Publications by authors named "Pierre Broué"

35Publications

Budd-Chiari syndrome.

Clin Res Hepatol Gastroenterol 2020 09 2;44(4):420-425. Epub 2020 Apr 2.

French Network for Rare Liver Diseases FILFOIE, Saint-Antoine Hospital, APHP, 184, rue du Faubourg Saint-Antoine, 75012 Paris, France; Department of Gastroenterology and Hepatology, Rangueil Hospital, University Hospital of Toulouse, 1, avenue du Professeur Jean-Poulhès, 31400 Toulouse, France.

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September 2020

Population and evolutionary genetics of the PAH locus to uncover overdominance and adaptive mechanisms in phenylketonuria: Results from a multiethnic study.

EBioMedicine 2020 Jan 7;51:102623. Epub 2020 Jan 7.

University of Lorraine, INSERM UMR_S 1256, Nutrition, Genetics, and Environmental Risk Exposure (NGERE), Faculty of Medicine of Nancy, Nancy, France; Department of Molecular Medicine, Division of Biochemistry, Molecular Biology, Nutrition, and Metabolism, University Hospital of Nancy, Nancy, France; Reference Centre for Inborn Errors of Metabolism (ORPHA67872), University Hospital of Nancy, Nancy F-54000, France.

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January 2020

First Report of a Patient with MPS Type VII, Due to Novel Mutations in , Who Underwent Enzyme Replacement and Then Hematopoietic Stem Cell Transplantation.

Int J Mol Sci 2019 Oct 28;20(21). Epub 2019 Oct 28.

Laboratoire de Biochimie Métabolique, Centre de Référence en Maladies Héréditaires du Métabolisme, Institut Fédératif de Biologie, CHU de Toulouse, 31059 Toulouse cedex 9, France.

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October 2019

Genetic contribution of ABCC2 to Dubin-Johnson syndrome and inherited cholestatic disorders.

Liver Int 2020 01 13;40(1):163-174. Epub 2019 Oct 13.

INSERM, Centre de Recherche Saint-Antoine (CRSA), Institut Hospitalo-Universitaire de Cardio-métabolisme et Nutrition (ICAN), Sorbonne Université, Paris, France.

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January 2020

Management of Biliary Atresia in France 1986 to 2015: Long-term Results.

J Pediatr Gastroenterol Nutr 2019 10;69(4):416-424

Observatoire Français de l'Atrésie des Voies Biliaires et Centre de Référence Atrésie des Voies Biliaires-Cholestases Génétiques, Hôpital Necker-Enfants Malades, Assistance Publique Hôpitaux de Paris.

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October 2019

Pregnancy outcome in Refsum disease: Affected fetuses and children born to an affected mother.

JIMD Rep 2019 Mar 14;46(1):11-15. Epub 2019 Mar 14.

Laboratoire de Biochimie Métabolique Centre de Référence en Maladies Héréditaires du Métabolisme, Institut Fédératif de Biologie, CHU de Toulouse Toulouse France.

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March 2019

Long-term liver disease in methylmalonic and propionic acidemias.

Mol Genet Metab 2018 04 7;123(4):433-440. Epub 2018 Feb 7.

Biochemistry Laboratory, APHP, Robert Debré University Hospital, Paris, France; Paris Sud University, Chatenay Malabry, France. Electronic address:

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April 2018

An Early Viral Response Predicts the Virological Response to Ribavirin in Hepatitis E Virus Organ Transplant Patients.

Transplantation 2015 Oct;99(10):2124-31

1 Department of Nephrology and Organ Transplantation, CHU Rangueil, Toulouse, France. 2 INSERM U1043, IFR-BMT, CHU Purpan, Toulouse, France. 3 Université Paul Sabatier, Toulouse, France. 4 Laboratory of Virology, CHU Purpan, Toulouse, France. 5 Department of Thoracic Surgery and Lung Transplantation, CHU Rangueil-Larrey, Toulouse, France. 6 Pediatric Hepatology, Hôpital des enfants, Toulouse, France. 7 Laboratory of Toxicology, CHU Purpan, Toulouse, France.

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October 2015

Transient neonatal liver disease after maternal antenatal intravenous Ig infusions in gestational alloimmune liver disease associated with neonatal haemochromatosis.

