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Radiologic measurement of cochlea and hearing preservation rate using slim straight electrode (CI422) and round window approach

Acta otorhino-laryngologica italica, 2018-10, Vol.38 (5), p.468-475

2018

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Malnutrition Risk in Kidney Recipients Treated With Mycophenolate Mofetil Is Associated With IMPDH1 rs2278294 Polymorphism

Transplantation proceedings, 2018-07, Vol.50 (6), p.1794-1797

2018

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Novel sporadic and recurrent mutations in KRT5 and KRT14 genes in Polish epidermolysis bullosa simplex patients: further insights into epidemiology and genotype–phenotype correlation

Journal of applied genetics, 2016-05, Vol.57 (2), p.175-181

2016

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Genotype and phenotype correlation of monogenic corneal dystrophies in population of central Poland

Acta ophthalmologica (Oxford, England), 2015-10, Vol.93 (S255), p.n/a

2015

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Association of MYH9 rs3752462 and rs5756168 Polymorphisms With Transplanted Kidney Artery Stenosis

Transplantation proceedings, 2016-06, Vol.48 (5), p.1561-1565

2016

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A variant rs613872 in TCF4 gene is responsible for the higher risk for Fuchs endothelial corneal dystrophy development‐ the results of study in Polish patients

Acta ophthalmologica (Oxford, England), 2015-10, Vol.93 (S255), p.n/a

2015

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Recipient Uridine 5′-Diphospho-glucuronosyltransferase UGT1A9 c.98T>C Variant Determines Transplanted Kidney Filtration Rate

Transplantation proceedings, 2014-10, Vol.46 (8), p.2678-2682

2014

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GJB2 and hearing impairment: promoter defects do not explain the excess of monoallelic mutations

Journal of medical genetics, 2008-09, Vol.45 (9), p.607-608

2008

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7. GENETIC TESTING FOR COPY NUMBER VARIATIONS IN FIRST POLAR BODIES AND OOCYTES BY SINGLE-CELL NEXT-GENERATION SEQUENCING

Reproductive biomedicine online, 2019-08, Vol.39, p.e30-e31

2019

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Multidrug Resistance-Associated Protein 2 Gene ( ABCC2 ) Variant in Kidney Allograft Recipients

Transplantation proceedings, 2009-10, Vol.41 (8), p.3009-3010

2009

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Uridine Diphosphate Glucuronosyltransferase 2B7 Variant p.His268Tyr as a Predictor of Kidney Allograft Early Acute Rejection

Transplantation proceedings, 2013-05, Vol.45 (4), p.1516-1519

2013

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A variant rs613872 in TCF 4 gene is responsible for the higher risk for Fuchs endothelial corneal dystrophy development‐ the results of study in Polish patients

Acta ophthalmologica (Oxford, England), 2015-10, Vol.93 (S255)

2015

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Clinical aspects of disrupted Hedgehog signaling (Review)

International journal of molecular medicine, 2001-10, Vol.8 (4), p.445

2001

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Lymphocyte Counts in Kidney Allograft Recipients Are Associated With IMPDH2 3757T>C Gene Polymorphism

Transplantation proceedings, 2011-10, Vol.43 (8), p.2943-2945

2011

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Molecular activity of sirolimus and its possible application in tuberous sclerosis treatment

Medicinal research reviews, 2006-03, Vol.26 (2), p.160-180

2006

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Fibular aplasia with ectrodactyly—broadening the clinical spectrum

European journal of medical genetics, 2006, Vol.49 (1), p.83-86

2006

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The Papillomavirus E2 Protein Binds to and Synergizes with C/EBP Factors Involved in Keratinocyte Differentiation

Journal of Virology, 2003-05, Vol.77 (9), p.5253-5265

2003

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Pentoxifylline inhibits perforin-dependent natural cytotoxicity in vitro

Oncology reports, 2002-03, Vol.9 (2), p.423

2002

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Congenital anomalies and developmental delay in a boy with double chromosome 6 derived supernumerary marker

