Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
---|---|---|---|
1 |
Material Type: Artigo
|
EAA/EMQN best practice guidelines for molecular diagnosis of Y‐chromosomal microdeletions: state‐of‐the‐art 2013Krausz, C. ; Hoefsloot, L. ; Simoni, M. ; Tüttelmann, F.Andrology (Oxford), 2014-01, Vol.2 (1), p.5-19 [Periódico revisado por pares]Schaumburg, IL: American Society of AndrologyTexto completo disponível |
|
2 |
Material Type: Artigo
|
Severe male factor in in vitro fertilization: definition, prevalence, and treatment. An updateMazzilli, Rossella ; Vaiarelli, Alberto ; Dovere, Lisa ; Cimadomo, Danilo ; Ubaldi, Nicolò ; Ferrero, Susanna ; Rienzi, Laura ; Lombardo, Francesco ; Lenzi, Andrea ; Tournaye, Herman ; Ubaldi, FilippoAsian journal of andrology, 2022-03, Vol.24 (2), p.125-134 [Periódico revisado por pares]China: Wolters Kluwer India Pvt. LtdTexto completo disponível |
|
3 |
Material Type: Artigo
|
Recent advances in the genetics of testicular failureSong, Seung-Hun ; Chiba, Koji ; Ramasamy, Ranjith ; Lamb, DoloresAsian journal of andrology, 2016-05, Vol.18 (3), p.350-355 [Periódico revisado por pares]China: Wolters Kluwer - Medknow PublicationsTexto completo disponível |
|
4 |
Material Type: Artigo
|
SARS‐CoV‐2 pandemic and repercussions for male infertility patients: A proposal for the individualized provision of andrological servicesEsteves, Sandro C. ; Lombardo, Francesco ; Garrido, Nicolás ; Alvarez, Juan ; Zini, Armand ; Colpi, Giovanni M. ; Kirkman‐Brown, Jackson ; Lewis, Sheena E. M. ; Björndahl, Lars ; Majzoub, Ahmad ; Cho, Chak‐Lam ; Vendeira, Pedro ; Hallak, Jorge ; Amar, Edouard ; Cocuzza, Marcello ; Bento, Fabiola C. ; Figueira, Rita C. ; Sciorio, Romualdo ; Laursen, Rita J. ; Metwalley, Ahmad M. ; Jindal, Sunil K. ; Parekattil, Sijo ; Ramasamy, Ranjith ; Alviggi, Carlo ; Humaidan, Peter ; Yovich, John L. ; Agarwal, AshokAndrology (Oxford), 2021-01, Vol.9 (1), p.10-18 [Periódico revisado por pares]England: Wiley Subscription Services, IncTexto completo disponível |
|
5 |
Material Type: Artigo
|
Investigation of the genetic etiology in male infertility with apparently balanced chromosomal structural rearrangements by genome sequencingChau, Matthew ; Li, Ying ; Dai, Peng ; Shi, Mengmeng ; Zhu, Xiaofan ; Wah Chung, Jacqueline ; Kwok, Yvonne ; Choy, Kwong ; Kong, Xiangdong ; Dong, ZiruiAsian journal of andrology, 2022-05, Vol.24 (3), p.248-254 [Periódico revisado por pares]China: Wolters Kluwer India Pvt. LtdTexto completo disponível |
|
6 |
Material Type: Artigo
|
Reference range and cutoff value of serum inhibin B to predict successful sperm retrieval: A cross‐sectional study of 30 613 Chinese menWang, Jian ; Lu, Na ; Zhang, Shuolei ; Tang, Zhangming ; Huang, Yifei ; Li, Weina ; Liu, GangClinical endocrinology (Oxford), 2020-03, Vol.92 (3), p.232-240 [Periódico revisado por pares]England: Wiley Subscription Services, IncTexto completo disponível |
|
7 |
Material Type: Artigo
|
EAA/EMQN best practice guidelines for molecular diagnosis of Y‐chromosomal microdeletions: State of the art 2023Krausz, Csilla ; Navarro‐Costa, Paulo ; Wilke, Martina ; Tüttelmann, FrankAndrology (Oxford), 2024-03, Vol.12 (3), p.487-504 [Periódico revisado por pares]England: Wiley Subscription Services, IncTexto completo disponível |
|
8 |
Material Type: Artigo
|
Rescue of male infertility through correcting a genetic mutation causing meiotic arrest in spermatogonial stem cellsWang, Ying-Hua ; Yan, Meng ; Zhang, Xi ; Liu, Xin-Yu ; Ding, Yi-Fu ; Lai, Chong-Ping ; Tong, Ming-Han ; Li, Jin-SongAsian journal of andrology, 2021-11, Vol.23 (6), p.590-599 [Periódico revisado por pares]China: Wolters Kluwer India Pvt. LtdTexto completo disponível |
|
9 |
Material Type: Artigo
|
Using microRNAs as molecular biomarkers for the evaluation of male infertilityAsadpour, Reza ; Mofidi Chelan, EhsanAndrologia, 2022-03, Vol.54 (2), p.e14298-n/a [Periódico revisado por pares]Germany: Wiley Subscription Services, IncTexto completo disponível |
|
10 |
Material Type: Artigo
|
Loss-of-function CFTR p.G970D missense mutation might cause congenital bilateral absence of the vas deferens and be associated with impaired spermatogenesisHou, Jian-Wen ; Li, Xiao-Liang ; Wang, Li ; Dai, Cong-Ling ; Li, Na ; Jiang, Xiao-Hui ; Tan, Yue-Qiu ; Tian, Er-Po ; Li, Qin-Tong ; Xu, Wen-MingAsian journal of andrology, 2023-01, Vol.25 (1), p.58-65 [Periódico revisado por pares]China: Wolters Kluwer India Pvt. LtdTexto completo disponível |