All Stories

  1. Antisense Oligonucleotide Therapy for Spinocerebellar Ataxias: Good News for Terrible Diseases
  2. Sleep disorders in spinocerebellar ataxia type 10
  3. Imaging and Clinical Worsening After Penicillamine Treatment in Wilson's Disease
  4. Differential diagnosis of sporadic adult-onset ataxia: The role of REM sleep behavior disorder
  5. Non-motor signs in Parkinson’s disease: a review
  6. Diffusion tensor imaging and tract-based spatial statistics analysis in Friedreich's ataxia patients
  7. The genetics of the dystonias – a review based on the new classification of the dystonias
  8. Neurological examination: history, problems and facts in the 21st century
  9. REM sleep behaviour disorder: How useful is it for the differential diagnosis of parkinsonism?
  10. Genetic evaluation for TOR1-A (DYT1) in Brazilian patients with dystonia
  11. Ataxia espinocerebelar tipo 6: relato de caso
  12. ‘Pseudo-Dominant’ Inheritance in Friedreich's Ataxia: Clinical and Genetic Study of a Brazilian Family
  13. Spinocerebellar ataxia type 3: subphenotypes in a cohort of brazilian patients
  14. Neurology in Federico Fellini?s work and life
  15. Psychogenic movement disorders: an unusual presentation in childhood with improvement after placebo test
  16. Postural instability in Parkinson?s disease ? 120 years after Charcot?s death
  17. 126 hysterical years - the contribution of Charcot
  18. Freezing of Gait 3 Years After Bilateral Globus Pallidus Internus Deep Brain Stimulation in Generalized Dystonia
  19. Pull test performance and correlation with falls risk in Parkinson?s disease
  20. Evolution of the concept of dystonia
  21. Jean-Baptiste Charcot, the French Antarctic expedition and scurvy
  22. Edgar Allan Poe and neurology
  23. The relationship between Marcel Proust and Joseph Babinski: the encounter of two geniuses
  24. The physical, social and emotional aspects are the most affected in the quality of life of the patients with cervical dystonia
  25. Jean-Baptiste Charcot and Brazil
  26. Niemann-Pick disease type C: a case series of Brazilian patients
  27. Identifying novel interruption motifs in spinocerebellar ataxia type 10 expansions
  28. Cervical dystonia: about familial and sporadic cases in 88 patients
  29. Pathogenic compound heterozygous ATP7B mutations with hypoceruloplasminaemia without clinical features of Wilson’s disease
  30. The evaluation of swallowing in patients with spinocerebellar ataxia and oropharyngeal dysphagia: A comparison study of videofluoroscopic and sonar doppler
  31. Chorea in Inherited Ataxias
  32. Proust, Neurology and Stendhal's Syndrome
  33. Psychogenic nonepileptic seizures and psychogenic movement disorders: two sides of the same coin?
  34. Movement Disorders in Spinocerebellar Ataxias in a Cohort of Brazilian Patients
  35. Repeat interruptions in spinocerebellar ataxia type 10 expansions are strongly associated with epileptic seizures
  36. Expansion of the Spinocerebellar Ataxia Type 10 (SCA10) Repeat in a Patient with Sioux Native American Ancestry
  37. Professor Abraham Akerman
  38. Avaliação audiológica na ataxia espinocerebelar
  39. Professor Elio Lugaresi's contributions to neurology and sleep disorders
  40. Delusional misidentification syndrome and other unusual delusions in advanced Parkinson's disease
  41. Wilson's disease in Southern Brazil: genotype-phenotype correlation and description of two novel mutations in ATP7B gene
