Recurrent APC gene mutations in Polish FAP families

Por Pławski, Andrzej, Podralska, Marta, Słomski, Ryszard
Publicado em 2007

Juvenile polyposis syndrome

Por Cichy, Wojciech, Klincewicz, Beata, Plawski, Andrzej
Publicado em 2014

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

Por Boruń, Paweł, Plawski, Andrzej, Bartkowiak, Anna, Cichy, Wojciech
Publicado em 2012

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...

Por Stec, Rafał, Pławski, Andrzej, Synowiec, Agnieszka, Mączewski, Michał, Szczylik, Cezary
Publicado em 2010

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

Por Krawczuk-Rybak, Maryna, Jakubiuk-Tomaszuk, Anna, Skiba, Elżbieta, Pławski, Andrzej
Publicado em 2012

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

Por Borun, Pawel, Salanowski, Kacper, Godlewski, Dariusz, Walkowiak, Jaroslaw, Plawski, Andrzej
Publicado no Mol Diagn Ther (2015)

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

Por Borun, Pawel, De Rosa, Marina, Nedoszytko, Boguslaw, Walkowiak, Jaroslaw, Plawski, Andrzej
Publicado no Fam Cancer (2015)

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

Por Tomys, Michalina, Skrzypczak-Zielinska, Marzena, Jasinowska, Marzena, Plawski, Andrzej, Froster, Ursula
Publicado no Hered Cancer Clin Pract (2015)

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

Por Borun Pawel, Jerzy Sowinski, Ziemnicka Katarzyna, Kubaszewski Lukasz, Lipinski Daniel, Plawski Andrzej
Publicado em 2012-10-01

First Polish Cowden syndrome patient with confirmed PTEN gene mutation

Por Podralska, Marta, Nowakowska, Dorota, Steffen, Jan, Cichy, Wojciech, Slomski, Ryszard, Plawski, Andrzej
Publicado em 2010

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

Por Borun, Pawel, Jerzy, Sowinski, Ziemnicka, Katarzyna, Kubaszewski, Lukasz, Lipinski, Daniel, Plawski, Andrzej
Publicado em 2012

MYH Gene Status in Polish FAP Patients without APC Gene Mutations

Por Skrzypczak, Marzena, Podralska, Marta, Heinritz, Wolfram, Froster, Ursula G, Lipiński, Daniel, Słomski, Ryszard, Pławski, Andrzej
Publicado em 2006

Familial adenomatous polyposis of the colon

Por Plawski, Andrzej, Banasiewicz, Tomasz, Borun, Pawel, Kubaszewski, Lukasz, Krokowicz, Piotr, Skrzypczak-Zielinska, Marzena, Lubinski, Jan
Publicado em 2013

Hamartomatous polyposis syndromes

Por Stojcev, Zoran, Borun, Pawel, Hermann, Jacek, Krokowicz, Piotr, Cichy, Wojciech, Kubaszewski, Lukasz, Banasiewicz, Tomasz, Plawski, Andrzej
Publicado em 2013

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

Por Borun, Pawel, Kubaszewski, Lukasz, Banasiewicz, Tomasz, Walkowiak, Jaroslaw, Skrzypczak-Zielinska, Marzena, Kaczmarek-Rys, Marta, Plawski, Andrzej
Publicado em 2013

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

Por Kaczmarek-Ryś, Marta, Ziemnicka, Katarzyna, Budny, Bartłomiej, Szkudlarek, Małgorzata, Hryhorowicz, Szymon, Skrzypczak-Zielińska, Marzena, Pławski, Andrzej
Publicado no Hered Cancer Clin Pract (2015)

Familial Adenomatous Polyposis in Three Generations of a Single Family: A Case Study

Por Murgic, Jure, Kirac, Iva, Soldic, Zeljko, Tomas, Davor, Zovak, Mario, Bolanca, Ante, Plawski, Andrzej, Banasiewicz, y, Kusic, Zvonko
Publicado em 2014

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...

Por Banasiewicz, Tomasz, Marciniak, Ryszard, Kaczmarek, Elzbieta, Krokowicz, Piotr, Paszkowski, Jacek, Lozynska-Nelke, Aleksandra, Gronek, Piotr, Plawski, Andrzej, Drews, Michal
Publicado em 2011

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

Por Lipinski, Daniel, Zeyland, Joanna, Szalata, Marlena, Plawski, Andrzej, Jarmuz, Malgorzata, Jura, Jacek, Korcz, Aleksandra, Smorag, Zdzislaw, Pienkowski, Marek, Slomski, Ryszard
Publicado em 2012

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

Por Nowak, Jan K., Grzybowska-Chlebowczyk, Urszula, Landowski, Piotr, Szaflarska-Poplawska, Anna, Klincewicz, Beata, Adamczak, Daria, Banasiewicz, Tomasz, Plawski, Andrzej, Walkowiak, Jaroslaw
Publicado em 2014