BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

236 related articles for article (PubMed ID: 17223894)

  • 1. Incontinentia pigmenti in a newborn with a novel nonsense mutation in the NEMO gene.
    Has C; Danescu S; Volz A; Nöh F; Technau K; Bruckner-Tuderman L
    Br J Dermatol; 2007 Feb; 156(2):392-3. PubMed ID: 17223894
    [No Abstract]   [Full Text] [Related]  

  • 2. Incontinentia pigmenti revisited. A novel nonsense mutation of the IKBKG gene.
    Fryssira H; Kakourou T; Valari M; Stefanaki K; Amenta S; Kanavakis E
    Acta Paediatr; 2011 Jan; 100(1):128-33. PubMed ID: 20586999
    [TBL] [Abstract][Full Text] [Related]  

  • 3. NEMO mutational analysis in a Japanese family with incontinentia pigmenti.
    Tada H; Yoshida S; Yamaji Y; Fujisawa K; Ishibashi T
    Eye (Lond); 2007 Jun; 21(6):888-90. PubMed ID: 17401323
    [No Abstract]   [Full Text] [Related]  

  • 4. De novo NEMO gene deletion (delta4-10)--a cause of incontinentia pigmenti in a female infant: a case report.
    Culić V; Gabrić D; Puizina-Ivić N; Rozman K; Peterlin B; Pavelić J
    Coll Antropol; 2008 Dec; 32(4):1259-62. PubMed ID: 19149237
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [An incontinentia pigmenti family with deletion in both NEMO gene and pseudogene DeltaNEMO].
    Zhang G; Shi H; Du X; Shao M; Zhou Q
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):573-5. PubMed ID: 18841575
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A genetic cause for neonatal encephalopathy: incontinentia pigmenti with NEMO mutation.
    Loh NR; Jadresic LP; Whitelaw A
    Acta Paediatr; 2008 Mar; 97(3):379-81. PubMed ID: 18241293
    [TBL] [Abstract][Full Text] [Related]  

  • 7. De Novo incontinentia pigmenti in female twins.
    Su PH; Chen JY; Yu JS; Su CM; Huang TC; Chen SJ
    Acta Paediatr Taiwan; 2004; 45(3):178-80. PubMed ID: 15493740
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Skin lesion development in a mouse model of incontinentia pigmenti is triggered by NEMO deficiency in epidermal keratinocytes and requires TNF signaling.
    Nenci A; Huth M; Funteh A; Schmidt-Supprian M; Bloch W; Metzger D; Chambon P; Rajewsky K; Krieg T; Haase I; Pasparakis M
    Hum Mol Genet; 2006 Feb; 15(4):531-42. PubMed ID: 16399796
    [TBL] [Abstract][Full Text] [Related]  

  • 9. NEMO, NFkappaB signaling and incontinentia pigmenti.
    Nelson DL
    Curr Opin Genet Dev; 2006 Jun; 16(3):282-8. PubMed ID: 16647846
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Proposal for a protocol for the staging of incontinentia pigmenti in pediatric age].
    Portaleone D; Taroni F; Micheli S; Moioli M; Pedrazzini A; Cognizzoli P; Carnelli V
    Minerva Pediatr; 2007 Jun; 59(3):255-65. PubMed ID: 17519871
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Incontinentia pigmenti: three new cases that demonstrate it is not only a matter of women].
    Feito-Rodríguez M; García-Macarrón J; Bravo-Burguillos ER; Vera-Casaño A; de Lucas-Laguna R
    Actas Dermosifiliogr; 2007 Mar; 98(2):112-5. PubMed ID: 17397599
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A rare cause of neonatal seizure: incontinentia pigmenti.
    Türkmen M; Eliaçik K; Temoçin K; Savk E; Tosun A; Dikicioğlu E
    Turk J Pediatr; 2007; 49(3):327-30. PubMed ID: 17990592
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical diagnosis of incontinentia pigmenti in a cohort of male patients.
    Fusco F; Fimiani G; Tadini G; Michele D; Ursini MV
    J Am Acad Dermatol; 2007 Feb; 56(2):264-7. PubMed ID: 17224368
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Case no. 8. Bullous dermatosis].
    Fraitag S
    Ann Pathol; 2013 Jun; 33(3):211-5. PubMed ID: 23790664
    [No Abstract]   [Full Text] [Related]  

  • 15. Incontinentia pigmenti in a newborn with NEMO mutation.
    Lee Y; Kim S; Kim K; Chang M
    J Korean Med Sci; 2011 Feb; 26(2):308-11. PubMed ID: 21286028
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Abnormal white matter in a neurologically intact child with incontinentia pigmenti.
    Bryant SA; Rutledge SL
    Pediatr Neurol; 2007 Mar; 36(3):199-201. PubMed ID: 17352958
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Incontinetia pigmenti-related myopathy or unsolved "double trouble"?
    Huttner HB; Richter G; Jünemann A; Kress W; Weis J; Schröder JM; Gal A; Doerfler A; Udd B; Schröder R
    Neuromuscul Disord; 2010 Feb; 20(2):139-41. PubMed ID: 20064724
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Insight into IKBKG/NEMO locus: report of new mutations and complex genomic rearrangements leading to incontinentia pigmenti disease.
    Conte MI; Pescatore A; Paciolla M; Esposito E; Miano MG; Lioi MB; McAleer MA; Giardino G; Pignata C; Irvine AD; Scheuerle AE; Royer G; Hadj-Rabia S; Bodemer C; Bonnefont JP; Munnich A; Smahi A; Steffann J; Fusco F; Ursini MV
    Hum Mutat; 2014 Feb; 35(2):165-77. PubMed ID: 24339369
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Incontinentia pigmenti with retinal vascular anomaly and deletion of exons 4-10 in NEMO.
    Araki Y; Abe Y; Takeda Y; Nakano H; Sawamura D; Yamashita H; Suzuki T
    J Dermatol; 2017 Aug; 44(8):976-977. PubMed ID: 27666948
    [No Abstract]   [Full Text] [Related]  

  • 20. Incontinentia pigmenti with NEMO mutation in a Japanese family.
    Okita M; Nakanishi G; Fujimoto N; Kishida M; Tanaka T
    J Dermatol; 2012 Nov; 39(11):940-1. PubMed ID: 22300264
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 12.