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Items: 1 to 20 of 100

1.

Cerebrospinal Fluid Total Prion Protein in the Spectrum of Prion Diseases.

Villar-Piqué A, Schmitz M, Lachmann I, Karch A, Calero O, Stehmann C, Sarros S, Ladogana A, Poleggi A, Santana I, Ferrer I, Mitrova E, Žáková D, Pocchiari M, Baldeiras I, Calero M, Collins SJ, Geschwind MD, Sánchez-Valle R, Zerr I, Llorens F.

Mol Neurobiol. 2018 Jul 30. doi: 10.1007/s12035-018-1251-1. [Epub ahead of print]

PMID:
30062673
2.

Neurodegeneration as the presenting symptom in 2 adults with xeroderma pigmentosum complementation group F.

Shanbhag NM, Geschwind MD, DiGiovanna JJ, Groden C, Godfrey R, Yousefzadeh MJ, Wade EA, Niedernhofer LJ, Malicdan MCV, Kraemer KH, Gahl WA, Toro C.

Neurol Genet. 2018 Jun 8;4(3):e240. doi: 10.1212/NXG.0000000000000240. eCollection 2018 Jun.

3.

Differential diagnosis with other rapid progressive dementias in human prion diseases.

Geschwind MD, Murray K.

Handb Clin Neurol. 2018;153:371-397. doi: 10.1016/B978-0-444-63945-5.00020-9. Review.

PMID:
29887146
4.

Distinct HLA associations of LGI1 and CASPR2-antibody diseases.

Binks S, Varley J, Lee W, Makuch M, Elliott K, Gelfand JM, Jacob S, Leite MI, Maddison P, Chen M, Geschwind MD, Grant E, Sen A, Waters P, McCormack M, Cavalleri GL, Barnardo M, Knight JC, Irani SR.

Brain. 2018 May 18. doi: 10.1093/brain/awy109. [Epub ahead of print]

5.

Expanding the global prevalence of spinocerebellar ataxia type 42.

Ngo K, Aker M, Petty LE, Chen J, Cavalcanti F, Nelson AB, Hassin-Baer S, Geschwind MD, Perlman S, Italiano D, Laganà A, Cavallaro S, Coppola G, Below JE, Fogel BL.

Neurol Genet. 2018 Apr 5;4(3):e232. doi: 10.1212/NXG.0000000000000232. eCollection 2018 Jun. No abstract available. Erratum in: Neurol Genet. 2018 May 18;4(3):e238.

6.

Prion disease.

Takada LT, Kim MO, Metcalf S, Gala II, Geschwind MD.

Handb Clin Neurol. 2018;148:441-464. doi: 10.1016/B978-0-444-64076-5.00029-6. Review.

PMID:
29478593
7.

The importance of early immunotherapy in patients with faciobrachial dystonic seizures.

Thompson J, Bi M, Murchison AG, Makuch M, Bien CG, Chu K, Farooque P, Gelfand JM, Geschwind MD, Hirsch LJ, Somerville E, Lang B, Vincent A, Leite MI, Waters P, Irani SR; Faciobrachial Dystonic Seizures Study Group .

Brain. 2018 Feb 1;141(2):348-356. doi: 10.1093/brain/awx323.

8.

Neuroimaging in Dementia.

Staffaroni AM, Elahi FM, McDermott D, Marton K, Karageorgiou E, Sacco S, Paoletti M, Caverzasi E, Hess CP, Rosen HJ, Geschwind MD.

Semin Neurol. 2017 Oct;37(5):510-537. doi: 10.1055/s-0037-1608808. Epub 2017 Dec 5. No abstract available.

9.

Dystonia and ataxia progression in spinocerebellar ataxias.

Kuo PH, Gan SR, Wang J, Lo RY, Figueroa KP, Tomishon D, Pulst SM, Perlman S, Wilmot G, Gomez CM, Schmahmann JD, Paulson H, Shakkottai VG, Ying SH, Zesiewicz T, Bushara K, Geschwind MD, Xia G, Subramony SH, Ashizawa T, Kuo SH.

Parkinsonism Relat Disord. 2017 Dec;45:75-80. doi: 10.1016/j.parkreldis.2017.10.007. Epub 2017 Oct 23.

