Akademisyen
OKAN DOĞU
PROFESÖR
MERSİN ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
- Ana Dal Sağlık Bilimleri Temel Alanı
- Yan Dal Nöroloji
Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.
- Makale 26
- Proje 0
- Kitap 5
- Bildiri 3
- Patent 0
- Sanatsal 0
Scopus (SJR)
Q1
16
Q2
5
Q3
3
Q4
0
WoS (JCR)
Q1
15
Q2
3
Q3
3
Q4
3
TR Index
2
makale
Alan+yıl+tür normalize OpenAlex yüzdelik — Clarivate ESI / SciVal değildir.
Üst %1 makale
0
Üst %10 makale
0
Ort. yüzdelik
70.5%
Üst %1 payı
0.0%
Üst %10 payı
0.0%
Makaleler
YÖKSİS ve OpenAlex kaynak ayrımıyla makaleler; quartile ve TR Index ile daraltabilirsiniz.
Makale listesi
- 2020 Multicenter study of levodopa carbidopa intestinal gel in Parkinson’s disease: the Turkish experince YÖKSİS TR Index SJR Q3 JCR Q4
- 2019 Correction to: How satisfied are cervical dystonia patients after 3 years of botulinum toxin type A treatment? Results from a prospective, long-term observational study YÖKSİS SJR Q1 JCR Q1
- 2019 Multicenter study of levodopa carbidopa intestinal gel in Parkinson’s disease:the Turkish experience YÖKSİS TR Index SJR Q3 JCR Q4 OpenAlex 55.1%
- 2019 Retinal nerve fiber layer thickness in patients with essential tremor and Parkinson’s disease YÖKSİS
- 2018 INTEREST IN CD2, a global patient-centred study of long-term cervical dystonia treatment with botulinum toxin YÖKSİS SJR Q1 JCR Q1
- 2017 The p.Thr11Met mutation in c19orf12 is frequent among adult Turkish patients with MPAN YÖKSİS SJR Q1 JCR Q1
- 2017 Turkish Standardization of Movement Disorders Society Unified Parkinson's Disease Rating Scale and Unified Dyskinesia Rating Scale YÖKSİS SJR Q3 JCR Q2 OpenAlex 74.2%
- 2017 F-18 FDG PET/CT image of alzheimer like primaryprogressive aphasia YÖKSİS
- 2017 The p.Thr11Met mutation in c19orf12 is frequent among adult Turkish patients with MPAN YÖKSİS SJR Q1 JCR Q1
- 2017 The p.Thr11Met mutation in c19orf12 is frequent among adult Turkish patients with MPAN YÖKSİS SJR Q1 JCR Q1
- 2017 title Epigenetic approach to early-onset Parkinson’s disease: low methylation status of iSNCA/i and iPARK2/i promoter regions/title YÖKSİS SJR Q2 JCR Q4 OpenAlex 82.2%
- 2016 Mutation analysis of the PARKIN, PINK1, DJ1, and SNCA genes in Turkish early-onset Parkinson’s patients and genotype-phenotype correlations YÖKSİS SJR Q2 JCR Q3
- 2014 Mitochondrial serine protease HTRA2 p G399S in a kindred with essential tremor and Parkinson disease YÖKSİS SJR Q1 JCR Q1
- 2013 Rapid disease progression in adult onset mitochondrial membrane protein associated neurodegeneration YÖKSİS SJR Q2 JCR Q2
- 2012 Genetic bases and phenotypes of autosomal recessive Parkinson disease in a Turkish population YÖKSİS SJR Q1 JCR Q1
- 2012 Prevalence of Blepharospasm and Apraxia of Eyelid Opening in Patients with Parkinsonism Cervical Dystonia and Essential Tremor YÖKSİS SJR Q2 JCR Q3
- 2010 Identification of sleepwalking gene s Not yet but soon YÖKSİS SJR Q1 JCR Q1
- 2010 Subclinical tremor in normal controls with versus without a family history of essential tremor data from the United States and Turkey YÖKSİS SJR Q1 JCR Q1
- 2009 Isolated head tremor Part of the clinical spectrum of essential tremor Data from population based and clinic based case samples YÖKSİS SJR Q1 JCR Q1
- 2008 SPG11 mutations are common in familial cases of complicated hereditary spastic paraplegia YÖKSİS SJR Q1 JCR Q1