  42. Clinical relevance of "bulging eyes" for the differential diagnosis of spinocerebellar ataxias
  43. Lentiform fork sign and fluctuating, reversible parkinsonism in a patient with uremic encephalopathy
  44. Nonmotor and extracerebellar features in Machado-Joseph disease: A review
  45. Early onset cerebellar ataxia with retained reflexes: a clinical and genetic conundrum
  46. Reabilitação vestibular com realidade virtual na ataxia espinocerebelar
  47. Where is Gilles? Or, the little mistake in a copy of Brouillet's painting: "A clinical lesson at the Salpêtrière"
  48. Spontaneous intracerebral hemorrhage in Urbach-Wiethe disease
  49. Is San Francisco's “The Shaking Man” an urban depiction of parkinsonism?
  50. Paradoxical effects of repeat interruptions on spinocerebellar ataxia type 10 expansions and repeat instability
  51. Parakinesia brachialis oscitans during thrombolytic therapy
  52. Darkening of white hair in Parkinson's disease during use of levodopa rich Mucuna pruriens extract powder
  53. Long-duration Parkinson's disease: Role of lateralization of motor features
  54. MacDonald Critchley
  55. Vestibular findings in autosomal recessive ataxia
  56. Acute onset of cerebellar ataxia in a spinocerebellar ataxia type 10 patient after use of steroids
  57. Reversible parkinsonism associated with neurocysticercosis
  58. Charcot's skepticism
  59. Parkinson's disease and body mass index: too much or too little?
  60. Pramipexole-related chronic lower limb oedema in a patient with Parkinson’s disease
  61. Neurological disorders associated with glutamic acid decarboxylase antibodies: a Brazilian series
  62. Dopamine transporter imaging in clinically unclear cases of parkinsonism and the importance of Scans Without Evidence of Dopaminergic Deficit (SWEDDs)
  63. Isolated frontalis, corrugator and procerus dystonia: a blepharospasm variant
  64. Letters from Dom Pedro II to professor Brown-Séquard: imperial correspondence and neurophysiology
  65. Tourette's syndrome: from demonic possession and psychoanalysis to the discovery of gene
  66. Movement disorders emergencies: a review
  67. Jaw-opening oromandibular dystonia secondary to Wilson's Disease treated with botulinum toxin type A
  68. Electrophysiological characteristics in four patients from Brazil with stiff person syndrome
  69. Progression of Idiopathic Late Onset Cerebellar Ataxia (S12.006)
  70. Charcot's son, commander Jean-Baptiste Charcot: from neurology to "Pourquoi Pas?"
  71. An upper limb variant of RLS? Report of 2 cases
  72. Cerebellar ataxia as the first manifestation of Alexander's disease
  73. Inherited and Sporadic Ataxias
  74. Acquired cerebellar ataxia due to statin use
  75. Parakinesia brachialis oscitans: Report of three cases
  76. Essential tremor: phenotypes
  77. 2.13.3 ESSENTIAL TREMOR: PHENOTYPES
  78. 1.102 FACTORS ASSOCIATED WITH FUNCTIONAL PERFORMANCE IN ELDERLY PEOPLE WITH PARKINSON'S DISEASE
  79. 2.287 ROTIGOTINE-INDUCED NAIL DYSCHROMIA IN A PATIENT WITH PARKINSONS DISEASE
  80. Spinocerebellar ataxia type 10 – A review
  81. Lees' syndrome: a case series
  82. Neuroleptic malignant syndrome
  83. Electronystagmography findings in spinocerebellar ataxia type 3 (SCA3) and type 2 (SCA2)
  84. Spinocerebellar ataxia type 10: disproportionate cerebellar symptoms among at-risk subjects induced by small amounts of alcohol
