Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Laurant Kollçaku"'
Autor:
Agim Gjikopulli, Sonila Tomori, Donjeta Bali, Paskal Cullufi, Laurant Kollcaku, Mirela Tabaku, Anila Babameto
Publikováno v:
International Journal of Biomedicine, Vol 14, Iss 2, Pp 275-281 (2024)
Background: There is no doubt that the use of rhGH in patients with TS brings satisfactory results regarding the improvement of height growth, realizing the improvement of the final adult height. This study aimed to evaluate the influence of the type
Externí odkaz:
https://doaj.org/article/58e57ac111d3459c8ed2e23469d6c612
Autor:
Virtut Velmishi, Erjon Troja, Marjeta Tanka, Donjeta Bali, Ermira Dervishi, Afërdita Tako, Laurant Kollcaku, Paskal Cullufi
Publikováno v:
Journal of Osteoporosis, Vol 2023 (2023)
Gaucher disease is a rare, genetic lysosomal disorder leading to lipid accumulation and dysfunctions in multiple organs. Bone involvement is one of the most prevalent aspects of Gaucher disease. Pain, disability, and reduced quality of life remain th
Externí odkaz:
https://doaj.org/article/346eaba71eb0486694872dfc8a99569a
Autor:
Paskal Cullufi, Renald Meçani, Agim Gjikopulli, Laurant Kollçaku, Sonila Tomori, Armand Shehu, Aida Bushati, Kristi Aleksi, Afërdita Tako Kumaraku
Publikováno v:
Journal of Advances in Medicine and Medical Research. :46-50
Sotos syndrome is a rare genetic disorder with autosomal dominant inheritance, marked by overgrowth with macrocephaly, a distinctive facial appearance, and intellectual impairment. It occurs due to pathogenic variants encompassing the NSD1 gene. In a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c94b639ec588d060099b861e464027f7
https://doi.org/10.9734/jammr/2023/v35i34953
https://doi.org/10.9734/jammr/2023/v35i34953
Autor:
null Laurant Kollçaku
Publikováno v:
South Eastern European Journal of Public Health (SEEJPH)
Aim: Diabetes mellitus is a major public health problem worldwide. Type 1 diabetes mellitus (T1DM) is the most common metabolic chronic disease in genetically susceptible children and adolescents, due to an autoimmune process characterized by a selec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db92540a5a40178b5ee5eb518950ebf5
https://doi.org/10.56801/seejph.vi.293
https://doi.org/10.56801/seejph.vi.293