Malgorzata Krajewska: search on Z-Library

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1

Environmental contaminants—Occurrence of coccidiostats in poultry manure

Teresa Szprengier-Juszkiewicz, Malgorzata Olejnik, Piotr Jedziniak, Joanna Frischke-Krajewska

Journal:

Toxicology Letters

Year:

2008

Language:

english

File:

PDF, 89 KB

english, 2008

2

History and molecular characteristics of a patient with terminal deletion of 14q. Is this another syndrome with a striking phenotype?

Jezela-Stanek, Aleksandra, Kucharczyk, Marzena, Gutkowska, Anna, Pelc, Magdalena, Ciara, Elżbieta, Chrzanowska, Krystyna H., Krajewska-Walasek, Małgorzata

Journal:

Clinical Dysmorphology

Year:

2012

Language:

english

File:

PDF, 230 KB

english, 2012

3

Urease activity and l -ascorbic acid

Krajewska, Barbara, Brindell, Małgorzata

Journal:

Journal of Enzyme Inhibition and Medicinal Chemistry

Year:

2011

Language:

english

File:

PDF, 893 KB

english, 2011

4

Risk of food losses and potential of food recovery for social purposes

Bilska, Beata, Wrzosek, Małgorzata, Kołożyn-Krajewska, Danuta, Krajewski, Karol

Journal:

Waste Management

Year:

2016

Language:

english

File:

PDF, 684 KB

english, 2016

5

Współpraca genetyka klinicznego i biologa molekularnego – wczoraj i dziś

Jezela-Stanek, Aleksandra, Kucharczyk, Marzena, Jurkiewicz, Dorota, Ciara, Elżbieta, Krajewska-Walasek, Małgorzata

Journal:

Pediatria Polska

Year:

2015

Language:

polish

File:

PDF, 1.78 MB

polish, 2015

6

Additional data on the clinical phenotype of Helsmoortel-Van der Aa syndrome associated with a novel truncating mutation in ADNP gene

Krajewska-Walasek, Małgorzata, Jurkiewicz, Dorota, Piekutowska-Abramczuk, Dorota, Kucharczyk, Marzena, Chrzanowska, Krystyna H., Jezela-Stanek, Aleksandra, Ciara, Elżbieta

Journal:

American Journal of Medical Genetics Part A

Year:

2016

Language:

english

File:

PDF, 179 KB

english, 2016

7

Alagille syndrome associated with a paracentric inversion 20p12.2p13 disrupting the JAG1 gene

Paweł Stankiewicz, Jolanta Rujner, Christiane Löffler, Antje Krüger, Manjunath Nimmakayalu, Bożena Piłacik, Małgorzata Krajewska-Walasek, Anna Gutkowska, Ingo Hansmann, Ioannis Giannakudis

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 330 KB

english, 2001

8

Identification of a nuclear antigen with molecular weight of 48 000 differentially expressed in tumour and normal cells

Wanda M. Krajewska, Anna Lipińska, Małgorzata Marszałek, Zofia Kiliańska, Zbigniew Wojtkowiak, Leokadia Kłyszejko-Stefanowicz

Journal:

Cell Biochemistry and Function

Year:

1990

Language:

english

File:

PDF, 985 KB

english, 1990

9

Twelve novel JAG1 gene mutations in polish Alagille syndrome patients

Dorota Jurkiewicz, Ewa Popowska, Christiane Gläser, Ingo Hansmann, Małgorzata Krajewska-Walasek

Journal:

Year:

2005

Language:

english

File:

PDF, 119 KB

english, 2005

10

Carrier frequency of mutation 657del5 in the NBS1 gene in a population of polish pediatric patients with sporadic lymphoid malignancies

Krystyna H. Chrzanowska, Dorota Piekutowska-Abramczuk, Ewa Popowska, Małgorzata Gładkowska-Dura, Jadwiga Małdyk, Małgorzata Syczewska, Małgorzata Krajewska-Walasek, Bożenna Goryluk-Kozakiewicz, Halina

Journal:

International Journal of Cancer

Year:

2006

Language:

english

File:

PDF, 94 KB

english, 2006

11

Growth-related changes of non-histone chromatin proteins from Kirkman-Robbins hepatoma

Zofia Kilianska, Wanda M. Krajewska, Marek Gaczynski, Malgorzata Marszalek, Leokadia Klyszejko-Stefanowicz

Journal:

International Journal of Biochemistry

Year:

1989

Language:

english

File:

