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Results 1 to 25 of 29

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Valproate reduces spontaneous generalized spikes and waves but not photoparoxysmal reactions in patients with idiopathic generalized epilepsiesMUHLE, Hiltrud; ETTLE, Esther; BOOR, Rainer et al.Epilepsia (Copenhagen). 2011, Vol 52, Num 7, pp 1297-1302, issn 0013-9580, 6 p.Article

Hashimoto Encephalopathy in a 15-Year-Old-Girl: EEG Findings and Follow-UpMUHLE, Hiltrud; VAN BAALEN, Andreas; RIEPE, Felix G et al.Pediatric neurology. 2009, Vol 41, Num 4, pp 301-304, issn 0887-8994, 4 p.Article

Absence seizures: Individual patterns revealed by EEG-fMRIMOELLER, Friederike; LEVAN, Pierre; MUHLE, Hiltrud et al.Epilepsia (Copenhagen). 2010, Vol 51, Num 10, pp 2000-2010, issn 0013-9580, 11 p.Article

Iterative phenotyping of 15q11.2, 15q13.3 and 16p13.11 microdeletion carriers in pediatric epilepsiesJAHN, Johanna A; VON SPICZAK, Sarah; MUHLE, Hiltrud et al.Epilepsy research. 2014, Vol 108, Num 1, pp 109-116, issn 0920-1211, 8 p.Article

Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsyHEMPELMANN, Anne; COBILANSCHI, Joana; HEILS, Armin et al.Epilepsy research. 2007, Vol 74, Num 1, pp 28-32, issn 0920-1211, 5 p.Article

Association of BRD2 polymorphisms with photoparoxysmal responseLORENZ, Susanne; TAYLOR, Kirsten P; GEHRMANN, Anne et al.Neuroscience letters. 2006, Vol 400, Num 1-2, pp 135-139, issn 0304-3940, 5 p.Article

EEG-fMRI in myoclonic astatic epilepsy (Doose syndrome)MOELLER, Friederike; GROENING, Kristina; MOEHRING, Jan et al.Neurology. 2014, Vol 82, Num 17, pp 1508-1513, issn 0028-3878, 6 p.Article

Spreading photoparoxysmal EEG response is associated with an abnormal cortical excitability patternSINIATCHKIN, Michael; GROPPA, Sergey; JEROSCH, Bettina et al.Brain. 2007, Vol 130, pp 78-87, issn 0006-8950, 10 p., 1Article

Recurrent de novo mutations of SCN1A in severe myoclonic epilepsy of infancyKEARNEY, Jennifer A; WISTE, Anna K; MEISLER, Miriam H et al.Pediatric neurology. 2006, Vol 34, Num 2, pp 116-120, issn 0887-8994, 5 p.Article

Genetic dissection of photosensitivity and its relation to idiopathic generalized epilepsyTAUER, Ulrike; LORENZ, Susanne; STRAUCH, Konstantin et al.Annals of neurology. 2005, Vol 57, Num 6, pp 866-873, issn 0364-5134, 8 p.Article

Impact of ABCC2 genotype on antiepileptic drug response in Caucasian patients with childhood epilepsyUFER, Mike; VON STÜLPNAGEL, Celina; MUHLE, Hiltrud et al.Pharmacogenetics and genomics (Print). 2011, Vol 21, Num 10, pp 624-630, issn 1744-6872, 7 p.Article

Mapping brain activity on the verge of a photically induced generalized tonic―clonic seizureMOELLER, Friederike; SIEBNER, Hartwig R; WOLFF, Stephan et al.Epilepsia (Copenhagen). 2009, Vol 50, Num 6, pp 1632-1637, issn 0013-9580, 6 p.Article

Simultaneous EEG-fMRl in drug-naive children with newly diagnosed absence epilepsyMOELLER, Friederike; SIEBNER, Hartwig R; WOLFF, Stephan et al.Epilepsia (Copenhagen). 2008, Vol 49, Num 9, pp 1510-1519, issn 0013-9580, 10 p.Article

