SCOPUS 정보 검색 플랫폼

Seminars in Pediatric Neurology

Volumn 15, Issue 4, 2008, Pages 151-153

Hypotonia, Weakness, and Pontocerebellar Hypoplasia in Siblings

(5) Tsao, Chang Yong a Mendell, Jerry a Sahenk, Zarife a Rusin, Jerome b Boue, Daniel a

a OHIO STATE UNIVERSITY (United States)

b THE OHIO STATE UNIVERSITY WEXNER MEDICAL CENTER (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AREFLEXIA; ARTICLE; AUTOPSY; CASE REPORT; CAUSE OF DEATH; CEREBELLUM HYPOPLASIA; FACE DYSMORPHIA; FASCICULATION; FEMALE; GASTROESOPHAGEAL REFLUX; HEREDITARY SPINAL MUSCULAR ATROPHY; HIGH ARCHED PALATE; HUMAN; HUMAN TISSUE; INFANT; LOBAR PNEUMONIA; MALE; MICROCEPHALY; MICROGNATHIA; MUSCLE HYPOTONIA; NEUROIMAGING; PRESCHOOL CHILD; SIBLING; STOMACH TUBE; WEAKNESS;

ABNORMALITIES, MULTIPLE; CEREBELLUM; FEMALE; HUMANS; INFANT; MALE; MUSCLE HYPOTONIA; MUSCLE WEAKNESS; PONS; SIBLINGS; SPINAL MUSCULAR ATROPHIES OF CHILDHOOD;

EID: 57349158515 PISSN: 10719091 EISSN: None Source Type: Journal
DOI: 10.1016/j.spen.2008.09.001 Document Type: Article

Times cited : (3)

References (8)

1
- 0002513078
- Cerebellar hypoplasia in Werdnig-Hoffmann disease
- Norman R.M. Cerebellar hypoplasia in Werdnig-Hoffmann disease. Arch Dis Child 36 (1961) 96-101
- (1961) Arch Dis Child , vol.36 , pp. 96-101
- Norman, R.M.¹

2
- 0027771377
- Pontocerebellar hypoplasias. An overview of a group of inherited neurodegenerative disorders with fetal onset
- Barth P.G. Pontocerebellar hypoplasias. An overview of a group of inherited neurodegenerative disorders with fetal onset. Brain Dev 15 (1993) 411-422
- (1993) Brain Dev , vol.15 , pp. 411-422
- Barth, P.G.¹

3
- 0017687503
- Anterior horn cell disease associated with pontocerebellar hypoplasia in infants
- Goutieres F., Aicardi J., and Farkas E. Anterior horn cell disease associated with pontocerebellar hypoplasia in infants. J Neurol Neurosurg Psychiatry 40 (1977) 370-378
- (1977) J Neurol Neurosurg Psychiatry , vol.40 , pp. 370-378
- Goutieres, F.¹ Aicardi, J.² Farkas, E.³

4
- 0025320510
- Infantile olivopontocerebellar atrophy with spinal muscular atrophy (infantile OPCA + SMA)
- Chou S.M., Gilbert E.F., Chun R.W.M., et al. Infantile olivopontocerebellar atrophy with spinal muscular atrophy (infantile OPCA + SMA). Clin Neuropathol 9 (1990) 21-32
- (1990) Clin Neuropathol , vol.9 , pp. 21-32
- Chou, S.M.¹ Gilbert, E.F.² Chun, R.W.M.³

5
- 0032911790
- Familial pontocerebellar hypoplasia type 1 with anterior horn cell disease
- Gorgen-Pauly U., Sperner J., Reiss I., et al. Familial pontocerebellar hypoplasia type 1 with anterior horn cell disease. Eur J Paediatr Neurol 3 (1999) 33-38
- (1999) Eur J Paediatr Neurol , vol.3 , pp. 33-38
- Gorgen-Pauly, U.¹ Sperner, J.² Reiss, I.³

6
- 0032726302
- Clinical spectrum and diagnostic difficulties of infantile ponto-cerebellar hypoplasia type 1
- Muntoni F., Goodwin F., Sewry C., et al. Clinical spectrum and diagnostic difficulties of infantile ponto-cerebellar hypoplasia type 1. Neuropediatrics 30 (1999) 243-248
- (1999) Neuropediatrics , vol.30 , pp. 243-248
- Muntoni, F.¹ Goodwin, F.² Sewry, C.³

7
- 0038069233
- Pontocerebellar hypoplasia type 1: New leads for an earlier diagnosis
- Salman M.S., Buncic J.R., and Becker L. Pontocerebellar hypoplasia type 1: New leads for an earlier diagnosis. J Child Neurol 18 (2003) 220-225
- (2003) J Child Neurol , vol.18 , pp. 220-225
- Salman, M.S.¹ Buncic, J.R.² Becker, L.³

8
- 0037736585
- Extended phenotype of pontocerebellar hypoplasia with infantile spinal muscular atrophy
- Rudnik-Schoneborn S., Sztriha L., Aithala G.R., et al. Extended phenotype of pontocerebellar hypoplasia with infantile spinal muscular atrophy. Am J Med Genet 117A (2003) 10-17
- (2003) Am J Med Genet , vol.117 A , pp. 10-17
- Rudnik-Schoneborn, S.¹ Sztriha, L.² Aithala, G.R.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.