BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

126 related articles for article (PubMed ID: 38700761)

  • 1. [Ectopia lentis].
    Britz L; Auffarth GU; Khoramnia R
    Ophthalmologie; 2024 May; ():. PubMed ID: 38700761
    [No Abstract]   [Full Text] [Related]  

  • 2. Hereditary ectopia lentis. A series of 10 cases of ectopia lentis et pupillae.
    Meire FM
    Bull Soc Belge Ophtalmol; 1991; 241():25-36. PubMed ID: 1840993
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Classifying Ectopia Lentis in Marfan Syndrome into Five Grades of Increasing Severity.
    Zech JC; Putoux A; Decullier E; Fargeton AE; Edery P; Plauchu H; Dupuis-Girod S
    J Clin Med; 2020 Mar; 9(3):. PubMed ID: 32155956
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Craniosynostosis with ectopia lentis and a homozygous 20-base deletion in ADAMTSL4.
    Chandra A; Aragon-Martin JA; Sharif S; Parulekar M; Child A; Arno G
    Ophthalmic Genet; 2013; 34(1-2):78-82. PubMed ID: 22871183
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The eye as a window to a rare disease: ectopia lentis and homocystinuria, a Pakistani perspective.
    Shafique M; Muzaffar W; Ishaq M
    Int Ophthalmol; 2016 Feb; 36(1):79-83. PubMed ID: 25982157
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Early onset ectopia lentis due to a FBN1 mutation with non-penetrance.
    Zhang L; Lai YH; Capasso JE; Han S; Levin AV
    Am J Med Genet A; 2015 Jun; 167(6):1365-8. PubMed ID: 25900864
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The Role of Genetic Testing in Children Requiring Surgery for Ectopia Lentis.
    Musleh M; Bull A; Linton E; Liu J; Waller S; Hardcastle C; Clayton-Smith J; Sharma V; Black GC; Biswas S; Ashworth JL; Sergouniotis PI
    Genes (Basel); 2023 Mar; 14(4):. PubMed ID: 37107549
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel ADAMTSL4 compound heterozygous mutation in isolated ectopia lentis: a case report and review of the literature.
    Wei H; Meng X; Qin H; Li X
    J Med Case Rep; 2023 Dec; 17(1):532. PubMed ID: 38146062
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The phenotypic spectrum of
    Knight LSW; Mullany S; Taranath DA; Ruddle JB; Barnett CP; Sallevelt SCEH; Berry EC; Marshall HN; Hollitt GL; Souzeau E; Craig JE; Siggs OM
    Mol Vis; 2022; 28():257-268. PubMed ID: 36284667
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel p.G1344E mutation in
    Yang Y; Zhou YL; Yao TT; Pan H; Gu P; Wang ZY
    Br J Ophthalmol; 2021 Mar; 105(3):341-347. PubMed ID: 32404357
    [TBL] [Abstract][Full Text] [Related]  

  • 11. How far is observation allowed in patients with ectopia lentis?
    Matsuo T
    Springerplus; 2015; 4():461. PubMed ID: 26339562
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Corneal biomechanical properties and intraocular pressure measurement in Marfan patients.
    Kara N; Bozkurt E; Baz O; Altinkaynak H; Dundar H; Yuksel K; Yazici AT; Demirok A; Candan S
    J Cataract Refract Surg; 2012 Feb; 38(2):309-14. PubMed ID: 22153358
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A recurrent FBN1 mutation in an autosomal dominant ectopia lentis family of Indian origin.
    Vanita V; Singh JR; Singh D; Varon R; Robinson PN; Sperling K
    Mol Vis; 2007 Oct; 13():2035-40. PubMed ID: 18079676
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Evaluation of surgical intervention in familial isolated simple ectopia lentis: younger v. older generations.
    Galvin JA; Baker JD; Bawle EV
    Binocul Vis Strabismus Q; 2002; 17(3):229-34. PubMed ID: 12171597
    [TBL] [Abstract][Full Text] [Related]  

  • 15. ADAMTSL4-related ectopia lentis: A case of pseudodominance with an asymptomatic parent.
    Scanga HL; Nischal KK
    Am J Med Genet A; 2022 Jun; 188(6):1853-1857. PubMed ID: 35218299
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Hereditary ectopia lentis].
    Neuhann TM
    Klin Monbl Augenheilkd; 2015 Mar; 232(3):259-65. PubMed ID: 25654236
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetics of ectopia lentis.
    Sadiq MA; Vanderveen D
    Semin Ophthalmol; 2013; 28(5-6):313-20. PubMed ID: 24138040
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Ectopia lentis in Loeys-Dietz syndrome type 4.
    Braverman AC; Blinder KJ; Khanna S; Willing M
    Am J Med Genet A; 2020 Aug; 182(8):1957-1959. PubMed ID: 32462795
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A homozygous mutation in ADAMTSL4 causes autosomal-recessive isolated ectopia lentis.
    Ahram D; Sato TS; Kohilan A; Tayeh M; Chen S; Leal S; Al-Salem M; El-Shanti H
    Am J Hum Genet; 2009 Feb; 84(2):274-8. PubMed ID: 19200529
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Incidence and de novo mutation rate of Marfan syndrome and risk of ectopia lentis.
    Cui RZ; Hodge DO; Mohney BG
    J AAPOS; 2023 Oct; 27(5):273.e1-273.e4. PubMed ID: 37716433
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.