Results 171 to 180 of about 23,359 (243)

Heparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadism. [PDF]

Proc Natl Acad Sci U S A, 2011
Tornberg J, Sykiotis GP, Keefe K, Plummer L, Hoang X, Hall JE, Quinton R, Seminara SB, Hughes V, Van Vliet G, Van Uum S, Crowley WF, Habuchi H, Kimata K, Pitteloud N, Bülow HE.   +15 more
europepmc   +1 more source

PROKR2 mutations and SPRY4 variants with uncertain significance in a Kallmann syndrome family: Incomplete penetrance. [PDF]

Glob Med Genet
Yuan Y, Huang Q, Zhang J, Zhou Z, Wan Q, Chen L, Zeng T, Li H, Zhang Q, Hu X.   +9 more
europepmc   +1 more source

The influence of the pharmaceutical industry on the development of gonadotrophins and ovarian stimulation protocols in assisted reproductive technologies. [PDF]

Front Endocrinol (Lausanne)
Child T, Bassett R, Howles CM.
europepmc   +1 more source

Consider CUX1 variants in children with a variation of sex development: a case report and review of the literature. [PDF]

BMC Med Genomics
Tan L, Young SG, Sinclair AH, Hunter MF, Ayers KL.   +4 more
europepmc   +1 more source

Gonadal Function in Boys with Bilateral Undescended Testes. [PDF]

J Endocr Soc
Lucas-Herald AK, Alkanhal KI, Caney E, Malik I, Alimussina M, McNeilly JD, Bradnock T, Lee B, Steven M, Flett M, O'Toole S, McGowan R, Faisal Ahmed S.   +12 more
europepmc   +1 more source

46 XX male syndrome with hypogonadotrophic hypogonadism: a case report

, 2018
Mehmet Muhittin Yalçın
openalex   +1 more source

Low libido despite high normal testosterone levels in a male with an FSH-secreting pituitary macroadenoma. [PDF]

Endocrinol Diabetes Metab Case Rep
Ghazal Asswad R, Khan MI, Elizabeth Gilkes C, Daousi C, Thondam SK.   +4 more
europepmc   +1 more source

Childhood obesity from the genes to the epigenome. [PDF]

Front Endocrinol (Lausanne)
Sivakumar S, Lama D, Rabhi N.
europepmc   +1 more source

Case Report: A rare chromosomal imbalance with dup 7q36.3-qter and del 7pter-p22.3 arising from parental pericentric inversion. [PDF]

Front Genet
Lin R, Zhang W, Huang M, Shen Y, Liao J, Song P, Qi Y, He J, Xia Y, Duan J, Ye Y, Yi Q, Lan P, Kong L, Hu Z.   +14 more
europepmc   +1 more source

Abnormality of pituitary gonadal axis among Nigerian males with infertility: study of patterns and possible etiologic interrelationships

core   +1 more source