Works matching DE "HEPATOLENTICULAR degeneration diagnosis"
Results: 133
Wilson disease tissue classification and characterization using seven artificial intelligence models embedded with 3D optimization paradigm on a weak training brain magnetic resonance imaging datasets: a supercomputer application.
- Published in:
- Medical & Biological Engineering & Computing, 2021, v. 59, n. 3, p. 511, doi. 10.1007/s11517-021-02322-0
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- Publication type:
- Article
Biochemical diagnosis of Wilson's disease: an update.
- Published in:
- Advances in Laboratory Medicine / Avances en Medicina de Laboratorio, 2022, v. 3, n. 2, p. 103, doi. 10.1515/almed-2022-0020
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- Publication type:
- Article
Abstract- Poster.
- Published in:
- 2022
- Publication type:
- Abstract
Abstract- Poster.
- Published in:
- 2022
- Publication type:
- Abstract
Adolescent onset Wilson's disease misdiagnosed as psychosis.
- Published in:
- 2016
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- Publication type:
- Case Study
A child with abdominal pain, arthralgia, palpable skin rash, hepatosplenomegaly, and pancytopenia: Answers.
- Published in:
- Pediatric Nephrology, 2023, v. 38, n. 6, p. 1771, doi. 10.1007/s00467-022-05750-8
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- Publication type:
- Article
Nephrotic range proteinuria in an adolescent with a diagnosis of Wilson's disease: Questions.
- Published in:
- 2021
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- Publication type:
- Test/Instrument
A special case of recurrent gross hematuria: Answers.
- Published in:
- Pediatric Nephrology, 2017, v. 32, n. 2, p. 273, doi. 10.1007/s00467-015-3265-5
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- Publication type:
- Article
Gross hematuria in a case of Wilson disease: Answers.
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- Pediatric Nephrology, 2012, v. 27, n. 6, p. 919, doi. 10.1007/s00467-011-2011-x
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- Publication type:
- Article
Gross hematuria in a case of Wilson disease: Questions.
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- Pediatric Nephrology, 2012, v. 27, n. 6, p. 917, doi. 10.1007/s00467-011-2007-6
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- Publication type:
- Article
Molecular Genetics Diagnosis of Wilson Disease: the First Reported Case of ATP7B Gene Mutation at Codon 778 in Southwest Iran.
- Published in:
- 2012
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- Publication type:
- Case Study
Comparison of MRI, EEG, EPs and ECD-SPECT in Wilson's disease.
- Published in:
- Acta Neurologica Scandinavica, 2001, v. 103, n. 2, p. 71, doi. 10.1034/j.1600-0404.2001.103002071.x
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- Publication type:
- Article
Kayser-Fleischer rings of acute Wilson's disease.
- Published in:
- Baylor University Medical Center Proceedings, 2013, v. 26, n. 2, p. 166, doi. 10.1080/08998280.2013.11928948
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- Publication type:
- Article
Morbus Wilson und Multiple Sklerose. Eine Koinzidenz.
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- Der Nervenarzt, 2010, v. 81, n. 2, p. 226, doi. 10.1007/s00115-009-2876-0
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- Publication type:
- Article
A study of the non-motor neurological symptoms of Wilson's disease and its correlation with global disease severity and motor symptoms.
- Published in:
- 2022
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- Publication type:
- Abstract
Unusual Confluence: Exploring the Association of Biliary Atresia, Wilson Disease, and Iron Overload.
- Published in:
- ACG Case Reports Journal, 2024, v. 11, n. 10, p. 1, doi. 10.14309/crj.0000000000001500
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- Publication type:
- Article
Dysregulation of Copper Metabolism in a Patient With Acute-on-Chronic Liver Failure Worked up for Fulminant Wilson Disease.
- Published in:
- ACG Case Reports Journal, 2023, v. 10, n. 7, p. 1, doi. 10.14309/crj.0000000000001084
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- Publication type:
- Article
A Novel Mutation in the ATP7B Gene: A Rare Manifestation of Wilson Disease With Liver Failure.
- Published in:
- ACG Case Reports Journal, 2023, v. 10, n. 2, p. 1, doi. 10.14309/crj.0000000000000977
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- Publication type:
- Article
A Rare Case of Wilson Disease in a 72-Year-Old Patient.
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- ACG Case Reports Journal, 2019, v. 6, n. 3, p. 1, doi. 10.14309/crj.0000000000000024
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- Publication type:
- Article
Value of histochemical stains for copper in the diagnosis of paediatric copper storage disorders.
- Published in:
- Histopathology, 1999, v. 34, n. 5, p. 471, doi. 10.1046/j.1365-2559.1999.00676.x
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- Publication type:
- Article
Maligniteyi Taklit Eden Wilson Hastalığı Olgusu.
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- Medical Bulletin of Haseki / Haseki Tip Bulteni, 2014, v. 52, n. 1, p. 64, doi. 10.4274/Haseki.1297
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- Publication type:
- Article
Case 1: A 12-year-old boy with acute liver failure.
- Published in:
- 2016
- By:
- Publication type:
- Case Study
Case 2: A teenager with nausea, vomiting and dysarthria.
- Published in:
- 2013
- By:
- Publication type:
- Case Study
Psychological Signs as the Only Presentation of Wilson's Disease in an 11-Year-Old Boy.
- Published in:
- Iranian Journal of Child Neurology, 2018, v. 12, n. 2, p. 113
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- Publication type:
- Article
Rare Initial Presentation of Wilson's Disease as Acute Encephalopathy with Recurrent Seizure.
