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

Year Number of Results
1945 6
1946 12
1947 18
1948 29
1949 50
1950 56
1951 81
1952 70
1953 72
1954 75
1955 64
1956 108
1957 60
1958 91
1959 83
1960 102
1961 150
1962 123
1963 189
1964 202
1965 197
1966 173
1967 213
1968 227
1969 283
1970 512
1971 567
1972 505
1973 430
1974 372
1975 359
1976 361
1977 304
1978 288
1979 263
1980 269
1981 289
1982 299
1983 371
1984 473
1985 489
1986 574
1987 716
1988 669
1989 773
1990 912
1991 846
1992 891
1993 1045
1994 967
1995 1044
1996 1057
1997 1275
1998 1284
1999 1577
2000 1750
2001 1707
2002 1932
2003 2216
2004 2107
2005 2307
2006 2714
2007 2818
2008 3037
2009 3346
2010 3614
2011 3825
2012 4046
2013 4204
2014 4283
2015 4581
2016 4791
2017 4963
2018 4921
2019 5192
2020 5734
2021 5725
2022 5655
2023 5573
2024 5765
2025 5699
2026 2086

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113,713 results

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Page 1
Autosomal recessive parkinsonism.
Bonifati V. Bonifati V. Parkinsonism Relat Disord. 2012 Jan;18 Suppl 1:S4-6. doi: 10.1016/S1353-8020(11)70004-9. Parkinsonism Relat Disord. 2012. PMID: 22166450 Review.
Several forms of autosomal recessive parkinsonism are known. In three forms, caused by mutations in parkin (PARK2), PINK1 (PARK6), or DJ-1 (PARK7), the phenotype is usually characterized by levodopa-responsive parkinsonism without atypical features. .. …
Several forms of autosomal recessive parkinsonism are known. In three forms, caused by mutations in parkin (PARK2), PIN …
Autosomal recessive juvenile parkinsonism.
Saito M, Maruyama M, Ikeuchi K, Kondo H, Ishikawa A, Yuasa T, Tsuji S. Saito M, et al. Brain Dev. 2000 Sep;22 Suppl 1:S115-7. doi: 10.1016/s0387-7604(00)00137-6. Brain Dev. 2000. PMID: 10984671 Review.
Autosomal recessive juvenile parkinsonism (AR-JP) is a hereditary neurodegenerative disorder characterized by levodopa-responsive parkinsonism with onset before age 40 years and a slowly progressive course. Families with this condition have been descri …
Autosomal recessive juvenile parkinsonism (AR-JP) is a hereditary neurodegenerative disorder characterized by levodopa- …
Monogenic Parkinson's Disease: Genotype, Phenotype, Pathophysiology, and Genetic Testing.
Jia F, Fellner A, Kumar KR. Jia F, et al. Genes (Basel). 2022 Mar 7;13(3):471. doi: 10.3390/genes13030471. Genes (Basel). 2022. PMID: 35328025 Free PMC article. Review.
Well-established Parkinson's disease genes include autosomal dominant forms (SNCA, LRRK2, and VPS35) and autosomal recessive forms (PRKN, PINK1 and DJ1). ...Additionally, we discuss the role of heterozygous mutations in autosomal recessive genes …
Well-established Parkinson's disease genes include autosomal dominant forms (SNCA, LRRK2, and VPS35) and autosomal recessiv …
A Practical Approach to Early-Onset Parkinsonism.
Riboldi GM, Frattini E, Monfrini E, Frucht SJ, Di Fonzo A. Riboldi GM, et al. J Parkinsons Dis. 2022;12(1):1-26. doi: 10.3233/JPD-212815. J Parkinsons Dis. 2022. PMID: 34569973 Free PMC article. Review.
Early-onset parkinsonism (EO parkinsonism), defined as subjects with disease onset before the age of 40 or 50 years, can be the main clinical presentation of a variety of conditions that are important to differentiate. ...Here we summarize the most important conditi …
Early-onset parkinsonism (EO parkinsonism), defined as subjects with disease onset before the age of 40 or 50 years, can be th …
Parkinson's disease - genetic cause.
Cherian A, K P D, Vijayaraghavan A. Cherian A, et al. Curr Opin Neurol. 2023 Aug 1;36(4):292-301. doi: 10.1097/WCO.0000000000001167. Epub 2023 May 24. Curr Opin Neurol. 2023. PMID: 37366140 Review.
