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Genes
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October 23, 2021
Two Decades after Mandibuloacral Dysplasia Discovery: Additional Cases and Comprehensive View of Disease Characteristics
Isabelle Jéru, Amira Nabil, Gehad El-Makkawy, et al.
Reproductive Sciences (Thousand Oaks, Calif.)
|
November 13, 2023
Conservative Hypomethylation of Mesenchymal Stem Cells and Their Secretome Restored the Follicular Development in Cisplatin-Induced Premature Ovarian Failure Mice
Amira Nabil Salama, Eman Abd El-Fatah Badr, Nanis Shawky Holah, et al.
European Journal of Medical Genetics
|
March 24, 2020
A familial PLCB4 mutation causing auriculocondylar syndrome 2 with variable severity
Amira Nabil, Sahar El Shafei, Nihal M El Shakankiri, et al.
Cureus
|
February 6, 2026
Diagnostic Challenges in Seronegative Celiac Disease: A Case of Massive Splenomegaly and Persistent Metabolic Imbalance
Mathab Adam, Ahmed H Ahmed, Aia A Ibrahim, et al.
Journal of Inherited Metabolic Disease
|
March 11, 2016
On the phenotypic spectrum of serine biosynthesis defects
Ayman W El-Hattab, Ranad Shaheen, Jozef Hertecant, et al.
Frontiers in Genetics
|
June 6, 2022
Genomics in Egypt: Current Status and Future Aspects
Eman Ahmed El-Attar, Rasha Mohamed Helmy Elkaffas, Sarah Ahmed Aglan, et al.
European Journal of Pediatrics
|
October 4, 2014
Kyphoscoliotic type of Ehlers-Danlos Syndrome (EDS VIA) in six Egyptian patients presenting with a homogeneous clinical phenotype
Ebtesam M Abdalla, Marianne Rohrbach, Céline Bürer, et al.
Molecular Vision
|
April 9, 2026
Exploring the molecular basis of microphthalmia and anophthalmia: Insights from an Egyptian cohort
Gehad Elmakkawy, Amira Nabil, Karim Nabil, et al.
Clinical Dysmorphology
|
August 30, 2023
Clinical and molecular study of Egyptian patients with Treacher Collins syndrome
Nagham M Elbagoury, Amira Nabil, Asmaa F Abdel-Aleem, et al.
Journal of Assisted Reproduction and Genetics
|
January 26, 2024
A report of two homozygous TERB1 protein-truncating variants in two unrelated women with primary infertility
Zeynep Yalcin, Manqi Liang, Ibrahim M Abdelrazek, et al.
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Search research articles
Search
Showing results (1-10 of 17) with videos related to
Sort By:
Page
of 2
Genes
|
October 23, 2021
Two Decades after Mandibuloacral Dysplasia Discovery: Additional Cases and Comprehensive View of Disease Characteristics
Isabelle Jéru, Amira Nabil, Gehad El-Makkawy, et al.
Reproductive Sciences (Thousand Oaks, Calif.)
|
November 13, 2023
Conservative Hypomethylation of Mesenchymal Stem Cells and Their Secretome Restored the Follicular Development in Cisplatin-Induced Premature Ovarian Failure Mice
Amira Nabil Salama, Eman Abd El-Fatah Badr, Nanis Shawky Holah, et al.
European Journal of Medical Genetics
|
March 24, 2020
A familial PLCB4 mutation causing auriculocondylar syndrome 2 with variable severity
Amira Nabil, Sahar El Shafei, Nihal M El Shakankiri, et al.
Cureus
|
February 6, 2026
Diagnostic Challenges in Seronegative Celiac Disease: A Case of Massive Splenomegaly and Persistent Metabolic Imbalance
Mathab Adam, Ahmed H Ahmed, Aia A Ibrahim, et al.
Journal of Inherited Metabolic Disease
|
March 11, 2016
On the phenotypic spectrum of serine biosynthesis defects
Ayman W El-Hattab, Ranad Shaheen, Jozef Hertecant, et al.
Frontiers in Genetics
|
June 6, 2022
Genomics in Egypt: Current Status and Future Aspects
Eman Ahmed El-Attar, Rasha Mohamed Helmy Elkaffas, Sarah Ahmed Aglan, et al.
European Journal of Pediatrics
|
October 4, 2014
Kyphoscoliotic type of Ehlers-Danlos Syndrome (EDS VIA) in six Egyptian patients presenting with a homogeneous clinical phenotype
Ebtesam M Abdalla, Marianne Rohrbach, Céline Bürer, et al.
Molecular Vision
|
April 9, 2026
Exploring the molecular basis of microphthalmia and anophthalmia: Insights from an Egyptian cohort
Gehad Elmakkawy, Amira Nabil, Karim Nabil, et al.
Clinical Dysmorphology
|
August 30, 2023
Clinical and molecular study of Egyptian patients with Treacher Collins syndrome
Nagham M Elbagoury, Amira Nabil, Asmaa F Abdel-Aleem, et al.
Journal of Assisted Reproduction and Genetics
|
January 26, 2024
A report of two homozygous TERB1 protein-truncating variants in two unrelated women with primary infertility
Zeynep Yalcin, Manqi Liang, Ibrahim M Abdelrazek, et al.
Page
of 2