Results 51 to 60 of about 28,795 (192)

Neonatal Bullous Urticaria Pigmentosa: Case Report

open access: yes, 2010
Mastocytosis is a heterogeneous group of diseases characterized by the abnormal infiltration of mast cells in the skin and other organs. The most common type of cutaneous mastocytosis in children is urticaria pigmentosa.
Ozkara, Sevgiye   +3 more
core   +1 more source

Mastocitose Mastocytosis

open access: yesAnais Brasileiros de Dermatologia, 2009
A mastocitose é caracterizada pelo acúmulo patológico e ativação de mastócitos nos tecidos e órgãos. Embora a classificação da mastocitose e seus critérios diagnósticos sejam bem aceitos, há necessidade de estabelecer parâmetros para aplicação de testes ...
Luciana Cirillo Maluf   +2 more
doaj   +1 more source

Urticaria Pigmentosa [PDF]

open access: yesThe Journal of Pediatrics, 2020
Avik Panigrahi   +2 more
openaire   +2 more sources

Gluten‐related skin disorders: clinical presentation, diagnostic and treatments

open access: yesJDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 7, Page 857-867, July 2025.
Summary Gluten‐related disorders (GRDs) encompass a spectrum of clinical manifestations triggered by gluten ingestion in genetically susceptible individuals. These disorders include celiac disease (CD) and non‐celiac gluten sensitivity (NCGS) and present with both intestinal and extraintestinal symptoms, including skin manifestations.
Dario Didona   +2 more
wiley   +1 more source

Scabies mimicking mastocytosis in two infants

open access: yesThe Turkish Journal of Pediatrics, 2013
Scabies is a common parasitic human infection in infants and children. However, diagnostic pitfalls are frequent in infants, in whom the clinical presentation is usually atypical and different from that in adults.
Emine Cölgeçen-Özel   +3 more
doaj  

Cutaneous Mastocytosis in Pediatric Patients With Skin of Color: A Retrospective Cohort Study

open access: yesPediatric Dermatology, Volume 42, Issue 4, Page 793-795, July/August 2025.
ABSTRACT Cutaneous mastocytosis (CM) is a rare skin disease with limited data on its prevalence across different racial groups. This retrospective cohort study examines the characteristics of CM at Nationwide Children's Hospital (NCH) from January 2010 to June 2022, identifying 192 confirmed cases of CM and further stratifying this cohort to 155 ...
Trent D. Walker   +4 more
wiley   +1 more source

The Report of a Very Rare Case of Peseudoxanthomatous Mastocytosis

open access: yesپزشکی بالینی ابن سینا, 2001
Diffuse cutaneous mastocytosis is very rare variety mast-cell disorder    which is called peseudoxanthomatous mastocytosis. Our case was a man    who was eighteen years old.
Mahmoud Farshchain   +2 more
doaj  

Illuminating Immunity: A Systematic Review of Immune Cell Autofluorescence

open access: yesJournal of Biophotonics, Volume 18, Issue 6, June 2025.
ABSTRACT Immunophenotyping provides valuable prognostic and diagnostic information, but is technically complex and expensive. The assessment of autofluorescence is label‐free and provides complex information on cell identity. However, research on its application to immunophenotyping has been heterogenous.
Aline Knab   +4 more
wiley   +1 more source

Clinical practice guidelines for the diagnosis and treatment of scabies

open access: yesInternational Journal of Dermatology, Volume 63, Issue 12, Page 1642-1656, December 2024.
Abstract Scabies, caused by the Sarcoptes scabiei var hominis mite burrowing into the skin, is a highly contagious disease characterized by intense nocturnal itching. Its global impact is considerable, affecting more than 200 million individuals annually and posing significant challenges to healthcare systems worldwide.
Soner Uzun   +24 more
wiley   +1 more source

Retinitis Pigmentosa GTPase Regulator (RPGR) protein isoforms in mammalian retina:insights into X-linked Retinitis Pigmentosa and associated ciliopathies [PDF]

open access: yes, 2008
Mutations in the cilia-centrosomal protein Retinitis Pigmentosa GTPase Regulator (RPGR) are a frequent cause of retinal degeneration. The RPGR gene undergoes complex alternative splicing and encodes multiple protein isoforms. To elucidate the function of
Hurd, Toby W   +6 more
core   +1 more source

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