Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Marwa Farid"'
Autor:
Ola M. Eid, Maha M. Eid, Marwa Farid, Rania M. A. Abdel Kader, Rana Mahrous, Sara H. El-Dessouky
Publikováno v:
Journal of Genetic Engineering and Biotechnology, Vol 20, Iss 1, Pp 1-7 (2022)
Abstract Background The prenatal diagnosis of syndromes caused by chromosomal abnormality is a long-established part of obstetric care. Several DNA-based molecular approaches have provided rapid prenatal diagnosis of of cytogenomic abnormalities. MLP
Externí odkaz:
https://doaj.org/article/c83d0b82f769483691c477f6ced6b73c
Autor:
Ola M. Eid, Maha M. Eid, Amany H. Abdelrahman, Rania M. A. Abdel kader, Marwa Farid, Rana Mahrous, Mona K. Mekkawy, Alaa K. Kamel, Inas Mazen, Hala T. El-Bassyouni
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 21, Iss 1, Pp 1-8 (2020)
Abstract Background Short stature is defined as a body height below the third percentile, based on chronological age, or 2 standard deviations (SD) below the national height standard. The prevalence of short stature is around 2% of children worldwide
Externí odkaz:
https://doaj.org/article/1c67282c8740459d9ef6171ea075d21b
Autor:
Oda Al -- Atbi, Marwa Farid1 marwaf758@gmail.com, Rasham Al Asadi, Safa Abdul - Amir1 safaa.al_asadi@uobasrah.edu.iq
Publikováno v:
Arab Gulf. 2022, Vol. 50 Issue 4, p421-464. 44p.
Publikováno v:
Middle East Journal of Medical Genetics. 11:19-28
Autor:
Rania M. A. Abdel kader, Marwa Farid, Maha M. Eid, Mona K. Mekkawy, Inas Mazen, Amany H. Abdelrahman, Ola M. Eid, Hala T. El-Bassyouni, Alaa K. Kamel, Rana Mahrous
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 21, Iss 1, Pp 1-8 (2020)
Background Short stature is defined as a body height below the third percentile, based on chronological age, or 2 standard deviations (SD) below the national height standard. The prevalence of short stature is around 2% of children worldwide. Several
Autor:
Hsin-Chieh Tsay, Qinggong Yuan, Asha Balakrishnan, Marina Kaiser, Selina Möbus, Emilia Kozdrowska, Marwa Farid, Pia-Katharina Tegtmeyer, Katharina Borst, Florian W.R. Vondran, Ulrich Kalinke, Andreas Kispert, Michael P. Manns, Michael Ott, Amar Deep Sharma
Publikováno v:
Journal of Hepatology. 77:269
Publikováno v:
Gene Reports. 18:100573
Introduction Neurofibromatosis 1 (NF1) is an autosomal dominant disorder characterized by the presence of certain clinical manifestation. The most common clinical features are, hyperpigmented areas, neurofibromas and Lisch nodules of the iris. The di
Autor:
Qinggong Yuan, Pia-Katharina Tegtmeyer, Emilia Kozdrowska, Florian W. R. Vondran, Marina Kaiser, Selina Möbus, Andreas Kispert, Asha Balakrishnan, Marwa Farid, Ulrich Kalinke, Hsin-Chieh Tsay, Katharina Borst, Amar Deep Sharma, Michael Ott, Michael P. Manns
Publikováno v:
Journal of hepatology
Background & Aims Fibrosis, a cardinal feature of a dysfunctional liver, significantly contributes to the ever-increasing mortality due to end-stage chronic liver diseases. The crosstalk between hepatocytes and hepatic stellate cells (HSCs) plays a k