| Ident. | Authors (with country if any) | Title |
|---|
| 000601 |
QINBO YANG [République populaire de Chine, États-Unis] ; LIN LI [États-Unis] ; RONG YANG [République populaire de Chine, États-Unis] ; Gong-Qing Shen [États-Unis] ; QIUYUN CHEN [États-Unis] ; Nancy Foldvary-Schaefer [États-Unis] ; William G. Ondo [États-Unis] ; Qing Kenneth Wang [République populaire de Chine, États-Unis] | Family-Based and Population-Based Association Studies Validate PTPRD as a Risk Factor for Restless Legs Syndrome |
| 001675 |
David Kemlink [Allemagne, République tchèque] ; Olli Polo [Finlande] ; Pasquale Montagna [Italie] ; Federica Provini [Italie] ; Karin Stiasny-Kolster [Allemagne] ; Wolfgang Oertel [Allemagne] ; Al De Weerd [Pays-Bas] ; Sona Nevsimalova [République tchèque] ; Karel Sonka [République tchèque] ; Birgit Högl [Autriche] ; Birgit Frauscher [Autriche] ; Werner Poewe [Autriche] ; Claudia Trenkwalder [Allemagne] ; Peter P. Pramstaller [Italie] ; Luigi Ferini-Strambi [Italie] ; Marco Zucconi [Italie] ; Eric Konofal [France] ; Isabelle Arnulf [France] ; Georgios M. Hadjigeorgiou [Grèce] ; Svenja Happe [Allemagne] ; Christine Klein [Allemagne] ; Anja Hiller [Allemagne] ; Peter Lichtner [Allemagne] ; Thomas Meitinger [Allemagne] ; Betram Müller-Myshok [Allemagne] ; Juliane Winkelmann [Allemagne] | Family-based association study of the restless legs syndrome loci 2 and 3 in a European Population |
| 001A95 |
Sun J. Kang [États-Unis] ; William K. Scott [États-Unis] ; Yi-Ju Li [États-Unis] ; Michael A. Hauser [États-Unis] ; Joelle M. Van Der Walt [États-Unis] ; Kenichiro Fujiwara [États-Unis] ; Gregory M. Mayhew [États-Unis] ; Sandra G. West [États-Unis] ; Jeffery M. Vance [États-Unis] ; Eden R. Martin [États-Unis] | Family-based case-control study of MAOA and MAOB polymorphisms in parkinson disease |
| 001B82 |
Renato P. Munhoz [Brésil] ; Toshitaka Kawarai [Canada] ; Helio A. Teive [Brésil] ; Salmo Raskin [Brésil] ; Christine Sato [Canada] ; YAN LIANG [Canada] ; Peter H. St. George-Hyslop [Canada] ; Ekaterina Rogaeva [Canada] | Clinical and genetic study of a Brazilian family with spastic paraplegia (SPG6 locus) |
| 002302 |
Aida M. Bertoli-Avella [Pays-Bas, Cuba] ; Jose L. Giroud-Benitez [Cuba] ; Vincenzo Bonifati [Pays-Bas, Italie] ; Eduardo Alvarez-Gonzalez [Cuba] ; Luis Heredero-Baute [Cuba] ; Cornelia M. Van Duijn [Pays-Bas] ; Peter Heutink [Pays-Bas] | Suggestive linkage to chromosome 19 in a large Cuban family with late-onset Parkinson's disease |
| 002350 |
José L. Molinuevo [Espagne] ; Maria J. Marti [Espagne] ; Rafael Blesa [Espagne] ; Eduardo Tolosa [Espagne] | Pure akinesia: An unusual phenotype of Hallervorden-Spatz syndrome |
| 002369 |
Ruth H. Walker [États-Unis] ; Joseph Jankovic [États-Unis] ; Elizabeth O'Hearn [États-Unis] ; Russell L. Margolis [États-Unis] | Phenotypic features of Huntington's disease-like 2 |
| 002385 |
Rainer Dziewas [Allemagne] ; Gregor Kuhlenb Umer [Allemagne] ; Angelika Okegwo [Allemagne] ; Peter Lüdemann [Allemagne] | Painless legs and moving toes in a mother and her daughter |
| 002398 |
