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Minerva Pediatrica
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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 myopathy
T 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 disease
M 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 proteinuria
I Pela, M A Donati, E Zammarchi
Neuropediatrics
|
December 1, 1995
Transient neonatal nonketotic hyperglycinemia: a 13-year follow-up
E 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 function
I Pela, S Gasperini, E Pasquini, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
May 1, 1996
Cryptogenic hepatitis masking the diagnosis of ornithine transcarbamylase deficiency
E Zammarchi, M A Donati, L Filippi, et al.
Pediatric Neurology
|
July 1, 1994
Self-mutilation in a patient with mucolipidosis III
E 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 hyperammonemia
E 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.
Page
of 9
Search research articles
Search
Showing results (1-10 of 85) with videos related to
Sort By:
Page
of 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 myopathy
T 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 disease
M 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 proteinuria
I Pela, M A Donati, E Zammarchi
Neuropediatrics
|
December 1, 1995
Transient neonatal nonketotic hyperglycinemia: a 13-year follow-up
E 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 function
I Pela, S Gasperini, E Pasquini, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
May 1, 1996
Cryptogenic hepatitis masking the diagnosis of ornithine transcarbamylase deficiency
E Zammarchi, M A Donati, L Filippi, et al.
Pediatric Neurology
|
July 1, 1994
Self-mutilation in a patient with mucolipidosis III
E 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 hyperammonemia
E 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.
Page
of 9