Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Emir Behluli"'
Publikováno v:
Research Results in Pharmacology, Vol 10, Iss 2, Pp 27-39 (2024)
Introduction: Acute lymphoblastic leukemia (ALL) is the most frequent pediatric leukemia; it can be defined according to chromosomic and genomic data. Cytogenetic analyses and determination of chromosomal numbers (such as hypo- or hyperdiploidy) and/
Externí odkaz:
https://doaj.org/article/e06b932a662b4d8eaa73c281f1f65503
Publikováno v:
Pharmacia, Vol 70, Iss 4, Pp 1005-1013 (2023)
Systemic lupus erythematosus (SLE) is a disease associated with an impaired autoimmune response; the immune system attacks erroneously own tissues, which leads to inflammation, tissue damage and complement activation. The latter plays a pivotal role
Externí odkaz:
https://doaj.org/article/f6a38544e49541b999be19d764e1fc43
Publikováno v:
Folia Medica, Vol 65, Iss 1, Pp 161-165 (2023)
Mucopolysaccharidosis type IIIB (MPS IIIB), also known as Sanfilippo syndrome type B, is a metabolic disease caused by mutations in both alleles of the NAGLU gene encoding for the enzyme α-N-acetylglucosaminidase. A malfunction of this enzyme causes
Externí odkaz:
https://doaj.org/article/889739d893ad41a7a283ab963bcfefa1
Publikováno v:
Folia Medica, Vol 64, Iss 4, Pp 649-654 (2022)
Introduction: Many authors in their research have suggested an association between vitamin D and asthma, but the results from these publications are sometimes confusing.Aim: Our aim was to assess the relationship between serum vitamin D and lung func
Externí odkaz:
https://doaj.org/article/9fb358c5958f42d88a45a76e93166c3e
Publikováno v:
F1000Research, Vol 11 (2023)
Background. Joubert syndrome (JS) is a rare autosomal recessive ciliopathy with an estimated prevalence of 1 in 100,000. JS is characterized by hyperpnoea, hypotonia, ataxia, developmental delay and various neuropathological abnormalities in the brai
Externí odkaz:
https://doaj.org/article/8d747da280bc493dbd61faa05b47dba0
Publikováno v:
Current Pediatric Reviews. 19:150-156
Abstract: Acute lymphoblastic leukemia is the most frequent pediatric malignancy in children, comprising 30% of all pediatric malignancies; adult ALL comprises 5% of all ALL cases, which have a 186.6 per 1 million incidence. In pediatric ALL (pALL),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e704cc537ff6e8910355d03340f89e6
https://doi.org/10.2174/1573396318666220901165247
https://doi.org/10.2174/1573396318666220901165247
Publikováno v:
Open Access Macedonian Journal of Medical Sciences. 10:2215-2219
Background/Objectives: To assess the effectiveness and safeness of Lactobacillus reuteri and additionally three other probiotics to conventional triple therapy against the Heliobacter pylori.Materials and Methods: We randomly selected 115 H. pylori p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00a1d419fa8329b268ceea2961c937ce
https://doi.org/10.3889/oamjms.2022.10733
https://doi.org/10.3889/oamjms.2022.10733
Publikováno v:
F1000Research. 11:388
Background. Joubert syndrome (JS) is a rare autosomal recessive ciliopathy with an estimated prevalence of 1 in 100,000. JS is characterized by hyperpnoea, hypotonia, ataxia, developmental delay and various neuropathological abnormalities in the brai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f541092d9d703643954a0b76618b992
https://doi.org/10.12688/f1000research.109628.2
https://doi.org/10.12688/f1000research.109628.2
Publikováno v:
Journal of mother and childReferences.
Children with Down syndrome (DS) are at markedly increased risk for acute lymphoblastic leukaemia (ALL). DS is caused by trisomy of chromosome 21 affecting approximately 1 in 732 newborns in the USA. ALL is the most common cancer in children and cons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7c3e94cabacefd67787ca68e2380ef03
https://pubmed.ncbi.nlm.nih.gov/35853737
https://pubmed.ncbi.nlm.nih.gov/35853737
Autor:
Rifat Hadziselimovic, Lidvana Spahiu, Hilada Nefic, Gazmend Temaj, Emir Behluli, Borut Peterlin, Thomas Liehr
Publikováno v:
Pediatric endocrinology, diabetes, and metabolism. 27(3)
Mucopolysaccharidoses (MPSs) are known as rare genetic diseases which are caused by mutation in the enzyme heparin sulfate, which normally leads to degradation and accumulation of glycosaminoglycans in the cells. There are 11 types of MPSs, whereby n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0299c910756c5431b6be740d9b62661
https://pubmed.ncbi.nlm.nih.gov/34743503
https://pubmed.ncbi.nlm.nih.gov/34743503