Pages that link to "Q30500546"
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The following pages link to Holger Lerche (Q30500546):
Displaying 38 items.
- De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome (Q24600816) (← links)
- Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1. (Q24648494) (← links)
- Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies (Q28213203) (← links)
- Molecular analysis of the A322D mutation in the GABA receptor alpha-subunit causing juvenile myoclonic epilepsy (Q28262624) (← links)
- Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies (Q28647874) (← links)
- Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32. (Q29417109) (← links)
- GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak (Q30481800) (← links)
- Axon initial segment dysfunction in a mouse model of genetic epilepsy with febrile seizures plus (Q30495760) (← links)
- Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies (Q33569995) (← links)
- Genetic testing in the epilepsies--report of the ILAE Genetics Commission (Q33794130) (← links)
- 15q13.3 microdeletions increase risk of idiopathic generalized epilepsy (Q34519312) (← links)
- Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A. (Q37200320) (← links)
- 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 (Q38471476) (← links)
- Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders. (Q38853247) (← links)
- Phenotypic spectrum of GABRA1: From generalized epilepsies to severe epileptic encephalopathies. (Q39493334) (← links)
- Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies (Q41543882) (← links)
- Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1. (Q43268196) (← links)
- Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy (Q46405759) (← links)
- Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy (Q46499520) (← links)
- Gain-of-function HCN2 variants in genetic epilepsy. (Q47590313) (← links)
- Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery (Q47639772) (← links)
- Mutations in GABRB3: From febrile seizures to epileptic encephalopathies. (Q47778090) (← links)
- Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes (Q47810400) (← links)
- Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation (Q47938595) (← links)
- Rare variants in γ-aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromes (Q48304242) (← links)
- 16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy (Q48710057) (← links)
- Exploration of the genetic architecture of idiopathic generalized epilepsies. (Q52929662) (← links)
- Analysis of shared heritability in common disorders of the brain (Q55128222) (← links)
- Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study (Q57573940) (← links)
- Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies (Q57905570) (← links)
- Reply (Q59591791) (← links)
- Clinical spectrum of STX1B-related epileptic disorders. (Q64948892) (← links)
- Intestinal-Cell Kinase and Juvenile Myoclonic Epilepsy (Q68446042) (← links)
- (Q98499112) (redirect page) (← links)
- Predicting functional effects of missense variants in voltage-gated sodium and calcium channels (Q98499117) (← links)
- Drug-resistant epilepsy - time to target mechanisms (Q100465339) (← links)
- Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With <i>KCNC2</i> Pathogenic Variants (Q112559770) (← links)
- Wikidata:University of Tübingen/Listeria/UTübingen employees (born after 1951 or unknown) (← links | edit)