Emotional closeness and emotional distance among schoolteachers: the case of Arab teachers who teach in Jewish schools

Autor: Izhar Oplatka, Alaa Afif Elmalak-Watted

Publikováno v: Journal of Professional Capital and Community. 7:193-208

PurposeThe aim of the current study was to explore emotional closeness and emotional distance between Arab teachers who teach in the Jewish State Educational System and their Jewish counterparts in the school.Design/methodology/approachThe research u

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::255ff02fd2640b733d4a200a381de500
https://doi.org/10.1108/jpcc-09-2021-0060

Relation between vitamin D level and severity, symptomatology and cognitive dysfunction of major depressive disorder—A sample of Egyptian patients

Autor: Mohamed A. Khalil, Alaa Afif, Akmal Mostafa, Tamer Goueli, Sandra W. Elseesy

Publikováno v: Neurology, Psychiatry and Brain Research. 35:10-15

Background Vitamin D helps in the regulation of neurotransmission and neuroprotection. Therefore, vitamin D deficiency might lead to inactivated receptors and may result in depression. Aim The study assessed the relation between serum level of vitami

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0e0dbdb62688586a7f4ebfcf73acde1d
https://doi.org/10.1016/j.npbr.2019.12.001

CYP21A2genetic profile in 14 Egyptian children with suspected congenital adrenal hyperplasia: a diagnostic challenge

Autor: Hend Soliman, Normeen Hany Rady, Mona Hafez, Yasmin Elshiwy, Amany Ibrahim, Fatma El-Mougy, Mona Abdullatif, Balsam Sherif, Sahar A. Sharaf, Heba Baz, Ahmed Khattab, Marwa Elsharkawy, Sherif Ekladious, Alaa Afif, Noha Musa, Hazem Abou-Yousef, Ghada Thabet

Publikováno v: Annals of the New York Academy of Sciences. 1415:11-20

CYP21A2 genotyping remains an important element in the diagnosis and management of congenital adrenal hyperplasia, and establishing accurate genotype-phenotype correlations has facillitated adequate genetic counseling and prenatal management for at-r

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::42fe288362122ec16232ea47b277379f
https://doi.org/10.1111/nyas.13540

De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies

Autor: Alaa Afif Mohammed, Yong-hui Jiang, Thalia Antoniadi, Cynthia J. Curry, Celia Zazo Seco, Dorine Bax, Slavé Petrovski, Samuel J.H. Clokie, Vandana Shashi, Stephen W. Wilson, Dianne Gerrelli, Nicola K. Ragge, Marco Tartaglia, Nicolas Chassaing, Andrea Ciolfi, Marleen Simon, Bruce D. Gelb, Helle Andersen, Zöe Powis, Patrick Calvas, Jennifer A. Sullivan, Fabiola Ceroni, Constance Smith-Hicks, Emanuele Bellacchio, Kristina Pilekær Sørensen, Rodrigo M. Young, Christina Fagerberg, Alessandro De Luca, Ellen van Binsbergen, Luigi Memo, William B. Dobyns, Anna Chassevent, Berta Crespo, Richard J. Holt

Publikováno v: Holt, R J, Young, R M, Crespo, B, Ceroni, F, Curry, C J, Bellacchio, E, Bax, D A, Ciolfi, A, Simon, M, Fagerberg, C R, van Binsbergen, E, De Luca, A, Memo, L, Dobyns, W B, Mohammed, A A, Clokie, S J H, Zazo Seco, C, Jiang, Y H, Sørensen, K P, Andersen, H, Sullivan, J, Powis, Z, Chassevent, A, Smith-Hicks, C, Petrovski, S, Antoniadi, T, Shashi, V, Gelb, B D, Wilson, S W, Gerrelli, D, Tartaglia, M, Chassaing, N, Calvas, P & Ragge, N K 2019, ' De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies ', American Journal of Human Genetics, vol. 105, no. 3, pp. 640-657 . https://doi.org/10.1016/j.ajhg.2019.07.005
American Journal of Human Genetics

The identification of genetic variants implicated in human developmental disorders has been revolutionized by second-generation sequencing combined with international pooling of cases. Here, we describe seven individuals who have diverse yet overlapp

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1ac6035c7582657339b72496940ad80
https://findresearcher.sdu.dk:8443/ws/files/153983581/De_Novo_Missense_Variants_in_FBXW11_Cause_Diverse_Developmental_Phenotypes_Including_Brain_Eye_and_Digit_Anomalies.pdf

CYP21A2 genetic profile in 14 Egyptian children with suspected congenital adrenal hyperplasia: a diagnostic challenge

Autor: Fatma, Elmougy, Sahar, Sharaf, Mona, Hafez, Ahmed, Khattab, Hazem, Abou-Yousef, Marwa, Elsharkawy, Heba, Baz, Sherif, Ekladious, Balsam, Sherif, Noha, Musa, Yasmin, Elshiwy, Alaa, Afif, Mona, Abdullatif, Ghada, Thabet, Normeen, Rady, Amany, Ibrahim, Hend, Soliman

Publikováno v: Annals of the New York Academy of Sciences. 1415(1)

CYP21A2 genotyping remains an important element in the diagnosis and management of congenital adrenal hyperplasia, and establishing accurate genotype-phenotype correlations has facillitated adequate genetic counseling and prenatal management for at-r

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9ad0e3166d53369a8e05159bba2fef4e
https://pubmed.ncbi.nlm.nih.gov/29266270