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Clinical and genetic characterization of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia associated with CSF1R mutation.
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- European Journal of Neurology, 2017, v. 24, n. 1, p. 37, doi. 10.1111/ene.13125
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- Article
Brain atrophy over time in genetic and sporadic frontotemporal dementia: a study of 198 serial magnetic resonance images.
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- European Journal of Neurology, 2015, v. 22, n. 5, p. 745, doi. 10.1111/ene.12675
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- Article
Genetic variants associated with myocardial infarction in the PSMA6 gene and Chr9p21 are also associated with ischaemic stroke.
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- European Journal of Neurology, 2013, v. 20, n. 2, p. 300, doi. 10.1111/j.1468-1331.2012.03846.x
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- Article
Death-associated protein kinase 1 variation and Parkinson's disease.
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- European Journal of Neurology, 2011, v. 18, n. 8, p. 1090, doi. 10.1111/j.1468-1331.2010.03255.x
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- Article
SNCA, MAPT, and GSK3B in Parkinson disease: a gene-gene interaction study.
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- European Journal of Neurology, 2011, v. 18, n. 6, p. 876, doi. 10.1111/j.1468-1331.2010.03297.x
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- Article
Frontotemporal dementia and parkinsonism linked to chromosome 17 - the first Polish family.
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- European Journal of Neurology, 2011, v. 18, n. 3, p. 535, doi. 10.1111/j.1468-1331.2010.03107.x
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- Article
Association of the MAPT locus with Parkinson’s disease.
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- European Journal of Neurology, 2010, v. 17, n. 3, p. 483, doi. 10.1111/j.1468-1331.2009.02847.x
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- Article
Calbindin-1 association and Parkinson’s disease.
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- European Journal of Neurology, 2010, v. 17, n. 2, p. 208, doi. 10.1111/j.1468-1331.2009.02769.x
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- Article
GRN 3′UTR+78 C>T is not associated with risk for Parkinson’s disease.
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- European Journal of Neurology, 2009, v. 16, n. 8, p. 909, doi. 10.1111/j.1468-1331.2009.02621.x
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- Article
Medications used to treat Parkinson’s disease and the risk of gambling.
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- European Journal of Neurology, 2008, v. 15, n. 4, p. 350, doi. 10.1111/j.1468-1331.2008.02081.x
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- Article
Interest in genetic testing in pallido-ponto-nigral degeneration (PPND): a family with frontotemporal dementia with Parkinsonism linked to chromosome 17.
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- European Journal of Neurology, 2001, v. 8, n. 2, p. 179, doi. 10.1046/j.1468-1331.2001.00198.x
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- Article
Cortical blindness and seizures in a patient receiving FK506 after bone marrow transplantation.
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- Bone Marrow Transplantation, 1999, v. 23, n. 9, p. 959, doi. 10.1038/sj.bmt.1701732
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- Article
Complex partial status epilepticus after bone marrow transplantation for non-Hodgkin’s lymphoma.
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- Bone Marrow Transplantation, 1997, v. 19, n. 6, p. 637, doi. 10.1038/sj.bmt.1700704
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- Article
Comparison of EEG background frequency analysis, psychologic test scores, short test of mental status, and quantitative SPECT in dementia.
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- 1992
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- Publication type:
- journal article
Clinicopathologic heterogeneity in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) due to microtubule-associated protein tau (MAPT) p.P301L mutation, including a patient with globular glial tauopathy.
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- Neuropathology & Applied Neurobiology, 2017, v. 43, n. 3, p. 200, doi. 10.1111/nan.12367
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- Article
Neurophysiologic evaluation of cyclosporine toxicity associated with bone marrow transplantation.
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- Acta Neurologica Scandinavica, 1996, v. 94, n. 5, p. 358, doi. 10.1111/j.1600-0404.1996.tb07081.x
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- Article
Neurophysiologic evaluation of cyclosporine toxicity associated with bone marrow transplantation.
