Diagnosis and phenotypic classification of Wilson disease<sup>1</sup>.
- Published in:
- Liver International, 2003, v. 23, n. 3, p. 139, doi. 10.1034/j.1600-0676.2003.00824.x
- By:
- Publication type:
- Article
Works by Loudianos, Georgios
Results: 15
1
2
Wilson's disease in Sardinian population: The experience of a pediatric referral center.
- Published in:
- Journal of Pediatric Gastroenterology & Nutrition, 2024, v. 79, n. 4, p. 807, doi. 10.1002/jpn3.12343
- By:
- Publication type:
- Article
3
Acute Liver Failure Because of Wilson Disease With Overlapping Autoimmune Hepatitis Features: The Coexistence of Two Diseases?
- Published in:
- 2016
- By:
- Publication type:
- journal article
4
WILSON'S DISEASE.
- Published in:
- Contributions / Prilozi (1857-9345), 2014, v. 35, n. 1, p. 93
- By:
- Publication type:
- Article
5
"Acquired" hepatocerebral degeneration in a patient heterozygote carrier for a novel mutation in ATP7B gene.
- Published in:
- 2009
- By:
- Publication type:
- Case Study
6
'Acquired' hepatocerebral degeneration in a patient heterozygote carrier for a novel mutation in ATP7B gene.
- Published in:
- Movement Disorders, 2009, v. 24, n. 11, p. 1706, doi. 10.1002/mds.22659
- By:
- Publication type:
- Article
7
The homozygosity index (HI) approach reveals high allele frequency for Wilson disease in the Sardinian population.
- Published in:
- European Journal of Human Genetics, 2014, v. 22, n. 2, p. 295, doi. 10.1038/ejhg.2013.261
- By:
- Publication type:
- Article
8
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
- By:
- Publication type:
- Article
9
Haplotype and mutation analysis in Greek patients with Wilson disease.
- Published in:
- European Journal of Human Genetics, 1998, v. 6, n. 5, p. 487, doi. 10.1038/sj.ejhg.5200219
- By:
- Publication type:
- Article
10
Gabapentin Can Improve Dystonia in Confirmed Wilson Disease.
- Published in:
- 2014
- By:
- Publication type:
- Case Study
11
Wilson's disease in an adult asymptomatic patient: a potential role for modifying factors of copper metabolism.
- Published in:
- Annals of Gastroenterology, 2016, v. 29, n. 1, p. 96
- By:
- Publication type:
- Article
12
Molecular characterization of Wilson disease in the Sardinian population-Evidence of a founder effect.
- Published in:
- Human Mutation, 1999, v. 14, n. 4, p. 294, doi. 10.1002/(SICI)1098-1004(199910)14:4<294::AID-HUMU4>3.0.CO;2-9
- By:
- Publication type:
- Article
13
Further delineation of the molecular pathology of Wilson disease in the Mediterranean population.
- Published in:
- Human Mutation, 1998, v. 12, n. 2, p. 89, doi. 10.1002/(SICI)1098-1004(1998)12:2<89::AID-HUMU3>3.0.CO;2-G
- By:
- Publication type:
- Article
14
A new δ-chain variant hemoglobin A<sub>2</sub>-puglia or α<sub>2</sub>δ<sub>2</sub> 26 Glu→Asp (B8), detected by DNA analysis in a family of Southern Italian origin.
- Published in:
- Human Mutation, 1993, v. 2, n. 4, p. 327, doi. 10.1002/humu.1380020417
- By:
- Publication type:
- Article
15
A novel mediterranean 'δβ-thalassemia' determinant containing the δ<sup>+</sup>27 and β°39 point mutations in cis.
- Published in:
- American Journal of Hematology, 1994, v. 45, n. 1, p. 81, doi. 10.1002/ajh.2830450113
- By:
- Publication type:
- Article