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2. Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals

3. Genetische Diagnostik

4. Genetische Epilepsien

7. Could the 2017 ILAE and the four-dimensional epilepsy classifications be merged to a new “Integrated Epilepsy Classification”?

11. NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns

19. The phenotypic and genotypic spectrum of epilepsy and intellectual disability in adults: Implications for genetic testing

23. Natural History Study of STXBP1-Developmental and Epileptic Encephalopathy Into Adulthood

25. Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals

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

28. Heterozygous variants in KCNC2 cause a broad spectrum of epilepsy phenotypes associated with characteristic functional alterations 2021.05.21.21257099

29. Heterozygous variants in KCNC2 cause a broad spectrum of epilepsy phenotypes associated with characteristic functional alterations 2021.05.21.21257099

30. Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals

31. 16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy

33. Heterozygous variants in KCNC2 cause a broad spectrum of epilepsy phenotypes associated with characteristic functional alterations

35. Epilepsy Subtype-Specific Copy Number Burden Observed in a Genome-Wide Study of 17 458 Subjects

36. Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A

37. Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32

38. The LaLiMo Trial: lamotrigine compared with levetiracetam in the initial 26 weeks of monotherapy for focal and generalised epilepsy—an open-label, prospective, randomised controlled multicenter study

39. From theory to practice: Critical points in the 2017 ILAE classification of epileptic seizures and epilepsies

41. Intranasal midazolam as first‐line inhospital treatment for status epilepticus: a pharmaco‐EEG cohort study

42. Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3

43. Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3

44. Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals

45. Efficacy, retention, and tolerability of Brivaracetam in patients with epileptic encephalopathies : a multicenter cohort study from Germany

49. Seizure Management and Prescription Patterns of Anticonvulsants in Dravet Syndrome: A Multicenter Cohort Study from Germany and Review of Literature

50. Seizure management and prescription patterns of anticonvulsants in Dravet syndrome: A multicenter cohort study from Germany and review of literature

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