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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1996 1
1998 1
1999 3
2000 2
2001 4
2002 2
2003 1
2004 2
2005 2
2006 17
2007 3
2008 4
2010 4
2011 3
2012 3
2013 4
2014 4
2015 2
2016 2
2017 1
2019 2
2020 2
2021 1
2022 0
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66 results
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Page 1
Clinical characterization of the HOXA1 syndrome BSAS variant.
Bosley TM, Salih MA, Alorainy IA, Oystreck DT, Nester M, Abu-Amero KK, Tischfield MA, Engle EC. Bosley TM, et al. Among authors: alorainy ia. Neurology. 2007 Sep 18;69(12):1245-53. doi: 10.1212/01.wnl.0000276947.59704.cf. Neurology. 2007. PMID: 17875913 Free PMC article.
Genetic and phenotypic characterization of NKX6-2-related spastic ataxia and hypomyelination.
Chelban V, Alsagob M, Kloth K, Chirita-Emandi A, Vandrovcova J, Maroofian R, Davagnanam I, Bakhtiari S, AlSayed MD, Rahbeeni Z, AlZaidan H, Malintan NT, Johannsen J, Efthymiou S, Ghayoor Karimiani E, Mankad K, Al-Shahrani SA, Beiraghi Toosi M, AlShammari M, Groppa S, Haridy NA, AlQuait L, Qari A, Huma R, Salih MA, Almass R, Almutairi FB, Hamad MH, Alorainy IA, Ramzan K, Imtiaz F, Puiu M, Kruer MC, Bierhals T, Wood NW, Colak D, Houlden H, Kaya N. Chelban V, et al. Among authors: alorainy ia. Eur J Neurol. 2020 Feb;27(2):334-342. doi: 10.1111/ene.14082. Epub 2019 Oct 17. Eur J Neurol. 2020. PMID: 31509304 Free PMC article.
The clinical spectrum of homozygous HOXA1 mutations.
Bosley TM, Alorainy IA, Salih MA, Aldhalaan HM, Abu-Amero KK, Oystreck DT, Tischfield MA, Engle EC, Erickson RP. Bosley TM, et al. Among authors: alorainy ia. Am J Med Genet A. 2008 May 15;146A(10):1235-40. doi: 10.1002/ajmg.a.32262. Am J Med Genet A. 2008. PMID: 18412118 Free PMC article.
Exome Sequencing Reveals Novel TTN Variants in Saudi Patients with Congenital Titinopathies.
Salih MA, Hamad MH, Savarese M, Alorainy IA, Al-Jarallah AS, Alkhalidi H, AlQudairy H, Albader A, Alotaibi AJ, Alsagob M, Al-Bakheet A, Colak D, Udd B, Kaya N. Salih MA, et al. Among authors: alorainy ia. Genet Test Mol Biomarkers. 2021 Dec;25(12):757-764. doi: 10.1089/gtmb.2021.0085. Genet Test Mol Biomarkers. 2021. PMID: 34918981
Senile scleral plaques.
Alorainy IA. Alorainy IA. Clin Radiol. 2001 Feb;56(2):167. doi: 10.1053/crad.2000.0607. Clin Radiol. 2001. PMID: 11222082 No abstract available.
Biallelic mutations in human DCC cause developmental split-brain syndrome.
Jamuar SS, Schmitz-Abe K, D'Gama AM, Drottar M, Chan WM, Peeva M, Servattalab S, Lam AN, Delgado MR, Clegg NJ, Zayed ZA, Dogar MA, Alorainy IA, Jamea AA, Abu-Amero K, Griebel M, Ward W, Lein ES, Markianos K, Barkovich AJ, Robson CD, Grant PE, Bosley TM, Engle EC, Walsh CA, Yu TW. Jamuar SS, et al. Among authors: alorainy ia. Nat Genet. 2017 Apr;49(4):606-612. doi: 10.1038/ng.3804. Epub 2017 Feb 27. Nat Genet. 2017. PMID: 28250456 Free PMC article.
Senile scleral plaques: CT.
Alorainy I. Alorainy I. Neuroradiology. 2000 Feb;42(2):145-8. doi: 10.1007/s002340050035. Neuroradiology. 2000. PMID: 10663495
Pai syndrome: a report of a case and review of the literature.
Al-Mazrou KA, Al-Rekabi A, Alorainy IA, Al-Kharfi T, Al-Serhani AM. Al-Mazrou KA, et al. Among authors: alorainy ia. Int J Pediatr Otorhinolaryngol. 2001 Nov 1;61(2):149-53. doi: 10.1016/s0165-5876(01)00555-9. Int J Pediatr Otorhinolaryngol. 2001. PMID: 11589982 Review.
66 results