Abu-Amero K - Search Results

1

Pregnancy after preimplantation genetic diagnosis for brachydactyly type B.

Hellani A, Abu-Amero K, Azouri J, Al-Sharif H, Barblet H, El-Akoum S. Hellani A, et al. Reprod Biomed Online. 2009 Jan;18(1):127-31. doi: 10.1016/s1472-6483(10)60434-8. Reprod Biomed Online. 2009. PMID: 19146779

2

Successful pregnancies after application of array-comparative genomic hybridization in PGS-aneuploidy screening.

Hellani A, Abu-Amero K, Azouri J, El-Akoum S. Hellani A, et al. Reprod Biomed Online. 2008 Dec;17(6):841-7. doi: 10.1016/s1472-6483(10)60413-0. Reprod Biomed Online. 2008. PMID: 19079969

3

G6PD Mediterranean S188F codon mutation is common among Saudi sickle cell patients and increases the risk of stroke.

Hellani A, Al-Akoum S, Abu-Amero KK. Hellani A, et al. Genet Test Mol Biomarkers. 2009 Aug;13(4):449-52. doi: 10.1089/gtmb.2009.0011. Genet Test Mol Biomarkers. 2009. PMID: 19594365

4

Successful pregnancies after combined human leukocyte antigen direct genotyping and preimplantation genetic diagnosis utilizing multiple displacement amplification.

Hellani AM, Akoum SM, Fadel ES, Yousef HM, Abu-Amero KK. Hellani AM, et al. Saudi Med J. 2012 Oct;33(10):1059-64. Saudi Med J. 2012. PMID: 23047205

5

Absence of mtDNA mutations in leukocytes of CADASIL patients.

Abu-Amero KK, Hellani A, Bohlega S. Abu-Amero KK, et al. BMC Res Notes. 2008 May 30;1:16. doi: 10.1186/1756-0500-1-16. BMC Res Notes. 2008. PMID: 18710532 Free PMC article.

6

Molecular spectrum of alpha-thalassemia mutations in microcytic hypochromic anemia patients from Saudi Arabia.

Hellani A, Fadel E, El-Sadadi S, El-Sweilam H, El-Dawood A, Abu-Amero KK. Hellani A, et al. Genet Test Mol Biomarkers. 2009 Apr;13(2):219-21. doi: 10.1089/gtmb.2008.0123. Genet Test Mol Biomarkers. 2009. PMID: 19371220

7

A t(5;16)(p15.32;q23.3) generating 16q23.3 --> qter duplication and 5p15.32 --> pter deletion in two siblings with mental retardation, dysmorphic features, and speech delay.

Hellani A, Mohamed S, Al-Akoum S, Bosley TM, Abu-Amero KK. Hellani A, et al. Am J Med Genet A. 2010 Jun;152A(6):1555-60. doi: 10.1002/ajmg.a.33400. Am J Med Genet A. 2010. PMID: 20503335

8

Isolated foveal hypoplasia: report of a new case and detailed genetic investigation.

Al-Saleh AA, Hellani A, Abu-Amero KK. Al-Saleh AA, et al. Int Ophthalmol. 2011 Apr;31(2):117-20. doi: 10.1007/s10792-011-9424-1. Epub 2011 Jan 25. Int Ophthalmol. 2011. PMID: 21264491

9

Preimplantation genetic diagnosis in isolated sulfite oxidase deficiency.

Salih MA, Bosley TM, Alorainy IA, Sabry MA, Rashed MS, Al-Yamani EA, El-Akoum S, Mohamed SH, Abu-Amero KK, Hellani AM. Salih MA, et al. Can J Neurol Sci. 2013 Jan;40(1):109-12. doi: 10.1017/s0317167100013081. Can J Neurol Sci. 2013. PMID: 23250141 No abstract available.

10

Five new consanguineous families with horizontal gaze palsy and progressive scoliosis and novel ROBO3 mutations.

Abu-Amero KK, al Dhalaan H, al Zayed Z, Hellani A, Bosley TM. Abu-Amero KK, et al. J Neurol Sci. 2009 Jan 15;276(1-2):22-6. doi: 10.1016/j.jns.2008.08.026. Epub 2008 Oct 1. J Neurol Sci. 2009. PMID: 18829051

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