These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

198 related articles for article (PubMed ID: 16509005)

  • 61. Rare pulmonary diseases: a common fight.
    Harari S; Humbert M
    Eur Respir Rev; 2017 Sep; 26(145):. PubMed ID: 28877977
    [TBL] [Abstract][Full Text] [Related]  

  • 62. [Reference center for rare vascular diseases of the eye and brain].
    Chabriat H;
    Rev Neurol (Paris); 2013 Feb; 169 Suppl 1():S28-32. PubMed ID: 23452768
    [TBL] [Abstract][Full Text] [Related]  

  • 63. [GPs: patients require you to doubt! Interview by Catherine Holué].
    Viollet V
    Rev Prat; 2012 Jan; 62(1):85-6. PubMed ID: 22335075
    [No Abstract]   [Full Text] [Related]  

  • 64. [Therapeutic strategies for hereditary retinal diseases].
    Rüther K; Bartsch U
    Ophthalmologe; 2005 Aug; 102(8):755-6. PubMed ID: 15999275
    [No Abstract]   [Full Text] [Related]  

  • 65. [The stakes of pre- and post-market authorization development and clinical assessment].
    Schwebig A
    Presse Med; 2012 May; 41 Suppl 1():S6-8. PubMed ID: 22483770
    [No Abstract]   [Full Text] [Related]  

  • 66. [New treatments of hereditary blindness].
    Bertelsen M; Rosenberg T; Larsen M
    Ugeskr Laeger; 2013 Sep; 175(36):2038-42. PubMed ID: 23992912
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Patients with rare diseases work to jump-start research; advocacy groups create their own tissue banks to aid in drug treatment.
    Marcus AD
    Wall St J (East Ed); 2006 Jul; ():D1, D2. PubMed ID: 16906687
    [No Abstract]   [Full Text] [Related]  

  • 68. Genetic manipulation for inherited neurodegenerative diseases: myth or reality?
    Yu-Wai-Man P
    Br J Ophthalmol; 2016 Oct; 100(10):1322-31. PubMed ID: 27002113
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Long-Term Macular Changes in the First Proband of Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC) Due to a Newly Identified Mutation in BEST1.
    Chen CJ; Kaufman S; Packo K; Stöhr H; Weber BH; Goldberg MF
    Ophthalmic Genet; 2016; 37(1):102-8. PubMed ID: 26849243
    [TBL] [Abstract][Full Text] [Related]  

  • 70. What Is Next for Retinal Gene Therapy?
    Vandenberghe LH
    Cold Spring Harb Perspect Med; 2015 Apr; 5(10):. PubMed ID: 25877395
    [TBL] [Abstract][Full Text] [Related]  

  • 71. [Introduction and welcome message].
    Schwebig A; Levy N; Ayme S
    Presse Med; 2012 May; 41 Suppl 1():S1-2. PubMed ID: 22483772
    [No Abstract]   [Full Text] [Related]  

  • 72.
    Guziewicz KE; Cideciyan AV; Beltran WA; Komáromy AM; Dufour VL; Swider M; Iwabe S; Sumaroka A; Kendrick BT; Ruthel G; Chiodo VA; Héon E; Hauswirth WW; Jacobson SG; Aguirre GD
    Proc Natl Acad Sci U S A; 2018 Mar; 115(12):E2839-E2848. PubMed ID: 29507198
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Clinical manifestation of a novel PAX6 mutation Arg128Pro.
    Bredrup C; Knappskog PM; Rødahl E; Boman H
    Arch Ophthalmol; 2008 Mar; 126(3):428-30. PubMed ID: 18332330
    [No Abstract]   [Full Text] [Related]  

  • 74. Clinical and molecular evaluation of probands and family members with familial exudative vitreoretinopathy.
    Boonstra FN; van Nouhuys CE; Schuil J; de Wijs IJ; van der Donk KP; Nikopoulos K; Mukhopadhyay A; Scheffer H; Tilanus MA; Cremers FP; Hoefsloot LH
    Invest Ophthalmol Vis Sci; 2009 Sep; 50(9):4379-85. PubMed ID: 19324841
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Towards efficiency in rare disease research: what is distinctive and important?
    Jia J; Shi T
    Sci China Life Sci; 2017 Jul; 60(7):686-691. PubMed ID: 28639105
    [TBL] [Abstract][Full Text] [Related]  

  • 76. [Extensive yellowish fundus changes in a 6-year-old child].
    Gottwalt S; Bergmann A; Kautza-Lucht M; Roider JB; Treumer F
    Ophthalmologe; 2017 Jun; 114(6):556-559. PubMed ID: 27503085
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Choroidal neovascularization, outer retinal tubulation and fundus autofluorescence findings in a patient with enhanced S-cone syndrome.
    Sambricio J; Tejada-Palacios P; Barceló-Mendiguchía A
    Clin Exp Ophthalmol; 2016; 44(1):69-71. PubMed ID: 26154701
    [No Abstract]   [Full Text] [Related]  

  • 78. [HERNS. A rare, hereditary, multisystemic disease with cerebral microangiopathy].
    Seifried C; Sitzer M; Jen J; Auburger G
    Nervenarzt; 2005 Oct; 76(10):1191-2, 1194-5. PubMed ID: 15856153
    [TBL] [Abstract][Full Text] [Related]  

  • 79. [Hereditary eye dieseas in the Entlebucher Mountaindog in Switzerland: a retrospective study from 1999 to 2009].
    Kuster N; Hässig M; Spiess B
    Schweiz Arch Tierheilkd; 2011 Jun; 153(6):269-75. PubMed ID: 21638263
    [TBL] [Abstract][Full Text] [Related]  

  • 80. [Optimising treatment for people with rare diseases].
    Lund AM; Skovby F
    Ugeskr Laeger; 2006 Apr; 168(15):1547-50. PubMed ID: 16640978
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.