BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

134 related articles for article (PubMed ID: 7327850)

  • 1. Hearing loss in Pfeiffer's syndrome.
    Cremers CW
    Int J Pediatr Otorhinolaryngol; 1981 Dec; 3(4):343-53. PubMed ID: 7327850
    [TBL] [Abstract][Full Text] [Related]  

  • 2. An autosomal dominant inherited syndrome with congenital stapes ankylosis.
    Teunissen B; Cremers WR
    Laryngoscope; 1990 Apr; 100(4):380-4. PubMed ID: 2319886
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Congenital conductive hearing loss in Apert syndrome.
    Phillips SG; Miyamoto RT
    Otolaryngol Head Neck Surg; 1986 Nov; 95(4):429-33. PubMed ID: 3106904
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hearing loss in the cervico-oculo-acoustic (Wildervanck) syndrome.
    Cremers CW; Hoogland GA; Kuypers W
    Arch Otolaryngol; 1984 Jan; 110(1):54-7. PubMed ID: 6689909
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The feet in Pfeiffer's syndrome.
    Anderson PJ; Hall CM; Evans RD; Jones BM; Hayward RD
    J Craniofac Surg; 1998 Jan; 9(1):83-7. PubMed ID: 9558574
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Proximal symphalangia and stapes ankylosis.
    Cremers C; Theunissen E; Kuijpers W
    Arch Otolaryngol; 1985 Nov; 111(11):765-7. PubMed ID: 4051868
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Surgery for congenital conductive deafness in Klippel-Feil syndrome.
    van Rijn PM; Cremers CW
    Ann Otol Rhinol Laryngol; 1988; 97(4 Pt 1):347-52. PubMed ID: 3408109
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Apert syndrome and hearing loss with ear anomalies: a case report and literature review.
    Huang F; Sweet R; Tewfik TL
    Int J Pediatr Otorhinolaryngol; 2004 Apr; 68(4):495-501. PubMed ID: 15013619
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Involvement of the incudostapedial joint anomaly in conductive deafness.
    Suzuki M; Kanebayashi H; Kawano A; Hagiwara A; Furuse H; Yamaguchi T; Shimizu M
    Acta Otolaryngol; 2008 May; 128(5):515-9. PubMed ID: 18421604
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Inner ear anomalies and conductive hearing loss in children with Apert syndrome: an overlooked otologic aspect.
    Zhou G; Schwartz LT; Gopen Q
    Otol Neurotol; 2009 Feb; 30(2):184-9. PubMed ID: 19169132
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Surgery for congenital stapes ankylosis with an associated congenital ossicular chain anomaly.
    Teunissen B; Cremers CW
    Int J Pediatr Otorhinolaryngol; 1991 May; 21(3):217-26. PubMed ID: 1869375
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Pfeiffer's syndrome family tree. Review of the literature.
    Lyon JR; Burgess RC
    Clin Orthop Relat Res; 1993 Sep; (294):294-8. PubMed ID: 8358932
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cervical spine in Pfeiffer's syndrome.
    Anderson PJ; Hall CM; Evans RD; Jones BM; Harkness W; Hayward RD
    J Craniofac Surg; 1996 Jul; 7(4):275-9. PubMed ID: 9133831
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Congenital stapes ankylosis associated with another ossicular chain anomaly: surgical results in 30 ears.
    Thomeer HG; Kunst HP; Cremers CW
    Arch Otolaryngol Head Neck Surg; 2011 Sep; 137(9):935-41. PubMed ID: 21930985
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hearing loss in the Saethre-Chotzen syndrome.
    Ensink RJ; Marres HA; Brunner HG; Cremers CW
    J Laryngol Otol; 1996 Oct; 110(10):952-7. PubMed ID: 8977861
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Unusual case of bilateral conductive deafness.
    Hoare TJ; Aldren CJ; Morgan DW; Bull TR
    J Laryngol Otol; 1990 Jul; 104(7):560-1. PubMed ID: 2384713
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Congenital stapes ankylosis: study of 28 cases and surgical results.
    Albert S; Roger G; Rouillon I; Chauvin P; Denoyelle F; Derbez R; Delattre J; Triglia JM; Garabedian EN
    Laryngoscope; 2006 Jul; 116(7):1153-7. PubMed ID: 16826051
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A case of congenital bilateral stapes agenesis.
    Keskin G; Ustündağ E; Almaç A
    Kulak Burun Bogaz Ihtis Derg; 2003 Dec; 11(6):175-8. PubMed ID: 15567932
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Pfeiffer syndrome associated with clover-leaf skull: 1st case described in Venezuela].
    Martínez-Basalo C; Alvarez-Nava F; González-Inciarte ME; González-Inciarte L; Delgado-Luengo W; Mora-La Cruz E; Peña J; Rodríguez B; Gómez-Polo G; Delgado-Luengo J
    Invest Clin; 1997 Jun; 38(2):95-106. PubMed ID: 9296644
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [A case of Pfeiffer syndrome with psychomotor delay. Part I - Physical and X-ray examination and psychomotor assessment. Part II - Notes about surgical treatment of Pfeiffer syndrome and other craniofacial stenosis types].
    Ronconi GF; Pesenti P; Cenzi R; Baciliero U; Zanardo V; Curioni C
    Pediatr Med Chir; 1982; 4(4):459-66. PubMed ID: 7170223
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.