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Ermira Dervishi

Observed names: Dervishi¹, Ermira, E Dervishi, E. Dervishi
ORCID: 0000-0003-3073-0277
Observed ORCID: 0000-0003-3073-0277
OpenAlex ID: A5064240664
A novel de novo pathogenic variant in KDM3B gene at the first Albanian case of Diets-Jongmans syndrome: DIJOS
2022 · Mirela Tabaku, Sonila Tomori, et al. · Molecular Genetics and Metabolism Reports · 9
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Congenital Hepatic Fibrosis as an Early Sign of Presentation of ADPKD
2022 · L. Sila, V. Velmishi, et al. · Balkan Journal of Medical Genetics · 6
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Delayed Diagnosis of Congenital Duodenal Stenosis in a 16-Year-Old Girl
2024 · Virtut Velmishi, Dritan Alushani, et al. · Case Reports in Medicine · 5
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Skeletal Manifestations, Bone Pain, and BMD Changes in Albanian Type 1 Gaucher Patients Treated with Taliglucerase Alfa
2023 · Virtut Velmishi, Erjon Troja, et al. · Journal of Osteoporosis · 5
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Genetic characterization of the Albanian Gaucher disease patient population
2020 · Paskal Cullufi, Mirela Tabaku, et al. · JIMD Reports · 5
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Treatment and follow up of children with chronic hepatitis C in Albania
2012 · Virtut Velmishi, Ermira Dervishi, et al. · Virology Journal · 5
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Taliglucerase alfa in the longterm treatment of children and adolescents with type 1 Gaucher disease: the Albanian experience
2024 · Paskal Cullufi, Sonila Tomori, et al. · Frontiers in Pediatrics · 4
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Seronegative celiac disease presented with a pronounced abdominal distention in a 4-year-old boy- Case report and review of literature
2020 · Virtut Velmishi, Laurant Kollçaku, et al. · Pediatrics & Therapeutics · 2
Constipation as an Atypical Sign of ARC Syndrome - Case Report.
2016 · V Velmishi, E Dervishi, et al. · PubMed Central · 2
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Phenotypic Spectrum of Type 2-3 Gaucher Disease: A Case Study in the Balkan Genotype
2025 · Paskal Cullufi, Virtut Velmishi, et al. · American Journal of Case Reports · 1
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Broadening the clinical spectrum of White-Sutton syndrome, implications for co-morbidity with celiac disease in a patient with a novel likely pathogenic variant in the POGZ gene
2025 · Mirela Tabaku, Sonila Tomori, et al. · Gene · 1
Epidemiology of Celiac Disease in Children in Albania and Psychological Implications of the Disease
2017 · Ermira Dervishi, Afërdita Tako, et al. · American Journal of Psychiatry and Neuroscience · 1
Real-world comparison of genome- and exome-based diagnostic workflows in a pediatric Albanian rare disease cohort
2026 · P. Cullufi, M. Tabaku, et al. · BMC Medical Genomics
Transition From Interferon‐Based Therapy to Direct‐Acting Antivirals in Albanian Children With Chronic Hepatitis C: A 17‐Year Real‐World Experience
2026 · Virtut Velmishi, Ermira Dervishi, et al. · Advances in Virology
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Ten-Year Follow-Up of Taliglucerase Alfa in Type 1 Gaucher Disease: Real-World Evidence from Albania
2025 · Paskal Cullufi, Virtut Velmishi, et al. · Journal of Clinical Medicine
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The First Reported Albanian Patient With Fructose‐1,6‐Bisphosphatase Deficiency: A Rare Disorder of Fructose Metabolism
2025 · Paskal Cullufi, Gladiola Hoxha, et al. · Case Reports in Medicine
Diagnostic tardiv de tulburare de spectru autist şi sindrom Sotos la un pacient cu simptomatologie atipică în copilăria timpurie
2023 · Sonila Tomori, Mirela Tabaku, et al. · Psihiatru ro
Correlation Between Tga-iga Levels and Hystopathologic Changes in Cd: a Study in Coeliac Children in Albania
2018 · Ermira Dervishi, Spiro Sila, et al. · International Journal of Ecosystems and Ecology Science (IJEES)
Multifocal Osteonecrosis after Short Term Methylprednysolon Therapy: A Case Report
2016 · Afërdita Tako Kumaraku, Aida Bushati, et al. · 55th ESPE Meeting
Follow up of Gaucher patients in “Mother Teresa Hospital” Tirana — Albania
2013 · Virtut Velmishi, Ermira Dervishi, et al. · Molecular Genetics and Metabolism
Works count: 21
Citation count: 46
H-index: 5
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