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J P Colombo

Showing results (121-130 of 159) with videos related to

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Revue Neurologique|January 1, 1990
[Late diagnosis of congenital argininemia during administration of sodium valproate]D Christmann, E Hirsch, V Mutschler, et al.
Journal De Genetique Humaine|March 1, 1972
Familial hyperargininemiaH G Terheggen, F Lavinha, J P Colombo, et al.
American Journal of Medical Genetics. Supplement|January 1, 1986
Biotin and Rett syndromeC Bachmann, J P Colombo, E Gugler, et al.
The Journal of Laboratory and Clinical Medicine|July 1, 1977
The defect of uric acid metabolism in Eck-fistula ratsB Lauterburg, V Sautter, R Herz, et al.
The New England Journal of Medicine|February 26, 1981
N-acetylglutamate synthetase deficiency: a disorder of ammonia detoxicationC Bachmann, S Krähenbühl, J P Colombo, et al.
Nephron|March 13, 1998
Urinary sodium, potassium, chloride, calcium, magnesium, phosphate, urate and urea in healthy subjects aged 5-18 yearsP Donati-Genet, R Donati, J P Colombo, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
A new neonatal case of N-acetylglutamate synthase deficiency treated by carbamylglutamateN Guffon, C Vianey-Saban, J Bourgeois, et al.
European Journal of Pediatrics|April 1, 1986
Rett syndrome revisited: a patient with biotin dependencyC Bachmann, J Schaub, J P Colombo, et al.
Schweizerische Medizinische Wochenschrift|June 29, 1974
[Mental retardation in childhood. Clinical, biochemical and epidemiological studies on 286 institutionalized children]A Schmid, H Moser, U Wälti, et al.
Pediatrics|June 1, 1992
Long-term follow-up of 12 patients with the late-onset variant of argininosuccinic acid lyase deficiency: no impairment of intellectual and psychomotor development during therapyK Widhalm, S Koch, S Scheibenreiter, et al.
Pageof 16

Showing results (121-130 of 159) with videos related to

Sort By:
Pageof 16
Revue Neurologique|January 1, 1990
[Late diagnosis of congenital argininemia during administration of sodium valproate]D Christmann, E Hirsch, V Mutschler, et al.
Journal De Genetique Humaine|March 1, 1972
Familial hyperargininemiaH G Terheggen, F Lavinha, J P Colombo, et al.
American Journal of Medical Genetics. Supplement|January 1, 1986
Biotin and Rett syndromeC Bachmann, J P Colombo, E Gugler, et al.
The Journal of Laboratory and Clinical Medicine|July 1, 1977
The defect of uric acid metabolism in Eck-fistula ratsB Lauterburg, V Sautter, R Herz, et al.
The New England Journal of Medicine|February 26, 1981
N-acetylglutamate synthetase deficiency: a disorder of ammonia detoxicationC Bachmann, S Krähenbühl, J P Colombo, et al.
Nephron|March 13, 1998
Urinary sodium, potassium, chloride, calcium, magnesium, phosphate, urate and urea in healthy subjects aged 5-18 yearsP Donati-Genet, R Donati, J P Colombo, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
A new neonatal case of N-acetylglutamate synthase deficiency treated by carbamylglutamateN Guffon, C Vianey-Saban, J Bourgeois, et al.
European Journal of Pediatrics|April 1, 1986
Rett syndrome revisited: a patient with biotin dependencyC Bachmann, J Schaub, J P Colombo, et al.
Schweizerische Medizinische Wochenschrift|June 29, 1974
[Mental retardation in childhood. Clinical, biochemical and epidemiological studies on 286 institutionalized children]A Schmid, H Moser, U Wälti, et al.
Pediatrics|June 1, 1992
Long-term follow-up of 12 patients with the late-onset variant of argininosuccinic acid lyase deficiency: no impairment of intellectual and psychomotor development during therapyK Widhalm, S Koch, S Scheibenreiter, et al.
Pageof 16