HbA(1c) levels in schoolchildren with type 1 diabetes are seasonally variable and dependent on weather conditions.Thiopurine S-methyltransferase (TPMT) polymorphisms in children with acute lymphoblastic leukemia, and the need for reduction or cessation of 6-mercaptopurine doses during maintenance therapy: the Polish multicenter analysis.FOXP3, IL-10, and TGF-β genes expression in children with IgE-dependent food allergyLess but better: cardioprotective lipid profile of patients with GCK-MODY despite lower HDL cholesterol level.MLL-rearranged B lymphoblastic leukemias selectively express the immunoregulatory carbohydrate-binding protein galectin-1.Polymorphism of the FTO Gene Influences Body Weight in Children with Type 1 Diabetes without Severe Obesity.Vitamin D receptor gene variability as a factor influencing bone mineral density in pediatric patients.Weekend admissions to paediatric/neonatal intensive care units are associated with longer hospitalisation time but not with greater mortality.Central nervous system PET-CT imaging reveals regional impairments in pediatric patients with Wolfram syndromeEURO-WABB: an EU rare diseases registry for Wolfram syndrome, Alström syndrome and Bardet-Biedl syndrome.Phenotype variability and neonatal diabetes in a large family with heterozygous mutation of the glucokinase gene.One-step nucleic acid amplification testing in medullary thyroid cancer lymph nodes: a case series.Availability and outcomes of radiotherapy in Central Poland during the 2005-2012 period - an observational study.Altered platelets' morphological parameters in children with type 1 diabetes – a case-control study.Assessment of insulin sensitivity in adults with permanent neonatal diabetes mellitus due to mutations in the KCNJ11 gene encoding Kir6.2.Influence of genomic variation in FTO at 16q12.2, MC4R at 18q22 and NRXN3 at 14q31 genes on breast cancer risk.Decreased FOXP3 mRNA expression in children with atopic asthma and IgE-mediated food allergy.Administration of CD4+CD25highCD127- regulatory T cells preserves β-cell function in type 1 diabetes in children.Prevalence of monogenic diabetes amongst Polish children after a nationwide genetic screening campaign.Glycemic variability in patients with Wolfram syndrome is lower than in type 1 diabetes.Is the SIOP-2001 Classification of Renal Tumors of Childhood accurate with regard to prognosis? A problem revisitedThree-year comparison of subcutaneous insulin pump treatment with multi-daily injections on HbA1c, its variability and hospital burden of children with type 1 diabetes.Efficacy of metabolic and psychological screening for mood disorders among children with type 1 diabetesDevelopment of treatment and clinical results in childhood acute myeloid leukemia in Poland.Dental Anomalies as Late Adverse Effect among Young Children Treated for Cancer.Differential regulation of serum microRNA expression by HNF1β and HNF1α transcription factors.Genetic polymorphisms in DNA base excision repair gene XRCC1 and the risk of squamous cell carcinoma of the head and neck.Impact of mTOR expression on clinical outcome in paediatric patients with B-cell acute lymphoblastic leukaemia - preliminary reportAbnormal serum microRNA profiles in tuberous sclerosis are normalized during treatment with everolimus: possible clinical implications.Can geneticists help clinicians to understand and treat non-autoimmune diabetes?Interleukin 18 as a marker of chronic nephropathy in children after anticancer treatment.L-thyroxine stabilizes autoimmune inflammatory process in euthyroid nongoitrous children with Hashimoto's thyroiditis and type 1 diabetes mellitus.Cystatin C is not a good candidate biomarker for HNF1A-MODY.The Role of Histone Protein Modifications and Mutations in Histone Modifiers in Pediatric B-Cell Progenitor Acute Lymphoblastic Leukemia.The first investigation of Wilms' tumour atomic structure-nitrogen and carbon isotopic composition as a novel biomarker for the most individual approach in cancer disease.Megaloblastic anaemia in infancy or early childhood and diabetes as leading symptoms of the TRMA syndrome.Factor XIII deficiency in Henoch-Schönlein purpura - report on two cases and literature review.Retinal thickness as a marker of disease progression in longitudinal observation of patients with Wolfram syndrome.Natural History and Current Treatment Options for Subependymal Giant Cell Astrocytoma in Tuberous Sclerosis Complex.Clinical course and therapeutic implications for lymphoid malignancies in Nijmegen breakage syndrome.
P50
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P50
description
Polish pediatrician
@en
polski lekarz, pediatra, hematolog i onkolog dziecięcy
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péidiatraí Polannach
@ga
name
Wojciech Młynarski
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Wojciech Młynarski
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Wojciech Młynarski
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Wojciech Młynarski
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Wojciech Młynarski
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Wojciech Młynarski
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Wojciech Młynarski
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Wojciech Młynarski
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Wojciech Młynarski
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Wojciech Młynarski
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Wojciech Młynarski
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Wojciech Młynarski
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Wojciech Młynarski
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Wojciech Młynarski
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Wojciech Młynarski
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Wojciech Młynarski
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Wojciech Młynarski
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Wojciech Młynarski
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Wojciech Młynarski
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Wojciech Młynarski
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Wojciech Michał Młynarski
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Wojciech Mlynarski
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prefLabel
Wojciech Młynarski
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Wojciech Młynarski
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Wojciech Młynarski
@de
Wojciech Młynarski
@en
Wojciech Młynarski
@es
Wojciech Młynarski
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Wojciech Młynarski
@ga
Wojciech Młynarski
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Wojciech Młynarski
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Wojciech Młynarski
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P106
P1412
P1559
Wojciech Młynarski
@pl
P21
P214
5950156317466102350005
P27
P31
P3124
P569
1971-12-12T00:00:00Z
P734
P7859
viaf-5950156317466102350005