BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

179 related articles for article (PubMed ID: 33367184)

  • 1. Goldenhar syndrome: the importance of an ophthalmological approach.
    Malta PG; Vilani DSRA; de Miranda CF; Fouad IL; Castro CC; Borgatti MÉ
    Rom J Ophthalmol; 2020; 64(4):444-448. PubMed ID: 33367184
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Severe bilateral ocular features in Goldenhar's syndrome.
    Mc Alister JC; Olver JM; Hatter T
    J Pediatr Ophthalmol Strabismus; 2001; 38(1):44-6. PubMed ID: 11201919
    [No Abstract]   [Full Text] [Related]  

  • 3. Distinguishing Goldenhar Syndrome from Craniofacial Microsomia.
    Tuin J; Tahiri Y; Paliga JT; Taylor JA; Bartlett SP
    J Craniofac Surg; 2015 Sep; 26(6):1887-92. PubMed ID: 26267577
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Goldenhar syndrome with limbal neoformation, microtia and skeletal deformities: a case report and literature review.
    Fu Y; Yu H; Zhang J; Zhou N
    BMC Ophthalmol; 2024 Feb; 24(1):81. PubMed ID: 38388885
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Goldenhar syndrome with unusual features.
    Mehta B; Nayak C; Savant S; Amladi S
    Indian J Dermatol Venereol Leprol; 2008; 74(3):254-6. PubMed ID: 18583796
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Three-generation family with resemblance to Townes-Brocks syndrome and Goldenhar/oculoauriculovertebral spectrum.
    Johnson JP; Poskanzer LS; Sherman S
    Am J Med Genet; 1996 Jan; 61(2):134-9. PubMed ID: 8669439
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Goldenhar syndrome: surgical management protocol in a reference center.
    Guevara-Valmaña OI; Nahas-Combina L; Andrade-Delgado L; Apellaniz-Campo AG; Leyva-Sotelo LM; Gaspar-Daniel Á
    Cir Cir; 2019; 87(5):516-527. PubMed ID: 31448792
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A case of Goldenhar-Gorlin syndrome with unusual association of hypoplastic thumb.
    Das A; Ray B; Das D; Das S
    Indian J Ophthalmol; 2008; 56(2):150-2. PubMed ID: 18292629
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Goldenhar syndrome (oculoauriculovertebral dysplasia): report of one case.
    Ng YY; Hu JM; Su PH; Chen JY; Yang MS; Chen SJ
    Acta Paediatr Taiwan; 2006; 47(3):142-5. PubMed ID: 17078468
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Goldenhar syndrome with blepharophimosis and limb deformities: a case report.
    Ding X; Wang X; Cao Y; Zhang J; Lin M; Fan X; Li J
    BMC Ophthalmol; 2018 Aug; 18(1):206. PubMed ID: 30134872
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Anterior segment dysgenesis and secondary glaucoma in Goldenhar syndrome.
    Dhingra D; Joshi G; Kaushik S; Pandav SS
    Indian J Ophthalmol; 2019 Oct; 67(10):1751-1753. PubMed ID: 31546553
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Late Recognition of a Case of Oculo-Auriculo-Vertebral Spectrum.
    El Mansoury J; Mbekeani JN
    Optom Vis Sci; 2016 Nov; 93(11):1449-1453. PubMed ID: 27755235
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Posterior fossa dermoid cyst in a patient with Goldenhar syndrome.
    Dange N; Bonde V; Goel A; Muzumdar D
    Pediatr Neurosurg; 2007; 43(6):522-5. PubMed ID: 17992045
    [TBL] [Abstract][Full Text] [Related]  

  • 14. An unusual association of Goldenhar syndrome.
    Seymenoğlu G; Başer E; Tansuğ N; Demireli P
    Int Ophthalmol; 2013 Feb; 33(1):91-4. PubMed ID: 23053767
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Trisomy 22 and facioauriculovertebral (Goldenhar) sequence.
    Kobrynski L; Chitayat D; Zahed L; McGregor D; Rochon L; Brownstein S; Vekemans M; Albert DL
    Am J Med Genet; 1993 Apr; 46(1):68-71. PubMed ID: 8494034
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Goldenhar Syndrome in a Young Girl.
    Kadakia N; Waghmare M; Gotmare S; Manoj R
    J Coll Physicians Surg Pak; 2019 Nov; 29(11):1108-1110. PubMed ID: 31659973
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Complex diagnosis of congenital cranial dysostosis in children].
    Iakubov RK; Azimov MI
    Stomatologiia (Mosk); 2002; 81(2):45-9. PubMed ID: 12056142
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Goldenhar syndrome and hemifacial microsomia: observations on three patients.
    Thomas P
    Eur J Pediatr; 1980 May; 133(3):287-92. PubMed ID: 7389743
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Oculo-auriculo-vertebral spectrum: clinical and molecular analysis of 51 patients.
    Beleza-Meireles A; Hart R; Clayton-Smith J; Oliveira R; Reis CF; Venâncio M; Ramos F; Sá J; Ramos L; Cunha E; Pires LM; Carreira IM; Scholey R; Wright R; Urquhart JE; Briggs TA; Kerr B; Kingston H; Metcalfe K; Donnai D; Newman WG; Saraiva JM; Tassabehji M
    Eur J Med Genet; 2015 Sep; 58(9):455-65. PubMed ID: 26206081
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Goldenhar Syndrome - ophthalmologist's perspective.
    Schmitzer S; Burcel M; Dăscălescu D; Popteanu IC
    Rom J Ophthalmol; 2018; 62(2):96-104. PubMed ID: 30206552
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.