Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
4 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Publication Date timeline is not available.
Page 1
Phenotypic and molecular insights into PQBP1-related intellectual disability.
Am J Med Genet A. 2018 Nov;176(11):2446-2450. doi: 10.1002/ajmg.a.40479. Epub 2018 Sep 23.
Am J Med Genet A. 2018.
PMID: 30244542
Magnetic resonance imaging of developmental facial paresis: a spectrum of complex anomalies.
Mohammad SA, Abdelaziz TT, Gadelhak MI, Afifi HH, Abdel-Salam GMH.
Mohammad SA, et al. Among authors: gadelhak mi.
Neuroradiology. 2018 Oct;60(10):1053-1061. doi: 10.1007/s00234-018-2063-8. Epub 2018 Aug 3.
Neuroradiology. 2018.
PMID: 30074067
Item in Clipboard
Further Evidence of a Continuum in the Clinical Spectrum of Dominant PIEZO2-Related Disorders and Implications in Cerebellar Anomalies.
Abdel-Salam GMH, Afifi HH, Saleem SN, Gadelhak MI, El-Serafy MA, Sayed ISM, Abdel-Hamid MS.
Abdel-Salam GMH, et al. Among authors: gadelhak mi.
Mol Syndromol. 2022 Dec;13(5):389-396. doi: 10.1159/000523956. Epub 2022 Apr 27.
Mol Syndromol. 2022.
PMID: 36588752
Free PMC article.
Item in Clipboard
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: gadelhak mi.
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.
Item in Clipboard
Cite
Cite
ARTICLE TYPE
ARTICLE LANGUAGE
AGE
Filters on the sidebar will be reset to the default list and any currently applied filters will be cleared.