메뉴 건너뛰기




Volumn 209, Issue 6, 1997, Pages 361-363

Severe hyponatremia as a sign of cystic fibrosis;Schwere hyponatriamie als diagnoseweisendes symptom der cystischen fibrose

Author keywords

Cystic fibrosis; Hypochloremic alkalosis; Hyponatremia; Pseudo Bartter Syndrome

Indexed keywords

ARTICLE; CASE REPORT; COMA; CYSTIC FIBROSIS; DEHYDRATION; FAILURE TO THRIVE; HUMAN; HUMAN CELL; HUMAN TISSUE; HYPONATREMIA; INFANT; SEIZURE; SODIUM DEPLETION; WEIGHT REDUCTION; BARTTER SYNDROME; BLOOD; DIFFERENTIAL DIAGNOSIS; FEMALE; GASTROENTERITIS; MALE; REFERENCE VALUE;

EID: 0031262247     PISSN: 03008630     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1043976     Document Type: Article
Times cited : (5)

References (7)
  • 1
    • 0028997099 scopus 로고
    • Wird die Diagnose "Pseudohypoaldosteronismus" zu selten gestellt? Monatsschr
    • Akkurt, I., U. Kuhnle: Wird die Diagnose "Pseudohypoaldosteronismus" zu selten gestellt? Monatsschr. Kinderheilkd. I43 (1995) 580-583
    • (1995) Kinderheilkd. , vol.I43 , pp. 580-583
    • Akkurt, I.1    Kuhnle, U.2
  • 4
    • 0029128156 scopus 로고
    • A specific cystic fibrosis mutation (T338I) associated with the phenotype of isolated hypotonic dehydration
    • Leoni, G. B., S. Pitzalis, R. Podda, M. Zanda, M. Silvetti, I., Caocci, A. Cao, M. C. Rosatelli: A specific cystic fibrosis mutation (T338I) associated with the phenotype of isolated hypotonic dehydration. J. Pediatr. 127 (1995) 281-283
    • (1995) J. Pediatr. , vol.127 , pp. 281-283
    • Leoni, G.B.1    Pitzalis, S.2    Podda, R.3    Zanda, M.4    Silvetti, M.5    Caocci, I.6    Cao, A.7    Rosatelli, M.C.8
  • 5
    • 0343370211 scopus 로고
    • Exocrine Glands
    • Taussig, L. M. (Hrsg.): Thieme-Stratton Inc. New York
    • Quinton, P. M.: Exocrine Glands. In: Taussig, L. M. (Hrsg.): Cystic Fibrosis. Thieme-Stratton Inc. New York (1984) 338-375
    • (1984) Cystic Fibrosis , pp. 338-375
    • Quinton, P.M.1
  • 7
    • 0027216088 scopus 로고
    • Zur Variabilität des Corticosteron-Methyl-Oxydase (Typ II)-Mangels
    • Rosendahl, W., M. König, D. Haack, P. Vecsei, S. Lewicka: Zur Variabilität des Corticosteron-Methyl-Oxydase (Typ II)-Mangels. Klin. Pädiatr. 205 (1993) 180-184
    • (1993) Klin. Pädiatr. , vol.205 , pp. 180-184
    • Rosendahl, W.1    König, M.2    Haack, D.3    Vecsei, P.4    Lewicka, S.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.