Genetic counseling, 2006, Vol.17 (1), p.29

2006

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Unusual phenotype in a family with the R124C mutation in the TGFBI gene

Acta ophthalmologica (Oxford, England), 2012-09, Vol.90 (s249), p.0-0

2012

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MTHFR 677T is a strong determinant of the degree of hearing loss among Polish males with postlingual sensorineural hearing impairment

DNA and cell biology, 2012-07, Vol.31 (7), p.1267

2012

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Influence of culture medium pH on cytotoxicity of CD95L in vitro

Folia histochemica et cytobiologica, 2001, Vol.39 (1), p.29

2001

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Detection of a novel premature stop codon in the OPA1 gene in autosomal dominant optic atrophy

Acta ophthalmologica (Oxford, England), 2012-09, Vol.90 (s249), p.0-0

2012

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The adenoviral E1A oncoprotein activates the Smad7 promoter: Requirement of a functional E-box

International journal of oncology, 2009-12, Vol.35 (6), p.1493-1498

2009

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Novel mutation in the TGFBI gene in a patient with a late‐onset lattice corneal dystrophy

Acta ophthalmologica (Oxford, England), 2010-09, Vol.88 (s246), p.0-0

2010

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Radiologic measurement of cochlea and hearing preservation rate using slim straight electrode (CI422) and round window approach

Malnutrition Risk in Kidney Recipients Treated With Mycophenolate Mofetil Is Associated With IMPDH1 rs2278294 Polymorphism

Novel sporadic and recurrent mutations in KRT5 and KRT14 genes in Polish epidermolysis bullosa simplex patients: further insights into epidemiology and genotype–phenotype correlation

Genotype and phenotype correlation of monogenic corneal dystrophies in population of central Poland

Association of MYH9 rs3752462 and rs5756168 Polymorphisms With Transplanted Kidney Artery Stenosis

A variant rs613872 in TCF4 gene is responsible for the higher risk for Fuchs endothelial corneal dystrophy development‐ the results of study in Polish patients

Recipient Uridine 5′-Diphospho-glucuronosyltransferase UGT1A9 c.98T>C Variant Determines Transplanted Kidney Filtration Rate

GJB2 and hearing impairment: promoter defects do not explain the excess of monoallelic mutations

7. GENETIC TESTING FOR COPY NUMBER VARIATIONS IN FIRST POLAR BODIES AND OOCYTES BY SINGLE-CELL NEXT-GENERATION SEQUENCING

Multidrug Resistance-Associated Protein 2 Gene ( ABCC2 ) Variant in Kidney Allograft Recipients

Uridine Diphosphate Glucuronosyltransferase 2B7 Variant p.His268Tyr as a Predictor of Kidney Allograft Early Acute Rejection

A variant rs613872 in TCF 4 gene is responsible for the higher risk for Fuchs endothelial corneal dystrophy development‐ the results of study in Polish patients

Clinical aspects of disrupted Hedgehog signaling (Review)

Lymphocyte Counts in Kidney Allograft Recipients Are Associated With IMPDH2 3757T>C Gene Polymorphism

Molecular activity of sirolimus and its possible application in tuberous sclerosis treatment

Fibular aplasia with ectrodactyly—broadening the clinical spectrum

The Papillomavirus E2 Protein Binds to and Synergizes with C/EBP Factors Involved in Keratinocyte Differentiation

Pentoxifylline inhibits perforin-dependent natural cytotoxicity in vitro

Congenital anomalies and developmental delay in a boy with double chromosome 6 derived supernumerary marker

Unusual phenotype in a family with the R124C mutation in the TGFBI gene

MTHFR 677T is a strong determinant of the degree of hearing loss among Polish males with postlingual sensorineural hearing impairment

Influence of culture medium pH on cytotoxicity of CD95L in vitro

Detection of a novel premature stop codon in the OPA1 gene in autosomal dominant optic atrophy

The adenoviral E1A oncoprotein activates the Smad7 promoter: Requirement of a functional E-box

Novel mutation in the TGFBI gene in a patient with a late‐onset lattice corneal dystrophy

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