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1. Developmental dysfunction in a preclinical model of Kcnq2 developmental and epileptic encephalopathy

2. Experience of the first adult-focussed undiagnosed disease program in Australia (AHA-UDP): solving rare and puzzling genetic disorders is ageless

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3. RNA variant assessment using transactivation and transdifferentiation

4. Expanding genotype–phenotype correlations in FOXG1 syndrome: results from a patient registry

5. P305: Evaluation of the feasibility, diagnostic yield, and utility of rapid genome sequencing in infantile epilepsy (Gene-STEPS): An international pilot study

7. Generation of seven iPSC lines from peripheral blood mononuclear cells suitable to investigate Autism Spectrum Disorder

8. Comparing saliva and blood for the detection of mosaic genomic abnormalities that cause syndromic intellectual disability

9. Does long-term phenytoin have a place in Dravet syndrome?

11. Diverse genetic causes of polymicrogyria with epilepsy

13. The Epilepsy Genetics Initiative: Systematic reanalysis of diagnostic exomes increases yield

16. Guidelines on the Diagnosis, Clinical Assessments, Treatment and Management for CLN2 Disease Patients

17. De novo variants in the alternative exon 5 of SCN8A cause epileptic encephalopathy

18. Assessing the genetic association between vitamin B6 metabolism and genetic generalized epilepsy

19. The 'maternal effect' on epilepsy risk: Analysis of familial epilepsies and reassessment of prior evidence

20. Intestinal-Cell Kinase and Juvenile Myoclonic Epilepsy. Reply

21. Epilepsy

22. Phenotypic and imaging features of FLNA-negative patients with bilateral periventricular nodular heterotopia and epilepsy

23. Racial and ethnic differences in epilepsy classification among probands in the Epilepsy Phenome/Genome Project (EPGP)

25. Febrile seizures

27. Quinidine in the treatment of KCNT1-positive epilepsies

28. The epilepsy phenome/genome project

29. Corrections

30. Epi4K: gene discovery in 4,000 genomes

31. Milder phenotypes of glucose transporter type 1 deficiency syndrome

33. Erratum

36. Clinical spectrum of early onset epileptic encephalopathies associated with STXBP1 mutations