Rare diseases, an emergent paradigm in the medicine of the XXI century

被引：22
作者：
Palau, Francesc [1 ]
机构：
[1] CSIC, IBV, CIBERER, ISCIII, Valencia, Spain
来源：
MEDICINA CLINICA | 2010年 / 134卷 / 04期
关键词：
HUNTINGTONS-DISEASE; CHALLENGE; DISORDERS; LESSONS;
D O I：
10.1016/j.medcli.2009.06.038
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
[No abstract available]
引用
收藏
页码：161 / 168
页数：8
相关论文
共 30 条
  • [1] [Anonymous], The voice of 12,000 patients: Experiences and expectations of rare disease patients on diagnosis and care in Europe
  • [2] [Anonymous], 1978, Historia de la medicina
  • [3] Opinion - Mendelian disorders deserve more attention
    Antonarakis, SE
    Beckmann, JS
    [J]. NATURE REVIEWS GENETICS, 2006, 7 (04) : 277 - 282
  • [4] ARMERO CE, 2008, TRATADO NEUROLOGIA C, P1
  • [5] Avellaneda A, 2007, AN SIST SANIT NAVAR, V30, P177
  • [6] Empowerment of patients:: lessons from the rare diseases community
    Ayme, Segolene
    Kole, Anna
    Groft, Stephen
    [J]. LANCET, 2008, 371 (9629) : 2048 - 2051
  • [7] Human monogenic disorders -: a source of novel drug targets
    Brinkman, RR
    Dubé, MP
    Rouleau, GA
    Orr, AC
    Samuels, ME
    [J]. NATURE REVIEWS GENETICS, 2006, 7 (04) : 249 - 260
  • [8] Clinical trials of orphan medicines
    Buckley, Brendan M.
    [J]. LANCET, 2008, 371 (9629) : 2051 - 2055
  • [9] Burguera JA, 1997, REV NEUROLOGIA, V25, P1845
  • [10] Childs B., 1999, Genetic medicine: A logic of disease
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