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Results of search for 'au:"Saudubray, J-M"', page 5 of 19
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Authors
Bonnefont, J P
Brivet, M
Brunelle, F
Charpentier, C
Demaugre, F
Frezal, J
Kamoun, P
Marsac, C
Munnich, A
Nihoul-Fékété, C
Ogier, H
Poggi, F
Poll-The, B T
Rabier, D
Rahier, J
Rustin, P
Rötig, A
Saudubray, J M
Touati, G
de Lonlay, P
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Adolescent
Adult
Amino Acid Metabolism, Inborn Errors
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Child, Preschool
Female
Fibroblasts
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Infant, Newborn
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Metabolism, Inborn Errors
blood
complications
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81.
Methylenetetrahydrofolate reductase deficiency: prenatal diagnosis and family studies.
[electronic resource]
by
Marquet, J
Chadefaux, B
Bonnefont, J P
Saudubray, J M
Zittoun, J
Producer:
19940610
In:
Prenatal diagnosis
vol. 14
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82.
Autosomal dominant deletions of the mitochondrial genome in a case of progressive encephalomyopathy.
[electronic resource]
by
Cormier, V
Rotig, A
Tardieu, M
Colonna, M
Saudubray, J M
Munnich, A
Producer:
19910515
In:
American journal of human genetics
vol. 48
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83.
Reference charts for respiratory chain activities in human tissues.
[electronic resource]
by
Chretien, D
Rustin, P
Bourgeron, T
Rötig, A
Saudubray, J M
Munnich, A
Producer:
19941202
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 228
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84.
Complementation analysis of carnitine palmitoyltransferase I and II defects.
[electronic resource]
by
Slama, A
Brivet, M
Boutron, A
Legrand, A
Saudubray, J M
Demaugre, F
Producer:
19970218
In:
Pediatric research
vol. 40
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85.
[Severe lactic acidosis disease disclosing milk-protein intolerance to cows' milk].
[electronic resource]
by
Rizk, C
Valdes, L
Ogier de Baulny, H
Saudubray, J M
Olivier, C
Producer:
19990524
In:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
vol. 6
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86.
Sudden child death and 'healthy' affected family members with medium-chain acyl-coenzyme A dehydrogenase deficiency.
[electronic resource]
by
Duran, M
Hofkamp, M
Rhead, W J
Saudubray, J M
Wadman, S K
Producer:
19870105
In:
Pediatrics
vol. 78
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87.
Studies on requirements for amino acids in infants with disorders of amino acid metabolism. I. Effect of alanine.
[electronic resource]
by
Kelts, D G
Ney, D
Bay, C
Saudubray, J M
Nyhan, W L
Producer:
19850320
In:
Pediatric research
vol. 19
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88.
[Nesidioblastosis and persistent neonatal hyperinsulinism].
[electronic resource]
by
Rahier, J
Sempoux, C
Poggi, F
Brunelle, F
Saudubray, J M
Fekete, C
Producer:
19950804
In:
Journees annuelles de diabetologie de l'Hotel-Dieu
p. 73-82
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89.
Nesidioblastosis and persistent neonatal hyperinsulinism.
[electronic resource]
by
Sempoux, C
Poggi, F
Brunelle, F
Saudubray, J M
Fekete, C
Rahier, J
Producer:
19960409
In:
Diabete & metabolisme
vol. 21
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90.
[Scleroderma-like lesions and phenylketonuria (PKU). Role of hyperphenylalaninemia, efficacy of diet (3 cases)].
[electronic resource]
by
Bodemer, C
Bonnefont, J P
Saudubray, J M
Teillac, D
De Prost, Y
Producer:
19900315
In:
Annales de dermatologie et de venereologie
vol. 116
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91.
Arginine remains an essential amino acid after liver transplantation in urea cycle enzyme deficiencies.
[electronic resource]
by
Rabier, D
Narcy, C
Bardet, J
Parvy, P
Saudubray, J M
Kamoun, P
Producer:
19920225
In:
Journal of inherited metabolic disease
vol. 14
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92.
Search for the biochemical basis of biotin dependent multiple carboxylase deficiencies: determination of biotin activation in cultured fibroblasts.
[electronic resource]
by
Zamboni, M
Gaudry, M
Marquet, A
Munnich, A
Saudubray, J M
Marsac, C
Producer:
19821029
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 122
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93.
[Treatment of phenylketonuria with a new phenylalanine-free protein hydrolysate (Albumaid XP). II. Practical application and effect on weight, height and bone development in 21 days].
[electronic resource]
by
Saudubray, J M
Boisse, J
Strouck, J
Caty, T
Lery, E
Mozziconacci, P
Producer:
19721108
In:
Annales de pediatrie
vol. 19
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94.
[Protocol of metabolic investigations in hereditary metabolic diseases].
[electronic resource]
by
Poggi, F
Rabier, D
Vassault, A
Charpentier, C
Kamoun, P
Saudubray, J M
Producer:
19950111
In:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
vol. 1
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95.
Clinical presentations and laboratory investigations in respiratory chain deficiency.
[electronic resource]
by
Munnich, A
Rötig, A
Chretien, D
Saudubray, J M
Cormier, V
Rustin, P
Producer:
19960917
In:
European journal of pediatrics
vol. 155
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96.
[Mitochondrial beta-oxidation of fatty acids: an essential metabolic pathway of muscular function].
[electronic resource]
by
de Lonlay, P
Djouadi, F
Bonnefont, J P
Saudubray, J M
Bastin, J
Producer:
20020917
In:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
vol. 9 Suppl 2
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97.
Localisation of focal lesion permitting partial pancreatectomy in infants.
[electronic resource]
by
Lyonnet, S
Bonnefont, J P
Saudubray, J M
Nihoule-Fekete, C
Brunelle, F
Producer:
19891018
In:
Lancet (London, England)
vol. 2
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98.
[Evaluation of the activity of a phenylketonuria detection center. Analysis of the results of 500,000 tests].
[electronic resource]
by
Barbesier, J
Boisse, J
Charpentier, C
Lemonnier, A
Mozziconacci, P
Saudubray, J M
Producer:
19710420
In:
La Presse medicale
vol. 79
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99.
[Alopecia, chronic candidodis, mental retardation and repeated ketoacidosic comas curable by biotin administration: multiple carboxylases deficiency (author's transl)].
[electronic resource]
by
Munnich, A
Saudubray, J M
Ogier, H
Marsac, C
Charpentier, C
Frezal, J
Producer:
19810613
In:
Annales de medecine interne
vol. 131
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100.
[Hereditary metabolic diseases in adults].
[electronic resource]
by
Saudubray, J M
Nuoffer, J M
de Lonlay, P
Castelnau, P
Touati, G
Producer:
19990210
In:
La Revue de medecine interne
vol. 19 Suppl 3
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