Lista de obras -

-308 G/A TNF-α gene polymorphism influences the course of basal cell carcinoma in a Polish population

artículo científico publicado en 2015

A case with 47,XXY,del(11)(q23) karotype-coexistence of Jacobsen and Klinefelter syndromes

artículo científico publicado en 2000

Aberrations of chromosome 22 and polysomy of chromosome 8 as non-random changes in clear cell sarcoma.

artículo científico publicado en 1994

Abnormal karyotypes in three carcinomas of the gallbladder

scientific article published on 01 August 1994

Absence of structural rearrangements of chromosome 11 in human primary malignant melanoma

artículo científico publicado el 1 de febrero de 1992

Accumulation of chromosomal changes in human glioma progression. A cytogenetic study of 50 cases

artículo científico publicado en 1995

Assessment of Interleukin 16 Serum Levels and Skin Expression in Psoriasis Patients in Correlation with Clinical Severity of the Disease.

artículo científico publicado en 2016

Association between the -1154 G/A promoter polymorphism of the vascular endothelial growth factor gene and atopic dermatitis

artículo científico publicado en 2009

Association of distinct IL-31 polymorphisms with pruritus and severity of atopic dermatitis

scientific article published on 24 July 2012

Association of mastocytosis with interleukin 31 gene polymorphism

artículo científico publicado en 2015

Association of psoriasis with the VEGF gene polymorphism in the northern Polish population.

artículo científico publicado en 2011

Association of single nucleotide polymorphism of interleukin-18 with atopic dermatitis

artículo científico publicado en 2009

Associations of promoter region polymorphisms in the tumour necrosis factor-alpha gene and early-onset psoriasis vulgaris in a northern Polish population

scientific article published on 06 June 2007

Bioactive forms of vitamin D selectively stimulate the skin analog of the hypothalamus-pituitary-adrenal axis in human epidermal keratinocytes

artículo científico publicado en 2016

COVID-19 Vaccination in Mastocytosis: Recommendations of the European Competence Network on Mastocytosis (ECNM) and American Initiative in Mast Cell Diseases (AIM)

artículo científico publicado en 2021

Chemokines and cytokines network in the pathogenesis of the inflammatory skin diseases: atopic dermatitis, psoriasis and skin mastocytosis

artículo científico publicado en 2014

Chromosome aberrations, spontaneous SCE, and growth kinetics in PHA-stimulated lymphocytes of five cases with Sézary syndrome ⬇️

artículo científico publicado el 1 de agosto de 1995

Clear cell sarcoma of tendons and aponeuroses with t(12;22) (q13;q12) diagnosed initially as malignant melanoma

scientific article published on 01 October 1996

Clinical aspects of paediatric mastocytosis: a review of 101 cases

artículo científico publicado en 2011

Comparative analysis of IL6 and IL6 receptor gene polymorphisms in mastocytosis

artículo científico publicado en 2012

Cutaneous manifestations in patients with mastocytosis: Consensus report of the European Competence Network on Mastocytosis; the American Academy of Allergy, Asthma & Immunology; and the European Academy of Allergology and Clinical Immunology

artículo científico

Cytogenetic and immunohistochemical profile of myxoid liposarcoma

scientific article published on 01 January 1995

Cytogenetic findings in malignant peripheral nerve sheath tumors

artículo científico publicado en 1995

Cytogenetic findings in two synovial sarcomas

scientific article published on 01 April 1989

Cytogenetic studies of families with reproductive failure

artículo científico publicado en 1989

Cytogenetics of synovial sarcoma: presentation of ten new cases and review of the literature

artículo científico publicado en 1991

Cytogenetics of uterine sarcomas: presentation of eight new cases and review of the literature

artículo científico publicado en 1998

Definitions, criteria and global classification of mast cell disorders with special reference to mast cell activation syndromes: a consensus proposal

artículo científico publicado en 2011

Diagnosis of Mastocytosis in Children and Adults in Daily Clinical Practice

artículo científico publicado en 2016

Diffuse cutaneous mastocytosis: analysis of 10 cases and a brief review of the literature

artículo científico publicado en 2011

Does the aberrant expression of CD2 and CD25 by skin mast cells truly correlate with systemic involvement in patients presenting with mastocytosis in the skin?

artículo científico publicado en 2014

European Competence Network on Mastocytosis (ECNM): 10-year jubilee, update, and future perspectives

artículo científico publicado en 2012

Evaluation of the effectiveness of isoprinosine in the treatment of patients with acute viral hepatitis. I. Clinical evaluation

artículo científico publicado en 1987

Evaluation of the effectiveness of isoprinosine in the treatment of patients with acute viral hepatitis. II. Immunological evaluation

artículo científico publicado en 1987

Gene expression analysis predicts insect venom anaphylaxis in indolent systemic mastocytosis.