PDF, 2.09 MB

english, 1989

12

Nuclear antigen with a molecular weight of 48,000 associated with malignant tranformation

Wanda M. Krajewska, Małgorzata Marszałek, Marek Gaczyński, Leokadia Kłszejko-Stefanowicz

Journal:

International Journal of Biochemistry

Year:

1991

Language:

english

File:

PDF, 1.31 MB

english, 1991

13

Lack of cross tolerance between pyrogenic effects of LPS and turpentine in rats

Dariusz Soszynski, Malgorzata Krajewska

Journal:

Journal of Thermal Biology

Year:

2002

Language:

english

File:

PDF, 324 KB

english, 2002

14

Time-course of changes in plasma nitric oxide following lipopolysaccharide and turpentine injection in rats

Dariusz Soszynski, Malgorzata Krajewska

Journal:

Journal of Thermal Biology

Year:

2002

Language:

english

File:

PDF, 105 KB

english, 2002

15

Timolol 0.5%/dorzolamide 2% fixed combination versus timolol 0.5%/pilocarpine 2% fixed combination in primary open-angle glaucoma or ocular hypertensive patients

Jakub J. Kałuz̊ny, Jerzy Szaflik, Krystyna Czechowicz-Janicka, Józef Kałuz̊ny, Alicja Orzalkiewicz, Anna Zaleska, Malgorzata Krajewska, Jeanette A. Stewart, Jessica N. Leech, William C. Stewart

Journal:

Acta Ophthalmologica (Blackwell)

Year:

2003

Language:

english

File:

PDF, 110 KB

english, 2003

16

Schimke immuno-osseous dysplasia: two cases

Anna Tylki-Szymańska, Antoni Pyrkosz, Małgorzata Krajewska-Walasek, Jacek Michałkiewicz, Aleksandra Kowalska, Dariusz Rokicki

Journal:

Pediatric Radiology

Year:

2003

Language:

english

File:

PDF, 211 KB

english, 2003

17

Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery

Lidia Ziolkowska, Wanda Kawalec, Anna Turska-Kmiec, Malgorzata Krajewska-Walasek, Grazyna Brzezinska-Rajszys, Jadwiga Daszkowska, Bogdan Maruszewski, Piotr Burczynski

Journal:

European Journal of Pediatrics

Year:

2008

Language:

english

File:

PDF, 115 KB

english, 2008

18

Maternal de novo triple mosaicism for two singleOCRLnucleotide substitutions (c.1736A>T, c.1736A>G) in a Lowe syndrome family

Markus Draaken, Carmen A. Giesen, Anne L. Kesselheim, Ronald Jabs, Stefan Aretz, Monika Kugaudo, Krystyna H. Chrzanowska, Malgorzata Krajewska-Walasek, Michael Ludwig

Journal:

Year:

2011

Language:

english

File:

PDF, 425 KB

english, 2011

19

A case of Prader – Willi syndrome arising as a result of familial unbalanced translocation t(11;15)(q25;q13)

Malgorzata Krajewska Walasek, Anna Gutkowska, Beata Bielińska, Bozenna Goryluk-Kozakiewicz, Ewa Popowska

Journal:

Clinical Genetics

Year:

1998

Language:

english

File:

PDF, 996 KB

english, 1998

20

10.1038/75629

Horsthemke, Bernhard, Bielinska, Beata, Blaydes, Susan M., Buiting, Karin, Yang, Tao, Krajewska-Walasek, Malgorzata, Brannan, Camilynn I.

Journal:

Nature Genetics

Year:

2000

Language:

english

File:

PDF, 623 KB

english, 2000

21

Clinical ascertainment of Nijmegen breakage syndrome (NBS) and prevalence of the major mutation, 657del5, in three Slav populations

Varon, Raymonda, Seemanova, Eva, Chrzanowska, Krystyna, Hnateyko, Oleg, Piekutowska-Abramczuk, Dorota, Krajewska-Walasek, Malgorzata, Sykut-Cegielska, Jolanta, Sperling, Karl, Reis, André

Journal:

European Journal of Human Genetics

Year:

2000

Language:

english

File:

PDF, 45 KB

english, 2000

22

Parental mosaicism of JAG1 mutations in families with Alagille syndrome

Giannakudis, Joannis, Röpke, Albrecht, Kujat, Annegret, Krajewska-Walasek, Malgorzata, Hughes, Helen, Fryns, Jean-Pierre, Bankier, Agnes, Amor, David, Schlicker, Mike, Hansmann, Ingo

Journal:

European Journal of Human Genetics

Year:

