First Report of a Patient with MPS Type VII, Due to Novel Mutations in GUSB , Who Underwent Enzyme Replacement and Then Hematopoietic Stem Cell Transplantation
Dubot, Patricia, Sabourdy, Frédérique, Plat, Geneviève, Jubert, Charlotte, Cancès, Claude, Broué, Pierre, Touati, Guy, Levade, Thierry
Published in International journal of molecular sciences (28.10.2019)
Published in International journal of molecular sciences (28.10.2019)
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Genetic contribution of ABCC2 to Dubin‐Johnson syndrome and inherited cholestatic disorders
Corpechot, Christophe, Barbu, Véronique, Chazouillères, Olivier, Broué, Pierre, Girard, Muriel, Roquelaure, Bertrand, Chrétien, Yves, Dong, Catherine, Lascols, Olivier, Housset, Chantal, Jéru, Isabelle
Published in Liver international (01.01.2020)
Published in Liver international (01.01.2020)
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Pediatric Wilson's Disease: Phenotypic, Genetic Characterization and Outcome of 182 Children in France
Couchonnal, Eduardo, Lion-François, Laurence, Guillaud, Olivier, Habes, Dalila, Debray, Dominique, Lamireau, Thierry, Broué, Pierre, Fabre, Alexandre, Vanlemmens, Claire, Sobesky, Rodolphe, Gottrand, Frederic, Bridoux-Henno, Laure, Dumortier, Jérôme, Belmalih, Abdelouahed, Poujois, Aurelia, Jacquemin, Emmanuel, Brunet, Anne Sophie, Bost, Muriel, Lachaux, Alain
Published in Journal of pediatric gastroenterology and nutrition (01.10.2021)
Published in Journal of pediatric gastroenterology and nutrition (01.10.2021)
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Clinical and biological features at diagnosis in mitochondrial fatty acid beta-oxidation defects: a French pediatric study of 187 patients
Baruteau, Julien, Sachs, Philippe, Broué, Pierre, Brivet, Michèle, Abdoul, Hendy, Vianey-Saban, Christine, Ogier de Baulny, Hélène
Published in Journal of inherited metabolic disease (01.09.2013)
Published in Journal of inherited metabolic disease (01.09.2013)
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Fructose‐1,6‐bisphosphatase deficiency causes fatty liver disease and requires long‐term hepatic follow‐up
Gorce, Magali, Lebigot, Elise, Arion, Alina, Brassier, Anaïs, Cano, Aline, De Lonlay, Pascale, Feillet, François, Gay, Claire, Labarthe, François, Nassogne, Marie‐Cécile, Roche, Sandrine, Roubertie, Agathe, Sacaze, Elise, Touati, Guy, Broué, Pierre
Published in Journal of inherited metabolic disease (01.03.2022)
Published in Journal of inherited metabolic disease (01.03.2022)
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Long-term liver disease in methylmalonic and propionic acidemias
Imbard, Apolline, Garcia Segarra, Nuria, Tardieu, Marine, Broué, Pierre, Bouchereau, Juliette, Pichard, Samia, de Baulny, Hélène Ogier, Slama, Abdelhamid, Mussini, Charlotte, Touati, Guy, Danjoux, Marie, Gaignard, Pauline, Vogel, Hannes, Labarthe, François, Schiff, Manuel, Benoist, Jean-François
Published in Molecular genetics and metabolism (01.04.2018)
Published in Molecular genetics and metabolism (01.04.2018)
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Relevance of C5b9 immunostaining in the diagnosis of neonatal hemochromatosis
Dubruc, Estelle, Nadaud, Béatrice, Ruchelli, Eduardo, Heissat, Sophie, Baruteau, Julien, Broué, Pierre, Debray, Dominique, Cordier, Marie-Pierre, Miossec, Pierre, Russo, Pierre, Collardeau-Frachon, Sophie
Published in Pediatric research (01.05.2017)
Published in Pediatric research (01.05.2017)
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Efficacy of Propranolol in Hepatic Infantile Hemangiomas with Diffuse Neonatal Hemangiomatosis
Mazereeuw-Hautier, Juliette, MD, PhD, Hoeger, Peter H., MD, Benlahrech, Sarah, MD, Ammour, Amir, MD, Broue, Pierre, MD, Vial, Julie, MD, Ohanessian, Gerard, MD, Léauté-Labrèze, Christine, MD, Labenne, Marc, MD, Vabres, Pierre, MD, PhD, Rössler, Jochen, MD, Bodemer, Christine, MD, PhD
Published in The Journal of pediatrics (01.08.2010)
Published in The Journal of pediatrics (01.08.2010)
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Budd-Chiari syndrome
Coilly, Audrey, Potier, Pascal, Broué, Pierre, Kounis, Ilias, Valla, Dominique, Hillaire, Sophie, Lambert, Vincent, Dutheil, Danielle, Hernández-Gea, Virginia, Plessier, Aurélie, Vilgrain, Valérie, Bureau, Christophe
Published in Clinics and research in hepatology and gastroenterology (01.09.2020)
Published in Clinics and research in hepatology and gastroenterology (01.09.2020)
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ATP7B variant spectrum in a French pediatric Wilson disease cohort
Couchonnal, Eduardo, Bouchard, Sophie, Sandahl, Thomas Damgaard, Pagan, Cecile, Lion-François, Laurence, Guillaud, Olivier, Habes, Dalila, Debray, Dominique, Lamireau, Thierry, Broué, Pierre, Fabre, Alexandre, Vanlemmens, Claire, Sobesky, Rodolphe, Gottrand, Frederic, Bridoux-Henno, Laure, Belmalih, Abdelouahed, Poujois, Aurelia, Brunet, Anne Sophie, Lachaux, Alain, Bost, Muriel
Published in European journal of medical genetics (01.10.2021)
