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Journal Abstract Search

300 related items for PubMed ID: 27021801

  • 1. Molecular diagnosis in patients with retinoblastoma: Report of a series of cases.
    Ossandón D, Zanolli M, López JP, Benavides F, Pérez V, Repetto GM.
    Arch Soc Esp Oftalmol; 2016 Aug; 91(8):379-84. PubMed ID: 27021801
    [Abstract] [Full Text] [Related]

  • 2. Genetic analysis in retinoblastoma and peripheral blood correlation.
    Ruiz del Río N, Abelairas Gómez JM, Alonso García de la Rosa FJ, Peralta Calvo JM, de las Heras Martín A.
    Arch Soc Esp Oftalmol; 2015 Dec; 90(12):562-5. PubMed ID: 26279484
    [Abstract] [Full Text] [Related]

  • 3. Identification of three new mutations in the RB1 gene in patients with sporadic retinoblastoma in Colombia.
    Serrano ML, Yunis JJ.
    Biomedica; 2013 Dec; 33(1):53-61. PubMed ID: 23715307
    [Abstract] [Full Text] [Related]

  • 4. Iris Hypoplasia as the Presenting Sign of Retinoblastoma in a Child With a 13q Deletion.
    Shah S, Koban Y, Le BHA, Bechtold M, Zolfaghari E, Kim JW, Berry JL.
    J Pediatr Ophthalmol Strabismus; 2018 Apr 23; 55():e10-e13. PubMed ID: 29684226
    [Abstract] [Full Text] [Related]

  • 5. Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastoma.
    Lohmann DR, Gerick M, Brandt B, Oelschläger U, Lorenz B, Passarge E, Horsthemke B.
    Am J Hum Genet; 1997 Aug 23; 61(2):282-94. PubMed ID: 9311732
    [Abstract] [Full Text] [Related]

  • 6. Detection of mutations in the RB1 gene by single strand conformation polymorphism (SSCP) analysis, amplification mismatch detection (AMD) analysis and polymerase chain reaction sequencing.
    Dundar M, Lanyon GW, Connor MJ.
    Proc Natl Sci Counc Repub China B; 2001 Jul 23; 25(3):166-73. PubMed ID: 11480772
    [Abstract] [Full Text] [Related]

  • 7. Simultaneous diagnosis of unilateral retinoblastoma and contralateral optic pathway glioma in a child with neurofibromatosis type 1.
    Das A, Ghosh P, Zameer L, Ramprasad VL, Bhaduri A.
    Pediatr Hematol Oncol; 2019 Mar 23; 36(2):82-85. PubMed ID: 30963792
    [No Abstract] [Full Text] [Related]

  • 8. RB1 germline mutation spectrum and clinical features in patients with unilateral retinoblastomas.
    Fang X, Chen J, Wang Y, Zhao M, Zhang X, Yang L, Ni X, Zhao J, Gallie BL.
    Ophthalmic Genet; 2021 Oct 23; 42(5):593-599. PubMed ID: 34190019
    [Abstract] [Full Text] [Related]

  • 9. Mutational analysis of the RB1 gene and the inheritance patterns of retinoblastoma in Jordan.
    Yousef YA, Tbakhi A, Al-Hussaini M, AlNawaiseh I, Saab A, Afifi A, Naji M, Mohammad M, Deebajah R, Jaradat I, Sultan I, Mehyar M.
    Fam Cancer; 2018 Apr 23; 17(2):261-268. PubMed ID: 28803391
    [Abstract] [Full Text] [Related]

  • 10. Next-Generation Sequencing of Retinoblastoma Identifies Pathogenic Alterations beyond RB1 Inactivation That Correlate with Aggressive Histopathologic Features.
    Afshar AR, Pekmezci M, Bloomer MM, Cadenas NJ, Stevers M, Banerjee A, Roy R, Olshen AB, Van Ziffle J, Onodera C, Devine WP, Grenert JP, Bastian BC, Solomon DA, Damato BE.
    Ophthalmology; 2020 Jun 23; 127(6):804-813. PubMed ID: 32139107
    [Abstract] [Full Text] [Related]