2001

Language:

english

File:

PDF, 179 KB

english, 2001

23

Parental mosaicism of JAG1 mutations in families with Alagille syndrome

Giannakudis, Joannis, Röpke, Albrecht, Kujat, Annegret, Krajewska-Walasek, Malgorzata, Hughes, Helen, Fryns, Jean-Pierre, Bankier, Agnes, Amor, David, Schlicker, Mike, Hansmann, Ingo

Journal:

European Journal of Human Genetics

Year:

2001

File:

PDF, 37 KB

2001

24

Recurrent rearrangements in the proximal 15q11–q14 region: a new breakpoint cluster specific to unbalanced translocations

Mignon-Ravix, Cécile, Depetris, Danielle, Luciani, Judith J, Cuoco, Cristina, Krajewska-Walasek, Malgorzata, Missirian, Chantal, Collignon, Patrick, Delobel, Bruno, Croquette, Marie-Françoise, Moncla,

Journal:

European Journal of Human Genetics

Year:

2007

Language:

english

File:

PDF, 207 KB

english, 2007

25

Minimal clinical findings in a patient with 15qter microdeletion syndrome: Delineation of the associated phenotype

Aleksandra Jezela-Stanek, Marzena Kucharczyk, Magdalena Pelc, Krystyna H. Chrzanowska, Małgorzata Krajewska-Walasek

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 224 KB

english, 2012

26

A girl with two syndromes: Turner syndrome and Costello syndrome. A case history

Agata Skórka, Elżbieta Ciara, Dorota Gieruszczak-Białek, Magdalena Pelc, Monika Kugaudo, Krystyna Chrzanowska, Małgorzata Krajewska-Walasek

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 146 KB

english, 2012

27

Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation

Monika B. Hartig, Arcangela Iuso, Tobias Haack, Tomasz Kmiec, Elzbieta Jurkiewicz, Katharina Heim, Sigrun Roeber, Victoria Tarabin, Sabrina Dusi, Malgorzata Krajewska-Walasek, Sergiusz Jozwiak, Maja H

Journal:

The American Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 899 KB

english, 2011

28

The new molecular p.M177T identified in two unrelated patients with clinical features of SCO2-dependent cytochrome c oxidase deficiency

Sylwia Łuczak, Dorota Piekutowska-Abramczuk, Paweł Kowalski, Elżbieta Ciara, Dorota Jurkiewicz, Maria Borucka-Mankiewicz, Anna Tańska, Magdalena Pelc, Joanna Trubicka, Małgorzata Krajewska-Walasek, Ew

Journal:

Biochimica et Biophysica Acta (BBA) - Bioenergetics

Year:

2010

Language:

english

File:

PDF, 57 KB

english, 2010

29

Biological evaluation of novel Pt(II) and Pd(II) complexes with pyrazole-containing ligands

Elzbieta Budzisz, Urszula Krajewska, Marek Rozalski, Agata Szulawska, Malgorzata Czyz, Barbara Nawrot

Journal:

European Journal of Pharmacology

Year:

2004

Language:

english

File:

PDF, 408 KB

english, 2004

30

High prevalence of SURF1 c.845_846delCT mutation in Polish Leigh patients

Dorota Piekutowska-Abramczuk, Ewa Popowska, Maciej Pronicki, Elzbieta Karczmarewicz, Dorota Tylek-Lemanska, Jolanta Sykut-Cegielska, Tamara Szymanska-Dembinska, Liliana Bielecka, Malgorzata Krajewska-

Journal:

European Journal of Paediatric Neurology

Year:

2009

Language:

english

File:

PDF, 498 KB

english, 2009

31

Effect of cancer procoagulant (CP) on the growth and adhesion of MCF-7 cells to vitronectin in vitro

Małgorzata Kamocka, Marek Różalski, Urszula Krajewska, Ryszard Wierzbicki, Wojciech P. Mielicki

Journal:

Year:

2005

Language:

english

File:

PDF, 145 KB

english, 2005

32

A case described as translocation 15;15 revised: maternal 15 UPD, resulting from isochromosome 15, in a PWS patient

Anna Gutkowska, Anna Tylki-Szymańska, Ewa Popowska, Beata Bielińska, Dorota Jurkiewicz, Małgorzata Krajewska-Walasek

Journal:

European Journal of Medical Genetics

Year:

2005

Language:

english

File:

