Hakami F - Search Results

1

The role of HOX genes in head and neck squamous cell carcinoma.

Platais C, Hakami F, Darda L, Lambert DW, Morgan R, Hunter KD. Platais C, et al. Among authors: hakami f. J Oral Pathol Med. 2016 Apr;45(4):239-47. doi: 10.1111/jop.12388. Epub 2015 Dec 14. J Oral Pathol Med. 2016. PMID: 26661059 Review.

2

The role of HOXB9 and miR-196a in head and neck squamous cell carcinoma.

Darda L, Hakami F, Morgan R, Murdoch C, Lambert DW, Hunter KD. Darda L, et al. Among authors: hakami f. PLoS One. 2015 Apr 10;10(4):e0122285. doi: 10.1371/journal.pone.0122285. eCollection 2015. PLoS One. 2015. PMID: 25860510 Free PMC article.

3

The roles of HOXD10 in the development and progression of head and neck squamous cell carcinoma (HNSCC).

Hakami F, Darda L, Stafford P, Woll P, Lambert DW, Hunter KD. Hakami F, et al. Br J Cancer. 2014 Aug 12;111(4):807-16. doi: 10.1038/bjc.2014.372. Epub 2014 Jul 10. Br J Cancer. 2014. PMID: 25010866 Free PMC article.

4

Retrospective study of prenatal ultrasound findings in newborns with a Noonan spectrum disorder.

Hakami F, Dillon MW, Lebo M, Mason-Suares H. Hakami F, et al. Prenat Diagn. 2016 May;36(5):418-23. doi: 10.1002/pd.4797. Epub 2016 Mar 28. Prenat Diagn. 2016. PMID: 26918529

5

Majewski dwarfism type II: an atypical neuroradiological presentation with a novel variant in the PCNT gene.

Alrajhi H, Alallah J, Shawli A, Alghamdi K, Hakami F. Alrajhi H, et al. Among authors: hakami f. BMJ Case Rep. 2019 May 30;12(5):e224197. doi: 10.1136/bcr-2018-224197. BMJ Case Rep. 2019. PMID: 31151966 Free PMC article.

6

Bi-allelic pathogenic variants in NDUFC2 cause early-onset Leigh syndrome and stalled biogenesis of complex I.

Alahmad A, Nasca A, Heidler J, Thompson K, Oláhová M, Legati A, Lamantea E, Meisterknecht J, Spagnolo M, He L, Alameer S, Hakami F, Almehdar A, Ardissone A, Alston CL, McFarland R, Wittig I, Ghezzi D, Taylor RW. Alahmad A, et al. Among authors: hakami f. EMBO Mol Med. 2020 Nov 6;12(11):e12619. doi: 10.15252/emmm.202012619. Epub 2020 Sep 24. EMBO Mol Med. 2020. PMID: 32969598 Free PMC article.

7

A case of atypical systemic primary carnitine deficiency in Saudi Arabia.

Alghamdi A, Almalki H, Shawli A, Waggass R, Hakami F. Alghamdi A, et al. Among authors: hakami f. Pediatr Rep. 2018 Jun 27;10(2):7705. doi: 10.4081/pr.2018.7705. eCollection 2018 May 24. Pediatr Rep. 2018. PMID: 30069296 Free PMC article.

8

Prenatal exome sequencing and chromosomal microarray analysis in fetal structural anomalies in a highly consanguineous population reveals a propensity of ciliopathy genes causing multisystem phenotypes.

Al-Hamed MH, Kurdi W, Khan R, Tulbah M, AlNemer M, AlSahan N, AlMugbel M, Rafiullah R, Assoum M, Monies D, Shah Z, Rahbeeni Z, Derar N, Hakami F, Almutairi G, AlOtaibi A, Ali W, AlShammasi A, AlMubarak W, AlDawoud S, AlAmri S, Saeed B, Bukhari H, Ali M, Akili R, Alquayt L, Hagos S, Elbardisy H, Akilan A, Almuhana N, AlKhalifah A, Abouelhoda M, Ramzan K, Sayer JA, Imtiaz F. Al-Hamed MH, et al. Among authors: hakami f. Hum Genet. 2022 Jan;141(1):101-126. doi: 10.1007/s00439-021-02406-9. Epub 2021 Dec 1. Hum Genet. 2022. PMID: 34853893

9

A Novel Variant in the AGPS Gene Causes the Rare Rhizomelic Chondrodysplasia Punctata Type 3: A Case Report.

Shawli AM, Nazer AT, Khayyat Y, Alqurashi MG, Hakami F. Shawli AM, et al. Among authors: hakami f. Cureus. 2021 Dec 20;13(12):e20543. doi: 10.7759/cureus.20543. eCollection 2021 Dec. Cureus. 2021. PMID: 35070570 Free PMC article.

10

A Novel Variant of Adenosine Deaminase 2 Deficiency Presented With Chronic Thrombocytopenia, Anemia, and Early-Onset Stroke.

Al-Hebshi A, Aljohani M, AlShenaifi N, Aloqbi M, Turkistani W, Hakami F. Al-Hebshi A, et al. Among authors: hakami f. Cureus. 2021 May 28;13(5):e15288. doi: 10.7759/cureus.15288. Cureus. 2021. PMID: 34221752 Free PMC article.

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