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

Motor Nerve Transfer for Voluntary Physiological Voiding: Scientific Foundations, Historical Review, and Case Report

运动神经移植术治疗自主生理性排尿:科学基础、历史回顾及病例报告

Brown, Justin M; De, Elise; Johnston, Benjamin R; Bazarek, Stanley F; Sten, Margaret; Blaivas, Jerry G; McGovern, Frank; Barbe, Mary F; Ruggieri, Michael R Sr

Genomic insights into within-farm persistence and global phylogenetic relatedness of Shiga toxin-producing Escherichia coli O26 in a dairy cattle farm in the UK

英国某奶牛场产志贺毒素大肠杆菌O26的农场内持久性和全球系统发育相关性的基因组学研究

Vesga, Daniela A; Rodrigues, Rafaela C; Ferreira, Christina R; Torrecilhas, Juliana A; Carvalho, Pedro H V; Rovadoski, Gregori; Coutinho, Marcelo A S; Pereira, Guilherme L; Torres, Rodrigo N S; Machado Neto, Otávio R; Chardulo, Luis Artur L; Baldassini, Welder A; Condon, Jaedyn M; Phelps, Sarah L; Culbertson, Miranda M; Phelps, Sarah L; Dahlke, Garland; Wall, Patrick B; Culbertson, Miranda; Costa, Thais C; Lopes, Mariana; Knapper, Emily; Jiang, Mingjia; Li, Zitling K; Gastaldo, Mariana; Silva, Walmir; Verado, Lucas L; Serao, Nick; Duarte, Marcio S; Eckhardt, Megan E; Mayer, Jenna; Tennant, Travis; Lucherk, Loni W; Lawrence, Ty E; Ghnenis, Adel; II, Jerome C Peel; Dinegdie, Gemechu; Prieto, Nuria; Segura, Jose; Tayengwa, Tawanda; Attema, Haley; López-Campos, Óscar; Barrett, Tessa L; Belk, Aeriel D; Bass, Phillip D; Bertino, Antonino; Natalello, Antonio; Musati, Martino; Mangano, Fabrizio; Mangione, Guido; Cannone, Marco Sebastiano; Priolo, Alessandro; Luciano, Giuseppe; Ladeira, Marcio M; Laura, Sara; Oliveira, Jose Maria; Gionbelli, Tathyane R S; Horta, Artur; Souza, Marcela M; Souza, Paloma; Kim, Brad; Alambarrio, Daniela A; Li, Xiaohan; Zedonek, Siara; Willis, Sophia E; Proctor, Jordan; Gonzalez, John M; Mangano, Fabrizio; Bessa, Rui J B; Alves, Susana P; Musati, Martino; Mangione, Guido; Bertino, Antonino; Priolo, Alessandro; Natalello, Antonio; Luciano, Giuseppe; Dobbins, Thomas W; Hardcastle, Nicholas C; Johnson, Bradley J; Ramanathan, Ranjith; Woerner, Dale R; Legako, Jerrad F; Li, Xiaohan; Drouillard, James S; Farney, Jaymelynn K; Proctor, Jordan; Alambarrio, Daniela A; Zedonek, Siara; Gonzalez, John M; Sexton-Bowser, Sarah; Smolensky, Dmitriy; Peterson, Jaymi; Santana, Adina; Johnson, Harleigh; Block, Payton; Berkmeyer, Paige; McCann, Joshua C; Chawdhury, Md Nahid Hassan; Rahman, Md Zillur; Pasha, Md Mahmudul Hasan; Afrin, Sadia; Yankocy, Samantha; Stenhouse, Claire; Hines, Elizabeth A; Tarochione, Audrey; Culbertson, Miranda M; Felix, Tara L; Wang, Yifei; Bohrer, Benjamin M; Cooper, Charle; Hoffmann, Carly; Kelley, Stanley F; Nicholson, Kristin; Wise, Kamlynn; Greiner, Kaylee; Deeney, Alannah S; Raj Kumari, Sanjukta; Withenshaw, Susan M; Bare, Harriet L; Duggett, Nicholas A; Kirchner, Miranda; Smith, Richard P; Davies, Robert H; Rodgers, John D; Anjum, Muna F

The Genetic Architecture of Congenital Diarrhea and Enteropathy

先天性腹泻和肠病的遗传结构

Gaibee, Zeenat; Warner, Neil; Bugda Gwilt, Katlynn; Li, Wenjuan; Guan, Rei; Yourshaw, Michael; Whittaker Hawkins, Ryder; Zorbas, Christiane; St-Germain, Jonathan; Tabatabaie, Mahdi; Mao, Suli; Pinsk, Vered; Yerushalmi, Baruch; Wang, Lee-Kai; Nelson, Stanley F; Wozniak, Laura; Shouval, Dror S; Matar, Manar; Assa, Amit; Frost, Nathaniel; Jimenez, Lissette; Acra, Sari; Walters, Thomas; Mouat, Stephen; Li, Michael; Lafontaine, Denis L J; Tyska, Matthew; Raught, Brian; Avitzur, Yaron; Lencer, Wayne I; Goldenring, James R; Martín, Martín G; Thiagarajah, Jay R; Muise, Aleixo M

Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations

联合、多方面的基因组分析能够诊断各种极其罕见的单基因疾病。

Kobren, Shilpa Nadimpalli; Moldovan, Mikhail A; Reimers, Rebecca; Traviglia, Daniel; Li, Xinyun; Barnum, Danielle; Veit, Alexander; Corona, Rosario I; Carvalho Neto, George de V; Willett, Julian; Berselli, Michele; Ronchetti, William; Nelson, Stanley F; Martinez-Agosto, Julian A; Sherwood, Richard; Krier, Joel; Kohane, Isaac S; Sunyaev, Shamil R

Genetic variants in DDX53 contribute to autism spectrum disorder associated with the Xp22.11 locus

DDX53基因的遗传变异与Xp22.11位点相关的自闭症谱系障碍有关。

Scala, Marcello; Bradley, Clarrisa A; Howe, Jennifer L; Trost, Brett; Salazar, Nelson Bautista; Shum, Carole; Mendes, Marla; Reuter, Miriam S; Anagnostou, Evdokia; MacDonald, Jeffrey R; Ko, Sangyoon Y; Frankland, Paul W; Charlebois, Jessica; Elsabbagh, Mayada; Granger, Leslie; Anadiotis, George; Pullano, Verdiana; Brusco, Alfredo; Keller, Roberto; Parisotto, Sarah; Pedro, Helio F; Lusk, Laina; McDonnell, Pamela Pojomovsky; Helbig, Ingo; Mullegama, Sureni V; Douine, Emilie D; Corona, Rosario Ivetth; Russell, Bianca E; Nelson, Stanley F; Graziano, Claudio; Schwab, Maria; Simone, Laurie; Zara, Federico; Scherer, Stephen W

Developing a disease-specific accessible transcriptional signature as a biomarker for ataxia with oculomotor apraxia type 2

开发疾病特异性的、易于获取的转录特征作为2型眼动失用性共济失调的生物标志物

Ngo, Kathie J; Wong, Darice Y; Huang, Alden Y; Lee, Hane; Nelson, Stanley F; Fogel, Brent L

ELFN1 deficiency: The mechanistic basis and phenotypic spectrum of a neurodevelopmental disorder with epilepsy.

ELFN1 缺陷:一种伴有癫痫的神经发育障碍的机制基础和表型谱

Dore Rhys, Chang Chu-Ting, Declève Amber, Brunori Gloria, Ludlam W Grant, Huang Alden, Movahedinia Mojtaba, Damseh Nadirah S, Anwar Ijaz, Vahidi Mehrjardi Mohammad Yahya, Ny Annelii, Khorrami Mehdi, Kheirollahi Majid, Frederiksen Helen, Eghbal Fatemeh, Mirjalili Mohammad Reza, Dehghani Mohammadreza, Karimiani Ehsan Ghayoor, Oreshkov Sergey, Alves Cesar, Striano Pasquale, Suri Mohnish, Martinez-Agosto Julian, Ansar Muhammad, Zahid Muhammad, Akram Samra, Ansar Muhammad, Nelson Stanley F, Antonarakis Stylianos E, Houlden Henry, Copmans Daniëlle, Martemyanov Kirill A, Maroofian Reza

Diaphragmatic pacing after cervical spinal cord injury due to gunshot wound: a 14-year institutional experience

枪伤导致颈髓损伤后膈肌起搏:一项为期14年的机构经验

Labak, Collin M; Herring, Eric Z; Crooks, Elliot; Bazarek, Stanley F; Smith, Gabriel A; Onders, Raymond

Real-world treatment and health care utilization among patients with Duchenne muscular dystrophy by race and ethnicity in a Medicaid population

在医疗补助人群中,杜氏肌营养不良症患者按种族和族裔划分的真实世界治疗和医疗保健利用情况

Posner, Nathaniel; Manjelievskaia, Janna; Talaga, Anna K; Richards, Megan; Lew, Carolyn R; Merla, Valeria; Alvir, Jose Maria Jimenez; Nelson, Stanley F

Novel Technologies to Address the Lower Motor Neuron Injury and Augment Reconstruction in Spinal Cord Injury

用于治疗下运动神经元损伤和增强脊髓损伤重建的新技术

Bazarek, Stanley F; Krenn, Matthias J; Shah, Sameer B; Mandeville, Ross M; Brown, Justin M