Chin S - 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: chin s. 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

A subtype of sporadic prion disease mimicking fatal familial insomnia.

Parchi P, Capellari S, Chin S, Schwarz HB, Schecter NP, Butts JD, Hudkins P, Burns DK, Powers JM, Gambetti P. Parchi P, et al. Among authors: chin s. Neurology. 1999 Jun 10;52(9):1757-63. doi: 10.1212/wnl.52.9.1757. Neurology. 1999. PMID: 10371520

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: chin ss. Neurology. 1998 Sep;51(3):844-9. doi: 10.1212/wnl.51.3.844. Neurology. 1998. PMID: 9748037

4

Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJD.

Pastore M, Chin SS, Bell KL, Dong Z, Yang Q, Yang L, Yuan J, Chen SG, Gambetti P, Zou WQ. Pastore M, et al. Among authors: chin ss. Am J Pathol. 2005 Dec;167(6):1729-38. doi: 10.1016/S0002-9440(10)61254-0. Am J Pathol. 2005. PMID: 16314483 Free PMC article.

5

MRI of Creutzfeldt-Jakob disease: asymmetric high signal intensity of the basal ganglia.

Yoon SS, Chan S, Chin S, Lee K, Goodman RR. Yoon SS, et al. Among authors: chin s. Neurology. 1995 Oct;45(10):1932-3. doi: 10.1212/wnl.45.10.1932. Neurology. 1995. PMID: 7477998

6

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: chin ss. Stroke. 1999 Jun;30(6):1230-3. doi: 10.1161/01.str.30.6.1230. Stroke. 1999. PMID: 10356105

7

Woman with a 26-year history of parkinsonism, supranuclear ophthalmoplegia, and loss of postural reflexes.

Gordon PH, Fahn S, Chin S, Golbe LI, Lynch T, Eidelberg D. Gordon PH, et al. Among authors: chin s. Mov Disord. 2004 Aug;19(8):950-61. doi: 10.1002/mds.20139. Mov Disord. 2004. PMID: 15300663

8

Sporadic fatal insomnia masquerading as a paraneoplastic cerebellar syndrome.

Mehta LR, Huddleston BJ, Skalabrin EJ, Burns JB, Zou WQ, Gambetti P, Chin SS. Mehta LR, et al. Among authors: chin ss. Arch Neurol. 2008 Jul;65(7):971-3. doi: 10.1001/archneur.65.7.971. Arch Neurol. 2008. PMID: 18625868

9

Presenilin 1 mutation in an african american family presenting with atypical Alzheimer dementia.

Rippon GA, Crook R, Baker M, Halvorsen E, Chin S, Hutton M, Houlden H, Hardy J, Lynch T. Rippon GA, et al. Among authors: chin s. Arch Neurol. 2003 Jun;60(6):884-8. doi: 10.1001/archneur.60.6.884. Arch Neurol. 2003. PMID: 12810495

10

Prospective magnetic resonance imaging identification of focal cortical dysplasia, including the non-balloon cell subtype.

Chan S, Chin SS, Nordli DR, Goodman RR, DeLaPaz RL, Pedley TA. Chan S, et al. Among authors: chin ss. Ann Neurol. 1998 Nov;44(5):749-57. doi: 10.1002/ana.410440508. Ann Neurol. 1998. PMID: 9818930

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