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

Year Number of Results
1990 1
1991 4
1992 6
1993 10
1994 4
1995 7
1996 6
1997 5
1998 13
1999 10
2000 7
2001 7
2002 8
2003 10
2004 4
2005 10
2006 7
2007 11
2008 11
2009 15
2010 10
2011 18
2012 16
2013 16
2014 28
2015 26
2016 19
2017 15
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2020 36
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2023 36
2024 11

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437 results

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Page 1
Pearson syndrome.
Farruggia P, Di Marco F, Dufour C. Farruggia P, et al. Expert Rev Hematol. 2018 Mar;11(3):239-246. doi: 10.1080/17474086.2018.1426454. Epub 2018 Jan 23. Expert Rev Hematol. 2018. PMID: 29337599 Review.
Pearson syndrome (PS) is a sporadic and very rare syndrome classically associated with single large-scale deletions of mitochondrial DNA and characterized by refractory sideroblastic anemia during infancy. ...
Pearson syndrome (PS) is a sporadic and very rare syndrome classically associated with single large-scale deletions of mitocho
Pearson syndrome: a multisystem mitochondrial disease with bone marrow failure.
Yoshimi A, Ishikawa K, Niemeyer C, Grünert SC. Yoshimi A, et al. Orphanet J Rare Dis. 2022 Oct 17;17(1):379. doi: 10.1186/s13023-022-02538-9. Orphanet J Rare Dis. 2022. PMID: 36253820 Free PMC article. Review.
Pearson syndrome (PS) is a rare fatal mitochondrial disorder caused by single large-scale mitochondrial DNA deletions (SLSMDs). ...
Pearson syndrome (PS) is a rare fatal mitochondrial disorder caused by single large-scale mitochondrial DNA deletions (SLSMDs)
Pearson syndrome.
Tedjaseputra A, Radhakrishnan K, Martin M, Downie P, Stergiotis M, Bain BJ. Tedjaseputra A, et al. Am J Hematol. 2023 Mar;98(3):527-528. doi: 10.1002/ajh.26794. Epub 2022 Dec 5. Am J Hematol. 2023. PMID: 36436195 Free article. No abstract available.
[Pearson syndrome].
Goto Y. Goto Y. Nihon Rinsho. 2002 Apr;60 Suppl 4:270-2. Nihon Rinsho. 2002. PMID: 12013863 Review. Japanese. No abstract available.
Pearson Syndrome: Spontaneously Recovering Anemia and Hypoparathyroidism.
Nilay M, Phadke SR. Nilay M, et al. Indian J Pediatr. 2020 Dec;87(12):1070-1072. doi: 10.1007/s12098-020-03333-9. Epub 2020 Jun 15. Indian J Pediatr. 2020. PMID: 32537709
Pearson syndrome is a genetic disorder caused by mutations in the mitochondrial genome, characterized by failure to thrive with hematological and gastrointestinal abnormalities. Individuals with Pearson syndrome may develop the symptoms and signs of Ke
Pearson syndrome is a genetic disorder caused by mutations in the mitochondrial genome, characterized by failure to thrive wit
Juvenile Pearson syndrome.
Blaw ME, Mize CE. Blaw ME, et al. J Child Neurol. 1990 Jul;5(3):187-90. J Child Neurol. 1990. PMID: 2398232
The clinical and magnetic resonance imaging findings of a 14-year-old boy with Pearson syndrome are presented. The patient represents the oldest living survivor of the original four patients described by Pearson and associates. ...Several mitochondrial myopathies ha …
The clinical and magnetic resonance imaging findings of a 14-year-old boy with Pearson syndrome are presented. The patient rep …
Pearson syndrome in a child transplanted for Diamond-Blackfan anemia.
Uygun V, Daloğlu H, Öztürkmen S, Karasu G, Yeşilipek A. Uygun V, et al. Arch Argent Pediatr. 2021 Oct;119(5):e559-e561. doi: 10.5546/aap.2021.eng.e559. Arch Argent Pediatr. 2021. PMID: 34569763 Free article. English, Spanish.
Pearson syndrome (PS), shares a number of overlapping features with Diamond-Blackfan anemia (DBA), including early onset of severe anemia, making differential diagnosis important. ...
Pearson syndrome (PS), shares a number of overlapping features with Diamond-Blackfan anemia (DBA), including early onset of se
Pearson syndrome-like anemia induced by accumulation of mutant mtDNA and anemia with imbalanced white blood cell lineages induced by Drp1 deletion in a murine model.
Ishikawa K, Honma Y, Yoshimi A, Katada S, Ishihara T, Ishihara N, Nakada K. Ishikawa K, et al. Pharmacol Res. 2022 Nov;185:106467. doi: 10.1016/j.phrs.2022.106467. Epub 2022 Sep 28. Pharmacol Res. 2022. PMID: 36179953 Free article.
The former showed signs of aberrant respiration, analogous to Pearson syndrome, while the latter showed signs of abnormal mitochondrial dynamics and was associated with changes in the relative proportions of leukocyte lineages. ...
The former showed signs of aberrant respiration, analogous to Pearson syndrome, while the latter showed signs of abnormal mito …
B-cell Immunodeficiency in a Patient with Pearson Syndrome.
Chen YC, Jou ST, Lee NC, Chiang BL, Yu HH. Chen YC, et al. J Clin Immunol. 2023 Feb;43(2):335-337. doi: 10.1007/s10875-022-01406-2. Epub 2022 Nov 15. J Clin Immunol. 2023. PMID: 36378425 No abstract available.
437 results