Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1945 5
1946 4
1947 4
1948 4
1949 6
1950 11
1951 12
1952 14
1953 17
1954 8
1955 11
1956 13
1957 10
1958 33
1959 16
1960 13
1961 28
1962 7
1963 29
1964 18
1965 24
1966 18
1967 22
1968 25
1969 20
1970 23
1971 17
1972 20
1973 21
1974 21
1975 32
1976 40
1977 41
1978 28
1979 52
1980 24
1981 38
1982 44
1983 35
1984 45
1985 42
1986 48
1987 49
1988 65
1989 76
1990 67
1991 77
1992 81
1993 122
1994 123
1995 118
1996 161
1997 150
1998 168
1999 132
2000 170
2001 215
2002 230
2003 256
2004 283
2005 365
2006 419
2007 473
2008 583
2009 651
2010 739
2011 880
2012 904
2013 946
2014 1070
2015 1174
2016 1180
2017 1268
2018 1426
2019 1507
2020 1768
2021 1979
2022 1860
2023 1784
2024 633

Text availability

Article attribute

Article type

Publication date

Search Results

22,247 results

Results by year

Filters applied: . Clear all
The following term was not found in PubMed: Kethelyn
Page 1
Machado-Joseph disease/spinocerebellar ataxia type 3.
Paulson H. Paulson H. Handb Clin Neurol. 2012;103:437-49. doi: 10.1016/B978-0-444-51892-7.00027-9. Handb Clin Neurol. 2012. PMID: 21827905 Free PMC article. Review.
Machado-Joseph disease (MJD), also known as spinocerebellar ataxia type 3 (SCA3), may be the most common dominantly inherited ataxia in the world. ...
Machado-Joseph disease (MJD), also known as spinocerebellar ataxia type 3 (SCA3), may be the most common dominantly inherited ataxia …
Manuel Machado Macedo.
Fragata J, Roquette J. Fragata J, et al. Port J Card Thorac Vasc Surg. 2021 Nov 7;28(3):15-19. doi: 10.48729/pjctvs.189. Port J Card Thorac Vasc Surg. 2021. PMID: 35333474 No abstract available.
Animal Models of Machado-Joseph Disease.
Schmidt J, Schmidt T. Schmidt J, et al. Adv Exp Med Biol. 2018;1049:289-308. doi: 10.1007/978-3-319-71779-1_15. Adv Exp Med Biol. 2018. PMID: 29427110 Review.
Animal models are an important tool to study the pathophysiology of Machado-Joseph Disease (MJD). So far, animal models using simple organisms (like the round worm Caenorhabditis elegans or the fruit fly drosophila) but also mammalian models (mouse and even a non-human pri …
Animal models are an important tool to study the pathophysiology of Machado-Joseph Disease (MJD). So far, animal models using simple …
Reconstructing the History of Machado-Joseph Disease.
Meira AT, Pedroso JL, Boller F, Franklin GL, Barsottini OGP, Teive HAG. Meira AT, et al. Eur Neurol. 2020;83(1):99-104. doi: 10.1159/000507191. Epub 2020 Apr 28. Eur Neurol. 2020. PMID: 32344416 Free article. Review.
Machado-Joseph disease (MJD), or spinocerebellar ataxia type 3, was originally described in members of the families of Machado, Thomas, and Joseph from Sao Miguel Island, Azores, Portugal, in 1972. ...
Machado-Joseph disease (MJD), or spinocerebellar ataxia type 3, was originally described in members of the families of Machado …
Recent therapeutic prospects for Machado-Joseph disease.
Costa MDC. Costa MDC. Curr Opin Neurol. 2020 Aug;33(4):519-526. doi: 10.1097/WCO.0000000000000832. Curr Opin Neurol. 2020. PMID: 32657894 Review.
PURPOSE OF REVIEW: Machado-Joseph disease (MJD), also known as spinocerebellar ataxia type 3 (SCA3), is a fatal, dominantly inherited, neurodegenerative disease caused by expansion of a CAG repeat in the coding region of the ATXN3 gene. ...
