Clinical and molecular spectrum of a large Egyptian cohort with ALS2‐related disorders of infantile‐onset of clinical continuum IAHSP/JPLS
Zaki, Maha S., Sharaf‐Eldin, Wessam E., Rafat, Karima, Elbendary, Hasnaa M., Kamel, Mona, Elkhateeb, Nour, Noureldeen, Mahmoud M., Abdeltawab, Mohamed A., Sadek, Abdelrahim A., Essawi, Mona L., Lau, Tracy, Murphy, David, Abdel‐Hamid, Mohamed S., Holuden, Henry, Issa, Mahmoud Y., Gleeson, Joseph G.
Published in Clinical genetics (01.08.2023)
Published in Clinical genetics (01.08.2023)
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Journal Article
MLPA analysis for molecular diagnosis of spinal muscular atrophy and correlation of 5q13.2 genes with disease phenotype in Egyptian patients
Hassan, Heba A., Fahmy, Nagia A., El-Bagoury, Nagham M., Eissa, Noura R., Sharaf-Eldin, Wessam E., Issa, Mahmoud Y., Zaki, Maha S., Essawi, Mona L.
Published in Egyptian Journal of Medical Human Genetics (01.12.2022)
Published in Egyptian Journal of Medical Human Genetics (01.12.2022)
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Journal Article
Is trofinetide a future treatment for Rett syndrome? A comprehensive systematic review and meta-analysis of randomized controlled trials
Mohammed, Hazem E, Bady, Zeyad, Haseeb, Mohamed E, Aboeldahab, Heba, Sharaf-Eldin, Wessam E, Zaki, Maha S
Published in BMC medicine (18.07.2024)
Published in BMC medicine (18.07.2024)
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Journal Article
Extracellular miR-145, miR-223 and miR-326 expression signature allow for differential diagnosis of immune-mediated neuroinflammatory diseases
Sharaf-Eldin, Wessam E., Kishk, Nirmeen A., Gad, Yehia Z., Hassan, Heba, Ali, Mohamed A.M., Zaki, Maha S., Mohamed, Mohamed R., Essawi, Mona L.
Published in Journal of the neurological sciences (15.12.2017)
Published in Journal of the neurological sciences (15.12.2017)
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Journal Article
The Modulatory Effects of Mesenchymal Stem Cells on Osteoclastogenesis
El-Badri, Nagwa, Mahmoud, Marwa, Abu-Shahba, Nourhan, Sharaf-Eldin, Wessam E.
Published in Stem Cells International (01.01.2016)
Published in Stem Cells International (01.01.2016)
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Journal Article
Clinical and Molecular Profiles of a Cohort of Egyptian Patients with Collagen VI-Related Dystrophy
Sharaf-Eldin, Wessam E., Rafat, Karima, Issa, Mahmoud Y., Elbendary, Hasnaa M., Eissa, Noura R., Hawaary, Bahaa, Gaboon, Nagwa E. A., Maroofian, Reza, Gleeson, Joseph G., Essawi, Mona L., Zaki, Maha S.
Published in Journal of molecular neuroscience (05.10.2024)
Published in Journal of molecular neuroscience (05.10.2024)
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Journal Article
Expanding the phenotypic spectrum in ESRRB related sensorineural hearing loss: Evidence provided via detecting novel nonsense mutation in an Egyptian family
Elbagoury, Nagham M., Ashaat, Engy A., Sharaf-Eldin, Wessam E., Hassib, Nehal, Ashaat, Neveen A., Youssef, Ragaey, El Ruby, Mona O., Esswai, Mona L.
Published in Human gene (Amsterdam, Netherlands) (01.12.2022)
Published in Human gene (Amsterdam, Netherlands) (01.12.2022)
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Journal Article
Case report: Homozygous PRRT2 mutation in ICCA Egyptian family with reduced penetrance
Kishk, Nirmeen A., Sharaf-Eldin, Wessam E., Saher, Heba, Essawi, Mona
Published in Meta Gene (01.02.2017)
Published in Meta Gene (01.02.2017)
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Journal Article