메뉴 건너뛰기




Volumn 168, Issue 3, 2009, Pages 311-315

Early neurological impairment and severe anemia in a newborn with Pearson syndrome

Author keywords

Aregenerative anemia; Brain MRI; Cerebral lesions; Mitochondrial encephalopathy; Pearson syndrome

Indexed keywords

BICARBONATE;

EID: 59449093145     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00431-008-0756-4     Document Type: Article
Times cited : (15)

References (11)
  • 9
    • 0029018848 scopus 로고
    • Phenotypic expression of mitochondrial genotypes in cultured skin fibroblasts and in Epstein-Barr virus-transformed lymphocytes in Pearson syndrome
    • A Rötig T Bourgeron P Rustin A Munnich 1995 Phenotypic expression of mitochondrial genotypes in cultured skin fibroblasts and in Epstein-Barr virus-transformed lymphocytes in Pearson syndrome Muscle Nerve 3 S159 S164
    • (1995) Muscle Nerve , vol.3
    • Rötig, A.1    Bourgeron, T.2    Rustin, P.3    Munnich, A.4
  • 10
    • 0027310104 scopus 로고
    • 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
    • A Superti-Furga E Schoenle P Tuchschmid R Caduff V Sabato D DeMattia R Gitzelmann B Steinmann 1993 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 Eur J Pediatr 152 44 50
    • (1993) Eur J Pediatr , vol.152 , pp. 44-50
    • Superti-Furga, A.1    Schoenle, E.2    Tuchschmid, P.3    Caduff, R.4    Sabato, V.5    Demattia, D.6    Gitzelmann, R.7    Steinmann, B.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.