Congenital myasthenic syndrome in a cohort of patients with ‘double’ seronegative myasthenia gravis
Peripheral polyneuropathy from electrodiagnostic tests: a 10-year etiology and neurophysiology overview
Seventy years since the invention of the averaging technique in Neurophysiology: Tribute to George Duncan Dawson
Correlation between specific histological and electromyographic findings in neuromuscular disorders
Distrofia muscular de Duchenne em menina com translocação cromossômica
Biópsias de nervos periféricos: análise de 89 casos
Muscle biopsy correlated with electromyography: study of 100 cases
Miopatia por deficiência de succinato-citocromo-C-redutase: possível defeito no complexo II da cadeia respiratória
Distrofina na diferenciação das distrofias de duchenne e becker estudo imuno-histoquímico comparado com o estádio clínico, enzimas séricas e biópsia muscular
Miastenia grave tratamento clínico x cirúrgico
Hematomas intracerebral espontâneos estudo de 121 casos
Cognitive function assessment in idiopathic Parkinson's disease
Myasthenia gravis during pregnancy: what care should be taken?
Horner syndrome: tribute to Professor Horner on his 190th birthday
Somatosensory evoked potentials in clinical practice: a review
When should MELAS (Mitochondrial myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like episodes) be the diagnosis?
Diagnosis of limb-girdle muscular dystrophies in the molecular biology era: do clinical findings still matter?
Myasthenia gravis and thymus: long-term follow-up screening of thymectomized and non-thymectomized patients
Miopatia nemalinica: relato de um caso com estudo histoquimico e microscopia eletrônica
Miopatia por deficiência de carnitina-palmitil-transferase: relato de 2 casos com dosagens enzimáticas no tecido muscular