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 *

167 related articles for article (PubMed ID: 16374328)

  • 61. Autosomal Recessive Bestrophinopathy Is Not Associated With the Loss of Bestrophin-1 Anion Channel Function in a Patient With a Novel BEST1 Mutation.
    Johnson AA; Bachman LA; Gilles BJ; Cross SD; Stelzig KE; Resch ZT; Marmorstein LY; Pulido JS; Marmorstein AD
    Invest Ophthalmol Vis Sci; 2015 Jul; 56(8):4619-30. PubMed ID: 26200502
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Spontaneous regression of juvenile retinoschisis.
    Boucher MC
    Can J Ophthalmol; 1997 Oct; 32(6):392-5. PubMed ID: 9363344
    [No Abstract]   [Full Text] [Related]  

  • 63. Pigmented paravenous retinochoroidal atrophy with macular involvement.
    Romero R; Castaño A; Moriche M; Poyales B; Granados M
    Arch Soc Esp Oftalmol; 2013 Feb; 88(2):77-9. PubMed ID: 23433195
    [TBL] [Abstract][Full Text] [Related]  

  • 64. [Gene Replacement Therapy for Inherited Retinal Dystrophies].
    Mühlfriedel R; Sothilingam V; Tanimoto N; Seeliger MW
    Klin Monbl Augenheilkd; 2017 Mar; 234(3):320-328. PubMed ID: 28355661
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Evaluation of the norrie disease gene in a family with incontinentia pigmenti.
    Shastry BS; Trese MT
    Ophthalmic Res; 2000; 32(4):181-4. PubMed ID: 10828739
    [TBL] [Abstract][Full Text] [Related]  

  • 66. A Novel Pathogenic Variant in NDP Gene With Incomplete Penetrance Manifests as X-Linked Familial Exudative Vitreoretinopathy.
    Scott NL; Tran KD; Russell JF; Hinkle JW; Cernichiaro-Espinosa LA; Lauer A; Berrocal AM
    Ophthalmic Surg Lasers Imaging Retina; 2019 Feb; 50(2):120-124. PubMed ID: 30768221
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Ocular gene therapy: the basic science and current state of research.
    da Cruz L; Rakoczy P; Constable I
    Aust N Z J Ophthalmol; 1997 May; 25(2):97-104. PubMed ID: 9267594
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Optical Coherence Tomography Angiography in Familial Exudative Vitreoretinopathy: Clinical Features and Phenotype-Genotype Correlation.
    Chen C; Liu C; Wang Z; Sun L; Zhao X; Li S; Luo X; Zhang A; Chong V; Lu L; Ding X
    Invest Ophthalmol Vis Sci; 2018 Dec; 59(15):5726-5734. PubMed ID: 30513533
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Whole Genome Sequencing Increases Molecular Diagnostic Yield Compared with Current Diagnostic Testing for Inherited Retinal Disease.
    Ellingford JM; Barton S; Bhaskar S; Williams SG; Sergouniotis PI; O'Sullivan J; Lamb JA; Perveen R; Hall G; Newman WG; Bishop PN; Roberts SA; Leach R; Tearle R; Bayliss S; Ramsden SC; Nemeth AH; Black GC
    Ophthalmology; 2016 May; 123(5):1143-50. PubMed ID: 26872967
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Bestrophinopathy: An RPE-photoreceptor interface disease.
    Guziewicz KE; Sinha D; Gómez NM; Zorych K; Dutrow EV; Dhingra A; Mullins RF; Stone EM; Gamm DM; Boesze-Battaglia K; Aguirre GD
    Prog Retin Eye Res; 2017 May; 58():70-88. PubMed ID: 28111324
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Diffuse infiltrating retinoblastoma: an inherited case.
    Kao LY
    Retina; 2000; 20(2):217-9. PubMed ID: 10783961
    [No Abstract]   [Full Text] [Related]  

  • 72. Novel and recurrent NDP gene mutations in familial cases of Norrie disease and X-linked exudative vitreoretinopathy.
    Pelcastre EL; Villanueva-Mendoza C; Zenteno JC
    Clin Exp Ophthalmol; 2010 May; 38(4):367-74. PubMed ID: 20491809
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Genotype-based databases for variants causing rare diseases.
    Lanthaler B; Wieser S; Deutschmann A; Schossig A; Fauth C; Zschocke J; Witsch-Baumgartner M
    Gene; 2014 Oct; 550(1):136-40. PubMed ID: 25111118
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Oligocone trichromacy: clinical and molecular genetic investigations.
    Andersen MK; Christoffersen NL; Sander B; Edmund C; Larsen M; Grau T; Wissinger B; Kohl S; Rosenberg T
    Invest Ophthalmol Vis Sci; 2010 Jan; 51(1):89-95. PubMed ID: 19797231
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Disappearance of puncta after uveitis in an eye with fundus albipunctatus.
    Imaizumi M; Tatewaki SY; Kimoto K; Takaki Y; Nakatsuka K; Furushima M; Matsumoto CS; Choshi T
    Retina; 2005 Dec; 25(8):1096-8. PubMed ID: 16340543
    [No Abstract]   [Full Text] [Related]  

  • 76. [Rare diseases: an "exceptional field of research. Interview by Catherine Holué].
    Dolfus H; Lévy N
    Rev Prat; 2012 Jan; 62(1):89-90. PubMed ID: 22335076
    [No Abstract]   [Full Text] [Related]  

  • 77. 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]  

  • 78. Wnt-Spectrum Vitreoretinopathy Masquerading as Congenital Toxoplasmosis.
    Callaway NF; Berrocal AM
    Ophthalmic Surg Lasers Imaging Retina; 2018 Jun; 49(6):446-450. PubMed ID: 29927473
    [TBL] [Abstract][Full Text] [Related]  

  • 79. BESTROPHINOPATHY: A Spectrum of Ocular Abnormalities Caused by the c.614T>C Mutation in the BEST1 Gene.
    Toto L; Boon CJ; Di Antonio L; Battaglia Parodi M; Mastropasqua R; Antonucci I; Stuppia L; Mastropasqua L
    Retina; 2016 Aug; 36(8):1586-95. PubMed ID: 26716959
    [TBL] [Abstract][Full Text] [Related]  

  • 80. [Rare diseases: "a public health priorty". Interview by Catherine Holué].
    Podeur A
    Rev Prat; 2012 Jan; 62(1):79-80. PubMed ID: 22335073
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.