  • 11. A novel de-novo RB1 mutation identified in a patient with bilateral retinoblastoma.
    Fukushima H, Suzuki R, Hiraoka T, Suzuki S, Noguchi E, Takada H.
    Jpn J Clin Oncol; 2023 Aug 30; 53(9):863-865. PubMed ID: 37345682
    [Abstract] [Full Text] [Related]

  • 12. Clinical characteristics and germline mutation spectrum of RB1 in Chinese patients with retinoblastoma: A dual-center study of 145 patients.
    Chai P, Luo Y, Yu J, Li Y, Yang J, Zhuang A, Fan J, Han M, Jia R.
    Exp Eye Res; 2021 Apr 30; 205():108456. PubMed ID: 33493472
    [Abstract] [Full Text] [Related]

  • 13. [Genetic analysis results of patients with a retinoblastoma refractory to systemic chemotherapy].
    Ruiz del Río N, Abelairas Gómez JM, Alonso García de la Rosa FJ, Peralta Calvo JM, de las Heras Martín A.
    Arch Soc Esp Oftalmol; 2015 Sep 30; 90(9):414-20. PubMed ID: 25817468
    [Abstract] [Full Text] [Related]

  • 14. Impact of RB1 gene mutation type in retinoblastoma patients on clinical presentation and management outcome.
    Mehyar M, Mosallam M, Tbakhi A, Saab A, Sultan I, Deebajah R, Jaradat I, AlJabari R, Mohammad M, AlNawaiseh I, Al-Hussaini M, Yousef YA.
    Hematol Oncol Stem Cell Ther; 2020 Sep 30; 13(3):152-159. PubMed ID: 32222358
    [Abstract] [Full Text] [Related]

  • 15. Lack of correlation between age at diagnosis and RB1 mutations for unilateral retinoblastoma: the importance of genetic testing.
    Berry JL, Lewis L, Zolfaghari E, Green S, Le BHA, Lee TC, Murphree AL, Kim JW, Jubran R.
    Ophthalmic Genet; 2018 Jun 30; 39(3):407-409. PubMed ID: 29286867
    [No Abstract] [Full Text] [Related]

  • 16. Prenatal genetic diagnosis of retinoblastoma and report of RB1 gene mutation from India.
    Shah PK, Sripriya S, Narendran V, Pandian AJ.
    Ophthalmic Genet; 2016 Dec 30; 37(4):430-433. PubMed ID: 26914665
    [Abstract] [Full Text] [Related]

  • 17. Detection of mutations of the RB1 gene in retinoblastoma patients by using exon-by-exon PCR-SSCP analysis.
    Shimizu T, Toguchida J, Kato MV, Kaneko A, Ishizaki K, Sasaki MS.
    Am J Hum Genet; 1994 May 30; 54(5):793-800. PubMed ID: 8178820
    [Abstract] [Full Text] [Related]

  • 18. Retinoblastoma in Patients with 13q deletion syndrome - case series.
    Jedrychowska-Jamborska J, Morawski K, Kubicka-Trzaska A, Romanowska-Dixon B.
    Klin Oczna; 2016 Aug 30; 118(1):32-35. PubMed ID: 29715405
    [Abstract] [Full Text] [Related]

  • 19. Mosaicism and prenatal diagnosis options: insights from retinoblastoma.
    Dehainault C, Golmard L, Millot GA, Charpin A, Laugé A, Tarabeux J, Aerts I, Cassoux N, Stoppa-Lyonnet D, Gauthier-Villars M, Houdayer C.
    Eur J Hum Genet; 2017 Feb 30; 25(3):381-383. PubMed ID: 28000698
    [Abstract] [Full Text] [Related]

  • 20. Impact of RB1 gene screening from blood collected on a single day from 411 family members of 113 Retinoblastoma survivors in India.
    Vanniarajan A, Maitra P, Saraswathi KK, Shah PK.
    Eye (Lond); 2024 Jun 30; 38(8):1575-1580. PubMed ID: 38341497
    [Abstract] [Full Text] [Related]

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