Stoessl AJ - Search Results

1

A scan without evidence is not evidence of absence: Scans without evidence of dopaminergic deficit in a symptomatic leucine-rich repeat kinase 2 mutation carrier.

Wile DJ, Dinelle K, Vafai N, McKenzie J, Tsui JK, Schaffer P, Ding YS, Farrer M, Sossi V, Stoessl AJ. Wile DJ, et al. Among authors: stoessl aj. Mov Disord. 2016 Mar;31(3):405-9. doi: 10.1002/mds.26450. Epub 2015 Dec 21. Mov Disord. 2016. PMID: 26685774 Free PMC article.

2

Cerebral metabolism of glucose in benign hereditary chorea.

Suchowersky O, Hayden MR, Martin WR, Stoessl AJ, Hildebrand AM, Pate BD. Suchowersky O, et al. Among authors: stoessl aj. Mov Disord. 1986;1(1):33-44. doi: 10.1002/mds.870010105. Mov Disord. 1986. PMID: 2973557

3

Unilateral pallidotomy for reduction of parkinsonian pain.

Honey CR, Stoessl AJ, Tsui JK, Schulzer M, Calne DB. Honey CR, et al. Among authors: stoessl aj. J Neurosurg. 1999 Aug;91(2):198-201. doi: 10.3171/jns.1999.91.2.0198. J Neurosurg. 1999. PMID: 10433307

4

PET studies of parkinsonism associated with mutation in the alpha-synuclein gene.

Samii A, Markopoulou K, Wszolek ZK, Sossi V, Dobko T, Mak E, Calne DB, Stoessl AJ. Samii A, et al. Among authors: stoessl aj. Neurology. 1999 Dec 10;53(9):2097-102. doi: 10.1212/wnl.53.9.2097. Neurology. 1999. PMID: 10599788

5

In vivo positron emission tomographic evidence for compensatory changes in presynaptic dopaminergic nerve terminals in Parkinson's disease.

Lee CS, Samii A, Sossi V, Ruth TJ, Schulzer M, Holden JE, Wudel J, Pal PK, de la Fuente-Fernandez R, Calne DB, Stoessl AJ. Lee CS, et al. Among authors: stoessl aj. Ann Neurol. 2000 Apr;47(4):493-503. Ann Neurol. 2000. PMID: 10762161

6

Analysis of four dopaminergic tracers kinetics using two different tissue input function methods.

Sossi V, Holden JE, Chan G, Krzywinski M, Stoessl AJ, Ruth TJ. Sossi V, et al. Among authors: stoessl aj. J Cereb Blood Flow Metab. 2000 Apr;20(4):653-60. doi: 10.1097/00004647-200004000-00002. J Cereb Blood Flow Metab. 2000. PMID: 10779009

7

Positron emission tomography in pallido-ponto-nigral degeneration (PPND) family (frontotemporal dementia with parkinsonism linked to chromosome 17 and point mutation in tau gene).

Pal PK, Wszolek ZK, Kishore A, de la Fuente-Fernandez R, Sossi V, Uitti RJ, Dobko T, Stoessl AJ. Pal PK, et al. Among authors: stoessl aj. Parkinsonism Relat Disord. 2001 Apr;7(2):81-88. doi: 10.1016/s1353-8020(00)00026-2. Parkinsonism Relat Disord. 2001. PMID: 11248587

8

Biochemical variations in the synaptic level of dopamine precede motor fluctuations in Parkinson's disease: PET evidence of increased dopamine turnover.

de la Fuente-Fernández R, Lu JQ, Sossi V, Jivan S, Schulzer M, Holden JE, Lee CS, Ruth TJ, Calne DB, Stoessl AJ. de la Fuente-Fernández R, et al. Among authors: stoessl aj. Ann Neurol. 2001 Mar;49(3):298-303. doi: 10.1002/ana.65.abs. Ann Neurol. 2001. PMID: 11261503

9

Daytime somnolence in patients with Parkinson's disease.

Sanjiv CC, Schulzer M, Mak E, Fleming J, Martin WR, Brown T, Calne SM, Tsui J, Stoessl AJ, Lee CS, Calne DB. Sanjiv CC, et al. Among authors: stoessl aj. Parkinsonism Relat Disord. 2001 Oct;7(4):283-286. doi: 10.1016/s1353-8020(00)00076-6. Parkinsonism Relat Disord. 2001. PMID: 11344010

10

Alternating two finger tapping with contralateral activation is an objective measure of clinical severity in Parkinson's disease and correlates with PET.

Pal PK, Lee CS, Samii A, Schulzer M, Stoessl AJ, Mak EK, Wudel J, Dobko T, Tsui JK. Pal PK, et al. Among authors: stoessl aj. Parkinsonism Relat Disord. 2001 Oct;7(4):305-309. doi: 10.1016/s1353-8020(00)00048-1. Parkinsonism Relat Disord. 2001. PMID: 11344014

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