  85. Botulinum toxin type A and cervical dystonia: a seven-year follow-up
  86. Wittgenstein, medicine and neuropsychiatry
  87. Américo Negrette and Huntington's disease
  88. Hyperintense basal ganglia on MR imaging in hematopoietic stem cell transplantation recipient
  89. Huntington's disease like phenotype: new data from Brazil and what we know between heaven and earth
  90. Historical aphasia cases: "Tan-tan", "Vot-vot", and "Cré nom!"
  91. Avaliação do processamento auditivo central em pacientes com doença de Parkinson
  92. Rotigotine-induced nail dyschromia in a patient with Parkinson disease
  93. New gene of spinocerebellar ataxia
  94. Cross-cultural influences on psychogenic movement disorders – A comparative review with a Brazilian series of 83 cases
  95. Botulinum toxin type-A effect as a preemptive treatment in a model of acute trigeminal pain: a pre-clinical double-blind and placebo-controlled study
  96. Wilson's disease in southern Brazil: a 40-year follow-up study
  97. Tremor in X-linked recessive spinal and bulbar muscular atrophy (Kennedy's disease)
  98. Coma scales: a historical review
  99. Stereotypies after herpetic encephalitis with bitemporal lesions
  100. Spinocerebellar ataxia type 10: Frequency of epilepsy in a large sample of Brazilian patients
  101. Olfactory heterogeneity in LRRK2 related Parkinsonism
  102. How many Babinski's signs are there?
  103. CORRELAÇÃO ENTRE A QUALIDADE DE VIDA DE CUIDADORES FAMILIARES E OS NÍVEIS DE INDEPENDÊNCIA FUNCIONAL DOS CUIDADOS
  104. Inactivation of hnRNP K by Expanded Intronic AUUCU Repeat Induces Apoptosis Via Translocation of PKCδ to Mitochondria in Spinocerebellar Ataxia 10
  105. The differential diagnoses of parkinsonism: Findings from a cohort of 1528 patients and a 10 years comparison in tertiary movement disorders clinics
  106. Homage: Professor J.W. Sander
  107. Botulinum neurotoxin type-A for primary stabbing headache: an open study
  108. Hemibalismo-hemicoreia em estado hiperglicêmico não cetótico: distúrbio do movimento associado ao diabetes melito
  109. Stiff person syndrome as the initial manifestation of systemic lupus erythematosus
  110. Video-EEG in the pursuit of documented coexistence of epileptic and psychogenic nonepileptic seizures: how long is too long? - a case report
  111. Spinocerebellar ataxias
  112. Spinocerebellar ataxias: microsatellite and allele frequency in unaffected and affected individuals
  113. P3.023 Parakinesia Brachialis Oscitans due to brainstem stroke. Report of two cases
  114. P3.134 Infectious causes of parkinsonism
  115. P1.080 Genetic mutations in ataxia–telangiectasia patients
  116. Singing-induced cervical dystonia
  117. Catamenial and oral contraceptive-induced exacerbation of chorea in chorea-acanthocytosis: Case report
  118. Cerebellar cryptococcoma simulating metastatic neoplasm
  119. Fulminant idiopathic intracranial hypertension in a pediatric patient following a minor head trauma
  120. Flunarizine and cinnarizine-induced parkinsonism: 25 years of de Melo-Souza's syndrome
  121. Attention deficit hyperactivity disorder and the behavior of “Che” Guevara
  122. Complex hyperkinetic movement disorders: an unusual presentation in multiple sclerosis
  123. Professor Charles David Marsden
  124. Did darwin have syncope caused by chagas' disease?
  125. Vestibular rehabilitation: clinical benefits to patients with Parkinson's disease
  126. Professor Karl-Axel Ekbom and restless legs syndrome
  127. Increased Frequency and Range of Sexual Behavior in a Patient with Parkinson's Disease After Use of Pramipexole: A Case Report
  128. Karl-Axel Ekbom and iron deficiency in restless legs syndrome
  129. Botulinum toxin type A in the treatment of lower-limb spasticity in children with cerebral palsy
  130. Progressive Ataxia, Palatal Tremor, and the Romberg Sign
  131. CTA/CTG expansions at the SCA 8 locus in multiple system atrophy
  132. Stiff-three limbs syndrome
  133. Spinocerebellar Degenerations in Japan
  134. Charcot's contribution to the study of Tourette's syndrome
  135. Huntington's disease-like 2 in Brazil-Report of 4 patients
