Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: Syndrome and STS[original query] |
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Polymorphisms of N-acetyltransferases, glutathione S-transferases, microsomal epoxide hydrolase and sulfotransferases: influence on cancer susceptibility. Recent results in cancer research. Fortschritte der Krebsforschung. Progre?s dans les recherches sur le cancer 1998 154 47-85. Hengstler J G, Arand M, Herrero M E, Oesch |
Genes for enzymes regulating dehydroepiandrosterone sulfonation are associated with levels of dehydroepiandrosterone sulfate in polycystic ovary syndrome. The Journal of clinical endocrinology and metabolism 2007 Jul 92 (7): 2659-64. Goodarzi Mark O, Antoine Heath J, Azziz Ricar |
Variants in SULT2A1 affect the DHEA sulphate to DHEA ratio in patients with polycystic ovary syndrome but not the hyperandrogenic phenotype. The Journal of clinical endocrinology and metabolism 2013 Sep 98 (9): 3848-55. Louwers Yvonne V, de Jong Frank H, van Herwaarden Nathalie A A, Stolk Lisette, Fauser Bart C J M, Uitterlinden André G, Laven Joop S |
Correlation of genetic results with testicular histology, hormones and sperm retrieval in nonobstructive azoospermia patients with testis biopsy. Andrologia 2016 Dec . Liu W, Gao X, Ma G, Yan L, Chen T, Li T, Yu R-M, Ma J |
[Genetic analysis of two cases with Dandy-Walker deformed fetus]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2017 10 34 (5): 666-670. Yao Juan, Fang Rong, Shen Xueping, Shen Guosong, Zhang |
Incidence of Y chromosome microdeletions in patients with Klinefelter syndrome. Journal of endocrinological investigation 2018 12 42 (7): 833-842. Sciarra F, Pelloni M, Faja F, Pallotti F, Martino G, Radicioni A F, Lenzi A, Lombardo F, Paoli |
[The incidence of AZF deletions, CFTR mutations and long alleles of the ar CAG repeats during the primary laboratory diagnostics in a heterogeneous group of infertily men]. Urologiia (Moscow, Russia : 1999) 2019 Jul (3): 101-107. Mikhaylenko D S, Sobol I Y, Safronova N Y, Simonova O A, Efremov E A, Efremov G D, Alekseev B Y, Kaprin A D, Nemtsova M |
Role of 11? HSD 1, rs12086634, and rs846910 single-nucleotide polymorphisms in metabolic-related skin diseases: a clinical, biochemical, and genetic study. Clinical, cosmetic and investigational dermatology 2019 12 91-102. Farag Azza Gaber Antar, Badr Eman Ae, Eltorgoman Abdel Monem A, Assar Mohamed Fa, Elshafey Eman N, Tayel Nermin Reda, Aboutaleb Hossam |
Clinical and genetic characteristics of patients with Doose syndrome. Epilepsia open 2020 9 5 (3): 442-450. Hinokuma Nodoka, Nakashima Mitsuko, Asai Hideyuki, Nakamura Kazuyuki, Akaboshi Shinjiro, Fukuoka Masataka, Togawa Masami, Oana Shingo, Ohno Koyo, Kasai Mariko, Ogawa Chikako, Yamamoto Kazuna, Okumiya Kiyohito, Chong Pin Fee, Kira Ryutaro, Uchino Shumpei, Fukuyama Tetsuhiro, Shinagawa Tomoe, Miyata Yohane, Abe Yuichi, Hojo Akira, Kobayashi Kozue, Maegaki Yoshihiro, Ishikawa Nobutsune, Ikeda Hiroko, Amamoto Masano, Mizuguchi Takeshi, Iwama Kazuhiro, Itai Toshiyuki, Miyatake Satoko, Saitsu Hirotomo, Matsumoto Naomichi, Kato Mitsuhi |
Pulmonary fibrosis in non-mutation carriers of families with short telomere syndrome gene mutations. Respirology (Carlton, Vic.) 2021 9 26 (12): 1160-1170. van der Vis Joanne J, van der Smagt Jasper J, van Batenburg Aernoud A, Goldschmeding Roel, van Es H Wouter, Grutters Jan C, van Moorsel Coline H |
Outcomes of early repeat sweat testing in infants with cystic fibrosis transmembrane conductance regulator-related metabolic syndrome/CF screen-positive, inconclusive diagnosis. Pediatric pulmonology 2021 Sep . Terlizzi Vito, Claut Laura, Colombo Carla, Tosco Antonella, Castaldo Alice, Fabrizzi Benedetta, Lucarelli Marco, Cimino Giuseppe, Carducci Carla, Dolce Daniela, Biffi Arianna, Bonomi Paolo, Timpano Silviana, Padoan Ri |
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- Page last updated:Mar 25, 2024
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