Zobrazeno 1 - 10
of 24
pro vyhledávání: '"M L Givner"'
Autor:
M L Givner, L Lehmann, R Douglas, E C Abbott, M H Tan, S R Salisbury, S E York, A H Shlossberg, S Reddy, R S Rittmaster
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 83:814-818
Medical treatment of Graves' disease involves antithyroid drugs with or without the addition of exogenous T4. There have been conflicting reports as to whether the addition of T4 improves remission rates or delays relapse. To evaluate this issue in a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2b508dea872fcf58d6af1e9fd9d2df5
https://doi.org/10.1210/jcem.83.3.4613
https://doi.org/10.1210/jcem.83.3.4613
Publikováno v:
The Journal of clinical endocrinology and metabolism. 83(3)
Testolactone, an aromatase inhibitor, blocks conversion of androgens to estrogens. In familial male precocious puberty, slowing of pubertal progression and growth velocity occurs with testolactone and spironolactone. Girls with McCune-Albright syndro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c710b64a921366c0da9bb353294d36f2
https://pubmed.ncbi.nlm.nih.gov/9506727
https://pubmed.ncbi.nlm.nih.gov/9506727
Autor:
I S, Sketris, J G, Lawen, L, Beauregard-Zollinger, P, Belitsky, D, Landsberg, M L, Givner, P, Keown
Publikováno v:
Transplantation proceedings. 26(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::24649127bd17506bcc9580b1213d1469
https://pubmed.ncbi.nlm.nih.gov/7940935
https://pubmed.ncbi.nlm.nih.gov/7940935
Autor:
M. L. Givner, M. A. Hirsch
Publikováno v:
Canadian Journal of Physiology and Pharmacology. 54:405-408
An in vivo method for the determination of biological potency of luteinizing hormone -releasing hormone (LH–RH) antiserum is described. The procedure involves antiserum blockade of LH–RH induced ovulation in immature rats primed with pregnant mar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcd7dc4362a93f0e70876251fdaf6817
https://doi.org/10.1139/y76-056
https://doi.org/10.1139/y76-056
Autor:
M. L. Givner, C. Auclair
Publikováno v:
Archives of Andrology. 8:21-24
Treatment (5 mg/kg s.c. for 1 to 4 weeks) of adult male rats with medrogestone (Colprone), a compound with progestational and antiandrogenic properties, induced significant atrophy of the ventral prostate without affecting testicular weight, testicul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6771ce8436b8ebf16919af22eb30f122
https://doi.org/10.3109/01485018208987013
https://doi.org/10.3109/01485018208987013
Autor:
M. L. Givner, U. K. Banik
Publikováno v:
Reproduction. 44:87-94
Pro-oestrous rats, treated with fluphenazine dihydrochloride to block ovulation, were used to compare the ovulation-inducing activity of synthetic LH-RH with one of its analogues, [D-Ala-6, des-Gly-NH2-10]-LH-RH ethylamide (AY-25,205). The lowest dos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6db72b5cee2f1231c9375d95bb3628f5
https://doi.org/10.1530/jrf.0.0440087
https://doi.org/10.1530/jrf.0.0440087
Autor:
N. Jagarinec, M. L. Givner
Publikováno v:
Archives of Andrology. 7:39-44
Medrogestone (MDG), viz., 6,17-dimethyl-4,6-pregnadiene-3,20-dione (Colprone), a synthetic compound with progestational and antiandrogenic properties was studied for its effect on the conversion of testosterone (T) to 5 alpha-dihydrotestosterone (DHT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21844258914d609bc7abeeb7c22f2e20
https://doi.org/10.3109/01485018109009374
https://doi.org/10.3109/01485018109009374
Publikováno v:
Endocrinology. 83:555-564
Oral administration of the cholesterol biosynthesis inhibitor AY-9944 [trans-1,4- bis(2-chlorobenzylaminomethyl)cyclohexane dihydrochloride] did not affect the steroidogenic response to injected ACTH in hypophysectomized rats nor to laparotomy stress
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ea0b950c9440c66add0d8712ffb35fb
https://doi.org/10.1210/endo-83-3-555
https://doi.org/10.1210/endo-83-3-555
Publikováno v:
Endocrinology. 81:976-980
AY-9944 [trans-1,4-bis(2-chlorobenzylaminomethyl) cyclohexane dihydroohloride], an inhibitor of cholesterol biosynthesis, was studied for its effect on adrenal corticoid synthesis. In rat adrenal homogenates AY-9944 inhibited the production of cortic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b58b804920e7cfeeed4c2aa40679158
https://doi.org/10.1210/endo-81-5-976
https://doi.org/10.1210/endo-81-5-976
Autor:
J. G. Rochefort, M. L. Givner
Publikováno v:
Endocrinology. 90:1238-1244
Medroxyprogesterone acetate, chlormadinone acetate, AY-11,497 and clogestone acetate (AY-11,440) reduced adrenal and ovarian weights, serum and adrenal corticosterone in the rat. Adrenal homogenates from rats treated with medroxyprogesterone acetate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b1798a1946286f263e3ba8fbab61439
https://doi.org/10.1210/endo-90-5-1238
https://doi.org/10.1210/endo-90-5-1238