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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 1028
1994 966
1995 1044
1996 1056
1997 1275
1998 1281
1999 1573
2000 1745
2001 1704
2002 1931
2003 2209
2004 2103
2005 2300
2006 2704
2007 2812
2008 3025
2009 3332
2010 3603
2011 3816
2012 4036
2013 4194
2014 4267
2015 4573
2016 4780
2017 4947
2018 4908
2019 5172
2020 5716
2021 5704
2022 5633
2023 5552
2024 5748
2025 5695
2026 2205

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113,567 results

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8 articles found by citation matching

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Page 1
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.
Although rarer than classical late-onset Parkinson's disease (PD) and not infrequently overlapping with forms of juvenile onset PD, a correct diagnosis of the specific cause of EO parkinsonism is critical for offering appropriate counseling to patients, for f …
Although rarer than classical late-onset Parkinson's disease (PD) and not infrequently overlapping with forms of juvenile
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 …
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.
The contribution of genetic factors to the pathogenesis of Parkinson's disease (PD) is supported by the demonstration of the high concordance in twins studies using positron emission tomography (PET), the increased risk among relatives of PD patients in case-control …
The contribution of genetic factors to the pathogenesis of Parkinson's disease (PD) is supported by the demonstration of the h …
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 …
Maladie de Parkinson et syndromes parkinsoniens : les signes moteurs.
Grabli D. Grabli D. Presse Med. 2017 Mar;46(2 Pt 1):187-194. doi: 10.1016/j.lpm.2017.01.003. Epub 2017 Feb 21. Presse Med. 2017. PMID: 28233705 Review. French.
The clinical analysis of motor symptoms may guide clinical diagnosis. Parkinson's disease is characterized by a pure asymmetric parkinsonian syndrome, responsive to dopaminergic treatment. ...Gait disturbances (postural instability and freezing) are late in …
The clinical analysis of motor symptoms may guide clinical diagnosis. Parkinson's disease is characterized by a pure asymmetri …
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 described pre
Autosomal recessive juvenile parkinsonism (AR-JP) is a hereditary neurodegenerative disorder characterized by levodopa-
Atypical Parkinsonian Disorders.
Olfati N, Akhoundi FH, Litvan I. Olfati N, et al. Neurol Clin. 2025 May;43(2):249-277. doi: 10.1016/j.ncl.2024.12.006. Epub 2025 Jan 22. Neurol Clin. 2025. PMID: 40185521 Review.
Atypical parkinsonian disorders (APD) include progressive supranuclear palsy, corticobasal degeneration, and multiple system atrophy. Identifying APD is important because they have different pathogenesis, disease course, and prognosis than Parkinson's …
Atypical parkinsonian disorders (APD) include progressive supranuclear palsy, corticobasal degeneration, and multiple system a …
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 b …
Parkinsonism is a clinical syndrome, which is characterized by bradykinesia, rigidity, rest tremor, and postural instability. Idiopathic …
Parkin-associated Parkinson's disease.
von Coelln R, Dawson VL, Dawson TM. von Coelln R, et al. Cell Tissue Res. 2004 Oct;318(1):175-84. doi: 10.1007/s00441-004-0924-4. Epub 2004 Jul 30. Cell Tissue Res. 2004. PMID: 15503153 Review.
Mutations in the PARK2 gene coding for parkin cause autosomal recessive juvenile parkinsonism (AR-JP), a familial form of Parkinson's disease (PD). ...
Mutations in the PARK2 gene coding for parkin cause autosomal recessive juvenile parkinsonism (AR-JP), a familial form …
Non-motor parkinsonism.
Pfeiffer RF. Pfeiffer RF. Parkinsonism Relat Disord. 2007;13 Suppl 3:S211-20. doi: 10.1016/S1353-8020(08)70004-X. Parkinsonism Relat Disord. 2007. PMID: 18267238 Review.
Recent years have brought increased awareness of and attention to the non-motor aspects of Parkinson's disease. Non-motor features encompass a surprisingly broad clinical spectrum that includes sensory dysfunction, behavioral abnormalities, autonomic impairment, sle …
Recent years have brought increased awareness of and attention to the non-motor aspects of Parkinson's disease. Non-motor feat …
113,567 results
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