Zobrazeno 1 - 10
of 128
pro vyhledávání: '"A. M. Wakil"'
Publikováno v:
International Journal of One Health, Vol 5, Pp 1-8 (2019)
Aim: Bovine tuberculosis (bTB) is an important milk-borne zoonosis that affects cattle production and poses serious threat to public health. This study aimed at assessing the risk factors as well as the level of awareness, attitude, and practices of
Externí odkaz:
https://doaj.org/article/09d59294235b4d5baad306ed8af36e72
Autor:
Sibtain Afzal, Khushnooda Ramzan, Sajjad Ullah, Salma M. Wakil, Arshad Jamal, Sulman Basit, Ahmed Bilal Waqar
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-7 (2020)
Abstract Background X-linked ichthyosis (XLI; OMIM# 308100) is a recessive keratinization disorder characterized by the presence of dark brown, polygonal, adherent scales on different parts of the body surface. It almost exclusively affects males and
Externí odkaz:
https://doaj.org/article/5ab2066d1a5d425dbce17cff495e67c6
Autor:
Salma M. Wakil, Safa Alhissi, Haya Al Dossari, Ayesha Alqahtani, Sherin Shibin, Brahim T. Melaiki, Josef Finsterer, Amal Al-Hashem, Saeed Bohlega, Anas M. Alazami
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-6 (2019)
Abstract Background Mutations in ARL6IP1, which encodes a tetraspan membrane protein localized to the endoplasmic reticulum (ER), have been recently described in a large family with a complicated form of hereditary spastic paraplegia (HSP). Case pres
Externí odkaz:
https://doaj.org/article/71bceb16ca6a4a7f80e01f6087f9cb35
Autor:
Maysoon Alsagob, Mustafa A. Salih, Muddathir H. A. Hamad, Yusra Al-Yafee, Jawaher Al-Zahrani, Albandary Al-Bakheet, Michael Nester, Nadia Sakati, Salma M. Wakil, Ali AlOdaib, Dilek Colak, Namik Kaya
Publikováno v:
Molecular Cytogenetics, Vol 12, Iss 1, Pp 1-6 (2019)
Abstract 15q13.3 syndrome is associated with a wide spectrum of neurological disorders. Among a cohort of 150 neurodevelopmental cases, we identified two patients with two close proximity interstitial hemizygous deletions on chromosome 15q13. Using h
Externí odkaz:
https://doaj.org/article/74f03fe71e934a9d8b9467422ded30d0
Autor:
Dorota Monies, Hussam Abou Al-Shaar, Ewa A. Goljan, Banan Al-Younes, Muna Monther Abdullah Al-Breacan, Maher Mohammed Al-Saif, Salma M. Wakil, Brian F. Meyer, Khalid S. A. Khabar, Saeed Bohlega
Publikováno v:
Human Genomics, Vol 11, Iss 1, Pp 1-10 (2017)
Abstract Background Five affected individuals with syndromic tremulous dystonia, spasticity, and white matter disease from a consanguineous extended family covering a period of over 24 years are presented. A positional cloning approach utilizing geno
Externí odkaz:
https://doaj.org/article/5b7cbc4813c3447b8ee52ae99170fc61
Autor:
Razek Georges Coussa, Susan M. Wakil, Hady Saheb, David E. Lederer, Karin M. Oliver, Devinder P. Cheema
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 5, Iss C, Pp 16-19 (2017)
Purpose: To report the occurrence and management of severe infectious scleritis in a 75 year-old woman following intravitreal ranibizumab injection. Observations: A 75 year-old monocular woman receiving monthly intravitreal ranibizumab injection for
Externí odkaz:
https://doaj.org/article/e6dfadae1e7049459ea6562065f9e794
Autor:
Salma M. Wakil, Ramesh Ram, Nzioka P. Muiya, Munish Mehta, Editha Andres, Nejat Mazhar, Batoul Baz, Samya Hagos, Maie Alshahid, Brian F. Meyer, Grant Morahan, Nduna Dzimiri
Publikováno v:
Data in Brief, Vol 7, Iss , Pp 172-176 (2016)
The data shows results acquired in a large cohort of 5668 ethnic Arabs involved in a common variants association study for coronary artery disease (CAD) and myocardial infarction (MI) using the Affymetrix Axiom Genotyping platform (“A genome-wide a
Externí odkaz:
https://doaj.org/article/be66429f563a46519585684c4c63b7f8
Autor:
Salma M. Wakil, Dorota Monies, Samya Hagos, Fahad Al-Ajlan, Josef Finsterer, Aisha Al Qahtani, Khushnooda Ramzan, Rawan Al Humaidy, Mohamed A. Al-Muhaizea, Brian Meyer, Saeed A. Bohlega
Publikováno v:
Case Reports in Genetics, Vol 2018 (2018)
Hereditary sensory and autonomic neuropathies (HSANs) are a clinically and genetically heterogeneous group of disorders involving various sensory and autonomic dysfunctions. The most common symptoms of HSANs include loss of sensations of pain and tem
Externí odkaz:
https://doaj.org/article/4e810ac4986442648d13395431f8d886
Autor:
Mada Yateem, Dorota Monies, Haya Al-Dusery, Sulaiman M. Al-Mayouf, Raed Alzyoud, Boshra Aladaileh, Brian F. Meyer, Salma M. Wakil, Abdullatif Alenazi, Manal AlShiakh
Publikováno v:
International Journal of Pediatrics & Adolescent Medicine
International Journal of Pediatrics and Adolescent Medicine, Vol 8, Iss 1, Pp 44-47 (2021)
International Journal of Pediatrics and Adolescent Medicine, Vol 8, Iss 1, Pp 44-47 (2021)
Background The classification and pathogenic basis of juvenile idiopathic arthritis (JIA) are a subject of some controversy. Essentially, JIA is an exclusion diagnosis that represents a phenotypically heterogeneous group of arthritis of unknown origi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9304deab67f20f762b658159f26c6f9f
http://europepmc.org/articles/PMC7922844
http://europepmc.org/articles/PMC7922844
Publikováno v:
Asian Food Science Journal. :32-42
Aim: This work was carried out to investigate the influence of Lactic Acid Bacteria (LAB) on organoleptic quality and proximate composition of yoghurt, and viability of starter cultures in yoghurt. Methods: The LAB starter cultures were selected base
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0538914c613ef83f9916b4e2d06a5549
https://doi.org/10.9734/afsj/2020/v16i330173
https://doi.org/10.9734/afsj/2020/v16i330173