Lynch T - Search Results

1

Type 1 protease resistant prion protein and valine homozygosity at codon 129 of PRNP identify a subtype of sporadic Creutzfeldt-Jakob disease.

Worrall BB, Herman ST, Capellari S, Lynch T, Chin S, Gambetti P, Parchi P. Worrall BB, et al. Among authors: lynch t. J Neurol Neurosurg Psychiatry. 1999 Nov;67(5):671-4. doi: 10.1136/jnnp.67.5.671. J Neurol Neurosurg Psychiatry. 1999. PMID: 10519879 Free PMC article.

2

The neuropathology of chromosome 17-linked dementia.

Sima AA, Defendini R, Keohane C, D'Amato C, Foster NL, Parchi P, Gambetti P, Lynch T, Wilhelmsen KC. Sima AA, et al. Among authors: lynch t. Ann Neurol. 1996 Jun;39(6):734-43. doi: 10.1002/ana.410390609. Ann Neurol. 1996. PMID: 8651645 Free article.

3

CADASIL in a North American family: clinical, pathologic, and radiologic findings.

Desmond DW, Moroney JT, Lynch T, Chan S, Chin SS, Shungu DC, Naini AB, Mohr JP. Desmond DW, et al. Among authors: lynch t. Neurology. 1998 Sep;51(3):844-9. doi: 10.1212/wnl.51.3.844. Neurology. 1998. PMID: 9748037

4

The natural history of CADASIL: a pooled analysis of previously published cases.

Desmond DW, Moroney JT, Lynch T, Chan S, Chin SS, Mohr JP. Desmond DW, et al. Among authors: lynch t. Stroke. 1999 Jun;30(6):1230-3. doi: 10.1161/01.str.30.6.1230. Stroke. 1999. PMID: 10356105

5

Leukoencephalopathy and raised brain lactate from heroin vapor inhalation ("chasing the dragon").

Kriegstein AR, Shungu DC, Millar WS, Armitage BA, Brust JC, Chillrud S, Goldman J, Lynch T. Kriegstein AR, et al. Among authors: lynch t. Neurology. 1999 Nov 10;53(8):1765-73. doi: 10.1212/wnl.53.8.1765. Neurology. 1999. PMID: 10563626

6

Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex.

Lynch T, Sano M, Marder KS, Bell KL, Foster NL, Defendini RF, Sima AA, Keohane C, Nygaard TG, Fahn S, et al. Lynch T, et al. Neurology. 1994 Oct;44(10):1878-84. doi: 10.1212/wnl.44.10.1878. Neurology. 1994. PMID: 7936241

7

Biopsy-proven isolated sarcoid meningitis. Case report.

Mayer SA, Yim GK, Onesti ST, Lynch T, Faust PL, Marder K. Mayer SA, et al. Among authors: lynch t. J Neurosurg. 1993 Jun;78(6):994-6. doi: 10.3171/jns.1993.78.6.0994. J Neurosurg. 1993. PMID: 8487086

8

Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy.

Wilhelmsen KC, Blake DM, Lynch T, Mabutas J, De Vera M, Neystat M, Bernstein M, Hirano M, Gilliam TC, Murphy PL, Sola MD, Bonilla E, Schotland DL, Hays AP, Rowland LP. Wilhelmsen KC, et al. Among authors: lynch t. Ann Neurol. 1996 Apr;39(4):507-20. doi: 10.1002/ana.410390413. Ann Neurol. 1996. PMID: 8619529 Review.

9

Delayed-onset cerebellar syndrome.

Louis ED, Lynch T, Ford B, Greene P, Bressman SB, Fahn S. Louis ED, et al. Among authors: lynch t. Arch Neurol. 1996 May;53(5):450-4. doi: 10.1001/archneur.1996.00550050080027. Arch Neurol. 1996. PMID: 8624221

10

Clinical genetics of familial progressive supranuclear palsy.

Rojo A, Pernaute RS, Fontán A, Ruíz PG, Honnorat J, Lynch T, Chin S, Gonzalo I, Rábano A, Martínez A, Daniel S, Pramstaller P, Morris H, Wood N, Lees A, Tabernero C, Nyggard T, Jackson AC, Hanson A, de Yébenes JG. Rojo A, et al. Among authors: lynch t. Brain. 1999 Jul;122 ( Pt 7):1233-45. doi: 10.1093/brain/122.7.1233. Brain. 1999. PMID: 10388790

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