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536 results on '"Macaya, Alfons"'

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1. Child-to-adult transition: a survey of current practices within the European Reference Network for Rare Neurological Diseases (ERN-RND)

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

4. ClinPrior: an algorithm for diagnosis and novel gene discovery by network-based prioritization

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

6. Developmental outcome of electroencephalographic findings in SYNGAP1 encephalopathy

8. Clinical phenotypes of infantile onset CACNA1A-related disorder

9. Clinical and Molecular Spectrum of Autosomal Recessive CA8‐Related Cerebellar Ataxia.

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

11. Clinical course of sly syndrome (mucopolysaccharidosis type VII)

12. Correction to: A guide to writing systematic reviews of rare disease treatments to generate FAIRcompliant datasets: building a Treatabolome

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

17. Epilepsy with migrating focal seizures: KCNT1 mutation hotspots and phenotype variability

20. A guide to writing systematic reviews of rare disease treatments to generate FAIR-compliant datasets: building a Treatabolome

24. Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome

25. Headache and Vomiting in an 8-Year-Old Girl

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

27. The Expanding Phenotypical Spectrum of WARS2-Related Disorder: Four Novel Cases with a Common Recurrent Variant

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

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

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

32. AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders

34. Preterm Birth and Early Life Environmental Factors: Neuropsychological Profiles at Adolescence and Young Adulthood

35. Longitudinal volumetric and 2D assessment of cerebellar atrophy in a large cohort of children with phosphomannomutase deficiency (PMM2-CDG)

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

38. TSC-associated neuropsychiatric disorders (TAND): findings from the TOSCA natural history study

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

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

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

47. Diagnosis of Genetic White Matter Disorders by Singleton Whole-Exome and Genome Sequencing Using Interactome-Driven Prioritization

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