Works matching DE "RAPP-Hodgkin syndrome"
Results: 24
Gene p63: In ectrodactyly-ectodermal dysplasia clefting, ankyloblepharon-ectodermal dysplasia, Rapp-Hodgkin syndrome.
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- Annals of Maxillofacial Surgery, 2013, v. 3, n. 1, p. 58, doi. 10.4103/2231-0746.110085
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- Publication type:
- Article
Syndromes and Genetics.
- Published in:
- 2021
- Publication type:
- Abstract
Cicatricial external auditory canal stenosis caused by ectodermal dysplasia: Rapp-Hodgkin syndrome.
- Published in:
- 2013
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- Publication type:
- Journal Article
Let-7b regulates alpaca hair growth by downregulating ectodysplasin A.
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- Molecular Medicine Reports, 2018, v. 17, n. 3, p. 4688, doi. 10.3892/mmr.2018.8442
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- Publication type:
- Article
The novel EDAR p.L397H missense mutation causes autosomal dominant hypohidrotic ectodermal dysplasia.
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- Journal of the European Academy of Dermatology & Venereology, 2017, v. 31, n. 1, p. e17, doi. 10.1111/jdv.13587
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- Publication type:
- Article
Non-invasive diagnosis of sweat gland dysplasia using optical coherence tomography and reflectance confocal microscopy in a family with anhidrotic ectodermal dysplasia (Christ-Siemens-Touraine syndrome).
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- Journal of the European Academy of Dermatology & Venereology, 2016, v. 30, n. 4, p. 677, doi. 10.1111/jdv.13085
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- Publication type:
- Article
High-Potency Topical Steroids: An Effective Therapy for Chronic Scalp Inflammation in Rapp-Hodgkin Ectodermal Dysplasia.
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- Pediatric Dermatology, 2016, v. 33, n. 2, p. e84, doi. 10.1111/pde.12784
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- Publication type:
- Article
Death Due to Complications of Anhidrotic Ectodermal Dysplasia.
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- Journal of Forensic Sciences, 2014, v. 59, n. 6, p. 1672, doi. 10.1111/1556-4029.12564
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- Publication type:
- Article
A Case of Anhidrotic Ectodermal Dysplasia.
- Published in:
- 2013
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- Publication type:
- Case Study
XL-EDA-ID Presenting with Congenital Duodenal Atresia and Perforations.
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- Journal of Clinical Immunology, 2018, v. 38, n. 7, p. 733, doi. 10.1007/s10875-018-0544-5
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- Publication type:
- Article
Autosomal Dominant Anhidrotic Ectodermal Dysplasia with Immunodeficiency Caused by a Novel NFKBIA Mutation, p.Ser36Tyr, Presents with Mild Ectodermal Dysplasia and Non-Infectious Systemic Inflammation.
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- Journal of Clinical Immunology, 2013, v. 33, n. 7, p. 1165, doi. 10.1007/s10875-013-9924-z
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- Publication type:
- Article
Christ-Siemens-Touraine Syndrome: A Case Report and Review of the Literature.
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- Case Reports in Dentistry, 2012, p. 1, doi. 10.1155/2012/586418
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- Publication type:
- Article
EDA-ID and IP, Two Faces of the Same Coin: How the Same IKBKG / NEMO Mutation Affecting the NF-κB Pathway Can Cause Immunodeficiency and/or Inflammation.
- Published in:
- International Reviews of Immunology, 2015, v. 34, n. 6, p. 445, doi. 10.3109/08830185.2015.1055331
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- Publication type:
- Article
Rapp-Hodgkin Syndrome: Clinical and Dental Findings.
- Published in:
- 2009
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- Publication type:
- Case Study
Autosomal Recessive Anhidrotic Ectodermal Dysplasia: A Rare Entity.
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- Indian Journal of Dermatology, 2014, v. 59, n. 4, p. 1, doi. 10.4103/0019-5154.135541
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- Publication type:
- Article
Buphthalmos development in adult: case report.
- Published in:
- Arquivos Brasileiros de Oftalmologia, 2012, v. 75, n. 5, p. 361, doi. 10.1590/S0004-27492012000500015
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- Publication type:
- Article
Dental management of Rapp-Hodgkin syndrome associated with oral cleft and hypodontia.
- Published in:
- 2016
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- Publication type:
- journal article
Dental management of hypohidrotic ectodermal dysplasia: A report of two cases.
- Published in:
- 2015
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- Publication type:
- Case Study
Avaliação do NF-kB na regulação gênica do sistema NADPH oxidase em pacientes com displasia ectodérmica com imunodeficiência.
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- ConScientiae Saúde, 2016, v. 15, n. 1, p. 114, doi. 10.5585/ConsSaude.v15n1.6259
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- Publication type:
- Article
Ending diagnostic odyssey using clinical whole-exome sequencing (CWES).
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- Journal of Laboratory Medicine, 2021, v. 45, n. 6, p. 259, doi. 10.1515/labmed-2021-0127
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- Publication type:
- Article
A Rare Cause of Fever in the Emergency Department: Anhidrotic Ectodermal Dysplasia.
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- Turkish Journal of Emergency Medicine, 2013, v. 13, n. 2, p. 89, doi. 10.5505/1304.7361.2013.54366
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- Publication type:
- Article
Autosomal Recessive Anhidrotic Ectodermal Dysplasia: A Rare Disease.
- Published in:
- 2018
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- Publication type:
- Letter to the Editor
Rapp Hodgkin Syndrome.
- Published in:
- Indian Dermatology Online Journal, 2017, v. 8, n. 3, p. 215, doi. 10.4103/idoj.IDOJ_100_16
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- Publication type:
- Article
Christ-Siemens-Touraine syndrome with palmoplantar keratoderma: A rare association.
- Published in:
- 2016
- By:
- Publication type:
- Case Study