Cargando…

Dermoscopic and Onychoscopic Features of Dyskeratosis Congenita

Detalles Bibliográficos
Autores principales:	Vasani, Resham, Baddireddy, Kavya
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer - Medknow 2022
Materias:	Letter to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9650737/ https://www.ncbi.nlm.nih.gov/pubmed/36386733 http://dx.doi.org/10.4103/idoj.idoj_23_22

Ejemplares similares

Dyskeratosis congenita
por: Gitto, Lorenzo, et al.
Publicado: (2020)

Are Dyskeratosis Congenita patients at higher risk of symptomatic COVID-19?
por: Dorgaleleh, Saeed, et al.
Publicado: (2022)

Dyskeratosis congenita presenting with dysphagia
por: Gupta, Kalpana, et al.
Publicado: (2016)

Dermoscopic View of Papular Acantholytic Dyskeratosis of the Genitocrural Region
por: Cebeci, Dua, et al.
Publicado: (2022)

Dyskeratosis congenita, stem cells and telomeres
por: Kirwan, Michael, et al.
Publicado: (2009)

Dyskeratosis congenita and the DNA damage response
por: Kirwan, Michael, et al.
Publicado: (2011)

Dyskeratosis congenita in a Nigerian boy
por: Ibrahim, Aliyu, et al.
Publicado: (2014)

Oral and Dental Findings of Dyskeratosis Congenita
por: Koruyucu, Mine, et al.
Publicado: (2014)

Dyskeratosis Congenita and Corneal Refractive Surgery
por: Heiland, Madeline B., et al.
Publicado: (2019)

Dermoscopic clues to diagnose acantholytic dyskeratosis
por: Specchio, Francesca, et al.
Publicado: (2015)

Demystifying the Stinking Reddish Brown Stains Through the Dermoscope: Cydnidae Pigmentation
por: Poojary, Shital, et al.
Publicado: (2019)

Bullous Aplasia Cutis Congenita—Description of a Novel Dermoscopic Feature
por: Rout, Aradhana, et al.
Publicado: (2021)

Cytomegalovirus Retinitis as a Presenting Feature of Multisystem Disorder: Dyskeratosis Congenita
por: Parchand, Swapnil, et al.
Publicado: (2017)

The diagnosis and treatment of dyskeratosis congenita: a review
por: Fernández García, M Soledad, et al.
Publicado: (2014)

Dyskeratosis Congenita: A Report of Two Cases
por: Karunakaran, Anila, et al.
Publicado: (2013)

Long tails, short telomeres: Dyskeratosis congenita
por: Tummala, Hemanth, et al.
Publicado: (2015)

Dyskeratosis congenita: rare case report of Syria
por: Hussein, Firas, et al.
Publicado: (2021)

Case Report: A Missense Mutation in Dyskeratosis Congenita 1 Leads to a Benign Form of Dyskeratosis Congenita Syndrome With the Mucocutaneous Triad
por: Wang, Liqing, et al.
Publicado: (2022)

Multisystemic Manifestations in Rare Diseases: The Experience of Dyskeratosis Congenita
por: Callea, Michele, et al.
Publicado: (2022)

Interstitial Lung Disease in a Patient with Dyskeratosis Congenita
por: Kim, Hyun Jung, et al.
Publicado: (2013)

DNA Damage Responses and Oxidative Stress in Dyskeratosis Congenita
por: Pereboeva, Larisa, et al.
Publicado: (2013)

DNA methylation in PRDM8 is indicative for dyskeratosis congenita
por: Weidner, Carola I., et al.
Publicado: (2016)

Pagetoid dyskeratosis of the forehead
por: Salphale, Pankaj, et al.
Publicado: (2014)

Molecular insight of dyskeratosis congenita: Defects in telomere length homeostasis
por: Dorgaleleh, Saeed, et al.
Publicado: (2022)

A CASE OF DYSKERATOSIS CONGENITA WITH PRIMARY AMENORRHEA AND ADENOCARCINOMA OF STOMACH
por: Chakrabarti, Nandini, et al.
Publicado: (2011)

Constitutional Mutations in RTEL1 Cause Severe Dyskeratosis Congenita
por: Walne, Amanda J., et al.
Publicado: (2013)

Dyskeratosis congenita induced cirrhosis for liver transplantation-perioperative management
por: Singh, Anshuman, et al.
Publicado: (2015)

A Case Report on a Rare Disease: Dyskeratosis Congenita
por: Shiferaw, Bethel, et al.
Publicado: (2015)

Dyskeratosis Congenita with DKC1 Mutation: A Case Report
por: Zhao, Xing-Yun, et al.
Publicado: (2020)

A Case of Membranous Aplasia Cutis Congenita and Dermoscopic Features
por: Lozano-Masdemont, Belén
Publicado: (2017)

Fatal bilateral pneumothoraces complicating dyskeratosis congenita: a case report
por: Boueiz, Adel, et al.
Publicado: (2009)

Novel Mutation of the TINF2 Gene in a Patient with Dyskeratosis Congenita
por: Panichareon, Benjaporn, et al.
Publicado: (2015)

The limitations of qPCR telomere length measurement in diagnosing dyskeratosis congenita
por: Gadalla, Shahinaz M., et al.
Publicado: (2016)

Frosted Branch Angiitis in Pediatric Dyskeratosis Congenita: A Case Report
por: Zheng, Xiao-Yu, et al.
Publicado: (2016)

p53 Mediates Failure of Human Definitive Hematopoiesis in Dyskeratosis Congenita
por: Fok, Wilson Chun, et al.
Publicado: (2017)

Dyskeratosis Congenita with Portal Hypertension and Oesophageal Webs: A Case Report
por: Khuraiya, Sandeep, et al.
Publicado: (2021)

Lipoprotein particle alterations due to androgen therapy in individuals with dyskeratosis congenita
por: Thompson, Mone't B., et al.
Publicado: (2021)

Dyskeratosis Congenita Links Telomere Attrition to  Age-Related Systemic Energetics
por: James, Emma Naomi, et al.
Publicado: (2023)

Incidental Focal Acantholytic Dyskeratosis in the Setting of Rosacea
por: Park, Sang-Yeon, et al.
Publicado: (2013)

Germline thymidylate synthase deficiency impacts nucleotide metabolism and causes dyskeratosis congenita
por: Tummala, Hemanth, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_6tkms1o3s7t2t72018eomsv2g7