J Pediatr Gastroenterol Nutr 2014 Nov;59(5):629-35

*Pediatric Hepatology and Inborn Metabolic Diseases Unit, University Children's Hospital, Toulouse †Department of Pediatric Gastroenterology, Hepatology and Nutrition ‡Pathology Department, Hopital Femme Mère Enfant, Bron §Pathology Department, Institut Gustave Roussy ||Sorbonne Universités, UPMC Univ Paris 06, Paris ¶Internal Medicine Department #Special Care Baby Unit, Poissy-Saint Germain en Laye Hospital, Poissy **Clinical Genetics, Hopital Femme Mère Enfant, Bron ‡‡Pediatric Hepatology and Gastroenterology Unit §§Special Care Baby Unit, University Children's Hospital, Bordeaux ||Fetal Medicine, Saint Nicolas Hospital, Blaye ¶¶Neonatal Intensive Care Unit, Armand Trousseau Hospital, Paris ##Neonatal Intensive Care Unit, General Hospital, Saint-Brieuc ***Pediatric Surgery, Saint-Brieuc †††Clinical Genetics, University Hospital, Rennes, France ‡‡‡Metabolic Medicine Department, Great Ormond Street Hospital, London, UK §§§Department of Pediatric Surgery, Hepatology, and Transplantation, Necker Enfants Malades Hospital, Paris ||||||Pediatrics, University Hospital, Limoges, France.

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November 2014

Improving outcomes of biliary atresia: French national series 1986-2009.

J Hepatol 2013 Jun 8;58(6):1209-17. Epub 2013 Feb 8.

Observatoire français de l'atrésie des voies biliaires, Hôpital Necker - Enfants malades, Université Paris Descartes, Paris, France.

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June 2013

Clinical and biological features at diagnosis in mitochondrial fatty acid beta-oxidation defects: a French pediatric study of 187 patients.

J Inherit Metab Dis 2013 Sep 3;36(5):795-803. Epub 2012 Oct 3.

Hépatologie Pédiatrique et Maladies Métaboliques, Hôpital des Enfants-CHU Toulouse, Toulouse, France.

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September 2013

Hypoketotic hypoglycemia with myolysis and hypoparathyroidism: an unusual association in medium chain acyl-CoA desydrogenase deficiency (MCADD).

J Pediatr Endocrinol Metab 2009 Dec;22(12):1175-7

APHP, Hôpital Robert Debré, Service de Neurologie Pédiatrique et Maladies Héréditaires du Métabolisme, Paris, France.

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December 2009

Hereditary fructose intolerance: frequency and spectrum mutations of the aldolase B gene in a large patients cohort from France--identification of eight new mutations.

Mol Genet Metab 2008 Aug 9;94(4):443-7. Epub 2008 Jun 9.

Laboratoire de Biochimie, CHU de Bicêtre, Assistance Publique-Hôpitaux de Paris, 78, rue du Général Leclerc, 94275 Le Kremlin Bicêtre Cedex, France et Université Paris XI, IFR Bicêtre, France.

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August 2008

Endoscopic cystostomy for posttraumatic pseudocyst in children.

J Pediatr Gastroenterol Nutr 2007 Jul;45(1):121-4

Division of Gastroenterology, Hepatology and Nutrition, Children's Hospital, Toulouse, France.

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July 2007

Intractable diarrhea with "phenotypic anomalies" and tricho-hepato-enteric syndrome: two names for the same disorder.

Am J Med Genet A 2007 Mar;143A(6):584-8

Multidisciplinary Paediatric Department, Children Hospital of "La Timone", Boulevard Jean Moulin, Marseille Cedex, France.

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March 2007

Thrombotic microangiopathy in a child with acute pancreatitis.

J Pediatr Gastroenterol Nutr 2007 Jan;44(1):149-51

Division of Gastroenterology, Hepatology and Nutrition, Department of Paediatrics, Children's Hospital, Toulouse, France.

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January 2007

Ulcerative esophagitis: a complication of a self-expanding metal-stent in a child.

J Pediatr Gastroenterol Nutr 2006 Feb;42(2):229-31

Division of Gastroenterology, Hepatology and Nutrition, Department of Pediatrics, Children's Hospital, Toulouse University Hospital, 330 Avenue de Grande-Bretagne, TSA 70034, 31059 Toulouse Cedex 9, France.

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February 2006