- Published in:
- Oman Medical Journal, 2023, v. 38, n. 2, p. 33, doi. 10.5001/omj.2023.17
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- Publication type:
- Article
Exchangeable copper: a reflection of the neurological severity in Wilson's disease.
- Published in:
- European Journal of Neurology, 2017, v. 24, n. 1, p. 154, doi. 10.1111/ene.13171
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- Publication type:
- Article
Autoimmune Hepatitis or Wilson's Disease, a Clinical Dilemma.
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- Hepatitis Monthly, 2013, v. 13, n. 5, p. 1, doi. 10.5812/hepatmon.7872
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- Publication type:
- Article
Hypercalciuria and Nephrocalcinosis as Early Feature of Wilson Disease Onset: Description of a Pediatric Case and Literature Review.
- Published in:
- Hepatitis Monthly, 2012, v. 12, n. 8, p. 1, doi. 10.5812/hepatmon.6233
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- Publication type:
- Article
Wilson disease in children and young adults - State of the art.
- Published in:
- Saudi Journal of Gastroenterology, 2022, v. 28, n. 1, p. 21, doi. 10.4103/sjg.sjg_501_21
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- Publication type:
- Article
Presentation, Diagnosis and Outcome of Predominantly Hepatic Wilson's Disease in Adult Saudi Patients: A Single Centre Experience.
- Published in:
- Saudi Journal of Gastroenterology, 2012, v. 18, n. 5, p. 334, doi. 10.4103/1319-3767.101135
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- Publication type:
- Article
Genetic analysis of 55 northern Vietnamese patients with Wilson disease: seven novel mutations in ATP7B.
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- Journal of Genetics, 2017, v. 96, n. 6, p. 933, doi. 10.1007/s12041-017-0857-9
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- Publication type:
- Article
Wilson’s disease with superimposed autoimmune features: Report of two cases and review.
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- Journal of Gastroenterology & Hepatology, 2000, v. 15, n. 5, p. 570, doi. 10.1046/j.1440-1746.2000.02158.x
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- Publication type:
- Article
Uneven distribution of hepatic copper concentration and diagnostic value of double-sample biopsy in Wilson's disease.
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- Scandinavian Journal of Gastroenterology, 2013, v. 48, n. 12, p. 1452, doi. 10.3109/00365521.2013.845904
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- Publication type:
- Article
ERKEN ÇOCUKLUK ÇAĞINDA WILSON HASTALARIN TANISAL ZORLUKLARI.
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- Journal of Current Pediatrics / Guncel Pediatri, 2020, v. 18, n. 1, p. 41, doi. 10.4274/jcp.2020.0004
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- Publication type:
- Article
Wilson disease: a most unusual patient.
- Published in:
- QJM: An International Journal of Medicine, 2016, v. 109, n. 2, p. 117, doi. 10.1093/qjmed/hcv142
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- Publication type:
- Article
Decompensated Liver Disease in a Patient with Neurocysticercosis.
- Published in:
- 2017
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- Publication type:
- journal article
Wilson's Disease Presents as Recurrent Hypokalemic Muscle Paralysis.
- Published in:
- Indian Journal of Nephrology, 2023, v. 33, n. 4, p. 292, doi. 10.4103/ijn.ijn_143_22
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- Publication type:
- Article
IgA Nephropathy with Wilson's Disease: A Case Report and Literature Review.
- Published in:
- Indian Journal of Nephrology, 2021, v. 31, n. 5, p. 474, doi. 10.4103/ijn.IJN_227_20
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- Publication type:
- Article
D‑penicillamine‑induced membranous nephropathy.
- Published in:
- 2014
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- Publication type:
- Letter to the Editor
A WEB SERVICE-BASED MOBILE APPLICATION FOR DETECTING KAYSER-FLEISCHER RING IN EYE CORNEA.
- Published in:
- Instrumentation Science & Technology, 2014, v. 42, n. 1, p. 95, doi. 10.1080/10739149.2013.841190
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- Publication type:
- Article
Epigenomic signatures in liver and blood of Wilson disease patients include hypermethylation of liver-specific enhancers.
- Published in:
- Epigenetics & Chromatin, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13072-019-0255-z
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- Publication type:
- Article
The homozygosity index (HI) approach reveals high allele frequency for Wilson disease in the Sardinian population.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 11, p. 1308, doi. 10.1038/ejhg.2013.43
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- Publication type:
- Article
Dysphagia as the First Symptom in Wilson Disease: A Case Report.
- Published in:
- 2013
- By:
- Publication type:
- Case Study
Study on Lesion Assessment of Cerebello-Thalamo-Cortical Network in Wilson’s Disease with Diffusion Tensor Imaging.
- Published in:
- Neural Plasticity, 2017, p. 1, doi. 10.1155/2017/7323121
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- Publication type:
- Article
Characteristics of a newly diagnosed Polish cohort of patients with neurological manifestations of Wilson disease evaluated with the Unified Wilson's Disease Rating Scale.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Comparative assessment of clinical rating scales in Wilson's disease.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Clinical features and outcome in patients with osseomuscular type of Wilson's disease.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Accuracy of the radioactive copper incorporation test in the diagnosis of Wilson disease.
- Published in:
- Liver International, 2018, v. 38, n. 10, p. 1860, doi. 10.1111/liv.13715
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- Publication type:
- Article
Relative exchangeable copper: A valuable tool for the diagnosis of Wilson disease.
- Published in:
- Liver International, 2018, v. 38, n. 2, p. 350, doi. 10.1111/liv.13520
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- Publication type:
- Article
Unique CT imaging findings of liver in Wilson's disease.
- Published in:
- 2011
- By:
- Publication type:
- journal article