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Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes.
Cortese A, Zhu Y, Rebelo AP, Negri S, Courel S, Abreu L, Bacon CJ, Bai Y, Bis-Brewer DM, Bugiardini E, Buglo E, Danzi MC, Feely SME, Athanasiou-Fragkouli A, Haridy NA; Inherited Neuropathy Consortium; Isasi R, Khan A, Laurà M, Magri S, Pipis M, Pisciotta C, Powell E, Rossor AM, Saveri P, Sowden JE, Tozza S, Vandrovcova J, Dallman J, Grignani E, Marchioni E, Scherer SS, Tang B, Lin Z, Al-Ajmi A, Schüle R, Synofzik M, Maisonobe T, Stojkovic T, Auer-Grumbach M, Abdelhamed MA, Hamed SA, Zhang R, Manganelli F, Santoro L, Taroni F, Pareyson D, Houlden H, Herrmann DN, Reilly MM, Shy ME, Zhai RG, Zuchner S. Cortese A, et al. Among authors: abdelhamed ma. Nat Genet. 2020 May;52(5):473-481. doi: 10.1038/s41588-020-0615-4. Epub 2020 May 4. Nat Genet. 2020. PMID: 32367058 Free PMC article.
Securing Internet-of-Medical-Things networks using cancellable ECG recognition.
El-Moneim Kabel SA, El-Banby GM, Abou Elazm LA, El-Shafai W, El-Bahnasawy NA, El-Samie FEA, Elazm AA, Siam AI, Abdelhamed MA. El-Moneim Kabel SA, et al. Among authors: abdelhamed ma. Sci Rep. 2024 May 13;14(1):10871. doi: 10.1038/s41598-024-54830-2. Sci Rep. 2024. PMID: 38740777 Free PMC article.
Construction and Standardization of Dementia Arabic Scale.
Farghaly WM, El Tallawy HN, Mohamed H, El Tallawy SH, Abdelhamed MA. Farghaly WM, et al. Among authors: abdelhamed ma. Neuropsychiatr Dis Treat. 2021 Mar 3;17:721-729. doi: 10.2147/NDT.S291392. eCollection 2021. Neuropsychiatr Dis Treat. 2021. PMID: 33716503 Free PMC article.
Efficient implementation of optical scanning holography in cancelable biometrics.
Abd El-Samie FE, Nassar RM, Safan M, Abdelhamed MA, Khalaf AAM, El Banby GM, Zahran O, El-Rabaie EM, Mohamed AA, El-Dokany IM, H Ahmed H, El-Khamy S, Ramadan N, Soliman RF, El-Shafai W. Abd El-Samie FE, et al. Among authors: abdelhamed ma. Appl Opt. 2021 May 1;60(13):3659-3667. doi: 10.1364/AO.415523. Appl Opt. 2021. PMID: 33983298
Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes.
Cortese A, Zhu Y, Rebelo AP, Negri S, Courel S, Abreu L, Bacon CJ, Bai Y, Bis-Brewer DM, Bugiardini E, Buglo E, Danzi MC, Feely SME, Athanasiou-Fragkouli A, Haridy NA; Inherited Neuropathy Consortium; Isasi R, Khan A, Laurà M, Magri S, Pipis M, Pisciotta C, Powell E, Rossor AM, Saveri P, Sowden JE, Tozza S, Vandrovcova J, Dallman J, Grignani E, Marchioni E, Scherer SS, Tang B, Lin Z, Al-Ajmi A, Schüle R, Synofzik M, Maisonobe T, Stojkovic T, Auer-Grumbach M, Abdelhamed MA, Hamed SA, Zhang R, Manganelli F, Santoro L, Taroni F, Pareyson D, Houlden H, Herrmann DN, Reilly MM, Shy ME, Zhai RG, Zuchner S. Cortese A, et al. Among authors: abdelhamed ma. Nat Genet. 2020 Jun;52(6):640. doi: 10.1038/s41588-020-0649-7. Nat Genet. 2020. PMID: 32457452
12 results