Results 31 to 40 of about 7,686 (174)

Synthetic Ligands of Myeloid C‐Type Lectin Receptors

open access: yesChemBioChem, Volume 27, Issue 13, 14 July 2026.
Binding of ligands to C‐type lectin receptors (CLRs) on myeloid cells can lead to an array of cellular responses. Exploitation of these receptors for therapeutic purposes requires high‐affinity ligands. This review surveys the diversity of synthetic ligands of myeloid CLRs in the context of binding, signaling, and downstream effects, as well as ...
James Suri, Bernd Lepenies
wiley   +1 more source

LANGERHANS CELLS HISTIOCYTOSIS IN ONE FAMILY [PDF]

open access: yesActa Medica Iranica, 2004
Histiocytosis of Langerhans cells (class 1 histiocytosis) consists of a range of clinical manifestations, including bone eosinophilic granuloma, Hand-Schüller-Christian syndrome, and Letterer-Siwe disease. These syndromes represent a spectrum of severity
Sh. Ansari   +1 more
doaj   +1 more source

Periodontitis and Periodontal Conditions in Systemically Healthy Children and Adolescents

open access: yesJournal of Clinical Periodontology, Volume 53, Issue 7, Page 1100-1198, July 2026.
ABSTRACT Objective To answer the PICoS question ‘in systemically healthy children and adolescents (Population), what are the main features of periodontitis, necrotising periodontal diseases (NPD) and other periodontal conditions (periodontal abscesses, endo‐periodontal lesions, traumatic occlusal forces, prosthesis‐ and tooth‐related factors ...
Inbar Eshkol‐Yogev   +5 more
wiley   +1 more source

COMPROMISO OSEO EN HISTIOCITOSIS DE CELULAS DE LANGERHANS EN EL NIÑO: ESTUDIO RADIOLOGICO SIMPLE. PRESENTACION CLINICA Y DIAGNOSTICO RADIOLOGICO

open access: yesRevista Chilena de Radiología
Introducción. La Histiocitosis de células de Langerhans (HCL) es una patología poco frecuente, con diferentes manifestaciones radio-lógicas. Su causa es desconocida y se caracteriza por una proliferación de las células de Langerhans.
Raúl Rojas C   +7 more
doaj   +1 more source

Adult Langerhans cell histiocytosis with pulmonary and colorectoanal involvement: a case report

open access: yesJournal of Medical Case Reports, 2017
Background Langerhans cell histiocytosis is a rare systemic disease characterized by the abnormal overproduction of histiocytes that tend to infiltrate single or multiple organ systems leading to significant tissue damage. It mainly affects – by order of
Mohamad Jihad Mansour   +4 more
doaj   +1 more source

Gingival and Periodontal Diseases and Conditions in Children and Adolescents: Consensus Report

open access: yesJournal of Clinical Periodontology, Volume 53, Issue 7, Page 1068-1099, July 2026.
ABSTRACT Background The objectives of this Focused Workshop were to update the epidemiology, aetiology, risk factors, diagnosis and management of gingival and periodontal diseases and conditions in children and adolescents, and to explore the applicability of the 2018 Classification in children and adolescents.
Iain Chapple   +30 more
wiley   +1 more source

Diagnostic problems and surgical treatment of histiocytosis X [PDF]

open access: yesMedicinski Glasnik, 2007
A 16-year-old boy, with swelling and pain in the left submandibular region was treated at the Clinic for Maxillofacial Surgery. The x-ray examination showed destructive bone lesion of the mandibulae left side and oval lesions on the left hand bone and ...
Alkhalil M, A. Redžić, A. Smajilagić
doaj  

Pulmonary langerhans cell granulomatosis (histiocytosis X)

open access: yesТуберкулез и болезни лёгких, 2014
Pulmonary Langerhans cell granulomatosis is a rare disease. Its causes are unknown and accurate data on its prevalence are lacking. This disease is characterized by the formation of lung tissue granulomas consisting of activated Langerhans cells ...
A. A. Sadovnikov, K. I. Panchenko
doaj  

Clinical experience in an infant with Langerhans cell histiocytosis

open access: yesUniversidad Médica Pinareña, 2021
Introduction: Langerhans cell histiocytosis (LCH) or Histiocytosis X is a benign proliferative disease affecting dendritic cells. It presents a wide clinical spectrum, from isolated eosinophilic bone granuloma to multisystem involvement with multiple ...
Yamilka Pita Barrios   +2 more
doaj  

Secondary aneurysmal bone cyst in Langerhans cell histiocytosis: Case report, literature review

open access: yesEuropean Journal of Radiology Open, 2019
Langerhans cell histiocytosis (LCH) is a rare disease of the myeloid precursor cells, it predominantly occurs in the skull and long bones as unifocal bone lesions. Aneurysmal bone cysts (ABC) are benign, expansive and lytic bone. Reports of secondary ABC
P. Lomoro   +6 more
doaj   +1 more source

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