Georgios Loudianos
ScholarGPS® ID: 25453796181827
Affiliation History
Field
Life Sciences
Discipline
Biomedical Sciences
Top Specialties
Mutation | Thalassemia | Beta Thalassemia | Medical Genetics | Human Genetics | Genetic Testing | Mutation Testing | Human Mutation | Liver Disease
Metrics Summary
Publication Count
87
Predicted Citations
2,953
Predicted h-index
27
Ranking
Publications and Citation History
Publications based on Top Specialties
Types of Publication
- Publications
- Books
- Patents
- NIH/NSF
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Cost analysis of Wilson's disease in Italy: a retrospective cohort study (journal article) Digestive and Liver Disease, volume 56 (2024). |
PRO114 Wilson Disease: Unmet NEEDS Emerging from the Italian Population - a Qualitative Survey Study (journal article) Value in Health, volume 23 (2020). |
Wilson Disease in the Mediterranean Region (book chapter) In Clinical and Translational Perspectives on WILSON DISEASE Elsevier (2019) |
P057 Persistent hypertransaminasemia in an obese child with asymptomatic Wilson disease and familiarity for parkinsonism and cardiomyopathy: a case report (journal article) Digestive and Liver Disease, volume 50, issue 4, pages e379- (2018). |
Wilson Disease (book chapter) In Zakim and Boyer's Hepatology Elsevier (2018) |
Acute Liver Failure Because of Wilson Disease With Overlapping Autoimmune Hepatitis Features (journal article) Journal of Pediatric Gastroenterology and Nutrition, volume 63, issue 2 (2016). |
ATP7B Gene Mutations in Croatian Patients with Wilson Disease (journal article) Genetic Testing and Molecular Biomarkers, volume 20, issue 3, pages 112-117 (2016). |
Wilson's disease in an adult asymptomatic patient: a potential role for modifying factors of copper metabolism. (journal article) Annals of gastroenterology : quarterly publication of the Hellenic Society of Gastroenterology, volume 29, issue 1 (2016). |
Wilson's disease caused by alternative splicing and Alu exonization due to a homozygous 3039-bp deletion spanning from intron 1 to exon 2 of the ATP7B gene (journal article) Gene, volume 569, issue 2, pages 276-279 (2015). |
Gabapentin Can Improve Dystonia in Confirmed Wilson Disease (journal article) Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, volume 41, issue 2, pages 284-285 (2014). |
Erratum: The homozygosity index (HI) approach reveals high allele frequency for Wilson disease in the Sardinian population (journal article) European Journal of Human Genetics, volume 22, issue 2, pages 295-295 (2014). |
Wilson's disease. (journal article) Prilozi (Makedonska akademija na naukite i umetnostite. Oddelenie za medicinski nauki), volume 35, issue 1 (2014). |
The homozygosity index (HI) approach reveals high allele frequency for Wilson disease in the Sardinian population (journal article) European Journal of Human Genetics, volume 21, issue 11, pages 1308-1311 (2013). |
Wilson's disease in two consecutive generations: The detection of three mutated alleles in the ATP7B gene in two Sardinian families (journal article) Digestive and Liver Disease, volume 45, issue 4, pages 342-345 (2013). |
European Journal of Medical Genetics, volume 56, issue 4, pages 207-210 (2013). |
A new deletion in 5′-end of dystrophin gene removing M and P promoters and dystrophin muscle enhancers (journal article) Gene, volume 511, issue 2, pages 437-440 (2012). |
Mutation analysis of the ATP7B gene in a new group of Wilson's disease patients: Contribution to diagnosis (journal article) Molecular and Cellular Probes, volume 26, issue 4, pages 147-150 (2012). |
Feasibility of RNA studies on illegitimate transcription for molecular characterization of splicing mutations in the ATP7B gene: A case report (journal article) Molecular and Cellular Probes, volume 26, issue 2, pages 63-65 (2012). |
Molecular and Cellular Probes, volume 25, issue 5-6, pages 195-198 (2011). |
Allan–Herndon–Dudley syndrome (AHDS) caused by a novel SLC16A2 gene mutation showing severe neurologic features and unexpectedly low TRH-stimulated serum TSH (journal article) European Journal of Medical Genetics, volume 53, issue 6, pages 392-395 (2010). |