416 related articles for article (PubMed ID: 15719880)
1. 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]
2. Hypohidrotic (anhidrotic) ectodermal dysplasia in female twins.
Ogunrinde GO; Zubair RO; Ajike SO; Ige SO
Niger J Clin Pract; 2012; 15(1):98-100. PubMed ID: 22437101
[TBL] [Abstract][Full Text] [Related]
3. Autosomal recessive hypohidrotic ectodermal dysplasia with subclinical manifestation in the heterozygote.
Passarge E; Fries E
Birth Defects Orig Artic Ser; 1977; 13(3C):95-100. PubMed ID: 890117
[TBL] [Abstract][Full Text] [Related]
4. Aplasia cutis congenita, congenital heart lesions, and frontonasal cysts in four successive generations.
Rodrigues RG
Clin Genet; 2007 Jun; 71(6):558-60. PubMed ID: 17539905
[TBL] [Abstract][Full Text] [Related]
5. Hypohidrotic ectodermal dysplasia: argument against an autosomal recessive form clinically indistinguishable from X-linked hypohidrotic ectodermal dysplasia (Christ-Siemens-Touraine syndrome).
Sybert VP
Pediatr Dermatol; 1989 Jun; 6(2):76-81. PubMed ID: 2748478
[TBL] [Abstract][Full Text] [Related]
6. X-linked anhidrotic ectodermal dysplasia with some unusual features.
Settineri WM; Salzano FM; Fretas MJ
J Med Genet; 1976 Jun; 13(3):212-6. PubMed ID: 933122
[TBL] [Abstract][Full Text] [Related]
7. [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]
8. X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein.
Kere J; Srivastava AK; Montonen O; Zonana J; Thomas N; Ferguson B; Munoz F; Morgan D; Clarke A; Baybayan P; Chen EY; Ezer S; Saarialho-Kere U; de la Chapelle A; Schlessinger D
Nat Genet; 1996 Aug; 13(4):409-16. PubMed ID: 8696334
[TBL] [Abstract][Full Text] [Related]
9. Clinical and radiographic dental findings in X linked hypohidrotic ectodermal dysplasia.
Crawford PJ; Aldred MJ; Clarke A
J Med Genet; 1991 Mar; 28(3):181-5. PubMed ID: 2051453
[TBL] [Abstract][Full Text] [Related]
10. [Anhidrotic ectodermal dysplasia. Clinico-genetic study of 4 families].
Balestrazzi P; Solli R; Salami P; Corrini L; Mattioli M; Bernasconi S
Minerva Pediatr; 1979 Feb; 31(4):265-74. PubMed ID: 460084
[No Abstract] [Full Text] [Related]
11. A gene for autosomal dominant hypohidrotic ectodermal dysplasia (EDA3) maps to chromosome 2q11-q13.
Ho L; Williams MS; Spritz RA
Am J Hum Genet; 1998 May; 62(5):1102-6. PubMed ID: 9545409
[TBL] [Abstract][Full Text] [Related]
12. Novel mutations in the EDAR gene in two Pakistani consanguineous families with autosomal recessive hypohidrotic ectodermal dysplasia.
Naeem M; Muhammad D; Ahmad W
Br J Dermatol; 2005 Jul; 153(1):46-50. PubMed ID: 16029325
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. Ear nose throat manifestations in hypoidrotic ectodermal dysplasia.
Callea M; Teggi R; Yavuz I; Tadini G; Priolo M; Crovella S; Clarich G; Grasso DL
Int J Pediatr Otorhinolaryngol; 2013 Nov; 77(11):1801-4. PubMed ID: 24080322
[TBL] [Abstract][Full Text] [Related]
15. [Anhidrotic ectodermal dysplasia. Apropos of a case report of quadruplets].
Delaire J; Schmidt J; Lumineau JP; Pressard J; Billet J
Rev Stomatol Chir Maxillofac; 1984; 85(1):34-7. PubMed ID: 6584956
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Two novel mutations in the gene EDAR causing autosomal recessive hypohidrotic ectodermal dysplasia.
Naqvi SK; Wasif N; Javaid H; Ahmad W
Orthod Craniofac Res; 2011 Aug; 14(3):156-9. PubMed ID: 21771270
[TBL] [Abstract][Full Text] [Related]
19. A new autosomal dominant syndrome of hypohidrotic ectodermal dysplasia and unusual facies.
Bocian M; Rimoin DL
Birth Defects Orig Artic Ser; 1979; 15(5B):239-51. PubMed ID: 526580
[No Abstract] [Full Text] [Related]
20. Autosomal dominant ectodermal dysplasia.
Jorgenson RJ; Dowben JS; Dowben SL
J Craniofac Genet Dev Biol; 1987; 7(4):403-12. PubMed ID: 3429615
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
