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22. Fluorescence in situ hybridization analysis of peripheral blood cells in Pearson marrow-pancreas syndrome. Yanagihara I; Inui K; Yanagihara K; Park YD; Tanaka J; Ozono K; Okada S; Kurahashi H J Pediatr; 2001 Sep; 139(3):452-5. PubMed ID: 11562629 [TBL] [Abstract][Full Text] [Related]
23. Familial childhood onset neuropathy and cirrhosis with the 4977bp mitochondrial DNA deletion. McDonald DG; McMenamin JB; Farrell MA; Droogan O; Green AJ Am J Med Genet; 2002 Aug; 111(2):191-4. PubMed ID: 12210349 [TBL] [Abstract][Full Text] [Related]
24. Deletion in blood mitochondrial DNA in Kearns-Sayre syndrome. Fischel-Ghodsian N; Bohlman MC; Prezant TR; Graham JM; Cederbaum SD; Edwards MJ Pediatr Res; 1992 Jun; 31(6):557-60. PubMed ID: 1635816 [TBL] [Abstract][Full Text] [Related]
26. mtDNA Deletion in an Iranian Infant with Pearson Marrow Syndrome. Arzanian MT; Eghbali A; Karimzade P; Ahmadi M; Houshmand M; Rezaei N Iran J Pediatr; 2010 Mar; 20(1):107-12. PubMed ID: 23056691 [TBL] [Abstract][Full Text] [Related]
27. The neurological evolution of Pearson syndrome: case report and literature review. Lee HF; Lee HJ; Chi CS; Tsai CR; Chang TK; Wang CJ Eur J Paediatr Neurol; 2007 Jul; 11(4):208-14. PubMed ID: 17434771 [TBL] [Abstract][Full Text] [Related]
29. Atypical presentation of Pearson syndrome in an infant with suspected myelodysplastic syndrome. Tajan A; Riebel A; Zavala MJ; Quiroz L; Monzón P; Ardiles L; Krall P; Lehmann P Pediatr Nephrol; 2024 Feb; 39(2):447-450. PubMed ID: 37682370 [TBL] [Abstract][Full Text] [Related]
30. A novel mitochondrial DNA deletion in a patient with Pearson syndrome and neonatal diabetes mellitus provides insight into disease etiology, severity and progression. Chen XY; Zhao SY; Wang Y; Wang D; Dong CH; Yang Y; Wang ZH; Wu YM Mitochondrial DNA A DNA Mapp Seq Anal; 2016 Jul; 27(4):2492-5. PubMed ID: 26016877 [TBL] [Abstract][Full Text] [Related]
31. Pearson syndrome in the neonatal period: two case reports and review of the literature. Manea EM; Leverger G; Bellmann F; Stanescu PA; Mircea A; Lèbre AS; Rötig A; Munnich A J Pediatr Hematol Oncol; 2009 Dec; 31(12):947-51. PubMed ID: 19881395 [TBL] [Abstract][Full Text] [Related]
32. Pearson syndrome. Farruggia P; Di Marco F; Dufour C Expert Rev Hematol; 2018 Mar; 11(3):239-246. PubMed ID: 29337599 [TBL] [Abstract][Full Text] [Related]
33. [Hematologic improvement of Pearson's syndrome confirmed by mitochondrial DNA analysis]. Park YD; Yanagihara I; Saitoh S; Momoi MY; Yoshioka A Rinsho Ketsueki; 1999 May; 40(5):390-5. PubMed ID: 10390887 [TBL] [Abstract][Full Text] [Related]
34. Pearson marrow-pancreas syndrome with worsening cardiac function caused by pleiotropic rearrangement of mitochondrial DNA. Krauch G; Wilichowski E; Schmidt KG; Mayatepek E Am J Med Genet; 2002 Jun; 110(1):57-61. PubMed ID: 12116272 [TBL] [Abstract][Full Text] [Related]
35. Tubulopathy and pancytopaenia with normal pancreatic function: a variant of Pearson syndrome. Atale A; Bonneau-Amati P; Rötig A; Fischer A; Perez-Martin S; de Lonlay P; Niaudet P; De Parscau L; Mousson C; Thauvin-Robinet C; Munnich A; Huet F; Faivre L Eur J Med Genet; 2009; 52(1):23-6. PubMed ID: 19026771 [TBL] [Abstract][Full Text] [Related]
36. Hematologic features and clinical course of an infant with Pearson syndrome caused by a novel deletion of mitochondrial DNA. Knerr I; Metzler M; Niemeyer CM; Holter W; Gerecke A; Baumann I; Trollmann R; Repp R J Pediatr Hematol Oncol; 2003 Dec; 25(12):948-51. PubMed ID: 14663277 [TBL] [Abstract][Full Text] [Related]
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38. Detection of mtDNA deletion in Pearson syndrome by two independent PCR assays from Guthrie card. Tóth T; Bókay J; Szönyi L; Nagy B; Papp Z Clin Genet; 1998 Mar; 53(3):210-3. PubMed ID: 9630077 [TBL] [Abstract][Full Text] [Related]
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40. [Pearson's syndrome. Pancytopenia with exocrine pancreatic insufficiency: new mitochondrial disease in the first childhood]. Cormier V; Rötig A; Bonnefont JP; Mechinand F; Berthou C; Goulet O; Schmitz J; Blanche S; Vassaut A; Maier M Arch Fr Pediatr; 1991 Mar; 48(3):171-8. PubMed ID: 2048956 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]