Abou Al-Shaar H - Search Results

1

Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families.

Bohlega SA, Al-Mubarak BR, Alyemni EA, Abouelhoda M, Monies D, Mustafa AE, Khalil DS, Al Haibi S, Abou Al-Shaar H, Faquih T, El-Kalioby M, Tahir AI, Al Tassan NA. Bohlega SA, et al. BMC Res Notes. 2016 Jun 7;9:295. doi: 10.1186/s13104-016-2102-7. BMC Res Notes. 2016. PMID: 27268037 Free PMC article.

2

Parkinson's Disease in Saudi Patients: A Genetic Study.

Al-Mubarak BR, Bohlega SA, Alkhairallah TS, Magrashi AI, AlTurki MI, Khalil DS, AlAbdulaziz BS, Abou Al-Shaar H, Mustafa AE, Alyemni EA, Alsaffar BA, Tahir AI, Al Tassan NA. Al-Mubarak BR, et al. PLoS One. 2015 Aug 14;10(8):e0135950. doi: 10.1371/journal.pone.0135950. eCollection 2015. PLoS One. 2015. PMID: 26274610 Free PMC article. Clinical Trial.

3

Levodopa-Carbidopa Intestinal Gel Infusion Therapy in Advanced Parkinson's Disease: Single Middle Eastern Center Experience.

Bohlega S, Abou Al-Shaar H, Alkhairallah T, Al-Ajlan F, Hasan N, Alkahtani K. Bohlega S, et al. Eur Neurol. 2015;74(5-6):227-36. doi: 10.1159/000442151. Epub 2015 Dec 1. Eur Neurol. 2015. PMID: 26618531

4

Phenotypic comparison of individuals with homozygous or heterozygous mutation of NOTCH3 in a large CADASIL family.

Abou Al-Shaar H, Qadi N, Al-Hamed MH, Meyer BF, Bohlega S. Abou Al-Shaar H, et al. J Neurol Sci. 2016 Aug 15;367:239-43. doi: 10.1016/j.jns.2016.05.061. Epub 2016 Jun 1. J Neurol Sci. 2016. PMID: 27423596

5

Ultrasound-guided botulinum toxin A injection in the treatment of belly dancer's dyskinesia.

Alshubaili A, Abou-Al-Shaar H, Santhamoorthy P, Attia H, Bohlega S. Alshubaili A, et al. BMC Neurol. 2016 Nov 17;16(1):226. doi: 10.1186/s12883-016-0746-5. BMC Neurol. 2016. PMID: 27855646 Free PMC article.

6

Identification of a novel genetic locus underlying tremor and dystonia.

Monies D, Abou Al-Shaar H, Goljan EA, Al-Younes B, Al-Breacan MMA, Al-Saif MM, Wakil SM, Meyer BF, Khabar KSA, Bohlega S. Monies D, et al. Hum Genomics. 2017 Nov 6;11(1):25. doi: 10.1186/s40246-017-0123-5. Hum Genomics. 2017. PMID: 29110692 Free PMC article.

7

LGMD1D myopathy with cytoplasmic and nuclear inclusions in a Saudi family due to DNAJB6 mutation.

Bohlega SA, Alfawaz S, Abou-Al-Shaar H, Al-Hindi HN, Murad HN, Bohlega MS, Meyer BF, Monies D. Bohlega SA, et al. Acta Myol. 2018 Sep 1;37(3):221-226. eCollection 2018 Sep. Acta Myol. 2018. PMID: 30838352 Free PMC article.

8

Autosomal recessive ADCY5-Related dystonia and myoclonus: Expanding the genetic spectrum of ADCY5-Related movement disorders.

Bohlega SA, Abou-Al-Shaar H, AlDakheel A, Alajlan H, Bohlega BS, Meyer BF, Monies D, Cupler EJ, Al-Saif AM. Bohlega SA, et al. Parkinsonism Relat Disord. 2019 Jul;64:145-149. doi: 10.1016/j.parkreldis.2019.02.039. Epub 2019 Feb 28. Parkinsonism Relat Disord. 2019. PMID: 30975617

9

A novel missense mutation in the TBX5 gene in a Saudi infant with Holt-Oram syndrome.

Al-Qattan MM, Abou Al-Shaar H. Al-Qattan MM, et al. Saudi Med J. 2015 Aug;36(8):980-2. doi: 10.15537/smj.2015.8.11891. Saudi Med J. 2015. PMID: 26219450 Free PMC article.

10

The role of RNA metabolism in neurological diseases.

Alaqeel AM, Abou Al-Shaar H, Shariff RK, Albakr A. Alaqeel AM, et al. Balkan J Med Genet. 2016 Jul 9;18(2):5-14. doi: 10.1515/bjmg-2015-0080. eCollection 2015 Dec 1. Balkan J Med Genet. 2016. PMID: 27785391 Free PMC article.

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

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

204 results

Search Page