Correction: Comparison of clinical characteristics of a pediatric cohort with combined pituitary hormone deficiency caused by mutation of the PROP1 gene or of other origins.

Zygmunt-Górska, Agata; Wójcik, Malgorzata; Gilis-Januszewska, Aleksandra; Starmach, Anna; Bik-Multanowski, Miroslaw; Starzyk, Jerzy B

Zygmunt-Górska, Agata; Wójcik, Malgorzata; Gilis-Januszewska, Aleksandra; Starmach, Anna; Bik-Multanowski, Miroslaw; Starzyk, Jerzy B.

Afiliación

Zygmunt-Górska A; Department of Pediatric and Adolescent Endocrinology, University Children's Hospital in Cracow, Cracow, Poland.
Wójcik M; Department of Pediatric and Adolescent Endocrinology, University Children's Hospital in Cracow, Cracow, Poland. malgorzata.wojcik@uj.edu.pl.
Gilis-Januszewska A; Department of Pediatric and Adolescent Endocrinology, Chair of Pediatrics, Pediatric Institute, Jagiellonian University Medical College, Ul. Wielicka 265, Cracow, 30-663, Poland. malgorzata.wojcik@uj.edu.pl.
Starmach A; Chair and Department of Endocrinology, Jagiellonian University Medical College, Cracow, Poland.
Bik-Multanowski M; Department of Pediatric and Adolescent Endocrinology, University Children's Hospital in Cracow, Cracow, Poland.
Starzyk JB; Department of Pediatric and Adolescent Endocrinology, Chair of Pediatrics, Pediatric Institute, Jagiellonian University Medical College, Ul. Wielicka 265, Cracow, 30-663, Poland.

Hormones (Athens) ; 23(2): 357, 2024 Jun.

Article en En | MEDLINE | ID: mdl-38498234

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Hormones (Athens) Asunto de la revista: ENDOCRINOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Polonia

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