Published in European journal of medical genetics (01.10.2021)
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Management of patients with biliary atresia in France: Results of a decentralized policy 1986‐2002
Serinet, Marie‐Odile, Broué, Pierre, Jacquemin, Emmanuel, Lachaux, Alain, Sarles, Jacques, Gottrand, Frédéric, Gauthier, Frédéric, Chardot, Christophe
Published in Hepatology (Baltimore, Md.) (01.07.2006)
Published in Hepatology (Baltimore, Md.) (01.07.2006)
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Recommended respiratory tests are not routinely performed for mucopolysaccharidosis patients
Denamur, Sophie, Touati, Guy, Debelleix, Stéphane, Damaj, Léna, Barth, Magalie, Tardieu, Marine, Gorce, Magali, Broué, Pierre, Lacombe, Didier, Labarthe, François
Published in ERJ open research (2022)
Published in ERJ open research (2022)
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Management of Biliary Atresia in France 1986 to 2015
Fanna, Martina, Masson, Guillaume, Capito, Carmen, Girard, Muriel, Guerin, Florent, Hermeziu, Bogdan, Lachaux, Alain, Roquelaure, Bertrand, Gottrand, Frédéric, Broue, Pierre, Dabadie, Alain, Lamireau, Thierry, Jacquemin, Emmanuel, Chardot, Christophe
Published in Journal of pediatric gastroenterology and nutrition (01.10.2019)
Published in Journal of pediatric gastroenterology and nutrition (01.10.2019)
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Clinical and biological features at diagnosis in mitochondrial fatty acid beta-oxidation defects: a French pediatric study from 187 patients. Complementary data
Baruteau, Julien, Sachs, Philippe, Broué, Pierre, Brivet, Michele, Abdoul, Hendy, Vianey-Saban, Christine, Ogier de Baulny, Hélène
Published in Journal of inherited metabolic disease (2014)
Published in Journal of inherited metabolic disease (2014)
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Liver Disease Associated with ZZ α1‐Antitrypsin Deficiency and Ursodeoxycholic Acid Therapy in Children
Lykavieris, Panayotis, Ducot, Béatrice, Lachaux, Alain, Dabadie, Alain, Broué, Pierre, Sarles, Jacques, Bernard, Olivier, Jacquemin, Emmanuel
Published in Journal of pediatric gastroenterology and nutrition (01.11.2008)
Published in Journal of pediatric gastroenterology and nutrition (01.11.2008)
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Impact of age at Kasai operation on its results in late childhood and adolescence: a rational basis for biliary atresia screening
Serinet, Marie-Odile, Wildhaber, Barbara E, Broué, Pierre, Lachaux, Alain, Sarles, Jacques, Jacquemin, Emmanuel, Gauthier, Frédéric, Chardot, Christophe
Published in Pediatrics (Evanston) (01.05.2009)
Published in Pediatrics (Evanston) (01.05.2009)
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Improving outcomes of biliary atresia: French national series 1986–2009
Chardot, Christophe, Buet, Chantal, Serinet, Marie-Odile, Golmard, Jean-Louis, Lachaux, Alain, Roquelaure, Bertrand, Gottrand, Frédéric, Broué, Pierre, Dabadie, Alain, Gauthier, Frédéric, Jacquemin, Emmanuel
Published in Journal of hepatology (01.06.2013)
Published in Journal of hepatology (01.06.2013)
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Phase I/II Trial of Liver-derived Mesenchymal Stem Cells in Pediatric Liver-based Metabolic Disorders: A Prospective, Open Label, Multicenter, Partially Randomized, Safety Study of One Cycle of Heterologous Human Adult Liver-derived Progenitor Cells (HepaStem) in Urea Cycle Disorders and Crigler-Najjar Syndrome Patients
Smets, Françoise, Dobbelaere, Dries, McKiernan, Patrick, Dionisi-Vici, Carlo, Broué, Pierre, Jacquemin, Emmanuel, Lopes, Ana Isabel, Gonçalves, Isabel, Mandel, Hanna, Pawlowska, Joanna, Kamińska, Diana, Shteyer, Eyal, Torre, Giuliano, Shapiro, Riki, Eyskens, François, Clapuyt, Philippe, Gissen, Paul, Pariente, Danièle, Grunewald, Stephanie, Yudkoff, Marc, Binda, Maria Mercedes, Najimi, Mustapha, Belmonte, Nathalie, de Vos, Beatrice, Thonnard, Joelle, Sokal, Etienne
Published in Transplantation (01.09.2019)
Published in Transplantation (01.09.2019)
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Transition care to adolescent hepatology in a tertiary center for rare adult–child liver disease
Laborde, Nolwenn, Barange, Karl, Girard, Chloé, Marbach, Clothilde, Bureau, Christophe, Broué, Pierre
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.01.2024)
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.01.2024)
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An Early Viral Response Predicts the Virological Response to Ribavirin in Hepatitis E Virus Organ Transplant Patients
Kamar, Nassim, Lhomme, Sebastien, Abravanel, Florence, Cointault, Olivier, Esposito, Laure, Cardeau-Desangles, Isabelle, Del Bello, Arnaud, Dörr, Gaëlle, Lavayssière, Laurence, Nogier, Marie Béatrice, Guitard, Joelle, Ribes, David, Goin, Anne Laure, Broué, Pierre, Metsu, David, Sauné, Karine, Rostaing, Lionel, Izopet, Jacques
Published in Transplantation (01.10.2015)
Published in Transplantation (01.10.2015)
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