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 *

202 related articles for article (PubMed ID: 10964838)

  • 1. Ophthalmologic findings in Cohen syndrome. A long-term follow-up.
    Kivitie-Kallio S; Summanen P; Raitta C; Norio R
    Ophthalmology; 2000 Sep; 107(9):1737-45. PubMed ID: 10964838
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pediatric ophthalmologic findings of Cohen syndrome in twins.
    Mrugacz M; Sredzinska-Kita D; Bakunowicz-Lazarczyk A
    J Pediatr Ophthalmol Strabismus; 2005; 42(1):54-6. PubMed ID: 15724900
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Ophthalmologic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation: a new type of hereditary metabolic chorioretinopathy.
    Tyni T; Kivelä T; Lappi M; Summanen P; Nikoskelainen E; Pihko H
    Ophthalmology; 1998 May; 105(5):810-24. PubMed ID: 9593380
    [TBL] [Abstract][Full Text] [Related]  

  • 4. IMPG2-associated retinitis pigmentosa displays relatively early macular involvement.
    van Huet RA; Collin RW; Siemiatkowska AM; Klaver CC; Hoyng CB; Simonelli F; Khan MI; Qamar R; Banin E; Cremers FP; Theelen T; den Hollander AI; van den Born LI; Klevering BJ
    Invest Ophthalmol Vis Sci; 2014 May; 55(6):3939-53. PubMed ID: 24876279
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Neurological and psychological findings in patients with Cohen syndrome: a study of 18 patients aged 11 months to 57 years.
    Kivitie-Kallio S; Larsen A; Kajasto K; Norio R
    Neuropediatrics; 1999 Aug; 30(4):181-9. PubMed ID: 10569209
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Ocular findings in Brazilian identical twins with Cohen syndrome: case report.
    Rim PH; Figueirêdo ES; Hirata FE; Steiner CE; Marques-de-Faria AP
    Arq Bras Oftalmol; 2009; 72(6):815-8. PubMed ID: 20098905
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The Cohen syndrome. Retinal lesions and granulocytopenia.
    Warburg M; Pedersen SA; Hørlyk H
    Ophthalmic Paediatr Genet; 1990 Mar; 11(1):7-13. PubMed ID: 2348983
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cohen syndrome: essential features, natural history, and heterogeneity.
    Kivitie-Kallio S; Norio R
    Am J Med Genet; 2001 Aug; 102(2):125-35. PubMed ID: 11477603
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mechanisms of myopia in Cohen syndrome mapped to chromosome 8q22.
    Summanen P; Kivitie-Kallio S; Norio R; Raitta C; Kivelä T
    Invest Ophthalmol Vis Sci; 2002 May; 43(5):1686-93. PubMed ID: 11980891
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Long-term visual outcome of methylmalonic aciduria and homocystinuria, cobalamin C type.
    Gizicki R; Robert MC; Gómez-López L; Orquin J; Decarie JC; Mitchell GA; Roy MS; Ospina LH
    Ophthalmology; 2014 Jan; 121(1):381-386. PubMed ID: 24126030
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Ophthalmic features of retinitis pigmentosa in Cohen syndrome caused by pathogenic variants in the VPS13B gene.
    Nasser F; Kurtenbach A; Biskup S; Weidensee S; Kohl S; Zrenner E
    Acta Ophthalmol; 2020 May; 98(3):e316-e321. PubMed ID: 31580008
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Ocular manifestations of microcephaly with or without chorioretinopathy, lymphedema or intellectual disability (MCLID) syndrome associated with mutations in KIF11.
    Balikova I; Robson AG; Holder GE; Ostergaard P; Mansour S; Moore AT
    Acta Ophthalmol; 2016 Feb; 94(1):92-8. PubMed ID: 25996076
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Dominant cystoid macular dystrophy.
    Saksens NT; van Huet RA; van Lith-Verhoeven JJ; den Hollander AI; Hoyng CB; Boon CJ
    Ophthalmology; 2015 Jan; 122(1):180-91. PubMed ID: 25267528
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Ophthalmic manifestations of Smith-Magenis syndrome.
    Chen RM; Lupski JR; Greenberg F; Lewis RA
    Ophthalmology; 1996 Jul; 103(7):1084-91. PubMed ID: 8684798
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The ophthalmic findings in Cohen syndrome.
    Chandler KE; Biswas S; Lloyd IC; Parry N; Clayton-Smith J; Black GC
    Br J Ophthalmol; 2002 Dec; 86(12):1395-8. PubMed ID: 12446373
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cohen syndrome in the Ohio Amish.
    Falk MJ; Feiler HS; Neilson DE; Maxwell K; Lee JV; Segall SK; Robin NH; Wilhelmsen KC; Träskelin AL; Kolehmainen J; Lehesjoki AE; Wiznitzer M; Warman ML
    Am J Med Genet A; 2004 Jul; 128A(1):23-8. PubMed ID: 15211651
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical features and natural history of the acute idiopathic enlarged blind spot syndrome.
    Watzke RC; Shults WT
    Ophthalmology; 2002 Jul; 109(7):1326-35. PubMed ID: 12093658
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Long-term pattern of progression of myopic maculopathy: a natural history study.
    Hayashi K; Ohno-Matsui K; Shimada N; Moriyama M; Kojima A; Hayashi W; Yasuzumi K; Nagaoka N; Saka N; Yoshida T; Tokoro T; Mochizuki M
    Ophthalmology; 2010 Aug; 117(8):1595-611, 1611.e1-4. PubMed ID: 20207005
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Allelic heterogeneity in the COH1 gene explains clinical variability in Cohen syndrome.
    Hennies HC; Rauch A; Seifert W; Schumi C; Moser E; Al-Taji E; Tariverdian G; Chrzanowska KH; Krajewska-Walasek M; Rajab A; Giugliani R; Neumann TE; Eckl KM; Karbasiyan M; Reis A; Horn D
    Am J Hum Genet; 2004 Jul; 75(1):138-45. PubMed ID: 15154116
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cohen Syndrome-Associated Cataract Is Explained by VPS13B Functions in Lens Homeostasis and Is Modified by Additional Genetic Factors.
    Lhussiez V; Dubus E; Cesar Q; Acar N; Nandrot EF; Simonutti M; Audo I; Lizé E; Nguyen S; Geissler A; Bouchot A; Ansar M; Picaud S; Thauvin-Robinet C; Olivier-Faivre L; Duplomb L; Da Costa R
    Invest Ophthalmol Vis Sci; 2020 Sep; 61(11):18. PubMed ID: 32915983
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.