Primary congenital Hypothyroidism

被引：1
|
作者：
Baumgartner-Parzer, Sabina [1 ]
机构：
[1] Med Univ Wien, Univ Klin Innere Med 3, Wahringer Gurtel 18-20, A-1090 Vienna, Austria
来源：
AUSTRIAN JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM | 2019年 / 12卷 / 02期
关键词：
CAUSATIVE GENES; MUTATIONS; PAX8; MANAGEMENT;
D O I：
10.1007/s41969-019-0068-5
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
[No abstract available]
引用
收藏
页码：70 / 72
页数：3
相关论文
共 50 条
  • [41] High Prevalence of Hearing Impairment in Primary Congenital Hypothyroidism
    Almagor, Tal
    Rath, Shoshana
    Nachtigal, Dan
    Sharroni, Zohara
    Elias-Assad, Ghadir
    Hess, Ora
    Havazelet, Gilad
    Zehavi, Yoav
    Spiegel, Ronen
    Bercovich, Dani
    Almashanu, Shlomo
    Tenenbaum-Rakover, Yardena
    EUROPEAN THYROID JOURNAL, 2021, 10 (03) : 215 - 221
  • [42] HIGHER SENSITIVITY OF PRIMARY THYROTROPIN IN SCREENING FOR CONGENITAL HYPOTHYROIDISM - A MYTH
    DUSSAULT, JH
    MORISSETTE, J
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1983, 56 (04): : 849 - 852
  • [43] Dependence of pituitary gland abnormalities on the cause of primary congenital hypothyroidism
    Rajewska, J.
    Czyzyk, Adam
    EUROPEAN JOURNAL OF MEDICAL RESEARCH, 2009, 14 : 25 - 26
  • [44] Iatrogenic hyperthyroidism in primary congenital hypothyroidism: prevalence and predictive factors
    Chooprasertsuk, Nuanpan
    Dejkhamron, Prapai
    Unachak, Kevalee
    Wejaphikul, Karn
    JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 2022, 35 (10): : 1250 - 1256
  • [45] Incidence of primary congenital hypothyroidism over 24 years in Finland
    Danner, Emmi
    Niuro, Laura
    Huopio, Hanna
    Niinikoski, Harri
    Viikari, Liisa
    Kero, Jukka
    Jaaskelainen, Jarmo
    PEDIATRIC RESEARCH, 2023, 93 (03) : 649 - 653
  • [46] ANEMIA AND ITS PLACE IN PRIMARY CONGENITAL HYPOTHYROIDISM DIAGNOSTIC ASSESSMENT
    Dobrota, L.
    Neamtu, M. L.
    Bodrug, N.
    Istrate, V.
    EUROPEAN JOURNAL OF PEDIATRICS, 2016, 175 (11) : 1788 - 1788
  • [47] Recent advances in understanding the molecular basis of primary congenital hypothyroidism
    Macchia, PE
    MOLECULAR MEDICINE TODAY, 2000, 6 (01): : 36 - 42
  • [48] EVOLUTION OF HEIGHT AND BONE-AGE IN PRIMARY CONGENITAL HYPOTHYROIDISM
    DEFRIAS, EC
    RUIBAL, JL
    REVERTE, F
    BUENO, G
    CLINICAL PEDIATRICS, 1993, 32 (07) : 426 - 432
  • [49] Incidence of primary congenital hypothyroidism over 24 years in Finland
    Emmi Danner
    Laura Niuro
    Hanna Huopio
    Harri Niinikoski
    Liisa Viikari
    Jukka Kero
    Jarmo Jääskeläinen
    Pediatric Research, 2023, 93 : 649 - 653
  • [50] Revised guidelines for neonatal screening programmes for primary congenital hypothyroidism
    Toublanc, JE
    Grüters-Kieslich, A
    Donaldson, M
    Ferrandez-Longas, A
    Giovannelli, G
    Honour, JW
    Hnikova, O
    Klett, M
    Larsson, A
    Keizer-Schrama, SMPFD
    Torresani, T
    HORMONE RESEARCH, 1999, 52 (01) : 49 - 52
12345