Sergei N. Illarioshkin [Russie] ; Magali Periquet [France] ; Nina Rawal [France] ; Christoph B. Lücking [France] ; Tatyana B. Zagorovskaya [Russie] ; Pyotr A. Slominsky [Russie] ; Olga V. Miloserdova [Russie] ; Elena D. Markova [Russie] ; Svetlana A. Limborska [Russie] ; Irina A. Ivanova-Smolenskaya [Russie] ; Alexis Brice [France] | Mutation analysis of the parkin gene in Russian families with autosomal recessive juvenile parkinsonism |
| 002409 |
Louis C. Tan [États-Unis] ; Caroline M. Tanner [États-Unis] ; RONG CHEN [États-Unis] ; PIU CHAN [États-Unis] ; Matthew Farrer [États-Unis] ; John Hardy [États-Unis] ; J. William Langston [États-Unis] | Marked variation in clinical presentation and age of onset in a family with a heterozygous parkin mutation |
| 002445 |
Stefan Evers [Allemagne] ; Florian Stögbauer [Allemagne] | Genetic association of Huntington's disease and restless legs syndrome? A family report |
| 002454 |
Giovanni Defazio [Italie] ; Francesco Brancati [Italie] ; Enza Maria Valente [Italie] ; Viviana Caputo [Italie] ; Antonio Pizzuti [Italie] ; Davide Martino [Italie] ; Giovanni Abbruzzese [Italie] ; Paolo Livrea [Italie] ; Alfredo Berardelli [Italie] ; Bruno Dallapiccola [Italie] | Familial Blepharospasm is inherited as an autosomal dominant trait and relates to a novel unassigned gene |
| 002516 |
Saeed Bohlega [Arabie saoudite] ; Adel Al-Jishi [Bahreïn] ; Carol Dobson-Stone [Royaume-Uni] ; Luca Rampoldi [Royaume-Uni, Italie] ; Parthasarathi Saha [Arabie saoudite] ; Hatem Murad [Arabie saoudite] ; Abid Kareem [Arabie saoudite] ; George Roberts [Arabie saoudite] ; Anthony P. Monaco [Royaume-Uni] | Chorea-acanthocytosis: Clinical and genetic findings in three families from the arabian peninsula |
| 002657 |
Anna Rita Bentivoglio [Italie] ; Mario Loi [Italie] ; Enza M. Valente [Italie] ; Tamara Ialongo [Italie] ; Pietro Tonali [Italie] ; Alberto Albanese [Italie] | Phenotypic variability of DYTI-PTD: Does the clinical spectrum include psychogenic dystonia? |
| 002676 |
Francesco Brancati [Italie] ; Giovanni Defazio [Italie] ; Viviana Caputo [Italie] ; Enza Maria Valente [Italie, Royaume-Uni] ; Antonio Pizzuti [Italie] ; Paolo Livrea [Italie] ; Alfredo Berardelli [Italie] ; Bruno Dallapiccola [Italie] | Novel Italian family supports clinical and genetic heterogeneity of primary adult-onset torsion dystonia |
| 002713 |
David A. Grimes [Canada] ; J. David Grimes [Canada] ; Lem Racacho [Canada] ; Kylie A. Scoggan [Canada] ; Fabin Han [Canada] ; Betty Anne Schwarz [Canada] ; John Woulfe [Canada] ; Dennise Bulman [Canada] | Large French-Canadian family with Lewy body parkinsonism: Exclusion of known loci |
| 002724 |
Puneet Opal [États-Unis] ; Ron Tintner [États-Unis] ; Joseph Jankovic [États-Unis] ; Joanne Leung [États-Unis] ; Xandra O. Breakefield [États-Unis] ; Jennifer Friedman [États-Unis] ; Laurie Ozelius [États-Unis] | Intrafamilial phenotypic variability of the DYT1 dystonia: From asymptomatic TOR1A gene carrier status to dystonic storm |
| 002735 |
David A. Grimes [Canada] ; Fabin Han [Canada] ; Dennise Bulman [Canada] ; Mary Lou Nicolson [Canada] ; Oksana Suchowersky [Canada] | Hereditary chin trembling: A new family with exclusion of the chromosome 9q13-q21 locus |
| 002736 |
