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Syndromic classification of hereditary lymphedema.

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Traumatic injury of the thoracic duct.

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An imaging evaluation of angiodysplasia syndromes.

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Segregation analyses and a genome-wide linkage search confirm genetic heterogeneity and suggest oligogenic inheritance in some Milroy congenital primary lymphedema families.

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Pharmacokinetic Predictor of Infection in Patients With Inflammatory Bowel Disease Treated With Intravenous and Subcutaneous Infliximab.

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Sloughing Esophagitis: A Self-Limited Condition Associated With Debilitation and Polypharmacy? A Large Sample Analysis.

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Global Action in Addressing the Challenge of Environmental Change and Digestive Health: A Report Card on Progress.

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Transformer-Based Deep Learning Framework for Automated Lesion Detection in Capsule Endoscopy: A Comparative Study With CNN Architectures.

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Real-World Study of Clinical Outcomes in Patients With Spontaneous Bacterial Peritonitis Receiving Albumin: Impact of Multidrug-Resistant Organisms From 2012 to 2022.

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Suspected Small Bowel Bleeding: A Single-Center Retrospective Study on Long-Term Prognosis and Predictive Factors.

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Vexas Syndrome: A Multisystem Challenge with Sweet Syndrome and Myelodysplastic Syndrome.

European journal of case reports in internal medicine·2026

Soft tissue sarcoma invasion of the humerus via the nutrient foramen in a dog.

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Blood pressure, electrolyte and fluid balance in horses with insulin dysregulation after short-term treatment with canagliflozin.

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Rare forms of small intestinal diverticulum and diagnostic features. A clinical case report.

Frontiers in surgery·2026

Characterisation of Haemolytic Uropathogenic Escherichia coli Isolated From Dogs and Cats.

Veterinary medicine and science·2026

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Is vagotomy and gastrectomy still justified for gastroduodenal ulcer?

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Lymphedema-distichiasis syndrome without FOXC2 mutation: evidence for chromosome 16 duplication upstream of FOXC2.

Syndromic classification of hereditary lymphedema.

Traumatic injury of the thoracic duct.

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Segregation analyses and a genome-wide linkage search confirm genetic heterogeneity and suggest oligogenic inheritance in some Milroy congenital primary lymphedema families.

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