artículo científico

Gene expression profile, pathways, and transcriptional system regulation in indolent systemic mastocytosis.

artículo científico publicado en 2010

Genetic and Epigenetic Aspects of Atopic Dermatitis

artículo científico publicado en 2020

Global Classification of Mast Cell Activation Disorders: An ICD-10-CM–Adjusted Proposal of the ECNM-AIM Consortium

artículo científico publicado en 2022

Granulocyte-macrophage colony-stimulating factor (GM-CSF)-677C/a promoter gene polymorphism is not associated with acne vulgaris in Polish population

scientific article published on 01 January 2012

HLA-C locus alleles distribution in patients from northern Poland with psoriatic arthritis--preliminary report

artículo científico publicado en 2005

Hereditary alpha tryptasemia is a valid genetic biomarker for severe mediator-related symptoms in mastocytosis

scientific article published on 10 August 2020

High Resolution Melting analysis as a rapid and efficient method of screening for small mutations in the STK11 gene in patients with Peutz-Jeghers syndrome.

artículo científico publicado en 2013

High prevalence of carriers of variant c.1528G>C of HADHA gene causing long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD) in the population of adult Kashubians from North Poland.

artículo científico publicado en 2017

How to diagnose Mast Cell Activation Syndrome? Practical considerations

artículo científico publicado en 2020

Immune response against HtrA proteases in children with cutaneous mastocytosis.

artículo científico publicado en 2018

Interleukin-13 promoter gene polymorphism -1112 C/T is associated with atopic dermatitis in Polish patients

artículo científico publicado en 2012

Interleukin-13 promoter gene polymorphism -1112C/T is associated with the systemic form of mastocytosis

artículo científico publicado en 2009

Interleukin-31 Polymorphisms and Serum IL-31 Level in Patients with Mastocytosis: Correlation with Clinical Presen-tation and Pruritus.

artículo científico publicado en 2016

International prognostic scoring system for mastocytosis (IPSM): a retrospective cohort study

artículo científico publicado en 2019

Lack of association between the promoter polymorphisms at positions -238 and -308 of the tumour necrosis factor alpha gene and acne vulgaris in Polish patients

scientific article published on 26 June 2008

Mast cells in mastocytosis and allergy - Important player in metabolic and immunological homeostasis

scientific article published on 11 January 2019

Mastocytosis in children and adults: clinical disease heterogeneity

artículo científico publicado en 2012

Mediator-Related Symptoms and Anaphylaxis in Children with Mastocytosis

artículo científico publicado en 2021

Mediator-Related Symptoms and Anaphylaxis in Children with Mastocytosis

artículo científico publicado en 2021

Molecular Background, Clinical Features and Management of Pediatric Mastocytosis: Status 2021

artículo científico publicado en 2021

Monilethrix in monozygotic twins with very rare mutation in KRT 86 gene

scientific article published on 01 June 2017

New Approach to Paediatric Mastocytosis: Implications of KIT D816V Mutation Detection in Peripheral Blood

artículo científico publicado en 2020

Nonrandom secondary chromosome-aberrations in synovial sarcomas with t(x-18) ⬇️

artículo científico publicado el 1 de septiembre de 1995

On the significance of trisomy 7 and sex chromosome loss in renal cell carcinoma

artículo científico publicado en 1990

Parachordoma--a clinicopathologic, immunohistochemical, electron microscopic, flow cytometric, and cytogenetic study

artículo científico publicado en 1995

Pathogenesis of psoriasis in the "omic" era. Part I. Epidemiology, clinical manifestation, immunological and neuroendocrine disturbances

scientific article published on 01 April 2020

Pathogenesis of psoriasis in the "omic" era. Part II. Genetic, genomic and epigenetic changes in psoriasis

artículo científico publicado en 2020

Pathogenesis of psoriasis in the "omic" era. Part III. Metabolic disorders, metabolomics, nutrigenomics in psoriasis

artículo científico publicado en 2020

Pathogenesis of psoriasis in the "omic" era. Part IV. Epidemiology, genetics, immunopathogenesis, clinical manifestation and treatment of psoriatic arthritis

artículo científico publicado en 2020

Polymorphism in interleukin 1A but not in interleukin 8 gene predisposes to acne vulgaris in Polish population

artículo científico publicado en 2011

Polymorphism of the TAP1 gene in Polish patients with psoriasis vulgaris

scientific article published on 01 January 2004

Presence of Chlamydophila pneumoniae DNA in blood cells is a frequent event in patients with the late stage of primary cutaneous lymphomas and with atopic dermatitis.

