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2. Deletion of the mitochondrial DNA in a case of de Toni-Debré-Fanconi syndrome and Pearson syndrome. Niaudet P; Heidet L; Munnich A; Schmitz J; Bouissou F; Gubler MC; Rötig A Pediatr Nephrol; 1994 Apr; 8(2):164-8. PubMed ID: 8018492 [TBL] [Abstract][Full Text] [Related]
4. Pearson's marrow/pancreas syndrome: a histological and genetic study. Morikawa Y; Matsuura N; Kakudo K; Higuchi R; Koike M; Kobayashi Y Virchows Arch A Pathol Anat Histopathol; 1993; 423(3):227-31. PubMed ID: 8236818 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. Mitochondrial cytopathy combined with Fanconi's syndrome. Wang LC; Lee WT; Tsai WY; Tsau YK; Shen YZ Pediatr Neurol; 2000 May; 22(5):403-6. PubMed ID: 10913735 [TBL] [Abstract][Full Text] [Related]
7. Pearson's marrow/pancreas syndrome: haematological features associated with deletion and duplication of mitochondrial DNA. Smith OP; Hann IM; Woodward CE; Brockington M Br J Haematol; 1995 Jun; 90(2):469-72. PubMed ID: 7794775 [TBL] [Abstract][Full Text] [Related]
8. [A case of transitory Fanconi syndrome associated with acute renal insufficiency and hypoplasia of the bone marrow]. Benigno V; Scuderi F; Puccio G; Accomando A; Mogavero S Pediatr Med Chir; 1988; 10(3):335-7. PubMed ID: 3186517 [TBL] [Abstract][Full Text] [Related]
9. Renal Fanconi syndrome associated with monoclonal κ free light chain in a patient with Waldenström macroglobulinemia. Ugai T; Tsuda K; Sugihara H; Nishida Y; Yamakura M; Takeuchi M; Matsue K Br J Haematol; 2013 Jul; 162(1):1. PubMed ID: 23758066 [No Abstract] [Full Text] [Related]
11. Clinical, biochemical, and pathological features in a patient with plasma cell dyscrasia and Fanconi syndrome. Lajoie G; Leung R; Bargman JM Ultrastruct Pathol; 2000; 24(4):221-6. PubMed ID: 11013962 [TBL] [Abstract][Full Text] [Related]
12. Brain lesions of the Leigh-type distribution associated with a mitochondriopathy of Pearson's syndrome: light and electron microscopic study. Yamadori I; Kurose A; Kobayashi S; Ohmori M; Imai T Acta Neuropathol; 1992; 84(3):337-41. PubMed ID: 1414284 [TBL] [Abstract][Full Text] [Related]
17. Mitochondrial DNA deletion in a girl with Fanconi's syndrome. Au KM; Lau SC; Mak YF; Lai WM; Chow TC; Chen ML; Chiu MC; Chan AY Pediatr Nephrol; 2007 Jan; 22(1):136-40. PubMed ID: 16967281 [TBL] [Abstract][Full Text] [Related]
18. [On a case of cystine thesaurismosis]. Genova R Minerva Pediatr; 1974 Nov; 26(35):1782-9. PubMed ID: 4427587 [No Abstract] [Full Text] [Related]
19. 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]
20. Bilateral zonular cataract associated with the mitochondrial cytopathy of Pearson syndrome. Cruysberg JR Am J Ophthalmol; 1999 Feb; 127(2):243-4. PubMed ID: 10030587 [No Abstract] [Full Text] [Related] [Next] [New Search]