Mutation screening in patients with hereditary haemorrhagic telangiectasia

被引:0
|
作者
Toydemir, PB [1 ]
McDonald, J [1 ]
Ward, K [1 ]
Mao, R [1 ]
机构
[1] Univ Utah, DNA Diagnost Lab, Salt Lake City, UT USA
关键词
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
2398
引用
收藏
页码:577 / 577
页数:1
相关论文
共 50 条
  • [41] Quality of life in patients with hereditary haemorrhagic telangiectasia (HHT)
    Roberto Zarrabeitia
    Concepción Fariñas-Álvarez
    Miguel Santibáñez
    Blanca Señaris
    Ana Fontalba
    Luisa María Botella
    José Antonio Parra
    Health and Quality of Life Outcomes, 15
  • [42] Neurovascular Manifestations in Pediatric Patients With Hereditary Haemorrhagic Telangiectasia
    Azma, Roxana
    Dmytriw, Adam A.
    Biswas, Asthik
    Pollak, Mordechai
    Ratjen, Felix
    Amirabadi, Afsaneh
    Branson, Helen M.
    V. Kulkarni, Abhaya
    Dirks, Peter
    Muthusami, Prakash
    PEDIATRIC NEUROLOGY, 2022, 129 : 24 - 30
  • [43] Followup of thalidomide treatment in patients with hereditary haemorrhagic telangiectasia
    Hosman, A. E.
    Westermann, C. J. J.
    Snijder, R.
    Disch, F.
    Mummery, C. L.
    Mager, J. J.
    ANGIOGENESIS, 2015, 18 (04) : 560 - 561
  • [44] Quality of life in patients with hereditary haemorrhagic telangiectasia (HHT)
    Zarrabeitia, Roberto
    Farinas-Alvarez, Concepcion
    Santibanez, Miguel
    Senaris, Blanca
    Fontalba, Ana
    Maria Botella, Luisa
    Antonio Parra, Jose
    HEALTH AND QUALITY OF LIFE OUTCOMES, 2017, 15
  • [45] Screening for pulmonary and cerebral arteriovenous malformations in children with hereditary haemorrhagic telangiectasia
    Al-Saleh, S.
    Mei-Zahav, M.
    Faughnan, M. E.
    MacLusky, I. B.
    Carpenter, S.
    Letarte, M.
    Ratjen, F.
    EUROPEAN RESPIRATORY JOURNAL, 2009, 34 (04) : 875 - 881
  • [46] Neurovascular screening in hereditary haemorrhagic telangiectasia: dilemmas for the paediatric neuroscience community
    Ganesan, Vijeya
    Robertson, Fergus
    Berg, Jonathan
    DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 2013, 55 (05): : 405 - 407
  • [47] Uptake and radiological findings of screening cerebral magnetic resonance scans in patients with hereditary haemorrhagic telangiectasia
    Fatania, Gavin
    Gilson, Clare
    Glover, Alan
    Alsafi, Ali
    Jackson, James E.
    Patel, Maneesh C.
    Shovlin, Claire L.
    INTRACTABLE & RARE DISEASES RESEARCH, 2018, 7 (04) : 236 - 244
  • [48] Treatment of tongue telangiectasia in a patient with hereditary haemorrhagic telangiectasia
    Bowers, Eve Mandisa Rader
    Lee, Stella
    BMJ CASE REPORTS, 2020, 13 (11)
  • [49] A natural obturator in hereditary haemorrhagic telangiectasia
    Soni-Jaiswal, A.
    Woolford, T. J.
    JOURNAL OF LARYNGOLOGY AND OTOLOGY, 2009, 123 (06): : 695 - 696
  • [50] Screening in hereditary hemorrhagic telangiectasia patients
    Faughnan, ME
    Hyland, RH
    Nanthakumar, K
    Redelmeier, DA
    CHEST, 2000, 118 (02) : 566 - 566