M. Odiévre

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Recurrent Enterocolitis‐Like Symptoms as the Possible Presenting Manifestations of Neonatal Brucella Melitensis Infection

J. Magny, M. Guibert, P. Labrune, 1990, Acta paediatrica Scandinavica.

Point mutations in the tyrosine aminotransferase gene in tyrosinemia type II.

M. Di Rocco, G. Scherer, M. Odiévre, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Failure of cefotaxime treatment in two children with meningitis caused by highly penicillin‐resistant Streptococcus pneumoniae

M. Guibert, P. Labrune, M. Odiévre, 1995, Acta paediatrica.

Influence of sex and breastfeeding on liver disease in α1‐antitrypsin deficiency

F. Ghishan, P. Labrune, M. Odiévre, 1989 .

Early assessment of evolution of liver disease associated with alpha 1-antitrypsin deficiency in childhood.

G. Nebbia, M. Odiévre, D. Alagille, 1983, The Journal of pediatrics.

Long-term outcome after surgery for biliary atresia. Study of 40 patients surviving for more than 10 years.

M. Hadchouel, F. Gauthier, M. Odiévre, 1990, Gastroenterology.

Long-term prognosis for infants with intrahepatic cholestasis and patent extrahepatic biliary tract.

P. Landrieu, M. Odiévre, D. Alagille, 1981, Archives of disease in childhood.

Hepatic ductular hypoplasia associated with characteristic facies, vertebral malformations, retarded physical, mental, and sexual development, and cardiac murmur.

M. Gautier, M. Odiévre, D. Alagille, 1975, The Journal of pediatrics.

Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): review of 80 cases.

M. Hadchouel, M. Gautier, M. Odiévre, 1987, The Journal of pediatrics.

Hepatocellular adenomas in glycogen storage disease type I and III: a series of 43 patients and review of the literature.

M. Odiévre, P. Labrune, P. Chevalier, 1997, Journal of pediatric gastroenterology and nutrition.

Decreased ketogenesis due to deficiency of hepatic carnitine acyl transferase.

P. Bougnères, J. Saudubray, J. Girard, 1980, The New England journal of medicine.

Infantile phytanic acid storage disease, a possible variant of Refsum's disease: Three cases, including ultrastructural studies of the liver

P. Beaune, O. Dulac, J. Saudubray, 1982, Journal of Inherited Metabolic Disease.

Diabetes mellitus 14 years after a subtotal pancreatectomy for neonatal hyperinsulinism.

P. Labrune, M. Odiévre, S. Lechevallier, 1990, Journal of pediatric surgery.

Fasting hypoglycemia resulting from hepatic carnitine palmitoyl transferase deficiency.

P. Bougnères, J. Saudubray, J. Girard, 1981, The Journal of pediatrics.

Portal obstruction in children. II. Results of surgical portosystemic shunts.

F. Brunelle, F. Alvarez, M. Odiévre, 1983, The Journal of pediatrics.

In vivo13C-NMR evaluation of glycogen content in a patient with glycogen storage disease

P. Jehenson, A. Syrota, M. Odiévre, 1992, Journal of Inherited Metabolic Disease.

Congenital abnormalities associated with extrahepatic portal hypertension.

M. Odiévre, D. Alagille, G. Pigé, 1977, Archives of disease in childhood.

Severe giant cell hepatitis with autoimmune hemolytic anemia in early childhood.

M. Odiévre, O. Bernard, J. Scotto, 1981, The Journal of pediatrics.

Nervous and Ocular Disorders in Children with Cholestasis and Vitamin A and E Deficiencies

P. Landrieu, M. Odiévre, D. Alagille, 2007, Hepatology.

Increased Levels of Hemostatic Proteins are Independent of Inflammation in Glycogen Storage Disease Type Ia

M. Wolf, D. Meyer, A. Marfaing-Koka, 2003, Journal of pediatric gastroenterology and nutrition.

Alpha1-antitrypsin deficiency and liver disease in children: phenotypes, manifestations, and prognosis.

