Results 61 to 70 of about 2,806 (197)

Natural history and outcomes in drug induced autoimmune hepatitis [PDF]

open access: yes, 2016
Aim: Drug-induced autoimmune hepatitis (DIAIH) remains poorly characterized. Our aim was to assess natural history and outcomes in DIAIH. Methods: This was a retrospective cohort study.
Alla   +33 more
core   +1 more source

Diagnostics of Autoimmune Hepatitis Enabled by Non‐Invasive Clinical Proteomics

open access: yesAlimentary Pharmacology &Therapeutics, Volume 62, Issue 9, Page 901-919, November 2025.
Mass‐spectrometry‐based proteomic analyses of paired liver‐plasma samples from patients with AIH enabled discovery of numerous proteins showing high diagnostic accuracy. Proteomics may constitute a novel non‐invasive diagnostic tool for AIH if validated in larger, age‐ and sex‐matched cohorts.
Anne‐Sofie Houlberg Jensen   +20 more
wiley   +1 more source

Cytological diagnosis of Rosai–Dorfman disease: A study of twelve cases with emphasis on diagnostic challenges

open access: yesJournal of Cytology, 2020
Context: Rosai–Dorfman disease, also known as Sinus histiocytosis with massive lymphadenopathy, is a benign proliferative disorder of histiocytes. It typically affects lymph nodes; however, extranodal disease is being increasingly reported.
Rallapalli Rajyalakshmi   +5 more
doaj   +1 more source

Ultraviolet B (UVB) Radiation Induces Skin Alterations, Emperipolesis and Decreases the Erythroid-to-myeloid Ratio in Rats

open access: yesIndonesian Biomedical Journal
BACKGROUND: Ultraviolet B (UVB) radiation is commonly known to be related to skin inflammation. The inflammation process is orchestrated by many cell types, including immune cells.
Verda Farida   +3 more
doaj   +1 more source

Intrathoracic Rosai–Dorfman Disease in Elderly Patients: A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Rosai–Dorfman disease (RDD), a rare form of histiocytosis, predominantly affects young individuals. Clinically categorized into nodal and extranodal subtypes, the disease primarily involves systemic lymph nodes with possible involvement of other organs.
JianFeng Xiao, Li Ma, Wei Cao
wiley   +1 more source

A 50‐year‐old man with a 12‐year history of extensive pachymeningeal thickening

open access: yes
Brain Pathology, EarlyView.
Alyssa M. Lee   +3 more
wiley   +1 more source

Autoimmune gastrointestinal complications in patients with Systemic Lupus Erythematosus: case series and literature review [PDF]

open access: yes, 2016
The association of systemic lupus erythematosus (SLE) with gastrointestinal autoimmune diseases is rare, but has been described in the literature, mostly as case reports.
Agmon-Levin N   +101 more
core   +1 more source

Haga usted el diagnóstico: parte I

open access: yesRevista de la Asociación Colombiana de Dermatología y Cirugía Dermatológica
Haga usted el diagnóstico: parte I. Se trata de un trastorno proliferativo histiocítico, raro y generalmente benigno que afecta principalmente los ganglios linfáticos cervicales, sin embargo, puede tener afectación de la piel en el 10% de los casos, se
Erika Muñoz-Herrera   +2 more
doaj   +1 more source

Recommendations for the standardization of bone marrow disease assessment and reporting in children with neuroblastoma; on behalf of the International Neuroblastoma Response Criteria Bone Marrow Working Group [PDF]

open access: yes, 2017
BACKGROUND: The current study was conducted to expedite international standardized reporting of bone marrow disease in children with neuroblastoma and to improve equivalence of care.
Aronica   +39 more
core   +1 more source

Isolated localization of Rosai Dorfman disease as renal mass: a case report and review of literature

open access: yesThe Pan African Medical Journal, 2016
We report a rare case of an elderly woman presented with right renal mass with invasion of renal vein and several small lymphadenopathy in the hilar area .the diagnosis of kidney cancer is suspected and the patient underwent open radical nephrectomy ...
Aziz El Majdoub   +5 more
doaj   +1 more source

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