Kerstin Hallmann

Kerstin Hallmann

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Kerstin Hallmann

Kerstin Hallmann

Publications by authors named "Kerstin Hallmann"

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Functional variants in and may contribute to genetic generalized epilepsy.

Epilepsia Open 2017 09 5;2(3):334-342. Epub 2017 Aug 5.

Department of Neurology and Epileptology Hertie-Institute for Clinical Brain-Research University of Tübingen Tübingen Germany.

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http://dx.doi.org/10.1002/epi4.12068DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5862120PMC
September 2017

Do Glut1 (glucose transporter type 1) defects exist in epilepsy patients responding to a ketogenic diet?

Epilepsy Res 2015 Aug 1;114:47-51. Epub 2015 May 1.

Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.eplepsyres.2015.04.012DOI Listing
August 2015

A homozygous splice-site mutation in CARS2 is associated with progressive myoclonic epilepsy.

Neurology 2014 Dec 31;83(23):2183-7. Epub 2014 Oct 31.

From the Department of Epileptology and Life & Brain Center (K.H., G.Z., S.M.-H., C.E.E., W.S.K.), University of Bonn; Department of Neuropediatrics and Muscle Disorders (J.K., R.K.), University of Freiburg; Cologne Center for Genomics (A.-K.R., H.T., P.N., T.S.), Center for Molecular Medicine Cologne (P.N.), and Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (P.N.), University of Cologne, Germany; Genetic Department (O.O.), Institute of Experimental Medicine (DETAE), Istanbul University, Turkey; Department of Neurology and Epileptology (Y.W., F.B., H.L.), Hertie Institute for Clinical Brain Research, University of Tübingen, Germany.

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http://dx.doi.org/10.1212/WNL.0000000000001055DOI Listing
December 2014

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

Brain 2013 Oct 6;136(Pt 10):3140-50. Epub 2013 Sep 6.

1 NIHR University College London Hospitals Biomedical Research Centre, Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK.

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https://academic.oup.com/brain/article/136/10/3140/330027
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http://dx.doi.org/10.1093/brain/awt233DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3784283PMC
October 2013

POLG mutations cause decreased mitochondrial DNA repopulation rates following induced depletion in human fibroblasts.

Biochim Biophys Acta 2011 Mar 5;1812(3):321-5. Epub 2010 Dec 5.

Mitochondrial Research Group, Institute of Human Genetics, Newcastle University, Central Parkway, Newcastle upon Tyne, NE1 3BZ, UK.

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http://dx.doi.org/10.1016/j.bbadis.2010.11.012DOI Listing
March 2011

Distinct patterns of mitochondrial genome diversity in bonobos (Pan paniscus) and humans.

BMC Evol Biol 2010 Sep 2;10:270. Epub 2010 Sep 2.

Division of Neurochemistry, Department of Epileptology and Life&Brain Center, University Bonn, Sigmund-Freud-Str. 25, 53105 Bonn, Germany.

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http://dx.doi.org/10.1186/1471-2148-10-270DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2942848PMC
September 2010

A splice-site mutation in GABRG2 associated with childhood absence epilepsy and febrile convulsions.

Arch Neurol 2002 Jul;59(7):1137-41

Institute of Human Genetics, University Hospital Bonn, Rheinische Friedrich Wilhelms-University Bonn, Germany.

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http://dx.doi.org/10.1001/archneur.59.7.1137DOI Listing
July 2002