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 *

153 related articles for article (PubMed ID: 34897795)

  • 1. An epidemiological survey of anhidrotic/hypohidrotic ectodermal dysplasia in Japan: High prevalence of allergic diseases.
    Inazawa-Terada M; Namiki T; Omigawa C; Fujimoto T; Munetsugu T; Ugajin T; Shimomura Y; Ohshima Y; Yoshida K; Niizeki H; Hayashi R; Nakano H; Yokozeki H
    J Dermatol; 2022 Apr; 49(4):422-431. PubMed ID: 34897795
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hypohidrotic ectodermal dysplasia, osteopetrosis, lymphedema, and immunodeficiency in an infant with multiple opportunistic infections.
    Carlberg VM; Lofgren SM; Mann JA; Austin JP; Nolt D; Shereck EB; Davila-Saldana B; Zonana J; Krol AL
    Pediatr Dermatol; 2014; 31(6):716-21. PubMed ID: 23405946
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The prevalence of X-linked hypohidrotic ectodermal dysplasia (XLHED) in Denmark, 1995-2010.
    Nguyen-Nielsen M; Skovbo S; Svaneby D; Pedersen L; Fryzek J
    Eur J Med Genet; 2013 May; 56(5):236-42. PubMed ID: 23416623
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Characterization of X-linked hypohidrotic ectodermal dysplasia (XL-HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging.
    Jones KB; Goodwin AF; Landan M; Seidel K; Tran DK; Hogue J; Chavez M; Fete M; Yu W; Hussein T; Johnson R; Huttner K; Jheon AH; Klein OD
    Am J Med Genet A; 2013 Jul; 161A(7):1585-93. PubMed ID: 23687000
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal Genetic Testing for X-Linked Hypohidrotic Ectodermal Dysplasia.
    Yapijakis C; Gintoni I; Chrousos G
    Adv Exp Med Biol; 2021; 1339():337-340. PubMed ID: 35023123
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hypohidrotic Ectodermal Dysplasia: A Case Report.
    Shamim H; Hanif S
    Cureus; 2023 Oct; 15(10):e46530. PubMed ID: 37927739
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Should we consider hypohidrotic ectodermal dysplasia as a possible risk factor for malignant melanoma?
    Gregoriou S; Rigopoulos D; Vergou T; Korfitis C; Menegakis G; Kontochristopoulos G
    J Cutan Med Surg; 2007; 11(5):188-90. PubMed ID: 17942030
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Quantification of taurodontism: interests in the early diagnosis of hypohidrotic ectodermal dysplasia.
    Gros CI; Clauss F; Obry F; Manière MC; Schmittbuhl M
    Oral Dis; 2010 Apr; 16(3):292-8. PubMed ID: 20374512
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ocular and non-ocular manifestations of hypohidrotic ectodermal dysplasia.
    Tyagi P; Tyagi V; Hashim AA
    BMJ Case Rep; 2011 Apr; 2011():. PubMed ID: 22700604
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hypohidrotic ectodermal dysplasia: a case report.
    Chandravanshi SL
    Orbit; 2020 Aug; 39(4):298-301. PubMed ID: 31694435
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical, trichoscopy, and light microscopic findings in hypohidrotic ectodermal dysplasia: Report of 21 patients and a review of the literature.
    Peña-Romero AG; Sáez-de-Ocariz M; Toussaint-Caire S; Morán-Villaseñor E; Orozco-Covarrubias L; Durán-McKinster C
    Pediatr Dermatol; 2021 Mar; 38(2):442-448. PubMed ID: 33085121
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A new mutation in EDA gene in X-linked hypohidrotic ectodermal dysplasia associated with keratoconus.
    Piccione M; Serra G; Sanfilippo C; Andreucci E; Sani I; Corsello G
    Minerva Pediatr; 2012 Feb; 64(1):59-64. PubMed ID: 22350046
    [TBL] [Abstract][Full Text] [Related]  

  • 14. EDA, EDAR, EDARADD and WNT10A allelic variants in patients with ectodermal derivative impairment in the Spanish population.
    Martínez-Romero MC; Ballesta-Martínez MJ; López-González V; Sánchez-Soler MJ; Serrano-Antón AT; Barreda-Sánchez M; Rodriguez-Peña L; Martínez-Menchon MT; Frías-Iniesta J; Sánchez-Pedreño P; Carbonell-Meseguer P; Glover-López G; Guillén-Navarro E;
    Orphanet J Rare Dis; 2019 Dec; 14(1):281. PubMed ID: 31796081
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Anhidrotic/hypohidrotic ectodermal dysplasia: ten cases].
    Ezzine Sebai N; Khaled A; Kharfi M; Bouzgarrou A; M'halla H; Jones M; Fazaa B; Kamoun MR
    Tunis Med; 2009 Dec; 87(12):805-9. PubMed ID: 20209845
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prosthetic rehabilitation in a pediatric patient with hypohidrotic ectodermal dysplasia: a case report.
    Quintanilha LELP; Carneiro-Campos LE; Antunes LAA; Antunes LS; Fernandes CP; Abreu FV
    Gen Dent; 2017; 65(5):72-76. PubMed ID: 28862593
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel splicing mutation of ectodysplasin A gene responsible for hypohidrotic ectodermal dysplasia.
    Liu G; Wang X; Qin M; Sun L; Zhu J
    Oral Dis; 2018 Sep; 24(6):1101-1106. PubMed ID: 29676859
    [TBL] [Abstract][Full Text] [Related]  

  • 18. X-linked hypohidrotic ectodermal dysplasia by a de novo recurrent variant in a Mexican patient.
    Noriega-Juárez MA; García-Delgado C; Villaseñor-Domínguez A; Mena-Cedillos CA; Toledo-Bahena M; Valencia-Herrera A; Baeza-Capetillo P; Cervantes A; Morán-Barroso VF; Monroy-Jaramillo N
    Bol Med Hosp Infant Mex; 2020; 77(4):212-217. PubMed ID: 32713954
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hypohidrotic ectodermal dysplasia: clinical and molecular review.
    Reyes-Reali J; Mendoza-Ramos MI; Garrido-Guerrero E; Méndez-Catalá CF; Méndez-Cruz AR; Pozo-Molina G
    Int J Dermatol; 2018 Aug; 57(8):965-972. PubMed ID: 29855039
    [TBL] [Abstract][Full Text] [Related]  

  • 20. First report of X-linked hypohidrotic ectodermal dysplasia with a hemizygous c.1142G > C in the EDA gene: variant of uncertain significance or new pathogenic variant?
    Tumminello M; Gangemi A; Matina F; Guardino M; Giuffrè BL; Corsello G
    Ital J Pediatr; 2021 Jun; 47(1):128. PubMed ID: 34078430
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.