Found: 4
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Rapidly progressive spastic paraplegia due to hyperhomocysteinemia in child with MTHFR gene mutation and mitochondrial Complex I deficiency: A rare association.
- Published in:
- Journal of Pediatric Neurosciences, 2021, v. 16, n. 2, p. 153, doi. 10.4103/jpn.JPN_96_20
- By:
- Publication type:
- Article
Parkinsonism, Olivary Hypertrophy and Cerebellar Atrophy with TTC19 Gene Mutation.
- Published in:
- 2021
- By:
- Publication type:
- Case Study
Upbeat Nystagmus in Late Onset Cerebellar Ataxia: Think of Anti-Glutamate Decarboxylase 65 Antibody-Associated Cerebellar Ataxia.
- Published in:
- 2021
- By:
- Publication type:
- Literary Criticism
Autosomal Dominant Cerebral Small Vessel Disease in HTRA1 Gene Mutation.
- Published in:
- 2021
- By:
- Publication type:
- Letter to the Editor