Anna-pauliina Iivonen
Helsinki, 00014, Finland
Last Updated: 09/26/2026
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Found 8 publications
Presentation and diagnosis of childhood-onset combined pituitary hormone deficiency: A single center experience from over 30 years.
Journal: EClinicalMedicine
Published: February 10, 2022
Kallmann syndrome in a patient with Weiss-Kruszka syndrome and a de novo deletion in 9q31.2.
Journal: European journal of endocrinology
Published: December 03, 2020
Familial central precocious puberty: two novel MKRN3 mutations.
Journal: Pediatric research
Published: April 06, 2020
Loss-of-Function Variants in TBC1D32 Underlie Syndromic Hypopituitarism.
Journal: The Journal of clinical endocrinology and metabolism
Published: December 06, 2019
Screening for mutations in selected miRNA genes in hypogonadotropic hypogonadism patients.
Journal: Endocrine connections
Published: March 27, 2019
Screening for germline KCNQ1 and KCNE2 mutations in a set of somatotropinoma patients.
Journal: Endocrine connections
Published: March 21, 2018
Showing 1-8 of 8
Last Updated: 09/26/2026