Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Eman M. Sherif"'
Autor:
Amal El-Beshlawy, Azza A. G. Tantawy, Rabah M. Shawky, Solaf M. Elsayed, Iman M. Marzouk, S. Elgawhary, Hadeer Abdelghaffar, Usama El Safy, Khaled Eid, Khalid I. EISayh, Ahmed Megahed, Amira Adly, Eman M. Sherif, Mervat A. M. Youssef, Manar Mohamed Fathy, Nouran Yousef Salah, Sherine M. Elzeiny, Eslam Rabie Abdel Aziz EI Bakky, Ekram Fateen
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-16 (2024)
Abstract Background Gaucher disease (GD), an autosomal recessive, lysosomal storage disorder, is caused due to mutations in the glucocerebrosidase (GBA) gene. GD can occur at any age and is classified as type 1 (non-neurologic), type 2 (infantile for
Externí odkaz:
https://doaj.org/article/40af8925d1554eb7ab90e6b492f1c684
Publikováno v:
BMC Endocrine Disorders, Vol 24, Iss 1, Pp 1-11 (2024)
Abstract Background This study aimed to assess the anthropometric measures and pubertal growth of children and adolescents with Type 1 diabetes mellitus (T1DM) and to detect risk determinants affecting these measures and their link to glycemic contro
Externí odkaz:
https://doaj.org/article/7d3732aba66649ac9575eb5eaeacc914
Autor:
Eman M. Sherif, Randa M. Matter, Nouran Yousef Salah, Nour Eldin H. Abozeid, Heba M. Atif, Nermien M. Tantawy
Publikováno v:
Diabetes/Metabolism Research and Reviews. 39
Current diagnostic and treatment modalities target late stages of diabetic retinopathy (DR) when retinopathy has already been established. Novel and more sensitive strategies are needed. Optical coherence tomography angiography (OCTA) permits non-inv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bda98572a879e0f2a9ee314b031f2cd
https://doi.org/10.1002/dmrr.3598
https://doi.org/10.1002/dmrr.3598
Publikováno v:
Egyptian Journal of Hospital Medicine; Vol. 85 No. 1 (2021); 2730-2733
Background: Diabetic patients need to maintain tight glycemic control to avoid long term complications. Children need to achieve tight control without the risk of hypoglycemic excursions. Objective: To assess the safety and efficacy of insulin glargi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6663416fb18afddc274dac8e9fb1d0d
https://doi.org/10.21608/ejhm.2021.189839
https://doi.org/10.21608/ejhm.2021.189839
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 15, Iss 4, Pp 361-367 (2014)
Background: Advanced glycation end products (AGEs) are a heterogeneous and complex group of biochemical compounds, resulting from nonenzymatic glycation and oxidation of protein, nucleic acids, and lipids. Aim of the study: To assess sRAGE and CIMT i
Externí odkaz:
https://doaj.org/article/cc2e5010dc044c048c2a5366fa02400c
Autor:
Eman M. Sherif, Omneya Ibrahim Youssef, Ola Khaled Mohamed Khater, Nouran Yousef Salah El-Din, Abeer Ahmed Abd El Maksood
Publikováno v:
Journal of diabetes and its complications. 33(9)
Endothelial dysfunction caused by chronic inflammation is the cornerstone of vascular complications in type 1 Diabetes-Mellitus (T1DM). Soluble Urokinase Plasminogen Activator Receptor (SuPAR) is a novel marker of inflammation and endothelial dysfunc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::068f386971a88a69ca330484b59810ae
https://pubmed.ncbi.nlm.nih.gov/31301955
https://pubmed.ncbi.nlm.nih.gov/31301955
Autor:
Nevin M. Habeeb, Ahmed Ibrahim, Abeer A. Abdelmaksoud, Galila M. Mokhtar, Enas M. Hamed, Eman M. Sherif, Eman A. Elghoroury
Publikováno v:
Hematology. 21:46-53
Estimating the prevalence of glutathione S-transferase gene polymorphism (GSTM1) null genotype among patients with beta thalassemia major (β-TM) in relation to myocardial status assessed by tissue Doppler and cardiac siderosis assessed by cardiac ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a8db10b020a2710e39f9d8dc3fb3c98
https://doi.org/10.1179/1607845415y.0000000046
https://doi.org/10.1179/1607845415y.0000000046
Publikováno v:
Egyptian Journal of Pediatrics. 32:155-179
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::528a803c4e7f8c6f2785ea943ac56c80
https://doi.org/10.12816/0029192
https://doi.org/10.12816/0029192
Publikováno v:
Blood Coagulation & Fibrinolysis. 25:451-457
Thrombin-activatable fibrinolysis inhibitor (TAFI) is a potent inhibitor of fibrinolysis isolated from human plasma. This study was designed to investigate the association between TAFI levels in relation to metabolic control, microvascular complicati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::958bcaf52a260a2d79559c84a33aaccd
https://doi.org/10.1097/mbc.0000000000000080
https://doi.org/10.1097/mbc.0000000000000080
Autor:
Amina Hafez Awad, Sahar Hassanine, Azza A.G. Tantawy, Amira Abdel Moneam Adly, Eman M. Sherif
Publikováno v:
Journal of Inherited Metabolic Disease. 36:1025-1037
Effectiveness of enzyme replacement therapy (ERT) in reverting hematologic, skeletal, and visceral symptoms in Gaucher disease (GD) has been demonstrated, although, its efficacy in neurologic involvement is still debated.We evaluated the extent of ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6529e58d0670078a6f39235243e50db0
https://doi.org/10.1007/s10545-013-9597-z
https://doi.org/10.1007/s10545-013-9597-z