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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.
Journal of Inherited Metabolic Disease
|
January 1, 1988
Laryngeal stridor as a leading symptom in a biotinidase-deficient patient
C Dionisi-Vici, C Bachmann, M C Graziani, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 15, 1988
Determination of medium chain fatty acids in serum
C Dionisi Vici, C Bachmann, M Gradwoht, et al.
American Journal of Medical Genetics
|
November 1, 1990
Jeune syndrome associated with cystinuria: report of two sisters
S Rinaldi, C Dionisi-Vici, B Goffredo, et al.
Pediatric Research
|
September 1, 1987
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome: low creatine excretion and effect of citrulline, arginine, or ornithine supplement
C Dionisi Vici, C Bachmann, M Gambarara, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
February 1, 1985
Superior mesenteric artery syndrome: an unusual cause of Watson biopsy capsule retention
M Bonamico, M Roggini, A Pierro, et al.
Human Mutation
|
October 23, 2001
Seven novel mutations in the ORNT1 gene (SLC25A15) in patients with hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome
S Salvi, C Dionisi-Vici, E Bertini, et al.
Journal of Inherited Metabolic Disease
|
July 18, 2002
Successful pregnancy in a woman with mut- methylmalonic acidaemia
F Deodato, C Rizzo, S Boenzi, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 29, 1999
A simple and rapid HPLC method for simultaneous determination of plasma 7-dehydrocholesterol and vitamin E: its application in Smith-Lemli-Opitz patients
C Rizzo, C Dionisi-Vici, M D'Ippoliti, et al.
Page
of 10
Search research articles
Search
Showing results (1-10 of 92) with videos related to
Sort By:
Page
of 10
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.
Journal of Inherited Metabolic Disease
|
January 1, 1988
Laryngeal stridor as a leading symptom in a biotinidase-deficient patient
C Dionisi-Vici, C Bachmann, M C Graziani, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 15, 1988
Determination of medium chain fatty acids in serum
C Dionisi Vici, C Bachmann, M Gradwoht, et al.
American Journal of Medical Genetics
|
November 1, 1990
Jeune syndrome associated with cystinuria: report of two sisters
S Rinaldi, C Dionisi-Vici, B Goffredo, et al.
Pediatric Research
|
September 1, 1987
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome: low creatine excretion and effect of citrulline, arginine, or ornithine supplement
C Dionisi Vici, C Bachmann, M Gambarara, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
February 1, 1985
Superior mesenteric artery syndrome: an unusual cause of Watson biopsy capsule retention
M Bonamico, M Roggini, A Pierro, et al.
Human Mutation
|
October 23, 2001
Seven novel mutations in the ORNT1 gene (SLC25A15) in patients with hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome
S Salvi, C Dionisi-Vici, E Bertini, et al.
Journal of Inherited Metabolic Disease
|
July 18, 2002
Successful pregnancy in a woman with mut- methylmalonic acidaemia
F Deodato, C Rizzo, S Boenzi, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 29, 1999
A simple and rapid HPLC method for simultaneous determination of plasma 7-dehydrocholesterol and vitamin E: its application in Smith-Lemli-Opitz patients
C Rizzo, C Dionisi-Vici, M D'Ippoliti, et al.
Page
of 10