SCOPUS 정보 검색 플랫폼

Pediatric and Developmental Pathology

Volumn 7, Issue 6, 2004, Pages 620-624

Neonatal mitochondrial cardiomyopathy

(1) Taylor, G P a

a HOSPITAL FOR SICK CHILDREN (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOPSY; CARDIOMYOPATHY; CASE REPORT; CLINICAL EXAMINATION; CLINICAL FEATURE; DISEASE COURSE; HUMAN; IMMUNOHISTOCHEMISTRY; LABORATORY TEST; LETHAL NEONATAL MITOCHONDRIAL CARDIOMYOPATHY; MALE; NEWBORN; PRIORITY JOURNAL; PROGNOSIS;

CARDIOMYOPATHIES; DIAGNOSIS, DIFFERENTIAL; HUMANS; INFANT, NEWBORN; MALE; MICROSCOPY, ELECTRON, TRANSMISSION; MITOCHONDRIA, HEART; MITOCHONDRIA, MUSCLE; MITOCHONDRIAL MYOPATHIES; MUSCLE, SKELETAL; MYOCARDIUM;

EID: 12544253824 PISSN: 10935266 EISSN: None Source Type: Journal
DOI: 10.1007/s10024-004-5050-5 Document Type: Article

Times cited : (12)

References (11)

1
- 0032699506
- Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene
- Papdopoulou LC, Sue CM, Davidson MM, et al. Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene. Nat Genet 1999;23:333-337.
- (1999) Nat Genet , vol.23 , pp. 333-337
- Papdopoulou, L.C.¹ Sue, C.M.² Davidson, M.M.³

2
- 0024042701
- A newborn infant with respiratory distress and persistent stridulous breathing
- Hart Z, Chang C-H. A newborn infant with respiratory distress and persistent stridulous breathing. J Pediatr 1988;113:150-155.
- (1988) J Pediatr , vol.113 , pp. 150-155
- Hart, Z.¹ Chang, C.-H.²

3
- 0022975558
- Myopathy and fatal cardiopathy due to cytochrome c oxidase deficiency
- Zeviani M, Van Dyke DH, Servidei S, et al. Myopathy and fatal cardiopathy due to cytochrome c oxidase deficiency. Arch Neurol 1986;43:1198-1202.
- (1986) Arch Neurol , vol.43 , pp. 1198-1202
- Zeviani, M.¹ Van Dyke, D.H.² Servidei, S.³

4
- 0028969540
- Cardiomyopathy in respiratory chain disorders
- Guenthard J, Wyler F, Fowler B, Baumgartner R. Cardiomyopathy in respiratory chain disorders. Arch Dis Child 1995;72:223-226.
- (1995) Arch Dis Child , vol.72 , pp. 223-226
- Guenthard, J.¹ Wyler, F.² Fowler, B.³ Baumgartner, R.⁴

5
- 0011894893
- Immature myocardium
- Moller JH, Neal WA, Eds. Norwalk CT: Appleton & Lange.
- Anderson PAW. Immature myocardium. In: Moller JH, Neal WA, Eds. Fetal, Neonatal, Infant Cardiac Disease. Norwalk CT: Appleton & Lange. 1990;35-71.
- (1990) Fetal, Neonatal, Infant Cardiac Disease , pp. 35-71
- Anderson, P.A.W.¹

6
- 0024366601
- Cytochrome-c-oxidase deficient cardiomyocytes in the human heart - An age-related phenomenon. A histochemical and ultracytochemical study
- Muller-Hocker J. Cytochrome-c-oxidase deficient cardiomyocytes in the human heart - an age-related phenomenon. A histochemical and ultracytochemical study. Am J Pathol 1989;134:1167-1173.
- (1989) Am J Pathol , vol.134 , pp. 1167-1173
- Muller-Hocker, J.¹

7
- 0021345994
- Mitochondrial myopathies: Clinical, morphological and biochemical aspects
- Sengers RCA, Stadhouders AM, Trijbels JMF. Mitochondrial myopathies: clinical, morphological and biochemical aspects. Eur J Pediatr 1984;141:192-207.
- (1984) Eur J Pediatr , vol.141 , pp. 192-207
- Sengers, R.C.A.¹ Stadhouders, A.M.² Trijbels, J.M.F.³

8
- 0021798888
- Mitochondrial myopathies
- DiMauro S, Bonilla E, Zeviani M, Nakagawa M, DeVivo DC. Mitochondrial myopathies. Ann Neurol 1985;17:521-538.
- (1985) Ann Neurol , vol.17 , pp. 521-538
- DiMauro, S.¹ Bonilla, E.² Zeviani, M.³ Nakagawa, M.⁴ DeVivo, D.C.⁵

9
- 18244413442
- Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy
- Arbustini E, Diegoli M, Fasani R, et al. Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy. Am J Pathol 1998;153:1501-1510.
- (1998) Am J Pathol , vol.153 , pp. 1501-1510
- Arbustini, E.¹ Diegoli, M.² Fasani, R.³

10
- 0014231726
- The heart muscle in functional overload and hypoxia. A biochemical and ultrastructural study
- Pelosi G, Agliati G. The heart muscle in functional overload and hypoxia. A biochemical and ultrastructural study. Lab Invest 1968;18:86-93.
- (1968) Lab Invest , vol.18 , pp. 86-93
- Pelosi, G.¹ Agliati, G.²

11
- 0035077977
- Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases
- Brega A, Narula J, Arbustini E. Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases. J Nucl Cardiol 2001;8:89-97.
- (2001) J Nucl Cardiol , vol.8 , pp. 89-97
- Brega, A.¹ Narula, J.² Arbustini, E.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.