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Orphanet Journal of Rare Diseases
|
January 11, 2013
Syndromic diarrhea/Tricho-hepato-enteric syndrome
Alexandre Fabre, Christine Martinez-Vinson, Olivier Goulet, et al.
Pediatrics
|
June 2, 2021
Children's Drawings of Coronavirus
Laetitia Martinerie, Delphine Bernoux, Lisa Giovannini-Chami, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 2, 2023
Oral findings in children with congenital cholestatic disease: A systematic review of case reports and case series
Florence Reynal, Ariane Camoin, Corinne Tardieu, et al.
Brazilian Journal of Anesthesiology (Elsevier)
|
June 5, 2020
[General anesthesia for Crisponi syndrome: case report]
Chloé Allary, Marco Caruselli, Alexandre Fabre, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
April 9, 2026
Pediatric oral and dental manifestations of biliary atresia and Alagille syndrome: a comparative retrospective study
Florence Reynal, Ariane Camoin, Corinne Tardieu, et al.
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology
|
April 19, 2023
Proposed mechanism for the selection of lactase persistence in childhood
Alexandre Fabre, Anne Fabre, Céline Bon, et al.
Intractable & Rare Diseases Research
|
June 5, 2024
Systematic review of phenotypes and genotypes of patients with gastrointestinal defects and immunodeficiency syndrome-1 (GIDID1) (related to TTC7A)
Amelie Busolin, Frederic Vely, Gilles Eymard-Duvernay, et al.
American Journal of Medical Genetics. Part A
|
February 24, 2007
Intractable diarrhea with "phenotypic anomalies" and tricho-hepato-enteric syndrome: two names for the same disorder
Alexandre Fabre, Nicolas André, Anne Breton, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
January 4, 2026
Age and feeding method dependence of gamma-glutamyltransferase levels in non-jaundiced newborns
Audrey Ollivier-Garcia Cano, Marion Marlinge, Paul Guerry, et al.
European Journal of Medical Genetics
|
January 22, 2025
Hepatic manifestations in VPS53-related pontocerebellar hypoplasia type 2E: A case report
Auriane Mouchez, Célia Hoebeke, Béatrice Desnous, et al.
Page
of 8
Search research articles
Search
Showing results (11-20 of 73) with videos related to
Sort By:
Page
of 8
Orphanet Journal of Rare Diseases
|
January 11, 2013
Syndromic diarrhea/Tricho-hepato-enteric syndrome
Alexandre Fabre, Christine Martinez-Vinson, Olivier Goulet, et al.
Pediatrics
|
June 2, 2021
Children's Drawings of Coronavirus
Laetitia Martinerie, Delphine Bernoux, Lisa Giovannini-Chami, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 2, 2023
Oral findings in children with congenital cholestatic disease: A systematic review of case reports and case series
Florence Reynal, Ariane Camoin, Corinne Tardieu, et al.
Brazilian Journal of Anesthesiology (Elsevier)
|
June 5, 2020
[General anesthesia for Crisponi syndrome: case report]
Chloé Allary, Marco Caruselli, Alexandre Fabre, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
April 9, 2026
Pediatric oral and dental manifestations of biliary atresia and Alagille syndrome: a comparative retrospective study
Florence Reynal, Ariane Camoin, Corinne Tardieu, et al.
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology
|
April 19, 2023
Proposed mechanism for the selection of lactase persistence in childhood
Alexandre Fabre, Anne Fabre, Céline Bon, et al.
Intractable & Rare Diseases Research
|
June 5, 2024
Systematic review of phenotypes and genotypes of patients with gastrointestinal defects and immunodeficiency syndrome-1 (GIDID1) (related to TTC7A)
Amelie Busolin, Frederic Vely, Gilles Eymard-Duvernay, et al.
American Journal of Medical Genetics. Part A
|
February 24, 2007
Intractable diarrhea with "phenotypic anomalies" and tricho-hepato-enteric syndrome: two names for the same disorder
Alexandre Fabre, Nicolas André, Anne Breton, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
January 4, 2026
Age and feeding method dependence of gamma-glutamyltransferase levels in non-jaundiced newborns
Audrey Ollivier-Garcia Cano, Marion Marlinge, Paul Guerry, et al.
European Journal of Medical Genetics
|
January 22, 2025
Hepatic manifestations in VPS53-related pontocerebellar hypoplasia type 2E: A case report
Auriane Mouchez, Célia Hoebeke, Béatrice Desnous, et al.
Page
of 8