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3. Current practice in diagnostic genetic testing of the epilepsies.

4. Precision medicine for genetic epilepsy on the horizon: Recent advances, present challenges, and suggestions for continued progress

5. Ictal Electroencephalographic Characteristics of Nodding Syndrome: A Comparative Case‐Series from South Sudan, Tanzania, and Uganda

6. Missense variants in ANO4 cause sporadic encephalopathic or familial epilepsy with evidence for a dominant-negative effect

10. Distinct gene-set burden patterns underlie common generalized and focal epilepsies.

11. Shared genetic basis between genetic generalized epilepsy and background electroencephalographic oscillations

12. Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia

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

14. Polygenic burden in focal and generalized epilepsies

17. Optimizing clinical interpretability of functional evidence in epilepsy-related ion channel variants

18. Clinical spectrum of STX1B-related epileptic disorders.

20. Electrophysiological signatures of a developmental delay in a stem cell model ofKCNQ2developmental and epileptic encephalopathy

21. Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy

24. Differential excitatory vs inhibitory SCN expression at single cell level regulates brain sodium channel function in neurodevelopmental disorders

26. Complex biophysical changes and reduced neuronal firing in anSCN8Avariant associated with developmental delay and epilepsy

32. De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies

33. Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy

34. Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study

35. Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy

39. Hyperexcitable interneurons trigger cortical spreading depression in an Scn1a migraine model

42. Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia

43. Bi-allelic PRRT2variants may predispose to Self-limited Familial Infantile Epilepsy

44. Homozygous mutation in TXNRD1 is associated with genetic generalized epilepsy

46. GAA-FGF14 ataxia (SCA27B): phenotypic profile, natural history progression and 4-aminopyridine treatment response.

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

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