Delayed Diagnosis of Congenital Duodenal Stenosis in a 16-Year-Old Girl.

Authors: Velmishi, Virtut¹ (AUTHOR), Alushani, Dritan² (AUTHOR), Dervishi, Ermira¹ (AUTHOR), Heta, Saimir² (AUTHOR), Sila, Spiro² (AUTHOR), Cullufi, Paskal¹ (AUTHOR)

Source: Case Reports in Medicine. 5/4/2024, Vol. 2024, p1-4. 4p.

Subject Terms: *ANEMIA diagnosis, *PHYSICAL diagnosis, *POSTOPERATIVE care, *MALNUTRITION, *BLOOD testing, *DIGESTIVE system endoscopic surgery, *ABDOMINAL pain, *TREATMENT effectiveness, *OMEPRAZOLE, *ENTERAL feeding, *SEROLOGY, *DELAYED diagnosis, *DUODENAL obstructions, *VOMITING, *ABDOMINAL radiography, DIGESTIVE organ abnormalities

Skeletal Manifestations, Bone Pain, and BMD Changes in Albanian Type 1 Gaucher Patients Treated with Taliglucerase Alfa.

Authors: Velmishi, Virtut¹ (AUTHOR), Troja, Erjon² (AUTHOR), Tanka, Marjeta³ (AUTHOR), Bali, Donjeta³ (AUTHOR), Dervishi, Ermira¹ (AUTHOR), Tako, Afërdita³ (AUTHOR), Kollcaku, Laurant³ (AUTHOR), Cullufi, Paskal¹ (AUTHOR)

Source: Journal of Osteoporosis. 12/4/2023, p1-8. 8p.

Subject Terms: *LUMBAR vertebrae, *GAUCHER'S disease, *LYSOSOMAL storage diseases, *BONE density, *GLYCOGEN storage disease type II, *BONE fractures, *GENETIC disorders, *DUAL-energy X-ray absorptiometry

Taliglucerase alfa in the longterm treatment of children and adolescents with type 1 Gaucher disease: the Albanian experience.

Authors: Cullufi, Paskal, Tomori, Sonila, Velmishi, Virtut, Gjikopulli, Agim, Akshija, Ilir, Tako, Aferdita, Dervishi, Ermira, Hoxha, Gladiola, Tanka, Marjeta, Troja, Erjon, Tabaku, Mirela

Source: Frontiers in Pediatrics; 2024, p1-9, 9p

Dysphagia lusoria caused by aberrant right subclavian artery associated with truncus bicaroticus in an 8-month-old girl. Case report and review of literature.

Authors: Bizhga, Melpomeni, Velmishi, Virtut, Sila, Lorena, Koja, Albert, Hoxha, Stiljan

Source: Medical & Surgical Pediatrics / Pediatria Medica e Chirurgica; 2024, Vol. 46 Issue 1, p12-14, 3p

Subject Terms: DEGLUTITION disorders in infants, SUBCLAVIAN artery, HUMAN abnormalities, PEDIATRIC diagnosis, HOSPITAL admission & discharge

The First Familiar Case of PTEN-Related Disorder Reported in Albania.

Authors: Bali, Donjeta, Tabaku, Mirela, Gjikopulli, Agim, Velmishi, Virtut, Tocilla, Behar, Godo, Anila, Cullufi, Paskal

Source: Turkish Archives of Pediatrics; Sep2023, Vol. 58 Issue 5, p559-561, 3p

Subject Terms: GENETIC disorder diagnosis, COWDEN syndrome, TRACHEAL fistula, PHYSICAL diagnosis, GENETIC mutation, HYPERPIGMENTATION, MAGNETIC resonance imaging, NEURAL development, TUMOR suppressor genes, CASE studies, PROTEUS syndrome, AUTISM, ESOPHAGEAL atresia, CALF muscles, GLUTEAL muscles, CEREBRAL cortex abnormalities, LIPOMATOSIS

Geographic Terms: ALBANIA

Constipation as an Atypical Sign of ARC Syndrome - Case Report.

Authors: VELMISHI, VIRTUT¹ tutimodh@yahoo.com, DERVISHI, ERMIRA¹, BALI, DONJETA², SHEHU, ARMAND³, CULLUFI, PASKAL¹

Source: Current Health Sciences Journal. Apr-Jun2016, Vol. 42 Issue 2, p203-206. 4p.

Subject Terms: *ARTHROGRYPOSIS, *CHOLESTASIS, *RENAL tubular transport disorders, *GLYCOSURIA, *CONSTIPATION

A new phenotype of aldolase a deficiency in a 14 year-old boy with epilepsy and rhabdomyolysis – case report.

Authors: Santoro, Lucia, Pjetraj, Dorina, Velmishi, Virtut, Campana, Carmen, Catassi, Carlo, Dionisi-Vici, Carlo, Maiorana, Arianna

Source: Italian Journal of Pediatrics; 3/4/2022, Vol. 48 Issue 1, p1-5, 5p

Subject Terms: EPILEPSY prevention, ANTICONVULSANTS, KETOGENIC diet, RHABDOMYOLYSIS, SKELETAL muscle, NEURONS, LYASES, TREATMENT effectiveness, GLYCOGEN storage disease, SEIZURES (Medicine), PATIENT compliance, PHENOTYPES, ADOLESCENCE

Treatment and follow up of children with chronic hepatitis C in Albania

Authors: Velmishi Virtut, Dervishi Ermira, Cullufi Paskal, Bali Donjeta, Durro Vjollca

Source: Virology Journal, Vol 9, Iss 1, p 17 (2012)

Subject Terms: Chronic Hepatitis C = CHC, HCV = Hepatitis C Virus, SVR = Sustained Viral Response, ETVR = End Treatment Viral Response, Infectious and parasitic diseases, RC109-216

File Description: electronic resource

Relation: http://www.virologyj.com/content/9/1/17; https://doaj.org/toc/1743-422X

Access URL: https://doaj.org/article/cd7e6caa940c42fe8fd610be58dfa442

Genetic characterization of the Albanian Gaucher disease patient population.

Authors: Cullufi, Paskal, Tabaku, Mirela, Velmishi, Virtut, Gjikopulli, Agim, Tomori, Sonila, Dervishi, Ermira, Tako, Aferdita, Leubauer, Anika, Westenberger, Ana, Cozma, Claudia, Beetz, Christian, Bauer, Peter, Wirth, Stefan, Rolfs, Arndt

Source: Journal of Inherited Metabolic Disease Reports; Jan2021, Vol. 57 Issue 1, p52-57, 6p

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Follow up of Gaucher patients in “Mother Teresa Hospital” Tirana — Albania

Authors: Velmishi, Virtut, Dervishi, Ermira, Cullufi, Paskal

Source: In Molecular Genetics and Metabolism February 2013 108(2):S95-S95

Treatment Efficiency in Gaucher Patients Can Reliably Be Monitored by Quantification of Lyso-Gb1 Concentrations in Dried Blood Spots.

Authors: Cozma, Claudia, Cullufi, Paskal, Kramp, Guido, Hovakimyan, Marina, Velmishi, Virtut, Gjikopulli, Agim, Tomori, Sonila, Fischer, Steffen, Oppermann, Sebastian, Grittner, Ulrike, Bauer, Peter, Beetz, Christian, Rolfs, Arndt

Source: International Journal of Molecular Sciences; Jul2020, Vol. 21 Issue 13, p4577-4577, 1p

Subject Terms: INVOLUNTARY treatment, LYSOSOMAL storage diseases, MASS spectrometry, BIOMARKERS, BLOOD

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