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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1992 1
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1998 2
1999 1
2002 1
2003 2
2007 3
2008 2
2012 1
2013 1
2014 1
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2018 4
2019 1
2022 1
2024 0

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26 results

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Page 1
Genetics of Synucleinopathies.
Nussbaum RL. Nussbaum RL. Cold Spring Harb Perspect Med. 2018 Jun 1;8(6):a024109. doi: 10.1101/cshperspect.a024109. Cold Spring Harb Perspect Med. 2018. PMID: 28213435 Free PMC article. Review.
Parkinson's disease (PD), diffuse Lewy body disease (DLBD), and multiple system atrophy (MSA) constitute the three major neurodegenerative disorders referred to as synucleinopathies because both genetic and pathological results implicate the alpha-synuclein p
Parkinson's disease (PD), diffuse Lewy body disease (DLBD), and multiple system atrophy (MSA) constitute the three majo
Diet, Gut Microbiome, and Cognitive Decline.
Ettinger S. Ettinger S. Curr Nutr Rep. 2022 Dec;11(4):643-652. doi: 10.1007/s13668-022-00435-y. Epub 2022 Aug 26. Curr Nutr Rep. 2022. PMID: 36018501 Review.
PURPOSE OF REVIEW: An epidemic of age-associated cognitive decline, most commonly ascribed to neurodegenerative conditions such as Alzheimer's and Parkinson's disease, is causing healthcare costs to soar and devastating caregivers. An estimated 6.5 million Americans …
PURPOSE OF REVIEW: An epidemic of age-associated cognitive decline, most commonly ascribed to neurodegenerative conditions such as Alzheimer …
Dopa-responsive dystonia.
Nygaard TG. Nygaard TG. Curr Opin Neurol. 1995 Aug;8(4):310-3. doi: 10.1097/00019052-199508000-00011. Curr Opin Neurol. 1995. PMID: 7582048 Review.
A pathological study has confirmed the 'developmental' nature of the disease. Finally, mutations causing the autosomal dominant form of dopa-responsive dystonia have been identified in the gene coding for GTP cyclohydrolase I. Mutations in tyrosine hydroxylas …
A pathological study has confirmed the 'developmental' nature of the disease. Finally, mutations causing the autosomal domi
The synuclein family.
Lavedan C. Lavedan C. Genome Res. 1998 Sep;8(9):871-80. doi: 10.1101/gr.8.9.871. Genome Res. 1998. PMID: 9750188 Free article. Review.
The synuclein gene family recently came into the spotlight, when one of its members, alpha-synuclein, was found to be mutated in several families with autosomal dominant Parkinson's disease (PD). A peptide of the alpha-synuclein protein had been charac …
The synuclein gene family recently came into the spotlight, when one of its members, alpha-synuclein, was found to be mutated in several fam …
LRRK2 and vesicle trafficking.
Sanna G, Del Giudice MG, Crosio C, Iaccarino C. Sanna G, et al. Biochem Soc Trans. 2012 Oct;40(5):1117-22. doi: 10.1042/BST20120117. Biochem Soc Trans. 2012. PMID: 22988875 Review.
Mutations in LRRK2 (leucine-rich repeat kinase 2) (also known as PARK8 or dardarin) are responsible for the autosomal-dominant form of PD (Parkinson's disease). LRRK2 mutations were found in approximately 3-5% of familial and 1-3% of sporadic PD cases …
Mutations in LRRK2 (leucine-rich repeat kinase 2) (also known as PARK8 or dardarin) are responsible for the autosomal-dominant
Molecular Pathogenesis of Familial Wolff-Parkinson-White Syndrome.
Miyamoto L. Miyamoto L. J Med Invest. 2018;65(1.2):1-8. doi: 10.2152/jmi.65.1. J Med Invest. 2018. PMID: 29593177 Free article. Review.
Familial Wolff-Parkinson-White (WPW) syndrome is an autosomal dominant inherited disease and consists of a small percentage of WPW syndrome which exhibits ventricular pre-excitation by development of accessory atrioventricular pathway. ...This review f …
Familial Wolff-Parkinson-White (WPW) syndrome is an autosomal dominant inherited disease and consists of a small …
The Role of TMEM230 Gene in Parkinson's Disease.
Deng H, Fan K, Jankovic J. Deng H, et al. J Parkinsons Dis. 2018;8(4):469-477. doi: 10.3233/JPD-181421. J Parkinsons Dis. 2018. PMID: 30175983 Free PMC article. Review.
Parkinson's disease (PD) is a common neurodegenerative disease whose pathogenesis remains unknown. TMEM230 gene, encoding a transmembrane protein in secretory and recycling vesicle, has been recently identified as a novel disease-causing gene of aut
Parkinson's disease (PD) is a common neurodegenerative disease whose pathogenesis remains unknown. TMEM230 gene, encodi
Mitochondrial CHCHD-Containing Proteins: Physiologic Functions and Link with Neurodegenerative Diseases.
Zhou ZD, Saw WT, Tan EK. Zhou ZD, et al. Mol Neurobiol. 2017 Sep;54(7):5534-5546. doi: 10.1007/s12035-016-0099-5. Epub 2016 Sep 8. Mol Neurobiol. 2017. PMID: 27631878 Review.
Mutations of CHCHD10 are associated with amyotrophic lateral sclerosis (ALS) and/or frontotemporal lobe dementia (FTD), motor neuron disease, and late-onset spinal muscular atrophy and autosomal dominant mitochondrial myopathy. ...In patients with CHCHD10 mut …
Mutations of CHCHD10 are associated with amyotrophic lateral sclerosis (ALS) and/or frontotemporal lobe dementia (FTD), motor neuron dise
Modeling Parkinson's disease with induced pluripotent stem cells harboring alpha-synuclein mutations.
Singh Dolt K, Hammachi F, Kunath T. Singh Dolt K, et al. Brain Pathol. 2017 Jul;27(4):545-551. doi: 10.1111/bpa.12526. Brain Pathol. 2017. PMID: 28585381 Free PMC article. Review.
Parkinson's disease (PD) is a common neurodegenerative condition affecting more than 8 million people worldwide. ...Many of these familial mutations give rise to a condition that is clinically and neuropathologically similar, if not identical, to sporadic PD.
Parkinson's disease (PD) is a common neurodegenerative condition affecting more than 8 million people worldwide. ...Man
Genes associated with Parkinson syndrome.
Biskup S, Gerlach M, Kupsch A, Reichmann H, Riederer P, Vieregge P, Wüllner U, Gasser T. Biskup S, et al. J Neurol. 2008 Sep;255 Suppl 5:8-17. doi: 10.1007/s00415-008-5005-2. J Neurol. 2008. PMID: 18787878 Review.
Genetic findings have changed our views on Parkinson's disease (PD) and parkinsonism, which will be collectively referred to as Parkinsonian Syndrome (PS) in the present manuscript. ...Point mutations, duplications and triplications in the alpha-synuclein gene cause …
Genetic findings have changed our views on Parkinson's disease (PD) and parkinsonism, which will be collectively referred to a …
26 results