Bik-Multanowski, Mirosław.
Mirosław Bik-Multanowski
VIAF ID: 164208462 (Personal)
Permalink: http://viaf.org/viaf/164208462
Preferred Forms
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- 100 1 _ ‡a Bik-Multanowski, Mirosław
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- 100 0 _ ‡a Mirosław Bik-Multanowski
4xx's: Alternate Name Forms (9)
Works
Title | Sources |
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208 Bone Morphogenetic Proteins Genes and Neural Tube Defects | |
Additional risk factor for the development of ALL. | |
Amino acid profile in blood plasma of young boys with autism | |
Analiza mutacji genu hydroksylazy fenyloalaninowej u polskich pacjentów z fenyloketonurią jako wstęp do terapii tetrahydrobiopteryną | |
AO-14. Whole genome expression in very low birth weight | |
Brain phenylalanine measurement in patients with phenylketonuria: a serious diagnostic method or just reading tea leaves? | |
Cardiovascular Anomalies among 1005 Fetuses Referred to Invasive Prenatal Testing—A Comprehensive Cohort Study of Associated Chromosomal Aberrations | |
Carriership of the rs113883650/rs2287120 haplotype of the SLC7A5 (LAT1) gene increases the risk of obesity in infants with phenylketonuria | |
Case report of endoprosthesis -Y implantation in severe respiratory failure in the MPSII patient; comparison with literature data | |
Choroba Gauchera – zalecenia dotyczące rozpoznawania, leczenia i monitorowania | |
Choroby okresu noworodkowego, choroby układu oddechowego, choroby alergiczne, choroby tkanki łącznej, genetyka kliniczna | |
The clinical role of vascular endothelial growth factor (VEGF) system in the pathogenesis of retinopathy of prematurity | |
Comparison of whole genome expression profile between preterm and full-term newborns. | |
COVID-19 Pandemic and Patients with Rare Inherited Metabolic Disorders and Rare Autoinflammatory Diseases-Organizational Challenges from the Point of View of Healthcare Providers | |
Development and maturation of the immune system in preterm neonates: results from a whole genome expression study | |
Development of a model for assessment of phenylalanine hydroxylase activity in newborns with phenylketonuria receiving tetrahydrobiopterin: a potential for practical implementation | |
Developmental delay with hypotrophy associated with homozygous functionally relevant REV3L variant | |
Diagnostyka genetyczna pacjentów z opóźnieniem rozwoju psychomotorycznego, niepełnosprawnością intelektualną i zaburzeniami ze spektrum autyzmu | |
Dynamics of hyperphenylalaninemia and intellectual outcome in teenagers with phenylketonuria | |
[Early enzyme replacement therapy - hope for patients with mucopolysaccharidosis Type II]. | |
The Expression of Genes Related to Lipid Metabolism and Metabolic Disorders in Children before and after Hematopoietic Stem Cell Transplantation-A Prospective Observational Study | |
Expression of SCGB1C1 gene as a potential marker of susceptibility to upper respiratory tract infections in elite athletes - a pilot study | |
Galaktozemia | |
Gene expression profiling in preterm infants: new aspects of bronchopulmonary dysplasia development | |
[Genotyping and treatment modification in patients with phenylketonuria: an introduction to pharmacogenomics]. | |
Genotypowanie a zmiana rodzaju leczenia u pacjentów z fenyloketonurią jako wstęp do farmakogenomiki | |
High Frequency of Fusion Gene Transcript Resulting From t(10;11)(p12;q23) Translocation in Pediatric Acute Myeloid Leukemia in Poland | |
Human Induced Pluripotent Stem Cell-Derived Microvesicles Transmit RNAs and Proteins to Recipient Mature Heart Cells Modulating Cell Fate and Behavior. | |
Hypermethylation of NRG1 gene correlates with the presence of heart defects in Down's syndrome | |
Hyperoxia induces epigenetic changes in newborn mice lungs. | |
Immune System Regulation Affected by a Murine Experimental Model of Bronchopulmonary Dysplasia: Genomic and Epigenetic Findings | |
Impact of antenatal glucocorticosteroids on whole-genome expression in preterm babies | |
Influence of therapeutic proton beam on glioblastoma multiforme proliferation index : a preliminary study | |
[Inherited hyperammonemia] | |
The Insight into Insulin-Like Growth Factors and Insulin-Like Growth-Factor-Binding Proteins and Metabolic Profile in Pediatric Obesity | |
Intima media thickness of common carotids and abdominal aorta in children and adolescents with congenital adrenal hyperplasia due to 21-hydroxylase deficiency in relation to their genotypes. | |