Thomas D. Bird [États-Unis] | Hereditary benign chorea |
| 002743 |
Sian D. Spacey [Royaume-Uni, Canada] ; Enza-Maria Valente [Royaume-Uni, Italie] ; Gurusidheshwar M. Wali [Inde] ; Thomas T. Warner [Royaume-Uni] ; Paul R. Jarman [Royaume-Uni] ; Anthony H. V. Schapira [Royaume-Uni] ; Peter H. Dixon [Royaume-Uni] ; Mary B. Davis [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] ; Nicholas W. Wood [Royaume-Uni] | Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: Evidence for a third EKD gene |
| 002759 |
Thomas D. Bird [États-Unis] | Familial dyskinesia and facial myokymia |
| 002824 |
Anne Thiriaux [France] ; Anne De St Martin [France] ; Laurent Vercueil [France] ; Fabrice Battaglia [France] ; Jean-Paul Armspach [France] ; Edouard Hirsch [France] ; Christian Marescaux [France] ; Izzie J. Namer [France] | Co-occurrence of infantile epileptic seizures and childhood paroxysmal choreoathetosis in one family: Clinical, EEG, and SPECT characterization of episodic events |
| 002828 |
Ruey-Meei Wu [Taïwan] ; Din-E Shan [Taïwan] ; Chen-Ming Sun [Taïwan] ; Ren-Shyan Liu [Taïwan] ; Wuh-Liang Hwu [Taïwan] ; Chun-Hwei Tai [Taïwan] ; Jennifer Hussey [États-Unis] ; Andrew West [États-Unis] ; Katrina Gwinn-Hardy [États-Unis] ; John Hardy [États-Unis] ; Judy Chen [États-Unis] ; Matt Farrer [États-Unis] ; Sarah Lincoln [États-Unis] | Clinical, 18F-dopa PET, and genetic analysis of an ethnic Chinese kindred with early-onset parkinsonism and parkin gene mutations |
| 002852 |
Peter C. G. Nijssen [Pays-Bas] ; Esther Brusse [Pays-Bas] ; Antonius C. M. Leyten [Pays-Bas] ; J. J. Martin [Belgique] ; Johannes L. J. M. Teepen [Pays-Bas] ; Raymund A. C. Roos [Pays-Bas] | Autosomal dominant adult neuronal ceroid lipofuscinosis: Parkinsonism due to both striatal and nigral dysfunction |
| 002928 |
Emilia Mabel Gatto [Argentine] ; Manuel Maria Fernandez Pardal [Argentine] ; Ricardo Claudio Reisin [Argentine] ; Ana Maria Pardal [Argentine] | Playing harp, another unusual task-specific dystonia |
| 002932 |
Anna R. Bentivoglio [Italie] ; Pietro Cortelli [Italie] ; Enza M. Valente [Italie] ; Tamara Ialongo [Italie] ; Alessandro Ferraris [Italie] ; Antonio Elia [Italie] ; Pasquale Montagna [Italie] ; Alberto Albanese [Italie] | Phenotypic characterisation of autosomal recessive PARK6-linked Parkinsonism in three unrelated Italian families |
| 002946 |
J. Hoenicka [Espagne] ; L. Vidal [Espagne] ; M. Godoy [Espagne] ; J. J. Ochoa [Espagne] ; J. Garcia De Yebenes [Espagne] | New nonsense mutation in the GTP-cyclohydrolase I gene in L-DOPA responsive dystonia-parkinsonism |
| 002974 |
Jorg Müller [Autriche] ; Gregor K. Wenning [Autriche] ; Jorg Wissel [Autriche] ; Werner Poewe [Autriche] | Intrafamilial heterogeneity of facial hyperkinesias : Chance association of tics, cranial dystonia, and huntington's disease? |
| 002976 |
D. A. Grimes [Canada] ; D. Bulman [Canada] ; P. St. George-Hyslop [Canada] ; A. E. Lang [Canada] | Inherited myoclonus-dystonia : Evidence supporting genetic heterogeneity |
| 002996 |
Zbigniew K. Wszolek [États-Unis] ; Randy H. Kardon [États-Unis] ; Erik Ch. Wolters [Pays-Bas] ; Ronald F. Pfeiffer [États-Unis] | Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17): PPND family. A longitudinal videotape demonstration |
