited Metabolic Disease
|
January 7, 2009
Clinical and molecular features of mitochondrial DNA depletion syndromes
A Spinazzola, F Invernizzi, F Carrara, et al.
Biochimica Et Biophysica Acta
|
December 4, 2004
Clinical and molecular findings in children with complex I deficiency
M 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 disease
M 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 spectrum
A 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 encephalopathy
R 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 diseases
M 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 disorders
R 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 Response
Jean-Denis Courcol, Cédric F Invernizzi, Zachary C Landry, et al.
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of 9
Search research articles
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Showing results (81-90 of 90) with videos related to
Sort By:
Page
of 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 deficiency
A Ribes, E Riudor, B Garavaglia, et al.
Journal of Inherited Metabolic Disease
|
January 7, 2009
Clinical and molecular features of mitochondrial DNA depletion syndromes
A Spinazzola, F Invernizzi, F Carrara, et al.
Biochimica Et Biophysica Acta
|
December 4, 2004
Clinical and molecular findings in children with complex I deficiency
M 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 disease
M 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 spectrum
A 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 encephalopathy
R 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 diseases
M 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 disorders
R 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 Response
Jean-Denis Courcol, Cédric F Invernizzi, Zachary C Landry, et al.
Page
of 9