Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Lyda Jadresic"'
Publikováno v:
Pediatric nephrology (Berlin, Germany). 36(1)
BACKGROUND: There is increasing evidence that maternal obesity is associated with several structural birth defects. Congenital abnormalities of the kidney and urinary tract (CAKUT) account for 30 to 50% of children starting kidney replacement therapy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5d5eb4cdad21c1e18bad529bd170ca7
https://pubmed.ncbi.nlm.nih.gov/32596798
https://pubmed.ncbi.nlm.nih.gov/32596798
Publikováno v:
Pediatric Nephrology. 34:2457-2477
Childhood overweight and obesity affects more and more children. Whilst associations of childhood overweight with later outcomes such as hypertension, diabetes and cardiovascular disease have been well documented, less is known about the association
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4178e85f373051da44b8af041d04975b
https://doi.org/10.1007/s00467-018-4108-y
https://doi.org/10.1007/s00467-018-4108-y
Autor:
Philippa Moore, James Larcombe, Neville Q. Verlander, Jan Dudley, Lyda Jadresic, Jaydip Banerjee, Cliodna A. M. McNulty
Publikováno v:
Journal of Medical Microbiology
The National Institute of Care Excellence (NICE) 2007 guidance CG54, on urinary tract infection (UTI) in children, states that clinicians should use urgent microscopy and culture as the preferred method for diagnosing UTI in the hospital setting for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b79993b663fee5dc3251e32836ebcd73
http://europepmc.org/articles/PMC4681043
http://europepmc.org/articles/PMC4681043
Autor:
Lyda Jadresic, James Larcombe, Gita Gyoffry, Caroline Platt, Cliodna A. M. McNulty, Jaydip Banerjee, Jan Dudley, Katie Pike
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 104(6)
Aim To audit compliance with the 2007 National Institute of Clinical Excellence guidelines on the management of urinary tract infection in children under the age of 16 years across primary and secondary care services in England. Methods A retrospecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::baf15a4ee607aec92ce7f96ee323c085
https://pubmed.ncbi.nlm.nih.gov/25974004
https://pubmed.ncbi.nlm.nih.gov/25974004
Publikováno v:
Research. 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0f94607c290bda788eedb4f16493278
https://doi.org/10.13070/rs.en.1.1085
https://doi.org/10.13070/rs.en.1.1085
Publikováno v:
Acta Paediatrica. 97:379-381
UNLABELLED Incontinentia pigmenti (IP) is not generally recognized as a cause of neonatal encephalopathy. A full-term infant developed a rash and encephalopathy with lesions in the basal ganglia and periventricular white matter 3 days after a normal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef3cc2dcbd8d8f19212c966970eda709
https://doi.org/10.1111/j.1651-2227.2007.00630.x
https://doi.org/10.1111/j.1651-2227.2007.00630.x
Publikováno v:
Human Molecular Genetics. 1:301-305
The Denys-Drash syndrome is characterised by a typical nephropathy, genital abnormalities and also predisposes to the development of Wilms' tumor. These patients eventually go into end stage renal failure. A candidate Wilms' tumor gene, WT1, from the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11c90b70bdbb39227c2ed8a1123c1642
https://doi.org/10.1093/hmg/1.5.301
https://doi.org/10.1093/hmg/1.5.301
Publikováno v:
Archives of Disease in Childhood. 98:A59-A60
Aims Children and families should expect to receive NICE compliant care before and after diagnosis of UTI and independently of where this diagnosis is made. We aim to highlight the challenges faced by different healthcare providers in the diagnosis a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a39b46c8b0b96a56fd77cac21a1e2b6b
https://doi.org/10.1136/archdischild-2013-304107.137
https://doi.org/10.1136/archdischild-2013-304107.137
Publikováno v:
Case Reports. 2014:bcr2013200937-bcr2013200937
We present the case of a young boy with Dent's disease, identified as having a mutation in the kidney-specific chloride-proton antitransporter CLCN5 during investigation for nephrotic-range proteinuria. He went on to develop growth hormone deficiency
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb22894be43848990288aec3429e33e5
https://doi.org/10.1136/bcr-2013-200937
https://doi.org/10.1136/bcr-2013-200937
OBJECTIVES--To determine the number of laboratory confirmed urinary tract infections in children and to ascertain general practitioners' practices and attitudes towards their investigation and management. DESIGN--Prospective one year survey of urine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::175fbb7dd97628f358ebf4ad97b5555a
https://europepmc.org/articles/PMC1696421/
https://europepmc.org/articles/PMC1696421/
