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hypothyroidism screening. [A veleszületett hypothyreosis szűrővizsgálatának első 13 éve.] Gyermekgyógyászat, 1997, 48 , 133–135. [Hungarian] Blatniczky L. The first 13 year of the congenital

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thyroid development: how many genes for congenital hypothyroidism? Topical Endocrinol., 2001, 7 , 26–27. Lauro R. Transcription factors of thyroid development: how many genes for

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Orvosi Hetilap
Authors: Edina Flach, Richárd Kellermayer, Tibor Ertl, Gabriella Vida, Ilona Sárkány, Simone Funke, and Judit Gyarmati

congenital hypothyroidism. Pediatr. Dermatol., 1993, 10 , 6–11. Moroz B. Cutis marmorata telangiectatica congenita: long-term follow-up, review of the literature, and report of a case

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receptor properties in congenital hypothyroid rat under thyroxine or vasopressin therapy. Horm. Metab. Res. 19 , 624–628. Clos J. A comparative study of plasma vasopressin levels and

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Ali, M., Guillon, G., Cantau, B., Balestre, M. N., Chicot, D., Clos, J. (1987) A comparative study of plasma vasopressin levels and V1 and V2 vasopressin receptor properties in congenital hypothyroid rat under

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. Robinson , W. F. , Shaw , S. E. , Stanley , B. and Wyburn , R. S. ( 1988 ): Congenital hypothyroidism in Scottish deerhound puppies . Aust. Vet. J. 65 , 368 – 389 . Rudas , P

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-vizsgálatok Hajdú-Bihar megyében.] Gyermekgyógyászat 2006; 57: 535–542. [Hungarian] 47 Delange F. Screening for congenital hypothyroidism used as an indicator of

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