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Dopa-responsive dystonia: The story so farBANDMANN, O; WOOD, N. W.Neuropediatrics. 2002, Vol 33, Num 1, pp 1-5, issn 0174-304XArticle

Neurodegenerative disorders : Parkinson's disease and Huntington's diseaseHAGUE, S. M; KLAFFKE, S; BANDMANN, O et al.Journal of neurology, neurosurgery and psychiatry. 2005, Vol 76, Num 8, pp 1058-1063, issn 0022-3050, 6 p.Article

A contrast enhanced lesion of the III nerve on MR of a patient with ophthalmoplegic migraine as evidence for a Tolosa-Hunt syndromeSTRAUBE, A; BANDMANN, O; BÜTTNER, U et al.Headache. 1993, Vol 33, Num 8, pp 446-448, issn 0017-8748Article

Genetic aspects of Parkinson's diseaseBANDMANN, O; MARSDEN, C. D; WOOD, N. W et al.Movement disorders. 1998, Vol 13, Num 2, pp 203-211, issn 0885-3185Article

GTP cyclohydrolase I mutations in patients with dystonia responsive to anticholinergic drugsJARMAN, P. R; BANDMANN, O; MARSDEN, C. D et al.Journal of neurology, neurosurgery and psychiatry. 1997, Vol 63, Num 3, pp 304-308, issn 0022-3050Article

The human homologue of the weaver mouse gene in familial and sporadic Parkinson's diseaseBANDMANN, O; DAVIS, M. B; MARSDEN, C. D et al.Neuroscience. 1996, Vol 72, Num 4, pp 877-879, issn 0306-4522Article

CNS involvement in hereditary neuropathy with pressure palsies (HNPP)TACKENBERG, B; MÖLLER, J. C; RINDOCK, H et al.Neurology. 2006, Vol 67, Num 12, pp 2250-2252, issn 0028-3878, 3 p.Article

The tau gene A0 polymorphism in progressive supranuclear palsy and related neurodegenerative diseasesMORRIS, H. R; JANSSEN, J. C; BANDMANN, O et al.Journal of neurology, neurosurgery and psychiatry. 1999, Vol 66, Num 5, pp 665-667, issn 0022-3050Article

3H-spiperone binding to lymphocytes fails in the differential diagnosis of de novo Parkinson syndromesARNOLD, G; BONDY, B; BANDMANN, O et al.Journal of neural transmission - Parkinson's disease and dementia section. 1993, Vol 5, Num 2, pp 107-116, issn 0936-3076Article

Lack of association with TorsinA haplotype in German patients with sporadic dystoniaHAGUE, S; KLAFFKE, S; CLARIMON, J et al.Neurology. 2006, Vol 66, Num 6, pp 951-952, issn 0028-3878, 2 p.Article

Copper genes are not implicated in the pathogenesis of focal dystoniaBANDMANN, O; ASMUS, F; SIBBING, D et al.Neurology. 2002, Vol 59, Num 5, pp 782-783, issn 0028-3878Article

GTP cyclohydrolase deficiency; intrafamilial variation in clinical phenotype, including levodopa responsivenessROBINSON, R; MCCARTHY, G. T; BANDMANN, O et al.Journal of neurology, neurosurgery and psychiatry. 1999, Vol 66, Num 1, pp 86-89, issn 0022-3050Article

Dopa-responsive dystonia in British patients : new mutations of the GTP-cyclohydrolase I gene and evidence for genetic heterogeneityBANDMANN, O; NYGAARD, T. G; SURTEES, R et al.Human molecular genetics (Print). 1996, Vol 5, Num 3, pp 403-406, issn 0964-6906Article

Corpus Callosum Morphology and Microstructure Assessed Using Structural MR Imaging and Diffusion Tensor Imaging: Initial Findings in Adults with Neurofibromatosis Type 1WIGNALL, E. L; GRIFFITHS, P. D; PAPADAKIS, N. G et al.American journal of neuroradiology. 2010, Vol 31, Num 5, pp 856-861, issn 0195-6108, 6 p.Article

The phenylalanine loading test in the differential diagnosis of dystoniaBANDMANN, O; GOERTZ, M; ZSCHOCKE, J et al.Neurology. 2003, Vol 60, Num 4, pp 700-702, issn 0028-3878, 3 p.Article

Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's diseaseBANDMANN, O; VAUGHAN, J; HOLMANS, P et al.Lancet (British edition). 1997, Vol 350, Num 9085, pp 1136-1139, issn 0140-6736Article

Multiple-system atrophy is genetically distinct from identified inherited causes of spinocerebellar degenerationBANDMANN, O; SWEENEY, M. G; DANIEL, S. E et al.Neurology. 1997, Vol 49, Num 6, pp 1598-1604, issn 0028-3878Article

Sequence of the superoxide dismutase 1 (SOD 1) gene in familial Parkinson's diseaseBANDMANN, O; DAVIS, M. B; MARSDEN, C. D et al.Journal of neurology, neurosurgery and psychiatry. 1995, Vol 59, Num 1, pp 90-91, issn 0022-3050Article

The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy : data from the EMSA study groupKAMM, C; HEALY, D. G; TOLOSA, E et al.Brain. 2005, Vol 128, pp 1855-1860, issn 0006-8950, 6 p., 8Article

Candidate gene studies in focal dystoniaSIBBING, D; ASMUS, F; BANDMANN, O et al.Neurology. 2003, Vol 61, Num 8, pp 1097-1101, issn 0028-3878, 5 p.Article

Mitochondrial DNA polymorphisms in pathologically proven Parkinson's diseaseBANDMANN, O; SWEENEY, M. G; DANIEL, S. E et al.Journal of neurology. 1997, Vol 244, Num 4, pp 262-265, issn 0340-5354Article

The GTP-cyclohydrolase I gene in atypical Parkinsonian patients : a clinico-genetic studyBANDMANN, O; DANIEL, S; MARSDEN, C. D et al.Journal of the neurological sciences. 1996, Vol 141, Num 1-2, pp 27-32, issn 0022-510XArticle

Signal changes on MRI and increases in reactive microgliosis, astrogliosis, and iron in the putamen of two patients with multiple system atrophySCHWARZ, J; WEIS, S; KRAFT, E et al.Journal of neurology, neurosurgery and psychiatry. 1996, Vol 60, Num 1, pp 98-101, issn 0022-3050Conference Paper

Slow N-acetyltransferase 2 status leads to enhanced intrastriatal dopamine depletion in 6-hydroxydopamine-lesioned ratsGRUNDMANN, M; EARL, C. D; SAUTTER, J et al.Experimental neurology (Print). 2004, Vol 187, Num 1, pp 199-202, issn 0014-4886, 4 p.Article

Steele-richardson-olszewski-syndrome: the relation of dopamine D2 receptor binding and subcortical lesions in MRIARNOLD, G; SCHWARZ, J; TATSCH, K et al.Journal of neural transmission. 2002, Vol 109, Num 4, pp 503-512, issn 0300-9564Article

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