SCOPUS 정보 검색 플랫폼

Archives of Otolaryngology - Head and Neck Surgery

Volumn 123, Issue 12, 1997, Pages 1348-1350

Obstructive sleep apnea in Schwartz-Jampel syndrome

(2) Cook, Steven P a Borkowski, Winslow J a

a NEMOURS ALFRED I DUPONT HOSPITAL FOR CHILDREN (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHILD; HOME CARE; HUMAN; HYPOXIA; MALE; PALATOPLASTY; POLYSOMNOGRAPHY; POSITIVE END EXPIRATORY PRESSURE; SCHWARTZ JAMPEL SYNDROME; SLEEP APNEA SYNDROME; SNORING; TONSILLECTOMY;

EID: 0031437087 PISSN: 08864470 EISSN: None Source Type: Journal
DOI: 10.1001/archotol.1997.01900120098017 Document Type: Article

Times cited : (5)

References (15)

1
- 0015739133
- The Schwartz syndrome in Southern Africa
- Beighton P. The Schwartz syndrome in Southern Africa. Clin Genet. 1973;4:548-555
- (1973) Clin Genet , vol.4 , pp. 548-555
- Beighton, P.¹

2
- 13344257514
- Congenital blepharophimosis associated with a unique generalized myopathy
- Schwartz O, Jampel RS. Congenital blepharophimosis associated with a unique generalized myopathy. Arch Ophthalmol. 1962;68 82-87.
- (1962) Arch Ophthalmol , vol.68 , pp. 82-87
- Schwartz, O.¹ Jampel, R.S.²

3
- 0025953839
- Schwartz-Jampel syndrome
- Pascuzzi RM. Schwartz-Jampel syndrome. Semin Neurol. 1991;11:267-273.
- (1991) Semin Neurol , vol.11 , pp. 267-273
- Pascuzzi, R.M.¹

4
- 0017873273
- Schwariz-Jampel syndrome
- Cao A, Cianchetti C, Calisti L, De Virgiliis S, Ferreli A, Tangheroni W. Schwariz-Jampel syndrome. J Neurol Sci. 1978;35:175-187.
- (1978) J Neurol Sci , vol.35 , pp. 175-187
- Cao, A.¹ Cianchetti, C.² Calisti, L.³ De Virgiliis, S.⁴ Ferreli, A.⁵ Tangheroni, W.⁶

5
- 0019991712
- Chondrodystrophic myotonia (Schwartz-Jampel syndrome): Report of a new case and follow-up of patients initially reported in 1969
- Edwards WC, Root AW. Chondrodystrophic myotonia (Schwartz-Jampel syndrome): report of a new case and follow-up of patients initially reported in 1969. Am J Med Genet. 1982;13:51-56.
- (1982) Am J Med Genet , vol.13 , pp. 51-56
- Edwards, W.C.¹ Root, A.W.²

6
- 0027435531
- Schwartz-Jampel syndrome: An atypical form?
- Figuera LE, Jimenez-Gil FJ, Garcia-Cruz MO, Cantu JM. Schwartz-Jampel syndrome: an atypical form? Am J Med Genet. 1993;47:526-528.
- (1993) Am J Med Genet , vol.47 , pp. 526-528
- Figuera, L.E.¹ Jimenez-Gil, F.J.² Garcia-Cruz, M.O.³ Cantu, J.M.⁴

7
- 0014626845
- Osteo-chondro-muscular dystrophy: A disorder manifested by multiple skeletal deformities, myotonia, and dystrophic changes in muscle
- Huttenlocher PR, Landwirth J, Hanson V, Gailagher BB, Bensch K. Osteo-chondro-muscular dystrophy: a disorder manifested by multiple skeletal deformities, myotonia, and dystrophic changes in muscle. Pediatrics. 1969;44:945-958.
- (1969) Pediatrics , vol.44 , pp. 945-958
- Huttenlocher, P.R.¹ Landwirth, J.² Hanson, V.³ Gailagher, B.B.⁴ Bensch, K.⁵

8
- 0014494514
- Myotonia, shortness of stature, and hip dysplasia: Schwartz-Jampel syndrome
- Mereu TR, Porter IH, Hug G. Myotonia, shortness of stature, and hip dysplasia: Schwartz-Jampel syndrome. AJDC. 1969;117:470-478.
- (1969) AJDC , vol.117 , pp. 470-478
- Mereu, T.R.¹ Porter, I.H.² Hug, G.³

9
- 0023270834
- Neonatal manifestations of Schwartz-Jampel syndrome
- Farrell SA, Davidson RG, Thorp P. Neonatal manifestations of Schwartz-Jampel syndrome. Am J Med Genet. 1987;27:799-805.
- (1987) Am J Med Genet , vol.27 , pp. 799-805
- Farrell, S.A.¹ Davidson, R.G.² Thorp, P.³

10
- 0013951887
- A new generalized connective tissue syndrome
- Warden PM, Walker WA. A new generalized connective tissue syndrome. AJDC. 1966;112:225-228
- (1966) AJDC , vol.112 , pp. 225-228
- Warden, P.M.¹ Walker, W.A.²

11
- 0026528904
- Schwartz-Jampel syndrome (chondroaystrophic myotonia)
- Viljoen D, Beighton P. Schwartz-Jampel syndrome (chondroaystrophic myotonia). J Med Genet. 1992;29:58-62.
- (1992) J Med Genet , vol.29 , pp. 58-62
- Viljoen, D.¹ Beighton, P.²

12
- 0019522601
- Congenital myopathy with oculo-facial and skeletal abnormalities
- Ferguson SD, Young ID, Teoh R. Congenital myopathy with oculo-facial and skeletal abnormalities. Dev Med Child Neurol. 1981;23:237-241.
- (1981) Dev Med Child Neurol , vol.23 , pp. 237-241
- Ferguson, S.D.¹ Young, I.D.² Teoh, R.³

13
- 0016208133
- The Schwartz-Jampel syndrome: Its clinical, physiological, and histological expressions
- Fowler WM, Layzer RB, Taylor RG, et al. The Schwartz-Jampel syndrome: its clinical, physiological, and histological expressions. J Neurol Sci. 1974;22:127-146.
- (1974) J Neurol Sci , vol.22 , pp. 127-146
- Fowler, W.M.¹ Layzer, R.B.² Taylor, R.G.³

14
- 0027086904
- Le syndrome de Schwartz-Jampel (dystrophie osteochondromusculaire)
- Ben Becher S, El Mabrouk J, Debbiche A, et al. Le syndrome de Schwartz-Jampel (dystrophie osteochondromusculaire). Arch Fr Pediatr. 1992; 49:799-802.
- (1992) Arch Fr Pediatr , vol.49 , pp. 799-802
- Ben Becher, S.¹ El Mabrouk, J.² Debbiche, A.³

15
- 0025260168
- Schwartz-Jampel syndrome with dominant inheritance
- Pascuzzi RM, Gratianne R, Azzarelli B, Kincaid JC. Schwartz-Jampel syndrome with dominant inheritance. Muscle Nerve. 1990;13:1152-1163.
- (1990) Muscle Nerve , vol.13 , pp. 1152-1163
- Pascuzzi, R.M.¹ Gratianne, R.² Azzarelli, B.³ Kincaid, J.C.⁴

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.