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Results of search for 'au:"Saudubray, J-M"', page 2 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
Humans
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Infant, Newborn
Male
Metabolism, Inborn Errors
blood
complications
deficiency
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etiology
genetics
metabolism
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21.
[Pheochromocytomas and paroxysmal hypertension].
[electronic resource]
by
Chiche, P
Benaïm, R
Saudubray, J M
Producer:
19660305
In:
Coeur et medecine interne
vol. 4
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22.
Ornithine carbamyl transferase: the effects of pH on the kinetics of a mutant human enzyme.
[electronic resource]
by
Cathelineau, L
Saudubray, J M
Polonovski, C
Producer:
19730305
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 41
Online resources:
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23.
[Enzymopathic congenital hyperlactacidemia].
[electronic resource]
by
Leroux, J P
Marsac, C
Saudubray, J M
Producer:
19761201
In:
Annales de biologie clinique
vol. 34
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24.
[After PKU and hypothyroidism, what other screening?].
[electronic resource]
by
Frézal, J
Briard, M L
Saudubray, J M
Producer:
19820521
In:
Journal de genetique humaine
vol. 29
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25.
Clinical approach to treatable inborn metabolic diseases: an introduction.
[electronic resource]
by
Saudubray, J-M
Sedel, F
Walter, J H
Producer:
20070109
In:
Journal of inherited metabolic disease
vol. 29
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26.
[Treatable hereditary neuro-metabolic diseases].
[electronic resource]
by
Sedel, F
Lyon-Caen, O
Saudubray, J-M
Producer:
20080116
In:
Revue neurologique
vol. 163
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27.
[Value of peritoneal dialysis in the emergency treatment of metabolic diseases of constitutional origin revealed in the neonatal period].
[electronic resource]
by
Saudubray, J M
Fournet, J P
Cloup, M
Producer:
19720913
In:
Annales de medecine interne
vol. 122
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28.
[Molecular tests and metabolic diseases].
[electronic resource]
by
de Lonlay, P
Giurgea, I
Saudubray, J M
Producer:
20031125
In:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
vol. 10 Suppl 1
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29.
[SUDDEN DEATH AND RESUSCITATION IN MYOCARDIAL INFARCT].
[electronic resource]
by
CHICHE, P
SAUDUBRAY, J M
MARCANTONI, J P
Producer:
19961201
In:
Coeur et medecine interne
vol. 25
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30.
[Phenylalanine-restricted diet: the substitutes].
[electronic resource]
by
Ogier, H
Depondt, E
Munnich, A
Saudubray, J M
Producer:
19830923
In:
Archives francaises de pediatrie
vol. 40 Suppl 1
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31.
X-linked transmission of structural gene mutations responsible for ornithine-transcarbamylase deficiencies.
[electronic resource]
by
Cathelineau, L
Navarro, J
Polonovski, C
Saudubray, J M
Producer:
19730323
In:
Lancet (London, England)
vol. 1
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32.
Letter: The presence of the homoanalogues of substrates of the urea cycle in the presence of argininosuccinate synthetase deficiency.
[electronic resource]
by
Cathelineau, L
Saudubray, J M
Charpentier, C
Polonovski, C
Producer:
19741206
In:
Pediatric research
vol. 8
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33.
[An electroencephalographic study of disorders of amino-acid metabolism during the first days of life (author's transl)].
[electronic resource]
by
Mises, J
Moussalli, F
Plouin, P
Saudubray, J M
Producer:
19780127
In:
Revue d'electroencephalographie et de neurophysiologie clinique
vol. 7
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34.
CT scans of infants with glutaric aciduria.
[electronic resource]
by
Aicardi, J
Goutieres, F
Saudubray, J M
Ogier, H
Producer:
19850828
In:
Developmental medicine and child neurology
vol. 27
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35.
Plasma lysine concentration and availability of 2-ketoglutarate in liver mitochondria.
[electronic resource]
by
Kamoun, P
Richard, V
Rabier, D
Saudubray, J M
Producer:
20021119
In:
Journal of inherited metabolic disease
vol. 25
Online resources:
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36.
Liver transplantation in maple syrup urine disease.
[electronic resource]
by
Wendel, U
Saudubray, J M
Bodner, A
Schadewaldt, P
Producer:
20000106
In:
European journal of pediatrics
vol. 158 Suppl 2
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37.
Disorders of phospholipids, sphingolipids and fatty acids biosynthesis: toward a new category of inherited metabolic diseases.
[electronic resource]
by
Lamari, F
Mochel, F
Sedel, F
Saudubray, J M
Producer:
20131231
In:
Journal of inherited metabolic disease
vol. 36
Online resources:
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38.
Genetic complementation analysis of mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency in cultured fibroblasts.
[electronic resource]
by
Søvik, O
Saudubray, J M
Munnich, A
Sweetman, L
Producer:
19921116
In:
Journal of inherited metabolic disease
vol. 15
Online resources:
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39.
[Phenylalanine-restricted diet. The portion-by-weight system].
[electronic resource]
by
Depondt, E
Ogier, H
Munnich, A
Saudubray, J M
Producer:
19830923
In:
Archives francaises de pediatrie
vol. 40 Suppl 1
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40.
[Biochemistry of peroxisome and peroxisomal diseases].
[electronic resource]
by
Vamecq, J
Poll-The, B T
Saudubray, J M
Producer:
19880803
In:
Annales de biologie clinique
vol. 46
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