Lista de obras - Andrzej Pławski - Dominio Público Uruguay

A Simple Method for TPMT and ITPA Genotyping Using Multiplex HRMA for Patients Treated with Thiopurine Drugs.

artículo científico publicado en 2016

A case of late breast cancer metastases to both suprarenal glands 28 years after mastectomy

artículo científico publicado en 2012

A case of late breast cancer metastases to both suprarenal glands 28 years after mastectomy

scientific article published on 19 October 2011

A method of rapid and cost-effective screening for small mutations in patients with Peutz-Jeghers Syndrome

APC gene mutations causing familial adenomatous polyposis in Polish patients

artículo científico publicado en 2008

Absence of the RET+3:T allele in the MTC patients

artículo científico publicado en 2012

Allel RET+3 : T a medullary thyroid cancer

CCND1 gene polymorphic variants in patients with differentiated thyroid carcinoma

artículo científico publicado en 2014

Colorectal cancer in the course of familial adenomatous polyposis syndrome ("de novo" pathogenic mutation of APC gene): case report, review of the literature and genetic commentary

artículo científico publicado en 2010

Colorectal carcinoma in the course of inflammatory bowel diseases

artículo científico publicado en 2019

Combined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch syndrome and FAP patients

artículo científico publicado en 2009

Combined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch syndrome and FAP patients

artículo científico publicado en 2011

Comparative‑high resolution melting: a novel method of simultaneous screening for small mutations and copy number variations

artículo científico publicado en 2014

Comparison of fecal pyruvate kinase isoform M2 and calprotectin in assessment of pediatric inflammatory bowel disease severity and activity.

artículo científico publicado en 2014

Conflicting results of non-invasive methods for detection of Helicobacter pylori infection in children with celiac disease - a preliminary study

artículo científico publicado en 2016

Controversial aspect of using GFP as a marker for the production of transgenic cattle

artículo científico publicado en 2004

Crohn's Disease Susceptibility and Onset Are Strongly Related to Three Gene Haplotypes

artículo científico publicado en 2021

Cyclin D1 and CHEK2 polymorphic variants as low risk susceptibility alleles in DTC patients.

artículo científico publicado en 2015

DNA bank for Polish patients with predispositions to occurrence of colorectal polyposis.

artículo científico publicado en 2011

European context of the diversity and phylogenetic position of SARS-CoV-2 sequences from Polish COVID-19 patients

artículo científico publicado en 2021

Expression of human growth hormone in the milk of transgenic rabbits with transgene mapped to the telomere region of chromosome 7q.

artículo científico publicado en 2012

Familial adenomatous polyposis in three generations of a single family: a case study

artículo científico publicado en 2014

Familial adenomatous polyposis of the colon

artículo científico publicado en 2013

First Polish Cowden syndrome patient with confirmed PTEN gene mutation

artículo científico publicado en 2010

Generation of transgenic rabbits by the novel technique of chimeric somatic cell cloning

artículo científico publicado en 2006

Germline MSH2 and MLH1 mutational spectrum in HNPCC families from Poland and the Baltic States

artículo científico publicado en 2002

Germline MSH2 and MLH1 mutational spectrum including large rearrangements in HNPCC families from Poland (update study)

artículo científico publicado en 2005

Hamartomatous polyposis syndromes

scientific article published on 01 June 2013

Hepatoblastoma as a result of APC gene mutation.

artículo científico publicado en 2012

Heterozygous carriers of the I171V mutation of the NBS1 gene have a significantly increased risk of solid malignant tumours.

artículo científico publicado en 2008

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-resolution melting analysis of the TPMT gene: a study in the Polish population.

artículo científico publicado en 2012

Identification of the rate of chimerism of different tissues with microsatellite markers in chicken chimeras.

artículo científico publicado en 2010

In-silico analysis of Thr767Ile pathogenic variant in the MSH6 gene in family with endometrial cancer

artículo científico publicado en 2019

Influence of lactose intolerance on colorectal cancer incidence in the Polish population.

artículo científico publicado en 2015

Juvenile polyposis syndrome.

artículo científico publicado en 2014

MYH Gene Status in Polish FAP Patients without APC Gene Mutations

artículo científico publicado en 2006

Meeting abstracts from the Annual Conference on Hereditary Cancers 2015: Szczecin, Poland. 24-25 September, 2015.

