Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Ali Shaltout"'
Publikováno v:
Central European Journal of Immunology, Vol 43, Iss 3, Pp 248-254 (2018)
Down syndrome (DS) is the commonest genetic disorder and more liable for recurrent infections. We aimed to determine the differences in lymphocyte subgroups between DS children and the healthy population and to study the pattern and likelihood for re
Externí odkaz:
https://doaj.org/article/b55fca0037d145db8461253ec0284e5a
Autor:
Mohammad Al-Haggar, Ashraf Bakr, Yahya Wahba, Paul J Coucke, Fatma El-Hussini, Mona Hafez, Riham Eid, Abdel-Rahman Eid, Amr Sarhan, Ali Shaltout, Ayman Hammad, Sohier Yahia, Ahmad El-Rifaie, Dina Abdel-Hadi
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 28, Iss 1, Pp 141-148 (2017)
Marfan syndrome (MFS), the founding member of connective tissue disorder, is an autosomal dominant disease; it is caused by a deficiency of the microfibrillar protein fibrillin-1 (FBN1) and characterized by involvement of three main systems; skeletal
Externí odkaz:
https://doaj.org/article/1243858dedaa4cd682a50f0b8764c30f
Autor:
Mohammad Al-Haggar, Osamu Sakamoto, Ali Shaltout, Amany El-Hawary, Yahya Wahba, Dina Abdel-Hadi
Publikováno v:
Case Reports in Nephrology, Vol 2011 (2011)
Background. Fanconi-Bickel syndrome (FBS) is an autosomal recessive disorder caused by defects in facilitative glucose transporter 2 (GLUT2 or SLC2A2) gene mapped on chromosome 3q26.1-26.3, that codes for the glucose transporter protein 2. Methods. T
Externí odkaz:
https://doaj.org/article/4bc57789affa4e5baf01cf2c625eb082
Publikováno v:
Journal of Orthopaedic Science. 25:529-532
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fcbbcc95f63ca76411cdc16cf8166d4
https://doi.org/10.1016/j.jos.2017.09.004
https://doi.org/10.1016/j.jos.2017.09.004
Publikováno v:
Indian J Hematol Blood Transfus
Cluster of differentiation 96 (CD96) is an important leukemic stem cells (LSCs) surface marker. We evaluated CD96 expression in children with acute leukemia (AL) and described its relation with treatment response. We conducted a prospective cohort st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3768b381f61b18fe596e4a7c35477f4a
https://doi.org/10.1007/s12288-019-01145-2
https://doi.org/10.1007/s12288-019-01145-2
Publikováno v:
Central European Journal of Immunology, Vol 43, Iss 3, Pp 248-254 (2018)
Central-European Journal of Immunology
Central-European Journal of Immunology
Down syndrome (DS) is the commonest genetic disorder and more liable for recurrent infections. We aimed to determine the differences in lymphocyte subgroups between DS children and the healthy population and to study the pattern and likelihood for re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f89b3464cb782263024a5cb9355ade8
https://www.termedia.pl/Lymphocyte-subgroups-and-recurrent-infections-in-children-with-Down-syndrome-a-prospective-case-control-study,10,34284,1,1.html
https://www.termedia.pl/Lymphocyte-subgroups-and-recurrent-infections-in-children-with-Down-syndrome-a-prospective-case-control-study,10,34284,1,1.html
Autor:
Basma Shouman, Mohamed M. Abdelaziz, Ali Shaltout, Tahmina Ahmad, Mohamed T. Khashaba, Bothina M. Hasanein, Hany Aly, Hala Almarsafawy
Publikováno v:
Journal of Pediatric Neurology. :299-304
Proinflammatory cytokines play a role in the pathogenesis of hypoxic-ischemic encephalopathy (HIE). We aimed: 1) to characterize the expression of interleukin-1 β (IL-1 β ), IL-6 and tumor necrosis factor- α (TNF- α ) in the cerebrospinal fluid (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::177b44b6889d80be2477869f22e42bfa
https://doi.org/10.3233/jpn-2011-0501
https://doi.org/10.3233/jpn-2011-0501
Autor:
Osama Elbaz, Ali Shaltout
Publikováno v:
Hematology (Amsterdam, Netherlands). 5(5)
Granulocyte-macrophage colony stimulating factor (GM-CSF) and Interleukin-3 (IL-3) are increasingly used to stimulate granulopoiesis in neutropenic patients but these are rarely used in the lights of knowledge of the endogenous CSF-levels. In this st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74bf106f230d2b3027e9ad71beef5e1f
https://pubmed.ncbi.nlm.nih.gov/27420929
https://pubmed.ncbi.nlm.nih.gov/27420929
Autor:
Mohammad Al-Haggar, Yahya Wahba, Osamu Sakamoto, Dina Abdel-Hadi, Ali Shaltout, Amani Al-Hawari
Publikováno v:
Clinical and Experimental Nephrology. 16:604-610
Fanconi–Bickel syndrome (FBS) is an autosomal recessive disorder caused by defects in the facilitative glucose transporter 2 (GLUT2 or SLC2A2) gene which codes for the glucose transporter protein 2 expressed in hepatocytes and renal tubular cells c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df23f2d0faf7efdd1c0ba7d98f86a441
https://doi.org/10.1007/s10157-012-0603-9
https://doi.org/10.1007/s10157-012-0603-9
Publikováno v:
Alexandria Journal of Pediatrics. 31:141
Background Early recognition and management of sepsis is a challenge facing intensivists. Many biomarkers were investigated but none is optimal. Aim Appraise the value of presepsin as a biomarker for the diagnosis, differentiation of severity, and pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09a4626881845a736e47a1fbaa1f7763
https://doi.org/10.4103/ajop.ajop_32_18
https://doi.org/10.4103/ajop.ajop_32_18