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 *

79 related articles for article (PubMed ID: 11528739)

  • 1. [Nephritis-deafness(sensorineural), hereditary type].
    Sakazume S
    Ryoikibetsu Shokogun Shirizu; 2001; (34 Pt 2):279-80. PubMed ID: 11528739
    [No Abstract]   [Full Text] [Related]  

  • 2. [Congenital and hereditary hearing disorders in population of the Nakhichevan Autonomous Republic].
    Panakhiian VM
    Vestn Otorinolaringol; 2004; (6):22-4. PubMed ID: 15699983
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Phenotypic characterization of hereditary hearing impairment linked to DFNA25.
    Thirlwall AS; Brown DJ; McMillan PM; Barker SE; Lesperance MM
    Arch Otolaryngol Head Neck Surg; 2003 Aug; 129(8):830-5. PubMed ID: 12925340
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hereditary chronic nephritis.
    Bĕlobrádková J; Peychl L
    Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove; 1970; 13(2):177-84. PubMed ID: 5275071
    [No Abstract]   [Full Text] [Related]  

  • 5. Congenital hereditary endothelial dystrophy with progressive sensorineural deafness (Harboyan syndrome).
    Desir J; Abramowicz M
    Orphanet J Rare Dis; 2008 Oct; 3():28. PubMed ID: 18922146
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Medico-genetic consultation in monosymptomatic sensorineural deafness].
    Bliumina MG
    Vestn Otorinolaringol; 1985; (1):65-8. PubMed ID: 3969776
    [No Abstract]   [Full Text] [Related]  

  • 7. [Sensorineural deafness in the May Hegglin anomaly].
    Montaguti M; Gugliotta L
    Acta Otorhinolaryngol Ital; 1983; 3(1):71-6. PubMed ID: 6880705
    [No Abstract]   [Full Text] [Related]  

  • 8. Hereditary gingival fibromatosis and sensorineural hearing loss in a 42-year-old man with Jones syndrome.
    Kasaboğlu O; Tümer C; Balci S
    Genet Couns; 2004; 15(2):213-8. PubMed ID: 15287422
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Niikawa-Kuroki (Kabuki) syndrome with congenital sensorineural deafness: evidence for a wide spectrum of inner ear abnormalities.
    Tekin M; Fitoz S; Arici S; Cetinkaya E; Incesulu A
    Int J Pediatr Otorhinolaryngol; 2006 May; 70(5):885-9. PubMed ID: 16325926
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Classification of hereditary sensorineural deafness].
    Bliumina MG
    Vestn Otorinolaringol; 1986; (1):25-8. PubMed ID: 3952927
    [No Abstract]   [Full Text] [Related]  

  • 11. DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21-12.1.
    Delmaghani S; Aghaie A; Compain-Nouaille S; Ataie A; Lemainque A; Zeinali S; Lathrop M; Weil D; Petit C
    Eur J Hum Genet; 2003 Oct; 11(10):816-8. PubMed ID: 14512974
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Evaluation of ESPN, MYO3A, SLC26A5 and USH1C as candidates for hereditary non-syndromic deafness (congenital sensorineural deafness) in Dalmatian dogs.
    Mieskes K; Distl O
    Anim Genet; 2007 Oct; 38(5):533-4. PubMed ID: 17614983
    [No Abstract]   [Full Text] [Related]  

  • 13. Letter: Sensorineural deafness in hereditary nephritis.
    N Engl J Med; 1975 Aug; 293(8):404-5. PubMed ID: 1097924
    [No Abstract]   [Full Text] [Related]  

  • 14. OPA1 R445H mutation in optic atrophy associated with sensorineural deafness.
    Amati-Bonneau P; Guichet A; Olichon A; Chevrollier A; Viala F; Miot S; Ayuso C; Odent S; Arrouet C; Verny C; Calmels MN; Simard G; Belenguer P; Wang J; Puel JL; Hamel C; Malthièry Y; Bonneau D; Lenaers G; Reynier P
    Ann Neurol; 2005 Dec; 58(6):958-63. PubMed ID: 16240368
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Chronic hereditary nephropathy with hypoacusia and ocular defects (study of a family)].
    Zavala C; Villar-Puig P; Garza R; Lisker R; Díes F
    Rev Invest Clin; 1969; 21(3):369-82. PubMed ID: 5317588
    [No Abstract]   [Full Text] [Related]  

  • 16. Familial hematuric nephritis.
    Rome L; Cuppage FE; Vertes V
    Pediatrics; 1966 Nov; 38(5):808-18. PubMed ID: 4959307
    [No Abstract]   [Full Text] [Related]  

  • 17. Etiological diagnosis of bilateral, sensorineural hearing impairment in a pediatric Greek population.
    Riga M; Psarommatis I; Lyra Ch; Douniadakis D; Tsakanikos M; Neou P; Apostolopoulos N
    Int J Pediatr Otorhinolaryngol; 2005 Apr; 69(4):449-55. PubMed ID: 15763280
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Clinical aspects of hereditary nephritis].
    Ignatova MS; Fokeeva VV; Degtiareva EM
    Sov Med; 1975 Jul; (7):31-6. PubMed ID: 1216047
    [No Abstract]   [Full Text] [Related]  

  • 19. [Chronic hereditary nephritis].
    Bĕlobrádková J; Peychl L
    Cesk Pediatr; 1972 Apr; 27(4):179-80. PubMed ID: 5023106
    [No Abstract]   [Full Text] [Related]  

  • 20. [Hereditary nephritis. A study in two Canadian families of Indian origin].
    Kalbe U; Gilchrist I; Delva PL
    Klin Padiatr; 1972 Jul; 184(4):322-7. PubMed ID: 4628129
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.