15 results on '"Schottlaender Lucia"'
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2. Feeding difficulties in children and adolescents with spinal muscular atrophy type 2
3. Deconstructing Fahr's disease/syndrome of brain calcification in the era of new genes
4. Chapter 12 - Stroke genetics
5. White matter relapsing remitting disease: “Susac’s syndrome”—An underdiagnosed entity
6. Contributors
7. Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification
8. Diagnostic clues and manifesting carriers in fukutin-related protein (FKRP) limb-girdle muscular dystrophy
9. Mutations in GBA2 Cause Autosomal-Recessive Cerebellar Ataxia with Spasticity
10. LRP10 in α-synucleinopathies
11. Analysis of the prion protein gene in multiple system atrophy
12. 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]
13. The analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonism
14. Nueva mutación en SPG11 en una paciente con paraplejía espástica hereditaria complicada: hallazgos clínicos-electrofisiológicos y moleculares
15. Síndrome de Susac. Actualización
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