150 related articles for article (PubMed ID: 23880572)
1. Familial ectodermal dysplasia: a peers' agony.
Hegde K; Kashyap RR; Nair G; Nair PP
BMJ Case Rep; 2013 Jul; 2013():. PubMed ID: 23880572
[TBL] [Abstract][Full Text] [Related]
2. Hypohidrotic and hidrotic ectodermal dysplasia: a report of two cases.
Vasconcelos Carvalho M; Romero Souto de Sousa J; Paiva Correa de Melo F; Fonseca Faro T; Nunes Santos AC; Carvalho S; Veras Sobral AP
Dermatol Online J; 2013 Jul; 19(7):18985. PubMed ID: 24010518
[TBL] [Abstract][Full Text] [Related]
3. Appearance Says It All; A Rare Case Of Hypohidrotic Ectodermal Dysplasia.
Kumar J; Ahmed A; Hussain T; Kumar D; Aslams T
J Ayub Med Coll Abbottabad; 2022; 34(4):895-897. PubMed ID: 36566424
[TBL] [Abstract][Full Text] [Related]
4. A genetic study of anodontia in X-linked hypohidrotic ectodermal dysplasia.
Nakata M; Koshiba H; Eto K; Nance WE
Am J Hum Genet; 1980 Nov; 32(6):908-19. PubMed ID: 7446529
[TBL] [Abstract][Full Text] [Related]
5. Mutation in the ED1 gene, Ala349Thr, in a Korean patient with X-linked hypohidrotic ectodermal dysplasia developing de novo.
Na GY; Kim DW; Lee SJ; Chung SL; Park DJ; Kim JC; Kim MK
Pediatr Dermatol; 2004; 21(5):568-72. PubMed ID: 15461765
[TBL] [Abstract][Full Text] [Related]
6. A clinico-pathologic presentation. Hereditary hypohidrotic ectodermal dysplasia, or HED.
Cataldo E; Santis HR
J Mass Dent Soc; 1996; 45(1):8. PubMed ID: 9520670
[No Abstract] [Full Text] [Related]
7. [Anhidrotic ectodermal dysplasia (apropos of 3 families). Abnormal hair, a sign of heterozygosity?].
Le Marec B; Roussey M; Chevrant-Breton J; Segalen J; Bourdinière J; Sénécal J
J Genet Hum; 1983 Dec; 31(4):279-93. PubMed ID: 6663288
[TBL] [Abstract][Full Text] [Related]
8. [Primary anodontia in X-linked hidrotic ectodermal dysplasia].
Beliakov IuA; Elizarova VM; Smirnova TA; Krotov VA
Stomatologiia (Mosk); 1998; 77(4):29-31. PubMed ID: 9752735
[TBL] [Abstract][Full Text] [Related]
9. A novel 7-bp deletion mutation in a Taiwanese family with X-linked hypohidrotic ectodermal dysplasia.
Lin TK; Huang CY; Lin MH; Chao SC
Clin Exp Dermatol; 2004 Sep; 29(5):536-8. PubMed ID: 15347342
[TBL] [Abstract][Full Text] [Related]
10. Recurrent fever and lack of tooth buds. a case of ectodermal dysplasia in a 9 months old boy.
Nijs EL; Huisman TA
JBR-BTR; 2001; 84(6):256-7. PubMed ID: 11817478
[TBL] [Abstract][Full Text] [Related]
11. A dental approach to carrier screening in X linked hypohidrotic ectodermal dysplasia.
Spfaer JA
J Med Genet; 1981 Dec; 18(6):459-60. PubMed ID: 7334506
[TBL] [Abstract][Full Text] [Related]
12. [Dental agenesis in anhidrotic ectodermal dysplasia].
Fucci G; Ciccarelli R; Elefante R; Volpe A
Minerva Stomatol; 1984; 33(5):791-5. PubMed ID: 6596491
[No Abstract] [Full Text] [Related]
13. Hypodontia and sweat pore counts in detecting carriers of X-linked hypohidrotic ectodermal dysplasia.
Sofaer JA
Br Dent J; 1981 Nov; 151(10):327-30. PubMed ID: 6946797
[No Abstract] [Full Text] [Related]
14. Three successive generations of women with anhidrotic/hypohidrotic ectodermal dysplasia.
Rodrigues RG
J Natl Med Assoc; 2005 Jan; 97(1):99-101. PubMed ID: 15719880
[TBL] [Abstract][Full Text] [Related]
15. X-linked hypohidrotic ectodermal dysplasia (XLHED): clinical and diagnostic insights from an international patient registry.
Fete M; Hermann J; Behrens J; Huttner KM
Am J Med Genet A; 2014 Oct; 164A(10):2437-42. PubMed ID: 24664614
[TBL] [Abstract][Full Text] [Related]
16. Oligodontia ectodermal dysplasia--on signs, symptoms, genetics, and outcomes of dental treatment.
Bergendal B
Swed Dent J Suppl; 2010; (205):13-78, 7-8. PubMed ID: 20626136
[TBL] [Abstract][Full Text] [Related]
17. [Syndromes 17. Hypohidrotic ectodermal dysplasia].
Baart JA; van Hagen JM
Ned Tijdschr Tandheelkd; 2000 Jan; 107(1):12-4. PubMed ID: 12621820
[TBL] [Abstract][Full Text] [Related]
18. Congenital absence of all primary and permanent lateral incisors in a carrier of X-linked hypohidrotic ectodermal dysplasia.
McLaughlin WS
Int J Paediatr Dent; 1991 Aug; 1(2):99-103. PubMed ID: 1782201
[TBL] [Abstract][Full Text] [Related]
19. Oral findings in ankyloblepharon-ectodermal dysplasia-cleft lip/palate (AEC) syndrome.
Farrington F; Lausten L
Am J Med Genet A; 2009 Sep; 149A(9):1907-9. PubMed ID: 19681142
[TBL] [Abstract][Full Text] [Related]
20. X-linked ectodermal dysplasia with immunodeficiency caused by NEMO mutation: early recognition and diagnosis.
Mancini AJ; Lawley LP; Uzel G
Arch Dermatol; 2008 Mar; 144(3):342-6. PubMed ID: 18347290
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]