Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Fatima, Saif"'
Autor:
Alblooshi, Fatima Saif Ahmed Kameel, author
Publikováno v:
Entrepreneurial Rise in the Middle East and North Africa: The Influence of Quadruple Helix on Technological Innovation
Publikováno v:
مجلة الآداب, Vol 1, Iss 138 (2021)
هدفت هذه الدراسة إلى معرفة تأثير عمل المرأة في جودة حياتها، والتعرُّف على كيفية تحقيق المرأة العاملة للتوازن بين عملها وحياتها، والكشف ع
Externí odkaz:
https://doaj.org/article/b322f83c989b47dc94e5c9f025403d34
Publikováno v:
مجلة الآداب, Vol 2, Iss 135 (2020)
هدفت هذه الدراسة إلى التعرف على واقع استخدام طالبات الثانوية العامة لشبكات التواصل الاجتماعي في مدينة العين، وذلك من خلال التعرف على الخ
Externí odkaz:
https://doaj.org/article/e84283ef0614429ea5ff6cc702f7dd27
Publikováno v:
مجلة الآداب, Vol 2, Iss 135 (2020)
هدفت هذه الدراسة إلى التعرف على واقع استخدام طالبات الثانوية العامة لشبكات التواصل الاجتماعي في مدينة العين، وذلك من خلال التعرف على الخ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac773417b9670ac4cb53a529f1763fd2
https://doi.org/10.31973/aj.v2i135.811
https://doi.org/10.31973/aj.v2i135.811
Autor:
Fatima Saif, Mahmoud Taleb Al-Ali, Sami Bizzari, Ethar Mustafa Malik, Pratibha Nair, Madiha Mohamed, Fatma Bastaki, Sana Hamici, Abdul Rezzak Hamzeh
Publikováno v:
Annals of Human Genetics. 82:35-47
Congenital disorders of glycosylation (CDG) represent an expanding group of conditions that result from defects in protein and lipid glycosylation. Different subgroups of CDG display considerable clinical and genetic heterogeneity due to the highly c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7a4cc2b4d067db73a373c36ecd8263f
https://doi.org/10.1111/ahg.12220
https://doi.org/10.1111/ahg.12220
Autor:
Madiha Mohamed, Fatma Bastaki, Nafisa Tawfiq, Pratibha Nair, Fatima Saif, Abdul Rezzak Hamzeh, Mahmoud Taleb Al-Ali, Manal Mustafa Khadora
Publikováno v:
Hormone Research in Paediatrics. 87:64-68
Background/Aims: This study aimed to identify, clinically and molecularly, the causality of Rabson-Mendenhall syndrome in an Emirati family. It is one of the monogenic syndromes of abnormal glucose homeostasis, which result from insulin receptor defe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2580b53e5962e2632d1a2dd2eff602e
https://doi.org/10.1159/000447090
https://doi.org/10.1159/000447090
Autor:
Fatma Bastaki, Nafisa Tawfiq, Abdul Rezzak Hamzeh, Mahmoud Taleb Al-Ali, Madiha Mohamed, Fatima Saif, Pratibha Nair, Majdi El Halik
Publikováno v:
American Journal of Medical Genetics Part A. 170:2127-2132
Microcephaly is a rare neurological condition, both in isolation and when it occurs as part of a syndrome. One of the syndromic forms of microcephaly is microcephaly, seizures and developmental delay (MCSZ) (OMIM #613402), a rare autosomal recessive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcd4e2e090c70317d98c58c5165349bb
https://doi.org/10.1002/ajmg.a.37766
https://doi.org/10.1002/ajmg.a.37766
Autor:
Abdul Rezzak Hamzeh, Pratibha Nair, Fatma Bastaki, Majdi El-Halik, Madiha Mohamed, Fatima Saif, Mahmoud Taleb Al-Ali, Nafisa Tawfiq, Gururaj Aithala
Publikováno v:
Congenital Anomalies. 56:135-137
The WDR62 gene encodes a scaffold protein of the c-Jun N-terminal kinase (JNK) pathway. It plays a critical role in laying out various cellular layers in the cerebral cortex during embryogenesis, and hence the dramatic clinical features resulting fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83431c4d7dbb7f94bb7bfa1ad0e27483
https://doi.org/10.1111/cga.12144
https://doi.org/10.1111/cga.12144
Autor:
Fatima Saif, Pratibha Nair, Madiha Mohamed, Tasneem Obeid, Fatma Bastaki, Mahmoud Taleb Al-Ali, Abdul Rezzak Hamzeh
Publikováno v:
Metabolic brain disease. 33(3)
The UNC80 gene encodes for a large component of the NALCN sodium-leak channel complex that regulates the basal excitability of the nervous system. In this study, we report on a novel homozygous mutation in UNC80 in a Palestinian-Emirati patient suffe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c70877dd4c3d364c436fdc079519be76
https://pubmed.ncbi.nlm.nih.gov/29430593
https://pubmed.ncbi.nlm.nih.gov/29430593