Taher MB - Search Results

1

Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families.

El-Kamah GY, Mehrez MI, Taher MB, El-Bassyouni HT, Gaber KR, Amr KS. El-Kamah GY, et al. Among authors: taher mb. Genes (Basel). 2023 Apr 12;14(4):900. doi: 10.3390/genes14040900. Genes (Basel). 2023. PMID: 37107657 Free PMC article.

2

Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation.

Abdel-Salam GMH, Abdel-Hamid MS, Mehrez MI, Kamal AM, Taher MB, Afifi HH. Abdel-Salam GMH, et al. Among authors: taher mb. Ophthalmic Genet. 2018 Apr;39(2):215-220. doi: 10.1080/13816810.2017.1401089. Epub 2017 Nov 15. Ophthalmic Genet. 2018. PMID: 29140751

3

Genetic Implications in High-Risk Pregnancy and Its Outcome: A 2-Year Study.

Afifi HH, Gaber KR, Thomas MM, Taher MB, Tosson AMS. Afifi HH, et al. Among authors: taher mb. Am J Perinatol. 2022 Nov;39(15):1659-1667. doi: 10.1055/s-0041-1724002. Epub 2021 Feb 26. Am J Perinatol. 2022. PMID: 33636738

4

Defining the molecular pathology and consequent phenotypes in Egyptian HB patients.

El-Kamah GY, Mosaad RM, Taher MB, Amr KS. El-Kamah GY, et al. Among authors: taher mb. J Genet Eng Biotechnol. 2021 May 17;19(1):75. doi: 10.1186/s43141-021-00165-8. J Genet Eng Biotechnol. 2021. PMID: 33999344 Free PMC article.

5

Expanding the phenotypic spectrum and clinical severity associated with WLS gene.

Abdel-Salam GMH, Afifi HH, Abdel-Hamid MS, Ahmed NEB, Taher MB, El-Kamah G, Thiele H, Nürnberg PN, Bolz HJ. Abdel-Salam GMH, et al. Among authors: taher mb. J Hum Genet. 2023 Sep;68(9):607-613. doi: 10.1038/s10038-023-01152-2. Epub 2023 Apr 28. J Hum Genet. 2023. PMID: 37106064

6

Studying the pathogenicity of 26 variants characterized in the first molecular analyses of Egyptian aplastic anemia patients.

Sokkar MF, Hamdy M, Erian PS, Mosaad RM, Elaraby NM, Taher MB, El-Sayed H, Al Komy M, Eid MM, Mohamed AM, Amr KS, El-Kamah GY. Sokkar MF, et al. Among authors: taher mb. J Genet Eng Biotechnol. 2023 Nov 29;21(1):149. doi: 10.1186/s43141-023-00585-8. J Genet Eng Biotechnol. 2023. PMID: 38017244 Free PMC article.

7

Corrigendum to "Defining the molecular pathology and consequent phenotypes in Egyptian HB patients" [J. Genet. Eng. Biotechnol. 19(1) (2021) 75].

El-Kamah GY, Mosaad RM, Taher MB, Amr KS. El-Kamah GY, et al. Among authors: taher mb. J Genet Eng Biotechnol. 2024 Jun;22(2):100374. doi: 10.1016/j.jgeb.2024.100374. Epub 2024 Apr 2. J Genet Eng Biotechnol. 2024. PMID: 38797548 Free PMC article. No abstract available.

8

Genetic Correlation of HBB, HFE and HAMP Genes to Endocrinal Complications in Egyptian Beta Thalassemia Major Patients.

Sokkar MF, Hamdy M, Taher MB, El-Sayed H, Bayomi EA, Amr KS, El-Kamah GY. Sokkar MF, et al. Among authors: taher mb. Biochem Genet. 2024 Jul 2. doi: 10.1007/s10528-024-10868-5. Online ahead of print. Biochem Genet. 2024. PMID: 38954212

9

Molecular and Clinical Characterization of a Cohort of Autosomal Recessive Sensorineural Hearing Loss in Egyptian Patients.

Sayed-Ahmed MM, El-Bassyouni HT, Afifi HH, Essawi ML, Taher MB, Gadelhak MI, Zaytoun RA, Abdelmonem AA, Elbagoury NM. Sayed-Ahmed MM, et al. Among authors: taher mb. J Mol Neurosci. 2024 Oct 28;74(4):102. doi: 10.1007/s12031-024-02279-3. J Mol Neurosci. 2024. PMID: 39467922 Free PMC article.

10

Evaluation of Sleep Difficulties in Egyptian Children with Down Syndrome: A Case-Control Study.

Sayed-Ahmed MM, Taher MB, Zaytoun RAH, Abdel Hady AF. Sayed-Ahmed MM, et al. Among authors: taher mb. Indian J Otolaryngol Head Neck Surg. 2024 Feb;76(1):97-102. doi: 10.1007/s12070-023-04090-9. Epub 2023 Aug 9. Indian J Otolaryngol Head Neck Surg. 2024. PMID: 38440482

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