Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Simin Sadeghi Bojd"'
Autor:
Maryam Najafi, Korbinian M. Riedhammer, Aboulfazl Rad, Paria Najarzadeh Torbati, Riccardo Berutti, Isabel Schüle, Sophie Schroda, Thomas Meitinger, Jasmina Ćomić, Simin Sadeghi Bojd, Tayebeh Baranzehi, Azadeh Shojaei, Anoush Azarfar, Mahmood Reza Khazaei, Anna Köttgen, Rolf Backofen, Ehsan Ghayoor Karimiani, Julia Hoefele, Miriam Schmidts
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundSteroid resistant nephrotic syndrome (SRNS) represents a significant renal disease burden in childhood and adolescence. In contrast to steroid sensitive nephrotic syndrome (SSNS), renal outcomes are significantly poorer in SRNS. Over the pa
Externí odkaz:
https://doaj.org/article/7e9cdafe92c94f5181a68955cd99abd7
Autor:
Maryam Esteghamati, Hadi Sorkhi, Hamid Mohammadjafari, Ali Derakhshan, Simin Sadeghi-Bojd, Hossein Emad Momtaz, Masoumeh Mohkam, Baranak Safaeian, Nakysa Hooman, Afshin Safaeiasl, Mohsen Akhavan Sepahi, Khadijeh Ghasemi, Zahra Bazargani, Elham Emami
Publikováno v:
BMC Nephrology, Vol 23, Iss 1, Pp 1-6 (2022)
Abstract Background Given the importance of the function of the remnant kidney in children with unilateral renal agenesis and the significance of timely diagnosis and treatment of reflux nephropathy to prevent further damage to the remaining kidney,
Externí odkaz:
https://doaj.org/article/4b5bcdbc8932462a8747df468133dc1e
Autor:
Maryam Najafi, Dor Mohammad Kordi-Tamandani, Farkhondeh Behjati, Simin Sadeghi-Bojd, Zeineb Bakey, Ehsan Ghayoor Karimiani, Isabel Schüle, Anoush Azarfar, Miriam Schmidts
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-11 (2019)
Abstract Background Bartter Syndrome is a rare, genetically heterogeneous, mainly autosomal recessively inherited condition characterized by hypochloremic hypokalemic metabolic alkalosis. Mutations in several genes encoding for ion channels localizin
Externí odkaz:
https://doaj.org/article/2f47bf6ab337423e85de68cca12ea5c1
Publikováno v:
Caspian Journal of Health Research, Vol 3, Iss 1, Pp 24-27 (2018)
Background: Urolithiasis in children is associated with metabolic disorders. The most important metabolic disorders are hypercalciuria, hyperoxaluria, hypocitraturia, cysitinuria and hyperuricosuria. This study aimed to evaluate the level of urinary
Externí odkaz:
https://doaj.org/article/c2e650716e88439e9141c9e51743dee4
Autor:
Maryam Najafi, Dor Mohammad Kordi Tamandani, Anoush Azarfar, Zeineb Bakey, Farkhondeh Behjati, Dinu Antony, Isabel Schüle, Simin Sadeghi-Bojd, Ehsan Ghayoor Karimiani, Miriam Schmidts
Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
Background: Nephropathic Cystinosis, the most common cause of renal Fanconi syndrome, is a lysosomal transport disorder with an autosomal recessive inheritance pattern. A large number of mutations in CTNS have been identified as causative to date. A
Externí odkaz:
https://doaj.org/article/47e923e36e70496ab694f4a0f9194284
Autor:
Farnaz Kamali, Mahnaz Jamee, John A. Sayer, Simin Sadeghi-Bojd, Zahra Golchehre, Reyhaneh Dehghanzad, Mohammad Keramatipour, Masoumeh Mohkam
Publikováno v:
CEN Case Reports.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db8248b3e65dd7ab25b268a7d54cc3d7
https://doi.org/10.1007/s13730-023-00785-8
https://doi.org/10.1007/s13730-023-00785-8
Publikováno v:
Journal of Comprehensive Pediatrics. 13
Background: Childhood voiding and defecation dysfunction are common problems in children of all ages worldwide. The prevalence of bowel and bladder dysfunction in children is reported to be approximately 47%. Objectives: Due to the different ethnic a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b50e9d18c1d6bf350514da8a6832773
https://doi.org/10.5812/compreped-117406
https://doi.org/10.5812/compreped-117406
Autor:
Neda Enayati Zadeh, Simin Sadeghi‐Bojd, Alireza Ansari‐Moghaddam, Amin Mashhadi, Mohadeseh Zadehmir
Publikováno v:
Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in MedicineReferences.
This study hypothesizes using color Doppler ultrasound to measure ureteral jet angles (UJA) as a diagnostic screening tool for reflux.The present prospective cohort study included 122 patients and 238 renal unit pediatric patients suspected of VUR wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7ba24cdf451e75a7a4dc3da0db892c3
https://pubmed.ncbi.nlm.nih.gov/36190168
https://pubmed.ncbi.nlm.nih.gov/36190168
Publikováno v:
Caspian Journal of Health Research, Vol 5, Iss 1, Pp 8-11 (2020)
Background: Obesity is a global problem and is associated with pathophysiological mechanisms related to kidneys which may result in microalbuminuria. The aim of this study was to compare the microalbuminuria in obese and normal-weight children. Metho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::72e90452d3e3c34f208eeef683cabe3d
http://cjhr.gums.ac.ir/article-1-143-en.html
http://cjhr.gums.ac.ir/article-1-143-en.html
Publikováno v:
Caspian Journal of Health Research. 5:8-11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6ade5c87f6c7f81660564d7f7cf3b6d
https://doi.org/10.29252/cjhr.5.1.8
https://doi.org/10.29252/cjhr.5.1.8