Search

Your search keyword '"Davoine, C. -S."' showing total 19 results

Search Constraints

Start Over You searched for: Author "Davoine, C. -S." Remove constraint Author: "Davoine, C. -S."
19 results on '"Davoine, C. -S."'

Search Results

1. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

2. Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics, (2021), 29, 9, (1332-1336), 10.1038/s41431-021-00901-1)

3. Efficacy of exome-targeted capture sequencing to detect mutations in known cerebellar ataxia genes

5. Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2

6. Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14q.

7. Loss of paraplegin drives spasticity rather than ataxia in SPG7: A European cohort analysis of 238 patients

8. Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2

9. Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related Autosomal Recessive Ectodermal Dysplasia 14

10. Solving patients with rare diseases through programmatic reanalysis of genome-phenome data

11. Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

12. Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment

13. Schwartz-Jampel syndrome and perlecan deficiency.

14. Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia).

15. Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia.

16. A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24-q34.

17. Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia.

18. A fine integrated map of the SPG4 locus excludes an expanded CAG repeat in chromosome 2p-linked autosomal dominant spastic paraplegia.

Catalog

Books, media, physical & digital resources