24 results on '"Camu, William"'
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2. Teriflunomide‐induced psoriasiform changes of fingernails: a new example of paradoxical side effect?
3. Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis
4. A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories
5. Switching From Natalizumab to Fingolimod in Multiple Sclerosis: A French Prospective Study
6. A phase II−III trial of olesoxime in subjects with amyotrophic lateral sclerosis
7. A Rare Motor Neuron Deleterious Missense Mutation in the DPYSL3 (CRMP4) Gene is Associated with ALS
8. Investigating the contribution of VAPB/ALS8 loss of function in amyotrophic lateral sclerosis
9. Subcutaneous IFN-β1a to treat relapsing–remitting multiple sclerosis
10. C9orf72 Hexanucleotide Repeat Expansions as the Causative Mutation for Chromosome 9p21–Linked Amyotrophic Lateral Sclerosis and Frontotemporal Dementia
11. Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes
12. Association of Long ATXN2 CAG Repeat Sizes With Increased Risk of Amyotrophic Lateral Sclerosis
13. Resequencing of 29 Candidate Genes in Patients With Familial and Sporadic Amyotrophic Lateral Sclerosis
14. TAR DNA-binding protein 43 (TDP-43) regulates stress granule dynamics via differential regulation of G3BP and TIA-1
15. SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations
16. Four familial ALS pedigrees discordant for two SOD1 mutations: are all SOD1 mutations pathogenic?
17. Analysis of the UNC13A Gene as a Risk Factor for Sporadic Amyotrophic Lateral Sclerosis
18. A Mutation that Creates a Pseudoexon in SOD1 Causes Familial ALS
19. Mutations of the ANG Gene in French Patients With Sporadic Amyotrophic Lateral Sclerosis
20. Three Families With Amyotrophic Lateral Sclerosis and Frontotemporal Dementia With Evidence of Linkage to Chromosome 9p
21. Mutation Screening of the ALS2 Gene in Sporadic and Familial Amyotrophic Lateral Sclerosis
22. A Clustering of Conjugal Amyotrophic Lateral Sclerosis in Southeastern France
23. Bullous Pemphigoid and Amyotrophic Lateral Sclerosis: A New Clue for Understanding the Bullous Disease?
24. Acute hepatitis after riluzole administration
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