Zobrazeno 1 - 2
of 2
pro vyhledávání: '"M A, Aguilera Llovet"'
Autor:
A, Gutiérrez Benjumea, J, Rojo García, M A, Aguilera Llovet, C, García Arqueza, J, Casanovas Lax, J, Aguayo Maldonado
Publikováno v:
Anales espanoles de pediatria. 55(2)
Peutz-Jeghers syndrome is a rare hereditary disease, although in about 20 % of patients there is no known family history. Its clinical hallmarks are facial mucocutaneous pigmentation and diffuse gastrointestinal polyposis of hamartomatous origin. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b2d602189abba090d0bdef947f1c033d
https://pubmed.ncbi.nlm.nih.gov/11472670
https://pubmed.ncbi.nlm.nih.gov/11472670
Autor:
C, Cintado Bueno, M A, Aguilera Llovet, M, Menéndez Ruiz, P, Macías Mardones, F, Gayoso Gómez, R, Torronteras Santiago
Publikováno v:
Anales espanoles de pediatria. 11(8-9)
Eighty cases of mumps meningitis are studied in children between the ages of one to seven years. The parotids were affected before, after and during the meningitis in all cases. In fifteen cases, when admitted to the hospital, levels of glucose were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::33907318d3236558a646734c1b348226
https://pubmed.ncbi.nlm.nih.gov/717915
https://pubmed.ncbi.nlm.nih.gov/717915