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Acute kidney injury requiring renal replacement therapy due to Clostridioides difficile infection in a 15-year-old boy

Epidemiologie, mikrobiologie, imunologie, 2022, Vol.71 (4), p.208

2022

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1037 Determination of Prealbumin, Selenium, Zinc and Iron Concentration in Serum for Monitoring the Nutrition Status of Phenylketonuric and Hyperphenylalaninemic Patients

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A297-A297

2012

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Juxtaglomerular cell tumor--a rare cause of secondary hypertension

Bratislavské lékarské listy, 2010, Vol.111 (12), p.653-655

2010

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Transplantation Outcomes in Primary Hyperoxaluria

American journal of transplantation, 2010-11, Vol.10 (11), p.2493-2501

2010

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Increased risk of vitamin B12 nutritional deficiency in long-term treated patients with phenylketonuria and hyperfenylalaninemia

Archives of disease in childhood, 2014-10, Vol.99 (10), p.A292

2014

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PO-0136Increased Risk Of Vitamin B12 Nutritional Deficiency In Long-term Treated Patients With Phenylketonuria And Hyperfenylalaninemia

Archives of disease in childhood, 2014-10, Vol.99 (Suppl 2), p.A292-A292

2014

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PO-0136 Increased Risk Of Vitamin B12 Nutritional Deficiency In Long-term Treated Patients With Phenylketonuria And Hyperfenylalaninemia

Archives of disease in childhood, 2014-10, Vol.99 (Suppl 2), p.A292-A292

2014

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Secondary pseudohypoaldosteronism in an infant with pyelonephritis

Bratislavské lékarské listy, 2004, Vol.105 (12), p.435-437

2004

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Compound Heterozygous Mutations in the Vitamin D Receptor in a Patient With Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets With Alopecia

Journal of bone and mineral research, 2009-04, Vol.24 (4), p.643-651

2009

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1016 Tetrahydrobiopterin Responsiveness After Loading Test of 21 Czech Hpa/Pku Patients and Correlations to Their Genotype

Pediatric research, 2010-11, Vol.68, p.505-505

2010

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The rare cause of hypokalaemia [Letters and Replies]

Nephrology, dialysis, transplantation, 2000-09, Vol.15 (9), p.1475-1476

2000

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The analysis of the risks for the development of tumour lysis syndrome in children

Bratislavské lékarské listy, 2002, Vol.103 (6), p.206-209

2002

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Is it possible to influence the mortality in children with hemolytic uremic syndrome?

Bratislavské lékarské listy, 2001, Vol.102 (2), p.59-65

2001

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Oral rehydration in the therapy of simple diarrhea in infants and toddlers

Bratislavské lékarské listy, 2001, Vol.102 (10), p.485-486

2001

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Effects of intravitreal pegaptanib or bevacizumab and laser in treatment of threshold retinopathy of prematurity in zone I and posterior zone II--four years results

Česká a slovenská oftalmologie, 2012-02, Vol.68 (1), p.29

2012

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Liddle syndrome caused by P616R mutation of the epithelial sodium channel beta subunit

Pediatric nephrology (Berlin, West), 2005-06, Vol.20 (6), p.837-838

2005

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Paroxysmal nocturnal hemoglobinuria in a girl with hemolysis and "hematuria"

Pediatric nephrology (Berlin, West), 2004-10, Vol.19 (10), p.1177-1179

2004

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Refractive Surgery in Children with Myopic Anisometropia and Amblyopia in Comparison with Conventional Treatment by Contact Lenses

Česká a slovenská oftalmologie, 2016, Vol.72 (2), p.12

2016

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Rare ocular manifestation with suspect alport syndrome

Česká a slovenská oftalmologie, 2014-06, Vol.70 (3), p.114

2014

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Diagnosis of acute pyelonephritis in childhood: comparison of ultrasonographic examination and renal scintigraphy using 99mTc DMSA

Bratislavské lékarské listy, 2000, Vol.101 (9), p.495-498

2000

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An addition to the algorithm for treatment of typical forms of the hemolytic-uremic syndrome in children

Československá pediatrie, 1992-06, Vol.47 (6), p.368

1992

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ECG in neonatal hypocalcemia

Československá pediatrie, 1984-09, Vol.39 (9), p.555

Dolezel, Z

1984

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An algorithm for the therapy of typical forms of the hemolytic-uremic syndrome in children

Československá pediatrie, 1988-11, Vol.43 (11), p.680

1988

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The hemolytic-uremic syndrome in enterocolitis caused by Campylobacter jejuni

Československá pediatrie, 1993-11, Vol.48 (11), p.659

1993

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Autoimmune adrenalitis--idiopathic Addison's disease

Československá pediatrie, 1993-05, Vol.48 (5), p.270

1993

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Acute kidney injury requiring renal replacement therapy due to Clostridioides difficile infection in a 15-year-old boy

1037 Determination of Prealbumin, Selenium, Zinc and Iron Concentration in Serum for Monitoring the Nutrition Status of Phenylketonuric and Hyperphenylalaninemic Patients

Juxtaglomerular cell tumor--a rare cause of secondary hypertension

Transplantation Outcomes in Primary Hyperoxaluria

Increased risk of vitamin B12 nutritional deficiency in long-term treated patients with phenylketonuria and hyperfenylalaninemia

PO-0136Increased Risk Of Vitamin B12 Nutritional Deficiency In Long-term Treated Patients With Phenylketonuria And Hyperfenylalaninemia

PO-0136 Increased Risk Of Vitamin B12 Nutritional Deficiency In Long-term Treated Patients With Phenylketonuria And Hyperfenylalaninemia

Secondary pseudohypoaldosteronism in an infant with pyelonephritis

Compound Heterozygous Mutations in the Vitamin D Receptor in a Patient With Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets With Alopecia

1016 Tetrahydrobiopterin Responsiveness After Loading Test of 21 Czech Hpa/Pku Patients and Correlations to Their Genotype

The rare cause of hypokalaemia [Letters and Replies]

The analysis of the risks for the development of tumour lysis syndrome in children

Is it possible to influence the mortality in children with hemolytic uremic syndrome?

Oral rehydration in the therapy of simple diarrhea in infants and toddlers

Effects of intravitreal pegaptanib or bevacizumab and laser in treatment of threshold retinopathy of prematurity in zone I and posterior zone II--four years results

Liddle syndrome caused by P616R mutation of the epithelial sodium channel beta subunit

Paroxysmal nocturnal hemoglobinuria in a girl with hemolysis and "hematuria"

Refractive Surgery in Children with Myopic Anisometropia and Amblyopia in Comparison with Conventional Treatment by Contact Lenses

Rare ocular manifestation with suspect alport syndrome

Diagnosis of acute pyelonephritis in childhood: comparison of ultrasonographic examination and renal scintigraphy using 99mTc DMSA

An addition to the algorithm for treatment of typical forms of the hemolytic-uremic syndrome in children

ECG in neonatal hypocalcemia

An algorithm for the therapy of typical forms of the hemolytic-uremic syndrome in children

The hemolytic-uremic syndrome in enterocolitis caused by Campylobacter jejuni

Autoimmune adrenalitis--idiopathic Addison's disease

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