PURPOSE OF REVIEW: Machado-Joseph disease (MJD), also known as spinocerebellar ataxia type 3 (SCA3), is a fatal, dominantly inherited …
Pharmacological Therapies for Machado-Joseph Disease.
Duarte-Silva S, Maciel P. Duarte-Silva S, et al. Adv Exp Med Biol. 2018;1049:369-394. doi: 10.1007/978-3-319-71779-1_19. Adv Exp Med Biol. 2018. PMID: 29427114 Review.
Machado-Joseph disease (MJD), also known as Spinocerebellar Ataxia type 3 (SCA3), is the most common autosomal dominant ataxia worldwide. ...
Machado-Joseph disease (MJD), also known as Spinocerebellar Ataxia type 3 (SCA3), is the most common autosomal dominant ataxia worldw …
Clinical Features of Machado-Joseph Disease.
Mendonça N, França MC Jr, Gonçalves AF, Januário C. Mendonça N, et al. Adv Exp Med Biol. 2018;1049:255-273. doi: 10.1007/978-3-319-71779-1_13. Adv Exp Med Biol. 2018. PMID: 29427108 Review.
Machado-Joseph disease (MJD) also known as Spinocerebellar ataxia type 3, is a hereditary neurodegenerative disease associated with severe clinical manifestations and premature death. ...
Machado-Joseph disease (MJD) also known as Spinocerebellar ataxia type 3, is a hereditary neurodegenerative disease associated with s …
Machado-Joseph shoe.
Liu CS, Hsieh M, Chen YY, Lo MC. Liu CS, et al. Mov Disord. 2005 Jan;20(1):66-8. doi: 10.1002/mds.20277. Mov Disord. 2005. PMID: 15390034
Machado-Joseph shoe (MJS), defined as a shoe/slipper with a deep hallux imprint at its base, and hyperostosis/osteoma toe were two early ataxic signs in 17 of 31 patients (55%) and 24 of 31 patients (77%) with Machado-Joseph disease (MJD), respectively. ...
Machado-Joseph shoe (MJS), defined as a shoe/slipper with a deep hallux imprint at its base, and hyperostosis/osteoma toe were two ea …
Machado-Joseph Deubiquitinases: From Cellular Functions to Potential Therapy Targets.
Zeng C, Zhao C, Ge F, Li Y, Cao J, Ying M, Lu J, He Q, Yang B, Dai X, Zhu H. Zeng C, et al. Front Pharmacol. 2020 Aug 26;11:1311. doi: 10.3389/fphar.2020.01311. eCollection 2020. Front Pharmacol. 2020. PMID: 32982735 Free PMC article. Review.
They mainly function by cutting ubiquitin chains of the substrates. The Machado-Joseph domain-containing proteases (MJDs) is one of the sub-families of DUBs, consisting of four members, namely, Ataxin-3, Ataxin-3L, JOSD1, and JOSD2. Recent studies have provided new insight …
They mainly function by cutting ubiquitin chains of the substrates. The Machado-Joseph domain-containing proteases (MJDs) is one of t …
Sleep disorders in Machado-Joseph disease.
Pedroso JL, Braga-Neto P, Martinez AR, Martins CR Junior, Rezende Filho FM, Sobreira-Neto MA, Prado LB, do Prado GF, França MC Junior, Barsottini OG. Pedroso JL, et al. Curr Opin Psychiatry. 2016 Nov;29(6):402-8. doi: 10.1097/YCO.0000000000000287. Curr Opin Psychiatry. 2016. PMID: 27584711 Review.
PURPOSE OF REVIEW: This article provides a description on clinical features and pathophysiology of the main sleep disorders observed in Machado-Joseph disease (MJD). RECENT FINDINGS: Pathological studies have clearly demonstrated that degenerative process in MJD is widespr …
PURPOSE OF REVIEW: This article provides a description on clinical features and pathophysiology of the main sleep disorders observed in M …
22,247 results
You have reached the last available page of results. Please see the User Guide for more information.