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.
127 related articles for article (PubMed ID: 37699567)
1. Recurrent Vascularizing Keratitis in Infants With Hereditary Mucoepithelial Dysplasia Related to SREBF1 Mutation. Kim S; Jeong H; Ko JM; Kwon O; Oh JY Cornea; 2023 Dec; 42(12):1586-1589. PubMed ID: 37699567 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Hereditary Mucoepithelial Dysplasia Results from Heterozygous Variants at p.Arg557 Mutational Hotspot in SREBF1, Encoding a Transcription Factor Involved in Cholesterol Homeostasis. Morice-Picard F; Michaud V; Lasseaux E; Rezvani HR; Plaisant C; Bessis D; Leauté-Labrèze C; Arveiler B; Taieb A; Trimouille A; Boralevi F J Invest Dermatol; 2020 Jun; 140(6):1289-1292.e2. PubMed ID: 31790666 [No Abstract] [Full Text] [Related]
5. Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants. Murase C; Takeichi T; Nomura T; Ogi T; Akiyama M J Invest Dermatol; 2021 Jun; 141(6):1596-1598. PubMed ID: 33253727 [No Abstract] [Full Text] [Related]
6. Long-term ocular follow-up in a case with hereditary mucoepithelial dysplasia. Avadhanam VS; Khaw PT; Martin KR J Pediatr Ophthalmol Strabismus; 2010 Nov; 47 Online():e1-4. PubMed ID: 21117525 [TBL] [Abstract][Full Text] [Related]
7. 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]
15. Acute diffuse and total alopecia of the female scalp. A new subtype of diffuse alopecia areata that has a favorable prognosis. Sato-Kawamura M; Aiba S; Tagami H Dermatology; 2002; 205(4):367-73. PubMed ID: 12444333 [TBL] [Abstract][Full Text] [Related]
16. Childhood Alopecia Areata: An Overview of Treatment and Recent Patents. Hon KL; Luk DCK; Leung AKC; Ng C; Loo SKF Recent Pat Inflamm Allergy Drug Discov; 2020; 14(2):117-132. PubMed ID: 32723274 [TBL] [Abstract][Full Text] [Related]
17. A novel dominant and a de novo mutation in the GJB2 gene (connexin-26) cause keratitis-ichthyosis-deafness syndrome: implication for cochlear implantation. Arndt S; Aschendorff A; Schild C; Beck R; Maier W; Laszig R; Birkenhäger R Otol Neurotol; 2010 Feb; 31(2):210-5. PubMed ID: 20101161 [TBL] [Abstract][Full Text] [Related]
18. Treatment of pediatric alopecia areata with anthralin: A retrospective study of 37 patients. Wu SZ; Wang S; Ratnaparkhi R; Bergfeld WF Pediatr Dermatol; 2018 Nov; 35(6):817-820. PubMed ID: 30338548 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. An Excellent Response to Tofacitinib in a Pediatric Alopecia Patient: A Case Report and Review. Brown L; Skopit S J Drugs Dermatol; 2018 Aug; 17(8):914-917. PubMed ID: 30124734 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]