artículo científico publicado en 2017

Meeting abstracts from the Annual Conference on Hereditary Cancers 2016: Szczecin, Poland. 14-15 September 2016.

artículo científico publicado en 2017

Modifying impact of RET gene haplotypes on medullary thyroid carcinoma clinical course

artículo científico publicado en 2018

Molecular Diagnostics of Genetic Diseases: Experience from Studies of DMD, APC, TSC1, and OPG Genes. Part 1

artículo científico publicado en 2000

Mutations spectrum in hereditary disorders predisposing to occurrence of intestine polyposis in Poland.

artículo científico publicado en 2012

New EPCAM founder deletion in Polish population

artículo científico publicado en 2017

Novel germline mutations in the adenomatous polyposis coli gene in Polish families with familial adenomatous polyposis

artículo científico publicado en 2004

Organ-sparing surgery of the bilateral testicular large cell calcifying sertoli cell tumor in patient with atypical Peutz-Jeghers syndrome

artículo científico publicado en 2011

Participation of miRNA in conditioning the incidence and modification of the course of FAP

Physical Activity and DNA Methylation in Humans

artículo científico publicado en 2021

Prevalence and correlates of vitamin K deficiency in children with inflammatory bowel disease.

artículo científico publicado en 2014

Prevalence of Helicobacter pylori infection in patients with cystic fibrosis.

artículo científico publicado en 2013

RET gene mutations spectrum in patients with medullary thyroid carcinoma (MTC) from Great Poland region.

artículo científico publicado en 2015

Rapid Detection Method for the Four Most Common CHEK2 Mutations Based on Melting Profile Analysis

artículo científico publicado en 2015

Rare case of intraintestinal stromal tumors in the patient with familial adenomatous polyposis.

artículo científico publicado en 2015

Reconstitution of a chicken breed by inter se mating of germline chimeric birds

artículo científico publicado en 2002

Recurrent APC gene mutations in Polish FAP families

artículo científico publicado en 2007

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

The AAPC case, with an early onset of colorectal cancer

artículo científico publicado en 2006

The c.470 T > C CHEK2 missense variant increases the risk of differentiated thyroid carcinoma in the Great Poland population

artículo científico publicado en 2015

The case of the youngest infant with hepatoblastoma with APC gene mutation.

artículo científico publicado en 2012

The prognosis of clinical course and the analysis of the frequency of the inflammation and dysplasia in the intestinal J-pouch at the patients after restorative proctocolectomy due to FAP.

artículo científico publicado en 2011

The spectrum of mutations in families with breast and ovarian cancer from the region of Saxony, Germany.

artículo científico publicado en 2015

Thyroid cancer in two siblings with FAP syndrome and APC mutation

scientific article published on 31 July 2007

Transgenic rabbit producing human growth hormone in milk.

artículo científico publicado en 2003

Variant of rare Hermansky - Pudlak syndrome associated with granulomatous colitis: diagnostics, clinical course and treatment

[Clinical applications of recombinant complement inhibitors]

scientific article published on 01 June 2004

[ST segment elevation typical for Brugada syndrome after intracoronary acetylocholine injection with retrosternal pain in history]

scientific article published on 01 January 2012

Lista de obras de Andrzej Pławski

A Simple Method for TPMT and ITPA Genotyping Using Multiplex HRMA for Patients Treated with Thiopurine Drugs.

A case of late breast cancer metastases to both suprarenal glands 28 years after mastectomy

A case of late breast cancer metastases to both suprarenal glands 28 years after mastectomy

A method of rapid and cost-effective screening for small mutations in patients with Peutz-Jeghers Syndrome

APC gene mutations causing familial adenomatous polyposis in Polish patients

Absence of the RET+3:T allele in the MTC patients

Allel RET+3 : T a medullary thyroid cancer

CCND1 gene polymorphic variants in patients with differentiated thyroid carcinoma

Colorectal cancer in the course of familial adenomatous polyposis syndrome ("de novo" pathogenic mutation of APC gene): case report, review of the literature and genetic commentary

Colorectal carcinoma in the course of inflammatory bowel diseases

Combined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch syndrome and FAP patients

Combined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch syndrome and FAP patients

Comparative‑high resolution melting: a novel method of simultaneous screening for small mutations and copy number variations

Comparison of fecal pyruvate kinase isoform M2 and calprotectin in assessment of pediatric inflammatory bowel disease severity and activity.

