Zobrazeno 1 - 10
of 176
pro vyhledávání: '"Raza Jamal"'
Autor:
Denise O Garrett, MD, Ashley T Longley, MPH, Kristen Aiemjoy, PhD, Mohammad T Yousafzai, MPH, Caitlin Hemlock, MS, Alexander T Yu, MD, Krista Vaidya, MSc, Dipesh Tamrakar, MD, Shampa Saha, MPH, Isaac I Bogoch, MD, Kashmira Date, MD, Senjuti Saha, PhD, Mohammad Shahidul Islam, MSPH, K M Ishtiaque Sayeed, MPH, Caryn Bern, MD, Sadia Shakoor, MD, Irum F Dehraj, MSc, Junaid Mehmood, MA, Mohammad S I Sajib, MSc, Maksuda Islam, BA, Rozina S Thobani, MSc, Aneeta Hotwani, MPH, Najeeb Rahman, MSc, Seema Irfan, FCPS, Shiva R Naga, BSc, Ashraf M Memon, MD, Sailesh Pradhan, ProfMD, Khalid Iqbal, MBA, Rajeev Shrestha, ProfPhD, Hafizur Rahman, MDT, Md Mahmudul Hasan, MPH, Saqib H Qazi, FACS, Abdul M Kazi, MPH, Nasir S Saddal, FCPS, Raza Jamal, FCPS, Mohammed J Hunzai, MSc, Tanvir Hossain, MSc, Florian Marks, PhD, Alice S Carter, BA, Jessica C Seidman, PhD, Farah N Qamar, FRCP, Samir K Saha, PhD, Jason R Andrews, MD, Stephen P Luby, ProfMD
Publikováno v:
The Lancet Global Health, Vol 10, Iss 7, Pp e978-e988 (2022)
Summary: Background: Precise enteric fever disease burden data are needed to inform prevention and control measures, including the use of newly available typhoid vaccines. We established the Surveillance for Enteric Fever in Asia Project (SEAP) to in
Externí odkaz:
https://doaj.org/article/fbcb233774f04ca9930d763303f41190
Autor:
Raza Jamal, Jonathan LaCombe, Roshni Patel, Matthew Blackwell, Jared R. Thomas, Kourtney Sloan, Joseph M. Wallace, Randall J. Roper
Publikováno v:
PLoS ONE, Vol 17, Iss 2 (2022)
Bone abnormalities affect all individuals with Down syndrome (DS) and are linked to abnormal expression of DYRK1A, a gene found in three copies in people with DS and Ts65Dn DS model mice. Previous work in Ts65Dn male mice demonstrated that both genet
Externí odkaz:
https://doaj.org/article/c7c5b83ec4dd49aaaaa857bdbd911e6c
Publikováno v:
BMC Endocrine Disorders, Vol 11, Iss 1, p 5 (2011)
Abstract Background Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive disorders caused by defects in the steroid 21 hydroxylase gene (CYP21A2). We studied the spectrum of mutations in CYP21A2 gene in a multi-ethnic population in
Externí odkaz:
https://doaj.org/article/2ef0d2ebf3394e7a9a9137b2721362df
Autor:
Goudar, Shivaprasad, Dhaded, Sangappa M, Nagmoti, Mahantesh B, Somannavar, Manjunath S, Yogeshkumar, S, Harakuni, Sheetal, Guruprasad, Gowdar, Aradhya, Gayathri H, Nadig, Naveen, Kusgur, Varun, Raghoji, Chaitali R, Sarvamangala, B, Prakash, Veena, Joish, Upendra Kumar, Mangala, G K, Rajashekhar, K S, Sunilkumar, K Byranahalli, Kulkarni, Vardendra, Siddartha, ES, Patil, Lingaraja Gowda C, Pujar, Sneharoopa, Dhananjaya, Shobha, Nagaraj, TS, Jeevika, MU, Harikiran, Reddy R, Saleem, Sarah, Tikmani, Shiyam Sunder, Zafar, Afia, Ahmed, Imran, Uddin, Zeeshan, Ghanchi, Najia, Roujani, Sana, Ariff, Shabina, Sheikh, Lumaan, Mirza, Waseem, Yasmin, Haleema, Raza, Jamal, Prakash, Jai, Haider, Furqan, Aceituno, Anna, Parlberg, Lindsay, Moore, Janet L, Hwang, Kay, Parepelli, Suchita, Kim, Jean, Bann, Carla, McClure, Elizabeth, Goldenberg, Robert, Silver, Robert, Goudar, Shivaprasad S, Kusagur, Varun B, Reza, Sayyeda, Moore, Janet, Bann, Carla M, Silver, Robert M, Goldenberg, Robert L, McClure, Elizabeth M *
Publikováno v:
In The Lancet Global Health November 2022 10(11):e1575-e1581
Autor:
Goudar, Shivaprasad, Dhaded, Sangappa M, Nagmoti, Mahantesh B, Somannavar, Manjunath S, Yogeshkumar, S, Guruprasad, Gowdar, Aradhya, Gayathri H, Nadig, Naveen, Kusgur, Varun, Raghoji, Chaitali R, Sarvamangala, B, Prakash, Veena, Joish, Upendra Kumar, Mangala, G K, Rajashekhar, K S, Kumar, Sunil, Kulkarni, Vardendra, Saleem, Sarah, Tikmani, Shiyam Sunder, Zafar, Afia, Ahmed, Imran, Uddin, Zeeshan, Ghanchi, Najia, Ariff, Shabina, Sheikh, Lumaan, Mirza, Waseem, Yasmin, Haleema, Raza, Jamal, Prakash, Jai, Haider, Furqan, Aceituno, Anna, Parlberg, Lindsay, Moore, Janet L, Hwang, Kay, Parepelli, Suchita, Kim, Jean, Bann, Carla, McClure, Elizabeth, Goldenberg, Robert, McClure, Elizabeth M *, Goudar, Shivaprasad S, Shobha, Dhananjaya, Roujani, Sana, Reza, Sayyeda, Bann, Carla M, Silver, Robert M, Goldenberg, Robert L
Publikováno v:
In The Lancet Global Health July 2022 10(7):e970-e977
Publikováno v:
In Best Practice & Research Clinical Endocrinology & Metabolism June 2019 33(3)
Autor:
Tikmani, Shiyam Sunder, Saleem, Sarah, Sadia, Afreen, M. Bann, Carla, Bozdar, Muhammad Hayat, Raza, Jamal, Dhaded, Sangappa M., Goudar, Shivaprasad S., Gowdar, Guruparasad, Yasmin, Haleema, McClure, Elizabeth M., Goldenberg, Robert L.
Publikováno v:
Global Pediatric Health; 3/13/2024, p1-13, 13p
Akademický článek
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Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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Autor:
Perera, Luke A, Hattersley, Andrew T, Harding, Heather P, Wakeling, Matthew N, Flanagan, Sarah E, Mohsina, Ibrahim, Raza, Jamal, Gardham, Alice, Ron, David, De Franco, Elisa
Dysfunction of the endoplasmic reticulum (ER) in insulin‐producing beta cells results in cell loss and diabetes mellitus. Here we report on five individuals from three different consanguineous families with infancy‐onset diabetes mellitus and sev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77d2cebaa3ac643d0d0cd398695f1d7f
