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M A Donati

Showing results (1-10 of 85) with videos related to

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Minerva Pediatrica|November 26, 2009
[The key-role of the pediatrician in the diagnosis of accumulation diseases: the example of Pompe's disease]M A Donati
The Journal of Clinical Pediatric Dentistry|January 1, 1997
Craniofacial abnormalities associated with congenital fiber type disproportion myopathyT Baccetti, E Defraia, M A Donati
The Journal of Pediatrics|July 1, 1987
Prospective controlled study of home and hospital therapy of cystic fibrosis pulmonary diseaseM A Donati, G Guenette, H Auerbach
Journal of Inherited Metabolic Disease|January 5, 2002
Effect of ramipril in a patient with glycogen storage disease type I and nephrotic-range proteinuriaI Pela, M A Donati, E Zammarchi
Neuropediatrics|December 1, 1995
Transient neonatal nonketotic hyperglycinemia: a 13-year follow-upE Zammarchi, M A Donati, F Ciani
Clinical Nephrology|August 2, 2006
Hyperkalemia after acute metabolic decompensation in two children with vitamin B12-unresponsive methylmalonic acidemia and normal renal functionI Pela, S Gasperini, E Pasquini, et al.
Journal of Pediatric Gastroenterology and Nutrition|May 1, 1996
Cryptogenic hepatitis masking the diagnosis of ornithine transcarbamylase deficiencyE Zammarchi, M A Donati, L Filippi, et al.
Pediatric Neurology|July 1, 1994
Self-mutilation in a patient with mucolipidosis IIIE Zammarchi, A Savelli, M A Donati, et al.
Metabolism: Clinical and Experimental|August 1, 1996
Biochemical evaluation of a patient with a familial form of leucine-sensitive hypoglycemia and concomitant hyperammonemiaE Zammarchi, L Filippi, E Novembre, et al.
Rivista Di Neurobiologia : Organo Ufficiale Della Societa Dei Neurologi, Neuroradiologi E Neurochirurghi Ospedalieri|July 1, 1981
[Results of screening the urine of 26,014 newborn infants for amino acid disorders]E Zammarchi, M R Bardini, M A Donati, et al.
Pageof 9

Showing results (1-10 of 85) with videos related to

Sort By:
Pageof 9
Minerva Pediatrica|November 26, 2009
[The key-role of the pediatrician in the diagnosis of accumulation diseases: the example of Pompe's disease]M A Donati
The Journal of Clinical Pediatric Dentistry|January 1, 1997
Craniofacial abnormalities associated with congenital fiber type disproportion myopathyT Baccetti, E Defraia, M A Donati
The Journal of Pediatrics|July 1, 1987
Prospective controlled study of home and hospital therapy of cystic fibrosis pulmonary diseaseM A Donati, G Guenette, H Auerbach
Journal of Inherited Metabolic Disease|January 5, 2002
Effect of ramipril in a patient with glycogen storage disease type I and nephrotic-range proteinuriaI Pela, M A Donati, E Zammarchi
Neuropediatrics|December 1, 1995
Transient neonatal nonketotic hyperglycinemia: a 13-year follow-upE Zammarchi, M A Donati, F Ciani
Clinical Nephrology|August 2, 2006
Hyperkalemia after acute metabolic decompensation in two children with vitamin B12-unresponsive methylmalonic acidemia and normal renal functionI Pela, S Gasperini, E Pasquini, et al.
Journal of Pediatric Gastroenterology and Nutrition|May 1, 1996
Cryptogenic hepatitis masking the diagnosis of ornithine transcarbamylase deficiencyE Zammarchi, M A Donati, L Filippi, et al.
Pediatric Neurology|July 1, 1994
Self-mutilation in a patient with mucolipidosis IIIE Zammarchi, A Savelli, M A Donati, et al.
Metabolism: Clinical and Experimental|August 1, 1996
Biochemical evaluation of a patient with a familial form of leucine-sensitive hypoglycemia and concomitant hyperammonemiaE Zammarchi, L Filippi, E Novembre, et al.
Rivista Di Neurobiologia : Organo Ufficiale Della Societa Dei Neurologi, Neuroradiologi E Neurochirurghi Ospedalieri|July 1, 1981
[Results of screening the urine of 26,014 newborn infants for amino acid disorders]E Zammarchi, M R Bardini, M A Donati, et al.
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