about
Recurrent EZH1 mutations are a second hit in autonomous thyroid adenomasX-Linked Adrenal Hypoplasia Congenita in a Boy due to a Novel Deletion of the Entire NR0B1 (DAX1) and MAGEB1-4 Genes.Pituitary Microsomal Autoantibodies in Patients with Childhood-Onset Combined Pituitary Hormone Deficiency: an Antigen Identification AttemptAdrenal function and MC1R gene analysis in a prepubertal girl with generalized hyperpigmentation: case report.Clinical relevance of thyroid-stimulating autoantibodies in pediatric graves' disease-a multicenter study.Guidelines of Polish National Societies Diagnostics and Treatment of Thyroid Carcinoma. 2018 Update.Diagnostics and treatment of differentiated thyroid carcinoma in children - Guidelines of Polish National Societies.Integrating clinical and genetic approaches in the diagnosis of 46,XY disorder of sex development
P50
Q37217469-4A9401B1-C10E-4745-918B-E2E72507C161Q37253219-65FD9112-756F-40D9-8684-8FCC1902BB59Q37377805-4F785396-445C-481E-84EF-E929BB095E63Q42134614-B1889BAE-A8C0-4E5B-84AB-8FA4D5AF9726Q43626915-803CA341-16ED-47FF-AA8C-FC6A08981031Q50016120-2417359A-6D63-4453-B3E8-4271E50A34A0Q54515394-EF01AB87-A9AD-4941-B9AD-B01831AC2599Q60931487-6168BDC3-C583-4F28-A8EE-89D2BD2BBFA9
P50
description
researcher (ORCID 0000-0001-8862-6937)
@en
wetenschapper
@nl
name
Marek Niedziela
@en
Marek Niedziela
@nl
type
label
Marek Niedziela
@en
Marek Niedziela
@nl
prefLabel
Marek Niedziela
@en
Marek Niedziela
@nl
P31
P496
0000-0001-8862-6937