Lista de obras - Basar Bilgic - Dominio Público Uruguay

A novel PNPLA6 mutation in a Turkish family with intractable Holmes tremor and spastic ataxia

artículo científico publicado en 2020

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

artículo científico publicado en 2016

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

artículo científico publicado en 2019

Achromatic temporal-frequency responses of human lateral geniculate nucleus and primary visual cortex

artículo científico publicado en 2016

Adult-onset phenylketonuria with rapidly progressive dementia and parkinsonism.

artículo científico publicado en 2016

Amyloid Beta Adsorption Problem with Transfer Plates in Amyloid Beta 1-42 IVD Kits

scientific article published on 11 January 2019

An assessment of Movement Disorder Society Task Force diagnostic criteria for mild cognitive impairment in Parkinson's disease.

artículo científico publicado en 2017

An investigation of affective theory of mind ability and its relation to neuropsychological functions in Alzheimer's disease

artículo científico publicado en 2020

Analysis of the tremor in juvenile myoclonic epilepsy.

artículo científico publicado en 2016

Are There Any Specific EEG Findings in Autoimmune Epilepsies?

artículo científico publicado en 2015

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

scientific article published on 25 January 2019

BDNF, TNFα, HSP90, CFH, and IL-10 serum levels in patients with early or late onset Alzheimer's disease or mild cognitive impairment.

artículo científico publicado en 2013

Brain Volume Changes in Patients with Acute Brain Dysfunction Due to Sepsis

scientific article published on 01 April 2020

Clozapine treatment in oromandibular dystonia

artículo científico publicado en 2004

Cognitive and anatomical correlates of anosognosia in amnestic mild cognitive impairment and early-stage Alzheimer's disease

artículo científico publicado en 2016

Cognitive impairment and dementia in Parkinson's disease: practical issues and management.

artículo científico

Comparison of Brain Atrophy, Cognition and Optical Coherence Tomography Results Between Multiple Sclerosis Patients and Healthy Controls

scientific article published on 19 March 2018

Comparison of Cognitive Parameters Between Bilateral and Unilateral Hippocampal Sclerosis.

artículo científico

Dementia and behavioral neurology: recent advances.

artículo científico publicado en 2012

Differentiating symptomatic Parkin mutations carriers from patients with idiopathic Parkinson's disease: contribution of automated segmentation neuroimaging method.

artículo científico publicado en 2012

Erratum to: GC and VDR SNPs and Vitamin D Levels in Parkinson's Disease: The Relevance to Clinical Features

artículo científico publicado en 2017

Erratum: Evaluation of Onabotulinum toxin A Treatment in Patients with Concomitant Chronic Migraine and Temporomandibular Disorders

artículo científico publicado en 2019

Evaluation of Onabotulinum toxin A Treatment in Patients with Concomitant Chronic Migraine and Temporomandibular Disorders

scientific article published on 06 July 2018

Evaluation of incidence and clinical features of antibody-associated autoimmune encephalitis mimicking dementia

artículo científico publicado en 2014

Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's disease

artículo científico publicado en 2012

Expression changes of genes associated with apoptosis and survival processes in Parkinson's disease

artículo científico publicado en 2016

FBXO7-R498X mutation: phenotypic variability from chorea to early onset parkinsonism within a family.

artículo científico publicado en 2014

First-episode psychotic disorder improving after immunotherapy

artículo científico publicado en 2015

GC and VDR SNPs and Vitamin D Levels in Parkinson's Disease: The Relevance to Clinical Features

artículo científico publicado en 2016

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

scientific article published on 25 August 2018

Identification of PSEN1 and PSEN2 gene mutations and variants in Turkish dementia patients

artículo científico publicado en 2012

Interleukin-1alpha -889 C/T polymorphism in Turkish patients with late-onset Alzheimer's disease.