M. Hadchouel, M. Odiévre, D. Alagille, 1976, Pediatrics.

Haemolytic uraemic syndrome and pulmonary hypertension in a patient with methionine synthase deficiency

P. Niaudet, J. Zittoun, J. Marquet, 1999, European Journal of Pediatrics.

Azathioprine-induced lung toxicity and efficacy of cyclosporin A in a young girl with type 2 autoimmune hepatitis.

F. Capron, D. Zénaty, M. Odiévre, 2000, Journal of Pediatric Gastroenterology and Nutrition - JPGN.

Radiation sensitivity of Bloom's syndrome lymphocytes during S and G2 phases.

B. Dutrillaux, A. Aurias, M. Odiévre, 1985, Cancer genetics and cytogenetics.

Hereditary fructose intolerance in childhood. Diagnosis, management, and course in 55 patients.

M. Gautier, M. Odiévre, D. Alagille, 1978, American journal of diseases of children.

Liver adenomas in glycogen storage disease in children

F. Brunelle, P. Chaumont, M. Odiévre, 2005, Pediatric Radiology.

[Pneumonia due to adenovirus type 7: a case report in a healthy infant].

C. Picard, B. Mesplès, M. Leruez-Ville, 2011, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Sweet Syndrome as the Presenting Manifestation of Chronic Granulomatous Disease in an Infant

C. Lebbé, J. Donadieu, P. Labrune, 1994, Pediatric dermatology.

Familial cutaneous photosensitivity and colitis with lethal outcome.

P. Labrune, M. Odiévre, D. Alagille, 1991, Journal of medical genetics.

[Richner-Hanhart's syndrome or oculo-cutaneous tyrosinosis (about one case) (author's transl)].

J. Bressieux, M. Odiévre, M. Larrégue, 1979, Annales de dermatologie et de venereologie.

Current therapy for Crigler‐Najjar syndrome type 1: Report of a world registry

P. Rosenthal, W. Sperl, J. Fevery, 1996, Hepatology.

Case of congenital nonobstructive, nonhaemolytic jaundice. Successful long-term phototherapy at home.

F. Trivin, M. Odiévre, D. Alagille, 1978, Archives of disease in childhood.

Antenatal diagnosis of infantile Refsum's disease

B. Poll-The, A. Poulos, J. Saudubray, 1985, Clinical genetics.

Progressive vitiligo, mental retardation, facial dysmorphism, and urethral duplication without chromosomal breakage or immunodeficiency.

M. Odiévre, R. Assathiany, P. Labrune, 1992, Journal of medical genetics.

The human tyrosine aminotransferase gene: characterization of restriction fragment length polymorphisms and haplotype analysis in a family with tyrosinemia type II

E. Westphal, G. Scherer, T. Grimm, 1988, Human Genetics.

Seroimmunologic Classification of Chronic Hepatitis in 57 Children

G. Maggiore, M. Hadchouel, M. Odiévre, 2007, Hepatology.

Specificity of the effects of a fructose-free diet on the activity of intestinal -glucosidases in man. A study in hereditary fructose intolerance.

J. Schmitz, M. Odiévre, J. Rey, 1972, Gastroenterology.

The long-term outcome of patients with glycogen storage diseases

J. Leonard, J. Fernandes, M. Odiévre, 1990, Journal of Inherited Metabolic Disease.

Infantile Refsum disease: an inherited peroxisomal disorder

R. Wanders, R. Schutgens, B. Poll-The, 1987, European Journal of Pediatrics.

Absence of hepatic peroxisomes in a case of infantile Refsum's disease.

F. Roels, M. Odiévre, J. Scotto, 1985, Scandinavian journal of clinical and laboratory investigation.

Long‐chain 3‐hydroxyacylCoA dehydrogenase deficiency: a new case presenting with liver dysfunction, cholestasis and fibrosis

R. Wanders, D. Rabier, C. Roe, 2002, Acta paediatrica.

[Long-term course of hepatic glycogenosis. A retrospective study of 76 cases].

