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P. Broué · SciRah

Researcher profile · Semantic Scholar

P. Broué

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P. Broué — researcher profile on SciRah

h-index: 25
Works: 64
Citations: 2,345

Most-cited papers

Impact of Age at Kasai Operation on Its Results in Late Childhood and Adolescence: A Rational Basis for Biliary Atresia Screening
M. Serinet, B. Wildhaber, P. Broué, A. Lachaux +4 more
2009Pediatrics435 citations Open access
Semantic Scholar
Improving outcomes of biliary atresia: French national series 1986-2009.
C. Chardot, C. Buet, M. Serinet, J. Golmard +7 more
2013Journal of Hepatology245 citations
Semantic Scholar
Management of patients with biliary atresia in France: Results of a decentralized policy 1986‐2002
M. Serinet, P. Broué, E. Jacquemin, A. Lachaux +4 more
2006Hepatology172 citations Open access
Semantic Scholar
Efficacy of propranolol in hepatic infantile hemangiomas with diffuse neonatal hemangiomatosis.
J. Mazereeuw-Hautier, P. Hoeger, S. Benlahrech, A. Ammour +8 more
2010Jornal de Pediatria162 citations
Semantic Scholar
High sustained virologic response rates in children with chronic hepatitis C receiving peginterferon alfa-2b plus ribavirin.
S. Wirth, C. Ribes-Koninckx, M. A. Calzado, F. Bortolotti +28 more
2010Journal of Hepatology149 citations
Semantic Scholar
Clinical and biological features at diagnosis in mitochondrial fatty acid beta-oxidation defects: a French pediatric study of 187 patients
J. Baruteau, P. Sachs, P. Broué, M. Brivet +3 more
2013Journal of Inherited Metabolic Disease113 citations
Semantic Scholar
Management of Biliary Atresia in France 1986-2015: Long Term Results.
Martina Fanna, G. Masson, C. Capito, M. Girard +10 more
2019Journal of Pediatric Gastroenterology and Nutrition - JPGN105 citations Open access
Semantic Scholar
Defining clinical subgroups and genotype–phenotype correlations in NBAS-associated disease across 110 patients
C. Staufner, B. Peters, M. Wagner, S. Alameer +47 more
2019Genetics in Medicine66 citations Open access
Semantic Scholar
An Early Viral Response Predicts the Virological Response to Ribavirin in Hepatitis E Virus Organ Transplant Patients
N. Kamar, S. Lhomme, F. Abravanel, O. Cointault +14 more
2015Transplantation66 citations Open access
Semantic Scholar
Orthotopic liver transplantation for mitochondrial respiratory chain disorders: a study of 5 children.
B. Dubern, P. Broué, C. Dubuisson, V. Cormier-Daire +5 more
2001Transplantation62 citations Open access
Semantic Scholar
Liver disease related to alpha1‐antitrypsin deficiency in French children: The DEFI‐ALPHA cohort
M. Ruiz, F. Lacaille, J. Berthiller, P. Joly +12 more
2019Liver international (Print)44 citations
Semantic Scholar
The German Revolution, 1917-1923
P. Broué
200441 citations
Semantic Scholar
Genetic contribution of ABCC2 to Dubin‐Johnson syndrome and inherited cholestatic disorders
C. Corpechot, V. Barbu, O. Chazouilleres, P. Broué +7 more
2020Liver international (Print)40 citations
Semantic Scholar
Liver Disease Associated with ZZ α1-Antitrypsin Deficiency and Ursodeoxycholic Acid Therapy in Children
P. Lykavieris, B. Ducot, A. Lachaux, A. Dabadie +4 more
2008Journal of Pediatric Gastroenterology and Nutrition - JPGN40 citations Open access
Semantic Scholar
Neonatal hemochromatosis: diagnostic work-up based on a series of 56 cases of fetal death and neonatal liver failure.
S. Heissat, S. Collardeau-Frachon, J. Baruteau, E. Dubruc +6 more
2015Jornal de Pediatria38 citations
Semantic Scholar
Clinical and biological features at diagnosis in mitochondrial fatty acid beta-oxidation defects: a French pediatric study from 187 patients. Complementary data
J. Baruteau, P. Sachs, P. Broué, M. Brivet +3 more
2014Journal of Inherited Metabolic Disease38 citations
Semantic Scholar
French Retrospective Multicentric Study of Neonatal Hemochromatosis: Importance of Autopsy and Autoimmune Maternal Manifestations
