Results 51 to 60 of about 118 (92)
La endocrinopatía múltiple Tipo I se caracteriza por la presencia simultánea de tumores, o hiperplasias, en hipófisis, paratiroides y páncreas, originando el cuadro clínico de hiperfunción endocrina múltiple.
Guido Lastra, Jaime de la Hoz
doaj
Se realiza una investigación, prospectiva, con el empleo de la eritropoyetina recombinante humana (EPOrHu) cubana EPOCIM, durante 9 meses en pacientes en hemodiálisis iterada, a los que se les corrigió la anemia renal.
Jorge F. Pérez-Oliva Díaz +3 more
doaj
Association between current major depressive episode and the occurrence of menstrual irregularities in the last six months in university students in Lima, Peru. [PDF]
Pantoja-Coronel X +5 more
europepmc +1 more source
Double pituitary adenomas in a large surgical series. [PDF]
Zieliński G +4 more
europepmc +1 more source
Combining targeted panel-based resequencing and copy-number variation analysis for the diagnosis of inherited syndromic retinopathies and associated ciliopathies. [PDF]
Sanchez-Navarro I +20 more
europepmc +1 more source
[Hyperprolactinemia secondary to hypotensive treatment with verapamil]. [PDF]
Ortega Calvo M +3 more
europepmc +1 more source
Multiple endocrine neoplasia type 1 in childhood and description of a novel variant. [PDF]
Sales MTA +7 more
europepmc +1 more source