P. Labrune, M. Odiévre, L. de Parscau, 1988, Archives francaises de pediatrie.

Glomerular mesangiolipidosis in Alagille syndrome (arteriohepatic dysplasia)

M. Gubler, M. Gautier, M. Odiévre, 1987, Pediatric Nephrology.

Molecular analysis of aldolase B genes in hereditary fructose intolerance

C. Romano, N. Cross, S. Musumeci, 1990, The Lancet.

Comparative use of glucose and fructose in cultured fibroblasts from patients with hereditary fructose intolerance

M. Couturier, M. Gautier, M. Odiévre, 1987, Journal of Inherited Metabolic Disease.

Portal obstruction in children. I. Clinical investigation and hemorrhage risk.

F. Brunelle, F. Alvarez, M. Odiévre, 1983, The Journal of pediatrics.

Effect of lactation in a mother with galactosemia.

M. Brivet, M. Odiévre, A. Lemonnier, 1989, The Journal of pediatrics.

Defective Galactose Oxidation in a Patient with Glycogen Storage Disease and Fanconi Syndrome

M. Brivet, N. Moatti, M. Odiévre, 1983, Pediatric Research.

Genetic heterogeneity of glycogen storage disease type Ia in France: A study of 48 patients

M. Odiévre, P. Labrune, J. Francoual, 2000, Human mutation.

Obstructive jaundice in children with histiocytosis X.

M. Hadchouel, M. Odiévre, D. Alagille, 1981, Gastroenterology.

Histological liver evaluation 5 years after surgery for extrahepatic biliary atresia: a study of 20 cases.

M. Gautier, M. Odiévre, J. Valayer, 1984, Journal of pediatric surgery.

[Sclerosing cholangitis revealing histiocytosis X].

J. Chaussain, D. Musset, P. Labrune, 1990, Archives francaises de pediatrie.

Antenatal thrombocytopenia in three patients with TAR (thrombocytopenia with absent radii) syndrome

R. Frydman, J. Pons, F. Daffos, 1993, Prenatal diagnosis.

Liver disease associated with anti-liver-kidney microsome antibody in children.

F. Alvarez, G. Maggiore, M. Hadchouel, 1986, The Journal of pediatrics.

Treatment of autoimmune chronic active hepatitis in childhood.

G. Maggiore, M. Hadchouel, M. Odiévre, 1984, The Journal of pediatrics.

Gunn rats: a reproducible experimental model to compare the different methods of measurements of bilirubin serum concentration and to evaluate the risk of bilirubin encephalopathy.

F. Trivin, P. Labrune, M. Odiévre, 1990, Clinica chimica acta; international journal of clinical chemistry.

Congenital hepatic fibrosis in children.

F. Brunelle, F. Alvarez, M. Hadchouel, 1981, The Journal of pediatrics.

Anomalies of the intrahepatic portal venous system in congenital hepatic fibrosis.

P. Chaumont, M. Odiévre, D. Alagille, 1977, Radiology.

Ultrasonographic diagnosis of portal cavernoma in children: a study of twelve cases.

P. Chaumont, D. Doyon, P. Douillet, 1980, The British journal of radiology.

Histologic study of biliary fibrous remnants in 48 cases of extrahepatic biliary atresia: correlation with postoperative bile flow restoration.

M. Gautier, M. Odiévre, P. Jehan, 1976, The Journal of pediatrics.

Liver and biliary tract disease in children

M. Odiévre, D. Alagille, 1979 .

Mutations in the phosphorylase kinase gene PHKA2 are responsible for X-linked liver glycogen storage disease.

E. Dams, P. Willems, P. Coucke, 1995, Human molecular genetics.

Tyrosine aminotransferase isoenzyme deficiency.

M. Odiévre, A. Lemonnier, C. Charpentier, 1979, The Journal of pediatrics.

Genetic heterogeneity of Crigler-Najjar syndrome type I: a study of 14 cases.

A. Munnich, N. Chowdhury, J. Chowdhury, 1993, Human genetics.

Neonatal cholestasis and hypoglycemia: possible role of cortisol deficiency.

