339 related articles for article (PubMed ID: 16086741)
1. Hereditary mucoepithelial dysplasia: clinical, ultrastructural and genetic study of eight patients and literature review.
Boralevi F; Haftek M; Vabres P; Lepreux S; Goizet C; Leaute-Labreze C; Taieb A
Br J Dermatol; 2005 Aug; 153(2):310-8. PubMed ID: 16086741
[TBL] [Abstract][Full Text] [Related]
2. Hereditary mucoepithelial dysplasia: report of two sporadic cases.
Hernández-Martín A; Colmenero I; Torrelo A
Pediatr Dermatol; 2012; 29(3):311-5. PubMed ID: 22122740
[TBL] [Abstract][Full Text] [Related]
3. Ichthyosis follicularis with alopecia and photophobia.
Eramo LR; Esterly NB; Zieserl EJ; Stock EL; Herrmann J
Arch Dermatol; 1985 Sep; 121(9):1167-74. PubMed ID: 4037843
[TBL] [Abstract][Full Text] [Related]
4. Clinical, histologic, cytologic, and ultrastructural characteristics of the oral lesions from hereditary mucoepithelial dysplasia. A disease of gap junction and desmosome formation.
Witkop CJ; White JG; Sauk JJ; King RA
Oral Surg Oral Med Oral Pathol; 1978 Nov; 46(5):645-57. PubMed ID: 213754
[TBL] [Abstract][Full Text] [Related]
5. Ichthyosis follicularis, atrichia and photophobia (IFAP) and hereditary mucoepithelial dysplasia: Two syndromes that share a common clinical spectrum.
Irurzun I; Natale MI; Agostinelli ML; Lamberti M; Montero D; Granda C; Mássimo JA; Manzur GB; Valinotto LE
Pediatr Dermatol; 2021 May; 38(3):568-574. PubMed ID: 33742461
[TBL] [Abstract][Full Text] [Related]
6. Hereditary mucoepithelial dysplasia: unique histopathological findings in skin lesions.
Leithauser LA; Mutasim DF
J Cutan Pathol; 2012 Apr; 39(4):431-9. PubMed ID: 22443394
[TBL] [Abstract][Full Text] [Related]
7. Hereditary mucoepithelial dysplasia. Case report and review of the literature.
Scheman AJ; Ray DJ; Witkop CJ; Dahl MV
J Am Acad Dermatol; 1989 Aug; 21(2 Pt 2):351-7. PubMed ID: 2666466
[TBL] [Abstract][Full Text] [Related]
8. New clinical aspects of hereditary mucoepithelial dysplasia.
Urban MD; Schosser R; Spohn W; Wentling WO; Robinow M
Am J Med Genet; 1991 Jun; 39(3):338-41. PubMed ID: 1867287
[TBL] [Abstract][Full Text] [Related]
9. Clinical and genetic heterogeneity in keratosis follicularis spinulosa decalvans.
Castori M; Covaciu C; Paradisi M; Zambruno G
Eur J Med Genet; 2009; 52(1):53-8. PubMed ID: 18984066
[TBL] [Abstract][Full Text] [Related]
10. Hereditary 'white nails': a genetic and structural study.
Norgett EE; Wolf F; Balme B; Leigh IM; Perrot H; Kelsell DP; Haftek M
Br J Dermatol; 2004 Jul; 151(1):65-72. PubMed ID: 15270873
[TBL] [Abstract][Full Text] [Related]
11. Ichthyosis follicularis with alopecia and photophobia in a girl with cataract: histological and electron microscopy findings.
Tsolia M; Aroni K; Konstantopoulou I; Karpathios T; Tsoukatou T; Paraskevakou H; Stavrinadis C; Fretzayas A
Acta Derm Venereol; 2005; 85(1):51-5. PubMed ID: 15848992
[TBL] [Abstract][Full Text] [Related]
12. White sponge nevus: report of a three-generation family.
Martelli H; Pereira SM; Rocha TM; Nogueira dos Santos PL; Batista de Paula AM; Bonan PR
Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2007 Jan; 103(1):43-7. PubMed ID: 17178493
[TBL] [Abstract][Full Text] [Related]
13. Child with manifestations of dermotrichic syndrome and ichthyosis follicularis-alopecia-photophobia (IFAP) syndrome.
Martino F; D'Eufemia P; Pergola MS; Finocchiaro R; Celli M; Giampà G; Frontali M; Giardini O
Am J Med Genet; 1992 Sep; 44(2):233-6. PubMed ID: 1456297
[TBL] [Abstract][Full Text] [Related]
14. Exome sequencing identifies a SREBF1 recurrent ARG557CYS mutation as the cause of hereditary mucoepithelial dysplasia in a family with high clinical variability.
Chacon-Camacho OF; Arce-Gonzalez R; Ordaz-Robles T; Perezpeña-Diazconti M; Nava-Castañeda A; Zenteno JC
Am J Med Genet A; 2020 Nov; 182(11):2773-2777. PubMed ID: 32902915
[TBL] [Abstract][Full Text] [Related]
15. [Keratosis follicularis spinulosa decalvans (Siemens' syndrome) associated with other abnormalities].
Domenech P; Ferrando J; Corretger M; Torras H; Valls X; González A
Med Cutan Ibero Lat Am; 1985; 13(2):175-81. PubMed ID: 3900603
[TBL] [Abstract][Full Text] [Related]
16. Keratosis follicularis spinulosa decalvans: report of a new pedigree.
Herd RM; Benton EC
Br J Dermatol; 1996 Jan; 134(1):138-42. PubMed ID: 8745901
[TBL] [Abstract][Full Text] [Related]
17. Atrichia, ichthyosis, follicular hyperkeratosis, chronic candidiasis, keratitis, seizures, mental retardation and inguinal hernia: a severe manifestation of IFAP syndrome?
Boente MC; Bibas-Bonet H; Coronel AM; Asial RA
Eur J Dermatol; 2000 Mar; 10(2):98-102. PubMed ID: 10694306
[TBL] [Abstract][Full Text] [Related]
18. Hereditary mucoepithelial dysplasia: a disease apparently of desmosome and gap junction formation.
Witkop CJ; White JG; King RA; Dahl MV; Young WG; Sauk JJ
Am J Hum Genet; 1979 Jul; 31(4):414-27. PubMed ID: 484550
[TBL] [Abstract][Full Text] [Related]
19. Keratosis follicularis spinulosa decalvans in a family.
Bellet JS; Kaplan AL; Selim MA; Olsen EA
J Am Acad Dermatol; 2008 Mar; 58(3):499-502. PubMed ID: 18280351
[TBL] [Abstract][Full Text] [Related]
20. Ichthyosis follicularis, alopecia, and photophobia syndrome: a case report and a pathological insight into pilosebaceous anomaly.
Kamo M; Ohyama M; Kosaki K; Amagai M; Ebihara T; Nakayama J; Ishiko A
Am J Dermatopathol; 2011 Jun; 33(4):403-6. PubMed ID: 21242756
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
