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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 hyperargininemia
H G Terheggen, F Lavinha, J P Colombo, et al.
American Journal of Medical Genetics. Supplement
|
January 1, 1986
Biotin and Rett syndrome
C 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 rats
B Lauterburg, V Sautter, R Herz, et al.
The New England Journal of Medicine
|
February 26, 1981
N-acetylglutamate synthetase deficiency: a disorder of ammonia detoxication
C 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 years
P 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 carbamylglutamate
N Guffon, C Vianey-Saban, J Bourgeois, et al.
European Journal of Pediatrics
|
April 1, 1986
Rett syndrome revisited: a patient with biotin dependency
C 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 therapy
K Widhalm, S Koch, S Scheibenreiter, et al.
Page
of 16
Search research articles
Search
Showing results (121-130 of 159) with videos related to
Sort By:
Page
of 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 hyperargininemia
H G Terheggen, F Lavinha, J P Colombo, et al.
American Journal of Medical Genetics. Supplement
|
January 1, 1986
Biotin and Rett syndrome
C 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 rats
B Lauterburg, V Sautter, R Herz, et al.
The New England Journal of Medicine
|
February 26, 1981
N-acetylglutamate synthetase deficiency: a disorder of ammonia detoxication
C 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 years
P 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 carbamylglutamate
N Guffon, C Vianey-Saban, J Bourgeois, et al.
European Journal of Pediatrics
|
April 1, 1986
Rett syndrome revisited: a patient with biotin dependency
C 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 therapy
K Widhalm, S Koch, S Scheibenreiter, et al.
Page
of 16