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C Acquaviva

Showing results (41-50 of 58) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 26, 2009
[Late onset 3-HMG-CoA lyase deficiency: a rare but treatable disorder]S Pierron, H Giudicelli, M Moreigne, et al.
Revue Du Rhumatisme Et Des Maladies Osteo-Articulaires|June 1, 1992
[Inflammatory myalgic syndrome and muscular mitochondrial abnormalities: 4 cases]G Serratrice, V Daumen-Legré, P Lafforgue, et al.
Neuropediatrics|July 4, 2007
Isolated sulfite oxidase deficiency in the newborn: lactic acidaemia and leukoencephalopathyS N Basheer, P J Waters, C W Lam, et al.
The Journal of Rheumatology|April 1, 1992
Elbow synovitis related to an intraarticular osteoid osteoma of the humerus, with immunologic and histochemical studiesP Lafforgue, E Senbel, J Boucraut, et al.
Revue Du Rhumatisme Et Des Maladies Osteo-Articulaires|May 1, 1992
[Aspects and role of spinal MRI in the assessment of solitary plasmacytoma and multiple myeloma. Apropos of 11 cases]P Lafforgue, D Clairet, C Chagnaud, et al.
Molecular Genetics and Metabolism|February 13, 2001
Molecular and structural analysis of two novel mutations in a patient with mut(-) methylmalonyl-CoA deficiencyJ F Benoist, C Acquaviva, I Callebaut, et al.
Revue Neurologique|July 14, 2009
[Multiple acyl-CoA dehydrogenase deficiency (MADD): a curable cause of genetic muscular lipidosis]E Maillart, C Acquaviva-Bourdain, O Rigal, et al.
Annales De Biologie Clinique|January 9, 2004
[RT-PCR in clinical diagnosis]H Cavé, C Acquaviva, I Bièche, et al.
European Journal of Human Genetics : EJHG|August 31, 2001
N219Y, a new frequent mutation among mut(degree) forms of methylmalonic acidemia in Caucasian patientsC Acquaviva, J F Benoist, I Callebaut, et al.
Case Reports in Critical Care|January 15, 2020
Myogenic Disease and Metabolic Acidosis: Consider Multiple Acyl-Coenzyme A Dehydrogenase DeficiencyA Dernoncourt, J Bouchereau, C Acquaviva-Bourdain, et al.
Pageof 6

Showing results (41-50 of 58) with videos related to

Sort By:
Pageof 6
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 26, 2009
[Late onset 3-HMG-CoA lyase deficiency: a rare but treatable disorder]S Pierron, H Giudicelli, M Moreigne, et al.
Revue Du Rhumatisme Et Des Maladies Osteo-Articulaires|June 1, 1992
[Inflammatory myalgic syndrome and muscular mitochondrial abnormalities: 4 cases]G Serratrice, V Daumen-Legré, P Lafforgue, et al.
Neuropediatrics|July 4, 2007
Isolated sulfite oxidase deficiency in the newborn: lactic acidaemia and leukoencephalopathyS N Basheer, P J Waters, C W Lam, et al.
The Journal of Rheumatology|April 1, 1992
Elbow synovitis related to an intraarticular osteoid osteoma of the humerus, with immunologic and histochemical studiesP Lafforgue, E Senbel, J Boucraut, et al.
Revue Du Rhumatisme Et Des Maladies Osteo-Articulaires|May 1, 1992
[Aspects and role of spinal MRI in the assessment of solitary plasmacytoma and multiple myeloma. Apropos of 11 cases]P Lafforgue, D Clairet, C Chagnaud, et al.
Molecular Genetics and Metabolism|February 13, 2001
Molecular and structural analysis of two novel mutations in a patient with mut(-) methylmalonyl-CoA deficiencyJ F Benoist, C Acquaviva, I Callebaut, et al.
Revue Neurologique|July 14, 2009
[Multiple acyl-CoA dehydrogenase deficiency (MADD): a curable cause of genetic muscular lipidosis]E Maillart, C Acquaviva-Bourdain, O Rigal, et al.
Annales De Biologie Clinique|January 9, 2004
[RT-PCR in clinical diagnosis]H Cavé, C Acquaviva, I Bièche, et al.
European Journal of Human Genetics : EJHG|August 31, 2001
N219Y, a new frequent mutation among mut(degree) forms of methylmalonic acidemia in Caucasian patientsC Acquaviva, J F Benoist, I Callebaut, et al.
Case Reports in Critical Care|January 15, 2020
Myogenic Disease and Metabolic Acidosis: Consider Multiple Acyl-Coenzyme A Dehydrogenase DeficiencyA Dernoncourt, J Bouchereau, C Acquaviva-Bourdain, et al.
Pageof 6