Found: 14
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Hepatic manifestations of hereditary haemorrhagic telangiectasia.
- Published in:
- Liver International, 2024, v. 44, n. 9, p. 2220, doi. 10.1111/liv.16008
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- Article
Analysis of ENG and ACVRL1 genes in 137 HHT Italian families identifies 76 different mutations (24 novel). Comparison with other European studies.
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- Journal of Human Genetics, 2007, v. 52, n. 10, p. 820, doi. 10.1007/s10038-007-0187-5
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- Article
Liver involvement in hereditary hemorrhagic telangiectasia.
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- Abdominal Radiology, 2018, v. 43, n. 8, p. 1920, doi. 10.1007/s00261-018-1671-4
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- Article
The Role of Endoscopic Ultrasound and Ancillary Techniques in the Diagnosis of Autoimmune Pancreatitis: A Comprehensive Review.
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- Diagnostics (2075-4418), 2024, v. 14, n. 12, p. 1233, doi. 10.3390/diagnostics14121233
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- Article
Endoscopic ultrasonography and small‐bowel endoscopy: Present and future.
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- Digestive Endoscopy, 2019, v. 31, n. 6, p. 627, doi. 10.1111/den.13429
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- Article
Upper Gastrointestinal Endoscopy Quality in Italy: A Nationwide Study.
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- Journal of Gastrointestinal & Liver Diseases, 2023, v. 32, n. 4, p. 433, doi. 10.15403/jgld-5059
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- Article
Oxytocin inhibits the stimulatory effect of ghrelin on circulating neuropeptide Y levels in humans.
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- Journal of Neural Transmission, 2008, v. 115, n. 9, p. 1265, doi. 10.1007/s00702-008-0057-0
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- Article
Focal Active Colitis: What Are Its Clinical Implications? A Narrative Review.
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- Biomedicines, 2023, v. 11, n. 10, p. 2631, doi. 10.3390/biomedicines11102631
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- Article
Adrenocorticotropin/Cortisol and Arginine-Vasopressin Secretory Patterns in Response to Ghrelin in Normal Men.
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- Neuroendocrinology, 2005, v. 81, n. 2, p. 103, doi. 10.1159/000085541
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- Article
Hereditary haemorrhagic telangiectasia in North African and sub-Saharan patients.
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- SAMJ: South African Medical Journal, 2014, v. 104, n. 4, p. 256, doi. 10.7196/SAMJ.7816
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- Article
Dietary iron intake and anemia: food frequency questionnaire in patients with hereditary hemorrhagic telangiectasia.
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- 2020
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- Publication type:
- journal article
European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT).
- Published in:
- 2020
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- Publication type:
- journal article
Natural history and outcome of hepatic vascular malformations in a large cohort of patients with hereditary hemorrhagic teleangiectasia.
- Published in:
- 2011
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- Publication type:
- journal article
Hereditary hemorrhagic telangiectasia: First demonstration of a founder effect in Italy; the ACVRL1 c.289_294del variant originated in the country of Bergamo 200 years ago.
- Published in:
- Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 8, p. 1, doi. 10.1002/mgg3.1972
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- Publication type:
- Article