Your browser doesn't support javascript.
loading
Multifocal gastric adenocarcinoma in a patient with LRBA deficiency.
Bratanic, Nina; Kovac, Jernej; Pohar, Katka; Trebusak Podkrajsek, Katarina; Ihan, Alojz; Battelino, Tadej; Avbelj Stefanija, Magdalena.
Afiliação
  • Bratanic N; Department of Pediatric Endocrinology, Diabetes and Metabolism, University Medical Centre, University Children's Hospital, Bohoriceva 20, 1000, Ljubljana, Slovenia.
  • Kovac J; University Medical Centre, University Children's Hospital, Unit for Special Laboratory Diagnostics, Vrazov trg 1, 1000, Ljubljana, Slovenia.
  • Pohar K; University of Ljubljana, Faculty of Medicine, Institute for Microbiology and Immunology, Zaloska 4, 1000, Ljubljana, Slovenia.
  • Trebusak Podkrajsek K; University Medical Centre, University Children's Hospital, Unit for Special Laboratory Diagnostics, Vrazov trg 1, 1000, Ljubljana, Slovenia.
  • Ihan A; University of Ljubljana, Faculty of Medicine, Vrazov trg 2, 1000, Ljubljana, Slovenia.
  • Battelino T; University of Ljubljana, Faculty of Medicine, Institute for Microbiology and Immunology, Zaloska 4, 1000, Ljubljana, Slovenia.
  • Avbelj Stefanija M; Department of Pediatric Endocrinology, Diabetes and Metabolism, University Medical Centre, University Children's Hospital, Bohoriceva 20, 1000, Ljubljana, Slovenia.
Orphanet J Rare Dis ; 12(1): 131, 2017 07 18.
Article em En | MEDLINE | ID: mdl-28720148

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Gástricas / Adenocarcinoma / Proteínas Adaptadoras de Transdução de Sinal / Síndromes de Imunodeficiência Tipo de estudo: Prognostic_studies Limite: Adult / Humans / Male Idioma: En Revista: Orphanet J Rare Dis Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Gástricas / Adenocarcinoma / Proteínas Adaptadoras de Transdução de Sinal / Síndromes de Imunodeficiência Tipo de estudo: Prognostic_studies Limite: Adult / Humans / Male Idioma: En Revista: Orphanet J Rare Dis Ano de publicação: 2017 Tipo de documento: Article