14 results on '"Pfeffer G"'
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2. Update on recent advances in amyotrophic lateral sclerosis
3. Aperiodic alternating nystagmus in adult-onset Alexander disease with a novel mutation
4. Co-occurrence of amyotrophic lateral sclerosis and Leber’s hereditary optic neuropathy: is mitochondrial dysfunction a modifier?
5. Unravelling the etiology of sporadic late-onset cerebellar ataxia in a cohort of 205 patients: a prospective study
6. Guillain–Barré-like syndrome: an uncommon feature of CASPR2 and LGI1 autoimmunity
7. Movement disorders associated with neuronal antibodies: a data-driven approach
8. Adult-onset mitochondrial movement disorders: a national picture from the Italian Network
9. Autosomal recessive adult onset ataxia
10. Mutations in MT-ATP6 are a frequent cause of adult-onset spinocerebellar ataxia
11. Neurophysiological and ophthalmological findings of SPG7-related spastic ataxia: a phenotype study in an Irish cohort
12. Whole-body muscle MRI of patients with MATR3-associated distal myopathy reveals a distinct pattern of muscular involvement and highlights the value of whole-body examination
13. Leber hereditary optic neuropathy plus dystonia, and transverse myelitis due to double mutations in MT-ND4 and MT-ND6
14. Non-motor symptoms are relevant and possibly treatable in hereditary spastic paraplegia type 4 (SPG4)
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