| 002A02 |
T. Perniola [Italie] ; L. Margari [Italie] ; M. G. De Iaco [Italie] ; A. Presicci [Italie] ; P. Ventura [Italie] ; E. Ferrannini [Italie] ; G. Illiceto [Italie] | Familial paroxysmal exercise-induced dyskinesia, epilepsy, and mental retardation in a family with autosomal dominant inheritance |
| 002A35 |
C.-S. Lu [Taïwan] ; J.-C. Wu [Taïwan] ; C.-H. Tsai [Taïwan] ; R.-S. Chen [Taïwan] ; Y.-H. Wu Chou [Taïwan] ; N. Hattori [Japon] ; H. Yoshino [Japon] ; Y. Mizuno [Japon] | Clinical and genetic studies on familial parkinsonism : The first report on a Parkin gene mutation in a Taiwanese family |
| 002B02 |
Alain Destée [France] ; Isabelle Delalande [France] ; Isabelle Vuillaume [France] ; Susanna Schraen-Maschke [France] ; Luc Defebvre [France] ; Bernard Sablonniere [France] | The first identified French family with dentatorubral-pallidoluysian atrophy |
| 002B41 |
J. J. Higgins [États-Unis] ; K. Kluetzman [États-Unis] ; J. Berciano [Espagne] ; O. Combarros [Espagne] ; J. M. Loveless [États-Unis] | Posterior column ataxia and retinitis pigmentosa : A distinct clinical and genetic disorder |
| 002B49 |
P. R. Jarman [Royaume-Uni] ; K. P. Bhatia [Royaume-Uni] ; C. Davie [Royaume-Uni] ; S. J. R. Heales [Royaume-Uni] ; N. Turjanski [Royaume-Uni] ; S. D. Taylor-Robinson [Royaume-Uni] ; C. D. Marsden [Royaume-Uni] ; N. W. Wood [Royaume-Uni] | Paroxysmal dystonic choreoathetosis : Clinical features and investigation of pathophysiology in a large family |
| 002B74 |
Matt Farrer [États-Unis, France] ; Alain Destée [France] ; Estelle Becquet ; Fabienne Wavrant-De Vrieze [États-Unis] ; Vincent Mouroux ; Florence Richard ; Luc Defebvre [France] ; Sarah Lincoln [États-Unis] ; John Hardy [États-Unis] ; Philippe Amouyel ; Marie-Christine Chartier-Harlin | Linkage exclusion in French families with probable Parkinson's disease |
| 002C11 |
J. N. Caviness [États-Unis] ; K. Gwinn-Hardy [États-Unis] ; C. H. Adler [États-Unis] ; M. D. Muenter [États-Unis] | Electrophysiological observations in hereditary parkinsonism-dementia with Lewy body pathology |
| 002C36 |
Sergei N. Illarioshkin [Russie] ; Irina A. Ivanova-Smolenskaya [Russie] ; Rahmatullo A. Rahmonov [Russie] ; Elena D. Markova [Russie] ; Giovanni Stevanin [France] ; Alexis Brice [France] | Clinical and genetic study of familial essential tremor in an isolate of Northern Tajikistan |
| 002C51 |
A. Schrag [Royaume-Uni] ; N. P. Quinn [Royaume-Uni] ; K. P. Bhatia [Royaume-Uni] ; C. D. Marsden [Royaume-Uni] | Benign hereditary chorea : Entity or syndrome? |
| 002C78 |
A. Münchau [Royaume-Uni] ; E. M. Valente [Royaume-Uni] ; M. B. Davis [Royaume-Uni] ; V. Stinton [Royaume-Uni] ; N. W. Wood [Royaume-Uni] ; N. P. Quinn [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] | A yorkshire family with adult-onset cranio-cervical primary torsion dystonia |
| 002D12 |