About 5-10% of all patients suffer from a monogenic form of Parkinson's disease. RECENT FINDINGS: Mutations in autosomal dominant genes (e.g. SNCA, LRRK2, VPS35) or autosomal recessive genes (e.g. PRKN, PINK1, DJ-1) can cause genetic Parkinson's disease. R …
About 5-10% of all patients suffer from a monogenic form of Parkinson's disease. RECENT FINDINGS: Mutations in autosomal dominant gen …
The roles of PINK1, parkin, and mitochondrial fidelity in Parkinson's disease.
Pickrell AM, Youle RJ. Pickrell AM, et al. Neuron. 2015 Jan 21;85(2):257-73. doi: 10.1016/j.neuron.2014.12.007. Neuron. 2015. PMID: 25611507 Free PMC article. Review.
Although mutations or variants in many genes increase the susceptibility to Parkinson's disease, only a handful of monogenic causes of parkinsonism have been identified. Biochemical and genetic studies reveal that the products of two genes that are mutated in autosomal …
Although mutations or variants in many genes increase the susceptibility to Parkinson's disease, only a handful of monogenic causes of pa …
Autosomal recessive juvenile parkinsonism: a key to understanding nigral degeneration in sporadic Parkinson's disease.
Hattori N, Shimura H, Kubo S, Kitada T, Wang M, Asakawa S, Minashima S, Shimizu N, Suzuki T, Tanaka K, Mizuno Y. Hattori N, et al. Neuropathology. 2000 Sep;20 Suppl:S85-90. doi: 10.1046/j.1440-1789.2000.00312.x. Neuropathology. 2000. PMID: 11037196 Review.
Alpha-synuclein is involved in a rare dominant form of familial PD with dopa-responsive parkinsonism features and Lewy body-positive pathology. In contrast, parkin is responsible for the autosomal recessive form (AR-JP) of early onset PD with Lewy body-negati …
Alpha-synuclein is involved in a rare dominant form of familial PD with dopa-responsive parkinsonism features and Lewy body-positive …
Clinical approach to tremor in children.
Torres-Russotto D. Torres-Russotto D. Parkinsonism Relat Disord. 2019 Feb;59:111-116. doi: 10.1016/j.parkreldis.2019.03.015. Epub 2019 Mar 23. Parkinsonism Relat Disord. 2019. PMID: 30952437 Review.
Pediatric Movement Disorders encompass a very large and complex group of diseases, among which Tremor is one of the least studied. Evaluation of tremors in kids carries significant challenges, in particular the fact that many tremor etiologies have other associated movemen …
Pediatric Movement Disorders encompass a very large and complex group of diseases, among which Tremor is one of the least studied. Ev …
Parkinsonism.
Keener AM, Bordelon YM. Keener AM, et al. Semin Neurol. 2016 Aug;36(4):330-4. doi: 10.1055/s-0036-1585097. Epub 2016 Sep 19. Semin Neurol. 2016. PMID: 27643900 Review.
Parkinsonism is a clinical syndrome, which is characterized by bradykinesia, rigidity, rest tremor, and postural instability. Idiopathic Parkinson disease (PD) is the most common cause of this syndrome, though there are several other important etiologies that must be consi …
Parkinsonism is a clinical syndrome, which is characterized by bradykinesia, rigidity, rest tremor, and postural instability. Idiopat …
Dopamine transporter SPECT imaging in Parkinson's disease and parkinsonian disorders.
Akdemir ÜÖ, Bora Tokçaer A, Atay LÖ. Akdemir ÜÖ, et al. Turk J Med Sci. 2021 Apr 30;51(2):400-410. doi: 10.3906/sag-2008-253. Turk J Med Sci. 2021. PMID: 33237660 Free PMC article. Review.
The dopamine transporter (DAT) imaging provides an objective tool for the assessment of dopaminergic function of presynaptic terminals which is valuable for the differential diagnosis of parkinsonian disorders related to a striatal dopaminergic deficiency from movem …
The dopamine transporter (DAT) imaging provides an objective tool for the assessment of dopaminergic function of presynaptic terminals which …
113,713 results
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