Gamze Guven

Gamze Guven

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Gamze Guven

Gamze Guven

Publications by authors named "Gamze Guven"

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A patient with early-onset Alzheimer's disease with a novel PSEN1 p.Leu424Pro mutation.

Neurobiol Aging 2019 Jun 13. Epub 2019 Jun 13.

Department of Neurology, Behavioral Neurology and Movement Disorders Unit, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.

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http://dx.doi.org/10.1016/j.neurobiolaging.2019.05.014DOI Listing
June 2019

Association between selected cholesterol-related gene polymorphisms and Alzheimer's disease in a Turkish cohort.

Mol Biol Rep 2019 Apr 25;46(2):1701-1707. Epub 2019 Jan 25.

Department of Genetics, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul, Turkey.

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http://dx.doi.org/10.1007/s11033-019-04619-8DOI Listing
April 2019

HPCA confirmed as a genetic cause of DYT2-like dystonia phenotype.

Mov Disord 2018 08 25;33(8):1354-1358. Epub 2018 Aug 25.

German Center for Neurodegenerative Diseases (DZNE)-Tübingen, Tübingen, Germany.

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http://dx.doi.org/10.1002/mds.27442DOI Listing
August 2018

Mutations in TYROBP are not a common cause of dementia in a Turkish cohort.

Neurobiol Aging 2017 10 28;58:240.e1-240.e3. Epub 2017 Jun 28.

Department of Molecular Neuroscience, Institute of Neurology, University College London, London, UK; Department of Medical Sciences, Institute of Biomedicine-iBiMED, University of Aveiro, Aveiro, Portugal; UK Dementia Research Institute at UCL (UK DRI), London, UK. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2017.06.019DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5985528PMC
October 2017

Unilateral complex syngnathia of the maxilla, mandible, and zygomatic complex in a newborn baby.

Br J Oral Maxillofac Surg 2017 02 30;55(2):211-212. Epub 2016 Jun 30.

Medipol University, TEM Avrupa Otoyolu Goztepe Cikisi No: 1 Bagcilar 34214 Istanbul, Turkey. Electronic address:

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http://dx.doi.org/10.1016/j.bjoms.2016.06.007DOI Listing
February 2017

A novel homozygous DJ1 mutation causes parkinsonism and ALS in a Turkish family.

Parkinsonism Relat Disord 2016 08 3;29:117-20. Epub 2016 Mar 3.

Istanbul University, Istanbul Faculty of Medicine, Department of Neurology, Behavioral Neurology and Movement Disorders Unit, Capa, 34390 Istanbul, Turkey; Dept. of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen, and DZNE, German Center for Neurodegenerative Diseases, Tübingen, Germany.

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http://dx.doi.org/10.1016/j.parkreldis.2016.03.001DOI Listing
August 2016

Histologic and Histomorphometric Comparison of Bone Regeneration Between Bone Morphogenetic Protein-2 and Platelet-Derived Growth Factor-BB in Experimental Groups.

J Craniofac Surg 2016 May;27(3):805-9

*Department of Oral Implantology, Istanbul University Faculty of Dentistry†Department of Oral and Maxillofacial Surgery, Medipol University Faculty of Dentistry‡Department of Histology and Embryology, Istanbul University Cerrahpasa Faculty of Medicine, Istanbul§Department of Histology and Embryology, Kocaeli University Faculty of Medicine, Kocaeli||Department of Oral Implantology, Istanbul University Faculty of Dentistry, Istanbul, Turkey.

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http://dx.doi.org/10.1097/SCS.0000000000002560DOI Listing
May 2016

PLA2G6 Mutations Related to Distinct Phenotypes: A New Case with Early-onset Parkinsonism.

Tremor Other Hyperkinet Mov (N Y) 2016 16;6:363. Epub 2016 Mar 16.

Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany; German Center for Neurodegenerative Diseases (DZNE)-Tübingen, Tübingen, Germany.

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http://dx.doi.org/10.7916/D81G0M12DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811020PMC
April 2016

Clinical variability in ataxia-telangiectasia.

J Neurol 2015 Jul 10;262(7):1724-7. Epub 2015 May 10.

Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen, and DZNE, German Center for Neurodegenerative Diseases, Hoppe-Seyler-Str. 3, 72076, Tübingen, Germany,

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http://dx.doi.org/10.1007/s00415-015-7762-zDOI Listing
July 2015

A new F-box protein 7 gene mutation causing typical Parkinson's disease.

Mov Disord 2015 Jul 23;30(8):1130-3. Epub 2015 May 23.

Sorbonne Université, UPMC Univ Paris 06, UM 1127, ICM, Paris, France; Inserm, U 1127, ICM, Paris, France; Cnrs, UMR 7225, ICM, Paris, France; ICM, Paris, F-75013, Paris, France.

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http://dx.doi.org/10.1002/mds.26266DOI Listing
July 2015

Novel compound heterozygous mutation in TREM2 found in a Turkish frontotemporal dementia-like family.

Neurobiol Aging 2013 Dec 17;34(12):2890.e1-5. Epub 2013 Jul 17.

Department of Molecular Neuroscience, Institute of Neurology, University College London, London, UK. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2013.06.005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3898264PMC
December 2013

A novel A781V mutation in the CSF1R gene causes hereditary diffuse leucoencephalopathy with axonal spheroids.

J Neurol Sci 2013 Sep 28;332(1-2):141-4. Epub 2013 Jun 28.

Dementia Research Centre, Department of Neurodegenerative Disease, University College London, Institute of Neurology, Queen Square, London, UK.

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http://dx.doi.org/10.1016/j.jns.2013.06.007DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3750216PMC
September 2013