RSRabah Mohamad Shawky
Rabah Mohamad Shawky
*This is an algorithmically generated author record based on publicly available information.
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Rabah Mohamad Shawky has a total of 104 co-authors. Here are the top co-authors by number of shared publications:
Radwa Gamal
14 shared publications- Solaf Mohamed Elsayed
Medical Genetics Department, Faculty of Medicine, Ain Shams University, Cairo, Egypt
11 shared publications Neveen S. Seifeldin
7 shared publicationsShaimaa Abdelsattar Mohammad
7 shared publicationsHeba Salah Abd-Elkhalek
5 shared publicationsSahar M. Nour El-Din
5 shared publications
Latest Publications
- Open Access
- 1 October 2018
- Published by Springer Nature in Egyptian Journal of Medical Human Genetics
- Vol. 19 (4) , 429-432
Cantu syndrome in an Egyptian child
- 1 October 2018
- Published by Springer Nature in Egyptian Journal of Medical Human Genetics
- Vol. 19 (4) , 429-432
Open AccessCantu syndrome in an Egyptian child
- Open Access
- 1 July 2018
- Published by Springer Nature in Egyptian Journal of Medical Human Genetics
- Vol. 19 (3) , 215-220
Genotyping of PPAR-γ gene polymorphism in Egyptian neonates affected with sepsis disease and its severity
- 1 July 2018
- Published by Springer Nature in Egyptian Journal of Medical Human Genetics
- Vol. 19 (3) , 215-220
Open AccessGenotyping of PPAR-γ gene polymorphism in Egyptian neonates affected with sepsis disease and its severity
- Open Access
- 1 January 2018
- Published by Springer Nature in Egyptian Journal of Medical Human Genetics
- Vol. 19 (1) , 7-12
Abnormal maternal biomarkers of homocysteine and methionine metabolism and the risk of congenital heart defects
- 1 January 2018
- Published by Springer Nature in Egyptian Journal of Medical Human Genetics
- Vol. 19 (1) , 7-12
Open AccessAbnormal maternal biomarkers of homocysteine and methionine metabolism and the risk of congenital heart defects
- Open Access
- 1 October 2017
- Published by Springer Nature in Egyptian Journal of Medical Human Genetics
- Vol. 18 (4) , 397-401
Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II
- 1 October 2017
- Published by Springer Nature in Egyptian Journal of Medical Human Genetics
- Vol. 18 (4) , 397-401
Open AccessMicrocephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II
- Open Access
- 1 January 2017
- Published by Springer Nature in Egyptian Journal of Medical Human Genetics
- Vol. 18 (1) , 93-97
C syndrome with skeletal anomalies, mental retardation, eyelid chalazion, Bitot’s spots and agenesis of the corpus callosum in an Egyptian child
- 1 January 2017
- Published by Springer Nature in Egyptian Journal of Medical Human Genetics
- Vol. 18 (1) , 93-97
Open AccessC syndrome with skeletal anomalies, mental retardation, eyelid chalazion, Bitot’s spots and agenesis of the corpus callosum in an Egyptian child
- Open Access
- 1 January 2017
- Published by Springer Nature in Egyptian Journal of Medical Human Genetics
- Vol. 18 (1) , 87-92
Kabuki make-up syndrome with genitourinary anomalies, ophthalmologic features and hyperpigmentation in an Egyptian child
- 1 January 2017
- Published by Springer Nature in Egyptian Journal of Medical Human Genetics
- Vol. 18 (1) , 87-92
Open AccessKabuki make-up syndrome with genitourinary anomalies, ophthalmologic features and hyperpigmentation in an Egyptian child
- Open Access
- 1 October 2016
- Published by Springer Nature in Egyptian Journal of Medical Human Genetics
- Vol. 17 (4) , 389-395
Christ-Siemens-Touraine syndrome with cleft palate, absent nipples, gallstones and mild mental retardation in an Egyptian child
- 1 October 2016
- Published by Springer Nature in Egyptian Journal of Medical Human Genetics
- Vol. 17 (4) , 389-395
Open AccessChrist-Siemens-Touraine syndrome with cleft palate, absent nipples, gallstones and mild mental retardation in an Egyptian child
- Open Access
- 1 October 2016
- Published by Springer Nature in Egyptian Journal of Medical Human Genetics
- Vol. 17 (4) , 397-400
Meier–Gorlin syndrome: An additional Egyptian patient with gastroesophageal reflux, hydronephrosis, renal stones and hypoplastic labia majora and minora with clitromegaly
- 1 October 2016
- Published by Springer Nature in Egyptian Journal of Medical Human Genetics
- Vol. 17 (4) , 397-400
Open AccessMeier–Gorlin syndrome: An additional Egyptian patient with gastroesophageal reflux, hydronephrosis, renal stones and hypoplastic labia majora and minora with clitromegaly
- Open Access
- 1 July 2016
- Published by Springer Nature in Egyptian Journal of Medical Human Genetics
- Vol. 17 (3) , 281-285
Treatment options for patients with Gaucher disease
- 1 July 2016
- Published by Springer Nature in Egyptian Journal of Medical Human Genetics
- Vol. 17 (3) , 281-285
Open AccessTreatment options for patients with Gaucher disease