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Your search keyword '"De Septenville A"' showing total 21 results

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21 results on '"De Septenville A"'

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1. Higher-order connections between stereotyped subsets

2. Immunoglobulin gene analysis in chronic lymphocytic leukemia in the era of next generation sequencing

3. Immunoglobulin Gene Mutational Status Assessment by Next Generation Sequencing in Chronic Lymphocytic Leukemia

4. [Watch out for a second train]

5. Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation

6. Reply: Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?

7. TBK1 mutation frequencies in French frontotemporal dementia and amyotrophic lateral sclerosis cohorts

8. Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis

9. Posterior cortical atrophy as an extreme phenotype of GRN mutations

10. Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis

11. Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?

12. Extensive white matter involvement in patients with frontotemporal lobar degeneration: think progranulin

13. Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease

14. A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement

15. Partial deletions of the GRN gene are a cause of frontotemporal lobar degeneration

16. Homozygous TREM2 mutation in a family with atypical frontotemporal dementia

17. SQSTM1 mutations in French patients with frontotemporal dementia or frontotemporal dementia with amyotrophic lateral sclerosis

18. TREM2 mutations are rare in a French cohort of patients with frontotemporal dementia

19. Genetic analysis of matrin 3 gene in French amyotrophic lateral sclerosis patients and frontotemporal lobar degeneration with amyotrophic lateral sclerosis patients

20. Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients

21. A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement

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