Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Lea Oletić"'
Publikováno v:
Children, Vol 10, Iss 10, p 1700 (2023)
Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disorder, estimated to affect 1 in 1000 people. It displays a high level of variability in terms of onset and severity among affected individuals within the sam
Externí odkaz:
https://doaj.org/article/d278c3a59dbb4f5f8055e934ac19d35e
Publikováno v:
Acta Clinica Croatica, Vol 60., Iss 1., Pp 141-145 (2021)
We report a rare case of nephritic syndrome underlying dense deposit disease (DDD) with alternative complement pathway dysfunction explained with both C3 nephritic factor (C3NeF) antibodies and DDD associated polymorphism of factor H. An 8-year-old
Externí odkaz:
https://doaj.org/article/c545c466b9bf43f99f877c085518ff48
Publikováno v:
Acta Clinica Croatica, Vol 60., Iss 2., Pp 184-190 (2021)
Vesicoureteral reflux (VUR) is one of the most common anomalies of the urinary system in children. Contrast-enhanced voiding urosonography (ceVUS) is one of the best methods in VUR diagnosis. This study compared characteristics associated with VUR
Externí odkaz:
https://doaj.org/article/55cf70f48c9646de88a3381622349f0b
Publikováno v:
Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b3af43aaefcc6094806aa46069d9e430
https://doi.org/10.1136/archdischild-2021-europaediatrics.494
https://doi.org/10.1136/archdischild-2021-europaediatrics.494
Publikováno v:
Acta Clinica Croatica
Acta Clinica Croatica, Vol 60., Iss 2., Pp 184-190 (2021)
Acta Clinica Croatica, Vol 60., Iss 2., Pp 184-190 (2021)
Vesicoureteral reflux (VUR) is an anatomical and functional abnormality caused by a non- physiological retrograde flow of urine from the bladder into the ureter and the renal canal system. VUR is one of the most common anomalies in children and it is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a16dcd1e80659ce7577efd561c95047
https://doi.org/10.1136/archdischild-2021-europaediatrics.356
https://doi.org/10.1136/archdischild-2021-europaediatrics.356
Publikováno v:
Minerva endocrinology. 46(1)
ACKGROUND: Turner Syndrome (TS) is a chromosomal disorder with short stature as the most common feature. The aim of this paper was to show the characteristics of TS patients treated at our Clinic, with an emphasis on their age at diagnosis and the ef
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f7f302fe2c2b12bb204a1ea95e37981
https://pubmed.ncbi.nlm.nih.gov/32623843
https://pubmed.ncbi.nlm.nih.gov/32623843