Results 181 to 190 of about 28,682 (252)

Sequence Analysis of Thyroid Transcription Factor-2 (TTF-2) Gene in Ten Patients with Congenital Hypothyroidism due to Thyroid Dysgenesis.

, 2000
Takeo Kuribayashi, Akira Hishinuma, Sanae Kanazawa, Yuko Nihei, Megumi Hoshi, Mariko Oyama, Akihisa Nitta, Tamio Ieiri, Osamu Arisaka   +8 more
openalex   +2 more sources

Age of menarche and final height in patients with permanent congenital hypothyroidism. [PDF]

Ann Pediatr Endocrinol Metab
Karimian P, Hovsepian S, Alinia T, Raispour H, Mirshahzadeh N, Hashemipour M.   +5 more
europepmc   +1 more source

Neonatal screening for congenital hypothyroidism in environmentally disadvantaged regions1

, 2000
В. Г. Помелова, С. Г. Калиненкова   +1 more
openalex   +1 more source

Efficacy of levothyroxine on growth and development in children with congenital hypothyroidism: A meta-analysis. [PDF]

Medicine (Baltimore)
Liang W, Tu L.
europepmc   +1 more source

Neonatal screening for congenital hypothyroidism: 28-year experience in the state of Minas Gerais, Brazil. [PDF]

J Pediatr (Rio J)
Braga NTP, Alves DPDSS, Colosimo EA, Dias VMA, Januário JN, Silva IN.   +5 more
europepmc   +1 more source

Mutation spectra and genotype‑phenotype analysis of congenital hypothyroidism in a neonatal population. [PDF]

Biomed Rep
Huang X, Shao Q, Weng S, Chen W, Yuan W, Tan J, Yang X, Su X.   +7 more
europepmc   +1 more source

SCREENING FOR CONGENITAL HYPOTHYROIDISM

The Lancet, 1986
openaire   +3 more sources

A National Survey on Congenital Hypothyroidism Newborn Screening in Pakistan. [PDF]

Glob Pediatr Health
Khan SA, Aftab S, Khan YN, Yasir M, Arshad K, Mehak NUA, Rehman SKU, Faiztalpur A, Bahar S, Abdul Razzaq A, Habibullah S, Naseem A, Hussain SS, Sattar H, Usman M, Ayub A, Waris R, Butt TA.   +17 more
europepmc   +1 more source

Paroxysmal Hypertension in Congenital Hypothyroidism: An Unusual Case of Pheochromocytoma. [PDF]

Cureus
Fagan P, McLaughlin CJ, Fugok KL, Desai T.   +3 more
europepmc   +1 more source

Investigating <i>TSHR</i> gene variants in consanguineous families: novel insights into variable expression in familial congenital hypothyroidism. [PDF]

Front Endocrinol (Lausanne)
Nadeali Z, Mohammadi-Zaniani Z, Biglari S, Molavi N, Zardoui K, Mirfendereski S, Hashemipour M, Tabatabaiefar MA, Polychronakos C.   +8 more
europepmc   +1 more source