Dopa-responsive dystonia : delineation of the clinical syndrome and clues to pathogenesisNYGAARD, T. G.Advances in neurology. 1993, Vol 60, pp 577-585, issn 0091-3952Article

Hereditary dystonia-parkinsonism syndrome of juvenile onsetNYGAARD, T. G; DUVOISIN, R. C.Neurology. 1986, Vol 36, Num 11, pp 1424-1428, issn 0028-3878Article

Dopa-responsive dystonia : long-term treatment response and prognosisNYGAARD, T. G; MARSDEN, C. D; FAHN, S et al.Neurology. 1991, Vol 41, Num 2, pp 174-181, issn 0028-3878, 8 p., p.1Article

Mitochondrial neurogastrointestinal encephalomyopathy syndrome maps to chromosome 22q13.32-qterHIRANO, M; GARCIA-DE-YEBENES, J; NYGAARD, T. G et al.American journal of human genetics. 1998, Vol 63, Num 2, pp 526-533, issn 0002-9297Article

Phenotypic expression of X-linked dystonia-parkinsonism (lubag) in two womenWATERS, C. H; TAKAHASHI, H; WILHELMSEN, K. C et al.Neurology. 1993, Vol 43, Num 8, pp 1555-1558, issn 0028-3878Article

Long-term treatment response and fluorodopa positron emission tomographic scanning of parkinsonism in a family with dopa-responsive dystoniaNYGAARD, T. G; TAKAHASHI, H; HEIMAN, G. A et al.Annals of neurology. 1992, Vol 32, Num 5, pp 603-608, issn 0364-5134Article

Identification of a highly polymorphic microsatellite VNTR within the argininosuccinate synthetase locus : exclusion of the dystonia gene on 9q32-34 as the cause of dopa-responsive dystonia in a large kindredKWIATKOWSKI, D. J; NYGAARD, T. G; FAHN, S et al.American journal of human genetics. 1991, Vol 48, Num 1, pp 121-128, issn 0002-9297, 8 p.Article

Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31NYGAARD, T. G; RAYMOND, D; OZELIUS, L. J et al.Annals of neurology. 1999, Vol 46, Num 5, pp 794-798, issn 0364-5134Article

Characterization of microsatellite polymorphisms DXS691 and DXS692 : genetic mapping to Xq26.2-Xq27 and Xq25-Xq26.2LASSER, D. M; WILHELMSEN, K. C; NYGAARD, T. G et al.Genomics (San Diego, Calif.). 1993, Vol 16, Num 3, pp 785-786, issn 0888-7543Article

Geentic mapping of lubag (X-linked dystonia-parkinsonism) in a filipino kindred to the pericentromeric region of the X chromosomeWIHELMSEN, K. C; WEEKS, D. E; NYGAARD, T. G et al.Annals of neurology. 1991, Vol 29, Num 2, pp 124-131, issn 0364-5134Article

Tyrosine hydroxylase and levodopa responsive dystoniaFLETCHER, N. A; HOLT, I. J; HARDING, A. E et al.Journal of neurology, neurosurgery and psychiatry. 1989, Vol 52, Num 1, pp 112-114, issn 0022-3050Article

Oral phenylalanine loading profiles in symptomatic and asymptomatic gene carriers with dopa-responsive dystonia due to dominantly inherited GTP cyclohydrolase deficiencyHYLAND, K; NYGAARD, T. G; TRUGMAN, J. M et al.Journal of inherited metabolic disease. 1999, Vol 22, Num 3, pp 213-215, issn 0141-8955Article

Clinical-genetic spectrum of primary dystoniaBRESSMAN, S. B; DE LEON, D; RAYMOND, D et al.Advances in neurology. 1998, Vol 78, pp 79-91, issn 0091-3952Conference Paper

Tetrahydrobiopterin metabolism and GTP cyclohydrolase I mutations in L-dopa-responsive dystoniaBEZIN, L; ANASTASIADIS, P. Z; NYGAARD, T. G et al.Advances in neurology. 1998, Vol 78, pp 291-300, issn 0091-3952Conference Paper

Idiopathic torsion dystonia linked to chromosome 8 in two Mennonite familiesALMASY, L; BRESSMAN, S. B; SAUNDERS-PULLMAN, R et al.Annals of neurology. 1997, Vol 42, Num 4, pp 670-673, issn 0364-5134Article

Dopa-responsive dystonia: the spectrum of clinical manifestations in a large North American familyNYGAARD, T. G; TRUGMAN, J. M; DE YEBENES, J. G et al.Neurology. 1990, Vol 40, Num 1, pp 66-69, issn 0028-3878Article

Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complexLYNCH, T; SANO, M; MAYEUX, R et al.Neurology. 2001, Vol 57, Num 10, pp S39-S45, issn 0028-3878, SUP3Article

Primary torsion dystonia : the search for genes is not overJARMAN, P. R; DEL GROSSO, N; FRONTALI, M et al.Journal of neurology, neurosurgery and psychiatry. 1999, Vol 67, Num 3, pp 395-397, issn 0022-3050Article

A high-resolution genetic linkage map of the pericentromeric region of the human X chromosomeWEEKS, D. E; NYGAARD, T. G; NEYSTAT, M et al.Genomics (San Diego, Calif.). 1995, Vol 26, Num 1, pp 39-46, issn 0888-7543Article

Report of the second international workshop on human chromosome 14 mapping 1994COX, D. W; GEDDE-DAHL, T. JR; MENON, A. G et al.Cytogenetics and cell genetics. 1995, Vol 69, Num 3-4, pp 160-174, issn 0301-0171Article

A study of idiopathic torsion dystonia in a non-Jewish family : evidence for genetic heterogeneityBRESSMAN, S. B; HEIMAN, G. A; FAHN, S et al.Neurology. 1994, Vol 44, Num 2, pp 283-287, issn 0028-3878Article

Exclusion of the DYT1 mocus in a non-jewish family with early-onset dystoniaBRESSMAN, S. B; HUNT, A. L; NYGAARD, T. G et al.Movement disorders. 1994, Vol 9, Num 6, pp 626-632, issn 0885-3185Article

Striatal biopterin and tyrosine hydroxylase protein reduction in dopa-responsive dystoniaFURUKAWA, Y; NYGAARD, T. G; HAYCOCK, J. W et al.Neurology. 1999, Vol 53, Num 5, pp 1032-1041, issn 0028-3878Article

Autosomal recessive juvenile parkinsonism maps to 6q25.2-q27 in four ethnic groups: Detailed genetic mapping of the linked regionJONES, A. C; YAMAMURA, Y; NYGAARD, T. G et al.American journal of human genetics. 1998, Vol 63, Num 1, pp 80-87, issn 0002-9297Article

Reduced lymphoblast neopterin detects GTP cyclohydrolase dysfunction in dopa-responsive dystoniaBEZIN, L; NYGAARD, T. G; NEVILLE, J. D et al.Neurology. 1998, Vol 50, Num 4, pp 1021-1027, issn 0028-3878Article