J. Chaussain, M. Hadchouel, D. Gendrel, 1981, The Journal of pediatrics.

Familial hypermethioninemia partially responsive to dietary restriction.

J. Saudubray, C. Brunet, J. Pérignon, 1990, The Journal of pediatrics.

Effects of postoperative cholestyramine and phenobarbital administration on bile flow restoration in infants with extrahepatic biliary atresia.

M. Couturier, P. Vajro, M. Odiévre, 1986, Journal of pediatric surgery.

Severe familial intrahepatic cholestasis TABLE I Principal biochemical data in 5 cases of severe familial intrahepatic cholestasis

M. Hadchouel, M. Gautier, M. Odiévre, 2006 .

Severe familial intrahepatic cholestasis

M. Hadchouel, M. Gautier, M. Odiévre, 1973, Archives of disease in childhood.

Bilirubin Uridine Diphosphate Glucuronosyltransferase Hepatic Activity in Jaundice Associated with Congenital Hypothyroidism

F. Trivin, P. Labrune, M. Odiévre, 1992, Journal of pediatric gastroenterology and nutrition.

Unusual cerebral manifestations in hereditary fructose intolerance.

P. Labrune, M. Odiévre, P. Huguet, 1990, Archives of neurology.

A secondary respiratory chain defect in a patient with Fanconi–Bickel syndrome

B. Chevallier, M. Brivet, R. Santer, 2002, Journal of Inherited Metabolic Disease.

Jaundice with hypertrophic pyloric stenosis as an early manifestation of Gilbert syndrome

M. Odiévre, P. Labrune, J. Francoual, 1999, Archives of disease in childhood.

The Rose Bengal test in neonatal cholestasis: Diagnostic and prognostic value

F. Alvarez, M. Odiévre, J. Yvart, 1981, European Journal of Pediatrics.

Breast Milk Jaundice: In Vitro Inhibition of Rat Liver Bilirubin-Uridine Diphosphate Glucuronyltransferase Activity and Z Protein-Bromosulfophthalein Binding by Human Breast Milk

M. Odiévre, R. Luzeau, A. Foliot, 1976, Pediatric Research.

Demonstration of a lipolytic activity in human milk that inhibits the glucuro-conjugation of bilirubin.

M. Odiévre, P. Levillain, A. Lemonnier, 1974, Biomedicine / [publiee pour l'A.A.I.C.I.G.].

Faster estimation of reserve bilirubin binding capacity of serum from the neonate by thin-layer chromatography on sephadex.

F. Trivin, M. Odiévre, A. Lemonnier, 1977, Clinical chemistry.

Genetic heterogeneitiy of Crigler-Najjar syndrome type I: A study of 14 cases

A. Munnich, F. Trivin, M. Odiévre, 1994, Human Genetics.

[Hereditary fructose intolerance with early onset].

J. Mercier, M. Odiévre, A. Bourrillon, 1976, Archives francaises de pediatrie.

Hepatic porto-enterostomy or cholecystostomy in the treatment of extrahepatic biliary atresia. A study of 49 cases.

M. Odiévre, J. Valayer, D. Alagille, 1976, The Journal of pediatrics.

Bacteriological Analysis of Jejunostomy Fluid After Surgery for Extrahepatic Biliary Atresia

E. Bingen, M. Odiévre, N. Lambert-Zechovsky, 1983, Journal of pediatric gastroenterology and nutrition.

"Uncorrectable" extrahepatic biliary atresia: relationship between intrahepatic bile duct pattern and surgery.

M. Gautier, M. Odiévre, G. Moitier, 1980, Journal of pediatric surgery.

Long-term results of surgical treatment of biliary atresia

M. Odiévre, 1978, World Journal of Surgery.

[Angioma in infants: favorable effect of intravenous hydrocortisone].

M. Odiévre, D. Alagille, M. Hamza, 1971, Archives francaises de pediatrie.

Apolipoprotein E polymorphism and serum concentrations in patients with glycogen storage disease type Ia

M. Odiévre, P. Labrune, J. Francoual, 2000, Journal of Inherited Metabolic Disease.