artículo científico publicado en 2009

Late-onset phenotype associated with a homozygous GJC2 missense mutation in a Turkish family

scientific article published on 31 July 2019

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

scientific journal article

Multicenter study of levodopa carbidopa intestinal gel in Parkinson’s disease: the Turkish experience

scientific article published on 13 February 2020

Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients

artículo científico publicado en 2016

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

artículo científico publicado en 2017

NMDA receptor encephalitis with cancer of unknown primary origin

artículo científico publicado en 2016

Neuroimaging and Dementia

artículo científico publicado en 2018

Non-convulsive status epilepticus associated with glutamic acid decarboxylase antibody.

artículo científico publicado en 2013

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

artículo científico publicado en 2013

Olfactory function and olfactory bulb volume in Wilson's disease

scientific article published on 22 November 2018

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

artículo científico publicado en 2016

Parkinson's Disease Dementia and Lewy Body Disease

artículo científico publicado en 2019

Peripheral GRN mRNA and Serum Progranulin Levels as a Potential Indicator for Both the Presence of Splice Site Mutations and Individuals at Risk for Frontotemporal Dementia

artículo científico publicado en 2019

Peripheral TREM2 mRNA levels in early and late-onset Alzheimer disease's patients

artículo científico publicado en 2020

Reduced orexin-A levels in frontotemporal dementia: possible association with sleep disturbance.

artículo científico publicado en 2013

Secondary paroxysmal kinesigenic dyskinesia associated with CLCN2 gene mutation

artículo científico publicado en 2015

Silent neurological involvement in biopsy-defined coeliac patients

scientific article published on 25 April 2013

The Association Between Clusterin and APOE Polymorphisms and Late-Onset Alzheimer Disease in a Turkish Cohort.

artículo científico publicado en 2016

The Relationship of White Matter Hyperintensities with Depressive Symptoms and Daily Living Activities in Early-Stage Alzheimer's Disease Patients

artículo científico publicado en 2013

The association between repeat number in C9orf72 and phenotypic variability in Turkish patients with frontotemporal lobar degeneration

scientific article published on 28 December 2018

The distinct genetic pattern of ALS in Turkey and novel mutations.

artículo científico publicado en 2015

The interleukin 1 alpha, interleukin 1 beta, interleukin 6 and alpha-2-macroglobulin serum levels in patients with early or late onset Alzheimer's disease, mild cognitive impairment or Parkinson's disease.

artículo científico publicado en 2015

The p.Thr11Met mutation in c19orf12 is frequent among adult Turkish patients with MPAN.

artículo científico publicado en 2017

The prevalence of dementia in an urban Turkish population.

artículo científico publicado en 2008

Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvement

artículo científico publicado en 2013

Vitamin D deficiency might pose a greater risk for ApoEɛ4 non-carrier Alzheimer's disease patients.

artículo científico publicado en 2016

Volumetric differences suggest involvement of cerebellum and brainstem in chronic migraine

artículo científico publicado en 2015

Wernicke's Encephalopathy due to Non-Alcoholic Gastrointestinal Tract Disease

scientific article published on 25 April 2018

Which cognitive dual-task walking causes most interference on the Timed Up and Go test in Parkinson's disease: a controlled study

artículo científico publicado en 2018

Lista de obras de Basar Bilgic

A novel PNPLA6 mutation in a Turkish family with intractable Holmes tremor and spastic ataxia

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

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

Achromatic temporal-frequency responses of human lateral geniculate nucleus and primary visual cortex

Adult-onset phenylketonuria with rapidly progressive dementia and parkinsonism.

Amyloid Beta Adsorption Problem with Transfer Plates in Amyloid Beta 1-42 IVD Kits

An assessment of Movement Disorder Society Task Force diagnostic criteria for mild cognitive impairment in Parkinson's disease.

An investigation of affective theory of mind ability and its relation to neuropsychological functions in Alzheimer's disease

Analysis of the tremor in juvenile myoclonic epilepsy.

Are There Any Specific EEG Findings in Autoimmune Epilepsies?

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

BDNF, TNFα, HSP90, CFH, and IL-10 serum levels in patients with early or late onset Alzheimer's disease or mild cognitive impairment.