A. Lazzarini [États-Unis] ; A. S. Walters [États-Unis] ; K. Hickey [États-Unis] ; G. Coccagna [Italie] ; E. Lugaresi [Italie] ; B. L. Ehrenberg [États-Unis] ; D. L. Picchietti [États-Unis] ; M. F. Brin [États-Unis] ; E. S. Stenroos [États-Unis] ; T. Verrico [États-Unis] ; W. G. Johnson [États-Unis] | Studies of penetrance and anticipation in five autosomal-dominant restless legs syndrome pedigrees |
| 002D77 |
S. Nagamitsu [Japon] ; T. Matsuishi [Japon] ; K. Hashimoto [Japon] ; Y. Yamashita [Japon] ; M. Aihara [Japon] ; K. Shimizu [Japon] ; M. Mizuguchi [Japon] ; H. Iwamoto [Japon] ; S. Saitoh [Japon] ; Y. Hirano [Japon] ; H. Kato [Japon] ; Y. Fukuyama [Japon] ; M. Shimada [Japon] | Multicenter study of paroxysmal dyskinesias in Japan : Clinical and pedigree analysis |
| 002D98 |
E. Cassetta [Italie] ; N. Del Grosso [Italie] ; A. R. Bentivoglio [Italie] ; E. M. Valente [Italie, Royaume-Uni] ; M. Frontali [Italie] ; A. Albanese [Italie, Suisse] | Italian family with cranial cervical dystonia : Clinical and genetic study |
| 002E05 |
S. Diaz [Argentine] ; M. C. Scorticati [Argentine] ; F. Micheli [Argentine] | Hereditary chin tremor/myoclonus : A report from Latin America |
| 002E35 |
A. H. Nemeth [Royaume-Uni] ; K. R. Mills [Royaume-Uni] ; J. S. Elston [Royaume-Uni] ; A. Williams [Royaume-Uni] ; E. Dunne [Royaume-Uni] ; N. M. Hyman [Royaume-Uni] | Do the same genes predispose to Gilles de la Tourette syndrome and dystonia? Report of a new family and review of the literature |
| 002E83 |
M. Fukuda [Japon] ; O. Hashimoto [Japon] ; S. Nagakubo [Japon] ; A. Hata [Japon] | A family with an atonic variant of paroxysmal kinesigenic choreoathetosis and hypercalcitoninemia |
| 002E92 |
M. W. Hayes [Australie] ; R. A. Ouvrier [Australie] ; W. Evans [Australie] ; E. Somerville [Australie] ; J. G. L. Morris [Australie] | X-linked Dystonia-Deafness syndrome |
| 002F37 |
S. E. Johnson [Norvège] ; A. Dahl [Norvège] ; O. Sjaastad [Norvège] | Progressive pseudobulbar paresis, early choreiform movements, and later rigidity : Appearance in two sets of dizygotic twins in the same family |
| 003001 |
E. Silber [Afrique du Sud] ; J. Kromberg [Afrique du Sud] ; J. A. Temlett [Afrique du Sud] ; A. Krause [Afrique du Sud] ; D. Saffer [Afrique du Sud] | Huntington's disease confirmed by genetic testing in five African families |
| 003006 |
O. Bandmann [Royaume-Uni] ; C. D. Marsden [Royaume-Uni] ; N. W. Wood [Royaume-Uni] | Genetic aspects of Parkinson's disease |
| 003019 |
R. Djaldetti [Israël] ; I. Ziv ; E. Melamed | Extreme anticipation in young-onset Parkinson's disease |
| 003022 |
J. J. Higgins [États-Unis] ; J. M. Loveless [États-Unis] ; Joseph Jankovic [États-Unis] ; P. I. Patel [États-Unis] | Evidence that a gene for essential tremor maps to chromosome 2p in four families |
| 003031 |
R. Mielke [Allemagne] ; R. Hilker [Allemagne] ; G. Weber-Luxenburger [Allemagne] ; J. Kessler [Allemagne] ; W.-D. Heiss [Allemagne] | Early-onset cerebellar ataxia (EOCA) with retained reflexes : Reduced cerebellar benzodiazepine-receptor binding, progressive metabolic and cognitive impairment |
| 003225 |
B. Leube [Allemagne] ; K. R. Kessler [Allemagne] ; T. Goecke [Allemagne] ; G. Auburger [Allemagne] ; R. Benecke [Allemagne] | Frequency of familial inheritance among 488 index patients with idiopathic focal dystonia and clinical variability in a large family |