  136. Unilateral pallidotomy in a patient with parkinsonism and G2019S LRRK2 mutation
  137. Professor Octávio de Silveira: the pioneer of neurology in the State of Paraná
  138. Pressure ulcers and Charcot's definitions: report on two cases
  139. Cerebellar ataxia in non-paraneoplastic Lambert–Eaton myasthenic syndrome
  140. Cerebellar ataxia, myoclonus, cervical lipomas, and MERRF syndrome. Case report
  141. Brazilian Academy of Neurology: first meeting: Curitiba, 1963
  142. Familial Behr syndrome-like phenotype with autosomal dominant inheritance
  143. Chorea due to gabapentin monotherapy in a not encephalopatic patient
  144. Cervical dystonia: clinical and therapeutic features in 85 patients
  145. Optic neuritis due to solvent abuse
  146. Spinocerebellar ataxia type 6 in Brazil
  147. Neurological complications of hematopoietic stem cell transplantation (HSCT): a retrospective study in a HSCT center in Brazil
  148. Cognitive function assessment in idiopathic Parkinson's disease
  149. The history of spinocerebellar ataxia type 10 in Brazil: travels of a gene
  150. A novel missense mutation pattern of the GCH1 gene in dopa-responsive dystonia
  151. The G2019S LRRK2 mutation in Brazilian patients with Parkinson's disease: Phenotype in monozygotic twins
  152. Uncontrolled headache induced by oxcarbazepine
  153. Trigeminal sensory neuropathy and facial contact dermatitis due to Anthurium sp
  154. Chronic inflammatory demyelinating polyradiculoneuropathy in chronic graft-versus-host disease following allogeneic hematopoietic stem cell transplantation: case report
  155. Non-choreic movement disorders as initial manifestations of Huntington's disease
  156. Reduced Penetrance in a Brazilian Family With Spinocerebellar Ataxia Type 10
  157. Early-onset Parkinson's disease and depression
  158. Comparison study of executive functions in Parkinson's disease and degenerative cerebellar disease's patients
  159. Intrathecal baclofen for spasticity in primary lateral sclerosis
  160. Little-known scientific contributions of J-M Charcot
  161. Worsening of motor symptoms and gynecomastia during spironolactone treatment in a patient with Parkinson's disease and congestive heart failure
  162. Deletion of theparkinandPACRGgene promoter in early-onset parkinsonism
  163. 1.258 Singing-induced cervical dystonia
  164. 1.259 Frontalis, corrugator and procerus dystonia: A blepharospasm variant?
  165. 3.239 Unilateral pallidotomy in a patient with parkinsonism and G2019S LRRK2 mutation
  166. 3.403 Activity and participation on Parkinson's disease
  167. 1.109 Early-onset Parkinson's disease and depression
  168. Botulinum-A toxin in the treatment of painful post-stroke nocturnal paroxysmal dystonia triggered by periodic limb movements of sleep: case report
  169. Topiramate-induced psychosis: report of two cases
  170. The Brazilian contribution to the study of neurocysticercosis: Moses and Lange’s role in cerebrospinal fluid diagnosis
  171. Atypical parkinsonism and SCA8
  172. Movement disorders in Latin America
  173. Bone marrow transplantation in patients with storage diseases: a developing country experience
  174. Síndrome da cabeça caída em doença do neurônio motor
  175. Clinical and genetic study of a Brazilian family with spastic paraplegia (SPG6 locus)
  176. Rosalie: the brazilian female monkey of Charcot
  177. Movement disorders secondary to long-term treatment with cyclosporine A
  178. Frequency of obsessive and compulsive symptoms in patients with blepharospasm and hemifacial spasm
  179. Kennedy's disease phenotype with positive genetic study for Kugelberg-Welander's disease: case report
  180. Status dystonicus: study of five cases
  181. Parkinsonism associated with neurocysticercosis
  182. Leber's hereditary optic neuropathy: case report and literature review
  183. Cerebrotendinous xanthomatosis: report of two Brazilian brothers
  184. Hypothyroidism and Parkinson's disease
  185. Hemorrhagic stroke after naphazoline exposition: case report
  186. Parkinson's disease and thyroid dysfunction
  187. Flunarizine and cinnarizine-induced parkinsonism: a historical and clinical analysis
