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Results of search for 'au:"Brivet, M"', page 1 of 4
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Authors
Abadi, N
Acquaviva-Bourdain, C
Baptista, J
Bonnefont, J P
Boutron, A
Brivet, M
Costa, C
Demaugre, F
Gautier, M
Kadhom, N
Legrand, A
Lemonnier, A
Moatti, N
Munnich, A
Rabier, D
Roe, C
Saudubray, J M
Slama, A
Soni, T
de Lonlay, P
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Topics
Adult
Carnitine O-Palmitoyltransferase
Cells, Cultured
Child
Fatty Acids
Female
Fibroblasts
Humans
Infant
Infant, Newborn
Lipid Metabolism, Inborn Errors
Male
Oxidation-Reduction
blood
deficiency
diagnosis
enzymology
etiology
genetics
metabolism
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Languages
English
French
Your search returned 70 results.
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1.
[Mitochondrial diseases. Mitochondria, the major cellular energy producing organelle, in vivo functional approach to mitochondrial diseases].
[electronic resource]
by
Brivet, M
Producer:
20070405
In:
Annales de biologie clinique
vol. 64
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2.
[Enzymatic determination of blood D-beta-hydroxybutyrate and acetoacetate during prolonged fasting tests in the child].
[electronic resource]
by
Brivet, M
Moatti, N
Producer:
19820225
In:
Annales de biologie clinique
vol. 39
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3.
[Hereditary abnormalities of galactose metabolism: diagnosis and biochemical supervision (author's transl)].
[electronic resource]
by
Brivet, M
Moatti, N
Lemonnier, A
Producer:
19800825
In:
Annales de biologie clinique
vol. 37
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4.
[Hereditary abnormalities of galactose metabolism: diagnosis and biochemical supervision (author's transl)].
[electronic resource]
by
Brivet, M
Moatti, N
Lemonnier, A
Producer:
19800825
In:
Annales de biologie clinique
vol. 37
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5.
The Philadelphia variant of galactokinase in human erythrocytes: physicochemical and catalytic properties.
[electronic resource]
by
Soni, T
Brivet, M
Moatti, N
Lemonnier, A
Producer:
19881103
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 175
Online resources:
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6.
Type Ib glycogen storage disease: an in vivo and in vitro study of two cases.
[electronic resource]
by
Baussan, C
Moatti, N
Brivet, M
Lemonnier, A
Producer:
19841119
In:
Journal of inherited metabolic disease
vol. 7 Suppl 2
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7.
[Occurrence and nature of hyperamylasemia in chronic alcoholics].
[electronic resource]
by
Pelletier, G
Née, N
Brivet, M
Ponsot, P
Producer:
19850401
In:
Gastroenterologie clinique et biologique
vol. 8
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8.
Partial effect of bromocriptine on lactose and galactose synthesis in a pregnant woman heterozygous for galactosaemia.
[electronic resource]
by
Odièvre, M
Brivet, M
Rivière, M F
Labrune, P
Producer:
20020221
In:
Journal of inherited metabolic disease
vol. 24
Online resources:
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9.
Lens hexitols and cataract formation during lactation in a woman heterozygote for galactosaemia.
[electronic resource]
by
Brivet, M
Migayron, F
Roger, J
Cheron, G
Lemonnier, A
Producer:
19900125
In:
Journal of inherited metabolic disease
vol. 12 Suppl 2
Online resources:
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10.
Cytosolic thymidine kinase activity in cultured human fibroblasts from individuals with galactokinase deficiency.
[electronic resource]
by
Baptista, J
Brivet, M
Kadhom, N
Gautier, M
Lemonnier, A
Producer:
19890928
In:
Biochemical genetics
vol. 27
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11.
Evidence for a short-chain carnitine-acylcarnitine translocase in mitochondria specifically related to the metabolism of branched-chain amino acids.
[electronic resource]
by
Roe, D S
Roe, C R
Brivet, M
Sweetman, L
Producer:
20000229
In:
Molecular genetics and metabolism
vol. 69
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12.
[Metabolic cooperation in cocultures of fibroblasts from patients with various abnormalities of galactose metabolism].
[electronic resource]
by
Kadhom, N
Brivet, M
Baptista, J
Gautier, M
Lemonnier, A
Producer:
19890718
In:
Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie
vol. 308
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13.
The Philadelphia variant of galactokinase: impaired [1-14C]galactose oxidation by intact erythrocytes.
[electronic resource]
by
Soni, T
Brivet, M
Moatti, N
Dahan, N
Lemonnier, A
Producer:
19880811
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 174
Online resources:
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14.
Screening of the Philadelphia variant of galactokinase in racially unmixed black Africans: first results.
[electronic resource]
by
Soni, T
Brivet, M
Blanc, M
Jaeger, G
Lemonnier, A
Producer:
19880223
In:
American journal of human genetics
vol. 42
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15.
Defective galactose oxidation in a patient with glycogen storage disease and Fanconi syndrome.
[electronic resource]
by
Brivet, M
Moatti, N
Corriat, A
Lemonnier, A
Odievre, M
Producer:
19830415
In:
Pediatric research
vol. 17
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16.
Study of some enzymatic activities in human liver cell cultures.
[electronic resource]
by
Lemonnier, F
Moatti, N
Brivet, M
Domange, C
Gautier, M
Producer:
19791024
In:
Biomedicine / [publiee pour l'A.A.I.C.I.G.]
vol. 30
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17.
Low efficiency of [14C]galactose incorporation by galactosemic skin fibroblasts: relationship with neurological sequelae.
[electronic resource]
by
Kadhom, N
Baptista, J
Brivet, M
Wolfrom, C
Gautier, M
Producer:
19950113
In:
Biochemical medicine and metabolic biology
vol. 52
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18.
Upper gastrointestinal endoscopy. An unrecognized cause of hyperamylasemia.
[electronic resource]
by
Pelletier, G
Nee, N
Brivet, M
Etienne, J P
Lemonnier, A
Producer:
19870409
In:
Digestive diseases and sciences
vol. 32
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19.
Rapid diagnosis of long chain and medium chain fatty acid oxidation disorders using lymphocytes.
[electronic resource]
by
Brivet, M
Slama, A
Saudubray, J M
Legrand, A
Lemonnier, A
Producer:
19950720
In:
Annals of clinical biochemistry
vol. 32 ( Pt 2)
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20.
Inexplicable infantile cataracts and partial maternal galactose disorder.
[electronic resource]
by
Brivet, M
Abadie, V
Soni, T
Cheron, G
Dufier, J L
Producer:
19860630
In:
Archives of disease in childhood
vol. 61
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