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Volumn 57, Issue 3, 2005, Pages 143-146

Therapeutic approach in a case of Pearson's syndrome

Author keywords

Adrenal insufficiency; De Toni Debr Fanconi syndrome; Kearns Sayre syndrome; Pearson's syndrome

Indexed keywords

BICARBONATE; CALCIUM; CARNITINE; CITRIC ACID; COLECALCIFEROL; ETIRACETAM; HYDROCORTISONE; PHOSPHORUS; UBIQUINONE; DRUG DERIVATIVE; ERGOCALCIFEROL; MITOCHONDRIAL DNA; NOOTROPIC AGENT; PIRACETAM;

EID: 33644621124     PISSN: 00264946     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (16)

References (13)
  • 1
    • 0018712317 scopus 로고
    • 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 et al. A new syndrome of refractory sideroblastic anemia with vacuolization of marrow precursors and exocrine pancreatic dysfunction. J Pediatr 1979;95:976-84.
    • (1979) J Pediatr , vol.95 , pp. 976-984
    • Pearson, H.A.1    Lobel, J.S.2    Kocoshis, S.A.3    Naiman, J.L.4    Windmiller, J.5    Lammi, A.T.6
  • 3
    • 0031656184 scopus 로고    scopus 로고
    • Multiple endocrine involvement in two pediatric patients with Kearns-Sayre syndrome
    • Artuch R, Pavia C, Playan A, Vilaseca MA, Colomer J, Valls C et al. Multiple endocrine involvement in two pediatric patients with Kearns-Sayre syndrome. Horm Res 1998;50:99-104.
    • (1998) Horm Res , vol.50 , pp. 99-104
    • Artuch, R.1    Pavia, C.2    Playan, A.3    Vilaseca, M.A.4    Colomer, J.5    Valls, C.6
  • 4
    • 0030670573 scopus 로고    scopus 로고
    • Clinical features, investigation, and management of patients with defects of mitochondrial DNA
    • Chinnery PF, Turnbull DM. Clinical features, investigation, and management of patients with defects of mitochondrial DNA. J Neurol Neurosurg Psychiatry 1997;63:559-63.
    • (1997) J Neurol Neurosurg Psychiatry , vol.63 , pp. 559-563
    • Chinnery, P.F.1    Turnbull, D.M.2
  • 8
    • 0027497228 scopus 로고
    • Identical mitochondrial DNA deletion in mother with progressive external ophtalmoplegia and son with Pearson marrow-pancreas syndrome
    • Bernes SM, Bacino C, Prezant TR, Pearson MA, Wood TS, Fournier P et al. Identical mitochondrial DNA deletion in mother with progressive external ophtalmoplegia and son with Pearson marrow-pancreas syndrome. J Pediatr 1993;123:598-602.
    • (1993) J Pediatr , vol.123 , pp. 598-602
    • Bernes, S.M.1    Bacino, C.2    Prezant, T.R.3    Pearson, M.A.4    Wood, T.S.5    Fournier, P.6
  • 9
    • 0028286575 scopus 로고
    • Are duplications of mitochondrial DNA characteristic of Kearns-Sayre syndrome?
    • Poulton J, Morten KJ, Weber K, Brown GK, Bindoff L. Are duplications of mitochondrial DNA characteristic of Kearns-Sayre syndrome? Hum Mol Genet 1994;3:947-51.
    • (1994) Hum Mol Genet , vol.3 , pp. 947-951
    • Poulton, J.1    Morten, K.J.2    Weber, K.3    Brown, G.K.4    Bindoff, L.5
  • 10
    • 0030930127 scopus 로고    scopus 로고
    • Identification of a large-scale mitochondrial deoxyribonucleic acid deletion in endocrinopathies and defness: Report of two unrelated cases with diabetes mellitus and adrenal insufficiency, respectively
    • Nicolino M, Ferlin T, Forest M, Godinot C, Carrier H, David M et al. Identification of a large-scale mitochondrial deoxyribonucleic acid deletion in endocrinopathies and defness: report of two unrelated cases with diabetes mellitus and adrenal insufficiency, respectively. J Clin Endocrinol Metab 1997;82:3063-7.
    • (1997) J Clin Endocrinol Metab , vol.82 , pp. 3063-3067
    • Nicolino, M.1    Ferlin, T.2    Forest, M.3    Godinot, C.4    Carrier, H.5    David, M.6
  • 11
    • 0031595077 scopus 로고    scopus 로고
    • Mitochondrial DNA deletion with Kearns Sayre syndrome in a child with Addison disease
    • Boles RG, Roe T, Senadheera D, Mahnovski V, Wong LJ. Mitochondrial DNA deletion with Kearns Sayre syndrome in a child with Addison disease. Eur J Pediatr. 1998;157:643-7.
    • (1998) Eur J Pediatr , vol.157 , pp. 643-647
    • Boles, R.G.1    Roe, T.2    Senadheera, D.3    Mahnovski, V.4    Wong, L.J.5
  • 12
    • 0028288589 scopus 로고
    • Deletion of the mithocondrial DNA in a case of de Toni-Debré- Fanconi sindrome and Pearson sindrome
    • Niaudet P, Heidet L, Munnich A, Schmitz J, Bouissou F, Gubler MC et al. Deletion of the mithocondrial DNA in a case of de Toni-Debré-Fanconi sindrome and Pearson sindrome. Pediatr Nephrol 1994;8:164-8.
    • (1994) Pediatr Nephrol , vol.8 , pp. 164-168
    • Niaudet, P.1    Heidet, L.2    Munnich, A.3    Schmitz, J.4    Bouissou, F.5    Gubler, M.C.6
  • 13
    • 0026084932 scopus 로고
    • Renal and skin involvement in a patient with complete Kearns-Sayre syndrome
    • Mori K, Narahara K, Ninomiya S, Goto Y, Nonaka I. Renal and skin involvement in a patient with complete Kearns-Sayre syndrome. Am J Med Genet 1991;38:583-7.
    • (1991) Am J Med Genet , vol.38 , pp. 583-587
    • Mori, K.1    Narahara, K.2    Ninomiya, S.3    Goto, Y.4    Nonaka, I.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.