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Rivista Di Neurobiologia : Organo Ufficiale Della Societa Dei Neurologi, Neuroradiologi E Neurochirurghi Ospedalieri
|
July 1, 1981
[Screening for amino acids disorders in newborn infants in the city of Florence and neighboring towns from 1973 to 1980. Organizational model]
E Zammarchi, M R Bardini, M A Donati, et al.
Journal of Inherited Metabolic Disease
|
September 10, 2005
Successful prenatal molecular diagnosis of carbamyl-phosphate synthetase I deficiency in two at-risk pregnancies
S Funghini, A Morrone, E Pasquini, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
July 1, 1994
Familial infantile myasthenia: a neuromuscular cause of respiratory failure
E Zammarchi, M A Donati, S Masi, et al.
Clinical Pediatrics
|
October 1, 1995
Fructose-1,6-diphosphatase deficiency misdiagnosed as Reye syndrome
E Zammarchi, M A Donati, F Ciani, et al.
Human Mutation
|
September 5, 2003
Structural organization of the human carbamyl phosphate synthetase I gene (CPS1) and identification of two novel genetic lesions
S Funghini, M A Donati, E Pasquini, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
March 1, 1997
[Hyperglycinemia in clinical-laboratory practice]
F Ciani, E Pasquini, A Ciardetti, et al.
Clinical Nutrition (Edinburgh, Scotland)
|
June 27, 2000
Prolonged exclusive breast-feeding from vegan mother causing an acute onset of isolated methylmalonic aciduria due to a mild mutase deficiency
F Ciani, G M Poggi, E Pasquini, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
July 1, 1983
[Case report of a stage IV S neuroblastoma regressing without any aggressive treatment]
A Milanesi, E Zammarchi, G Bernini, et al.
La Pediatria
|
March 31, 1981
[Thromboembolic manifestations in a case of homocystinuria]
E Zammarchi, M R Bardini, G Cotrozzi, et al.
Clinical Nephrology
|
July 5, 2011
Hemolytic uremic syndrome and rhabdomyolysis in a patient with succinate coenzyme Q reductase (complex II) deficiency
M V Micheletti, G Lavoratti, S Gasperini, et al.
Page
of 9
Search research articles
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Showing results (11-20 of 85) with videos related to
Sort By:
Page
of 9
Rivista Di Neurobiologia : Organo Ufficiale Della Societa Dei Neurologi, Neuroradiologi E Neurochirurghi Ospedalieri
|
July 1, 1981
[Screening for amino acids disorders in newborn infants in the city of Florence and neighboring towns from 1973 to 1980. Organizational model]
E Zammarchi, M R Bardini, M A Donati, et al.
Journal of Inherited Metabolic Disease
|
September 10, 2005
Successful prenatal molecular diagnosis of carbamyl-phosphate synthetase I deficiency in two at-risk pregnancies
S Funghini, A Morrone, E Pasquini, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
July 1, 1994
Familial infantile myasthenia: a neuromuscular cause of respiratory failure
E Zammarchi, M A Donati, S Masi, et al.
Clinical Pediatrics
|
October 1, 1995
Fructose-1,6-diphosphatase deficiency misdiagnosed as Reye syndrome
E Zammarchi, M A Donati, F Ciani, et al.
Human Mutation
|
September 5, 2003
Structural organization of the human carbamyl phosphate synthetase I gene (CPS1) and identification of two novel genetic lesions
S Funghini, M A Donati, E Pasquini, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
March 1, 1997
[Hyperglycinemia in clinical-laboratory practice]
F Ciani, E Pasquini, A Ciardetti, et al.
Clinical Nutrition (Edinburgh, Scotland)
|
June 27, 2000
Prolonged exclusive breast-feeding from vegan mother causing an acute onset of isolated methylmalonic aciduria due to a mild mutase deficiency
F Ciani, G M Poggi, E Pasquini, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
July 1, 1983
[Case report of a stage IV S neuroblastoma regressing without any aggressive treatment]
A Milanesi, E Zammarchi, G Bernini, et al.
La Pediatria
|
March 31, 1981
[Thromboembolic manifestations in a case of homocystinuria]
E Zammarchi, M R Bardini, G Cotrozzi, et al.
Clinical Nephrology
|
July 5, 2011
Hemolytic uremic syndrome and rhabdomyolysis in a patient with succinate coenzyme Q reductase (complex II) deficiency
M V Micheletti, G Lavoratti, S Gasperini, et al.
Page
of 9