Autosomal-dominant non-autoimmune hyperthyroidism presenting with neuromuscular symptoms

Acta Paediatrica, International Journal of Paediatrics

Volumn 94, Issue 8, 2005, Pages 1145-1148

  Elgadi, Aziz ^a   Arvidsson, C G ^b   Janson, Annika ^a   Marcus, Claude ^a   Costagliola, Sabine ^c   Norgren, Svante ^a  

^a KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

^b CENTRAL HOSPITAL   (Sweden)

^c UNIVERSITÉ LIBRE DE BRUXELLES   (Belgium)

Author keywords

Endocrinology; Neuromuscular symptoms; Non autoimmune hyperthyroidism; TSHR mutation

Indexed keywords

GLYCINE; LEVOTHYROXINE; SERINE; THIAMAZOLE; THYROTROPIN RECEPTOR;

ARTICLE; AUTOIMMUNE DISEASE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; GENE SEQUENCE; HUMAN; HYPERTHYROIDISM; MISSENSE MUTATION; MUTANT; NEUROMUSCULAR DISEASE; PATHOGENESIS; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SYMPTOM; THYROIDECTOMY;

CHILD; DIAGNOSIS, DIFFERENTIAL; GENES, DOMINANT; GERM-LINE MUTATION; HUMANS; HYPERTHYROIDISM; MALE; METHIMAZOLE; NEUROMUSCULAR DISEASES; RECEPTORS, THYROTROPIN; RISK ASSESSMENT; SEVERITY OF ILLNESS INDEX; THYROID FUNCTION TESTS;

EID: 23844450115     PISSN: 08035253     EISSN: 16512227     Source Type: Journal    
DOI: 10.1080/08035250510032925     Document Type: Article

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