Literature DB >> 7195932

Syndrome of refractory sideroblastic anemia with vacuolization of marrow precursors and exocrine pancreatic dysfunction presenting in the neonate.

R A Stoddard, D C McCurnin, S J Shultenover, J E Wright, R A deLemos.   

Abstract

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Year:  1981        PMID： 7195932     DOI： 10.1016/s0022-3476(81)80470-2

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  8 in total

1.  Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy.

Authors:  A Rötig; V Cormier; S Blanche; J P Bonnefont; F Ledeist; N Romero; J Schmitz; P Rustin; A Fischer; J M Saudubray
Journal:  J Clin Invest       Date:  1990-11       Impact factor: 14.808

2.  Pearson syndrome and mitochondrial encephalomyopathy in a patient with a deletion of mtDNA.

Authors:  M A McShane; S R Hammans; M Sweeney; I J Holt; T J Beattie; E M Brett; A E Harding
Journal:  Am J Hum Genet       Date:  1991-01       Impact factor: 11.025

3.  Pearson marrow-pancreas syndrome with cardiac conduction abnormality necessitating prophylactic pacemaker implantation.

Authors:  Mats Steffi Jennifer; Daniel Cortez
Journal:  Ann Noninvasive Electrocardiol       Date:  2019-09-01       Impact factor: 1.468

4.  Pearson's marrow/pancreas syndrome: a histological and genetic study.

Authors:  Y Morikawa; N Matsuura; K Kakudo; R Higuchi; M Koike; Y Kobayashi
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1993

5.  Severe lactic acidosis and neonatal death in Pearson syndrome.

Authors:  K Muraki; Y Goto; I Nishino; M Hayashidani; S Takeuchi; S Horai; N Sakura; K Ueda
Journal:  J Inherit Metab Dis       Date:  1997-03       Impact factor: 4.982

6.  Pearson bone marrow-pancreas syndrome with insulin-dependent diabetes, progressive renal tubulopathy, organic aciduria and elevated fetal haemoglobin caused by deletion and duplication of mitochondrial DNA.

Authors:  A Superti-Furga; E Schoenle; P Tuchschmid; R Caduff; V Sabato; D DeMattia; R Gitzelmann; B Steinmann
Journal:  Eur J Pediatr       Date:  1993-01       Impact factor: 3.183

7.  Deletion of the mitochondrial DNA in a case of de Toni-Debré-Fanconi syndrome and Pearson syndrome.

Authors:  P Niaudet; L Heidet; A Munnich; J Schmitz; F Bouissou; M C Gubler; A Rötig
Journal:  Pediatr Nephrol       Date:  1994-04       Impact factor: 3.714

8.  Brain lesions of the Leigh-type distribution associated with a mitochondriopathy of Pearson's syndrome: light and electron microscopic study.

Authors:  I Yamadori; A Kurose; S Kobayashi; M Ohmori; T Imai
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088
  8 in total

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