Zobrazeno 1 - 10
of 99
pro vyhledávání: '"E M, Ritzén"'
Publikováno v:
Pediatrics. 131:e1174-e1180
OBJECTIVE:To investigate whether in congenital unilateral cryptorchidism the growth of a spontaneously descended testis is normal, compared with the contralateral scrotal testis or similar to the growth of testes that failed to descend spontaneously
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cdeed132420dd59def7c4946ea0913c2
https://doi.org/10.1542/peds.2012-2902
https://doi.org/10.1542/peds.2012-2902
Autor:
Olle Söder, Mirja Nurmio, E. M. Ritzén, Agneta Nordenskjöld, Jorma Toppari, E. Sundqvist, T. Gustafsson, Jan-Bernd Stukenborg, Claude Kollin
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 97:4588-4595
A randomized controlled study was conducted comparing the outcome of surgery for congenital cryptorchidism at 9 months or 3 yr of age.The aim of the study was to investigate whether surgery at 9 months is more beneficial than at 3 yr and to identify
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9cb7b3e365663697afec697a2be2262
https://doi.org/10.1210/jc.2012-2325
https://doi.org/10.1210/jc.2012-2325
Publikováno v:
Experimental and Clinical Endocrinology & Diabetes. 92:137-144
The kinetic of changes in plasma concentrations and pituitary contents of FSH, LH, prolactin after hysterectomy and treatment with steroid-free uterine extracts were studied in adult, non-pregnant female rats. The post-castration rise of plasma and p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1eb3f8ab77f00123d45d896a67f1d7aa
https://doi.org/10.1055/s-0029-1210794
https://doi.org/10.1055/s-0029-1210794
Publikováno v:
Acta Medica Scandinavica. 215:461-466
Serum from a woman with a history of Hashimoto's thyroiditis, who had given birth to two children with congenital hypothyroidism, contained potent TSH blocking activity. Immunoglobulin preparation from this serum abolished completely TSH-stimulated c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b70192e6ade6e6d00490dd6845507ae
https://doi.org/10.1111/j.0954-6820.1984.tb17679.x
https://doi.org/10.1111/j.0954-6820.1984.tb17679.x
Publikováno v:
Journal of Endocrinology. 188:193-203
The importance of estrogens for the regulation of longitudinal bone growth is unequivocal. However, any local effect of estrogens in growth plate cartilage has been debated. Recently, several enzymes essential for estrogen synthesis were shown to be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59615d27298d0b1e6c7df9350df61f27
https://doi.org/10.1677/joe.1.06364
https://doi.org/10.1677/joe.1.06364
Publikováno v:
Karolinska Institutet
Glucocorticoids cause significant growth retardation in mammals and humans and decreased proliferation of chondrocytes has been considered as the main local mechanism. Death by apoptosis is an important regulator of homeostasis in multicellular organ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da2ead0d707ee5cda90883cf84266a4c
https://doi.org/10.1677/joe.0.1760331
https://doi.org/10.1677/joe.0.1760331
Publikováno v:
Karolinska Institutet
Estrogen regulates skeletal growth and promotes epiphyseal fusion. To explore the mechanisms underlying these effects we investigated the expression of estrogen receptor-alpha (ERalpha) and -beta (ERbeta) in rat and rabbit growth plates during postna
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60bc4706c123be4247083a5daf22fa89
https://doi.org/10.1677/joe.0.1730407
https://doi.org/10.1677/joe.0.1730407
Publikováno v:
Karolinska Institutet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9344a08979f32c65b0b082d561f01eb6
https://doi.org/10.1016/s0960-0760(00)00116-3
https://doi.org/10.1016/s0960-0760(00)00116-3
Publikováno v:
Karolinska Institutet
The most common form of congenital adrenal hyperplasia is due to a deficiency of 21-hydroxylase (21OHD) activity and is caused by a mutation in the CYP21 gene. By genotyping patients, new and important information can be gained, including presence or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f8e46d0efb594b45abe7572aec1f07b
https://doi.org/10.1159/000053202
https://doi.org/10.1159/000053202
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 84:1210-1213
Congenital adrenal hyperplasia in children is often treated with cortisone acetate and fludrocortisone. It is known that certain patients with congenital adrenal hyperplasia require very high substitution doses of cortisone acetate, and a few patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc17c78206457ad8f880d0d7951f2c6e
https://doi.org/10.1210/jcem.84.4.5584
https://doi.org/10.1210/jcem.84.4.5584