10.

Postural Tremor and Ataxia Progression in Spinocerebellar Ataxias.

Gan SR, Wang J, Figueroa KP, Pulst SM, Tomishon D, Lee D, Perlman S, Wilmot G, Gomez CM, Schmahmann J, Paulson H, Shakkottai VG, Ying SH, Zesiewicz T, Bushara K, Geschwind MD, Xia G, Subramony SH, Ashizawa T, Kuo SH.

Tremor Other Hyperkinet Mov (N Y). 2017 Oct 9;7:492. doi: 10.7916/D8GM8KRH. eCollection 2017.

11.

Mass Confusion.

Abad CL, Dhaliwal G, Geschwind MD, Saint S, Safdar N.

J Hosp Med. 2017 Sep;12(9):750-754. doi: 10.12788/jhm.2805. No abstract available.

PMID:
28914282
12.

Genetic PrP Prion Diseases.

Kim MO, Takada LT, Wong K, Forner SA, Geschwind MD.

Cold Spring Harb Perspect Biol. 2018 May 1;10(5). pii: a033134. doi: 10.1101/cshperspect.a033134. Review.

PMID:
28778873
13.

Clinical Neurology and Epidemiology of the Major Neurodegenerative Diseases.

Erkkinen MG, Kim MO, Geschwind MD.

Cold Spring Harb Perspect Biol. 2018 Apr 2;10(4). pii: a033118. doi: 10.1101/cshperspect.a033118. Review.

PMID:
28716886
14.

Egocentric and allocentric visuospatial working memory in premotor Huntington's disease: A double dissociation with caudate and hippocampal volumes.

Possin KL, Kim H, Geschwind MD, Moskowitz T, Johnson ET, Sha SJ, Apple A, Xu D, Miller BL, Finkbeiner S, Hess CP, Kramer JH.

Neuropsychologia. 2017 Jul 1;101:57-64. doi: 10.1016/j.neuropsychologia.2017.04.022. Epub 2017 Apr 17.

15.

Precipitous Deterioration of Motor Function, Cognition, and Behavior.

Fernández-Fournier M, Perry DC, Tartaglia MC, de May M, Boxer A, Coppola G, Christine CW, Huang EJ, Seeley WW, Miller BL, DeArmond SJ, Grinberg LT, Geschwind MD.

JAMA Neurol. 2017 May 1;74(5):591-596. doi: 10.1001/jamaneurol.2016.6159.

16.

Genetic prion disease: Experience of a rapidly progressive dementia center in the United States and a review of the literature.

Takada LT, Kim MO, Cleveland RW, Wong K, Forner SA, Gala II, Fong JC, Geschwind MD.

Am J Med Genet B Neuropsychiatr Genet. 2017 Jan;174(1):36-69. doi: 10.1002/ajmg.b.32505. Review.

PMID:
27943639
17.

Surface-based morphometry reveals caudate subnuclear structural damage in patients with premotor Huntington disease.

Kim H, Kim JH, Possin KL, Winer J, Geschwind MD, Xu D, Hess CP.

Brain Imaging Behav. 2017 Oct;11(5):1365-1372. doi: 10.1007/s11682-016-9616-4.

18.

Genetic Prion Disease Caused by PRNP Q160X Mutation Presenting with an Orbitofrontal Syndrome, Cyclic Diarrhea, and Peripheral Neuropathy.

Fong JC, Rojas JC, Bang J, Legati A, Rankin KP, Forner S, Miller ZA, Karydas AM, Coppola G, Grouse CK, Ralph J, Miller BL, Geschwind MD.

J Alzheimers Dis. 2017;55(1):249-258.

19.

A case cluster of variant Creutzfeldt-Jakob disease linked to the Kingdom of Saudi Arabia.

Coulthart MB, Geschwind MD, Qureshi S, Phielipp N, Demarsh A, Abrams JY, Belay E, Gambetti P, Jansen GH, Lang AE, Schonberger LB.

Brain. 2016 Oct;139(Pt 10):2609-2616.

20.

Dementia.

Ljubenkov PA, Geschwind MD.

Semin Neurol. 2016 Aug;36(4):397-404. doi: 10.1055/s-0036-1585096. Epub 2016 Sep 19. Review.

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