日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Sperm DNA integrity and sexual dysfunction among infertile men : DFI and sexual dysfunction

精子DNA完整性与不育男性性功能障碍:DFI与性功能障碍

Karavani, Gilad; Chan, Justin; Wilk Goldsher, Yulia; Lajkosz, Katherine; Lau, Susan; Lo, Kirk C; Grober, Ethan D; Krakowsky, Yonah; Jarvi, Keith

Genital graft versus host disease in women after allogeneic hematopoietic stem cell transplantation - a single center experience

异基因造血干细胞移植后女性生殖器移植物抗宿主病——单中心经验

Wilk Goldsher, Yulia; Cohen Sacher, Bina; Cohen, May; Yeshurun, Moshe; Sabah, Gad; Eitan, Ram; Krissi, Haim

The Analgesic Effects of a Saddle Block with Intrathecal Morphine for Penile-Inversion Vaginoplasty: A Retrospective Study

鞘内注射吗啡进行鞍区阻滞镇痛治疗阴茎倒置阴道成形术的镇痛效果:一项回顾性研究

Girón-Arango, Laura; Kirkham, Kyle Robert; Millman, Alexandra L; Krakowsky, Yonah; Wilk Goldsher, Yulia; Drodge, Olivia; Li, Qixuan; Huszti, Ella; Brull, Richard

Sequence variation in PPP1R13L results in a novel form of cardio-cutaneous syndrome

PPP1R13L基因序列变异导致一种新型心皮肤综合征。

Falik-Zaccai, Tzipora C; Barsheshet, Yiftah; Mandel, Hanna; Segev, Meital; Lorber, Avraham; Gelberg, Shachaf; Kalfon, Limor; Ben Haroush, Shani; Shalata, Adel; Gelernter-Yaniv, Liat; Chaim, Sarah; Raviv Shay, Dorith; Khayat, Morad; Werbner, Michal; Levi, Inbar; Shoval, Yishay; Tal, Galit; Shalev, Stavit; Reuveni, Eli; Avitan-Hersh, Emily; Vlodavsky, Eugene; Appl-Sarid, Liat; Goldsher, Dorit; Bergman, Reuven; Segal, Zvi; Bitterman-Deutsch, Ora; Avni, Orly

Joubert Syndrome in French Canadians and Identification of Mutations in CEP104

法裔加拿大人中的Joubert综合征及CEP104基因突变的鉴定

Srour, Myriam; Hamdan, Fadi F; McKnight, Dianalee; Davis, Erica; Mandel, Hanna; Schwartzentruber, Jeremy; Martin, Brissa; Patry, Lysanne; Nassif, Christina; Dionne-Laporte, Alexandre; Ospina, Luis H; Lemyre, Emmanuelle; Massicotte, Christine; Laframboise, Rachel; Maranda, Bruno; Labuda, Damian; Décarie, Jean-Claude; Rypens, Françoise; Goldsher, Dorith; Fallet-Bianco, Catherine; Soucy, Jean-François; Laberge, Anne-Marie; Maftei, Catalina; Boycott, Kym; Brais, Bernard; Boucher, Renée-Myriam; Rouleau, Guy A; Katsanis, Nicholas; Majewski, Jacek; Elpeleg, Orly; Kukolich, Mary K; Shalev, Stavit; Michaud, Jacques L

Neuropathic pain: long term follow-up

神经性疼痛:长期随访

Schiavone, Cosima; Romano, Marcello; Zaaroor, Menashe; Sinai, Alon; Eran, Ayelet; Goldsher, Dorit; Erikh, Ilana; Nassar, Maria; Schlesinger, Ilana; Parker, Dennis; Napoli, Alessandro; Zaccagna, Fulvio; Cartocci, Gaia; Giulia, Brachetti; Caliolo, Gianluca; Andrani, Fabrizio; Catalano, Carlo; McDannold, Nathan; Arvanitis, Costas; Vykhodtseva, Natalia; Livingstone, Margaret; Ando, Yuta; Timbie, Kelsie; Song, Ji; Larner, James; Price, Richard; Andarawewa, Kumari; Gelet, Albert; Crouzet, Sebastien; Rouviere, Olivier; Chapelon, Jean-Yves; Rabilloud, Murielle; Schmitt, Paul; Foley, Jessica; Kassell, Neal; Sheehan, Jason; Xu, Zhiyuan; Gertner, Michael; Crura, Francesco; Zhang, Jimin; Ranjan, Ashish; Maples, Danny; Newhardt, Ryan; Perumal, Venkatesan; Peek, Mirjam; Ahmed, Muneer; Scudder, Julie; Purushotham, Arnie; Kothari, Ashutosh; Hisham, Hamed; Kovacs, Tibor; McWilliams, Sarah; Pinder, Sarah; ten Haken, Bennie; Douek, Michael; Napoli, Alessandro; Zaccagna, Fulvio; Paolo, Pier Luigi Di; Sandolo, Francesco; Palla, Carola; Andrani, Fabrizio; Catalano, Carlo; Martin, Ernst; Werner, Beat; Bauer, Ronald

Delineation of C12orf65-related phenotypes: a genotype-phenotype relationship

C12orf65相关表型的界定:基因型-表型关系

Spiegel, Ronen; Mandel, Hanna; Saada, Ann; Lerer, Issy; Burger, Ayala; Shaag, Avraham; Shalev, Stavit A; Jabaly-Habib, Haneen; Goldsher, Dorit; Gomori, John M; Lossos, Alex; Elpeleg, Orly; Meiner, Vardiella

A prospective evaluation of a protocol for magnetic resonance imaging of patients with implanted cardiac devices

对植入心脏装置患者进行磁共振成像方案的前瞻性评估

Nazarian, Saman; Hansford, Rozann; Roguin, Ariel; Goldsher, Dorith; Zviman, Menekhem M; Lardo, Albert C; Caffo, Brian S; Frick, Kevin D; Kraut, Michael A; Kamel, Ihab R; Calkins, Hugh; Berger, Ronald D; Bluemke, David A; Halperin, Henry R

Mitochondrial hsp60 chaperonopathy causes an autosomal-recessive neurodegenerative disorder linked to brain hypomyelination and leukodystrophy

线粒体hsp60分子伴侣病会导致一种常染色体隐性遗传的神经退行性疾病,该疾病与脑髓鞘形成不足和脑白质营养不良有关。

Magen, Daniella; Georgopoulos, Costa; Bross, Peter; Ang, Debbie; Segev, Yardena; Goldsher, Dorit; Nemirovski, Alexandra; Shahar, Eli; Ravid, Sarit; Luder, Anthony; Heno, Bayan; Gershoni-Baruch, Ruth; Skorecki, Karl; Mandel, Hanna

A mutation in SNAP29, coding for a SNARE protein involved in intracellular trafficking, causes a novel neurocutaneous syndrome characterized by cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma

SNAP29 基因突变(编码参与细胞内运输的 SNARE 蛋白)可导致一种新型神经皮肤综合征,其特征为脑发育不良、神经病变、鱼鳞病和掌跖角化病

Eli Sprecher, Akemi Ishida-Yamamoto, Mordechai Mizrahi-Koren, Debora Rapaport, Dorit Goldsher, Margarita Indelman, Orit Topaz, Ilana Chefetz, Hanni Keren, Timothy J O'brien, Dani Bercovich, Stavit Shalev, Dan Geiger, Reuven Bergman, Mia Horowitz, Hanna Mandel