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5. Syndrome of pancreatic insufficiency, blood dyscrasia and metaphyseal dysplasia. Pringle EM; Young WF; Haworth EM Proc R Soc Med; 1968 Aug; 61(8):776-8. PubMed ID: 5673403 [No Abstract] [Full Text] [Related]
6. A new syndrome of refractory sideroblastic anemia with vacuolization of marrow precursors and exocrine pancreatic dysfunction. Pearson HA; Lobel JS; Kocoshis SA; Naiman JL; Windmiller J; Lammi AT; Hoffman R; Marsh JC J Pediatr; 1979 Dec; 95(6):976-84. PubMed ID: 501502 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Therapeutic approach in a case of Pearson's syndrome. Zaffanello M; Zamboni G Minerva Pediatr; 2005 Jun; 57(3):143-6. PubMed ID: 16170299 [TBL] [Abstract][Full Text] [Related]
9. Syndrome of refractory sideroblastic anemia with vacuolization of marrow precursors and exocrine pancreatic dysfunction presenting in the neonate. Stoddard RA; McCurnin DC; Shultenover SJ; Wright JE; deLemos RA J Pediatr; 1981 Aug; 99(2):259-61. PubMed ID: 7195932 [No Abstract] [Full Text] [Related]
13. New clinical aspects of Pearson's syndrome. Report of three cases. Favareto F; Caprino D; Micalizzi C; Rosanda C; Boeri E; Mori PG Haematologica; 1989; 74(6):591-4. PubMed ID: 2628242 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Syndrome of Shwachman and leukaemia. Huijgens PC; van der Veen EA; Meijer S; Muntinghe OG Scand J Haematol; 1977 Jan; 18(1):20-4. PubMed ID: 265092 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Detection of extremely low levels of wild-type mitochondrial DNA in the liver of a patient with Pearson syndrome by a sensitive PCR assay. de Vries DD; Ruitenbeek W; van Oost BA J Inherit Metab Dis; 1992; 15(3):307-10. PubMed ID: 1405463 [No Abstract] [Full Text] [Related]