| 003227 |
K. Terada [Japon] ; A. Ikeda [Japon] ; T. Mima [Japon] ; K. Kimura [Japon] ; Y. Nagahama [Japon] ; Y. Kamioka [Japon] ; I. Murone [Japon] ; J. Kimura [Japon] ; H. Shibasaki [Japon] | Familial cortical myoclonic tremor as a unique form of cortical reflex myoclonus |
| 003229 |
J. J. Higgins [États-Unis] ; L. T. Pho [États-Unis] ; S. E. Ide [États-Unis] ; L. E. Nee [États-Unis] ; M. H. Polymeropoulos [États-Unis] | Evidence for a new spinocerebellar ataxia locus |
| 003242 |
M. W. Becher [États-Unis] ; D. C. Rubinsztein [Royaume-Uni] ; J. Leggo [Royaume-Uni] ; M. V. Wagster [États-Unis] ; O. C. Stine [États-Unis] ; N. G. Ranen [États-Unis] ; M. L. Franz [États-Unis] ; M. H. Abbott [États-Unis] ; M. Sherr [États-Unis] ; J. C. Macmillan [Royaume-Uni] ; L. Barron [Royaume-Uni] ; M. Porteous [Royaume-Uni] ; P. S. Harper [Royaume-Uni] ; C. A. Ross [États-Unis] | Dentatorubral and pallidoluysian atrophy (DRPLA) : Clinical and neuropathological findings in genetically confirmed North American and European pedigrees |
| 003251 |
A. H. Rajput [Canada] ; M. E. Fenton [Canada] ; D. George [Canada] ; A. Rajput [États-Unis] ; W. Wilson [Canada] ; L. Mcculloch [Canada] | Concordance of common movement disorders among familial cases |
| 003293 |
J. J. Higgins [États-Unis] ; L. T. Pho [États-Unis] ; L. E. Nee [États-Unis] | A gene (ETM) for essential tremor maps to chromosome 2p22-p25 |
| 003303 |
A. Brashear [États-Unis] ; M. R. Farlow [États-Unis] ; I. J. Butler ; E. J. Kasarskis ; W. B. Dobyns | Variable phenotype of rapid-onset dystonia-parkinsonism |
| 003355 |
S. H. Subramony [États-Unis] ; R. D. Currier [États-Unis] | Intrafamilial variability in Machado-Joseph disease |
| 003363 |
V. L. Soland [Canada] ; K. P. Bhatia [Royaume-Uni] ; G. L. Sheean [Royaume-Uni] ; C. D. Marsden [Royaume-Uni] | Hereditary geniospasm : Two new families |
| 003370 |
D. T. Schloesser [États-Unis] ; T. N. Ward [États-Unis] ; P. D. Williamson [États-Unis] | Familial paroxysmal dystonic choreoathetosis revisited |
| 003380 |
S. H. Subramony [États-Unis] ; J. D. Fratkin ; B. V. Manyam ; R. D. Currier [États-Unis] | Dominantly inherited cerebello-olivary atrophy is not due to a mutation at the spinocerebellar ataxia-I, Machado-Joseph disease, or dentato-rubro-pallido-luysian atrophy locus |
| 003381 |
J. E. Nielsen [Danemark] ; S. A. S Rensen [Danemark] ; L. Hasholt [Danemark] ; A. N Rrem Lle [Danemark] | Dentatorubral-pallidoluysian atrophy. Clinical features of a five-generation Danish family |
| 003410 |
C. Klein [Royaume-Uni] ; G. K. Wenning [Royaume-Uni] ; N. P. Quinn [Royaume-Uni] ; C. D. Marsden [Royaume-Uni] | Ataxia without telangiectasia masquerading as benign hereditary chorea |
| 003483 |
J. J. Poza [Espagne] ; J. F. Marti Masso [Espagne] ; E. Amato | Late onset familial periodic cerebellar ataxia |
| 003498 |
S. Bohlega [Arabie saoudite] ; B. Stigsby [Arabie saoudite] ; M. Z. Al-Kawi [Arabie saoudite] ; D. R. Mclean [Arabie saoudite] ; P. Ozand ; S. Omer [Arabie saoudite] ; P. Coates | Familial tremulous and myoclonic dystonia with white matter changes in brain magnetic resonance imaging |
| 003536 |