Conflicting results of non-invasive methods for detection of Helicobacter pylori infection in children with celiac disease - a preliminary study

Controversial aspect of using GFP as a marker for the production of transgenic cattle

Crohn's Disease Susceptibility and Onset Are Strongly Related to Three Gene Haplotypes

Cyclin D1 and CHEK2 polymorphic variants as low risk susceptibility alleles in DTC patients.

DNA bank for Polish patients with predispositions to occurrence of colorectal polyposis.

European context of the diversity and phylogenetic position of SARS-CoV-2 sequences from Polish COVID-19 patients

Expression of human growth hormone in the milk of transgenic rabbits with transgene mapped to the telomere region of chromosome 7q.

Familial adenomatous polyposis in three generations of a single family: a case study

Familial adenomatous polyposis of the colon

First Polish Cowden syndrome patient with confirmed PTEN gene mutation

Generation of transgenic rabbits by the novel technique of chimeric somatic cell cloning

Germline MSH2 and MLH1 mutational spectrum in HNPCC families from Poland and the Baltic States

Germline MSH2 and MLH1 mutational spectrum including large rearrangements in HNPCC families from Poland (update study)

Hamartomatous polyposis syndromes

Hepatoblastoma as a result of APC gene mutation.

Heterozygous carriers of the I171V mutation of the NBS1 gene have a significantly increased risk of solid malignant tumours.

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-resolution melting analysis of the TPMT gene: a study in the Polish population.

Identification of the rate of chimerism of different tissues with microsatellite markers in chicken chimeras.

In-silico analysis of Thr767Ile pathogenic variant in the MSH6 gene in family with endometrial cancer

Influence of lactose intolerance on colorectal cancer incidence in the Polish population.

Juvenile polyposis syndrome.

MYH Gene Status in Polish FAP Patients without APC Gene Mutations

Meeting abstracts from the Annual Conference on Hereditary Cancers 2015: Szczecin, Poland. 24-25 September, 2015.

Meeting abstracts from the Annual Conference on Hereditary Cancers 2016: Szczecin, Poland. 14-15 September 2016.

Modifying impact of RET gene haplotypes on medullary thyroid carcinoma clinical course

Molecular Diagnostics of Genetic Diseases: Experience from Studies of DMD, APC, TSC1, and OPG Genes. Part 1

Mutations spectrum in hereditary disorders predisposing to occurrence of intestine polyposis in Poland.

New EPCAM founder deletion in Polish population

Novel germline mutations in the adenomatous polyposis coli gene in Polish families with familial adenomatous polyposis

Organ-sparing surgery of the bilateral testicular large cell calcifying sertoli cell tumor in patient with atypical Peutz-Jeghers syndrome

Participation of miRNA in conditioning the incidence and modification of the course of FAP

Physical Activity and DNA Methylation in Humans

Prevalence and correlates of vitamin K deficiency in children with inflammatory bowel disease.

Prevalence of Helicobacter pylori infection in patients with cystic fibrosis.

RET gene mutations spectrum in patients with medullary thyroid carcinoma (MTC) from Great Poland region.

Rapid Detection Method for the Four Most Common CHEK2 Mutations Based on Melting Profile Analysis

Rare case of intraintestinal stromal tumors in the patient with familial adenomatous polyposis.

Reconstitution of a chicken breed by inter se mating of germline chimeric birds

Recurrent APC gene mutations in Polish FAP families

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

The AAPC case, with an early onset of colorectal cancer

The c.470 T > C CHEK2 missense variant increases the risk of differentiated thyroid carcinoma in the Great Poland population

The case of the youngest infant with hepatoblastoma with APC gene mutation.

The prognosis of clinical course and the analysis of the frequency of the inflammation and dysplasia in the intestinal J-pouch at the patients after restorative proctocolectomy due to FAP.

The spectrum of mutations in families with breast and ovarian cancer from the region of Saxony, Germany.

Thyroid cancer in two siblings with FAP syndrome and APC mutation

Transgenic rabbit producing human growth hormone in milk.

Variant of rare Hermansky - Pudlak syndrome associated with granulomatous colitis: diagnostics, clinical course and treatment

[Clinical applications of recombinant complement inhibitors]

[ST segment elevation typical for Brugada syndrome after intracoronary acetylocholine injection with retrosternal pain in history]