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47 results on '"Marcé‐Grau, Anna"'

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1. De novo KCNA6 variants with attenuated KV1.6 channel deactivation in patients with epilepsy

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

4. Delineating the motor phenotype of SGCE-myoclonus dystonia syndrome

5. The genetic etiology in cerebral palsy mimics: The results from a Greek tertiary care center

7. Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14

8. Twist exome capture allows for lower average sequence coverage in clinical exome sequencing

9. Solving unsolved rare neurological diseases-a Solve-RD viewpoint

10. The Genetic Landscape of Complex Childhood‐Onset Hyperkinetic Movement Disorders

11. Early recognition of SGCE ‐myoclonus–dystonia in children

12. Systematic Collaborative Reanalysis of Genomic Data Improves Diagnostic Yield in Neurologic Rare Diseases

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

14. Early recognition of SGCE‐myoclonus–dystonia in children.

15. De novo KCNA6 variants with attenuated KV1.6 channel deactivation in patients with epilepsy.

17. Rare functional genetic variants in COL7A1, COL6A5, COL1A2 and COL5A2 frequently occur in Chiari Malformation Type 1

18. Biallelic PI4KA variants cause a novel neurodevelopmental syndrome with hypomyelinating leukodystrophy

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

21. Correction: Solving unsolved rare neurological diseases : A Solve-RD viewpoint

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

25. Impaired proteasome activity and neurodegeneration with brain iron accumulation in FBXO7 defect

27. Delineating the neurological phenotype in children with defects in the ECHS1 or HIBCH gene

28. GRP94 promotes brain metastasis by engaging pro-survival autophagy

29. Seqüenciació exòmica en l’estudi molecular de les encefalopaties epilèptiques d’inici precoç

33. Delineating the neurological phenotype in children with defects in the ECHS1 or HIBCH gene.

35. A Single Amino Acid Deletion (ΔF1502) in the S6 Segment of Ca2.1 Domain III Associated with Congenital Ataxia Increases Channel Activity and Promotes Ca 2+ Influx

36. Homomeric Kv7.2 current suppression is a common feature in KCNQ2 epileptic encephalopathy.

37. Secondary coenzyme Q 10 deficiencies in oxidative phosphorylation (OXPHOS) and non-OXPHOS disorders

39. A Single Amino Acid Deletion (ΔF1502) in the S6 Segment of CaV2.1 Domain III Associated with Congenital Ataxia Increases Channel Activity and Promotes Ca2+ Influx

41. A Single Amino Acid Deletion (ΔF1502) in the S6 Segment of CaV2.1 Domain III Associated with Congenital Ataxia Increases Channel Activity and Promotes Ca2+ Influx.

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

43. Childhood onset progressive myoclonic dystonia due to a de novo KCTD17 splicing mutation.

44. De novo KCNA6 variants with attenuated K V 1.6 channel deactivation in patients with epilepsy.

45. Impaired proteasome activity and neurodegeneration with brain iron accumulation in FBXO7 defect.

46. GRP94 promotes brain metastasis by engaging pro-survival autophagy.

47. Secondary coenzyme Q10 deficiencies in oxidative phosphorylation (OXPHOS) and non-OXPHOS disorders.

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