Genetic analysis in children with transient thyroid dysfunction or subclinical hypothyroidism detected on neonatal screening

Clinical Pediatric Endocrinology

Volumn 18, Issue 4, 2009, Pages 95-100

  Satoh, Mari ^a   Aso, Keiko ^a   Ogikubo, Sayaka ^a   Ogasawara, Atsuko ^b,c   Saji, Tsutomu ^a  

^a TOHO UNIVERSITY OMORI MEDICAL CENTER   (Japan)

^b Ibaraki Children's Hospital   (Japan)

^c Okinaka Memorial Institute for Medical Research   (Japan)

Author keywords

Neonatal screening; Subclinical hypothyroidism; Thyroid peroxidase; Transient hyperthyrotropinemia; TSH receptor

Indexed keywords

DUAL OXIDASE 2; LEVOTHYROXINE; OXIDOREDUCTASE; THYROID PEROXIDASE; THYROTROPIN; THYROTROPIN RECEPTOR; UNCLASSIFIED DRUG;

ADOLESCENT; ARTICLE; CHILD; CLINICAL ARTICLE; CONGENITAL HYPOTHYROIDISM; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; HETEROZYGOTE; HORMONE SUBSTITUTION; HUMAN; MALE; NEWBORN SCREENING; PRESCHOOL CHILD; SCHOOL CHILD; THYROID DISEASE; THYROID FUNCTION TEST; THYROTROPIN BLOOD LEVEL;

EID: 73949092973     PISSN: 09185739     EISSN: 13477358     Source Type: Journal    
DOI: 10.1297/cpe.18.95     Document Type: Article

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