Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Maurizio Bosio"'
We describe a familial syndrome in two brothers who were investigated after the casual discovery of tubular proteinuria in their 1st month of life. During a follow-up of 20 and 11 years, respectively, the two children grew well and were asymptomatic,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f725f47aae853ddf66a7d5228392063
https://ora.ox.ac.uk/objects/uuid:806e38d8-a2b3-4b2d-9bba-947b5184cf75
https://ora.ox.ac.uk/objects/uuid:806e38d8-a2b3-4b2d-9bba-947b5184cf75
Publikováno v:
Pediatric Nephrology. 19:638-643
The primary causes of renal insufficiency in Albanian children are reflux nephropathy and obstructive uropathies. The poor availability and technical quality of conventional radiological imaging in detecting vesicoureteral reflux (VUR) and lower urin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9a3251f8a93922d6d4d2c4f53f0f2d8
https://doi.org/10.1007/s00467-004-1439-7
https://doi.org/10.1007/s00467-004-1439-7
Publikováno v:
Pediatric Nephrology. 4:240-244
Twenty-seven children [2 with chronic renal failure (CRF)] with reflux or obstructive nephropathy underwent intravenous urography with iopamidol 370, a nonionic contrast medium 1 (CM), osmolality 796 mosmol/kg, for renal growth evaluation. Mean iopam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab1f6dd69d959289aa3ea94bf376130d
https://doi.org/10.1007/bf00857663
https://doi.org/10.1007/bf00857663
Autor:
Alberto Bettinelli, Silvio Maringhini, Mario G. Bianchetti, Maurizio Bosio, Anita Ammenti, CHIld, Sara Viganò, Angela La Manna, Luigi Avolio, Ivana Pela, I M Rätsch, Gianluigi Ardissino, Italkid, Emilio F. Fossali
Publikováno v:
Bianchetti, MG; Ammenti, A; Avolio, L; Bettinelli, A; Bosio, M; Fossali, E; La Manna, A; Maringhini, S; Pela, I; Ratsch, IM; Viganò, S; Ardissino, G; Italkid, Project; CHIld, Project (2007). Prescription of drugs blocking the renin-angiotensin system in Italian children. Pediatric nephrology, 22(1), pp. 144-8. Berlin: Springer 10.1007/s00467-006-0293-1
Little is known about the prescription pattern of antihypertensive drugs for children with impaired kidney function. We have therefore documented the use of antihypertensive drugs in this patient group by evaluating the Italian pediatric population-b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d5d0642fbcc88816a75660ae565b93a
Autor:
Sabina Lewicka, Paolo Mulatero, Tracy Ann Williams, Mario Palermo, Franco Veglio, Decio Armanini, Maurizio Bosio
Publikováno v:
The Journal of clinical endocrinology and metabolism. 89(7)
Aldosterone synthase deficiency (ASD) usually presents in infancy as a life-threatening electrolyte imbalance. A 4-wk-old child of unrelated parents was examined for failure to thrive and salt-wasting. Notable laboratory findings were hyperkalemia, h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f70bc0b922c61f54a7596edecc7ccb38
https://pubmed.ncbi.nlm.nih.gov/15240589
https://pubmed.ncbi.nlm.nih.gov/15240589
Autor:
Elodie Poisson, Anna Maria Fusco, Rémi Salomon, Ursula Kuhnle, Patrick Niaudet, Marc Lombès, Decio Armanini, Jean Pierre Chabrolle, Massimiliano Caprio, Maria-Christina Zennaro, Eliana Di Battista, Véronique Poulet-Young, Paola Loli, A. Naselli, Paola Sartorato, Yasmina Khaldi, Maurizio Bosio, Véronique Abadie, Marie Hélène Lecornec, Christiane De Gennes, Alain Racine, Anne Laure Lapeyraque
Publikováno v:
Scopus-Elsevier
We have analyzed the human mineralocorticoid receptor (hMR) gene in 14 families with autosomal dominant or sporadic pseudohypoaldosteronism (PHA1), a rare form of mineralocorticoid resistance characterized by neonatal renal salt wasting and failure t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2e447bc718f86893d0249a1eab0ea73
https://pubmed.ncbi.nlm.nih.gov/12788847
https://pubmed.ncbi.nlm.nih.gov/12788847
Autor:
Maurizio, Bosio
Publikováno v:
Rays. 27(2)
The intrinsic abnormalities of male urethra causing urinary obstruction are frequently responsible for renal insufficiency, sometimes present at birth. The rare but typical malformations such as the posterior urethral valves represent major deviation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::56fdd36cf44217e2acc83506ab745fa3
https://pubmed.ncbi.nlm.nih.gov/12696267
https://pubmed.ncbi.nlm.nih.gov/12696267
Autor:
Mario De Marchi, Francesca Mari, Ilaria Meloni, Giancarlo Lavoratti, Gianna Mazzucco, Maura Conti, Alessandra Renieri, Andrea Onetti Muda, Christelle Arrondel, Maurizio Bosio, Carla Deplano, Alfredo Brusco, Federica Fasciolo, Laura Massella, Laurence Heidet, Daniela Giachino, Dario Roccatello, Paola Porcedda, Giovanni M. Frascà, Ilaria Longo
Publikováno v:
Kidney international. 61(6)
COL4A3/COL4A4 mutations: From familial hematuria to autosomal-dominant or recessive Alport syndrome . Background Mutations of the type IV collagen COL4A5 gene cause X-linked Alport syndrome (ATS). Mutations of COL4A3 and COL4A4 have been reported bot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66628c2909adbc3e9ab6cc6b9b792ba9
https://pubmed.ncbi.nlm.nih.gov/12028435
https://pubmed.ncbi.nlm.nih.gov/12028435
Autor:
Amelia Thomson, Maurizio Bosio, S J Scheinman, Sarah E. Lloyd, Willy Günther, Ian W. Craig, Simon E. Fisher, Maria Luisa Bianchi, Rajesh V. Thakker, Simon H. S. Pearce, Thomas J. Jentsch, Oliver Wrong
Publikováno v:
Human Molecular Genetics
Mutations of the renal-specific chloride channel (CLCN5) gene, which is located on chromosome Xp11.22, are associated with hypercalciuric nephrolithiasis (kidney stones) in the Northern European and Japanese populations. CLCN5 encodes a 746 amino aci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69002c62463f4dc549f0c9a1a01e5f6f
https://hdl.handle.net/11858/00-001M-0000-0012-CBEE-811858/00-001M-0000-0012-CBED-A
https://hdl.handle.net/11858/00-001M-0000-0012-CBEE-811858/00-001M-0000-0012-CBED-A
Publikováno v:
Journal of Biomedical Materials Research. 13:477-496
The “quality” of poly(glycolic acid) as an absorbable suture material was investigated in comparison with catgut. Tissue reactions to poly(glycolic acid) and plain catgut were examined histomorphologically at different time intervals after implan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a095baaebf7f762afc3a7b99dad54040
https://doi.org/10.1002/jbm.820130312
https://doi.org/10.1002/jbm.820130312