Results 71 to 80 of about 4,466,969 (285)

The Functional Role of Langerhans Cells [PDF]

open access: yes, 1980
Langerhans cells represent a subpopulation of mammalian epidermal cells. The recent findings that these cells are the only epidermal cells which express Fc-IgG receptors, C3 receptors and La antigens support the early suggestion that they are related to ...
Stingl, Georg   +3 more
core   +1 more source

Nail Disorders in Systemic Conditions

open access: yesJEADV Clinical Practice, EarlyView.
ABSTRACT Nail findings in children can be indicative of an underlying systemic disease. Many of these findings are seen in multiple entities and are not specific to one disease. The importance of specifically examining for these nail changes cannot be overstated.
Jane Sanders Bellet
wiley   +1 more source

Nail Toxicities Associated With Anticancer Therapies in Children

open access: yesJEADV Clinical Practice, EarlyView.
ABSTRACT Nail toxicities are a frequent yet often underrecognized component of dermatologic adverse events in children receiving anticancer therapies. Both conventional cytotoxic chemotherapy and newer targeted agents can affect the nail matrix, nail bed and periungual tissues, producing a broad spectrum of clinical manifestations that range from ...
Luca Rapparini, Michela Starace
wiley   +1 more source

Indeterminate Cell Histiocytosis: A Case Report

open access: yesKaohsiung Journal of Medical Sciences, 2004
Indeterminate cell histiocytosis is a rare neoplasm composed of cells with mixed characteristics of Langerhans cells and non-Langerhans cells. An otherwise healthy, 36-year-old woman presented with asymptomatic generalized papules and nodules that had ...
Chun-Hua Wang, Gwo-Shing Chen
doaj   +1 more source

Surface Coating of Islets of Langerhans by Activated Polyethylene Glycol [PDF]

open access: yesعلوم و تکنولوژی پلیمر, 2008
The final treatment for diabetes is transplantation of islets of Langerhans. One of the new proposed methods for immunological preservation of transplanted cells is coating of cell surface by polyethylene glycol.
S. Hashemi Najafabadi   +3 more
doaj   +1 more source

Langerhans Cell Histiocytosis [PDF]

open access: yesCancer Control, 2014
Langerhans cell histiocytosis (LCH) is a rare histiocytic disorder of unknown etiopathogenesis. Its clinical presentation is variable and ranges from isolated skin or bone disease to a life-threatening multisystem condition. LCH can occur at any age but is more frequent in the pediatric population. A neoplastic origin of this disease has been suggested
openaire   +2 more sources

Immunohistochemical staining of Langerhans cells in HPV-positive and HPV-negative cases of oral squamous cells carcinoma

open access: yesJournal of Applied Oral Science, 2011
The Human Papillomavirus (HPV) has been strongly implicated in development of some cases of oral squamous cell carcinoma (OSCC). However, the immunological system somehow reacts against the presence of this virus.
Karuza Maria Alves Pereira   +4 more
doaj   +2 more sources

An insight into the origin, distribution, and techniques of demonstration of Langerhans cells

open access: yesSRM Journal of Research in Dental Sciences, 2017
Langerhans cells (LCs), first described by Paul Langerhans, a German physician in 1868, are dendritic cells predominantly observed in the suprabasal layers of the epidermis and the oral epithelium.
Sarangi Snehanjan, Aich Ritesh
doaj   +1 more source

HIV-Infected Langerhans Cells Constitute a Significant Proportion of the Epidermal Langerhans Cell Population Throughout the Course of HIV Disease [PDF]

open access: yes, 1996
Human immunodeficiency virus (HIV) is known to infect Langerhans cells, but controversy still exists about the occurrence of HIV-infected Langerhans cells in the skin of HIV-infected individuals and about the density of epidermal Langerhans cells during ...
Kupper, Thomas S.   +2 more
core   +1 more source

Cutaneous Rosai‐Dorfman Disease With MAP2K1 Mutation Treated With Encorafenib and Binimetinib

open access: yesJEADV Clinical Practice, EarlyView.
ABSTRACT Rosai‐Dorfman disease (RDD) is a rare histiocytic disorder with unifocal to multisystemic involvement. Activating mutations in the MAPK/ERK pathway can occur in up to 50% of RDD cases. We report a case of cutaneous RDD (C‐RDD) with facial and truncal lesions harboring an activating MAP2K1 (MEK1) mutation that showed a complete response to a ...
Melike Ak   +2 more
wiley   +1 more source

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