28 results on '"Hübers, Annemarie"'
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2. Publisher Correction: Altered perivascular fibroblast activity precedes ALS disease onset
3. Case Series of Acute Peripheral Neuropathies in Individuals Who Received COVID-19 Vaccination
4. Hot-spot KIF5A mutations cause familial ALS
5. sj-docx-1-taj-10.1177_20406223221109480 – Supplemental material for Relaxation-weighted 23Na magnetic resonance imaging maps regional patterns of abnormal sodium concentrations in amyotrophic lateral sclerosis
6. sj-docx-2-taj-10.1177_20406223221109480 – Supplemental material for Relaxation-weighted 23Na magnetic resonance imaging maps regional patterns of abnormal sodium concentrations in amyotrophic lateral sclerosis
7. Relaxation-weighted 23Na magnetic resonance imaging maps regional patterns of abnormal sodium concentrations in amyotrophic lateral sclerosis
8. Are nerve conduction studies altered in functional neurological disorders?
9. NEK1 mutations in familial amyotrophic lateral sclerosis
10. Screening for CHCHD10 mutations in a large cohort of sporadic ALS patients: no evidence for pathogenicity of the p.P34S variant
11. Management of transthyretin amyloidosis
12. Relaxation-weighted 23 Na magnetic resonance imaging maps regional patterns of abnormal sodium concentrations in amyotrophic lateral sclerosis.
13. Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease
14. The ipsilateral silent period: an early diagnostic marker of callosal disconnection in ALS
15. Relaxation-weighted 23Na magnetic resonance imaging maps regional patterns of abnormal sodium concentrations in amyotrophic lateral sclerosis.
16. Motor callosal disconnection in early relapsing-remitting multiple sclerosis
17. Mutation of the WARS2 Gene as the Cause of a Severe Hyperkinetic Movement Disorder
18. Phenotypes and malignancy risk of different FUS mutations in genetic amyotrophic lateral sclerosis
19. Acute DWI Reductions In Patients After Single Epileptic Seizures - More Common Than Assumed
20. Comprehensive analysis of the mutation spectrum in 301 German ALS families
21. NEK1mutations in familial amyotrophic lateral sclerosis
22. Mutation of the WARS2 Gene as the Cause of a Severe Hyperkinetic Movement Disorder.
23. Screening forCHCHD10mutations in a large cohort of sporadic ALS patients: no evidence for pathogenicity of the p.P34S variant: Table 1
24. Motor callosal disconnection in early relapsing-remitting multiple sclerosis
25. Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations.
26. Management of transthyretin amyloidosis.
27. Expert recommendation from the Swiss Amyloidosis Network (SAN) for systemic AL-amyloidosis.
28. Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations.
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