About: Karl Martin Klein

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researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) researcher (en) 연구원 (ko) 研究者 (ja) araştırmacı (tr) wetenschapper (nl) дослідник (uk) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy)
rdfs:label	Karl Martin Klein (en) Karl Martin Klein (es) Karl Martin Klein (nl) Karl Martin Klein (sl) Karl Martin Klein (ast) كارل مارتن كلاين (ar)
skos:prefLabel	Karl Martin Klein (en) Karl Martin Klein (es) Karl Martin Klein (nl) Karl Martin Klein (sl) Karl Martin Klein (ast) كارل مارتن كلاين (ar)
name	Karl Martin Klein (en) Karl Martin Klein (es) Karl Martin Klein (nl) Karl Martin Klein (sl) Karl Martin Klein (ast) كارل مارتن كلاين (ar)
given name	wds:Q55711787-92EB8CA7-9335-4888-AB04-45C6C9978F6F
given name	Karl
instance of	wds:Q55711787-5ECEC25E-B99B-4BCB-A296-F46A59ABC7DB
instance of	Homo sapiens
Loop ID	wds:Q55711787-C53A8BE1-7815-42DF-9ECE-8CEC2E26A530
Loop ID	459381
occupation	wds:Q55711787-A6EFFEF4-5BD8-45D8-BD76-095F1282B19A
employer	wds:Q55711787-377f08a2-4d08-216e-9341-812f4c098f39 wds:Q55711787-532f9da5-4e58-1440-ef5c-e895367a3065
sex or gender	wds:Q55711787-86DD2A31-F5E9-4D9B-8160-384B4301B431
family name	wds:Q55711787-14EC9321-B79D-4E1D-A4D5-6397BD1EB7E4
occupation	researcher
employer	Goethe University Frankfurt University of Marburg
sex or gender	male
family name	Klein
ORCID iD	wds:Q55711787-71146407-CCDA-4DE2-A626-3A5278325F44
ORCID iD	https://orcid.org/0000-0002-6654-1665
ORCID iD	0000-0002-6654-1665
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q55711787
is author of	15q13.3 microdeletions increase risk of idiopathic generalized epilepsy Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies A distinctive seizure type in patients with CDKL5 mutations: Hypermotor-tonic-spasms sequence A commonSCN1Asplice-site polymorphism modifies the effect of carbamazepine on cortical excitability-A pharmacogenetic transcranial magnetic stimulation study Autosomal dominant vasovagal syncope: clinical features and linkage to chromosome 15q26. Mutations in DEPDC5 cause familial focal epilepsy with variable foci Phenotypic spectrum of GABRA1: From generalized epilepsies to severe epileptic encephalopathies. Familial focal epilepsy with variable foci mapped to chromosome 22q12: expansion of the phenotypic spectrum 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 Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies Postmarketing experience with brivaracetam in the treatment of epilepsies: A multicenter cohort study from Germany. Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients. [Brivaracetam for add-on treatment in focal epilepsy]. Brivaracetam in the treatment of focal and idiopathic generalized epilepsies and of status epilepticus. Trends in resource utilization and prescription of anticonvulsants for patients with active epilepsy in Germany from 2003 to 2013 — A ten-year overview Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies The phenotypic spectrum of ARHGEF9 includes intellectual disability, focal epilepsy and febrile seizures. Neurodevelopmental Disorders Caused by De Novo Variants in KCNB1 Genotypes and Phenotypes. The ClinGen Epilepsy Gene Curation Expert Panel-Bridging the divide between clinical domain knowledge and formal gene curation criteria Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study Sustained seizure remission on perampanel in progressive myoclonic epilepsy (Lafora disease). Evidence for genetic factors in vasovagal syncope: a twin-family study Genetics of vasovagal syncope Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2-2q11.2. Precision medicine in genetic epilepsies: break of dawn? Personalized translational epilepsy research - Novel approaches and future perspectives: Part I: Clinical and network analysis approaches. Personalized translational epilepsy research - Novel approaches and future perspectives: Part II: Experimental and translational approaches. Non-invasive EEG evaluation in epilepsy diagnosis. Burden-of-illness and cost-driving factors in Dravet syndrome patients and carers: A prospective, multicenter study from Germany The role of mTOR inhibitors in preventing epileptogenesis in patients with TSC: Current evidence and future perspectives Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With <i>KCNC2</i> Pathogenic Variants Autosomal dominant epilepsy with auditory features: a new LGI1 family including a phenocopy with cortical dysplasia. Prescribing practice of pregabalin/gabapentin in pain therapy: an evaluation of German claim data Efficacy, Retention, and Tolerability of Brivaracetam in Patients With Epileptic Encephalopathies: A Multicenter Cohort Study From Germany Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2 Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3 Eslicarbazepine acetate as a therapeutic option in a patient with carbamazepine-induced rash and HLA-A*31:01. New aspects in the field of epilepsy Use of Emergency Medication in Adult Patients with Epilepsy: A Multicentre Cohort Study from Germany Invasive EEG-electrodes in presurgical evaluation of epilepsies: Systematic analysis of implantation-, video-EEG-monitoring- and explantation-related complications, and review of literature Primary care electronic medical records can be used to predict risk and identify potentially modifiable factors for early and late death in adult onset epilepsy The phenotypic spectrum of KCNT1: a new family with variable epilepsy syndromes including mild focal epilepsy Sleep but not hyperventilation increases the sensitivity of the EEG in patients with temporal lobe epilepsy. Intravenous lacosamide for treatment of absence status epilepticus in genetic generalized epilepsy: A case report and review of literature.
is author of	wds:Q33162665-64CE8710-DB4E-4E07-B760-22CDD64B5666 wds:Q38471476-D5886077-70EB-4860-AB8A-E6C78F17277E wds:Q57926706-0A391BAC-6368-47E5-BC25-44AA59E068F0 wds:Q33569995-819B5CF0-811A-41C3-9FA1-9129A8CDEBA1 wds:Q39638629-E4B7317C-D332-403D-91CD-46BAA5B36DF5 wds:Q112559770-4D4C923F-3CDA-4F6D-8744-8BE3C435E3C7

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