A. Ishikawa [Japon] ; T. Miyatake | A family with hereditary juvenile dystonia-parkinsonism |
| 003553 |
S. Micheli [Argentine] ; M. Fernandez-Pardal ; P. Quesada ; T. Brannan ; J. A. Obeso | Variable onset of adult inherited focal dystonia: a problem for genetic studies |
| 003615 |
P. Nisipeanu [Israël] ; A. Kuritzky ; A. D. Korczyn [Israël] | Familial levodopa-responsive parkinsonian-pyramidal syndrome |
| 003616 |
F. Micheli [Argentine] ; M. C. Scorticati ; E. Gatto ; G. Cersosimo ; J. Adi | Familial hemifacial spasm |
| 003620 |
S. B. Bressman [États-Unis] ; A. L. Hunt [États-Unis] ; G. A. Heiman [États-Unis] ; M. F. Brin [États-Unis] ; R. E. Burke [États-Unis] ; S. Fahn [États-Unis] ; J. M. Trugman ; D. De Leon [États-Unis] ; P. L. Kramer ; K. C. Wilhelmsen [États-Unis] ; T. G. Nygaard | Exclusion of the DYT1 mocus in a non-jewish family with early-onset dystonia |
| 003635 |
C. H. Adler [États-Unis] ; L. Wrabetz ; M. F. Brin ; H. I. Hurtig [États-Unis] | Cerebellar ataxia, dystonia, and tremor within a family: variable phenotypes of a single genetic disorder? |
| 003641 |
T. T. Warner [Royaume-Uni] ; G. G. Lennox ; I. Janota ; A. E. Harding [Royaume-Uni] | Autosomal-dominant dentatorubropallidoluysian atrophy in the United Kingdom |
| 003730 |
P. Martinelli [Italie] ; S. Giuliani [Italie] ; M. Ippoliti [Italie] ; A. Martinelli ; A. Sforza [Italie] ; S. Ferrari | Familial idiopathic strio-pallido-dentate calcifications with late onset extrapyramidal syndrome |
| 003758 |
R. J. Uitti [États-Unis] ; D. M. Maraganore | Adult onset familial cervical dystonia: report of a family including monozygotic twins |
| 003814 |
A. Guala [Italie] ; D. Mittino ; P. Fabbrocini ; T. Ghini | Familial metoclopramide-induced dystonic reactions |
| 003845 |
A. Berardelli ; P. D. Thompson ; M. Zaccagnini ; O. Giardini ; P. D'Eufemia ; R. Massoud ; M. Mandredi | Two sisters with generalized dystonia associated with homocystinuria |
| 003876 |
N. A. Fletcher [Royaume-Uni] ; A. E. Harding ; C. D. Marsden | Intrafamilial correlation in idiopathic torsion dystonia |
| 003883 |
S. Fahn ; O. Sjaastad | Hereditary essential myoclonus in a large Norwegian family |
| 003908 |
D. M. Maraganore ; A. E. Harding ; C. D. Marsden | A clinical and genetic study of familial Parkinson's disease |
| 003968 |
M. Kyllerman ; L. Forsgren ; G. Sanner ; G. Holmgren ; J. Wahlstroêm ; U. Drugge | Alcohol-responsive myoclonic dystonia in a large family: dominant inheritance and phenotypic variation |
| 003A05 |
A. Friedman ; Z. Jamrozik ; J. Bojakowski | Familial hemifacial spasm |
| 003A13 |
U. J. Kang ; S. Fahn ; H. Schwarz ; I. Shoulson ; H. Vallejos ; J. Goldman | Case 1, 1989: Juvenile-onset Parkinsonism, dystonia, and pyramidal tract signs |
| 003A48 |
V. P. Misra ; M. Baraitser ; A. E. Harding | Genetic prediction in Huntington's disease: what are the limitations imposed by pedigree structure? |
| 003A85 |
R. Kurlan ; J. Behr ; L. Medved ; I. Shoulson | Familial paroxysmal dystonic choreoathetosis: a family study |
| 003B01 |
L. G. Cohen ; M. Hallett ; L. Sudarsky | A single family with writer's cramp, essential tremor, and primary writing tremor |