GABRA1 and STXBP1: Novel genetic causes of Dravet syndromeCARVILL, Gemma L; WECKHUYSEN, Sarah; CLARKE, Alison et al.Neurology. 2014, Vol 82, Num 14, issn 0028-3878, 1245-1250, 1250-1253 [10 p.]Article

Childhood-onset Restless Legs Syndrome : Clinical and Genetic Features of 22 FamiliesMUHLE, Hiltrud; NEUMANN, Anja; STEPHANI, Ulrich et al.Movement disorders. 2008, Vol 23, Num 8, pp 1113-1121, issn 0885-3185, 9 p.Article

A retrospective population-based study on seizures related to childhood vaccinationVON SPICZAK, Sarah; HELBIG, Ingo; KELLER-STANISLAWSKI, Brigitte et al.Epilepsia (Copenhagen). 2011, Vol 52, Num 8, pp 1506-1512, issn 0013-9580, 7 p.Article

A duplication in Iq21.3 in a family with early onset and childhood absence epilepsyMUHLE, Hiltrud; STEINICH, Ines; MARINI, Carla et al.Epilepsia (Copenhagen). 2010, Vol 51, Num 12, pp 2453-2456, issn 0013-9580, 4 p.Article

Hemodynamic responses to interictal epileptiform discharges in children with symptomatic epilepsyJACOBS, Julia; KOBAYASHI, Eliane; SINIATCHKIN, Michael et al.Epilepsia (Copenhagen). 2007, Vol 48, Num 11, pp 2068-2078, issn 0013-9580, 11 p.Article

Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsiesCONSORTIUM, Epicure; LEU, Costin; GIALLONARDO, Anna Teresa et al.Epilepsia (Copenhagen). 2012, Vol 53, Num 2, pp 308-318, issn 0013-9580, 11 p.Article

Deletions in 16p13 including GRIN2A in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic regionREUTLINGER, Constanze; HELBIG, Ingo; STEFANOVA, Irina et al.Epilepsia (Copenhagen). 2010, Vol 51, Num 9, pp 1870-1873, issn 0013-9580, 4 p.Article

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32STEFFEN, Michael Steffen; LEU, Costin; LA NEVE, Angela et al.Human molecular genetics (Print). 2012, Vol 21, Num 24, pp 5359-5372, issn 0964-6906, 14 p.Article

Dyschromatosis ptychotropica: an unusual pigmentary disorder in a boy with epileptic encephalopathy and progressive atrophy of the central nervous system: a novel entity?HELBIG, Ingo; FÖLSTER-HOLST, Regina; BRASCH, Jochen et al.European journal of pediatrics. 2010, Vol 169, Num 4, pp 495-500, issn 0340-6199, 6 p.Article

Non-response to antiepileptic pharmacotherapy is associated with the ABCC2 -240T polymorphism in young and adult patients with epilepsyUFER, Mike; MOSYAGIN, Igor; RUNGE, Uwe et al.Pharmacogenetics and genomics (Print). 2009, Vol 19, Num 5, pp 353-362, issn 1744-6872, 10 p.Article

Candidate gene analysis of the succinic semialdehyde dehydrogenase gene (ALDH5A1) in patients with idiopathic generalized epilepsy and photosensitivityLORENZ, Susanne; HEILS, Armin; TAYLOR, Kirsten P et al.Neuroscience letters. 2006, Vol 397, Num 3, pp 234-239, issn 0304-3940, 6 p.Article

The role of SLC2A1 in early onset and childhood absence epilepsiesMUHLE, Hiltrud; HELBIG, Ingo; TOMMERUP, Niels et al.Epilepsy research. 2013, Vol 105, Num 1-2, pp 229-233, issn 0920-1211, 5 p.Article

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