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

Year Number of Results
2005 1
2007 1
2009 1
2010 1
2011 2
2012 2
2015 2
2017 1
2019 1
2020 1
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2023 1
2024 0

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Page 1
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort.
Vollstedt EJ, Schaake S, Lohmann K, Padmanabhan S, Brice A, Lesage S, Tesson C, Vidailhet M, Wurster I, Hentati F, Mirelman A, Giladi N, Marder K, Waters C, Fahn S, Kasten M, Brüggemann N, Borsche M, Foroud T, Tolosa E, Garrido A, Annesi G, Gagliardi M, Bozi M, Stefanis L, Ferreira JJ, Correia Guedes L, Avenali M, Petrucci S, Clark L, Fedotova EY, Abramycheva NY, Alvarez V, Menéndez-González M, Jesús Maestre S, Gómez-Garre P, Mir P, Belin AC, Ran C, Lin CH, Kuo MC, Crosiers D, Wszolek ZK, Ross OA, Jankovic J, Nishioka K, Funayama M, Clarimon J, Williams-Gray CH, Camacho M, Cornejo-Olivas M, Torres-Ramirez L, Wu YR, Lee-Chen GJ, Morgadinho A, Pulkes T, Termsarasab P, Berg D, Kuhlenbäumer G, Kühn AA, Borngräber F, de Michele G, De Rosa A, Zimprich A, Puschmann A, Mellick GD, Dorszewska J, Carr J, Ferese R, Gambardella S, Chase B, Markopoulou K, Satake W, Toda T, Rossi M, Merello M, Lynch T, Olszewska DA, Lim SY, Ahmad-Annuar A, Tan AH, Al-Mubarak B, Hanagasi H, Koziorowski D, Ertan S, Genç G, de Carvalho Aguiar P, Barkhuizen M, Pimentel MMG, Saunders-Pullman R, van de Warrenburg B, Bressman S, Toft M, Appel-Cresswell S, Lang AE, Skorvanek M, Boon AJW, Krüger R, Sammler EM, Tumas V, … See abstract for full author list ➔ Vollstedt EJ, et al. Mov Disord. 2023 Feb;38(2):286-303. doi: 10.1002/mds.29288. Epub 2023 Jan 24. Mov Disord. 2023. PMID: 36692014
Isolated Neurological Manifestation in Silent Celiac Disease.
Tarabzouni S, AlKhairallah T. Tarabzouni S, et al. Among authors: alkhairallah t. J Mov Disord. 2017 May;10(2):105-107. doi: 10.14802/jmd.16063. Epub 2017 Mar 24. J Mov Disord. 2017. PMID: 28352056 Free PMC article. No abstract available.
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. Among authors: alkhairallah ts. 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.
Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson's Disease.
Yemni EA, Monies D, Alkhairallah T, Bohlega S, Abouelhoda M, Magrashi A, Mustafa A, AlAbdulaziz B, Alhamed M, Baz B, Goljan E, Albar R, Jabaan A, Faquih T, Subhani S, Ali W, Shinwari J, Al-Mubarak B, Al-Tassan N. Yemni EA, et al. Among authors: alkhairallah t. Sci Rep. 2019 Mar 4;9(1):3344. doi: 10.1038/s41598-019-40102-x. Sci Rep. 2019. PMID: 30833663 Free PMC article.
Natural course of epilepsy concomitant with CNS tuberculomas.
AlSemari A, Baz S, Alrabiah F, Al-Khairallah T, Qadi N, Kareem A, Alrajhi AA. AlSemari A, et al. Epilepsy Res. 2012 Mar;99(1-2):107-11. doi: 10.1016/j.eplepsyres.2011.10.032. Epub 2011 Nov 26. Epilepsy Res. 2012. PMID: 22119105
CADASIL in Arabs: clinical and genetic findings.
Bohlega S, Al Shubili A, Edris A, Alreshaid A, Alkhairallah T, AlSous MW, Farah S, Abu-Amero KK. Bohlega S, et al. Among authors: alkhairallah t. BMC Med Genet. 2007 Nov 9;8:67. doi: 10.1186/1471-2350-8-67. BMC Med Genet. 2007. PMID: 17996090 Free PMC article.
12 results