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M. Brivet

Veröffentlichungen von M. Brivet zu Brivet, M. ->
weitere Veröffentlichungen von M. Brivet:
Cytosolic thymidine kinase activity in cultured human fibroblasts from individuals with galactokinase deficiency (1989)
Cytosolic thymidine kinase activity in cultured human fibroblasts from individuals with galactokinase deficiency (1989)
Low Efficiency of [^1^4C] Galactose Incorporation by Galactosemic Skin Fibroblasts: Relationship with Neurological Sequelae (1994)
Cloning by functional complementation, and inactivation, of theSchizosaccharomyces pombe homologue of theSaccharomyces cerevisiae geneABC1 (1996)
Group a streptococcal meningitis and toxic shock syndrome caused by a protein M type 3 strain producing exotoxin C (1997)
The Philadelphia variant of galactokinase: Impaired [1-^1^4C]galactose oxidation by intact erythrocytes (1988)
The Philadelphia variant of galactokinase in human erythrocytes: Physicochemical and catalytic properties (1988)
Normal expression of thymidine kinase and O6-methylguanine-DNA methyltransferase in cultured fibroblasts from individuals with hereditary galactokinase deficiency (1991)
Normal expression of thymidine kinase and O6-methylguanine-DNA methyltransferase in cultured fibroblasts from individuals with hereditary galactokinase deficiency (1991)
Riboflavin responsive ethylmalonic-adipic aciduria in a 9-month-old boy with liver cirrhosis, myopathy and encephalopathy (1991)
Diagnosis of carnitine acylcarnitine translocase deficiency by complementation analysis (1994)
Do criteria exist from urinary organic acids to distinguish β-oxidation defects? (1995)
Hyperchloremic acidosis during grand mal seizure lactic acidosis (1994)
Acute Pancreatitis Caused by Severe Legionella pneumophila Infection (2000)
Acute cyanide poisoning: Recovery with non-specific supportive therapy (1983)
Veröffentlichungen zu Brivet, M.
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1
Baptista, J., Brivet, M., ... Cytosolic thymidine kinase activity in cultured human fibroblasts from individuals with galactokinase deficiency
in: Biochemical genetics , ISSN 1573-4927, Vol. 27 (3/4. 1989), p. 219-228
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1989
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2
Baptista, J., Brivet, M., ... Cytosolic thymidine kinase activity in cultured human fibroblasts from individuals with galactokinase deficiency
in: Biochemical genetics , ISSN 1573-4927, Vol. 27 (3/4. 1989), p. 219-228
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1989
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3
Kadhom, N., Baptista, J., ... Low Efficiency of [^1^4C] Galactose Incorporation by Galactosemic Skin Fibroblasts: Relationship with Neurological Sequelae
in: Biochemical Medicine and Metabolic Biology, in: Biochemical Medicine and Metabolic Biology . - Amsterdam : Elsevier, ISSN 0885-4505, ZDB-ID 2023534-3 Vol. 52, No. 2 (1994), p. 140-144
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1994
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4
Bonnefoy, N., Kermorgant, M., ... Cloning by functional complementation, and inactivation, of theSchizosaccharomyces pombe homologue of theSaccharomyces cerevisiae geneABC1
in: Molecular genetics and genomics , ISSN 1617-4623, Vol. 251 (2. 1996), p. 204-210
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1996
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5
Guibert, M., Livartowski, J., ... Group a streptococcal meningitis and toxic shock syndrome caused by a protein M type 3 strain producing exotoxin C
in: European journal of clinical microbiology & infectious diseases , ISSN 1435-4373, Vol. 16 (4. 1997), p. 323-324
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1997
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6
Soni, T., Brivet, M., ... The Philadelphia variant of galactokinase: Impaired [1-^1^4C]galactose oxidation by intact erythrocytes
in: Clinica Chimica Acta, in: Clinica Chimica Acta . - Amsterdam : Elsevier, ISSN 0009-8981, ZDB-ID 1499920-1 Vol. 174, No. 1 (1988), p. 101-110
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1988
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7
Soni, T., Brivet, M., ... The Philadelphia variant of galactokinase in human erythrocytes: Physicochemical and catalytic properties
in: Clinica Chimica Acta, in: Clinica Chimica Acta . - Amsterdam : Elsevier, ISSN 0009-8981, ZDB-ID 1499920-1 Vol. 175, No. 1 (1988), p. 97-106
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1988
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8
Stephenson, C., Brivet, M., ... Normal expression of thymidine kinase and O6-methylguanine-DNA methyltransferase in cultured fibroblasts from individuals with hereditary galactokinase deficiency
in: Biochemical genetics , ISSN 1573-4927, Vol. 29 (3/4. 1991), p. 135-144
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1991
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9
Stephenson, C., Brivet, M., ... Normal expression of thymidine kinase and O6-methylguanine-DNA methyltransferase in cultured fibroblasts from individuals with hereditary galactokinase deficiency
in: Biochemical genetics , ISSN 1573-4927, Vol. 29 (3/4. 1991), p. 135-144
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1991
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10
Brivet, M., Tardieu, M., ... Riboflavin responsive ethylmalonic-adipic aciduria in a 9-month-old boy with liver cirrhosis, myopathy and encephalopathy
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 14 (3. 1991), p. 333-337
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1991
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11
Brivet, M., Slama, A., ... Diagnosis of carnitine acylcarnitine translocase deficiency by complementation analysis
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 17 (3. 1994), p. 271-274
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1994
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12
Rabier, D., Bardet, J., ... Do criteria exist from urinary organic acids to distinguish β-oxidation defects?
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 18 (2. 1995), p. 257-260
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1995
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13
Brivet, F., Bernardin, M., ... Hyperchloremic acidosis during grand mal seizure lactic acidosis
in: Intensive care medicine , ISSN 1432-1238, Vol. 20 (1. 1994), p. 27-31
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1994
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14
Mégarbane, B., Montambault, S., ... Acute Pancreatitis Caused by Severe Legionella pneumophila Infection
in: Infection , ISSN 1439-0973, Vol. 28 (5. 2000), p. 329-331
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2000
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15
Brivet, F., Delfraissy, J. F., ... Acute cyanide poisoning: Recovery with non-specific supportive therapy
in: Intensive care medicine , ISSN 1432-1238, Vol. 9 (1. 1983), p. 33-35
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1983
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16
Trugnan, G., Bereziat, G., ... Platelets fatty acid variation in patients with atherosclerosis
in: Clinica Chimica Acta, in: Clinica Chimica Acta . - Amsterdam : Elsevier, ISSN 0009-8981, ZDB-ID 1499920-1 Vol. 79, No. 3 (1977), p. 583-589
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1977
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17
Costa, C., Costa, J. M., ... Identification of the molecular defect in a severe case of carnitine-acylcarnitine carrier deficiency
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 22 (3. 1999), p. 267-270
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1999
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18
Nuoffer, J. -M., de Lonlay, P., ... Familial neonatal SIDS revealing carnitine-acylcarnitine translocase deficiency
in: European journal of pediatrics , ISSN 1432-1076, Vol. 159 (1/2. 2000), p. 82-85
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2000
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19
Jakobs, C., Kneer, J., ... In vivo stable isotope studies in three patients affected with mitochondrial fatty acid oxidation disorders: Limited diagnostic use of 1-13C fatty acid breath test using bolus...
in: European journal of pediatrics , ISSN 1432-1076, Vol. 156 (1. 1997), p. S78
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1997
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20
Brivet, M., Boutron, A., ... Defects in activation and transport of fatty acids
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 22 (4. 1999), p. 428-441
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1999