12 results on '"Schottlaender Lucia"'
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2. Feeding difficulties in children and adolescents with spinal muscular atrophy type 2
3. Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification
4. LRP10 in α-synucleinopathies
5. Deconstructing Fahr's disease/syndrome of brain calcification in the era of new genes
6. Analysis of the prion protein gene in multiple system atrophy
7. Erratum to “The analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonism” [Neurobiol. Aging 36 (2015) 1221.e1–1221.e6]
8. The analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonism
9. Diagnostic clues and manifesting carriers in fukutin-related protein (FKRP) limb-girdle muscular dystrophy
10. White matter relapsing remitting disease: “Susac’s syndrome”—An underdiagnosed entity
11. Mutations in GBA2 Cause Autosomal-Recessive Cerebellar Ataxia with Spasticity
12. High frequency of the expanded C9ORF72 hexanucleotide repeat in familial and sporadic Greek ALS patients
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