Normalization of Height in Girls with Turner Syndrome after Long-Term Growth Hormone Treatment: Results of a Randomized Dose-Response Trial1

Autor: Stenvert L. S. Drop, T. Stijnen, Barto J. Otten, M. Jansen, H. M. Reeser, Guy Massa, T. Vulsma, C.W. Rouwé, S.M.P.F. de Muinck Keizer-Schrama, J. J. G. Hoorweg-Nijman, C Rongen-Westerlaken, Willem J M Gerver, J. J. Gosen, Theo C. J. Sas

Publikováno v: The Journal of Clinical Endocrinology & Metabolism. 84:4607-4612

Short stature and ovarian failure are the main features in Turner syndrome (TS). To optimize GH and estrogen treatment, we studied 68 previously untreated girls with TS, age 2–11 yr, who were randomly assigned to one of three GH dosage groups: grou

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4cddce9a7a94f1f7c90eca0f05defbb9
https://doi.org/10.1210/jcem.84.12.6241

Genetic Analysis of Short Children with Apparent Growth Hormone Insensitivity

Autor: J. van Doorn, Monique Losekoot, Sitha A. Scheltinga, H.A. van Duyvenvoorde, P.J.H.M Stouthart, I.E. Bonapart, W. Oostdijk, Claudia A. L. Ruivenkamp, Alberto M. Pereira, E. Feigerlova, M.J.E. Walenkamp, Cees Noordam, J. J. Gosen, H. Claahsen-van de Grinten, Jan M. Wit, Horacio M. Domené, H.A. Delemarre-van de Waal, S. de Bruin, Martijn H. Breuning, Vivian Hwa, S.G. Kant, L. Hafkenscheid, Antoinet C.J. Gijsbers

Publikováno v: Hormone Research in Paediatrics, 77, 320-333
Hormone Research in Paediatrics, 77, 5, pp. 320-333
Hormone Research in Paediatrics, 77(5), 320-333
Hormone Research in Paediatrics, 77(5), 320-333. S. Karger AG
Wit, J M, van Duyvenvoorde, H A, Scheltinga, S A, de Bruin, S, Hafkenscheid, L, Kant, S G, Ruivenkamp, C A L, Gijsbers, A C J, van Doorn, J, Feigerlova, E, Noordam, C, Walenkamp, M J E, Claahsen-van de Grinten, H, Stouthart, P, Bonapart, I E, Pereira, A M, Gosen, J, Delemarre-van de Waal, H A, Hwa, V, Breuning, M H, Domene, H M, Oostdijk, W & Losekoot, M 2012, ' Genetic Analysis of Short Children with Apparent Growth Hormone Insensitivity ', Hormone Research in Paediatrics, vol. 77, no. 5, pp. 320-333 . https://doi.org/10.1159/000338462

Background/Aims: In short children, a low IGF-I and normal GH secretion may be associated with various monogenic causes, but their prevalence is unknown. We aimed at testing GH1, GHR, STAT5B, IGF1, and IGFALS in children with GH insensitivity. Subjec

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c5ebbb644ecb97d5be5049c71ff44e6
https://hdl.handle.net/1887/97204

Normalization of height in girls with Turner syndrome after long-term growth hormone treatment: results of a randomized dose-response trial

Autor: T C, Sas, S M, de Muinck Keizer-Schrama, T, Stijnen, M, Jansen, B J, Otten, J J, Hoorweg-Nijman, T, Vulsma, G G, Massa, C W, Rouwe, H M, Reeser, W J, Gerver, J J, Gosen, C, Rongen-Westerlaken, S L, Drop

Publikováno v: The Journal of clinical endocrinology and metabolism. 84(12)

Short stature and ovarian failure are the main features in Turner syndrome (TS). To optimize GH and estrogen treatment, we studied 68 previously untreated girls with TS, age 2-11 yr, who were randomly assigned to one of three GH dosage groups: group

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::534139ce2d79a4f7bdc09c842c077060
https://pubmed.ncbi.nlm.nih.gov/10599727

Genetic analysis of short children with apparent growth hormone insensitivity.

Autor: Wit JM; Department of Pediatrics, Leiden University Medical Center, Leiden, The Netherlands., van Duyvenvoorde HA, Scheltinga SA, de Bruin S, Hafkenscheid L, Kant SG, Ruivenkamp CA, Gijsbers AC, van Doorn J, Feigerlova E, Noordam C, Walenkamp MJ, Claahsen-van de Grinten H, Stouthart P, Bonapart IE, Pereira AM, Gosen J, Delemarre-van de Waal HA, Hwa V, Breuning MH, Domené HM, Oostdijk W, Losekoot M

Publikováno v: Hormone research in paediatrics [Horm Res Paediatr] 2012; Vol. 77 (5), pp. 320-33. Date of Electronic Publication: 2012 Jun 06.