Publications by authors named "Susannah T Bellows"

17Publications

Epilepsy in families: Age at onset is a familial trait, independent of syndrome.

Ann Neurol 2019 07 20;86(1):91-98. Epub 2019 May 20.

Epilepsy Research Centre, Department of Medicine, University of Melbourne (Austin Health), Heidelberg, Victoria, Australia.

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http://dx.doi.org/10.1002/ana.25499DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6565452PMC
July 2019

Genetic epilepsy with febrile seizures plus: Refining the spectrum.

Neurology 2017 Sep 25;89(12):1210-1219. Epub 2017 Aug 25.

From the Epilepsy Research Centre, Department of Medicine (Y.-H.Z., R.B., J.P.M., G.C.G., K.L.H., L.V., B.E.G., S.T.B., D.F.V., J.A.D., M.S.H., S.F.B., I.E.S.), The University of Melbourne, Austin Health, Australia; Department of Pediatrics (Y.-H.Z.), Peking University First Hospital, Beijing, China; Department of Neurology (L.V.), The University of Queensland Centre for Clinical Research, Royal Brisbane and Women's Hospital, Australia; Schneider Children's Medical Center of Israel (S.K., H.G.-S.), Petach Tikvah; Department of Neurology (Z.A.), Tel-Aviv Sourasky Medical Center, Tel Aviv, Israel; Westmead Hospital (A.B.), New South Wales, Australia; Department of Neurology (P.G.-S.), Sydney Children's Hospital, Australia; Department of Neurology (A.D.K.), Tel Aviv University, Israel; Women's and Children's Hospital (L.M.D.), University of Adelaide, South Australia; Center for Neurobehavioral Genetics (E.K.R.), Semel Institute, David Geffen School of Medicine, University of California, Los Angeles; Department of Paediatrics (I.E.S.), The University of Melbourne, Royal Children's Hospital, Victoria; and The Florey Institute of Neurosciences and Mental Health (I.E.S.), Melbourne, Australia.

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http://dx.doi.org/10.1212/WNL.0000000000004384DOI Listing
September 2017

Familial mesial temporal lobe epilepsy and the borderland of déjà vu.

Ann Neurol 2017 Aug 19;82(2):166-176. Epub 2017 Jul 19.

Epilepsy Research Centre, Department of Medicine, Austin Health, University of Melbourne, Melbourne, Victoria, Australia.

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http://dx.doi.org/10.1002/ana.24984DOI Listing
August 2017

Evaluation of GLUT1 variation in non-acquired focal epilepsy.

Epilepsy Res 2017 07 10;133:54-57. Epub 2017 Apr 10.

Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria, 3084, Australia. Electronic address:

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http://dx.doi.org/10.1016/j.eplepsyres.2017.04.007DOI Listing
July 2017

Dominant KCNA2 mutation causes episodic ataxia and pharmacoresponsive epilepsy.

Neurology 2016 Nov 12;87(19):1975-1984. Epub 2016 Oct 12.

From the School of Medicine and Robinson Research Institute (M.A.C., R.C., J.G.) and School of Biological Sciences (J.G.), The University of Adelaide; Epilepsy Research Centre, Department of Medicine (S.T.B., S. Micallef, S.F.B., I.E.S.), University of Melbourne, Austin Health, Heidelberg; Florey Institute of Neuroscience and Mental Health (M.L., S. Maljevic, E.V.G., S.P., I.E.S.), Melbourne; Division of Genetic Medicine, Department of Pediatrics (G.L.C., C.T.M., H.C.M.), University of Washington, Seattle; Department of Neurology (K.B.H., I.E.S.), Royal Children's Hospital; Neurosciences Group (K.B.H.), Murdoch Childrens Research Institute, Melbourne; Department of Paediatrics (K.B.H.), University of Melbourne, Royal Children's Hospital, Parkville, Australia; Department of Neurology and Epileptology (S. Maljevic, H.L.), Hertie Institute for Clinical Brain Research, University of Tübingen, Germany; The Walter and Eliza Hall Institute of Medical Research (M.B.); Department of Medical Biology (M.B.), The University of Melbourne, Parkville; and Department of Medicine, Royal Melbourne Hospital (S.P.), The University of Melbourne, Australia.

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http://dx.doi.org/10.1212/WNL.0000000000003309DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5109949PMC
November 2016

Evaluation of non-coding variation in GLUT1 deficiency.

Dev Med Child Neurol 2016 Dec 6;58(12):1295-1302. Epub 2016 Jun 6.

Department of Medicine, Epilepsy Research Centre, Austin Health, University of Melbourne, Heidelberg, Vic., Australia.

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http://dx.doi.org/10.1111/dmcn.13163DOI Listing
December 2016

Evaluation of multiple putative risk alleles within the 15q13.3 region for genetic generalized epilepsy.

Epilepsy Res 2015 Nov 9;117:70-3. Epub 2015 Sep 9.

Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria 3084, Australia. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S09201211153004
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http://dx.doi.org/10.1016/j.eplepsyres.2015.09.007DOI Listing
November 2015

Glucose metabolism transporters and epilepsy: only GLUT1 has an established role.

Epilepsia 2014 Feb 31;55(2):e18-21. Epub 2014 Jan 31.

Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria, Australia.

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http://dx.doi.org/10.1111/epi.12519DOI Listing
February 2014

Does variation in NIPA2 contribute to genetic generalized epilepsy?

Hum Genet 2014 May 10;133(5):673-4. Epub 2014 Jan 10.

Department of Medicine, Epilepsy Research Centre, University of Melbourne, Austin Health, Heidelberg, VIC, 3084, Australia.

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http://dx.doi.org/10.1007/s00439-013-1414-0DOI Listing
May 2014

Seizure semiology in autosomal dominant epilepsy with auditory features, due to novel LGI1 mutations.

Epilepsy Res 2013 Dec 8;107(3):311-7. Epub 2013 Oct 8.

Department of Paediatrics, School of Medicine and Health Sciences, University of Otago, Wellington, New Zealand. Electronic address:

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http://dx.doi.org/10.1016/j.eplepsyres.2013.09.008DOI Listing
December 2013

Familial adult myoclonic epilepsy: recognition of mild phenotypes and refinement of the 2q locus.

Arch Neurol 2012 Apr;69(4):474-81

Institute of Genetic Medicine, Faculty of Medical Sciences and Newcastle Biomedicine, Newcastle University, Central Parkway, Newcastle upon Tyne, England.

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http://dx.doi.org/10.1001/archneurol.2011.584DOI Listing
April 2012