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- Acta Neurologica Scandinavica, 1995, v. 92, n. 5, p. 423, doi. 10.1111/j.1600-0404.1995.tb00158.x
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- Article
Predominance of brain tumors in an extended Li-Fraumeni (SBLA) kindred, including a case of Sturge-Weber syndrome.
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- 2000
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- Publication type:
- journal article
Clinical, neuropathological and genotypic variability in SNCA A53T familial Parkinson’s disease.
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- Acta Neuropathologica, 2008, v. 116, n. 1, p. 25, doi. 10.1007/s00401-008-0372-4
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- Article
Neuropathology of two members of a German-American kindred (Family C) with late onset parkinsonism.
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- Acta Neuropathologica, 2002, v. 103, n. 4, p. 344, doi. 10.1007/s00401-001-0474-8
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- Publication type:
- Article
Iron in Alzheimer's and Control Hippocampi — Mössbauer, Atomic Absorption and ELISA Studies.
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- Acta Physica Polonica: A, 2011, v. 119, n. 1, p. 81
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- Article
Partial loss of function of colony‐stimulating factor 1 receptor in a patient with white matter abnormalities.
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- European Journal of Neurology, 2018, v. 25, n. 6, p. 875, doi. 10.1111/ene.13611
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- Publication type:
- Article
Diagnostic criteria for adult-onset leukoencephalopathy with axonal spheroids and pigmented glia due to CSF1R mutation.
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- European Journal of Neurology, 2018, v. 25, n. 1, p. 142, doi. 10.1111/ene.13464
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- Publication type:
- Article
Atypical parkinsonian syndromes: a general neurologist's perspective.
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- European Journal of Neurology, 2018, v. 25, n. 1, p. 41, doi. 10.1111/ene.13412
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- Article
PHENOCONVERSION AMONG PARKINSON'S DISEASE CONTROL COHORT.
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- Neurologijos Seminarai, 2018, v. 22, n. 3, p. 269
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- Publication type:
- Article
Reduced expression of the G209A alpha-synuclein allele in familial Parkinsonism.
- Published in:
- 1999
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- Publication type:
- journal article
A Greek-American kindred with autosomal dominant, levodopa-responsive parkinsonism and anticipation.
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- Annals of Neurology, 1995, v. 38, n. 3, p. 373, doi. 10.1002/ana.410380306
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- Article
Genetic linkage studies in autosomal dominant parkinsonism: Evaluation of seven candidate genes.
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- Annals of Neurology, 1994, v. 36, n. 3, p. 387, doi. 10.1002/ana.410360310
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- Publication type:
- Article
Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration.
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- 1992
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- Publication type:
- journal article
Epileptiform electroencephalographic abnormalities in liver transplant recipients.
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- Annals of Neurology, 1991, v. 30, n. 1, p. 37, doi. 10.1002/ana.410300108
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- Article
Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutation.
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- Journal of Neural Transmission, 2007, v. 114, n. 7, p. 947, doi. 10.1007/s00702-007-0632-9
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- Publication type:
- Article
Pathogenic Lrrk2 substitutions and Amyotrophic lateral sclerosis.
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- Journal of Neural Transmission, 2007, v. 114, n. 3, p. 327, doi. 10.1007/s00702-006-0525-3
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- Article
Clinical and genetic evaluation of 8 Polish families with levodopa-responsive parkinsonism.
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- Journal of Neural Transmission, 2005, v. 112, n. 11, p. 1487, doi. 10.1007/s00702-005-0290-8
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- Publication type:
- Article
Autosomal-dominant Parkinson's disease linked to 2p13 is not caused by mutations in transforming growth factor alpha (TGF alpha).
- Published in:
- Journal of Neural Transmission, 2001, v. 108, n. 8/9, p. 1029, doi. 10.1007/s007020170021
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- Publication type:
- Article