Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Sylva Skálová"'
Publikováno v:
Acta Medica, Vol 65, Iss 1, Pp 1-7 (2022)
This review article introduces the basic principles of infants’ neurophysiology, while summarizing the core knowledge of the anatomical structure of the auditory pathway, and presents previous findings on newborns’ neural speech processing and su
Externí odkaz:
https://doaj.org/article/931cfc7fb21a4bbdb2cd5a7ab74f1e5a
Publikováno v:
Acta Medica, Vol 64, Iss 3, Pp 187-192 (2021)
Introduction: Treatment with orally administered ibandronate is an effective way to increase bone mineral density (BMD) and reduce fracture rate in post-menopausal women and in men with osteoporosis. There are only very few reports concerning ibandro
Externí odkaz:
https://doaj.org/article/da761f76a1dc43e59a780af449ac0dc5
Publikováno v:
Developmental Cognitive Neuroscience, Vol 52, Iss , Pp 101023- (2021)
Prenatal learning of speech rhythm and melody is well documented. Much less is known about the earliest acquisition of segmental speech categories. We tested whether newborn infants perceive native vowels, but not nonspeech sounds, through some exist
Externí odkaz:
https://doaj.org/article/b4d8b0738ac446149cc0e18e67c2f491
Autor:
Martin Bezdíčka, Dana Zemková, Sylva Skálová, Eva Hovorková, Miroslav Podhola, Jan Burkert, Jakub Zieg
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Monogenic nephrotic syndrome (NS) is associated with a resistance to initial glucocorticoid therapy and causative variants, which may be found in several genes influencing podocyte stability and kidney development. The TTC21B gene, which encodes the
Externí odkaz:
https://doaj.org/article/76c93d0cacbe44bea1cd417d0d3b4726
Autor:
Jan Melek, Markéta Štanclová, Radek Štichhauer, Pavel Rozsíval, Jan Kopřiva, Jana Dědková, Eva Terifajova, Eva Šedivá, Petr Dědek, Sylva Skálová, Jan Bureš
Publikováno v:
Acta Medica, Vol 63, Iss 2, Pp 79-81 (2020)
A two-year-old girl with two weeks of abdominal pain, vomiting, and food refusal, ten months after percutaneous endoscopic gastrostomy insertion because of inadequate peroral intake, was admitted to a tertiary centre hospital. On admission, the extra
Externí odkaz:
https://doaj.org/article/be15958596354f13981e52469e11ba67
Publikováno v:
Acta Medica, Vol 52, Iss 4, Pp 141-147 (2009)
This report analyses data on 177 renal biopsies (RB) performed in 174 children in the East Bohemian region throughout 1997–2008. The primary aim was to evaluate the diagnostic benefit of the procedure, the secondary aim was to assess the safety of
Externí odkaz:
https://doaj.org/article/5111efbd59b54ea99693807fe3b1b9c8
Autor:
Sylva Skálová
Publikováno v:
Acta Medica, Vol 48, Iss 2, Pp 75-80 (2005)
The kidney function can be assessed by a number of methods. The urinary excretion of enzymes, in particular N-acetyl-β-D-glucosaminidase (NAG), is considered a relatively simple, cheap, fast and non-invasive method in the detection and follow-up of
Externí odkaz:
https://doaj.org/article/3189d632f5d74801815dc6452c3d2537
Autor:
Ziad Albahri, Eliška Marklová, Hubert Vaníček, Lenka Minxová, Petr Dědek, Sylva Skálová, Marika Talábová, Jaroslava Vávrová, Eva Rencová
Publikováno v:
Acta Medica, Vol 47, Iss 4, Pp 267-272 (2004)
The aim of this study is to report our 3years experience with the screening of congenital disorders of glycosylation. A common isoelectric focusing method with immunofixation was used for analysis of serum transferrin and α1-antitrypsin, apart from
Externí odkaz:
https://doaj.org/article/10cb0e0e5ddc440ba60e6d1d45ceeb56
Publikováno v:
Acta Medica, Vol 53, Iss 3, Pp 157-159 (2010)
Podocin mutations (NPHS2 gene) are mostly responsible for steroid-resistant nephrotic syndrome (SRNS) of childhood onset. Patients with NPHS2 gene mutations do not respond to corticoids and other immunosuppressive agents; partial remission can be rar
Externí odkaz:
https://doaj.org/article/2f110bd984444818a3d95761efad4f50
Autor:
Sylva Skálová, Štěpán Kutílek
Publikováno v:
Acta Medica, Vol 49, Iss 2, Pp 109-111 (2006)
Idiopathic hypercalciuria (IH) is defined as hypercalciuria that persists after correction of dietary inbalances and has no detectable cause. The excretion of urinary N-acetyl-beta-D-glucosaminidase (U-NAG), a marker of proximal tubular damage, has b
Externí odkaz:
https://doaj.org/article/5ec5afcbb7d94bf7a7a2d9929ac4af85