Abdulhadi K - Search Results

1

Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients.

Vozzi D, Morgan A, Vuckovic D, D'Eustacchio A, Abdulhadi K, Rubinato E, Badii R, Gasparini P, Girotto G. Vozzi D, et al. Among authors: abdulhadi k. Gene. 2014 Jun 1;542(2):209-16. doi: 10.1016/j.gene.2014.03.033. Epub 2014 Mar 20. Gene. 2014. PMID: 24657061

2

Linkage study and exome sequencing identify a BDP1 mutation associated with hereditary hearing loss.

Girotto G, Abdulhadi K, Buniello A, Vozzi D, Licastro D, d'Eustacchio A, Vuckovic D, Alkowari MK, Steel KP, Badii R, Gasparini P. Girotto G, et al. Among authors: abdulhadi k. PLoS One. 2013 Dec 2;8(12):e80323. doi: 10.1371/journal.pone.0080323. eCollection 2013. PLoS One. 2013. PMID: 24312468 Free PMC article. Clinical Trial.

3

Consanguinity and hereditary hearing loss in Qatar.

Girotto G, Mezzavilla M, Abdulhadi K, Vuckovic D, Vozzi D, Khalifa Alkowari M, Gasparini P, Badii R. Girotto G, et al. Among authors: abdulhadi k. Hum Hered. 2014;77(1-4):175-82. doi: 10.1159/000360475. Epub 2014 Jul 29. Hum Hered. 2014. PMID: 25060281 Free article. Review.

4

Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families.

Alkowari MK, Vozzi D, Bhagat S, Krishnamoorthy N, Morgan A, Hayder Y, Logendra B, Najjar N, Gandin I, Gasparini P, Badii R, Girotto G, Abdulhadi K. Alkowari MK, et al. Among authors: abdulhadi k. Mutat Res. 2017 Aug;800-802:29-36. doi: 10.1016/j.mrfmmm.2017.05.001. Epub 2017 May 4. Mutat Res. 2017. PMID: 28501645

5

GJB2 and GJB6 genes and the A1555G mitochondrial mutation are only minor causes of nonsyndromic hearing loss in the Qatari population.

Khalifa Alkowari M, Girotto G, Abdulhadi K, Dipresa S, Siam R, Najjar N, Badii R, Gasparini P. Khalifa Alkowari M, et al. Among authors: abdulhadi k. Int J Audiol. 2012 Mar;51(3):181-5. doi: 10.3109/14992027.2011.625983. Epub 2011 Nov 21. Int J Audiol. 2012. PMID: 22103400

6

The p.Cys169Tyr variant of connexin 26 is not a polymorphism.

Zonta F, Girotto G, Buratto D, Crispino G, Morgan A, Abdulhadi K, Alkowari M, Badii R, Gasparini P, Mammano F. Zonta F, et al. Among authors: abdulhadi k. Hum Mol Genet. 2015 May 1;24(9):2641-8. doi: 10.1093/hmg/ddv026. Epub 2015 Jan 26. Hum Mol Genet. 2015. PMID: 25628337 Free PMC article.

7

Increased rate of deleterious variants in long runs of homozygosity of an inbred population from Qatar.

Mezzavilla M, Vozzi D, Badii R, Alkowari MK, Abdulhadi K, Girotto G, Gasparini P. Mezzavilla M, et al. Among authors: abdulhadi k. Hum Hered. 2015;79(1):14-9. doi: 10.1159/000371387. Hum Hered. 2015. PMID: 25720536

8

Interaction between diabetes mellitus and hypertension on risk of hearing loss in highly endogamous population.

Bener A, Al-Hamaq AOAA, Abdulhadi K, Salahaldin AH, Gansan L. Bener A, et al. Among authors: abdulhadi k. Diabetes Metab Syndr. 2017 Nov;11 Suppl 1:S45-S51. doi: 10.1016/j.dsx.2016.09.004. Epub 2016 Sep 5. Diabetes Metab Syndr. 2017. PMID: 27614865

9

Universal neonatal hearing screening: Six years of experience in Qatar.

Abdul Hadi K, Salahaldin A, Al Qahtani A, Al Musleh Z, Al Sulaitin M, Bener A, Chandra P, Alawi F. Abdul Hadi K, et al. Qatar Med J. 2013 Nov 1;2012(2):42-50. doi: 10.5339/qmj.2012.2.12. eCollection 2012. Qatar Med J. 2013. PMID: 25003040 Free PMC article. No abstract available.

10

Low-level laser therapy in patients with complaints of tinnitus: a clinical study.

Salahaldin AH, Abdulhadi K, Najjar N, Bener A. Salahaldin AH, et al. Among authors: abdulhadi k. ISRN Otolaryngol. 2012 Apr 9;2012:132060. doi: 10.5402/2012/132060. Print 2012. ISRN Otolaryngol. 2012. PMID: 23724264 Free PMC article.

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