Stoessl AJ - Search Results

1

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.

Zimprich A, Biskup S, Leitner P, Lichtner P, Farrer M, Lincoln S, Kachergus J, Hulihan M, Uitti RJ, Calne DB, Stoessl AJ, Pfeiffer RF, Patenge N, Carbajal IC, Vieregge P, Asmus F, Müller-Myhsok B, Dickson DW, Meitinger T, Strom TM, Wszolek ZK, Gasser T. Zimprich A, et al. Among authors: stoessl aj. Neuron. 2004 Nov 18;44(4):601-7. doi: 10.1016/j.neuron.2004.11.005. Neuron. 2004. PMID: 15541309 Free article.

2

(+)-4-Propyl-9-hydroxynaphthoxazine (PHNO), a new dopaminomimetic, in treatment of parkinsonism.

Stoessl AJ, Mak E, Calne DB. Stoessl AJ, et al. Lancet. 1985 Dec 14;2(8468):1330-1. doi: 10.1016/s0140-6736(85)92627-3. Lancet. 1985. PMID: 2866388 Clinical Trial.

3

Transmitter receptor alterations in Parkinson's disease.

Calne DB, Stoessl AJ. Calne DB, et al. Among authors: stoessl aj. Adv Neurol. 1987;45:45-9. Adv Neurol. 1987. PMID: 2881449 No abstract available.

4

Early parkinsonism.

Calne DB, Stoessl AJ. Calne DB, et al. Among authors: stoessl aj. Clin Neuropharmacol. 1986;9 Suppl 2:S3-8. Clin Neuropharmacol. 1986. PMID: 3297316 Review.

5

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

6

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

7

Nigrostriatal dopamine system and motor lateralization.

de la Fuente-Fernández R, Kishore A, Calne DB, Ruth TJ, Stoessl AJ. de la Fuente-Fernández R, et al. Among authors: stoessl aj. Behav Brain Res. 2000 Jul;112(1-2):63-8. doi: 10.1016/s0166-4328(00)00165-0. Behav Brain Res. 2000. PMID: 10862936

8

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

9

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

10

Positron emission tomography of dopamine pathways in familial Parkinsonian syndromes.

Pal PK, Wszolek ZK, Uitti R, Markopoulou K, Calne SM, Stoessl AJ, Calne DB. Pal PK, et al. Among authors: stoessl aj. Parkinsonism Relat Disord. 2001 Sep;8(1):51-6. doi: 10.1016/s1353-8020(01)00008-6. Parkinsonism Relat Disord. 2001. PMID: 11472880 Review.

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