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The Journal of Pediatrics
|
April 1, 1988
Carnitine in lactic acidosis
C Dionisi Vici, E Bertini, A Bartuli, et al.
Acta Paediatrica Scandinavica
|
October 1, 1990
Early introduction of uncooked cornstarch for the treatment of glycogen storage disease type I
C Dionisi Vici, A Bartuli, M R Mazziotta, et al.
La Clinica Terapeutica
|
May 31, 1985
[Combination of thiazide diuretics and prostaglandins inhibitors in the treatment of nephrogenic diabetes insipidus]
D Pichetti, M L Pandolfi, A Bartuli, et al.
Pediatric Transplantation
|
December 6, 2011
Too late to say it is too early--how to get children with non-cirrhotic metabolic diseases transplanted at the right time?
M Macchiaiolo, A Bartuli, P McKiernan, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1990
Prenatal exclusion of ornithine transcarbamylase (OTC) by using RFLP analysis
S Liechti, C Dionisi Vici, C Bachmann, et al.
Neurology
|
December 25, 2002
A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation
A Fogli, C Dionisi-Vici, F Deodato, et al.
European Journal of Paediatric Dentistry
|
August 8, 2014
Ligneous periodontal lesions in a young child with severe plasminogen deficiency: a case report
A Galeotti, R Uomo, V D'Antò, et al.
Minerva Anestesiologica
|
November 15, 2013
Hypercapnic hypoventilation due to tracheobroncomalacia: the success of non-invasive respiratory support with continuous positive airway pressure
V Caldarelli, T Salerno, E Verrillo, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1995
Acute pancreatitis in propionic acidaemia
A B Burlina, C Dionisi-Vici, S Piovan, et al.
Clinical Genetics
|
April 19, 2003
Analysis of Sanfilippo A gene mutations in a large pedigree
P Di Natale, G R D Villani, C Di Domenico, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 23) with videos related to
Sort By:
Page
of 3
The Journal of Pediatrics
|
April 1, 1988
Carnitine in lactic acidosis
C Dionisi Vici, E Bertini, A Bartuli, et al.
Acta Paediatrica Scandinavica
|
October 1, 1990
Early introduction of uncooked cornstarch for the treatment of glycogen storage disease type I
C Dionisi Vici, A Bartuli, M R Mazziotta, et al.
La Clinica Terapeutica
|
May 31, 1985
[Combination of thiazide diuretics and prostaglandins inhibitors in the treatment of nephrogenic diabetes insipidus]
D Pichetti, M L Pandolfi, A Bartuli, et al.
Pediatric Transplantation
|
December 6, 2011
Too late to say it is too early--how to get children with non-cirrhotic metabolic diseases transplanted at the right time?
M Macchiaiolo, A Bartuli, P McKiernan, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1990
Prenatal exclusion of ornithine transcarbamylase (OTC) by using RFLP analysis
S Liechti, C Dionisi Vici, C Bachmann, et al.
Neurology
|
December 25, 2002
A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation
A Fogli, C Dionisi-Vici, F Deodato, et al.
European Journal of Paediatric Dentistry
|
August 8, 2014
Ligneous periodontal lesions in a young child with severe plasminogen deficiency: a case report
A Galeotti, R Uomo, V D'Antò, et al.
Minerva Anestesiologica
|
November 15, 2013
Hypercapnic hypoventilation due to tracheobroncomalacia: the success of non-invasive respiratory support with continuous positive airway pressure
V Caldarelli, T Salerno, E Verrillo, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1995
Acute pancreatitis in propionic acidaemia
A B Burlina, C Dionisi-Vici, S Piovan, et al.
Clinical Genetics
|
April 19, 2003
Analysis of Sanfilippo A gene mutations in a large pedigree
P Di Natale, G R D Villani, C Di Domenico, et al.
Page
of 3