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 *

169 related articles for article (PubMed ID: 31099403)

  • 21. Cochlear implantation in keratitis-ichthyosis-deafness syndrome: 10-year follow-up of two patients.
    Smyth CM; Sinnathuray AR; Hughes AE; Toner JG
    Cochlear Implants Int; 2012 Feb; 13(1):54-9. PubMed ID: 22340753
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Severe form of keratitis-ichthyosis-deafness (KID) syndrome associated with septic complications.
    Haruna K; Suga Y; Oizumi A; Mizuno Y; Endo H; Shimizu T; Hasegawa T; Ikeda S
    J Dermatol; 2010 Jul; 37(7):680-2. PubMed ID: 20629838
    [No Abstract]   [Full Text] [Related]  

  • 23. [Keratitis-ichthyosis-deafness (KID) syndrome].
    Mazereeuw-Hautier J
    Ann Dermatol Venereol; 2008 Jan; 135(1):80-2; quiz 79, 83. PubMed ID: 18342082
    [No Abstract]   [Full Text] [Related]  

  • 24. Novel mutations in GJB2 encoding connexin-26 in Japanese patients with keratitis-ichthyosis-deafness syndrome.
    Yotsumoto S; Hashiguchi T; Chen X; Ohtake N; Tomitaka A; Akamatsu H; Matsunaga K; Shiraishi S; Miura H; Adachi J; Kanzaki T
    Br J Dermatol; 2003 Apr; 148(4):649-53. PubMed ID: 12752120
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The pattern of inheritance in KID syndrome.
    Restano L; Cambiaghi S; Tadini G
    Pediatr Dermatol; 1999; 16(2):164-5. PubMed ID: 10337688
    [No Abstract]   [Full Text] [Related]  

  • 26. Connexin 26 (GJB2) mutation in an Argentinean patient with keratitis-ichthyosis-deafness (KID) syndrome: a case report.
    Dalamón VK; Buonfiglio P; Larralde M; Craig P; Lotersztein V; Choate K; Pallares N; Diamante V; Elgoyhen AB
    BMC Med Genet; 2016 May; 17(1):37. PubMed ID: 27141831
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A novel connexin 26 mutation in a patient diagnosed with keratitis-ichthyosis-deafness syndrome.
    van Steensel MA; van Geel M; Nahuys M; Smitt JH; Steijlen PM
    J Invest Dermatol; 2002 Apr; 118(4):724-7. PubMed ID: 11918723
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genetic heterogeneity of KID syndrome: identification of a Cx30 gene (GJB6) mutation in a patient with KID syndrome and congenital atrichia.
    Jan AY; Amin S; Ratajczak P; Richard G; Sybert VP
    J Invest Dermatol; 2004 May; 122(5):1108-13. PubMed ID: 15140211
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Connexin 26 (GJB2) mutations in keratitis-ichthyosis-deafness syndrome presenting with squamous cell carcinoma.
    Sakabe J; Yoshiki R; Sugita K; Haruyama S; Sawada Y; Kabashima R; Bito T; Nakamura M; Tokura Y
    J Dermatol; 2012 Sep; 39(9):814-5. PubMed ID: 22098592
    [No Abstract]   [Full Text] [Related]  

  • 30. Keratitis-ichthyosis-deafness syndrome-associated Cx26 mutants produce nonfunctional gap junctions but hyperactive hemichannels when co-expressed with wild type Cx43.
    García IE; Maripillán J; Jara O; Ceriani R; Palacios-Muñoz A; Ramachandran J; Olivero P; Perez-Acle T; González C; Sáez JC; Contreras JE; Martínez AD
    J Invest Dermatol; 2015 May; 135(5):1338-1347. PubMed ID: 25625422
    [TBL] [Abstract][Full Text] [Related]  

  • 31. HID and KID syndromes are associated with the same connexin 26 mutation.
    van Geel M; van Steensel MA; Küster W; Hennies HC; Happle R; Steijlen PM; König A
    Br J Dermatol; 2002 Jun; 146(6):938-42. PubMed ID: 12072059
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The human Cx26-D50A and Cx26-A88V mutations causing keratitis-ichthyosis-deafness syndrome display increased hemichannel activity.
    Mhaske PV; Levit NA; Li L; Wang HZ; Lee JR; Shuja Z; Brink PR; White TW
    Am J Physiol Cell Physiol; 2013 Jun; 304(12):C1150-8. PubMed ID: 23447037
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Possible modifier effects of keratin 17 gene mutation on keratitis-ichthyosis-deafness syndrome.
    Natsuga K; Shinkuma S; Kanda M; Suzuki Y; Chosa N; Narita Y; Setoyama M; Nishie W; Akiyama M; Shimizu H
    Br J Dermatol; 2012 Apr; 166(4):903-5. PubMed ID: 21999526
    [No Abstract]   [Full Text] [Related]  

  • 34. KID Syndrome: report of a Scandinavian patient with connexin-26 gene mutation.
    Bygum A; Betz RC; Kragballe K; Steiniche T; Peeters N; Wuyts W; Nöthen MM
    Acta Derm Venereol; 2005; 85(2):152-5. PubMed ID: 15823911
    [TBL] [Abstract][Full Text] [Related]  

  • 35. GJB2 mutations in keratitis-ichthyosis-deafness syndrome including its fatal form.
    Janecke AR; Hennies HC; Günther B; Gansl G; Smolle J; Messmer EM; Utermann G; Rittinger O
    Am J Med Genet A; 2005 Mar; 133A(2):128-31. PubMed ID: 15633193
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Auditory manifestations of Keratitis-Ichthyosis-Deafness (KID) syndrome.
    Szymko-Bennett YM; Russell LJ; Bale SJ; Griffith AJ
    Laryngoscope; 2002 Feb; 112(2):272-80. PubMed ID: 11889383
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Dandy-Walker malformation in patients with KID syndrome associated with a heterozygote mutation (p.Asp50Asn) in the GJB2 gene encoding connexin 26.
    Todt I; Mazereeuw-Hautier J; Binder B; Willems PJ
    Clin Genet; 2009 Oct; 76(4):404-8. PubMed ID: 19793313
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Missense mutations in GJB2 encoding connexin-26 cause the ectodermal dysplasia keratitis-ichthyosis-deafness syndrome.
    Richard G; Rouan F; Willoughby CE; Brown N; Chung P; Ryynänen M; Jabs EW; Bale SJ; DiGiovanna JJ; Uitto J; Russell L
    Am J Hum Genet; 2002 May; 70(5):1341-8. PubMed ID: 11912510
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Drowning out communication. Focus on "The human Cx26-D50A and Cx26-A88V mutations causing keratitis-ichthyosis-deafness syndrome display increased hemichannel activity".
    Koval M
    Am J Physiol Cell Physiol; 2013 Jun; 304(12):C1129-30. PubMed ID: 23576574
    [No Abstract]   [Full Text] [Related]  

  • 40. Diffuse hyperkeratosis in a deaf and blind 48-year-old woman--quiz case. Diagnosis: keratitis-ichthyosis-deafness (KID) syndrome with secondary dermatophytosis.
    Machan M; Kestenbaum T; Fraga GR
    Arch Dermatol; 2012 Oct; 148(10):1199-200. PubMed ID: 23069961
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.