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For: Farruggia P, Di Cataldo A, Pinto RM, Palmisani E, Macaluso A, Valvo LL, Cantarini ME, Tornesello A, Corti P, Fioredda F, Varotto S, Martire B, Moroni I, Puccio G, Russo G, Dufour C, Pillon M. Pearson Syndrome: A Retrospective Cohort Study from the Marrow Failure Study Group of A.I.E.O.P. (Associazione Italiana Emato-Oncologia Pediatrica). JIMD Rep 2016;26:37-43. [PMID: 26238250 DOI: 10.1007/8904_2015_470] [Cited by in Crossref: 20] [Cited by in F6Publishing: 18] [Article Influence: 2.9] [Reference Citation Analysis]
Number Citing Articles
1 Anteneová N, Kelifová S, Kolářová H, Vondráčková A, Tóthová I, Lišková P, Magner M, Zámečník J, Hansíková H, Zeman J, Tesařová M, Honzík T. The Phenotypic Spectrum of 47 Czech Patients with Single, Large-Scale Mitochondrial DNA Deletions. Brain Sci 2020;10:E766. [PMID: 33105723 DOI: 10.3390/brainsci10110766] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
2 Liu R, Mo GL, Song YZ. Identification of a novel large deletion of the mitochondrial DNA in an infant with Pearson syndrome: a case report. Transl Pediatr 2021;10:204-8. [PMID: 33633954 DOI: 10.21037/tp-20-138] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
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5 Gopan A, Sarma MS. Mitochondrial hepatopathy: Respiratory chain disorders- ‘breathing in and out of the liver’. World J Hepatol 2021; 13(11): 1707-1726 [PMID: 34904040 DOI: 10.4254/wjh.v13.i11.1707] [Reference Citation Analysis]
6 Long Z, Li H, Du Y, Han B. Congenital sideroblastic anemia: Advances in gene mutations and pathophysiology. Gene 2018;668:182-9. [DOI: 10.1016/j.gene.2018.05.074] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
7 Pronman L, Rondinelli M, Burkardt DD, Velayuthan S, Khalili AS, Bedoyan JK. Pearson Syndrome: A Rare Cause of Failure to Thrive in Infants. Clin Pediatr (Phila) 2019;58:819-24. [PMID: 30845838 DOI: 10.1177/0009922819834285] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
8 Gucek M, Sack MN. Proteomic and metabolomic advances uncover biomarkers of mitochondrial disease pathophysiology and severity. J Clin Invest 2021;131:145158. [PMID: 33463543 DOI: 10.1172/JCI145158] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Tesarova M, Vondrackova A, Stufkova H, Veprekova L, Stranecky V, Berankova K, Hansikova H, Magner M, Galoova N, Honzik T, Vodickova E, Stary J, Zeman J. Sideroblastic anemia associated with multisystem mitochondrial disorders. Pediatr Blood Cancer 2019;66:e27591. [PMID: 30588737 DOI: 10.1002/pbc.27591] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 1.8] [Reference Citation Analysis]
10 Sankararaman S, Schindler T, Sferra TJ. Management of Exocrine Pancreatic Insufficiency in Children. Nutrition in Clinical Practice 2019;34:S27-42. [DOI: 10.1002/ncp.10388] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
11 Duran J, Martinez A, Adler E. Cardiovascular Manifestations of Mitochondrial Disease. Biology (Basel) 2019;8:E34. [PMID: 31083569 DOI: 10.3390/biology8020034] [Cited by in Crossref: 7] [Cited by in F6Publishing: 3] [Article Influence: 2.3] [Reference Citation Analysis]
12 Björkman K, Vissing J, Østergaard E, Bindoff LA, de Coo IFM, Engvall M, Hikmat O, Isohanni P, Kollberg G, Lindberg C, Majamaa K, Naess K, Uusimaa J, Tulinius M, Darin N. Phenotypic spectrum and clinical course of single large-scale mitochondrial DNA deletion disease in the paediatric population: a multicentre study. J Med Genet 2021:jmedgenet-2021-108006. [PMID: 34872991 DOI: 10.1136/jmedgenet-2021-108006] [Reference Citation Analysis]
13 Nishimura T, Yamada A, Utoyama M, Saito Y, Moritake H. A useful method to diagnose Pearson syndrome mimicking Diamond-Blackfan anemia. Pediatr Int 2021;63:223-5. [PMID: 33586850 DOI: 10.1111/ped.14385] [Reference Citation Analysis]
14 Nishimura A, Hirabayashi S, Hasegawa D, Yoshida K, Shiraishi Y, Ashiarai M, Hosoya Y, Fujiwara T, Harigae H, Miyano S, Ogawa S, Manabe A. Acquisition of monosomy 7 and a RUNX1 mutation in Pearson syndrome. Pediatr Blood Cancer 2021;68:e28799. [PMID: 33200495 DOI: 10.1002/pbc.28799] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
15 Furutani E, Newburger PE, Shimamura A. Neutropenia in the age of genetic testing: Advances and challenges. Am J Hematol 2019;94:384-93. [PMID: 30536760 DOI: 10.1002/ajh.25374] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
16 Bhowmick SS, Lang AE. Movement Disorders and Renal Diseases. Mov Disord Clin Pract 2020;7:763-79. [PMID: 33043074 DOI: 10.1002/mdc3.13005] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
17 Yoshimi A, Grünert SC, Cario H, Fisch A, Gross-Wieltsch U, Timmermann K, Kontny U, Lobitz S, Odenthal HS, Schmid I, Uetz B, Höll T, Rötig A, Lücke T, Borkhardt A, Strauß G, Hohnecker A, Metzler M, Karall D, Niemeyer CM. Haematological characteristics and spontaneous haematological recovery in Pearson syndrome. Br J Haematol 2021;193:1283-7. [PMID: 33837965 DOI: 10.1111/bjh.17434] [Reference Citation Analysis]
18 Rius R, Compton AG, Baker NL, Welch AE, Coman D, Kava MP, Minoche AE, Cowley MJ, Thorburn DR, Christodoulou J. Application of Genome Sequencing from Blood to Diagnose Mitochondrial Diseases. Genes (Basel) 2021;12:607. [PMID: 33924034 DOI: 10.3390/genes12040607] [Reference Citation Analysis]
19 Tadiotto E, Maines E, Degani D, Balter R, Bordugo A, Cesaro S. Bone marrow features in Pearson syndrome with neonatal onset: A case report and review of the literature. Pediatr Blood Cancer 2018;65. [PMID: 29286581 DOI: 10.1002/pbc.26939] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.6] [Reference Citation Analysis]
20 Spoor J, Farajifard H, Rezaei N. Congenital neutropenia and primary immunodeficiency diseases. Critical Reviews in Oncology/Hematology 2019;133:149-62. [DOI: 10.1016/j.critrevonc.2018.10.003] [Cited by in Crossref: 16] [Cited by in F6Publishing: 8] [Article Influence: 5.3] [Reference Citation Analysis]