SCOPUS 정보 검색 플랫폼

European Journal of Pediatrics

Volumn 163, Issue 6, 2004, Pages 331-332

Spinal muscle atrophy type 1 (Werdnig-Hoffman disease) will complex cardiac malformation

(4) El Matary, Wael a Kotagiri, Sunanda a Cameron, Duncan a Peart, Ian b

a GLAN CLWYD HOSPITAL (United Kingdom)

b ALDER HEY CHILDREN'S NHS FOUNDATION TRUST (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADIPOSE TISSUE; AMNIOCENTESIS; ARTICLE; ARTIFICIAL VENTILATION; BLOOD CHEMISTRY; CASE REPORT; CHILD CARE; CONGENITAL HEART MALFORMATION; DEATH; DELIVERY; DNA DETERMINATION; ECHOCARDIOGRAPHY; ELECTROMYOGRAM; FAMILY HISTORY; FETUS MOVEMENT; GESTATIONAL AGE; HISTOPATHOLOGY; HUMAN; HYDRAMNIOS; INFANT; KARYOTYPE; LABORATORY TEST; MALE; MOLECULAR GENETICS; MUSCLE BIOPSY; NEWBORN; PRENATAL CARE; PRIORITY JOURNAL; SPINAL MUSCULAR ATROPHY; THORAX RADIOGRAPHY; VAGINAL DELIVERY;

HEART DEFECTS, CONGENITAL; HUMANS; INFANT, NEWBORN; MALE; SPINAL MUSCULAR ATROPHIES OF CHILDHOOD;

EID: 2642548220 PISSN: 03406199 EISSN: None Source Type: Journal
DOI: 10.1007/s00431-004-1437-6 Document Type: Article

Times cited : (19)

References (8)

1
- 0029113456
- SMN gene deletion in variant of infantile spinal muscular atrophy
- Burglen LR, Spiegel J, Ignatius J, Cobben JM, Landrieu P, Lefebvre S (1995) SMN gene deletion in variant of infantile spinal muscular atrophy. Lancet 346: 316-317
- (1995) Lancet , vol.346 , pp. 316-317
- Burglen, L.R.¹ Spiegel, J.² Ignatius, J.³ Cobben, J.M.⁴ Landrieu, P.⁵ Lefebvre, S.⁶

2
- 0029834810
- Clinical and molecular genetic features of congenital spinal muscle atrophy
- Devriendt K, Lammens M, Schollen E, Van Hole C, Dom R, Devlieger H (1996) Clinical and molecular genetic features of congenital spinal muscle atrophy. Ann Neurol 40: 731-738
- (1996) Ann Neurol , vol.40 , pp. 731-738
- Devriendt, K.¹ Lammens, M.² Schollen, E.³ Van Hole, C.⁴ Dom, R.⁵ Devlieger, H.⁶

3
- 0343729522
- Cardiac involvement in Werdnig-Hoffmann's spinal muscle atrophy
- Finsterer J, Sollberger C (1999) Cardiac involvement in Werdnig-Hoffmann's spinal muscle atrophy. Cardiology 92: 178-182
- (1999) Cardiology , vol.92 , pp. 178-182
- Finsterer, J.¹ Sollberger, C.²

4
- 0025310718
- Spinal muscle atrophy type I combined with atrial septal defect in three sibs
- Moller P, Saugstad OD, Skullerud K, Velken M, Berg K, Nitter-Hauge S (1990) Spinal muscle atrophy type I combined with atrial septal defect in three sibs. Clin Genet 38: 81-83
- (1990) Clin Genet , vol.38 , pp. 81-83
- Moller, P.¹ Saugstad, O.D.² Skullerud, K.³ Velken, M.⁴ Berg, K.⁵ Nitter-Hauge, S.⁶

5
- 0030478478
- Spinal muscle atrophy combined with congenital heart disease: A report of two cases
- Mulleners WM, van Ravenswaay CM, Gabreels FJM, Hamel BC, van Oort A, Sengers RCA (1996) Spinal muscle atrophy combined with congenital heart disease: a report of two cases. Neuropediatrics 27: 333-334
- (1996) Neuropediatrics , vol.27 , pp. 333-334
- Mulleners, W.M.¹ Van Ravenswaay, C.M.² Gabreels, F.J.M.³ Hamel, B.C.⁴ Van Oort, A.⁵ Sengers, R.C.A.⁶

6
- 44949282843
- Workshop report: International SMA Collaboration
- Munsat TL (1991) Workshop report: International SMA Collaboration. Neuromuscul Disord 1: 81
- (1991) Neuromuscul Disord , vol.1 , pp. 81
- Munsat, T.L.¹

7
- 0036301711
- Spinal muscle atrophy: Recent advances and future prospects
- Nicole S, Diaz CC, Frugier T, Melki J (2002) Spinal muscle atrophy: recent advances and future prospects. Muscle Nerve 26: 4-13
- (2002) Muscle Nerve , vol.26 , pp. 4-13
- Nicole, S.¹ Diaz, C.C.² Frugier, T.³ Melki, J.⁴

8
- 0016164162
- Syndrome of campodactyly, multiple ankyloses, facial anomalies and pulmonary hypoplasia: A lethal condition
- Pena SD, Shokeir MHK (1974) Syndrome of campodactyly, multiple ankyloses, facial anomalies and pulmonary hypoplasia: a lethal condition. J Pediatr 85: 373-375
- (1974) J Pediatr , vol.85 , pp. 373-375
- Pena, S.D.¹ Shokeir, M.H.K.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.