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Hasmet A Hanagasi

Showing results (11-20 of 39) with videos related to

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The International Journal of Neuroscience|November 20, 2009
Mitochondrial pathology in muscle of a patient with a novel parkin mutationHasmet A Hanagasi, Piraye Serdaroglu, Mehmet Ozansoy, et al.
Parkinsonism & Related Disorders|October 25, 2011
A homozygous frameshift mutation of sepiapterin reductase gene causing parkinsonism with onset in childhoodEbba Lohmann, Çiğdem Köroğlu, Hasmet A Hanagasi, et al.
Acta Neurologica Belgica|March 24, 2022
Medication management and treatment adherence in Parkinson's disease patients with mild cognitive impairmentBetul Sumbul-Sekerci, Hasmet A Hanagasi, Basar Bilgic, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 9, 2021
A novel SACS p.Pro4154GlnfsTer20 mutation in a family with autosomal recessive spastic ataxia of Charlevoix-SaguenayBedia Samanci, Ebru Erzurumluoglu Gokalp, Basar Bilgic, et al.
International Psychogeriatrics|February 10, 2006
The attitude of elderly lay people towards the symptoms of dementiaHuseyin A Sahin, I Hakan Gurvit, Murat Emre, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 26, 2013
Silent neurological involvement in biopsy-defined coeliac patientsBasar Bilgic, Demet Aygun, Ali Bilgin Arslan, et al.
Neuroscience Letters|August 2, 2008
Single nucleotide polymorphisms in base-excision repair genes hOGG1, APE1 and XRCC1 do not alter risk of Alzheimer's diseaseHande Parildar-Karpuzoğlu, Semra Doğru-Abbasoğlu, Hasmet A Hanagasi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 21, 2021
Neurological features and outcomes of Wilson's disease: a single-center experienceBedia Samanci, Erdi Sahin, Basar Bilgic, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 19, 2020
A novel PNPLA6 mutation in a Turkish family with intractable Holmes tremor and spastic ataxiaAhmed S Emekli, Bedia Samanci, Gülşah Şimşir, et al.
Parkinsonism & Related Disorders|August 30, 2014
FBXO7-R498X mutation: phenotypic variability from chorea to early onset parkinsonism within a familyAyşegül Gündüz, Aslı Gündoğdu Eken, Başar Bilgiç, et al.
Pageof 4

Showing results (11-20 of 39) with videos related to

Sort By:
Pageof 4
The International Journal of Neuroscience|November 20, 2009
Mitochondrial pathology in muscle of a patient with a novel parkin mutationHasmet A Hanagasi, Piraye Serdaroglu, Mehmet Ozansoy, et al.
Parkinsonism & Related Disorders|October 25, 2011
A homozygous frameshift mutation of sepiapterin reductase gene causing parkinsonism with onset in childhoodEbba Lohmann, Çiğdem Köroğlu, Hasmet A Hanagasi, et al.
Acta Neurologica Belgica|March 24, 2022
Medication management and treatment adherence in Parkinson's disease patients with mild cognitive impairmentBetul Sumbul-Sekerci, Hasmet A Hanagasi, Basar Bilgic, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 9, 2021
A novel SACS p.Pro4154GlnfsTer20 mutation in a family with autosomal recessive spastic ataxia of Charlevoix-SaguenayBedia Samanci, Ebru Erzurumluoglu Gokalp, Basar Bilgic, et al.
International Psychogeriatrics|February 10, 2006
The attitude of elderly lay people towards the symptoms of dementiaHuseyin A Sahin, I Hakan Gurvit, Murat Emre, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 26, 2013
Silent neurological involvement in biopsy-defined coeliac patientsBasar Bilgic, Demet Aygun, Ali Bilgin Arslan, et al.
Neuroscience Letters|August 2, 2008
Single nucleotide polymorphisms in base-excision repair genes hOGG1, APE1 and XRCC1 do not alter risk of Alzheimer's diseaseHande Parildar-Karpuzoğlu, Semra Doğru-Abbasoğlu, Hasmet A Hanagasi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 21, 2021
Neurological features and outcomes of Wilson's disease: a single-center experienceBedia Samanci, Erdi Sahin, Basar Bilgic, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 19, 2020
A novel PNPLA6 mutation in a Turkish family with intractable Holmes tremor and spastic ataxiaAhmed S Emekli, Bedia Samanci, Gülşah Şimşir, et al.
Parkinsonism & Related Disorders|August 30, 2014
FBXO7-R498X mutation: phenotypic variability from chorea to early onset parkinsonism within a familyAyşegül Gündüz, Aslı Gündoğdu Eken, Başar Bilgiç, et al.
Pageof 4