142 related articles for article (PubMed ID: 140825)
1. Anhidrotic (or hypohidrotic) ectodermal dysplasis.
Martin-Pascual A; De Unamuno P; Aparicio M; Herreros V
Dermatologica; 1977; 154(4):235-43. PubMed ID: 140825
[No Abstract] [Full Text] [Related]
2. Sebaceous gland papules in anhidrotic ectodermal dysplasia.
Katz SI; Penneys NS
Arch Dermatol; 1971 May; 103(5):507-9. PubMed ID: 5580292
[No Abstract] [Full Text] [Related]
3. [Autosomal recessive ectodermal dysplasia--a special nosologic entity? (author's transl)].
Lelis J
Dermatol Monatsschr; 1979 Aug; 165(8):587-92. PubMed ID: 159839
[No Abstract] [Full Text] [Related]
4. [Multiple sebaceous gland hyperplasias in X chromosome hypohidrotic ectodermal dysplasia].
Orge C; Bonsmann G; Hamm H
Hautarzt; 1991 Oct; 42(10):645-7. PubMed ID: 1757259
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Athelia in a female infant - heterozygous for anhidrotic ectodermal dysplasia.
Burck U; Held KR
Clin Genet; 1981 Feb; 19(2):117-21. PubMed ID: 7471507
[TBL] [Abstract][Full Text] [Related]
8. X-linked recessive hypohidrotic ectodermal dysplasia. Manifestations and management.
Wright JT; Finley WH
Ala J Med Sci; 1986 Jan; 23(1):84-7. PubMed ID: 3953980
[No Abstract] [Full Text] [Related]
9. [Keratosis palmoplantaris with clubbed fingers, hypotrichosis, hypohidrosis and dental dysplasia].
Koch HJ; Hübner U; Schaarschmidt E; Thiel W
Hautarzt; 1991 Jun; 42(6):399-401. PubMed ID: 1833360
[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. Hypohidrotic ectodermal dysplasia (Christ-Siemans-Touraine syndrome) in siblings.
Nathan V
West Indian Med J; 1984 Mar; 33(1):55-8. PubMed ID: 6730467
[No Abstract] [Full Text] [Related]
12. 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]
13. Autosomal recessive anhidrotic ectodermal dysplasia: report of a case and discrimination of diagnostic features.
Anton-Lamprecht I; Schleiermacher E; Wolf M
Birth Defects Orig Artic Ser; 1988; 24(2):183-95. PubMed ID: 3179426
[No Abstract] [Full Text] [Related]
14. Autosomal dominant hypohidrotic ectodermal dysplasia in a large family.
Aswegan AL; Josephson KD; Mowbray R; Pauli RM; Spritz RA; Williams MS
Am J Med Genet; 1997 Nov; 72(4):462-7. PubMed ID: 9375732
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. [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]
17. A new case of keratin 14 functional knockout causes severe recessive EBS and questions the haploinsufficiency model of Naegeli-Franceschetti-Jadassohn syndrome.
Titeux M; Décha A; Pironon N; Tonasso L; Gasc G; Mejía JE; Prost-Squarcioni C; Hovnanian A
J Invest Dermatol; 2011 Oct; 131(10):2131-3. PubMed ID: 21734713
[No Abstract] [Full Text] [Related]
18. 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]
19. 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]
20. Possible genetic heterogeneity in X linked hypohidrotic ectodermal dysplasia.
Goodship J; Malcolm S; Clarke A; Pembrey ME
J Med Genet; 1990 Jul; 27(7):422-5. PubMed ID: 2395159
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]