artículo científico publicado en 2018

Primary cutaneous T-cell lymphomas show a deletion or translocation affecting NAV3, the human UNC-53 homologue

artículo científico publicado en 2005

Proposed Diagnostic Algorithm for Patients with Suspected Mast Cell Activation Syndrome

scientific article published on 05 February 2019

Proposed diagnostic algorithm for patients with suspected mastocytosis: a proposal of the European Competence Network on Mastocytosis.

artículo científico publicado en 2014

Refined Treatment Response Criteria for Indolent Systemic Mastocytosis Proposed by the ECNM-AIM Consortium

artículo científico publicado en 2022

Results from a Genome-Wide Association Study (GWAS) in Mastocytosis Reveal New Gene Polymorphisms Associated with WHO Subgroups

artículo científico publicado en 2020

Risk and Management of Patients with Mastocytosis and MCAS in the SARS-CoV-2 (COVID-19) Pandemic: Expert Opinions

scientific article published on 16 June 2020

Risk factors for anaphylaxis in patients with mastocytosis

scientific article published on 12 January 2015

Selecting the Right Criteria and Proper Classification to Diagnose Mast Cell Activation Syndromes: A Critical Review

artículo científico publicado en 2021

Specific Alu elements involved in a significant percentage of copy number variations of the STK11 gene in patients with Peutz-Jeghers syndrome.

artículo científico publicado en 2015

Standards of Genetic Testing in the Diagnosis and Prognostication of Systemic Mastocytosis in 2022: Recommendations of the EU-US Cooperative Group

artículo científico publicado en 2022

Standards of Pathology in the Diagnosis of Systemic Mastocytosis: Recommendations of the EU-US Cooperative Group

artículo científico publicado en 2022

Th1 response and cytotoxicity genes are down-regulated in cutaneous T-cell lymphoma

artículo científico publicado en 2006

The -2518 A/G MCP-1 and -403 G/A RANTES promoter gene polymorphisms are associated with psoriasis vulgaris

artículo científico publicado en 2016

The Brain-Skin Axis in Psoriasis-Psychological, Psychiatric, Hormonal, and Dermatological Aspects

artículo científico publicado en 2022

The Possible Role of Gene Variant Coding Nonfunctional Toll-Like Receptor 2 in the Pathogenesis of Mastocytosis

artículo científico publicado en 2018

The Role of TRAF4 and B3GAT1 Gene Expression in the Food Hypersensitivity and Insect Venom Allergy in Mastocytosis.

scientific article published on 16 April 2016

The association of GM-CSF -677A/C promoter gene polymorphism with the occurrence and severity of atopic dermatitis in a Polish population.

artículo científico publicado en 2013

The frequencies of haplotypes defined by three polymorphisms of the IL-31 gene: -1066, -2057, and IVS2+12 in Polish patients with atopic dermatitis

artículo científico publicado en 2015

The role of KIT gene mutations in pathogenesis of pediatric mastocytosis

artículo científico publicado en 2015

The role of polymorphism of interleukin-2, -10, -13 and TNF-α genes in cutaneous T-cell lymphoma pathogenesis.

artículo científico publicado en 2016

The role of regulatory T cells and genes involved in their differentiation in pathogenesis of selected inflammatory and neoplastic skin diseases. Part I: Treg properties and functions

artículo científico publicado en 2017

The role of regulatory T cells and genes involved in their differentiation in pathogenesis of selected inflammatory and neoplastic skin diseases. Part II: The Treg role in skin diseases pathogenesis.

artículo científico publicado en 2017

The role of regulatory T cells and genes involved in their differentiation in pathogenesis of selected inflammatory and neoplastic skin diseases. Part III: Polymorphisms of genes involved in Tregs' activation and function.

artículo científico publicado en 2017

The role of serum tryptase in the diagnosis and monitoring of pediatric mastocytosis: a single-center experience.