S. Collardeau-Frachon, S. Heissat, R. Bouvier, M. Fabre +7 more
2012Pediatric and Developmental Pathology33 citations
Semantic Scholar
Long‐term outcome of methylmalonic aciduria after kidney, liver, or combined liver‐kidney transplantation: The French experience
A. Brassier, P. Krug, F. Lacaille, C. Pontoizeau +28 more
2020Journal of Inherited Metabolic Disease32 citations
Semantic Scholar
Long-term liver disease in methylmalonic and propionic acidemias.
A. Imbard, N. Garcia-Segarra, M. Tardieu, P. Broué +12 more
2018Molecular Genetics and Metabolism29 citations
Semantic Scholar
Hereditary fructose intolerance: frequency and spectrum mutations of the aldolase B gene in a large patients cohort from France--identification of eight new mutations.
A. Davit-Spraul, C. Costa, M. Zater, D. Habès +6 more
2008Molecular Genetics and Metabolism29 citations
Semantic Scholar
Intractable diarrhea with “phenotypic anomalies” and tricho‐hepato‐enteric syndrome: Two names for the same disorder
A. Fabre, N. André, A. Breton, P. Broué +2 more
2007American Journal of Medical Genetics. Part A29 citations
Semantic Scholar
Targeted-Capture Next-Generation Sequencing in Diagnosis Approach of Pediatric Cholestasis
M. Almes, A. Spraul, M. Ruiz, M. Girard +16 more
2022Diagnostics28 citations Open access
Semantic Scholar
Genotype-phenotype associations in French patients with phenylketonuria and importance of genotype for full assessment of tetrahydrobiopterin responsiveness
E. Jeannesson-Thivisol, F. Feillet, C. Chéry, P. Perrin +24 more
2015Orphanet Journal of Rare Diseases27 citations Open access
Semantic Scholar
Fulminant hepatic failure after herbal medicine ingestion in children.
H. Bagheri, P. Broué, I. Lacroix, D. Larrey +4 more
1998The´rapie (Paris)27 citations
Semantic Scholar
Psychiatric adult-onset of urea cycle disorders: A case-series
A. Bigot, P. Brunault, C. Lavigne, F. Feillet +7 more
2017Molecular Genetics and Metabolism Reports26 citations Open access
Semantic Scholar
Heterogeneity of follow-up procedures in French and Belgian patients with treated hereditary tyrosinemia type 1: results of a questionnaire and proposed guidelines
M. Schiff, P. Broué, B. Chabrol, C. de Laet +6 more
2012Journal of Inherited Metabolic Disease24 citations
Semantic Scholar
Pediatric Wilson's Disease: Phenotypic, Genetic Characterization and Outcome of 182 Children in France
E. Couchonnal, L. Lion-François, O. Guillaud, D. Habès +15 more
2021Journal of Pediatric Gastroenterology and Nutrition - JPGN23 citations Open access
Semantic Scholar
Relevance of C5b9 immunostaining in the diagnosis of neonatal hemochromatosis
E. Dubruc, B. Nadaud, E. Ruchelli, S. Heissat +7 more
2017Pediatric Research21 citations Open access
Semantic Scholar
Transient Neonatal Liver Disease After Maternal Antenatal Intravenous Ig Infusions in Gestational Alloimmune Liver Disease Associated With Neonatal Haemochromatosis
J. Baruteau, S. Heissat, P. Broué, S. Collardeau-Frachon +18 more
2014Journal of Pediatric Gastroenterology and Nutrition - JPGN19 citations Open access
Semantic Scholar
Fructose‐1,6‐bisphosphatase deficiency causes fatty liver disease and requires long‐term hepatic follow‐up
M. Gorce, É. Lebigot, A. Arion, A. Brassier +11 more
2021Journal of Inherited Metabolic Disease16 citations Open access
Semantic Scholar
Population and evolutionary genetics of the PAH locus to uncover overdominance and adaptive mechanisms in phenylketonuria: Results from a multiethnic study
A. Oussalah, E. Jeannesson-Thivisol, C. Chéry, P. Perrin +26 more
2020EBioMedicine16 citations Open access
Semantic Scholar
Budd-Chiari syndrome.
A. Coilly, P. Potier, P. Broué, I. Kounis +8 more
2020Clinics And Research in Hepatology and Gastroenterology16 citations Open access
Semantic Scholar
Neurocognitive profiles in MSUD school-age patients
Juliette Bouchereau, Julie Leduc-Leballeur, S. Pichard, A. Imbard +20 more
2017Journal of Inherited Metabolic Disease16 citations
