Results 81 to 90 of about 521,586 (254)

Exploration of common genomic signatures of systemic juvenile rheumatoid arthritis and type 1 diabetes. [PDF]

Sci Rep, 2023
Zheng J, Wang Y, Fang X, Hu J.
europepmc   +1 more source

Association of attention‐deficit/hyperactivity disorder and autism with inflammatory bowel disease activity

Journal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Objectives To estimate the effect of attention deficit hyperactivity disorder (ADHD) and autism on the disease activity of inflammatory bowel disease (IBD) in pediatric and young patients. Methods Patients diagnosed with IBD between the ages of 6 and 24 years were identified in Danish nationwide registries 1996–2022.
Sabine Jansson, Mads Damsgaard Wewer, Johan Burisch, Matthew P. Fox, Michael E. Benros, Charlotte Ulrikka Rask, Vibeke Wewer, Mikkel Malham   +7 more
wiley   +1 more source

Juvenile Rheumatoid Arthritis

, 2017
Juvenile Rheumatoid Arthritis (JRA) or usually also called Still's disease, is a chronic disease occurring in children with the clinical signs and symptoms of joint involvement and systemic manifestation.
S. Zulkifli, Maimunah Affandi, Bambang Madiono   +2 more
core   +1 more source

CNS Complications of Rheumatoid Arthritis

Pediatric Neurology Briefs, 1991
Mass lesions in the basal ganglia bilaterally and mainly involving the globus pallidus are reported in a two year old boy with juvenile rheumatoid arthritis from the Department of Pediatrics, Hokushin General Hospital, Nishi, Nagano, Japan.
J Gordon Millichap
doaj   +1 more source

Effectiveness of Early Physical Therapy Rehabilitation in Patient With Juvenile Rheumatoid Arthritis. [PDF]

Cureus, 2022
Meghe S, Chitale N, Phansopkar P, Joshi A.   +3 more
europepmc   +1 more source

A nationwide multicenter observational study on childhood scurvy in Japan

Journal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Objectives Although scurvy is rare in developed countries, cases in children with selective diets due to neurodevelopmental disorders have been increasingly reported in Japan. In this nationwide multicenter observational study, we aimed to clarify the clinical characteristics and diagnostic challenges faced by children with scurvy in Japan ...
Yu Masuda, Ryohei Fukatsu, Ryosuke Miyamoto, Hitoshi Honma, Yoshinori Ito, Hiromichi Shoji, Masanobu Kawai, Yuri Etani, Toshiaki Shimizu, Akihisa Okumura   +9 more
wiley   +1 more source

A Rare Occurrence of Scleromalacia Perforans With Juvenile Rheumatoid Arthritis: A Case Report. [PDF]

Cureus, 2022
Wanjari MB, Lohakare T, Potdukhe A, Munjewar PK, Kantode VV.   +4 more
europepmc   +1 more source

Temporal Trends in Janus Kinase Inhibitor (JAKi) Use Across Five European Countries: A DARWIN EU Network Study [PDF]

Pharmacoepidemiol Drug Saf
ABSTRACT Introduction Janus kinase inhibitors (JAKi) are increasingly used for autoimmune conditions despite existing safety concerns. This study aims to estimate the incidence of new JAKi use over time and characterise users in Europe to support future safety studies.
Chen X, Barbulescu A, Corby G, Hayati S, Jodicke A, Lehtonen T, Nordeng H, Pacurariu A, Sanfélix‐Gimeno G, Trinh N, Verhamme K, Vojinovic D, Prieto‐Alhambra D, Lam A, Burn E.   +14 more
europepmc   +2 more sources

Nail Psoriasis in Pediatric Populations

JEADV Clinical Practice, EarlyView.
ABSTRACT Pediatric nail psoriasis is an under‐recognized yet clinically important manifestation of psoriasis with both diagnostic and prognostic implications. Nail involvement in children is associated with greater overall disease severity, poorer treatment outcomes, and is a predictor for the development of psoriatic arthritis.
Aditya K. Gupta, Elizabeth Teasell, Federico Quadrelli, Bianca Maria Piraccini   +3 more
wiley   +1 more source

Familial Blau syndrome:First molecularly confirmed report from India

Indian Journal of Ophthalmology, 2019
Blau syndrome (BS) is a rare autoinflammatory disorder characterized by the clinical triad of arthritis, uveitis, and dermatitis due to heterozygous gain-of-function mutations in the NOD2 gene.
Mahesh Janarthanan, Chanchal Poddar, S Sudharshan, Luis Seabra, Yanick J Crow   +4 more
doaj   +1 more source