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Chronic mucocutaneous candidiasis: a rare disease

Cilt: 5 Sayı: 1 31 Mayıs 2022
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Chronic mucocutaneous candidiasis: a rare disease

Öz

The article type of "letter to editor" does not need to present an abstract for Mucosa.

Anahtar Kelimeler

Kaynakça

  1. Shamriz O, Tal Y, Talmon A, Nahum A. Chronic mucocutaneous candidiasis in early life: Insights into immune mechanisms and novel targeted therapies. Front Immunol 2020;11:593289.
  2. Green L, Dolen WK. Chronic candidiasis in children. Curr Allergy Asthma Rep 2017;17:31.
  3. Veverka KK, Feldman SR. Chronic mucocutaneous candidiasis: what can we conclude about IL-17 antagonism? J Dermatolog Treat 2018;29:475-80.
  4. Khosravi AR, Mansouri P, Saffarian Z, Vahedi G, Nikaein D. Chronic mucocutaneous candidiasis, a case study and literature review. J Mycol Med 2018;28:206-10.
  5. Ostadi V, Sherkat R, Migaud M, et al. Functional analysis of two STAT1 gain-of-function mutations in two Iranian families with autosomal dominant chronic mucocutaneous candidiasis. Med Mycol 2021;59:180-8.
  6. Wang X, Netea MG, van de Veerdonk FL. Genetics of chronic mucocutaneous candidiasis. Immunogenetics of fungal diseases. Springer, 2017, p.85-103.
  7. Lehman H, Gordon C. The skin as a window into primary immune deficiency diseases: Atopic dermatitis and chronic mucocutaneous candidiasis. J Allergy Clin Immunol Pract 2019;7:788-98.
  8. Kirkpatrick CH. Chronic mucocutaneous candidiasis. Pediatr Infect Dis J 2001;20:197-206.

Ayrıntılar

Birincil Dil

İngilizce

Konular

Klinik Tıp Bilimleri

Bölüm

Editöre Mektup

Yayımlanma Tarihi

31 Mayıs 2022

Gönderilme Tarihi

22 Haziran 2021

Kabul Tarihi

13 Kasım 2021

Yayımlandığı Sayı

Yıl 2022 Cilt: 5 Sayı: 1

Kaynak Göster

APA
Erat, T., An, İ., Öztürk, M., Aksoy, M., Ayhan, E., & Uçan, E. (2022). Chronic mucocutaneous candidiasis: a rare disease. Mucosa, 5(1), 30-32. https://doi.org/10.33204/mucosa.956198
AMA
1.Erat T, An İ, Öztürk M, Aksoy M, Ayhan E, Uçan E. Chronic mucocutaneous candidiasis: a rare disease. Mucosa. 2022;5(1):30-32. doi:10.33204/mucosa.956198
Chicago
Erat, Tuğba, İsa An, Murat Öztürk, Mustafa Aksoy, Erhan Ayhan, ve Egemen Uçan. 2022. “Chronic mucocutaneous candidiasis: a rare disease”. Mucosa 5 (1): 30-32. https://doi.org/10.33204/mucosa.956198.
EndNote
Erat T, An İ, Öztürk M, Aksoy M, Ayhan E, Uçan E (01 Mayıs 2022) Chronic mucocutaneous candidiasis: a rare disease. Mucosa 5 1 30–32.
IEEE
[1]T. Erat, İ. An, M. Öztürk, M. Aksoy, E. Ayhan, ve E. Uçan, “Chronic mucocutaneous candidiasis: a rare disease”, Mucosa, c. 5, sy 1, ss. 30–32, May. 2022, doi: 10.33204/mucosa.956198.
ISNAD
Erat, Tuğba - An, İsa - Öztürk, Murat - Aksoy, Mustafa - Ayhan, Erhan - Uçan, Egemen. “Chronic mucocutaneous candidiasis: a rare disease”. Mucosa 5/1 (01 Mayıs 2022): 30-32. https://doi.org/10.33204/mucosa.956198.
JAMA
1.Erat T, An İ, Öztürk M, Aksoy M, Ayhan E, Uçan E. Chronic mucocutaneous candidiasis: a rare disease. Mucosa. 2022;5:30–32.
MLA
Erat, Tuğba, vd. “Chronic mucocutaneous candidiasis: a rare disease”. Mucosa, c. 5, sy 1, Mayıs 2022, ss. 30-32, doi:10.33204/mucosa.956198.
Vancouver
1.Tuğba Erat, İsa An, Murat Öztürk, Mustafa Aksoy, Erhan Ayhan, Egemen Uçan. Chronic mucocutaneous candidiasis: a rare disease. Mucosa. 01 Mayıs 2022;5(1):30-2. doi:10.33204/mucosa.956198