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 *

171 related articles for article (PubMed ID: 27200154)

  • 1. Goldenhar syndrome with contralateral pulmonary aplasia: a rare association.
    Jugpal TS; Kumar J; Gupta S; Garg A
    J Radiol Case Rep; 2016 Jan; 10(1):35-40. PubMed ID: 27200154
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. An interesting case presentation: pulmonary malformations associated with oculoauriculovertebral dysplasia (Goldenhar anomalad).
    Downing GJ; Kilbride H
    J Perinatol; 1991 Jun; 11(2):190-2. PubMed ID: 1890482
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [A case report of Goldenhar's syndrome accompanied with aplasia of the right lung].
    Ikezoe J; Morimoto S; Sone S; Higashihara T; Arisawa J; Hamada S; Kuriyama K
    Rinsho Hoshasen; 1984 Aug; 29(8):897-900. PubMed ID: 6513064
    [No Abstract]   [Full Text] [Related]  

  • 5. Hemifacial microsomia: skeletal abnormalities evaluation using CBCT (case report).
    Kabak SL; Savrasova NA; Zatochnaya VV; Melnichenko YM
    J Radiol Case Rep; 2019 Nov; 13(11):1-9. PubMed ID: 32190180
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Goldenhar syndrome associated with contralateral agenesis of the internal carotid artery.
    Ventura E; Ormitti F; Crisi G; Sesenna E
    Neuroradiol J; 2014 Apr; 27(2):150-3. PubMed ID: 24750700
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A rare case of Goldenhar syndrome with radial aplasia.
    Biswas S; Adhikari A; Meyur R; Kundu P
    Folia Morphol (Warsz); 2013 Nov; 72(4):362-5. PubMed ID: 24402760
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Mixed hearing loss in the case of Goldenhar-Gorlin syndrome].
    Obrebowski A; Kraśny J; Wojnowski W; Kurywczak-Grykiel K
    Otolaryngol Pol; 1999; 53(5):639-41. PubMed ID: 10689927
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Treatment of otological features of the oculoauriculovertebral dysplasia (Goldenhar syndrome).
    Skarzyński H; Porowski M; Podskarbi-Fayette R
    Int J Pediatr Otorhinolaryngol; 2009 Jul; 73(7):915-21. PubMed ID: 19203801
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Infectious keratitis in a newborn with goldenhar syndrome.
    Mittal S; Mittal A; Meenakshi R; Bharathi JM; Rengappa R
    J Pediatr Ophthalmol Strabismus; 2010; 47(1):43-5. PubMed ID: 20128554
    [TBL] [Abstract][Full Text] [Related]  

  • 11. AIRWAY MANAGEMENT WITH DIRECT LARYNGOSCOPY IN A CHILD WITH GOLDENHAR SYNDROME.
    Vitković B; Milić M
    Acta Clin Croat; 2016 Mar; 55 Suppl 1():90-3. PubMed ID: 27276779
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Craniofacial and dental characteristics of Goldenhar syndrome: a report of two cases.
    Tuna EB; Orino D; Ogawa K; Yildirim M; Seymen F; Gencay K; Maeda T
    J Oral Sci; 2011 Mar; 53(1):121-4. PubMed ID: 21467824
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Goldenhar-associated conditions (hemifacial microsomia) and congenital deformities of the spine.
    Tsirikos AI; McMaster MJ
    Spine (Phila Pa 1976); 2006 Jun; 31(13):E400-7. PubMed ID: 16741440
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Thrombophilia gene mutations in oculoauriculovertebral spectrum.
    Tug E; Atasoy HI; Koybasi Sanal S
    Genet Couns; 2012; 23(1):65-72. PubMed ID: 22611644
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Anaesthetic Management in a Child with Goldenhar Syndrome.
    Khan WA; Salim B; Khan AA; Chughtai S
    J Coll Physicians Surg Pak; 2017 Mar; 27(3):S6-S7. PubMed ID: 28302228
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Report of an atypical case of Goldenhar syndrome].
    Fiore C; Santoni G; Lungarotti S; Signorini E
    Ophthalmologica; 1983; 186(3):162-8. PubMed ID: 6843966
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal diagnosis of hemifacial microsomia and ipsilateral cerebellar hypoplasia in a fetus with oculoauriculovertebral spectrum.
    Martinelli P; Maruotti GM; Agangi A; Mazzarelli LL; Bifulco G; Paladini D
    Ultrasound Obstet Gynecol; 2004 Aug; 24(2):199-201. PubMed ID: 15287060
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hemifacial Microsomia : Clinicoradiological Insight and Report of a Case.
    Chhabra N; Chhabra A
    Ethiop J Health Sci; 2017 Jan; 27(1):91-94. PubMed ID: 28458495
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Unusual presentation of hemifacial microsomia.
    Handler MZ; Alabi O; Miller J
    J Plast Reconstr Aesthet Surg; 2011 Dec; 64(12):e306-8. PubMed ID: 21624853
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Congenital absence of the portal vein in oculoauriculovertebral dysplasia (Goldenhar syndrome).
    Morse SS; Taylor KJ; Strauss EB; Ramirez E; Seashore JH
    Pediatr Radiol; 1986; 16(5):437-9. PubMed ID: 3529022
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.