Brain Volume Changes in Patients with Acute Brain Dysfunction Due to Sepsis

Clozapine treatment in oromandibular dystonia

Cognitive and anatomical correlates of anosognosia in amnestic mild cognitive impairment and early-stage Alzheimer's disease

Cognitive impairment and dementia in Parkinson's disease: practical issues and management.

Comparison of Brain Atrophy, Cognition and Optical Coherence Tomography Results Between Multiple Sclerosis Patients and Healthy Controls

Comparison of Cognitive Parameters Between Bilateral and Unilateral Hippocampal Sclerosis.

Dementia and behavioral neurology: recent advances.

Differentiating symptomatic Parkin mutations carriers from patients with idiopathic Parkinson's disease: contribution of automated segmentation neuroimaging method.

Erratum to: GC and VDR SNPs and Vitamin D Levels in Parkinson's Disease: The Relevance to Clinical Features

Erratum: Evaluation of Onabotulinum toxin A Treatment in Patients with Concomitant Chronic Migraine and Temporomandibular Disorders

Evaluation of Onabotulinum toxin A Treatment in Patients with Concomitant Chronic Migraine and Temporomandibular Disorders

Evaluation of incidence and clinical features of antibody-associated autoimmune encephalitis mimicking dementia

Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's disease

Expression changes of genes associated with apoptosis and survival processes in Parkinson's disease

FBXO7-R498X mutation: phenotypic variability from chorea to early onset parkinsonism within a family.

First-episode psychotic disorder improving after immunotherapy

GC and VDR SNPs and Vitamin D Levels in Parkinson's Disease: The Relevance to Clinical Features

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

Identification of PSEN1 and PSEN2 gene mutations and variants in Turkish dementia patients

Interleukin-1alpha -889 C/T polymorphism in Turkish patients with late-onset Alzheimer's disease.

Late-onset phenotype associated with a homozygous GJC2 missense mutation in a Turkish family

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

Multicenter study of levodopa carbidopa intestinal gel in Parkinson’s disease: the Turkish experience

Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients

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

NMDA receptor encephalitis with cancer of unknown primary origin

Neuroimaging and Dementia

Non-convulsive status epilepticus associated with glutamic acid decarboxylase antibody.

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

Olfactory function and olfactory bulb volume in Wilson's disease

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

Parkinson's Disease Dementia and Lewy Body Disease

Peripheral GRN mRNA and Serum Progranulin Levels as a Potential Indicator for Both the Presence of Splice Site Mutations and Individuals at Risk for Frontotemporal Dementia

Peripheral TREM2 mRNA levels in early and late-onset Alzheimer disease's patients

Reduced orexin-A levels in frontotemporal dementia: possible association with sleep disturbance.

Secondary paroxysmal kinesigenic dyskinesia associated with CLCN2 gene mutation

Silent neurological involvement in biopsy-defined coeliac patients

The Association Between Clusterin and APOE Polymorphisms and Late-Onset Alzheimer Disease in a Turkish Cohort.

The Relationship of White Matter Hyperintensities with Depressive Symptoms and Daily Living Activities in Early-Stage Alzheimer's Disease Patients

The association between repeat number in C9orf72 and phenotypic variability in Turkish patients with frontotemporal lobar degeneration

The distinct genetic pattern of ALS in Turkey and novel mutations.

The interleukin 1 alpha, interleukin 1 beta, interleukin 6 and alpha-2-macroglobulin serum levels in patients with early or late onset Alzheimer's disease, mild cognitive impairment or Parkinson's disease.

The p.Thr11Met mutation in c19orf12 is frequent among adult Turkish patients with MPAN.

The prevalence of dementia in an urban Turkish population.

Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvement

Vitamin D deficiency might pose a greater risk for ApoEɛ4 non-carrier Alzheimer's disease patients.

Volumetric differences suggest involvement of cerebellum and brainstem in chronic migraine

Wernicke's Encephalopathy due to Non-Alcoholic Gastrointestinal Tract Disease

Which cognitive dual-task walking causes most interference on the Timed Up and Go test in Parkinson's disease: a controlled study