Rodrigues B. De Paiva
Sao Paulo, SP, Brazil
Last Updated: 09/26/2026
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Found 11 publications
The clinical, radiological and genetic spectrum AARS2-related leukoencephalopathy: a case series of 15 patients and review of the literature.
Journal: Journal of neurology
Published: April 27, 2026
Hematopoietic Stem Cell Transplantation in an International Cohort of Colony Stimulating Factor-1 Receptor (CSF1R)-Related Disorder.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: April 18, 2025
Pregabalin Responsive Tongue and Arm Tremor after Guillain Barré Syndrome.
Journal: Movement disorders clinical practice
Published: June 24, 2023
Marked neuropsychiatric involvement and dysmorphic features in nemaline myopathy.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: April 23, 2023
Aseptic meningitis in Fabry disease due to a novel GLA variant: an expanded phenotype?
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: July 30, 2022
A rare cause of monogenic cerebral small vessel disease and stroke: Cathepsin A-related arteriopathy with strokes and leukoencephalopathy (CARASAL).
Journal: Journal of neurology
Published: July 08, 2022
Mystery solved after 23 years: M syndrome is PIGT-associated multiple congenital anomalies-hypotonia-seizures syndrome 3.
Journal: American journal of medical genetics. Part A
Published: June 29, 2022
Moyamoya associated with Turner syndrome in a patient with type 2 spinocerebellar ataxia-Occam's razor or Hickam's dictum: a case report.
Journal: BMC neurology
Published: January 27, 2022
Adult Leukodystrophies: A Step-by-Step Diagnostic Approach.
Journal: Radiographics : a review publication of the Radiological Society of North America, Inc
Published: January 09, 2019
PUS3 mutations are associated with intellectual disability, leukoencephalopathy, and nephropathy.
Journal: Neurology. Genetics
Published: August 13, 2018
A novel GFAP mutation in a type II (late-onset) Alexander disease patient.
Journal: Journal of neurology
Published: January 14, 2016
Showing 1-11 of 11
Last Updated: 09/26/2026