Zobrazeno 1 - 10
of 144
pro vyhledávání: '"O, Hníková"'
Autor:
Giuseppe LaTessah, J. Lebl, Joan M. Jacobi, Annamaria Colao, P. D. Lapatsanis, Bartolomeo Merola, Johan Auwerx, Dorit Eldar, E. Ivašková, Edith Schober, George Economou, J. Zikmund, Tamar Amit, P.D. Gluckman, O. Hníková, Fernández Catalina, G.R. Ambler, G. Benz, Yehudit Altman, Francesca S. Tripodi, M. Eberlein-Gonska, Andrade Olivié, Antonella DiSarno, R.V.G. García-Mayor, Stiliani Andronikou, Joseph Sack, Zung Amnon, Dominique Porquet, U. Heinrich, Alpha S. Yap, Dirk Vanderschueren, John P. Galligan, Donald A. Perry-Keene, Robin H. Mortimer, Igor Kaiserman, Gabriele Häusler, Gaetano Lombardi, Roger Bouillon, Yaacov Baruch, H.F. Otto, Gideon Shoshany, Anna Challa, D. Haack, Julia Peinado-Onsurbe, Zeev Hochberg, V. Cholevas, Noëlle Beau, Paolo Marzullo, Malka Chen, Rego Iraeta, Renato Spaziante, S.N. McCutcheon, B.H. Breier, Pnina Hertz, H. Frisch, Bart Staels, Moussa B.H. Youdim, L. Kupková, Zvi Zadik, H. Sajdlová, Vincenzo Esposito, M. Castro, Frederick A. Khafagi, A. Reparaz, Rafael Enat, Didier Chevenne, Juliane Léger, Susanne Sagmeister, P. Kračmar
Publikováno v:
Hormone Research. 40:I-IV
Autor:
K, Banghová, Taji E, Al, D, Novotná, J, Zapletalová, O, Hníková, J, Cáp, J, Klabochová, M, Kúseková, J, Lebl
Publikováno v:
Casopis lekaru ceskych. 147(12)
Pendred syndrome (OMIM274600) is one of the causes of congenital hypothyroidism due to thyroid dyshormonogenesis. It is an autosomal recessive disease classically characterized by dyshormonogenetic goitre and sensorineural deafness. It is caused by m
Publikováno v:
Hormone Research. 40:201-203
Partial thyroxine-binding globulin (TBG) deficiency, with a median TBG of 2.3 mg/l, was found in 25 mature babies with hypothyroxinaemia (3 girls and 22 boys) from our screening programme for congenit
Publikováno v:
Casopis lekaru ceskych. 138(9)
The worldwide elimination of iodine deficiency is at present one of the priorities of WHO. The highest risk group with regard to sequelae of inadequate iodine supplies are even in case of a milder iodine deficiency, human foetuses during the foetal a
Autor:
V, Zamrazil, J, Cerovská, R, Bílek, A, Simecková, J, Vrbíková, M, Dvoráková, O, Hníková, M, Janecková, F, Tomiska
Publikováno v:
Bratislavske lekarske listy. 96(11)
The supply of iodine indisputably affects the function of the thyroid gland. It is not clear, however, as to what extent a moderate iodopenia affects common thyroid parameters. OBJECTIVES, STARTING POINT AND MAIN PURPOSE: The aim of the study is to e
Autor:
O, Hníková
Publikováno v:
Casopis lekaru ceskych. 134(6)
Changes of thyroid function affect beyond doubt the growth rate and bone maturation. In particular thyroid hypofunction during the first months of life leads not only to irreversible disorders of the development of the CNS but causes also a significa
Autor:
Z, Pôbisová, V, Zamrazil, A, Simecková, J, Cerovská, O, Hníková, Z, Novák, P, Vlcek, M, Voborská, J, Vrbíková
Publikováno v:
Vnitrni lekarstvi. 40(1)
In 1991-1992 in the Czech Republic an epidemiological survey was conducted focused on prevention of iodine deficiency and the incidence of some thyropathies. The authors examined samples of the Prague and Vsetín population selected at random. The cl
Publikováno v:
Ceskoslovenska pediatrie. 49(1)
The authors submit their experience with the treatment of idiopathic precocious central puberty in two girls with the GnRH analog (Decapeptyl-Depot, Ferring Co.). The drug was administered for one an a half and two years resp., 80 mg/kg once per mont
Autor:
O, Hníková
Publikováno v:
Ceskoslovenska pediatrie. 48(7)
The pathophysiology of endemic thyreopathies in extensive endemies is well known. In recent years considerable attention has been attracted even by moderate iodine deficiency, the result of which is not only goiter but a number of health, social and
Publikováno v:
Hormone research. 40(5-6)
Partial thyroxine-binding globulin (TBG) deficiency, with a median TBG of 2.3 mg/l, was found in 25 mature babies with hypothyroxinaemia (3 girls and 22 boys) from our screening programme for congenital hypothyroidism during 1988-1990. Analysis of th