S. Skálová

发表

Serum homocysteine levels in children and adolescents with impaired bone health.

Š. Kutílek, Petra Rehackova, S. Skálová, 2013, Revista brasileira de reumatologia.

The diagnostic role of urinary N-acetyl-beta-D-glucosaminidase (NAG) activity in the detection of renal tubular impairment.

S. Skálová, 2005, Acta medica.

Vitamin D status of very low birth weight infants at birth and the effects of generally recommended supplementation on their vitamin D levels at discharge

V. Palička, J. Maly, J. Maláková, 2019, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Parathyroid hormone – reference values and association with other bone metabolism markers in very low birth weight infants – pilot study

Intravenous pamidronate in the treatment of severe idiopathic infantile hypercalcemia.

M. Konrad, K. Schlingmann, Š. Kutílek, 2013, Iranian journal of kidney diseases.

Severe vitamin D deficiency in preterm infants: possibly no association with clinical outcomes?

V. Palička, J. Maláková, E. Čermáková, 2020, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Paediatric renal biopsies in East Bohemia. single centre experience in the years 1997-2008.

M. Podhola, S. Skálová, P. Rejtar, 2009, Acta medica.

Chronic kidney disease in children

J. Zieg, S. Skálová, 2017 .

Tubuloglomerular Disease With Cone-Shaped Epiphyses Associated With Hypomorphic Variant and a Novel p.Cys14Arg in the TTC21B Gene: A Case Report

E. Hovorková, J. Burkert, J. Zieg, 2021, Frontiers in Pediatrics.

Rituximab resistant evans syndrome and autoimmunity in Schimke immuno-osseous dysplasia

C. Boerkoel, T. Seeman, E. Levtchenko, 2011, Pediatric rheumatology online journal.

Hypokalaemic Paralysis Revealing Sjogren's Syndrome in a 16-Year Old Girl.

R. Slezák, S. Skálová, L. Minxová, 2008, Ghana medical journal.

Diagnosis and treatment of nephrotic syndrome in children

J. Zieg, S. Skálová, 2017 .

Is cyclophosphamide effective in patients with IgM-positive minimal change disease?

J. Feber, P. Geier, S. Skálová, 2012, Pediatric Nephrology.

Plasmapheresis-induced clinical improvement in a patient with steroid-resistant nephrotic syndrome due to podocin (NPHS2) gene mutation.

G. Chernin, M. Podhola, S. Skálová, 2010, Acta medica.

Wegener's granulomatosis in a 15-year-old boy.

M. Podhola, S. Skálová, L. Minxová, 2003, The Turkish journal of pediatrics.

Newborns’ neural processing of native vowels reveals directional asymmetries

Jan Kremláček, K. Chládková, S. Skálová, 2021, Developmental Cognitive Neuroscience.

Transient hyperphosphatemia: a benign laboratory disorder in a boy with Gitelman syndrome.

Š. Kutílek, S. Skálová, 2016, Jornal brasileiro de nefrologia : 'orgao oficial de Sociedades Brasileira e Latino-Americana de Nefrologia.

Transient hyperphosphatasemia in pediatric renal transplant patients – Is there a need for concern and when?

J. Feber, Š. Kutílek, P. Geier, 2012, Pediatric transplantation.

Intracardiac Thromboembolic Complications in Nephrotic Syndrome

S. Skálová, 2017 .

The urofacial (Ochoa) syndrome--first case in the central European population.

V. Jüttnerová, S. Skálová, I. Rejtar, 2006, Prague medical report.

Intracardiac thrombus--a rare complication of the steroid resistant nephrotic syndrome.

A. Lukes, P. Dědek, J. Hak, 2008, Bratislavske lekarske listy.

Metamizol in paediatric pain management

M. Kopecká, P. Rozsival, S. Skálová, 2020, Pediatrie pro praxi.

Safety profile of paediatric percutaneous ultrasonography-guided renal biopsies.

S. Skálová, P. Rejtar, 2010, Singapore medical journal.

Acute postinfectious glomerulonephritis: one disease with many faces

J. Zieg, S. Skálová, 2021, Pediatrie pro praxi.

Urinary N-acetyl-beta-D-glucosaminidase (U-NAG) activity in children with vesicoureteral reflux.

Š. Kutílek, S. Skálová, P. Rejtar, 2009, Bratislavske lekarske listy.

Transient hyperphosphatasemia in a child with nephrolithiasis and severe prematurity.

Š. Kutílek, M. Šenkeřík, S. Skálová, 2017, Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia.

Gitelman syndrome as a cause of psychomotor retardation in a toddler.

J. Štekrová, S. Skálová, P. Lněnička, 2013, Arab journal of nephrology and transplantation.

Increased urinary N-acetyl-beta-D-glucosaminidase activity in children with hydronephrosis.

Š. Kutílek, S. Skálová, P. Rejtar, 2007, International braz j urol : official journal of the Brazilian Society of Urology.

Bone mineral density and urinary N‐acetyl‐β‐ d‐glucosaminidase activity in paediatric patients with idiopathic hypercalciuria

Š. Kutílek, V. Palička, S. Skálová, 2005, Nephrology.

Genetic variants of transferrin in the diagnosis of protein hypoglycosylation

P. Dědek, S. Skálová, E. Marklová, 2005, Journal of Inherited Metabolic Disease.

Mesalazine-Induced Interstitial Nephritis

O. Pozler, P. Dědek, M. Podhola, 2009, Renal failure.

The Development and Neurophysiological Assessment of Newborn Auditory Cognition: A Review of Findings and Their Application.

Jan Kremláček, K. Chládková, S. Skálová, 2022, Acta medica.

Erroneous diagnosis of rickets.

Š. Kutílek, S. Skálová, 2017, Turk pediatri arsivi.

Three Different Causes of Hypercalciuria

M. Konrad, Š. Kutílek, S. Skálová, 2009, Klinische Padiatrie.

Rituximab resistant evans syndrome and autoimmunity in Schimke immuno-osseous dysplasia

C. Boerkoel, T. Seeman, E. Levtchenko, 2011, Pediatric rheumatology online journal.

RENAL VEIN THROMBOSIS WITH PULMONARY EMBOLISM: FIRST MANIFESTATION OF LUPUS NEPHRITIS

A. Lukes, P. Dědek, M. Podhola, 2011, Journal of paediatrics and child health.