Al-Khalidi H - Search Results

1

EGFRvIII expression and isocitrate dehydrogenase mutations in patients with glioma.

Taher MM, Dairi G, Butt EM, Al-Quthami K, Al-Khalidi H, Jastania RA, Nageeti TH, Bogari NM, Athar M, Al-Allaf FA, Valerie K. Taher MM, et al. Oncol Lett. 2020 Dec;20(6):384. doi: 10.3892/ol.2020.12247. Epub 2020 Oct 23. Oncol Lett. 2020. PMID: 33193845 Free PMC article.

2

Next generation DNA sequencing of atypical choroid plexus papilloma of brain: Identification of novel mutations in a female patient by Ion Proton.

Taher MM, Hassan AA, Saeed M, Jastania RA, Nageeti TH, Alkhalidi H, Dairi G, Abduljaleel Z, Athar M, Bouazzaoui A, El-Bjeirami WM, Al-Allaf FA. Taher MM, et al. Oncol Lett. 2019 Nov;18(5):5063-5076. doi: 10.3892/ol.2019.10882. Epub 2019 Sep 19. Oncol Lett. 2019. PMID: 31612017 Free PMC article.

3

Adamantinomatous Craniopharyngioma in an Adult: A Case Report with NGS Analysis.

Jastania RA, Saeed M, Al-Khalidi H, AlQuthami K, Nageeti TH, Al-Allaf FA, Valerie K, Taher MM. Jastania RA, et al. Int Med Case Rep J. 2020 Apr 21;13:123-137. doi: 10.2147/IMCRJ.S243405. eCollection 2020. Int Med Case Rep J. 2020. PMID: 32368160 Free PMC article.

4

Status of mismatch repair genes hMSH2 and hMSH6 in colorectal cancer in Saudi patients: an immunohistochemical analysis.

Alkhalidi H, Kfoury H. Alkhalidi H, et al. East Mediterr Health J. 2012 Nov;18(11):1114-7. doi: 10.26719/2012.18.11.1114. East Mediterr Health J. 2012. PMID: 23301373 Free article.

5

A novel syndrome of hypohidrosis and intellectual disability is linked to COG6 deficiency.

Shaheen R, Ansari S, Alshammari MJ, Alkhalidi H, Alrukban H, Eyaid W, Alkuraya FS. Shaheen R, et al. J Med Genet. 2013 Jul;50(7):431-6. doi: 10.1136/jmedgenet-2013-101527. Epub 2013 Apr 20. J Med Genet. 2013. PMID: 23606727

6

New findings in a global approach to dissect the whole phenotype of PLA2G6 gene mutations.

Salih MA, Mundwiller E, Khan AO, AlDrees A, Elmalik SA, Hassan HH, Al-Owain M, Alkhalidi HM, Katona I, Kabiraj MM, Chrast R, Kentab AY, Alzaidan H, Rodenburg RJ, Bosley TM, Weis J, Koenig M, Stevanin G, Azzedine H. Salih MA, et al. PLoS One. 2013 Oct 9;8(10):e76831. doi: 10.1371/journal.pone.0076831. eCollection 2013. PLoS One. 2013. PMID: 24130795 Free PMC article.

7

Autozygosity reveals recessive mutations and novel mechanisms in dominant genes: implications in variant interpretation.

Monies D, Maddirevula S, Kurdi W, Alanazy MH, Alkhalidi H, Al-Owain M, Sulaiman RA, Faqeih E, Goljan E, Ibrahim N, Abdulwahab F, Hashem M, Abouelhoda M, Shaheen R, Arold ST, Alkuraya FS. Monies D, et al. Genet Med. 2017 Oct;19(10):1144-1150. doi: 10.1038/gim.2017.22. Epub 2017 Apr 6. Genet Med. 2017. PMID: 28383543 Free article.

8

Efficient identification of novel mutations in patients with limb girdle muscular dystrophy.

Boyden SE, Salih MA, Duncan AR, White AJ, Estrella EA, Burgess SL, Seidahmed MZ, Al-Jarallah AS, Alkhalidi HM, Al-Maneea WM, Bennett RR, Alshemmari SH, Kunkel LM, Kang PB. Boyden SE, et al. Neurogenetics. 2010 Oct;11(4):449-55. doi: 10.1007/s10048-010-0250-9. Epub 2010 Jul 13. Neurogenetics. 2010. PMID: 20623375 Free PMC article.

9

Prevalence of biopsy-proven nonalcoholic fatty liver among patients with gallstone disease.

Alsaif FA, Alqahtani SH, Alsadoon AM, Alswat KA, Abdo AA, Hassanain MM, Alsharabi AB, Aljuhani GR, Alkhalidi HM, Elsharkawy MS, Alotaibi MA, Sanai FM, Al-Hamoudi WK. Alsaif FA, et al. Saudi J Gastroenterol. 2020 Apr 14;26(4):204-9. doi: 10.4103/sjg.SJG_29_20. Online ahead of print. Saudi J Gastroenterol. 2020. PMID: 32341228 Free PMC article.

10

Neuronal Differentiation in a Pituitary Macroadenoma with Focal Small Blue Round Cell Morphology: Report of a Rare Pattern.

Alkhalidi H. Alkhalidi H. Case Rep Pathol. 2020 Apr 29;2020:6450930. doi: 10.1155/2020/6450930. eCollection 2020. Case Rep Pathol. 2020. PMID: 32455041 Free PMC article.

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