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Volumn 8, Issue 3, 1998, Pages 267-271

Anaesthesia and Prader-Willi syndrome

Author keywords

Anaesthesia; Complications; Prader Willi syndrome

Indexed keywords

ADOLESCENT; ANESTHESIA COMPLICATION; ARTICLE; BODY WEIGHT; CHILD; CLINICAL ARTICLE; FEMALE; HUMAN; INFANT; OBESITY; PRADER WILLI SYNDROME; PREOPERATIVE EVALUATION; PRIORITY JOURNAL; SCOLIOSIS; SLEEP APNEA SYNDROME;

EID: 0031800619     PISSN: 11555645     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1460-9592.1998.00689.x     Document Type: Article
Times cited : (24)

References (8)
  • 1
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    • Ein Syndrom von Adipositas, Kleinwuchs, Kryptorchidismus und Oligophrenia nach Myotonieartigem Zustand in Neugeborn alter
    • Prader A, Labhart A, Willi H. Ein Syndrom von Adipositas, Kleinwuchs, Kryptorchidismus und Oligophrenia nach Myotonieartigem Zustand in Neugeborn alter. Schweiz Medizin Wochenscrift 1956; 86: 260-261.
    • (1956) Schweiz Medizin Wochenscrift , vol.86 , pp. 260-261
    • Prader, A.1    Labhart, A.2    Willi, H.3
  • 2
    • 0019377986 scopus 로고
    • Deletion of chromosome 15 as a cause of the Prader-Willi Syndrome
    • Ledbetter DH, Riccardi VM, Anhart SD et al. Deletion of chromosome 15 as a cause of the Prader-Willi Syndrome. N Engl J Med 1981; 304: 325-329.
    • (1981) N Engl J Med , vol.304 , pp. 325-329
    • Ledbetter, D.H.1    Riccardi, V.M.2    Anhart, S.D.3
  • 3
    • 0026647855 scopus 로고
    • The frequency of uniparental disomy in Prader-Willi Syndrome
    • Mascari MJ, Gottlieb W, Rogan PK et al. The frequency of uniparental disomy in Prader-Willi Syndrome. N Engl J Med 1992; 326: 1599-1607.
    • (1992) N Engl J Med , vol.326 , pp. 1599-1607
    • Mascari, M.J.1    Gottlieb, W.2    Rogan, P.K.3
  • 4
    • 0024619007 scopus 로고
    • Angelman and Prader Willi syndromes share a common chromosome 15 deletion but differ in the parental origin of the deletion
    • Knoll JH, Nicholls RD, Magenis RE et al. Angelman and Prader Willi syndromes share a common chromosome 15 deletion but differ in the parental origin of the deletion. Am J Med Genet, 1989; 32: 285-290.
    • (1989) Am J Med Genet , vol.32 , pp. 285-290
    • Knoll, J.H.1    Nicholls, R.D.2    Magenis, R.E.3
  • 5
    • 0028938410 scopus 로고
    • Pulmonary function abnormalities in Prader-Willi syndrome
    • Hakonarson H, Moskovitz J, Daigle KL et al. Pulmonary function abnormalities in Prader-Willi syndrome. J Pediatr 1995; 126: 565-570.
    • (1995) J Pediatr , vol.126 , pp. 565-570
    • Hakonarson, H.1    Moskovitz, J.2    Daigle, K.L.3
  • 6
    • 0028075517 scopus 로고
    • Absent peripheral chemosensitivity in Prader-Willi Syndrome
    • Gozal D, Arens R, Omlin KJ,et al. Absent peripheral chemosensitivity in Prader-Willi Syndrome. J Appl Physiol 1994; 77: 2231-2236.
    • (1994) J Appl Physiol , vol.77 , pp. 2231-2236
    • Gozal, D.1    Arens, R.2    Omlin, K.J.3
  • 7
    • 0028298708 scopus 로고
    • The upper airway and sleep apnea in Prader Willi syndrome
    • Richards A, Quaghebeur G, Clifts S et al. The upper airway and sleep apnea in Prader Willi syndrome. Clin Otolaryngol 1994; 19: 193-197.
    • (1994) Clin Otolaryngol , vol.19 , pp. 193-197
    • Richards, A.1    Quaghebeur, G.2    Clifts, S.3
  • 8
    • 0020692984 scopus 로고
    • Anaesthetic consideration in the Prader-Willi syndrome: Report of four cases
    • Yamashita M, Koishi K, Yamaya R et al. Anaesthetic consideration in the Prader-Willi syndrome: report of four cases. Can Anaesth Soc J 1983, 30: 179-184.
    • (1983) Can Anaesth Soc J , vol.30 , pp. 179-184
    • Yamashita, M.1    Koishi, K.2    Yamaya, R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.