Nihal Almenabawy
5PUBLICATIONS
21CO-AUTHORS
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Publications (5)
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|Feb 13, 2026
Clinical and genetic spectrum of L-dopa responsive dystonia: insights from seven Egyptian cases.Nihal Almenabawy, Fawzia Amer, Laila Selim
|Oct 14, 2024
Clinical and Genetic Spectrum of Patients With Mitochondrial Disease in a Pediatric Egyptian Cohort: Novel Variants and Phenotypic Expansion.Hebatallah M Hassaan, Angela Pyle, Nihal Almenabawy
|Aug 19, 2023
Clinical, biochemical, and molecular characterization of mucopolysaccharidosis type III in 34 Egyptian patients.Nihal Almenabawy, Manal Ramadan, Mona Kamel
|Oct 20, 2020
Author Correction: Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology.Sahar Elouej, Karim Harhouri, Morgane Le Mao
|Sep 12, 2020
Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology.Sahar Elouej, Karim Harhouri, Morgane Le Mao
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Frequent Collaborators
3 joint publications
Laila Selim
3 joint publications
Fawzia Amer
2 joint publications
Karim Harhouri
2 joint publications
Hϋlya Kayserili
2 joint publications
Davor Lessel
2 joint publications
Jean-François Deleuze
2 joint publications
Agnes Rötig
2 joint publications
Nathalie Escande-Beillard
2 joint publications
Song-Hua Lee
2 joint publications
Philippe Manivet
