Psychiatry in Ireland

por Latif, Zahid
Publicado 2009

The Relationship Between Brain MR Spectroscopy and Disability in Multiple Sclerosis: 20‐Year Data from the U.S. Glatiramer Acetate Extension Study

por Khan, Omar, Seraji‐Bozorgzad, Navid, Bao, Fen, Razmjou, Sara, Caon, Christina, Santiago, Carla, Latif, Zahid, Aronov, Rimma, Zak, Imad, Ashtamker, Natalia, Kolodny, Scott, Ford, Corey, Sidi, Yulia
Publicado 2016

Retrospective Observational Study of Daytime Add-On Administration of Zopiclone to Difficult-to-Treat Psychiatric Inpatients With Unpredictable Aggressive Behavior, With or Without...

por Ceccherini-Nelli, Alfonso, Bucuci, Elena, Burback, Lisa, Li, Daniel, Alikouzehgaran, Maryam, Latif, Zahid, Morin, Kevin, Ganapathy, Karthikeyan, Salsali, Manhaz, Abdullah, Ubaid, Westwood, Wanda, Orris, Janice, White, Patrick J.
Publicado 2021

Sequencing and Characterization of Mitochondrial Protein-Coding Genes for Schizothorax niger (Cypriniformes: Cyprinidae) with Phylogenetic Consideration

por Akhtar, Tasleem, Ali, Ghazanfar, Shafi, Nuzhat, Akhtar, Wasim, Khan, Abdul Hameed, Latif, Zahid, Wali, Abdul, Ain-ul-Batool, Syeda, Khan, Abdul Rehman, Mumtaz, Sadia, Altaf, Syed Iftikhar, Khawaja, Sundus, Sadia, Khalid, Madiha, Rehman, Fazal Ur, Javid, Qudir
Publicado 2020

A Comparison of Magnetic Resonance Imaging Methods to Assess Multiple Sclerosis Lesions: Implications for Patient Characterization and Clinical Trial Design

por Haacke, Ewart Mark, Bernitsas, Evanthia, Subramanian, Karthik, Utriainen, David, Palutla, Vinay Kumar, Yerramsetty, Kiran, Kumar, Prashanth, Sethi, Sean K., Chen, Yongsheng, Latif, Zahid, Jella, Pavan, Gharabaghi, Sara, Wang, Ying, Zhang, Xiaomeng, Comley, Robert A., Beaver, John, Luo, Yanping
Publicado 2021

Confirmation of the Role of DHX38 in the Etiology of Early-Onset Retinitis Pigmentosa

por Latif, Zahid, Chakchouk, Imen, Schrauwen, Isabelle, Lee, Kwanghyuk, Santos-Cortez, Regie Lyn P., Abbe, Izoduwa, Acharya, Anushree, Jarral, Afeefa, Ali, Imran, Ullah, Ehsan, Khan, Muhammad Nasim, Ali, Ghazanfar, Tahir, Tufail Hussain, Bamshad, Michael J., Nickerson, Deborah A., Ahmad, Wasim, Ansar, Muhammad, Leal, Suzanne M.
Publicado 2018

Identification of a Novel Homozygous Missense (c.443A>T:p.N148I) Mutation in BBS2 in a Kashmiri Family with Bardet-Biedl Syndrome

por Ali, Ghazanfar, Sadia, Foo, Jia Nee, Nasir, Abdul, Chang, Chu-Hua, Chew, Elaine GuoYan, Latif, Zahid, Azeem, Zahid, Ain-ul-Batool, Syeda, Kazmi, Syed Akif Raza, Awan, Naheed Bashir, Khan, Abdul Hameed, Rehman, Fazal-Ur-, Khalid, Madiha, Wali, Abdul, Sarwar, Samina, Akhtar, Wasim, Ahmed Abbasi, Ansar, Nisar, Rameez
Publicado 2021