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M Candito

Showing results (51-60 of 67) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1993
Arginase deficiency in two brothersM Candito, B Bebin, C Vianey-Saban, et al.
Diabete & Metabolisme|September 1, 1994
Type 1 diabetes mellitus and homocyst(e)ineJ F Robillon, B Canivet, M Candito, et al.
Psychiatry Research|June 1, 1989
Circadian rhythms in depression and recovery: evidence for blunted amplitude as the main chronobiological abnormalityE Souêtre, E Salvati, J L Belugou, et al.
Electrophoresis|July 6, 2000
Plasma total homocysteine and other thiols analyzed by capillary electrophoresis/laser-induced fluorescence detection: comparison with two other methodsE Caussé, P Malatray, R Calaf, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Lysinuric protein intolerance. Urinary amino acid excretion at 2 and 9 days of ageM Candito, C Vianey-Saban, J P Ferraci, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Homocysteine response to methionine challenge in four obligate heterozygotes for homocystinuria and relationship with cystathionine beta-synthase mutationsM P Sperandeo, M Candito, G Sebastio, et al.
Journal of Inherited Metabolic Disease|July 10, 1999
Fasting, postprandial, and post-methionine-load homocysteinaemia and methylenetetrahydrofolate reductase polymorphism in vascular diseaseM Candito, P Bedoucha, P Gibelin, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Molecular analysis of patients affected by homocystinuria due to cystathionine beta-synthase deficiency: report of a new mutation in exon 8 and a deletion in intron 11M P Sperandeo, M Panico, A Pepe, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Abnormal alpha-aminoadipic acid excretion in a newborn with a defect in platelet aggregation and antenatal cerebral haemorrhageM Candito, C Richelme, P Parvy, et al.
Presse Medicale (Paris, France : 1983)|November 5, 1997
[Cerebral vascular complication of hyperhomocysteinemia. Controlling thromboembolic complications with folates]M Candito, P Bedoucha, D Jambou, et al.
Pageof 7

Showing results (51-60 of 67) with videos related to

Sort By:
Pageof 7
Journal of Inherited Metabolic Disease|January 1, 1993
Arginase deficiency in two brothersM Candito, B Bebin, C Vianey-Saban, et al.
Diabete & Metabolisme|September 1, 1994
Type 1 diabetes mellitus and homocyst(e)ineJ F Robillon, B Canivet, M Candito, et al.
Psychiatry Research|June 1, 1989
Circadian rhythms in depression and recovery: evidence for blunted amplitude as the main chronobiological abnormalityE Souêtre, E Salvati, J L Belugou, et al.
Electrophoresis|July 6, 2000
Plasma total homocysteine and other thiols analyzed by capillary electrophoresis/laser-induced fluorescence detection: comparison with two other methodsE Caussé, P Malatray, R Calaf, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Lysinuric protein intolerance. Urinary amino acid excretion at 2 and 9 days of ageM Candito, C Vianey-Saban, J P Ferraci, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Homocysteine response to methionine challenge in four obligate heterozygotes for homocystinuria and relationship with cystathionine beta-synthase mutationsM P Sperandeo, M Candito, G Sebastio, et al.
Journal of Inherited Metabolic Disease|July 10, 1999
Fasting, postprandial, and post-methionine-load homocysteinaemia and methylenetetrahydrofolate reductase polymorphism in vascular diseaseM Candito, P Bedoucha, P Gibelin, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Molecular analysis of patients affected by homocystinuria due to cystathionine beta-synthase deficiency: report of a new mutation in exon 8 and a deletion in intron 11M P Sperandeo, M Panico, A Pepe, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Abnormal alpha-aminoadipic acid excretion in a newborn with a defect in platelet aggregation and antenatal cerebral haemorrhageM Candito, C Richelme, P Parvy, et al.
Presse Medicale (Paris, France : 1983)|November 5, 1997
[Cerebral vascular complication of hyperhomocysteinemia. Controlling thromboembolic complications with folates]M Candito, P Bedoucha, D Jambou, et al.
Pageof 7