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Results by year

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

Year Number of Results
1993 20
1999 1
2000 1
2001 3
2002 1
2004 1
2005 2
2006 1
2007 2
2008 1
2010 1
2011 1
2012 1
2013 1
2014 1
2015 1
2016 2
2017 4
2018 3
2020 2
2021 6
2022 2
2023 4
2024 5
2025 1

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Related Articles by Review for PMID: 20301358

29 results

Results by year

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Page 1
Mitochondrial Neurogastrointestinal Encephalopathy Disease.
Hirano M. Hirano M. 2005 Apr 22 [updated 2016 Jan 14]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2005 Apr 22 [updated 2016 Jan 14]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 20301358 Free Books & Documents. Review.
RRM2B Mitochondrial DNA Maintenance Defects.
Lim AZ, McFarland R, Taylor RW, Gorman GS. Lim AZ, et al. 2014 Apr 17 [updated 2021 Jun 24]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2014 Apr 17 [updated 2021 Jun 24]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 24741716 Free Books & Documents. Review.
Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE-MTDPS1).
Filosto M, Cotti Piccinelli S, Caria F, Gallo Cassarino S, Baldelli E, Galvagni A, Volonghi I, Scarpelli M, Padovani A. Filosto M, et al. J Clin Med. 2018 Oct 26;7(11):389. doi: 10.3390/jcm7110389. J Clin Med. 2018. PMID: 30373120 Free PMC article. Review.
SLC6A3-Related Dopamine Transporter Deficiency Syndrome.
Spaull RVV, Kurian MA. Spaull RVV, et al. 2017 Jul 27 [updated 2023 Sep 28]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2017 Jul 27 [updated 2023 Sep 28]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 28749637 Free Books & Documents. Review.
MNGIE: from nuclear DNA to mitochondrial DNA.
Nishino I, Spinazzola A, Hirano M. Nishino I, et al. Neuromuscul Disord. 2001 Jan;11(1):7-10. doi: 10.1016/s0960-8966(00)00159-0. Neuromuscul Disord. 2001. PMID: 11166160 Review.
Phosphorylase Kinase Deficiency.
Herbert M, Goldstein JL, Rehder C, Austin S, Kishnani PS, Bali DS. Herbert M, et al. 2011 May 31 [updated 2018 Nov 1]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2011 May 31 [updated 2018 Nov 1]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 21634085 Free Books & Documents. Review.
POLG-Related Disorders.
Cohen BH, Chinnery PF, Copeland WC. Cohen BH, et al. 2010 Mar 16 [updated 2024 Feb 29]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2010 Mar 16 [updated 2024 Feb 29]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 20301791 Free Books & Documents. Review.
29 results