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Journal of Inherited Metabolic Disease
|
January 1, 1984
4-Hydroxybutyric aciduria: a new inborn error of metabolism. II. Biochemical findings
C Jakobs, J Kneer, D Rating, et al.
European Journal of Pediatrics
|
May 1, 1981
Serum orosomucoid concentration in newborn infants
L Sann, J Bienvenu, C Lahet, et al.
La Revue Du Praticien
|
November 20, 1997
[Hereditary diseases causing kidney calculi]
P Cochat, M Jouvenet, H Pellet, et al.
Archives Francaises De Pediatrie
|
December 1, 1988
[Protein intolerance with lysinuria. Value of orotic aciduria in adjusting treatment with citrulline]
L de Parscau, C Vianey-Liaud, M Hermier, et al.
The Journal of Pediatrics
|
June 1, 1987
Sudden infant death syndrome and multiple acyl-coenzyme A dehydrogenase deficiency, ethylmalonic-adipic aciduria, or systemic carnitine deficiency
J P Harpey, C Charpentier, M Coudé, et al.
European Neurology
|
February 25, 2000
An adult form of L-2-hydroxyglutaric aciduria revealed by tremor
C Clerc, M Bataillard, P Richard, et al.
Archives Francaises De Pediatrie
|
April 1, 1989
[The phenylpropionate loading test and medium-chain acyl CoA dehydrogenase deficiency]
L De Parscau, S Barrois, C Vianey-Liaud, et al.
Journal De Radiologie, D'Electrologie, Et De Medecine Nucleaire
|
April 1, 1978
[Trickling mucography under high pressure and with moderate contrast. First phase of gastroduodenal examinations (author's transl)]
C Tavernier, P Divry, V Regimbau, et al.
Lyon Medical
|
January 11, 1970
[Asthma treatment by a dialysable immunizing substance from the expectoration]
H Thiers, C Ollagnier, C Vallon, et al.
European Urology
|
January 1, 1980
Uric acid, monosodium urate and ammonium urate urinary relative saturations in normo-uricuric calcium oxalate stone formers
M Labeeuw, C Gerbaulet, N Pozet, et al.
Page
of 12
Search research articles
Search
Showing results (41-50 of 114) with videos related to
Sort By:
Page
of 12
Journal of Inherited Metabolic Disease
|
January 1, 1984
4-Hydroxybutyric aciduria: a new inborn error of metabolism. II. Biochemical findings
C Jakobs, J Kneer, D Rating, et al.
European Journal of Pediatrics
|
May 1, 1981
Serum orosomucoid concentration in newborn infants
L Sann, J Bienvenu, C Lahet, et al.
La Revue Du Praticien
|
November 20, 1997
[Hereditary diseases causing kidney calculi]
P Cochat, M Jouvenet, H Pellet, et al.
Archives Francaises De Pediatrie
|
December 1, 1988
[Protein intolerance with lysinuria. Value of orotic aciduria in adjusting treatment with citrulline]
L de Parscau, C Vianey-Liaud, M Hermier, et al.
The Journal of Pediatrics
|
June 1, 1987
Sudden infant death syndrome and multiple acyl-coenzyme A dehydrogenase deficiency, ethylmalonic-adipic aciduria, or systemic carnitine deficiency
J P Harpey, C Charpentier, M Coudé, et al.
European Neurology
|
February 25, 2000
An adult form of L-2-hydroxyglutaric aciduria revealed by tremor
C Clerc, M Bataillard, P Richard, et al.
Archives Francaises De Pediatrie
|
April 1, 1989
[The phenylpropionate loading test and medium-chain acyl CoA dehydrogenase deficiency]
L De Parscau, S Barrois, C Vianey-Liaud, et al.
Journal De Radiologie, D'Electrologie, Et De Medecine Nucleaire
|
April 1, 1978
[Trickling mucography under high pressure and with moderate contrast. First phase of gastroduodenal examinations (author's transl)]
C Tavernier, P Divry, V Regimbau, et al.
Lyon Medical
|
January 11, 1970
[Asthma treatment by a dialysable immunizing substance from the expectoration]
H Thiers, C Ollagnier, C Vallon, et al.
European Urology
|
January 1, 1980
Uric acid, monosodium urate and ammonium urate urinary relative saturations in normo-uricuric calcium oxalate stone formers
M Labeeuw, C Gerbaulet, N Pozet, et al.
Page
of 12