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Scientific Reports
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September 18, 2023
Importance of TREC and KREC as molecular markers for immunological evaluation of down syndrome children
Eman Eissa, Hanan H Afifi, Assem M Abo-Shanab, et al.
Biochemical Genetics
|
July 2, 2024
Genetic Correlation of HBB, HFE and HAMP Genes to Endocrinal Complications in Egyptian Beta Thalassemia Major Patients
Mona F Sokkar, Mona Hamdy, Mohamed B Taher, et al.
Ophthalmic Genetics
|
November 16, 2017
Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation
Ghada M H Abdel-Salam, Mohamed S Abdel-Hamid, Mennat I Mehrez, et al.
International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases
|
May 18, 2019
Prevalence and 30-day all-cause mortality of carbapenem-and colistin-resistant bacteraemia caused by Acinetobacter baumannii, Pseudomonas aeruginosa, and Klebsiella pneumoniae: Description of a decade-long trend
A Balkhair, Z Al-Muharrmi, B Al'Adawi, et al.
Journal of Neuroimmunology
|
May 8, 2021
Altered distributions and functions of natural killer T cells and γδ T cells in neonates with neonatal encephalopathy, in school-age children at follow-up, and in children with cerebral palsy
Nawal A B Taher, Lynne A Kelly, Alhanouf I Al-Harbi, et al.
Molecular Neurobiology
|
April 22, 2025
Insight into Apert Syndrome: Reporting on Six Patients and Increasing Awareness
Hala T El-Bassyouni, Ghada Y El-Kamah, Hanan H Afifi, et al.
Journal of Molecular Neuroscience : MN
|
October 29, 2024
Molecular and Clinical Characterization of a Cohort of Autosomal Recessive Sensorineural Hearing Loss in Egyptian Patients
Mohammed M Sayed-Ahmed, Hala T El-Bassyouni, Hanan H Afifi, et al.
Journal of Human Genetics
|
April 27, 2023
Expanding the phenotypic spectrum and clinical severity associated with WLS gene
Ghada M H Abdel-Salam, Hanan H Afifi, Mohamed S Abdel-Hamid, et al.
Narra J
|
March 7, 2024
Elevated serum malondialdehyde (MDA), insulin, follicle-stimulating hormone (FSH), luteinizing hormone (LH), and thyroid- stimulating hormone (TSH), and reduced antioxidant vitamins in polycystic ovarian syndrome patients
Abdullah A Mahmud, Umme H Anu, Kazi A Foysal, et al.
Plos One
|
April 20, 2026
Upregulation of CD1d and ULBP3 on B cells from healthy donors and chronic lymphocytic leukaemia patients does not prime them for killing by γδ T cells
Julie David, Amy Walsh, Ke Sin Seow, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
Scientific Reports
|
September 18, 2023
Importance of TREC and KREC as molecular markers for immunological evaluation of down syndrome children
Eman Eissa, Hanan H Afifi, Assem M Abo-Shanab, et al.
Biochemical Genetics
|
July 2, 2024
Genetic Correlation of HBB, HFE and HAMP Genes to Endocrinal Complications in Egyptian Beta Thalassemia Major Patients
Mona F Sokkar, Mona Hamdy, Mohamed B Taher, et al.
Ophthalmic Genetics
|
November 16, 2017
Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation
Ghada M H Abdel-Salam, Mohamed S Abdel-Hamid, Mennat I Mehrez, et al.
International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases
|
May 18, 2019
Prevalence and 30-day all-cause mortality of carbapenem-and colistin-resistant bacteraemia caused by Acinetobacter baumannii, Pseudomonas aeruginosa, and Klebsiella pneumoniae: Description of a decade-long trend
A Balkhair, Z Al-Muharrmi, B Al'Adawi, et al.
Journal of Neuroimmunology
|
May 8, 2021
Altered distributions and functions of natural killer T cells and γδ T cells in neonates with neonatal encephalopathy, in school-age children at follow-up, and in children with cerebral palsy
Nawal A B Taher, Lynne A Kelly, Alhanouf I Al-Harbi, et al.
Molecular Neurobiology
|
April 22, 2025
Insight into Apert Syndrome: Reporting on Six Patients and Increasing Awareness
Hala T El-Bassyouni, Ghada Y El-Kamah, Hanan H Afifi, et al.
Journal of Molecular Neuroscience : MN
|
October 29, 2024
Molecular and Clinical Characterization of a Cohort of Autosomal Recessive Sensorineural Hearing Loss in Egyptian Patients
Mohammed M Sayed-Ahmed, Hala T El-Bassyouni, Hanan H Afifi, et al.
Journal of Human Genetics
|
April 27, 2023
Expanding the phenotypic spectrum and clinical severity associated with WLS gene
Ghada M H Abdel-Salam, Hanan H Afifi, Mohamed S Abdel-Hamid, et al.
Narra J
|
March 7, 2024
Elevated serum malondialdehyde (MDA), insulin, follicle-stimulating hormone (FSH), luteinizing hormone (LH), and thyroid- stimulating hormone (TSH), and reduced antioxidant vitamins in polycystic ovarian syndrome patients
Abdullah A Mahmud, Umme H Anu, Kazi A Foysal, et al.
Plos One
|
April 20, 2026
Upregulation of CD1d and ULBP3 on B cells from healthy donors and chronic lymphocytic leukaemia patients does not prime them for killing by γδ T cells
Julie David, Amy Walsh, Ke Sin Seow, et al.
Page
of 3