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25. A case of Pearson syndrome associated with multiple renal cysts. Gürgey A; Ozalp I; Rötig A; Coşkun T; Tekinalp G; Erdem G; Akeören Z; Caglar M; Bakkaloglu A Pediatr Nephrol; 1996 Oct; 10(5):637-8. PubMed ID: 8897573 [TBL] [Abstract][Full Text] [Related]
26. Mitochondrial DNA deletion in Pearson's marrow/pancreas syndrome. Rotig A; Colonna M; Bonnefont JP; Blanche S; Fischer A; Saudubray JM; Munnich A Lancet; 1989 Apr; 1(8643):902-3. PubMed ID: 2564980 [No Abstract] [Full Text] [Related]
27. 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]
28. A novel 3670-base pair mitochondrial DNA deletion resulting in multi-systemic manifestations in a child. Liu HM; Tsai LP; Chien YH; Wu JF; Weng WC; Peng SF; Wu ET; Huang PH; Lee WT; Tsai IJ; Hwu WL; Lee NC Pediatr Neonatol; 2012 Aug; 53(4):264-8. PubMed ID: 22964285 [TBL] [Abstract][Full Text] [Related]
29. A novel mtDNA deletion in an infant with Pearson syndrome. Kapsa R; Thompson GN; Thorburn DR; Dahl HH; Marzuki S; Byrne E; Blok RB J Inherit Metab Dis; 1994; 17(5):521-6. PubMed ID: 7837757 [TBL] [Abstract][Full Text] [Related]
30. Schwachman or Pearson syndrome. Ozsoylu S Am J Hematol; 1998 Mar; 57(3):262. PubMed ID: 9495386 [No Abstract] [Full Text] [Related]
31. A 2 bp deletion in the mitochondrial ATP 6 gene responsible for the NARP (neuropathy, ataxia, and retinitis pigmentosa) syndrome. Mordel P; Schaeffer S; Dupas Q; Laville MA; Gérard M; Chapon F; Allouche S Biochem Biophys Res Commun; 2017 Dec; 494(1-2):133-137. PubMed ID: 29054413 [TBL] [Abstract][Full Text] [Related]
32. Two new cases with Pearson syndrome and review of Hacettepe experience. Topaloğlu R; Lebre AS; Demirkaya E; Kuşkonmaz B; Coşkun T; Orhan D; Gürgey A; Gümrük F Turk J Pediatr; 2008; 50(6):572-6. PubMed ID: 19227422 [TBL] [Abstract][Full Text] [Related]
33. Myopathology and a mitochondrial DNA deletion in the Pearson marrow and pancreas syndrome. de Vries DD; Buzing CJ; Ruitenbeek W; van der Wouw MP; Sperl W; Sengers RC; Trijbels JM; van Oost BA Neuromuscul Disord; 1992; 2(3):185-95. PubMed ID: 1483044 [TBL] [Abstract][Full Text] [Related]
34. High mitochondrial DNA T8993G mutation (<90%) without typical features of Leigh's and NARP syndromes. Tsao CY; Mendell JR; Bartholomew D J Child Neurol; 2001 Jul; 16(7):533-5. PubMed ID: 11453454 [TBL] [Abstract][Full Text] [Related]
35. 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]
36. [NARP syndrome--a less known mitochondrial disease]. Kuusisto H; Simola KO; Keränen T Duodecim; 2003; 119(16):1563-6. PubMed ID: 14535029 [No Abstract] [Full Text] [Related]
37. The frequency of mtDNA 8994 polymorphism and detection of the NARP 8993 mutation. Gray RG; Davies PA; Marshall A; Heath SK J Med Genet; 2002 Mar; 39(3):204-5. PubMed ID: 11897826 [No Abstract] [Full Text] [Related]
38. [Ophthalmoplegia-plus: clinical variability, biochemical defects of the mitochondria respiratory chain and deletions of the mitochondria genome]. Zierz S; von Wersebe O; Gerbitz KD; Jerusalem F Nervenarzt; 1990 Jun; 61(6):332-9. PubMed ID: 2377259 [No Abstract] [Full Text] [Related]
39. Kearns-Sayre syndrome with features of Pearson's marrow-pancreas syndrome and a novel 2905-base pair mitochondrial DNA deletion. Becher MW; Wills ML; Noll WW; Hurko O; Price DL Hum Pathol; 1999 May; 30(5):577-81. PubMed ID: 10333230 [TBL] [Abstract][Full Text] [Related]