Works matching DE "CAROLI disease"
Results: 20
Rare Cause of Cholestasis: Caroli's Syndrome.
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- Anatolian Journal of Family Medicine, 2021, v. 4, n. 1, p. 102, doi. 10.5505/anatoljfm.2020.39205
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- Article
Molecular profiling of intrahepatic cholangiocarcinoma: the search for new therapeutic targets.
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- Expert Review of Gastroenterology & Hepatology, 2017, v. 11, n. 4, p. 349, doi. 10.1080/17474124.2017.1292127
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- Article
Caroli综合征合并常染色体显性遗传性多囊肾1例报告.
- Published in:
- 2017
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- Publication type:
- Case Study
Identification of occult active infection using PET- CT in a combined liver-kidney transplant candidate.
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- Transplant Infectious Disease, 2017, v. 19, n. 6, p. n/a, doi. 10.1111/tid.12776
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- Article
Abernethy malformation associated with Caroli's syndrome in a patient with a PKHD1 mutation: a case report.
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- Diagnostic Pathology, 2017, v. 12, p. 1, doi. 10.1186/s13000-017-0647-y
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- Article
Imaging manifestations of Caroli disease with autosomal recessive polycystic kidney disease: a case report and literature review.
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- 2021
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- Publication type:
- journal article
Imaging of fibropolycystic liver disease.
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- Abdominal Radiology, 2022, v. 47, n. 7, p. 2356, doi. 10.1007/s00261-022-03565-7
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- Article
Magnetic resonance imaging of fibropolycystic liver disease: the spectrum of ductal plate malformations.
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- Abdominal Radiology, 2019, v. 44, n. 6, p. 2156, doi. 10.1007/s00261-019-01966-9
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- Article
Central dot sign.
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- Abdominal Radiology, 2016, v. 41, n. 11, p. 2289, doi. 10.1007/s00261-016-0836-2
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- Article
Should Caroli's disease be in the Todani classification?
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- 2016
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- Letter
Response to letter on Caroli disease.
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- 2016
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- Publication type:
- Letter
Diffuse-Type Caroli Disease with Characteristic Central Dot Sign Complicated by Multiple Intrahepatic and Common Bile Duct Stones.
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- 2017
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- Publication type:
- Case Study
Surgical treatment for monolobular Caroli's disease ? Report of a 30-year single center case series.
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- BioScience Trends, 2018, v. 12, n. 4, p. 426, doi. 10.5582/bst.2018.01162
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- Article
A child with hypertension and ascitis.
- Published in:
- 2016
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- Publication type:
- Case Study
Diversity of renal phenotypes in patients with WDR19 mutations: Two case reports.
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- Nephrology, 2017, v. 22, n. 7, p. 566, doi. 10.1111/nep.12996
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- Article
Severe Hepatopulmonary Syndrome in a Child with Caroli Syndrome.
- Published in:
- 2017
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- Publication type:
- Case Study
Abnormalities of the biliary tract in patients with autosomal recessive polycystic kidney disease (ARPKD).
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- Polish Journal of Pediatrics / Pediatria Polska, 2020, v. 95, n. 4, p. 207, doi. 10.5114/POLP.2020.103463
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- Publication type:
- Article
Anaesthetic management of a child with Caroli's disease presenting for incidental surgery: A case report.
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- 2018
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- Publication type:
- Letter to the Editor
Left-hemihepatectomy as a method of treatment of locally limited Caroli disease.
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- Polish Journal of Surgery, 2013, v. 85, n. 11, p. 663, doi. 10.2478/pjs-2013-0100
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- Publication type:
- Article
Images of the Month.
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- American Journal of Gastroenterology (Springer Nature), 2015, v. 110, n. 4, p. 497, doi. 10.1038/ajg.2014.253
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- Article