Cargando…

Familial Epidermolysis Bullosa Pruriginosa

Detalles Bibliográficos
Autores principales:	Trivedi, Madhvi, Gupta, Lalit Kumar, Mittal, Asit, Khare, Ashok Kumar
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/PMC10231695/ https://www.ncbi.nlm.nih.gov/pubmed/37266102 http://dx.doi.org/10.4103/idoj.idoj_288_22

Ejemplares similares

Epidermolysis bullosa pruriginosa responding to dupilumab
por: Clawson, Rebecca C., et al.
Publicado: (2021)

Koebner's Phenomenon in Epidermolysis Bullosa Pruriginosa in an Infant
por: Pathania, Yashdeep S., et al.
Publicado: (2023)

Epidermolysis bullosa pruriginosa: A report of two cases
por: Pai, Varadraj Vasant, et al.
Publicado: (2014)

Misdiagnosed dystrophic epidermolysis bullosa pruriginosa: A case report
por: Wang, Zi, et al.
Publicado: (2021)

Epidermolysis bullosa pruriginosa: A case report of two first cousins
por: Zahoor, Maria
Publicado: (2023)

Low-dose naltrexone as treatment for epidermolysis bullosa pruriginosa–associated refractory pruritus
por: LaMonica, Lauren C., et al.
Publicado: (2023)

Adult-Onset Epidermolysis Bullosa Pruriginosa in a 52-Year-Old Filipino Female: A Case Report
por: Serquiña, Brice Patangan, et al.
Publicado: (2023)

An Incompletely Penetrant Novel Mutation in COL7A1 Causes Epidermolysis Bullosa Pruriginosa and Dominant Dystrophic Epidermolysis Bullosa Phenotypes in an Extended Kindred
por: Yang, Catherine S, et al.
Publicado: (2012)

A rare case of epidermolysis bullosa
por: Narendra, S. M., et al.
Publicado: (2013)

Pseudo Acne Fulminans: An Under Recognized Entity
por: Meena, Manju, et al.
Publicado: (2018)

Novel heterozygous COL7A1 mutation in a patient with de-novo dominant dystrophic epidermolysis bullosa pruriginosa
por: Rakasiwi, Tasya, et al.
Publicado: (2021)

Identification of a novel COL7A1 variant associated with dystrophic epidermolysis bullosa pruriginosa responding effectively to dupilumab
por: Zhao, Caichou, et al.
Publicado: (2023)

Anaesthetic management of a rare case of paediatric epidermolysis bullosa
por: Singh, Shalendra, et al.
Publicado: (2019)

Herpes zoster in infancy
por: Gupta, Lalit Kumar, et al.
Publicado: (2013)

Dystrophic Epidermolysis Bullosa
por: Yadav, Randhir Sagar, et al.
Publicado: (2018)

Trigeminal trophic syndrome
por: Gupta, Lalit Kumar, et al.
Publicado: (2016)

Genetic diagnosis of a rare COL7A1 variant causing dystrophic epidermolysis bullosa pruriginosa through whole‑exome sequencing
por: Yang, Yanhui, et al.
Publicado: (2023)

Topical diacerein for epidermolysis bullosa: a randomized controlled pilot study
por: Wally, Verena, et al.
Publicado: (2013)

Gastrostomy for infants with severe epidermolysis bullosa simplex in neonatal intensive care
por: Marro, M., et al.
Publicado: (2021)

Tranilast Can be a Useful Addition to the Limited Anti-Epidermolysis Bullosa Weaponry
por: Parvizi, Mohammad Mahdi, et al.
Publicado: (2017)

EGFR inhibition for metastasized cutaneous squamous cell carcinoma in dystrophic epidermolysis bullosa
por: Diociaiuti, Andrea, et al.
Publicado: (2019)

Topical ropivacaine for analgesia of aplasia cutis congenita in newborns with hereditary epidermolysis bullosa
por: Chambelland, A., et al.
Publicado: (2020)

Role of regional anaesthesia in a patient with epidermolysis bullosa dystrophica for emergency surgery
por: Arikrishnan, Thirumurugan, et al.
Publicado: (2021)

Current Scenario of Childhood Leprosy at a Tertiary Care Hospital in Southern Rajasthan
por: Balai, Manisha, et al.
Publicado: (2017)

Nevoid Psoriasis Coexisting with Verrucous Epidermal Nevus
por: Masatkar, Vaishali, et al.
Publicado: (2017)

Epidermolysis bullosa acquisita()
por: Miyamoto, Denise, et al.
Publicado: (2022)

Inherited epidermolysis bullosa
por: Fine, Jo-David
Publicado: (2010)

Congenital Triangular Alopecia: A Close Mimicker of Alopecia Areata
por: Gupta, Lalit K, et al.
Publicado: (2011)

A study of postherpetic pruritus
por: Mittal, Asit, et al.
Publicado: (2016)

Sporadic form of epidermolysis bullosa simplex with mottled pigmentation()()
por: Ferreira, Flávia Regina, et al.
Publicado: (2020)

Basal pharmacokinetic parameters of topically applied diacerein in pediatric patients with generalized severe epidermolysis bullosa simplex
por: Ablinger, Michael, et al.
Publicado: (2018)

Digenic Mutations in Junctional Epidermolysis Bullosa in An Iranian Family
por: Riahi, Kourosh, et al.
Publicado: (2021)

Revertant Mosaicism in Epidermolysis Bullosa
por: Meyer-Mueller, Cameron, et al.
Publicado: (2022)

The Epidermolysis bullosa house in Salzburg
por: Pohla-Gubo, Gabriela
Publicado: (2010)

Pretibial dystrophic epidermolysis bullosa
por: Callegaro, Elisabeth de Albuquerque Cavalcanti, et al.
Publicado: (2017)

Dystonin modifiers of junctional epidermolysis bullosa and models of epidermolysis bullosa simplex without dystonia musculorum
por: Sproule, Thomas J., et al.
Publicado: (2023)

Dominant Dystrophic Epidermolysis Bullosa with a Mutation in COL7A1 Confirmed by Diagnostic Exome Sequencing
por: Won, Sang-Hyeon, et al.
Publicado: (2022)

A de novo missense mutation in the NC1 domain of type VII collagen leads to dystrophic epidermolysis bullosa
por: Cheng, Ping, et al.
Publicado: (2022)

Long-term follow-up of epidermolysis bullosa in real practice shows stability of the Epidermolysis Bullosa Disease Activity and Scarring Index and improvement with some off-label therapies
por: Ho, Genevieve, et al.
Publicado: (2022)

The risk of cardiomyopathy in inherited epidermolysis bullosa
por: Fine, J-D, et al.
Publicado: (2008)

Cannot write session to /tmp/vufind_sessions/sess_gnhjvf6pgjdh1g14llmb117d2j