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.
267 related articles for article (PubMed ID: 24636437)
1. Incontinentia pigmenti in an XY boy: case report and review of the literature. Mullan E; Barbarian M; Trakadis Y; Moroz B J Cutan Med Surg; 2014; 18(2):119-22. PubMed ID: 24636437 [TBL] [Abstract][Full Text] [Related]
2. Unusual Father-to-Daughter Transmission of Incontinentia Pigmenti Due to Mosaicism in IP Males. Fusco F; Conte MI; Diociaiuti A; Bigoni S; Branda MF; Ferlini A; El Hachem M; Ursini MV Pediatrics; 2017 Sep; 140(3):. PubMed ID: 28794079 [TBL] [Abstract][Full Text] [Related]
3. Incontinentia pigmenti inherited from a father with a low level atypical IKBKG deletion mosaicism: a case report. Kawai M; Sugimoto A; Ishihara Y; Kato T; Kurahashi H BMC Pediatr; 2022 Jun; 22(1):378. PubMed ID: 35768795 [TBL] [Abstract][Full Text] [Related]
4. Incontinentia pigmenti in a male (XY) infant with long-term follow up over 8 years. Matsuzaki Y; Rokunohe A; Minakawa S; Nomura K; Nakano H; Ito E; Sawamura D J Dermatol; 2018 Jan; 45(1):100-103. PubMed ID: 28791733 [TBL] [Abstract][Full Text] [Related]
5. Molecular analysis of low-level mosaicism of the IKBKG mutation using the X Chromosome Inactivation pattern in Incontinentia Pigmenti. Kawai M; Kato T; Tsutsumi M; Shinkai Y; Inagaki H; Kurahashi H Mol Genet Genomic Med; 2020 Dec; 8(12):e1531. PubMed ID: 33085210 [TBL] [Abstract][Full Text] [Related]
6. A Novel Frameshift Mutation of the IKBKG Gene Causing Typical Incontinentia Pigmenti. Minić S; Trpinac D; Obradović M Srp Arh Celok Lek; 2015; 143(11-12):752-4. PubMed ID: 26946775 [TBL] [Abstract][Full Text] [Related]
7. First IKBKG gene mutation study in Serbian incontinentia pigmenti patients. Minić S; Trpinac D; Gabriel H; Gencik M; Obradović M Srp Arh Celok Lek; 2013; 141(7-8):490-4. PubMed ID: 24073555 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Lack of interaction between NEMO and SHARPIN impairs linear ubiquitination and NF-κB activation and leads to incontinentia pigmenti. Bal E; Laplantine E; Hamel Y; Dubosclard V; Boisson B; Pescatore A; Picard C; Hadj-Rabia S; Royer G; Steffann J; Bonnefont JP; Ursini VM; Vabres P; Munnich A; Casanova JL; Bodemer C; Weil R; Agou F; Smahi A J Allergy Clin Immunol; 2017 Dec; 140(6):1671-1682.e2. PubMed ID: 28249776 [TBL] [Abstract][Full Text] [Related]
10. Analysis of IKBKG/NEMO gene in five Japanese cases of incontinentia pigmenti with retinopathy: fine genomic assay of a rare male case with mosaicism. Haque MN; Ohtsubo M; Nishina S; Nakao S; Yoshida K; Hosono K; Kurata K; Ohishi K; Fukami M; Sato M; Hotta Y; Azuma N; Minoshima S J Hum Genet; 2021 Feb; 66(2):205-214. PubMed ID: 32908217 [TBL] [Abstract][Full Text] [Related]
11. [NEMO Delta 4-10 deletion of NEMO gene in Chinese incontinentia pigmenti cases]. Li L; Song GW; DU JB; Liu JR; Xu FS; Liu XY; Zhang T Zhonghua Er Ke Za Zhi; 2005 Feb; 43(2):89-92. PubMed ID: 15833158 [TBL] [Abstract][Full Text] [Related]
12. Survival of male patients with incontinentia pigmenti carrying a lethal mutation can be explained by somatic mosaicism or Klinefelter syndrome. Kenwrick S; Woffendin H; Jakins T; Shuttleworth SG; Mayer E; Greenhalgh L; Whittaker J; Rugolotto S; Bardaro T; Esposito T; D'Urso M; Soli F; Turco A; Smahi A; Hamel-Teillac D; Lyonnet S; Bonnefont JP; Munnich A; Aradhya S; Kashork CD; Shaffer LG; Nelson DL; Levy M; Lewis RA; Am J Hum Genet; 2001 Dec; 69(6):1210-7. PubMed ID: 11673821 [TBL] [Abstract][Full Text] [Related]
14. The common NF-κB essential modulator (NEMO) gene rearrangement in Korean patients with incontinentia pigmenti. Song MJ; Chae JH; Park EA; Ki CS J Korean Med Sci; 2010 Oct; 25(10):1513-7. PubMed ID: 20890435 [TBL] [Abstract][Full Text] [Related]
15. Somatic mosaicism of a novel IKBKG mutation in a male patient with incontinentia pigmenti. Hull S; Arno G; Thomson P; Mutch S; Webster AR; Rai H; Hill V; Moore AT Am J Med Genet A; 2015 Jul; 167(7):1601-4. PubMed ID: 25944529 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome. Ghedira N; Lagarde A; Ben Ameur K; Elouej S; Sakka R; Kerkeni E; Chioukh FZ; Olschwang S; Desvignes JP; Abdelhak S; Delague V; Lévy N; Monastiri K; De Sandre-Giovannoli A BMC Pediatr; 2018 Aug; 18(1):286. PubMed ID: 30157809 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. Genomic architecture at the Incontinentia Pigmenti locus favours de novo pathological alleles through different mechanisms. Fusco F; Paciolla M; Napolitano F; Pescatore A; D'Addario I; Bal E; Lioi MB; Smahi A; Miano MG; Ursini MV Hum Mol Genet; 2012 Mar; 21(6):1260-71. PubMed ID: 22121116 [TBL] [Abstract][Full Text] [Related]
20. Improved molecular diagnosis of the common recurrent intragenic deletion mutation in IKBKG in a Filipino family with incontinentia pigmenti. Guevara BE; Hsu CK; Liu L; Feast A; Alabado KL; Lacuesta MP; Lee JY; McGrath JA Australas J Dermatol; 2016 May; 57(2):150-3. PubMed ID: 26437686 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]