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Homozygosity analysis in amyotrophic lateral sclerosis.
Eur J Hum Genet. 2013 Dec;21(12):1429-35. doi: 10.1038/ejhg.2013.59. Epub 2013 Apr 24.
Eur J Hum Genet. 2013.
PMID: 23612577
Free PMC article.
Genetic testing in familial and young-onset Alzheimer's disease: mutation spectrum in a Serbian cohort.
Dobricic V, Stefanova E, Jankovic M, Gurunlian N, Novakovic I, Hardy J, Kostic V, Guerreiro R.
Dobricic V, et al. Among authors: gurunlian n.
Neurobiol Aging. 2012 Jul;33(7):1481.e7-12. doi: 10.1016/j.neurobiolaging.2011.12.007. Epub 2012 Jan 4.
Neurobiol Aging. 2012.
PMID: 22221884
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Genetic analysis of inherited leukodystrophies: genotype-phenotype correlations in the CSF1R gene.
Guerreiro R, Kara E, Le Ber I, Bras J, Rohrer JD, Taipa R, Lashley T, Dupuits C, Gurunlian N, Mochel F, Warren JD, Hannequin D, Sedel F, Depienne C, Camuzat A, Golfier V, Du Boisguéheneuc F, Schottlaender L, Fox NC, Beck J, Mead S, Rossor MN, Hardy J, Revesz T, Brice A, Houlden H.
Guerreiro R, et al. Among authors: gurunlian n.
JAMA Neurol. 2013 Jul;70(7):875-882. doi: 10.1001/jamaneurol.2013.698.
JAMA Neurol. 2013.
PMID: 23649896
Free PMC article.
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Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvement.
Guerreiro RJ, Lohmann E, Brás JM, Gibbs JR, Rohrer JD, Gurunlian N, Dursun B, Bilgic B, Hanagasi H, Gurvit H, Emre M, Singleton A, Hardy J.
Guerreiro RJ, et al. Among authors: gurunlian n.
JAMA Neurol. 2013 Jan;70(1):78-84. doi: 10.1001/jamaneurol.2013.579.
JAMA Neurol. 2013.
PMID: 23318515
Free PMC article.
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Identification of PSEN1 and PSEN2 gene mutations and variants in Turkish dementia patients.
Lohmann E, Guerreiro RJ, Erginel-Unaltuna N, Gurunlian N, Bilgic B, Gurvit H, Hanagasi HA, Luu N, Emre M, Singleton A.
Lohmann E, et al. Among authors: gurunlian n.
Neurobiol Aging. 2012 Aug;33(8):1850.e17-27. doi: 10.1016/j.neurobiolaging.2012.02.020. Epub 2012 Apr 13.
Neurobiol Aging. 2012.
PMID: 22503161
Free PMC article.
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Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's disease.
Guerreiro RJ, Lohmann E, Kinsella E, Brás JM, Luu N, Gurunlian N, Dursun B, Bilgic B, Santana I, Hanagasi H, Gurvit H, Gibbs JR, Oliveira C, Emre M, Singleton A.
Guerreiro RJ, et al. Among authors: gurunlian n.
Neurobiol Aging. 2012 May;33(5):1008.e17-23. doi: 10.1016/j.neurobiolaging.2011.10.009. Epub 2011 Dec 6.
Neurobiol Aging. 2012.
PMID: 22153900
Free PMC article.
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Utility of a ready-to-use PCR system for neuroendocrine tumor diagnosis.
Kidd M, Drozdov IA, Matar S, Gurunlian N, Ferranti NJ, Malczewska A, Bennett P, Bodei L, Modlin IM.
Kidd M, et al. Among authors: gurunlian n.
PLoS One. 2019 Jun 27;14(6):e0218592. doi: 10.1371/journal.pone.0218592. eCollection 2019.
PLoS One. 2019.
PMID: 31247038
Free PMC article.
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