Results 101 to 110 of about 61,964 (279)
Arthritis &Rheumatology, Accepted Article.Objectives The Assessment of SpondyloArthritis international Society recently defined early axial spondyloarthritis (axSpA) as a duration ≤2 years of axial symptoms. Previous studies have shown no significant difference in short‐term outcomes between early and established axSpA patients treated with biologic/targeted synthetic disease‐modifying anti ...
Annik Steimer +18 more
wiley +1 more source
The localised scleroderma and associated autoimmune diseases
, 2015 A lokalizált scleroderma egy ritka, kötőszöveti megbetegedés, mely a bőr sclerosis-ában, különböző formájú, és alakú plakkokban nyilvánul meg a gyulladás, sclerosis, atrophia jeleivel.
Kocsis, Ivett
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European Eating Disorders Review, EarlyView.ABSTRACT Objective Chronic malnutrition, hypothermia, and hormonal imbalance in anorexia nervosa (AN) may impair capillary structure and perfusion. This study aimed to describe the nailfold videocapillaroscopy (NVC) findings in adolescents with AN and atypical AN (AAN), to assess their association with Raynaud's phenomenon (RP), and evaluate ...
Muserref Kasap‐Cuceoglu +9 more
wiley +1 more source
Emergency Surgery in a Patient with Scleroderma - Anaesthetic Challenges: A Case Report [PDF]
, 2013 Scleroderma (progressive systemic sclerosis) is a multisystem disease involving the skin, airway, musculoskeletal, gastrointestinal, pulmonary, renal and cardiac systems that can pose a significant challenge for the anaesthetist.
Teena Bansal Sarla Hooda
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Parenteral nutrition and hospital outcomes in Australian adults: A descriptive cohort study
Journal of Parenteral and Enteral Nutrition, EarlyView.Abstract Background There is limited information regarding real‐world use of parenteral nutrition in hospitals. The objective of the study was to provide a real‐world description of parenteral nutrition administration in hospitalized patients. Methods This was a descriptive cohort study in 507 hospitalized adults who received parenteral nutrition at ...
Frank M. P. van Haren +16 more
wiley +1 more source
Carcinoid Syndrome-Induced Scleroderma-Like Disease
Dermatopathology, 2019 Scleroderma is a rare complication of carcinoid syndrome and is usually encountered in the setting of a metastatic primary neuroendocrine tumour of the distal ileum.
Karen Koch, Wayne Grayson
doaj +1 more source
Nephrogenic Systemic Fibrosis: A Rare Contemporary Case After a Decade of Declining Incidence
JEADV Clinical Practice, EarlyView.ABSTRACT Nephrogenic systemic fibrosis (NSF) is a rare fibrosing disorder associated with exposure to gadolinium‐based contrast agents in patients with renal impairment. Although its incidence has markedly declined since the restriction of high‐risk linear gadolinium agents, sporadic cases may still occur.
Marta Sánchez Díaz +5 more
wiley +1 more source
Rosiglitazone alleviates the persistent fibrotic phenotype of lesional skin scleroderma fibroblasts
, 2010 Objective - The transcription factor peroxisome proliferator-activated receptor (PPAR)-γ plays an important role in controlling cell differentiation. The aim of the present study was to examine whether PPAR-γ expression was reduced in skin scleroderma ...
Stratton, R.J. +5 more
core +1 more source
Paraneoplastic scleroderma or neoplasia secondary to scleroderma [PDF]
, 2019 Scleroderma is one of the rare illnesses from the group of autoimmune diseases, with unclear etiology, that starts with skin involvement and leads to systemic complications.
Alexandru Arvunescu +1 more
core +2 more sources