artículo científico publicado en 2017

The significance of Toll-like receptor (TLR) 2 and 9 gene polymorphisms in psoriasis

artículo científico publicado en 2017

Translocation (6;16) in a case of granulosa cell tumor of the ovary

artículo científico publicado el 1 de mayo de 1992

Translocations t(X;7) and t(7; 14) in a synovial sarcoma ⬇️

artículo científico publicado el 1 de enero de 1991

Trisomy of chromosome 12 in a case of thecoma of the ovary

artículo científico publicado en 1990

Updated Diagnostic Criteria and Classification of Mast Cell Disorders: A Consensus Proposal

artículo científico publicado en 2021

Usefulness of cytogenetic analysis in the diagnosis of undifferentiated synovial sarcoma of the chest wall. A case report

artículo científico publicado en 1995

Vitamin D Signaling in Psoriasis: Pathogenesis and Therapy

artículo científico publicado en 2022

X-linked anhidrotic ectodermal dysplasia and de novo t(X;1) in a female ⬇️

artículo científico publicado el 1 de julio de 1991

Lista de obras de

-308 G/A TNF-α gene polymorphism influences the course of basal cell carcinoma in a Polish population

A case with 47,XXY,del(11)(q23) karotype-coexistence of Jacobsen and Klinefelter syndromes

Aberrations of chromosome 22 and polysomy of chromosome 8 as non-random changes in clear cell sarcoma.

Abnormal karyotypes in three carcinomas of the gallbladder

Absence of structural rearrangements of chromosome 11 in human primary malignant melanoma

Accumulation of chromosomal changes in human glioma progression. A cytogenetic study of 50 cases

Assessment of Interleukin 16 Serum Levels and Skin Expression in Psoriasis Patients in Correlation with Clinical Severity of the Disease.

Association between the -1154 G/A promoter polymorphism of the vascular endothelial growth factor gene and atopic dermatitis

Association of distinct IL-31 polymorphisms with pruritus and severity of atopic dermatitis

Association of mastocytosis with interleukin 31 gene polymorphism

Association of psoriasis with the VEGF gene polymorphism in the northern Polish population.

Association of single nucleotide polymorphism of interleukin-18 with atopic dermatitis

Associations of promoter region polymorphisms in the tumour necrosis factor-alpha gene and early-onset psoriasis vulgaris in a northern Polish population

Bioactive forms of vitamin D selectively stimulate the skin analog of the hypothalamus-pituitary-adrenal axis in human epidermal keratinocytes

COVID-19 Vaccination in Mastocytosis: Recommendations of the European Competence Network on Mastocytosis (ECNM) and American Initiative in Mast Cell Diseases (AIM)

Chemokines and cytokines network in the pathogenesis of the inflammatory skin diseases: atopic dermatitis, psoriasis and skin mastocytosis

Chromosome aberrations, spontaneous SCE, and growth kinetics in PHA-stimulated lymphocytes of five cases with Sézary syndrome ⬇️

Clear cell sarcoma of tendons and aponeuroses with t(12;22) (q13;q12) diagnosed initially as malignant melanoma

Clinical aspects of paediatric mastocytosis: a review of 101 cases

Comparative analysis of IL6 and IL6 receptor gene polymorphisms in mastocytosis

Cutaneous manifestations in patients with mastocytosis: Consensus report of the European Competence Network on Mastocytosis; the American Academy of Allergy, Asthma & Immunology; and the European Academy of Allergology and Clinical Immunology

Cytogenetic and immunohistochemical profile of myxoid liposarcoma

Cytogenetic findings in malignant peripheral nerve sheath tumors

Cytogenetic findings in two synovial sarcomas

Cytogenetic studies of families with reproductive failure

Cytogenetics of synovial sarcoma: presentation of ten new cases and review of the literature

Cytogenetics of uterine sarcomas: presentation of eight new cases and review of the literature

Definitions, criteria and global classification of mast cell disorders with special reference to mast cell activation syndromes: a consensus proposal

Diagnosis of Mastocytosis in Children and Adults in Daily Clinical Practice

Diffuse cutaneous mastocytosis: analysis of 10 cases and a brief review of the literature

Does the aberrant expression of CD2 and CD25 by skin mast cells truly correlate with systemic involvement in patients presenting with mastocytosis in the skin?

European Competence Network on Mastocytosis (ECNM): 10-year jubilee, update, and future perspectives

Evaluation of the effectiveness of isoprinosine in the treatment of patients with acute viral hepatitis. I. Clinical evaluation

Evaluation of the effectiveness of isoprinosine in the treatment of patients with acute viral hepatitis. II. Immunological evaluation

Gene expression analysis predicts insect venom anaphylaxis in indolent systemic mastocytosis.

Gene expression profile, pathways, and transcriptional system regulation in indolent systemic mastocytosis.

