Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Nadica Ristoska-Bojkovska"'
Publikováno v:
PRILOZI. 36:213-217
Background: Bardet-Biedl syndrome (BBS) is a multisystem genetic disorder characterized with central obesity, pigmentary retinopathy, polydactyly, mental retardation, and hypogenitalism. Renal abnormalities have been recognized as a cardinal feature
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac80e2230fe882c8f3a2506ed4456e75
https://doi.org/10.1515/prilozi-2015-0048
https://doi.org/10.1515/prilozi-2015-0048
Autor:
Nadica Ristoska-Bojkovska
Publikováno v:
Prilozi (Makedonska akademija na naukite i umetnostite. Oddelenie za medicinski nauki). 38(1)
Congenital anomalies of the kidneys and urinary tract (CAKUT) are found in 3-6 out of 1.000 of the newborns, or according to some statistics they are represented in 0.5% of all pregnancies. Congenital abnormalities of the kidneys and urinary tract pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fced5a09d518cc09d4d6a831fd2a396
https://pubmed.ncbi.nlm.nih.gov/28593883
https://pubmed.ncbi.nlm.nih.gov/28593883
Publikováno v:
World Journal of Pediatrics. 7:280-283
Oculocerebrorenal (Lowe) syndrome is an X-linked multisystem disease characterized by renal proximal tubulopathy, mental retardation, and congenital cataracts. We present a 19-year-old boy who was found to have low molecular weight proteinuria, hyper
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01fca78763d650fcb39ef0ed2e9c29b3
https://doi.org/10.1007/s12519-011-0312-6
https://doi.org/10.1007/s12519-011-0312-6
Autor:
Zoran Gucev, Petar Korneti, Nadica Ristoska-Bojkovska, Velibor Tasic, Vladimir J Lozanovski, Vesna Sabolic-Avramovska, Michael Ludwig
Publikováno v:
Pediatric Nephrology. 26:557-562
OCRL mutations, which are a hallmark of Lowe syndrome, have recently been found in patients with isolated renal phenotype (Dent-2 disease). In this report, we describe clinical and laboratory features in five Macedonian children with mutations in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83fc69fb48b72b15175aa553abad36cc
https://doi.org/10.1007/s00467-010-1758-9
https://doi.org/10.1007/s00467-010-1758-9
Publikováno v:
Renal failure. 37(9)
The objective of this study was to assess clinical course and outcome of children with congenital anomalies of the kidney and urinary tract (CAKUT) who had an attack of acute poststreptococcal glomerulonephritis (PSGN).Renal status including blood pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64d403fe363083c53be319e47e4b0ef7
https://pubmed.ncbi.nlm.nih.gov/26335537
https://pubmed.ncbi.nlm.nih.gov/26335537
Autor:
E Sukarova-Stefanovska, Zoran Gucev, Katerina Popovska-Jankovic, Dijana Plaseska-Karanfilska, Velibor Tasic, Nadica Ristoska-Bojkovska, Georgi D. Efremov
Publikováno v:
ResearcherID
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b296f201078684531f6f4ecb7016c741
https://doi.org/10.1007/s12041-011-0045-2
https://doi.org/10.1007/s12041-011-0045-2
Autor:
Velibor Tasic, Nadica Ristoska-Bojkovska, Aleksandra Janchevska, Hermann-Josef Lüdecke, Zoran Gucev
The tricho-rhino-phalangeal syndrome type III (TRPS III) is a rare autosomal dominantly inherited condition. The main clinical features are sparse and slow-growing hair and nails, a pear-shaped nose with a bulbous tip, elongated and flat philtrum, th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d27e209331d1d69ff0fa18f3cc122b2a
https://www.ncbi.nlm.nih.gov/pubmed/24502542
https://www.ncbi.nlm.nih.gov/pubmed/24502542
Autor:
Momir Polenakovic, Velibor Tasic, Petar Korneti, Nadica Ristoska-Bojkovska, Gordana Petrusevska
Publikováno v:
Pediatric Nephrology. 18:394-396
A 5-year-old boy was investigated after an episode of gross hematuria of non-glomerular origin and was found to have idiopathic hypercalciuria. Despite normalization of calciuria he had recurrent attacks of gross hematuria. Since SDS-PAGE analysis of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc3fcee44b220fb31fcd59b6e45753e1
https://doi.org/10.1007/s00467-003-1078-4
https://doi.org/10.1007/s00467-003-1078-4
Autor:
Zoran Gucev, Emilija Sahpazova, Nadica Ristoska-Bojkovska, Vladimir J Lozanovski, Velibor Tasic
Publikováno v:
European journal of pediatrics. 170(2)
Cystinuria is an autosomal recessive disorder characterized with abnormal tubular reabsorption of cystine and dibasic amino acids leading to cystine urolithiasis. The classical form is caused by mutations in the SLC3A1 gene (OMIM 220100). The corners
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dcd63ec38f39c838fdbc402ba07cb98
https://pubmed.ncbi.nlm.nih.gov/20924604
https://pubmed.ncbi.nlm.nih.gov/20924604
Publikováno v:
European journal of pediatrics. 168(2)
Autoimmune thyroiditis is rarely described in association with nephrotic syndrome. Herein we report a girl who developed autoimmune thyroiditis insidiously during the course of minimal change nephrotic syndrome. She was streroid-sensitive, but develo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd7f68274d9937d6e7f4e2639617719c
https://pubmed.ncbi.nlm.nih.gov/18461358
https://pubmed.ncbi.nlm.nih.gov/18461358