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Results of search for 'au:"Saudubray, J-M"', page 4 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
Child
Child, Preschool
Female
Fibroblasts
Humans
Infant
Infant, Newborn
Male
Metabolism, Inborn Errors
blood
complications
deficiency
diagnosis
enzymology
etiology
genetics
metabolism
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61.
Glycine/serine ratio and the prenatal diagnosis of non-ketotic hyperglycinaemia.
[electronic resource]
by
Parvy, P
Rabier, D
Boue, J
Saudubray, J M
Kamoun, P
Producer:
19900926
In:
Prenatal diagnosis
vol. 10
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62.
[Study of a case of methylmalonic acidemia of neonatal onset. Therapeutic value of peritoneal dialysis. Discussion of vitamin B 12 sensitivity].
[electronic resource]
by
Saudubray, J M
Boisse, J
Charpentier, C
Lemonnier, A
Mozziconacci, P
Producer:
19721221
In:
Archives francaises de pediatrie
vol. 29
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63.
[Diagnosis of states of ketosis in pediatrics].
[electronic resource]
by
Ogier de Baulny, H
Husson, I
Castelnau, P
Saudubray, J M
Producer:
19990729
In:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
vol. 6 Suppl 2
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64.
Remethylation defects: guidelines for clinical diagnosis and treatment.
[electronic resource]
by
Ogier de Baulny, H
Gérard, M
Saudubray, J M
Zittoun, J
Producer:
19980714
In:
European journal of pediatrics
vol. 157 Suppl 2
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65.
Movement disorders and inborn errors of metabolism in adults: a diagnostic approach.
[electronic resource]
by
Sedel, F
Saudubray, J-M
Roze, E
Agid, Y
Vidailhet, M
Producer:
20080909
In:
Journal of inherited metabolic disease
vol. 31
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66.
[Research methods in metabolic myopathies in children].
[electronic resource]
by
Lombes, A
Ogier, H
Bonnefont, J P
Munnich, A
Saudubray, J M
Producer:
19880310
In:
Annales de medecine interne
vol. 138
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67.
[Congenital hyperglycemia without ketosis].
[electronic resource]
by
Piussan, C
Saudubray, J M
Audebert, M
Van Poperinghe, M
Risbourg, B
Producer:
19751230
In:
Pediatrie
vol. 30
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68.
[The E.E.G. in non-ketotic hyperglycinaemia (author's transl)].
[electronic resource]
by
Mises, J
Moussali-Salefranque, F
Plouin, P
Temam, G
Saudubray, J M
Producer:
19780828
In:
Revue d'electroencephalographie et de neurophysiologie clinique
vol. 8
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69.
[Surgical treatment of dorso lumbar scoliosis in a homocystinuric child (author's transl)].
[electronic resource]
by
Merckx, J
Rigault, P
Padovani, J P
Saudubray, J M
Guyonvarch, G
Producer:
19820212
In:
Revue de chirurgie orthopedique et reparatrice de l'appareil moteur
vol. 67
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70.
[EEG in hyperphenylalaninemia].
[electronic resource]
by
Mises, J
Moussalli, F
Odell, A
Lerique-Koechlin, A
Saudubray, J M
Producer:
19761020
In:
Revue d'electroencephalographie et de neurophysiologie clinique
vol. 3
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71.
Propionylcarnitine excretion is not affected by metronidazole administration to patients with disorders of propionate metabolism.
[electronic resource]
by
Burns, S P
Iles, R A
Saudubray, J M
Chalmers, R A
Producer:
19961011
In:
European journal of pediatrics
vol. 155
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72.
Urea cycle defects: management and outcome.
[electronic resource]
by
Nassogne, M C
Héron, B
Touati, G
Rabier, D
Saudubray, J M
Producer:
20050818
In:
Journal of inherited metabolic disease
vol. 28
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73.
[Hemorrhagic shock syndrome with encephalopathy].
[electronic resource]
by
Hervé, F
Bakchine, H
Le Loc'h, H
Ogier, H
Saudubray, J M
Producer:
19870617
In:
Archives francaises de pediatrie
vol. 44
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74.
[E.E.G. appearances in hyperphenylalaninaemia (author's transl)].
[electronic resource]
by
Moussalli-Salefranque, F
Mises, J
Cheynel, A
Phelippeau, M
Saudubray, J M
Producer:
19780828
In:
Revue d'electroencephalographie et de neurophysiologie clinique
vol. 8
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75.
The effect of D-carnitine on palmitate oxidation in cultured fibroblasts.
[electronic resource]
by
Mitchell, G
Saudubray, J M
Pellet, A
Demaugre, F
Labarthe, J C
Producer:
19850115
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 143
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76.
Anatomo-pathological findings in a case of combined deficiency of sulphite oxidase and xanthine oxidase with a defect of molybdenum cofactor.
[electronic resource]
by
Roth, A
Nogues, C
Monnet, J P
Ogier, H
Saudubray, J M
Producer:
19850418
In:
Virchows Archiv. A, Pathological anatomy and histopathology
vol. 405
Online resources:
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77.
Inborn errors of amino acid metabolism. The best strategy for their diagnosis.
[electronic resource]
by
Durand-Zaleski, I
Saudubray, J M
Kamoun, P P
Blum-Boisgard, C
Producer:
19921125
In:
International journal of technology assessment in health care
vol. 8
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78.
Clinical approach to inherited peroxisomal disorders.
[electronic resource]
by
Poggi-Travert, F
Fournier, B
Poll-The, B T
Saudubray, J M
Producer:
19970313
In:
Journal of inherited metabolic disease
vol. 18 Suppl 1
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79.
[The child and his physician].
[electronic resource]
by
de Paillerets, F
Dehan, M
Beaufils, F
Badoual, J
Saudubray, J M
Producer:
19960117
In:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
vol. 2
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80.
[Protein glycosylation deficiency: clinical presentation].
[electronic resource]
by
Ogier de Baulny, H
Poggi-Travert, F
Besnard, M
Saudubray, J M
Producer:
19961023
In:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
vol. 3 Suppl 1
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