SCOPUS 정보 검색 플랫폼

Volumn , Issue , 2007, Pages 145-147

Developmental Neurology: A Molecular Perspective

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EID: 57649127679 PISSN: None EISSN: None Source Type: Book
DOI: 10.1016/B978-012369509-3.50011-1 Document Type: Chapter

Times cited : (1)

References (10)

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3
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- Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiency
- S. DiMauro, J.F. Nicholson, A.P. Hays, A.B. Eastwood, A. Papadimitriou, R. Koenigsberger and D.C. DeVivo (1983) Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiency. Ann Neurol. 14 226-234.
- (1983) Ann Neurol. , vol.14 , pp. 226-234
- DiMauro, S.¹ Nicholson, J.F.² Hays, A.P.³ Eastwood, A.B.⁴ Papadimitriou, A.⁵ Koenigsberger, R.⁶ DeVivo, D.C.⁷

4
- 29144463310
- Spinal muscular atrophy: A deficiency in a ubiquitous protein; a motor neuron-specific disease
- U.R. Monani (2005) Spinal muscular atrophy: A deficiency in a ubiquitous protein; a motor neuron-specific disease. Neuron 48 885-896.
- (2005) Neuron , vol.48 , pp. 885-896
- Monani, U.R.¹

5
- 2942699901
- GLUT1 deficiency and other glucose transporter diseases
- J.M. Pascual, D. Wang, B. Lecumberri, H. Yang, X. Mao, R. Yang and D.C. De Vivo (2004) GLUT1 deficiency and other glucose transporter diseases. Eur J Endocrinol. 150 627-633.
- (2004) Eur J Endocrinol. , vol.150 , pp. 627-633
- Pascual, J.M.¹ Wang, D.² Lecumberri, B.³ Yang, H.⁴ Mao, X.⁵ Yang, R.⁶ De Vivo, D.C.⁷

6
- 0036096893
- Cytochrome c oxidase deficiency due to a novel SCO2 mutation mimics Werdnig-Hoffmann disease
- L. Salviati, S. Sacconi, M.M. Rasalan, D.F. Kronn, A. Braun, P. Canoll, et al. (2002) Cytochrome c oxidase deficiency due to a novel SCO2 mutation mimics Werdnig-Hoffmann disease. Arch Neurol. 59 862-865.
- (2002) Arch Neurol. , vol.59 , pp. 862-865
- Salviati, L.¹ Sacconi, S.² Rasalan, M.M.³ Kronn, D.F.⁴ Braun, A.⁵ Canoll, P.⁶

7
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- Varying loads of the mitochondrial DNA A3243G mutation in different tissues: Implications for diagnosis
- S. Shanske, J. Pancrudo, P. Kaufmann, K. Engelstad, S. Jhung, J. Lu, et al. (2004) Varying loads of the mitochondrial DNA A3243G mutation in different tissues: Implications for diagnosis. Am J Med Genet A. 130 134-137.
- (2004) Am J Med Genet A. , vol.130 , pp. 134-137
- Shanske, S.¹ Pancrudo, J.² Kaufmann, P.³ Engelstad, K.⁴ Jhung, S.⁵ Lu, J.⁶

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- S. Thor (1995) The genetics of brain development: Conserved programs in flies and mice. Neuron 15 975-977.
- (1995) Neuron , vol.15 , pp. 975-977
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9
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- Genetic influences on outcome following acute neurological insults
- R.J. Waters and J.A. Nicoll (2005) Genetic influences on outcome following acute neurological insults. Curr Opin Crit Care 11 105-110.
- (2005) Curr Opin Crit Care , vol.11 , pp. 105-110
- Waters, R.J.¹ Nicoll, J.A.²

10
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- MeCP2 dysfunction in humans and mice
- H.Y. Zoghbi (2005) MeCP2 dysfunction in humans and mice. J Child Neurol. 20 736-740.
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