Semantic Scholar
ATP7B variant spectrum in a French pediatric Wilson disease cohort.
E. Couchonnal, S. Bouchard, T. Sandahl, C. Pagan +16 more
2021European Journal of Medical Genetics15 citations Open access
Semantic Scholar
Effects of miglustat therapy on neurological disorder and survival in early-infantile Niemann-Pick disease type C: a national French retrospective study
C. Freihuber, Bahia Dahmani-Rabehi, A. Brassier, P. Broué +10 more
2017Orphanet Journal of Rare Diseases15 citations Open access
Semantic Scholar
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
Patricia Dubot, F. Sabourdy, G. Plat, C. Jubert +4 more
2019International Journal of Molecular Sciences14 citations Open access
Semantic Scholar
Individual and family determinants for quality of life in parents of children with inborn errors of metabolism requiring a restricted diet: a multilevel analysis approach.
Abdoulaye Ouattara, N. Resseguier, A. Cano, P. de Lonlay +25 more
2022Jornal de Pediatria12 citations Open access
Semantic Scholar
Determinants of Quality of Life in Children with Inborn Errors of Metabolism Receiving a Restricted Diet.
Abdoulaye Ouattara, N. Resseguier, A. Cano, P. de Lonlay +25 more
2021Jornal de Pediatria11 citations Open access
Semantic Scholar
Health Status of French Young Patients with Inborn Errors of Metabolism with Lifelong Restricted Diet.
A. Cano, N. Resseguier, Abdoulaye Ouattara, P. de Lonlay +25 more
2020Jornal de Pediatria11 citations Open access
Semantic Scholar
Porto-Sinusoidal Vascular Disease: A Pediatric Study of 30 Patients
C. Girard, N. Laborde, Clothilde Marbach, E. Mas +2 more
2022Journal of Pediatric Gastroenterology and Nutrition - JPGN10 citations
Semantic Scholar
Endoscopic cystostomy for posttraumatic pseudocyst in children.
E. Mas, K. Barange, A. Breton, François de Maupéou +3 more
2007Journal of Pediatric Gastroenterology and Nutrition - JPGN10 citations Open access
Semantic Scholar
Ulcerative esophagitis: a complication of a self-expanding metal-stent in a child.
E. Mas, K. Barange, A. Breton, P. Vaysse +2 more
2006Journal of Pediatric Gastroenterology and Nutrition - JPGN6 citations Open access
Semantic Scholar
A retrospective multicentric study on 34 patients with Niemann-Pick type C disease and early liver involvement in France.
Antoine Gardin, C. Mussini, B. Héron, M. Schiff +8 more
2022Jornal de Pediatria5 citations Open access
Semantic Scholar
A retrospective study on the liver toxicity of oral retinoids in Chanarin–Dorfman syndrome
C. Valette, N. Jonca, J. Fischer, J. Pernin-Grandjean +24 more
2023Journal of the European Academy of Dermatology and Venereology3 citations
Semantic Scholar
Pregnancy outcome in Refsum disease: Affected fetuses and children born to an affected mother
Patricia Dubot, L. Astudillo, G. Touati, J. Baruteau +4 more
2019JIMD Reports3 citations Open access
Semantic Scholar
[Congenital galactosaemia: an unusual presentation].
M. Marcoux, E. Laporte-Turpin, C. Alberge, E. Fournié-Gardini +4 more
2005Archives de pédiatrie3 citations
Semantic Scholar
Recommended respiratory tests are not routinely performed for mucopolysaccharidosis patients
Sophie Denamur, G. Touati, S. Debelleix, L. Damaj +6 more
2021ERJ Open Research2 citations Open access
Semantic Scholar
Thrombotic microangiopathy in a child with acute pancreatitis.
E. Mas, C. Azéma, A. Breton, S. Décramer +3 more
2007Journal of Pediatric Gastroenterology and Nutrition - JPGN2 citations Open access
Semantic Scholar
[Simple and rapid determination of leucine by HPLC. Importance for extra-renal treatment of maple syrup urine disease].
J. Garcia, A. Galinier, B. Périquet, P. Broué +3 more
2002Annales de Biologie Clinique1 citations
Semantic Scholar
ORTHOTOPIC LIVER TRANSPLANTATION FOR MITOCHONDRIAL RESPIRATORY CHAIN DISORDERS: A STUDY OF 5 CHILDREN1
B. Dubern, P. Broué, C. Dubuisson, V. Cormier-Daire +5 more
20011 citations
Semantic Scholar

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