Radha Procopio

neuroscience research center

H指数:6

被引数:152

个人简介

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Preliminary insights into whole-blood mitochondrial DNA copy number and telomere length in Parkinson’s disease and multiple system atrophy

帕金森病和多系统萎缩患者全血线粒体DNA拷贝数和端粒长度的初步研究

Journal of Neurology

IF4.6

2026-09-290

PRE

Abrupt-onset cervico-truncal dystonia after Mycoplasma pneumoniae infection: Unmasking a possible CACNA1A-related susceptibility

肺炎支原体感染后突发的颈干肌张力障碍：揭示可能的CACNA1A相关易感性

PARKINSONISM & RELATED DISORDERS

IF3.4

2026-06-180

PRE

Assessment of Mitochondrial DNA Copy Number in Progressive Supranuclear Palsy Patients: Evidence From a Pilot Study

评估进行性核上性麻痹患者线粒体DNA拷贝数：一项初步研究的结果

European Journal of Neurology

IF3.9

2026-04-170

OAAI

Early-onset parkinsonism with intellectual disability in an Italian family associated with a PTRHD1 variant

意大利一个家族中与PTRHD1变异相关的早发性帕金森病伴智力障碍

PARKINSONISM & RELATED DISORDERS

IF3.4

2026-04-010

PRE

No evidence for the LRRK2 p.L1795F variant in a Southern Italian cohort with Parkinson’s disease

Gene

IF2.4

2026-01-050

PRE

Genetic analysis of GBA1 gene in a cohort of patients with Parkinson's disease

帕金森病患者队列中GBA1基因的遗传分析

Parkinsonism & Related Disorders

IF3.4

2025-08-190

PRE

Hereditary Transthyretin Amyloidosis: Genetic Characterization of the TTR P.Val142Ile Variant in a Calabrian Kindred

遗传性甲状腺素转运蛋白淀粉样变性：卡拉布里亚家族中TTR P.Val142Ile变异的遗传特征

genes

IF0

2025-08-150

Identification of Ser71Arg mutation in RAB32 gene in familial Parkinson's disease from Southern Italy

在意大利南部家族性帕金森病中鉴定出RAB32基因的Ser71Arg突变

NPJ PARKINSONS DISEASE

IF8.2

2025-03-210

Novel KCNQ2 Variants Related to a Variable Phenotypic Spectrum Ranging from Epilepsy with Auditory Features to Severe Developmental and Epileptic Encephalopathies

新型KCNQ2变异与表型谱相关的变异性，其范围从具有听觉特征的癫痫到严重发育性和癫痫性脑病。

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

IF4.9

2024-12-310

ANXA1 mutation analysis in Italian patients with early onset PD

NEUROBIOLOGY OF AGING

IF3.5

2023-05-010

PRE

Multiple system atrophy and C9orf72 hexanucleotide repeat expansions in a cohort of Italian patients

NEUROBIOLOGY OF AGING

IF3.5

2022-04-014

PRE

Mutation analysis of the ATP13A2 gene in patients with PD and MSA from Italy

JOURNAL OF THE NEUROLOGICAL SCIENCES

IF3.2

2021-11-013

PRE

Mild case of Unverricht-Lundborg disease presenting as Juvenile myoclonic epilepsy

JOURNAL OF THE NEUROLOGICAL SCIENCES

IF3.2

2021-10-010

PRE

Headache and sleep-related breathing disorders among patients with sclerosteosis and disease carriers

JOURNAL OF THE NEUROLOGICAL SCIENCES

IF3.2

2021-10-010

PRE

DCTN1 mutation analysis in Italian patients with PSP, MSA, and DLB

NEUROBIOLOGY OF AGING

IF3.5

2020-09-010

PREAI

Analysis of the TMEM230 gene in familial Parkinson's disease from south Italy

JOURNAL OF THE NEUROLOGICAL SCIENCES

IF3.2

2019-09-013

PREAI

Intracellular FMRpolyG-Hsp70 complex in fibroblast cells from a patient affected by fragile X tremor ataxia syndrome

HELIYON

IF3.6

2019-06-016

OAAI

Selectivity of the CUBAN domain in the recognition of ubiquitin and NEDD8

FEBS JOURNAL

IF4.2

2019-02-0519

OAAI

DNAJC13 mutation screening in patients with Parkinson's disease from South Italy

PARKINSONISM & RELATED DISORDERS

IF3.4

2018-10-0113

PREAI

Analysis of the TMEM230 gene in patients with multiple system atrophy

JOURNAL OF THE NEUROLOGICAL SCIENCES

IF3.2

2018-09-012

PREAI

Radha Procopio

个人简介

教育背景

工作经历

荣誉奖项

研究方向