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2. [Spontaneous abortion of male fetuses with incontinentia pigmenti (apropos of a family)]. Odent S; Le Marec B; Smahi A; Hors-Cayla C; Milon J; Jouan H; Laurent MC; Borg AM J Gynecol Obstet Biol Reprod (Paris); 1997; 26(6):633-6. PubMed ID: 9453982 [TBL] [Abstract][Full Text] [Related]
3. Gonadal mosaicism for incontinentia pigmenti in a healthy male. Kirchman TT; Levy ML; Lewis RA; Kanzler MH; Nelson DL; Scheuerle AE J Med Genet; 1995 Nov; 32(11):887-90. PubMed ID: 8592334 [TBL] [Abstract][Full Text] [Related]
4. [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]
5. Second trimester miscarriage of a male fetus with incontinentia pigmenti. Devriendt K; Matthijs G; Fryns JP; Ballegeer V Am J Med Genet; 1998 Nov; 80(3):298-9. PubMed ID: 9843060 [No Abstract] [Full Text] [Related]
6. The genetics of incontinentia pigmenti. Curth HO; Warburton D Arch Dermatol; 1965 Sep; 92(3):229-35. PubMed ID: 11851242 [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. Incontinentia pigmenti (Bloch-Sulzberger syndrome): seven case reports from one family. Spallone A Br J Ophthalmol; 1987 Aug; 71(8):629-34. PubMed ID: 3115288 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. High-dose glucocorticoid therapy in the management of seizures in neonatal incontinentia pigmenti: a case report. Wolf DS; Golden WC; Hoover-Fong J; Applegate C; Cohen BA; Germain-Lee EL; Goldberg MF; Crawford TO; Gauda EB J Child Neurol; 2015 Jan; 30(1):100-6. PubMed ID: 24682289 [TBL] [Abstract][Full Text] [Related]
11. De novo mutation in three families with multigenerational incontinentia pigmenti. Scheuerle A; Lewis RA; Levy ML; Nelson DL Am J Hum Genet; 1994 Dec; 55(6):1279-81. PubMed ID: 7977389 [No Abstract] [Full Text] [Related]
12. Linkage analysis in 16 families with incontinentia pigmenti. Jouet M; Stewart H; Landy S; Yates J; Yong SL; Harris A; Garret C; Hatchwell E; Read A; Donnai D; Kenwrick S Eur J Hum Genet; 1997; 5(3):168-70. PubMed ID: 9272741 [TBL] [Abstract][Full Text] [Related]
13. Interaction of incontinentia pigmenti and factor VIII mutations in a female with biased X inactivation, resulting in haemophilia. Coleman R; Genet SA; Harper JI; Wilkie AO J Med Genet; 1993 Jun; 30(6):497-500. PubMed ID: 8326493 [TBL] [Abstract][Full Text] [Related]
14. A novel IKBKG mutation in a patient with incontinentia pigmenti and features of hepatic ciliopathy. Danescu S; Has C; Baican C; Müller T; Baican A Australas J Dermatol; 2018 Nov; 59(4):e262-e265. PubMed ID: 29520766 [TBL] [Abstract][Full Text] [Related]
15. Vaccination as a probable cause of incontinentia pigmenti reactivation. Alikhan A; Lee AD; Swing D; Carroll C; Yosipovitch G Pediatr Dermatol; 2010; 27(1):62-4. PubMed ID: 20199413 [TBL] [Abstract][Full Text] [Related]
16. [Incontinentia pigmenti. Observations and research in 2 cases]. Bartoli D; Balagi C; Gramegna M; Occhi M; Racugno A; Oldani R; Cottafava F Minerva Pediatr; 1987 Apr; 39(8):329-35. PubMed ID: 3614161 [No Abstract] [Full Text] [Related]
17. A case of incontinentia pigmenti. Amsalu S Ethiop Med J; 2003 Apr; 41(2):185-8. PubMed ID: 15227977 [TBL] [Abstract][Full Text] [Related]
19. Case report: unusually high rates of aneuploid embryos in a 28-year old woman with incontinentia pigmenti. Munné S; Alonso ML; Grifo J Cytogenet Cell Genet; 1996; 72(1):43-5. PubMed ID: 8565631 [TBL] [Abstract][Full Text] [Related]
20. A pregnancy following PGD for X-linked dominant [correction of X-linked autosomal dominant] incontinentia pigmenti (Bloch-Sulzberger syndrome): case report. Pettigrew R; Kuo HC; Scriven P; Rowell P; Pal K; Handyside A; Braude P; Ogilvie CM Hum Reprod; 2000 Dec; 15(12):2650-2. PubMed ID: 11098039 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]