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Volumn 59, Issue SUPPL. 6, 2008, Pages 683-688

Recurrence of arterio-venous malformations with life-threatening complications in a pregnant woman with hereditary teleangiectasia

Author keywords

Hereditary hemorrhagic teleangiectasia; Pregnancy; Pulmonary insufficiency

Indexed keywords

ADULT; ARTERIOVENOUS FISTULA; ARTICLE; ARTIFICIAL EMBOLISM; CASE REPORT; CEREBROVASCULAR ACCIDENT; FEMALE; HEMATOTHORAX; HEMIPARESIS; HUMAN; LOBECTOMY; LUNG INSUFFICIENCY; MORBIDITY; MORTALITY; OSTEOARTHROPATHY; PREGNANCY; PREMATURE LABOR; PULMONARY SHUNT; RECURRENT DISEASE; RENDU OSLER WEBER DISEASE; ARTERIOVENOUS MALFORMATION; BRAIN ISCHEMIA; CESAREAN SECTION; GENETICS; LUNG; LUNG CIRCULATION; PARESIS; PATHOLOGY; PHYSIOLOGY; PREGNANCY COMPLICATION; PUERPERIUM; STROKE;

EID: 64549095953     PISSN: 08675910     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (9)

References (12)
  • 1
    • 33644870430 scopus 로고    scopus 로고
    • Genotype-phenotype correlation in hereditary hemorrhagic telangiectasia: Mutations and manifestations
    • Bayrak-Toydemir P, McDonald J, Markewitz B et al. Genotype-phenotype correlation in hereditary hemorrhagic telangiectasia: mutations and manifestations. Am J Med Genet A 2006, 140: 463-470.
    • (2006) Am J Med Genet A , vol.140 , pp. 463-470
    • Bayrak-Toydemir, P.1    McDonald, J.2    Markewitz, B.3
  • 2
    • 0022389192 scopus 로고
    • Cerebral embolism-first manifestation of pulmonary arteriovenous malformation in patients with hereditary hemorrhagic telangiectasia
    • Hewes RC, Auster M, White RI Jr. Cerebral embolism-first manifestation of pulmonary arteriovenous malformation in patients with hereditary hemorrhagic telangiectasia. Cardiovasc Intervent Radiol 1985; 8: 151-115.
    • (1985) Cardiovasc Intervent Radiol , vol.8 , pp. 151-115
    • Hewes, R.C.1    Auster, M.2    White Jr., R.I.3
  • 3
    • 0029563707 scopus 로고
    • Medical complications of pregnancy in hereditary haemorrhagic telangiectasia
    • Shovlin CL, Winstock AR, Peters AM, Jackson JE, Hughes JM. Medical complications of pregnancy in hereditary haemorrhagic telangiectasia. QJM. 1995; 88: 879-887.
    • (1995) QJM , vol.88 , pp. 879-887
    • Shovlin, C.L.1    Winstock, A.R.2    Peters, A.M.3    Jackson, J.E.4    Hughes, J.M.5
  • 4
    • 0037286297 scopus 로고    scopus 로고
    • Hereditary haemorrhagic telangiectasia (Osler-Weber- Rendu syndrome): A view from the 21st century
    • Begbie ME, Wallace GM, Shovlin CL. Hereditary haemorrhagic telangiectasia (Osler-Weber- Rendu syndrome): a view from the 21st century. Postgrad Med J 2003; 79: 18-24.
    • (2003) Postgrad Med J , vol.79 , pp. 18-24
    • Begbie, M.E.1    Wallace, G.M.2    Shovlin, C.L.3
  • 7
    • 47349107056 scopus 로고    scopus 로고
    • Estimates of maternal risks of pregnancy for women with hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): Suggested approach for obstetric services
    • Jun 2 [Epub ahead of print
    • Shovlin C, Sodhi V, McCarthy A, Lasjaunias P, Jackson J, Sheppard M. Estimates of maternal risks of pregnancy for women with hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): suggested approach for obstetric services. BJOG 2008; Jun 2 [Epub ahead of print].
    • (2008) BJOG
    • Shovlin, C.1    Sodhi, V.2    McCarthy, A.3    Lasjaunias, P.4    Jackson, J.5    Sheppard, M.6
  • 9
    • 34548423622 scopus 로고    scopus 로고
    • Hereditary hemorrhagic telangiectasia and pregnancy
    • Worda C, Lang I, Husslein P, Kneussl M. Hereditary hemorrhagic telangiectasia and pregnancy. Obstet Gynecol 2007; 110: 474-477.
    • (2007) Obstet Gynecol , vol.110 , pp. 474-477
    • Worda, C.1    Lang, I.2    Husslein, P.3    Kneussl, M.4
  • 10
    • 33745700371 scopus 로고    scopus 로고
    • Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): Correlation of genotype with phenotype
    • Bossler AD, Richards J, George C, Godmilow L, Ganguly A. Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype. Hum Mutat 2006; 27: 667-675.
    • (2006) Hum Mutat , vol.27 , pp. 667-675
    • Bossler, A.D.1    Richards, J.2    George, C.3    Godmilow, L.4    Ganguly, A.5
  • 11
    • 22244449292 scopus 로고    scopus 로고
    • A new locus for hereditary haemorrhagic telangiectasia (HHT3) maps to chromosome 5
    • Cole SG, Begbie ME, Wallace GM, Shovlin CL A new locus for hereditary haemorrhagic telangiectasia (HHT3) maps to chromosome 5. J Med Genet 2005; 42: 577-582.
    • (2005) J Med Genet , vol.42 , pp. 577-582
    • Cole, S.G.1    Begbie, M.E.2    Wallace, G.M.3    Shovlin, C.L.4
  • 12
    • 33749455646 scopus 로고    scopus 로고
    • A fourth locus for hereditary hemorrhagic telangiectasia maps to chromosome 7
    • Bayrak-Toydemir P, McDonald J, Akarsu N et al. A fourth locus for hereditary hemorrhagic telangiectasia maps to chromosome 7. Am J Med Genet A 2006; 140: 2155-2162.
    • (2006) Am J Med Genet A , vol.140 , pp. 2155-2162
    • Bayrak-Toydemir, P.1    McDonald, J.2    Akarsu, N.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.