LAT1 gene variants--potential factors influencing the clinical course of phenylketonuria. | |
Medycyna rodzinna | |
Methylation and Expression of and Genes in Childhood Obesity: Insight into Anthropometric Parameters and Glucose-Lipid Metabolism | |
Mikromacierze DNA nowym narzędziem diagnostycznym w pediatrii | |
Molecular genetics of PKU in Poland and potential impact of mutations on BH4 responsiveness | |
Molecular karyotyping in early miscarriages: potential for the routine use of cytogenetic microarrays. | |
MTRNR2L12: A Candidate Blood Marker of Early Alzheimer's Disease-Like Dementia in Adults with Down Syndrome | |
Mutacja Asp299Gly genu Toll-like receptor-4 u dzieci z nieswoistymi zapaleniami jelit w południowo-wschodniej Polsce | |
Najczęstsze choroby metaboliczne u noworodka | |
Neurodegenerative changes detected by neuroimaging in a patient with contiguous X-chromosome deletion syndrome encompassing BTK and TIMM8A genes | |
New insight into the pathogenesis of retinopathy of prematurity: assessment of whole-genome expression | |
Nowa mutacja (p. Leu700Phe) w genie receptora androgenowego – opis spokrewnionych pacjentek z wczesnym rozpoznaniem zespołu całkowitej niewrażliwości na androgeny | |
Patient's weight can decide about spending millions on enzyme replacement therapy in MPS II | |
Plasma levels of leptin and soluble leptin receptor and polymorphisms of leptin gene -18G > A and leptin receptor genes K109R and Q223R, in survivors of childhood acute lymphoblastic leukemia | |
Podstawowe techniki badań molelularnych | |
Polimorfizmy genów kodujących czynnik wzrostu śródbłonka naczyniowego (VEGF) i transformującego czynnika wzrostowego (TGFbeta-1) jako czynniki ryzyka retinopatii wcześniaczej | |
Polymorphisms of SLC19A1 80 G>A, MTHFR 677 C>T, and Tandem TS Repeats Influence Pharmacokinetics, Acute Liver Toxicity, and Vomiting in Children With Acute Lymphoblastic Leukemia Treated With High Doses of Methotrexate | |
Polymorphisms of the 5,10-methylenetetrahydrofolate and the methionine synthase reductase genes as independent risk factors for spina bifida | |
PP-185. Genome wide microarray analysis in very low birth weight (VLBW) infants with retinopathy of prematurity (ROP) — Preliminary results | |
Quality of life in noncompliant adults with phenylketonuria after resumption of the diet | |
Routine use of CANTAB system for detection of neuropsychological deficits in patients with PKU. | |
The rs113883650 variant of gene may alter brain phenylalanine content in PKU | |
The rs9939609T>A polymorphism of the FTO gene and overweight in survivors of ALL | |
Severe dystonic encephalopathy without hyperphenylalaninemia associated with an 18-bp deletion within the proximal GCH1 promoter | |
Short- and long-term impact of hyperoxia on the blood and retinal cells' transcriptome in a mouse model of oxygen-induced retinopathy | |
Single exon deletions in the PAH gene in Polish PKU-patients | |
Techniki w badaniach cytogenetycznych | |
Transcriptome analysis reveals dysregulation of genes involved in oxidative phosphorylation in a murine model of retinopathy of prematurity | |
Unfavorable Outcome of Neuroblastoma in Patients With 2p Gain | |
Untreated PKU Patients without Intellectual Disability: What Do They Teach Us? | |
[Use of computerized neuropsychological tests and of nuclear magnetic resonance spectroscopy in clinical assessment of adult patients with phenylketonuria]. | |
The Use of d2 and Benton Tests for Assessment of Attention Deficits and Visual Memory in Teenagers with Phenylketonuria. | |
[The use of microarrays for gene expression analysis in premature children--new strategy of searching for genetic basis of late complications of prematurity--preliminary research] | |
Whole Genome Expression in Newborn Mouse Brain Tissue after Hypoxia and Reoxygenation | |
Wybrane zagadnienia z pediatrii : podręcznik dla studentów medycyny i lekarzy. | |
Zaburzenia poznawcze i emocjonalne w przebiegu fenyloketonurii = Cognitive and emotional disorders in the course of phenylketonuria | |
Zastosowanie mikromacierzy do oceny ekspresji genów u wcześniaków : nowa strategia poszukiwania genetycznego podłoża odległych powikłań wcześniactwa : badania wstępne | |
Zastosowanie spektroskopii magnetycznego rezonansu jądrowego w celu oceny mózgowego stężenia fenyloalaniny u chorych na fenyloketonurię |