Ahmed MKH - Search Results

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Correction to: Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene.

Elaraby NM, Ahmed HA, Ashaat NA, Tawfik S, Ahmed MKH, Hassib NF, Ashaat EA. Elaraby NM, et al. Among authors: ahmed mkh. J Mol Neurosci. 2024 Jun 1;74(2):58. doi: 10.1007/s12031-024-02233-3. J Mol Neurosci. 2024. PMID: 38822216 Free PMC article. No abstract available.

Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene and Review of Literature.

Elaraby NM, Ahmed HA, Ashaat NA, Tawfik S, Ahmed MKH, Hassib NF, Ashaat EA. Elaraby NM, et al. Among authors: ahmed mkh. J Mol Neurosci. 2022 Nov;72(11):2242-2251. doi: 10.1007/s12031-022-02074-y. Epub 2022 Oct 17. J Mol Neurosci. 2022. PMID: 36251212 Free PMC article. Review.

Profound microcephaly, primordial dwarfism with developmental brain malformations: a new syndrome.

Abdel-Salam GM, Abdel-Hamid MS, Saleem SN, Ahmed MK, Issa M, Effat LK, Kayed HF, Zaki MS, Gaber KR. Abdel-Salam GM, et al. Am J Med Genet A. 2012 Aug;158A(8):1823-31. doi: 10.1002/ajmg.a.35480. Epub 2012 Jul 11. Am J Med Genet A. 2012. PMID: 22786707

Use of Telemedicine for Postdischarge Assessment of the Surgical Wound: International Cohort Study, and Systematic Review With Meta-analysis.

NIHR Global Health Research Unit on Global Surgery, GlobalSurg Collaborative. NIHR Global Health Research Unit on Global Surgery, GlobalSurg Collaborative. Ann Surg. 2023 Jun 1;277(6):e1331-e1347. doi: 10.1097/SLA.0000000000005506. Epub 2022 Jun 27. Ann Surg. 2023. PMID: 36626409 Free PMC article.

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