Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Abdelnaser Zalan"'
Autor:
Jacob Genizi, Lotan Berger, Muhammad Mahajnah, Yulia Shlonsky, Orit Golan-Shany, Azriel Romem, Ayelet Halevy, Keren Nathan, Rajech Sharkia, Abdelnaser Zalan, Aharon Kessel, Rony Cohen
Publikováno v:
Children, Vol 10, Iss 7, p 1122 (2023)
Pseudotumor cerebri (PTC) is a disorder characterized by increased intracranial pressure in the absence of a structural lesion or other identifiable cause. Cytokines, which are involved in the regulation of immune responses and inflammation, have bee
Externí odkaz:
https://doaj.org/article/3fbd9ec43c4c4ccba10da03a66134cab
Publikováno v:
Annals of Global Health, Vol 85, Iss 1 (2019)
Background: Type 2 Diabetes Mellitus (T2DM) is becoming increasingly prevalent and is considered to be a major public health threat worldwide. Behavioral and sociodemographic factors associated with T2DM vary within different societies. Objective: Th
Externí odkaz:
https://doaj.org/article/bdcd7e3c59d34f4e819338fb9e23069d
Autor:
Abdelnaser Zalan, Mohammad Khatib, Ahmad Sheikh Muhammad, Muhammad Mahajnah, Esmael Atamany, Rajech Sharkia
Publikováno v:
Advances in Anthropology. 12:137-148
Autor:
Abdelnaser Zalan
Publikováno v:
American Journal of Biomedical Science & Research. 15:66-76
Publikováno v:
Journal of Biosocial Science. 55:169-173
The aim of this study was to determine the trend of consanguineous marriage among the Arab population in Israel. Socio-demographic data for the Arab population were extracted from national health surveys conducted in Israel in 2007 and 2017. The prev
Autor:
Rajech Sharkia, Abdelnaser Zalan, Hazar Zahalka, Amit Kessel, Ayman Asaly, Wasif Al-Shareef, Muhammad Mahajnah
Publikováno v:
Genes; Volume 13; Issue 8; Pages: 1393
The CLN8 disease type refers to one of the neuronal ceroid lipofuscinoses (NCLs) which are the most common group of neurodegenerative diseases in childhood. The clinical phenotypes of this disease are progressive neurological deterioration that could
Autor:
Rajech Sharkia, Sahil Jain, Muhammad Mahajnah, Clair Habib, Abdussalam Azem, Wasif Al-Shareef, Abdelnaser Zalan
Publikováno v:
Genes; Volume 14; Issue 5; Pages: 1031
Peptidyl-tRNA hydrolase 2 (PTRH2) is an evolutionarily highly conserved mitochondrial protein. The biallelic mutations in the PTRH2 gene have been suggested to cause a rare autosomal recessive disorder characterized by an infantile-onset multisystem
Autor:
Abdelnaser Zalan, Rajech Sharkia
Publikováno v:
Handbook of Healthcare in the Arab World ISBN: 9783030368104
Handbook of Healthcare in the Arab World ISBN: 9783319743653
Handbook of Healthcare in the Arab World
Handbook of Healthcare in the Arab World ISBN: 9783319743653
Handbook of Healthcare in the Arab World
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8cda1dd2bd63e7e3e4916745e12cf79
https://doi.org/10.1007/978-3-030-36811-1_162
https://doi.org/10.1007/978-3-030-36811-1_162
Publikováno v:
Current diabetes reviews. 17(8)
Background: Diabetes mellitus (DM) is considered one of the main causes of mortality, morbidity, and health care expenditures. Effectively treating this disease is of crucial importance and imposes a global challenge. The incidence of Type 2 DM (T2DM
Autor:
William G. Newman, Ronen Spiegel, Jill E. Urquhart, Orly Elpeleg, Rajech Sharkia, Abdelnaser Zalan, Milit Marom-David, Muhammad Mahajnah, Simon G. Williams, Abdussalam Azem, Nathan Watemberg, Stavit A. Shalev, Sanjeev S. Bhaskar, Sarah B. Daly
Publikováno v:
American Journal of Medical Genetics Part A. 173:1051-1055
PTRH2 is an evolutionarily highly conserved mitochondrial protein that belongs to a family of peptidyl-tRNA hydrolases. Recently, patients from two consanguineous families with mutations in the PTRH2 gene were reported. Global developmental delay ass