Results 101 to 110 of about 6,997 (197)

Overlap of Primary Biliary Cholangitis and Systemic Sclerosis: A Case of Reynolds Syndrome

open access: yesClinical Case Reports, Volume 14, Issue 8, August 2026.
ABSTRACT Reynolds Syndrome should be suspected in CREST patients with persistent cholestatic liver enzymes, since delayed diagnosis allows portal hypertension and variceal bleeding to develop. Early anti‐mitochondrial antibody screening and prompt ursodeoxycholic acid therapy improve outcomes, and these patients need multidisciplinary follow‐up for ...
Ali Gohar   +9 more
wiley   +1 more source

SCLERODERMA IN PEDIATRIC AGE GROUP: REPORT OF 25 CASES [PDF]

open access: yesActa Medica Iranica, 1999
Scleroderma is a multisystem autoimmune connective tissue disease, cliaracterized by hardening of the skin. HV had 25 patients in the Iranian Pediatric Unit of Rheumatology over 10 years.
M.H.Moradi-Nejad
doaj  

Sex Differences in Social, Health, and Lifestyle Characteristics Associated With Binge‐Eating Behaviors: Results From a French National Random Population‐Based Study

open access: yesInternational Journal of Eating Disorders, Volume 59, Issue 8, Page 1814-1825, August 2026.
ABSTRACT Objective To explore sex differences in social, health and lifestyle characteristics associated with binge‐eating behaviors in a large population‐based study. Method This study included 84,995 participants (women 52.1%) aged ≥ 15 years from the French national random population‐based EpiCov cohort.
Junko Kose   +21 more
wiley   +1 more source

Nodular Scleroderma in a Patient With Anti–RNA Polymerase III–Antibody Positive Systemic Sclerosis: A Case Report and Literature Review

open access: yesThe Journal of Dermatology, Volume 53, Issue 8, Page 1213-1216, August 2026.
ABSTRACT Nodular scleroderma (NS) is a rare manifestation of systemic sclerosis (SSc) that can clinically resemble keloids, often leading to diagnostic difficulty. Herein we report a case of a 76‐year‐old woman with anti–RNA polymerase III antibody–positive SSc who developed progressive erythematous, pruritic, keloid‐like plaques 3 months after ...
Kyoko Kanno   +2 more
wiley   +1 more source

Interleukin‐40 in Systemic Sclerosis: A Treatment‐Sensitive Marker of Immune Modulation Rather Than Disease Activity

open access: yesClinical and Translational Science, Volume 19, Issue 8, August 2026.
ABSTRACT Interleukin‐40 (IL‐40) is a recently identified cytokine primarily produced by activated B cells and implicated in immune regulation across several autoimmune diseases. Although B cell–driven immune dysregulation plays a central role in systemic sclerosis (SSc), the circulating behavior and clinical relevance of IL‐40 in this disease remain ...
İbrahim Vasi   +13 more
wiley   +1 more source

Non-specific cutaneous lupus erythematosus and clinical significance: a literature review

open access: yesJournal of Rheumatic Diseases
Cutaneous lupus erythematosus (CLE) is classified into LE-specific cutaneous lesions and LE-non-specific cutaneous lesions. LE-specific lesions, which include acute cutaneous LE, sub-acute cutaneous LE, and chronic cutaneous LE have been well-described ...
Nattanicha Chaisrimaneepan   +3 more
doaj   +1 more source

Performance of Leptopilina japonica Novković and Kimura (Hymenoptera: Figitidae) Under Fluctuating Temperature and Humidity

open access: yesEntomologia Experimentalis et Applicata, Volume 174, Issue 8, Page 876-886, August 2026.
Temperature is an important factor to determine the activity of insects. We tested the performance of the non‐native larval parasitoid Leptopilina japonica (Hymenoptera: Figitidae) under realistic climatic conditions to improve understanding about its ongoing spread and seasonal abundance.
Jakob Martin   +2 more
wiley   +1 more source

Rosai-Dorfman Disease with nodal and extranodal involvements: A case report

open access: yesJournal of Research in Medical Sciences, 2011
Rosai-Dorfman disease (RDD) is a rare lymphoproliferative disorder with nodal and extranodal involvements. Here we report a case of RDD in a 15-year-old female who presented with epigastric pain, fatigue, Raynaud phenomenon in fingers, submandibular ...
Mehri Najafi-Sani   +2 more
doaj  

A Case of Multidisciplinary Treatment for Deficiency of Adenosine Deaminase 2

open access: yes罕见病研究
This case report presents a 16-year-old male patient with deficiency of adenosine deaminase 2(DADA2). The patient had a history of Raynaud′s phenomenon with digital ulcers since childhood.
ZHANG Jingyuan   +13 more
doaj   +1 more source

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