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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

113 related items for PubMed ID: 9895244

  • 1. Analysis of the IRBP gene as a cause of RP in 45 ARRP Spanish families. Autosomal recessive retinitis pigmentosa. Interstitial retinol binding protein. Spanish Multicentric and Multidisciplinary Group for Research into Retinitis Pigmentosa.
    Valverde D, Vázquez-Gundín F, del Rio E, Calaf M, Fernández JL, Baiget M.
    Ophthalmic Genet; 1998 Dec; 19(4):197-202. PubMed ID: 9895244
    [Abstract] [Full Text] [Related]

  • 2. Evaluation of RLBP1 in 50 autosomal recessive retinitis pigmentosa and 4 retinitis punctata albescens Spanish families.
    Bernal S, Calaf M, Adan A, Solans T, Valverde D, Ayuso C, Baiget M.
    Ophthalmic Genet; 2001 Mar; 22(1):19-25. PubMed ID: 11262646
    [Abstract] [Full Text] [Related]

  • 3. Homozygosity Mapping in Leber Congenital Amaurosis and Autosomal Recessive Retinitis Pigmentosa in South Indian Families.
    Srilekha S, Arokiasamy T, Srikrupa NN, Umashankar V, Meenakshi S, Sen P, Kapur S, Soumittra N.
    PLoS One; 2015 Mar; 10(7):e0131679. PubMed ID: 26147992
    [Abstract] [Full Text] [Related]

  • 4. Evidence against involvement of recoverin in autosomal recessive retinitis pigmentosa in 42 Spanish families.
    Bayés M, Valverde D, Balcells S, Grinberg D, Vilageliu L, Benítez J, Ayuso C, Beneyto M, Baiget M, Gonzàlez-Duarte R.
    Hum Genet; 1995 Jul; 96(1):89-94. PubMed ID: 7607661
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. A homozygous missense mutation in the IRBP gene (RBP3) associated with autosomal recessive retinitis pigmentosa.
    den Hollander AI, McGee TL, Ziviello C, Banfi S, Dryja TP, Gonzalez-Fernandez F, Ghosh D, Berson EL.
    Invest Ophthalmol Vis Sci; 2009 Apr; 50(4):1864-72. PubMed ID: 19074801
    [Abstract] [Full Text] [Related]

  • 7. Homozygosity mapping of autosomal recessive retinitis pigmentosa locus (RP22) on chromosome 16p12.1-p12.3.
    Finckh U, Xu S, Kumaramanickavel G, Schürmann M, Mukkadan JK, Fernandez ST, John S, Weber JL, Denton MJ, Gal A.
    Genomics; 1998 Mar 15; 48(3):341-5. PubMed ID: 9545639
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. A new autosomal recessive retinitis pigmentosa locus maps on chromosome 2q31-q33.
    Bayés M, Goldaracena B, Martínez-Mir A, Iragui-Madoz MI, Solans T, Chivelet P, Bussaglia E, Ramos-Arroyo MA, Baiget M, Vilageliu L, Balcells S, Gonzàlez-Duarte R, Grinberg D.
    J Med Genet; 1998 Feb 15; 35(2):141-5. PubMed ID: 9507394
    [Abstract] [Full Text] [Related]

  • 10. WDR19: an ancient, retrograde, intraflagellar ciliary protein is mutated in autosomal recessive retinitis pigmentosa and in Senior-Loken syndrome.
    Coussa RG, Otto EA, Gee HY, Arthurs P, Ren H, Lopez I, Keser V, Fu Q, Faingold R, Khan A, Schwartzentruber J, Majewski J, Hildebrandt F, Koenekoop RK.
    Clin Genet; 2013 Aug 15; 84(2):150-9. PubMed ID: 23683095
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Mutation analysis of 272 Spanish families affected by autosomal recessive retinitis pigmentosa using a genotyping microarray.
    Ávila-Fernández A, Cantalapiedra D, Aller E, Vallespín E, Aguirre-Lambán J, Blanco-Kelly F, Corton M, Riveiro-Álvarez R, Allikmets R, Trujillo-Tiebas MJ, Millán JM, Cremers FP, Ayuso C.
    Mol Vis; 2010 Dec 03; 16():2550-8. PubMed ID: 21151602
    [Abstract] [Full Text] [Related]

  • 15. Homozygosity mapping reveals null mutations in FAM161A as a cause of autosomal-recessive retinitis pigmentosa.
    Bandah-Rozenfeld D, Mizrahi-Meissonnier L, Farhy C, Obolensky A, Chowers I, Pe'er J, Merin S, Ben-Yosef T, Ashery-Padan R, Banin E, Sharon D.
    Am J Hum Genet; 2010 Sep 10; 87(3):382-91. PubMed ID: 20705279
    [Abstract] [Full Text] [Related]

  • 16. Mutations in TULP1, NR2E3, and MFRP genes in Indian families with autosomal recessive retinitis pigmentosa.
    Kannabiran C, Singh H, Sahini N, Jalali S, Mohan G.
    Mol Vis; 2012 Sep 10; 18():1165-74. PubMed ID: 22605927
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. [Molecular analysis of the RPE65 gene in 72 Spanish families with autosomal recessive retinitis pigmentosa].
    Marcos I, Ruiz A, Borrego S, Ayuso C, Baiget M, Antiñolo G.
    Med Clin (Barc); 2001 Jun 30; 117(4):121-3. PubMed ID: 11472682
    [Abstract] [Full Text] [Related]

  • 19. Genetic analysis of Indian families with autosomal recessive retinitis pigmentosa by homozygosity screening.
    Singh HP, Jalali S, Narayanan R, Kannabiran C.
    Invest Ophthalmol Vis Sci; 2009 Sep 30; 50(9):4065-71. PubMed ID: 19339744
    [Abstract] [Full Text] [Related]

  • 20. Retinitis pigmentosa in Spain. The Spanish Multicentric and Multidisciplinary Group for Research into Retinitis Pigmentosa.
    Ayuso C, Garcia-Sandoval B, Najera C, Valverde D, Carballo M, Antiñolo G.
    Clin Genet; 1995 Sep 30; 48(3):120-2. PubMed ID: 8556816
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 6.