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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 6895204)

  • 21. A child with hypohidrotic ectodermal dysplasia with features of a collodion membrane.
    Thomas C; Suranyi E; Pride H; Tyler W
    Pediatr Dermatol; 2006; 23(3):251-4. PubMed ID: 16780473
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Anhidrotic ectodermal dysplasia. Two cases in twins].
    González Rivera F; Sierra Córcoles C; Marín Patón M; Cabeza Ramírez A; Bonal Alguacil Y
    An Esp Pediatr; 1998 Feb; 48(2):173-4. PubMed ID: 9577028
    [No Abstract]   [Full Text] [Related]  

  • 23. Anhidrotic ectodermal dysplasia: a new mutation.
    Giancane G; Ferrari S; Carsetti R; Papoff P; Iacobini M; Duse M
    J Allergy Clin Immunol; 2013 Dec; 132(6):1451-3. PubMed ID: 23870671
    [No Abstract]   [Full Text] [Related]  

  • 24. Hypohidrotic ectodermal dysplasia of sisters in a family.
    Ghosh S; Das MK
    Indian Pediatr; 2004 Nov; 41(11):1176-7. PubMed ID: 15591678
    [No Abstract]   [Full Text] [Related]  

  • 25. [Anhydrotic ectodermal dysplasia: un uncommon cause of unexplained fever in infants].
    Khemiri M; Ben Rhouma A; Kharfi M; Borgi A; Ben Mansour F; Zouari S; Barsaoui S
    Tunis Med; 2008 Dec; 86(12):1089-90. PubMed ID: 19213521
    [No Abstract]   [Full Text] [Related]  

  • 26. [Clouston's syndrome].
    Divanian RS; Muradian AG
    Vestn Dermatol Venerol; 1980 Aug; (8):46-9. PubMed ID: 7245886
    [No Abstract]   [Full Text] [Related]  

  • 27. R298Q mutation of p63 gene in autosomal dominant ectodermal dysplasia associated with arrhythmogenic right ventricular cardiomyopathy.
    Valenzise M; Arrigo T; De Luca F; Privitera A; Frigiola A; Carando A; Garelli E; Silengo M
    Eur J Med Genet; 2008; 51(5):497-500. PubMed ID: 18603493
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Hair collar sign associated with scalp aplasia cutis congenita].
    Roche-Gamón E; Febrer-Bosch I; Alegre de Miquel V
    Actas Dermosifiliogr; 2007; 98(6):442-3. PubMed ID: 17663938
    [No Abstract]   [Full Text] [Related]  

  • 29. [Anhidrotic ectodermal dysplasia in a female newborn].
    Thivolet J; Hermier C; Jeune R
    Ann Dermatol Venereol; 1977 May; 104(5):417-8. PubMed ID: 921172
    [No Abstract]   [Full Text] [Related]  

  • 30. [The development of ozena in a child suffering from anhydrotic ectodermal dysplasia].
    Chistiakova VR; Toropchina LV; Chumicheva IV
    Vestn Otorinolaringol; 2001; (1):48-9. PubMed ID: 11247252
    [No Abstract]   [Full Text] [Related]  

  • 31. Hereditary anhidrotic ectodermal dysplasia in a Zambian family.
    Sehgal D; Chawla V; Maguire MJ
    East Afr Med J; 1981 May; 58(5):374-9. PubMed ID: 7285838
    [No Abstract]   [Full Text] [Related]  

  • 32. [Familial oligodontia with ectodermal dysplasia: a sex-linked recessive hereditary disease].
    Tong KQ
    Zhonghua Kou Qiang Ke Za Zhi; 1983 Sep; 18(3):151-3. PubMed ID: 6581021
    [No Abstract]   [Full Text] [Related]  

  • 33. Hypohydrotic ectodermal dysplasia affecting a female patient.
    Ellis SG; Ahmed H
    Dent Update; 1993 Dec; 20(10):447-50. PubMed ID: 8056096
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Hypohidrotic ectodermal dysplasia.
    Wang HC; Chen CC; Wang WJ; Ho WL
    Zhonghua Yi Xue Za Zhi (Taipei); 2000 Mar; 63(3):230-3. PubMed ID: 10746420
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Picture of the month. Cutis aplasia.
    Jones CH; Andrews C
    Arch Pediatr Adolesc Med; 2005 Dec; 159(12):1127-8. PubMed ID: 16330735
    [No Abstract]   [Full Text] [Related]  

  • 36. Anhidrotic ectodermal dysplasia; fever in a neonate.
    Estrada R; Schaeffer H; Rosenfeld W; Jhaveri R; Salazar D; Evans H
    N Y State J Med; 1981 Nov; 81(12):1791-3. PubMed ID: 6949060
    [No Abstract]   [Full Text] [Related]  

  • 37. Type II congenital dyserythropoietic anemia in a patient with ectodermal dysplasia. Distinction from dyskeratosis congenita.
    Sykora KW; Niedich J; Price J; Bussel J
    Am J Pediatr Hematol Oncol; 1994 May; 16(2):173-6. PubMed ID: 8166371
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Hereditary anhidrotic ectodermal dysplasia.
    Mohanta KD; Kar RS; Swain U; Nanda BK
    Indian Pediatr; 1970 Mar; 7(3):186-7. PubMed ID: 5519181
    [No Abstract]   [Full Text] [Related]  

  • 39. Truncal aplasia cutis congenita associated with ileal atresia and mesenteric defect.
    Al-Sawan RM; Soni AL; Al-Kobrosly AM; Shawkat MM; Al-Saleh Q; Al-Sabah HY; Tahmiscija DV
    Pediatr Dermatol; 1999; 16(5):408-9. PubMed ID: 10627221
    [No Abstract]   [Full Text] [Related]  

  • 40. [Case of ectodermal dysplasia in a 6-week-old infant with congenital heart disease and porencephaly].
    Pyda E; Pinkawa E; Koehler B
    Pediatr Pol; 1976 Aug; 51(8):1001-3. PubMed ID: 967589
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.