Virtut Velmishi
Tirana, Albania
Last Updated: 09/26/2026
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Found 18 publications
Phenotypic Spectrum of Type 2-3 Gaucher Disease: A Case Study in the Balkan Genotype.
Journal: The American journal of case reports
Published: January 15, 2026
Ten-Year Follow-Up of Taliglucerase Alfa in Type 1 Gaucher Disease: Real-World Evidence from Albania.
Journal: Journal of clinical medicine
Published: September 02, 2025
Medium-Chain Acyl-CoA Dehydrogenase Deficiency Disorder as a Cause of Acute Liver Failure in a 23-Month-Old Baby.
Journal: Journal of medical cases
Published: October 15, 2024
Delayed Diagnosis of Congenital Duodenal Stenosis in a 16-Year-Old Girl.
Journal: Case reports in medicine
Published: February 22, 2024
Dysphagia lusoria caused by aberrant right subclavian artery associated with truncus bicaroticus in an 8-month-old girl. Case report and review of literature.
Journal: La Pediatria medica e chirurgica : Medical and surgical pediatrics
Published: January 27, 2024
Taliglucerase alfa in the longterm treatment of children and adolescents with type 1 Gaucher disease: the Albanian experience.
Journal: Frontiers in pediatrics
Published: December 07, 2023
The First Familiar Case of PTEN-Related Disorder Reported in Albania.
Journal: Turkish archives of pediatrics
Published: August 03, 2023
Congenital Hepatic Fibrosis as an Early Sign of Presentation of ADPKD.
Journal: Balkan journal of medical genetics : BJMG
Published: June 02, 2023
A new phenotype of aldolase a deficiency in a 14 year-old boy with epilepsy and rhabdomyolysis - case report.
Journal: Italian journal of pediatrics
Published: May 14, 2021
Treatment Efficiency in Gaucher Patients Can Reliably Be Monitored by Quantification of Lyso-Gb1 Concentrations in Dried Blood Spots.
Journal: International journal of molecular sciences
Published: May 20, 2020
Last Updated: 09/26/2026