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Volumn 37, Issue 4, 2001, Pages 852-858

Von Hippel-Lindau disease masquerading as autosomal dominant polycystic kidney disease

Author keywords

Autosomal dominant polycystic kidney disease (ADPKD); Misdiagnosis; Pancreatic cysts; Pancreatic malignancy; Von Hippel Lindau (VHL) disease

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CLINICAL FEATURE; DIFFERENTIAL DIAGNOSIS; FAMILY HISTORY; FEMALE; GENE MUTATION; GENETIC SCREENING; HUMAN; KIDNEY CYST; KIDNEY POLYCYSTIC DISEASE; LIVER POLYCYSTIC DISEASE; PANCREAS CARCINOMA; PANCREAS CYST; PANCREAS ISLET CELL TUMOR; VON HIPPEL LINDAU DISEASE;

EID: 0035057549     PISSN: 02726386     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0272-6386(01)80136-0     Document Type: Article
Times cited : (19)

References (37)
  • 16
    • 85031534337 scopus 로고    scopus 로고
    • 193300 von Hippel-Lindau syndrome. Downloaded December
    • (1999)
  • 21
    • 0023630505 scopus 로고
    • Basic criteria for clinical diagnosis and genetic counselling in Von Hippel-Lindau syndrome
    • (1987) J Vasc Dis , vol.16 , pp. 220-227
    • Neumann, H.P.H.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.