Results 71 to 80 of about 8,597 (215)

Genetic models for the study of luteinizing hormone receptor function [PDF]

, 2015
The luteinizing hormone/chorionic gonadotropin receptor (LHCGR) is essential for fertility in men and women. LHCGR binds luteinizing hormone (LH) as well as the highly homologous chorionic gonadotropin.
Narayan, Prema
core   +3 more sources

Pseudohermafroditismo masculino disgenético.

Acta Médica Portuguesa, 2001
Dysgenetic male pseudohermaphroditism is the result of a defect of testis development that encompasses a large clinical heterogeneity. It is characterized by bilateral dysgenetic testis, absence of mullerian regression, ambiguous genitalia and/or ...
E Proença, S Freitas, M Fonseca, S Figueiredo, C Rodrigues   +4 more
doaj   +1 more source

Testiculaire aandoening van seksuele differentiatie (78,XX SRY-negatief) bij een vrouwelijke Franse buldog [PDF]

, 2015
A presumably female intact French bulldog of ten months old was presented to the Faculty of Veterinary Medicine of the Ghent University with an enlarged clitoris and purulent vaginal discharge. It was suggested to remove the enlarged clitoris as to avoid
De Rooster, Hilde, Stachowiak, M, Switonski, M, Szczerbal, I, Van Brantegem, Leen, Van Cleven, Alexia, Wydooghe, Eline   +6 more
core   +1 more source

Endocrine and molecular investigations in a cohort of 25 adolescent males with prominent/persistent pubertal gynecomastia [PDF]

, 2016
Pubertal gynecomastia is a common condition observed in up to 65% of adolescent males. It is usually idiopathic and tends to regress within 1–2 years.
Audran, F., Biason-Lauber, Anna, Gaspari, L., Mbou, F., Morel, Y., Paris, F., Philibert, P., Sultan, C..   +7 more
core   +1 more source

A rare form of male pseudohermaphroditism-Persistent Mullerian Duct Syndrome. [PDF]

J Surg Case Rep, 2022
Ramzan R, Khan NA, Khalique A, Aziz MA.
europepmc   +1 more source

Phenotypic variation in a family with partial androgen insensitivity syndrome explained by differences in 5alpha dihydrotestosterone availability [PDF]

, 2001
Mutations in the androgen receptor (AR) gene result in a wide range of phenotypes of the androgen insensitivity syndrome (AIS). Inter- and intrafamilial differences in the phenotypic expression of identical AR mutations are ...
Boehmer, A.L.M. (Annemie), Brinkmann, A.O. (Albert), Drop, S.L.S. (Stenvert), Niermeijer, M.F. (Martinus), Nijman, R.J.M. (Rien), Ruiter, P. de, Verleun-Mooijman, M.C.   +6 more
core  

Bones and Crohn's: Estradiol deficiency in men with Crohn's disease is not associated with reduced bone mineral density [PDF]

, 2008
Background Reduced bone mineral density (BMD) and osteoporosis are frequent in Crohn's disease (CD), but the underlying mechanisms are still not fully understood.
J Klaus, M Reinshagen, G Adler, BO Boehm, C von Tirpitz, JE Compston, V Abitbol, CN Bernstein, I Bjarnason, C von Tirpitz, JH Tobias, JS Siffiledeen, J Klaus, TP Van Staa, N Pooran, EV Loftus jr, TP Van Staa, C von Tirpitz, H Tilg, BL Riggs, B Ettinger, S Khosla, JE Compston, D Clements, S Khosla, S Khosla, RJ Robinson, M Szathmári, RH Straub, B de la Torre, CG Carlsen, EP Smith, FA Conte, A Morishima, P Gillberg, I Pottelbergh, WR Best, WHO Study Group, L Katznelson, SF Evans, CW Slemenda, A Rapado, BL Clarke   +42 more
core   +2 more sources

Complex clinico-endocrinological characterization of the idiopathic variant of congenital disorder of sex development in a child with male karyotype 46,XY

Клинический разбор в общей медицине
Background. Congenital disorders of sex development (DSD) represent a heterogeneous group of dysontogenetic conditions characterized by a discordance between chromosomal, gonadal, and phenotypic sex.
Svyatoslav M. Yurin, Dmitry A. Apalkov, Tatiana A. Minenkova , Natalia S. Razinkova, Kristina I. Ragulina, Alexandra V. Serezhkina   +5 more
doaj   +1 more source

From the individual to the community and beyond: water quality, stress indicators and key species in coastal waters [PDF]

, 1994
This review examines water quality and stress indicators at levels of organisation from the individual to the community and beyond by means of three case studies concentrating on rocky shores within the north-east Atlantic.
Hawkins, S.J., Proud, S.V., Southward, A.J., Spence, S.K.   +3 more
core  

Persistent Mullerian duct syndrome: A case report and review of the literature

African Journal of Paediatric Surgery, 2010
Persistent Mullerian duct syndrome is a rare form of internal male pseudohermaphroditism, in which Mullerian duct derivatives (uterus and fallopian tubes) are present in a genotypic (46XY) and phenotypic male.
Odi Temitope, Abdur-Rahman Lukman, Nasir Abdulrasheed   +2 more
doaj