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

Year Number of Results
1998 1
1999 3
2000 1
2001 4
2002 1
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 1
2021 1
2022 1
2024 0

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63 results

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Page 1
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.
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.
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.
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.
Cree leukoencephalopathy: neuroimaging findings.
Alorainy IA, Patenaude YG, O'Gorman AM, Black DN, Meagher-Villemure K. Alorainy IA, et al. Radiology. 1999 Nov;213(2):400-6. doi: 10.1148/radiology.213.2.r99oc28400. Radiology. 1999. PMID: 10551219
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.
Genomic, Proteomic, and Phenotypic Spectrum of Novel O-Sialoglycoprotein Endopeptidase Variant in Four Affected Individuals With Galloway-Mowat Syndrome.
Ali Alghamdi M, Benabdelkamel H, Masood A, Saheb Sharif-Askari N, Hachim MY, Alsheikh H, Hamad MH, Salih MA, Bashiri FA, Alhasan K, Kashour T, Guatibonza Moreno P, Schröder S, Karageorgou V, Bertoli-Avella AM, Alkhalidi H, Jamjoom DZ, Alorainy IA, Alfadda AA, Halwani R. Ali Alghamdi M, et al. Among authors: alorainy ia. Front Genet. 2022 Jun 23;13:806190. doi: 10.3389/fgene.2022.806190. eCollection 2022. Front Genet. 2022. PMID: 35812735 Free PMC article.
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.
Imaging findings of neuro-Behcet disease.
Hassan HH, Alorainy IA, Rabee HM, Daif AM. Hassan HH, et al. Among authors: alorainy ia. Neurosciences (Riyadh). 2004 Jul;9(3):180-5. Neurosciences (Riyadh). 2004. PMID: 23377424
63 results