Genetic and Epigenetic Aspects of Atopic Dermatitis

Global Classification of Mast Cell Activation Disorders: An ICD-10-CM–Adjusted Proposal of the ECNM-AIM Consortium

Granulocyte-macrophage colony-stimulating factor (GM-CSF)-677C/a promoter gene polymorphism is not associated with acne vulgaris in Polish population

HLA-C locus alleles distribution in patients from northern Poland with psoriatic arthritis--preliminary report

Hereditary alpha tryptasemia is a valid genetic biomarker for severe mediator-related symptoms in mastocytosis

High Resolution Melting analysis as a rapid and efficient method of screening for small mutations in the STK11 gene in patients with Peutz-Jeghers syndrome.

High prevalence of carriers of variant c.1528G>C of HADHA gene causing long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD) in the population of adult Kashubians from North Poland.

How to diagnose Mast Cell Activation Syndrome? Practical considerations

Immune response against HtrA proteases in children with cutaneous mastocytosis.

Interleukin-13 promoter gene polymorphism -1112 C/T is associated with atopic dermatitis in Polish patients

Interleukin-13 promoter gene polymorphism -1112C/T is associated with the systemic form of mastocytosis

Interleukin-31 Polymorphisms and Serum IL-31 Level in Patients with Mastocytosis: Correlation with Clinical Presen-tation and Pruritus.

International prognostic scoring system for mastocytosis (IPSM): a retrospective cohort study

Lack of association between the promoter polymorphisms at positions -238 and -308 of the tumour necrosis factor alpha gene and acne vulgaris in Polish patients

Mast cells in mastocytosis and allergy - Important player in metabolic and immunological homeostasis

Mastocytosis in children and adults: clinical disease heterogeneity

Mediator-Related Symptoms and Anaphylaxis in Children with Mastocytosis

Mediator-Related Symptoms and Anaphylaxis in Children with Mastocytosis

Molecular Background, Clinical Features and Management of Pediatric Mastocytosis: Status 2021

Monilethrix in monozygotic twins with very rare mutation in KRT 86 gene

New Approach to Paediatric Mastocytosis: Implications of KIT D816V Mutation Detection in Peripheral Blood

Nonrandom secondary chromosome-aberrations in synovial sarcomas with t(x-18) ⬇️

On the significance of trisomy 7 and sex chromosome loss in renal cell carcinoma

Parachordoma--a clinicopathologic, immunohistochemical, electron microscopic, flow cytometric, and cytogenetic study

Pathogenesis of psoriasis in the "omic" era. Part I. Epidemiology, clinical manifestation, immunological and neuroendocrine disturbances

Pathogenesis of psoriasis in the "omic" era. Part II. Genetic, genomic and epigenetic changes in psoriasis

Pathogenesis of psoriasis in the "omic" era. Part III. Metabolic disorders, metabolomics, nutrigenomics in psoriasis

Pathogenesis of psoriasis in the "omic" era. Part IV. Epidemiology, genetics, immunopathogenesis, clinical manifestation and treatment of psoriatic arthritis

Polymorphism in interleukin 1A but not in interleukin 8 gene predisposes to acne vulgaris in Polish population

Polymorphism of the TAP1 gene in Polish patients with psoriasis vulgaris

Presence of Chlamydophila pneumoniae DNA in blood cells is a frequent event in patients with the late stage of primary cutaneous lymphomas and with atopic dermatitis.

Primary cutaneous T-cell lymphomas show a deletion or translocation affecting NAV3, the human UNC-53 homologue

Proposed Diagnostic Algorithm for Patients with Suspected Mast Cell Activation Syndrome

Proposed diagnostic algorithm for patients with suspected mastocytosis: a proposal of the European Competence Network on Mastocytosis.

Refined Treatment Response Criteria for Indolent Systemic Mastocytosis Proposed by the ECNM-AIM Consortium

Results from a Genome-Wide Association Study (GWAS) in Mastocytosis Reveal New Gene Polymorphisms Associated with WHO Subgroups

Risk and Management of Patients with Mastocytosis and MCAS in the SARS-CoV-2 (COVID-19) Pandemic: Expert Opinions

Risk factors for anaphylaxis in patients with mastocytosis

Selecting the Right Criteria and Proper Classification to Diagnose Mast Cell Activation Syndromes: A Critical Review

Specific Alu elements involved in a significant percentage of copy number variations of the STK11 gene in patients with Peutz-Jeghers syndrome.

Standards of Genetic Testing in the Diagnosis and Prognostication of Systemic Mastocytosis in 2022: Recommendations of the EU-US Cooperative Group

Standards of Pathology in the Diagnosis of Systemic Mastocytosis: Recommendations of the EU-US Cooperative Group

Th1 response and cytotoxicity genes are down-regulated in cutaneous T-cell lymphoma