  188. Carotid transient ischemic attacks presenting as limb-shaking syndrome: report of two cases
  189. A família Drew de Walworth: um século após a avaliação inicial finalmente o diagnóstico doença de Machado-Joseph
  190. Uso do propranolol de ação prolongada em 40 pacientes com tremor essencial e virgens de tratamento: um ensaio clínico não controlado
  191. Botulinum toxin for treatment of Frey's syndrome: report of two cases
  192. Síndrome das pernas inquietas com herança autossômica dominante piorada pelo uso de mirtazapina: relato de caso
  193. Mielinólise pontina central e extra-pontina em paciente alcoolista sem distúrbios hidro-eletrolíticos: relato de caso
  194. Exclusion of the Nurr1 gene in autosomal recessive Parkinson's disease
  195. Parkinsonian syndrome induced by amlodipine: Case Report
  196. The uncinated crisis of George Gershwin
  197. Achados tomográficos em 1000 pacientes consecutivos com antecedentes de crises epilépticas
  198. Hemimasticatory spasm treated with botulinum toxin: case report
  199. Machado-Joseph disease versus hereditary spastic paraplegia: case report
  200. Cerebelite aguda causada por vírus Epstein-Barr: relato de caso
  201. Tics and Tourette syndrome: clinical evaluation of 44 cases
  202. Hereditary spastic paraplegia associated with thin corpus callosum
  203. The G209A mutation in the alpha-synuclein gene in Brazilian families with Parkinson's disease
  204. Reversible posterior leucoencephalopathy syndrome associated with bone marrow transplantation
  205. As contribuições de Charcot e de Marsden para o desenvolvimento dos distúrbios do movimento nos séculos XIX e XX
  206. Bilateral pallidotomy for generalized dystonia
  207. Charcot and Brazil
  208. Multiple sclerosis: report on 200 cases from Curitiba, Southern Brazil and comparison with other Brazilian series
  209. Neuro-Behçet: report of three clinically distinct cases
  210. Worsening of parkinsonism after the use of veralipride for treatment of menopause: case report
  211. O uso da toxina botulínica no tratamento da distonia laríngea (disfonia espasmódica): estudo preliminar com doze pacientes
  212. Huntington disease: DNA analysis in brazilian population
  213. Hemibalismo: relato de oito casos
  214. The Rolex sign - first manifestation of Parkinson's disease: case report
  215. Palatal myoclonus: report of two cases
  216. Doença de Lafora e distúrbios do movimento: relato de dois casos
  217. Hemicoréia-hemibalismo associado a granuloma criptocócico em paciente com SIDA: relato de caso
  218. Mudança no padrão biológico da migrânea com aura após a utilização da tetrabenazina: relato de caso
  219. Muscle involvement in leprosy: study of the anterior tibial muscle in 40 patients
  220. Doenças de Dupuytren e de Ledderhose associadas ao uso crônico de anticonvulsivantes: relato de caso
  221. Professor Antonio Austregésilo: o pioneiro da neurologia e do estudo dos distúrbios do movimento no Brasil
  222. Aspectos clínicos e terapêuticos em 135 pacientes com distonia: experiência do Setor de Distúrbios do Movimento do Hospital de Clínicas da Universidade Federal do Paraná
  223. Malformação de Chiari tipo I: relato de dois casos com apresentações clínicas pouco usuais
  224. Síndrome de Isaacs: relato de três casos
  225. Oclusão bilateral das artérias carótidas internas, sífilis meningovascular e SIDA: relato de caso
  226. Tratamento da espasticidade: uma atualização
  227. Neurofisiologia álgica na irritação tentorial: descrição de um caso secundário a meduloblastoma
  228. O papel de Charcot na doença de Parkinson
  229. Molecular characteristics of Machado-Joseph disease mutation in 25 newly described Brazilian families
  230. Ataxias cerebelares hereditárias: do martelo ao gen
  231. Frequency of the different mutations causing spinocerebellar ataxia (SCA1, SCA2, MJD/SCA3 and DRPLA) in a large group of Brazilian patients
  232. Doença de Machado-Joseph descrição de cinco membros de uma família
  233. Arterial Graft Reconstruction in an Aneurysm of the Middle Cerebral Artery
  234. Síndrome de Isaacs: relato de um caso
  235. Miastenia grave: avaliação clinica e terapêutica de 55 casos
  236. Movement disorders in endocrinological diseases