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Elbendary, Hasnaa
48
results:
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Format
Online (48)
Mediatypes
Articles (Online) (21)
OpenAccess-fulltext (27)
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1
THE LEUKODYSTROPHY SPECTRUM IN PEDIATRIC EGYPTIANS POPULATI..:
Elbendary, Hasnaa
IBRO Neuroscience Reports. 15 (2023) - p. S922 , 2023
Link:
https://doi.org/10.1016/..
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2
In-depth characterization of neuroradiological findings in ..:
Ambrosino, Sara
;
Elbendary, Hasnaa
;
Lequin, Maarten
...
NeuroImage: Clinical. 35 (2022) - p. 103118 , 2022
Link:
https://doi.org/10.1016/..
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3
The clinical and genetic landscape of developmental and epi..:
Elkhateeb, Nour
;
Issa, Mahmoud Y.
;
Elbendary, Hasnaa M.
...
Clinical Genetics. 105 (2024) 5 - p. 510-522 , 2024
Link:
https://doi.org/10.1111/..
?
4
The clinical and genetic spectrum of inherited glycosylphos..:
Sidpra, Jai
;
Sudhakar, Sniya
;
Biswas, Asthik
...
Brain. 147 (2024) 8 - p. 2775-2790 , 2024
Link:
https://doi.org/10.1093/..
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5
Spondyloenchondrodysplasia in five new patients: identifica..:
Elhossini, Rasha M.
;
Elbendary, Hasnaa M.
;
Rafat, Karima
..
Molecular Genetics and Genomics. 298 (2023) 3 - p. 709-720 , 2023
Link:
https://doi.org/10.1007/..
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6
Clinical and molecular spectrum of a large Egyptian cohort ..:
Zaki, Maha S.
;
Sharaf‐Eldin, Wessam E.
;
Rafat, Karima
...
Clinical Genetics. 104 (2023) 2 - p. 238-244 , 2023
Link:
https://doi.org/10.1111/..
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7
Brain monoamine vesicular transport disease caused by homoz..:
Saida, Ken
;
Maroofian, Reza
;
Sengoku, Toru
...
Genetics in Medicine. 25 (2023) 1 - p. 90-102 , 2023
Link:
https://doi.org/10.1016/..
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8
Biallelic missense variants in COG3 cause a congenital diso..:
Duan, Ruizhi
;
Marafi, Dana
;
Xia, Zhi‐Jie
...
Journal of Inherited Metabolic Disease. 46 (2023) 6 - p. 1195-1205 , 2023
Link:
https://doi.org/10.1002/..
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9
Erratum to ' Taking action on climate change: Testimonials ..:
Aledo-Serrano, Angel
;
Battaglia, Giulia
;
Blenkinsop, Stephen
...
Seizure: European Journal of Epilepsy. 111 (2023) - p. 164 , 2023
Link:
https://doi.org/10.1016/..
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10
Novel LSS variants in alopecia and intellectual disability ..:
Elbendary, Hasnaa M.
;
Marafi, Dana
;
Saad, Ahmed K.
...
Clinical Genetics. 104 (2023) 3 - p. 344-349 , 2023
Link:
https://doi.org/10.1111/..
?
11
Taking action on climate change: Testimonials and position ..:
Aledo-Serrano, Angel
;
Battaglia, Giulia
;
Blenkinsop, Stephen
...
Seizure: European Journal of Epilepsy. 106 (2023) - p. 68-75 , 2023
Link:
https://doi.org/10.1016/..
?
12
First LIPA Mutational Analysis in Egyptian Patients Reveals..:
Elaraby, Nesma M.
;
Galal, Eman Reda
;
Abdel-Hamid, Mohamed
...
Journal of Molecular Neuroscience. 73 (2023) 7-8 - p. 598-607 , 2023
Link:
https://doi.org/10.1007/..
?
13
El‐Hattab‐Alkuraya syndrome caused by biallelic WDR45B path..:
Almannai, Mohammed
;
Marafi, Dana
;
Abdel‐Salam, Ghada M. H.
...
Clinical Genetics. 101 (2022) 5-6 - p. 530-540 , 2022
Link:
https://doi.org/10.1111/..
?
14
Mutation spectrum in the gene encoding methyl-CpG-binding p..:
Sharaf-Eldin, Wessam E.
;
Soliman, Hala N.
;
Abdel-Aziz, Nahla N.
...
Meta Gene. 24 (2020) - p. 100620 , 2020
Link:
https://doi.org/10.1016/..
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15
A founder mutation in PEX12 among Egyptian patients in pero..:
Zaki, Maha S.
;
Issa, Mahmoud Y.
;
Thomas, Manal M.
...
Neurological Sciences. 42 (2020) 7 - p. 2737-2745 , 2020
Link:
https://doi.org/10.1007/..
1-15