PDF, 92 KB

english, 2005

33

Four novel RSK2 mutations in females with Coffin–Lowry syndrome

Dorota Jurkiewicz, Aleksandra Jezela-Stanek, Elżbieta Ciara, Dorota Piekutowska-Abramczuk, Monika Kugaudo, Maria Gajdulewicz, Krystyna Chrzanowska, Ewa Popowska, Małgorzata Krajewska-Walasek

Journal:

European Journal of Medical Genetics

Year:

2010

Language:

english

File:

PDF, 839 KB

english, 2010

34

Molecular investigations of mitochondrial deletions: Evaluating the usefulness of different genetic tests

Katarzyna Tońska, Dorota Piekutowska-Abramczuk, Magdalena Kaliszewska, Paweł Kowalski, Anna Tańska, Ewa Bartnik, Ewa Pronicka, Małgorzata Krajewska-Walasek

Journal:

Year:

2012

Language:

english

File:

PDF, 483 KB

english, 2012

35

Cryptic X; Autosome Translocation in a Boy—Delineation of the Phenotype

Aleksandra Jezela-Stanek, Elżbieta Ciara, Marzena Juszczak, Magdalena Pelc, Anna Materna-Kiryluk, Małgorzata Krajewska-Walasek

Journal:

Pediatric Neurology

Year:

2011

Language:

english

File:

PDF, 480 KB

english, 2011

36

Allelic Heterogeneity in the COH1 Gene Explains Clinical Variabilityin Cohen Syndrome

Hans Christian Hennies, Anita Rauch, Wenke Seifert, Christian Schumi, Elisabeth Moser, Eva Al-Taji, Gholamali Tariverdian, Krystyna H. Chrzanowska, Malgorzata Krajewska-Walasek, Anna Rajab, Roberto Gi

Journal:

The American Journal of Human Genetics

Year:

2004

Language:

english

File:

PDF, 1.49 MB

english, 2004

37

1.15 Mb microdeletion in chromosome band 20p13 associated with moderate developmental delay-Additional case and data's review

Jezela-Stanek, Aleksandra, Kucharczyk, Marzena, Pelc, Magdalena, Gutkowska, Anna, Krajewska-Walasek, Małgorzata

Journal:

American Journal of Medical Genetics Part A

Year:

2013

Language:

english

File:

PDF, 339 KB

english, 2013

38

Structure of Escherichia coli RutC, a member of the YjgF family and putative aminoacrylate peracid reductase of the rut operon

Knapik, Aleksandra Alicja, Petkowski, Janusz Jurand, Otwinowski, Zbyszek, Cymborowski, Marcin Tadeusz, Cooper, David Robert, Chruszcz, Maksymilian, Krajewska, Wanda Małgorzata, Minor, Wladek

Journal:

Acta Crystallographica Section F Structural Biology and Crystallization Communications

Year:

2012

Language:

english

File:

PDF, 1.18 MB

english, 2012

39

Genetic causes of syndromic craniosynostoses

Jezela-Stanek, Aleksandra, Krajewska-Walasek, Małgorzata

Journal:

European Journal of Paediatric Neurology

Year:

2013

Language:

english

File:

PDF, 109 KB

english, 2013

40

The DNA damage response during mitosis

Heijink, Anne Margriet, Krajewska, Małgorzata, van Vugt, Marcel A.T.M.

Journal:

Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis

Year:

2013

Language:

english

File:

PDF, 2.36 MB

english, 2013

41

Zespół delecji 22q13 w praktyce klinicznej i cytogenetycznej: opis nowego przypadku (zespół Phelan i McDermid)

Grabowska, Ewa, Jezela-Stanek, Aleksandra, Marczak-Hałupka, Anna, Marczak, Aleksandra, Gutkowska, Anna, Gajdulewicz, Maria, Spodar, Krystyna, Chrzanowska, Krystyna H., Krajewska-Walasek, Małgorzata

Journal:

Pediatria Polska

Year:

2008

Language:

polish

File:

PDF, 285 KB

polish, 2008

42

Tetraploidy in the era of molecular karyotyping – What we need to remember

Bothur-Nowacka, Joanna, Jezela-Stanek, Aleksandra, Zaniuk, Katarzyna, Goryluk-Kozakiewicz, Bożenna, Krajewska-Walasek, Małgorzata, Dobrzańska, Anna

Journal:

Pediatria Polska

Year:

2013

Language:

english

File:

PDF, 833 KB

english, 2013

43

Mutacje genów kompleksu BAF jako nowy czynnik etiologiczny izolowanej oraz syndromicznej niepełnosprawności intelektualnej w zespołach Coffina i Siris oraz Nicolaidesa i Baraitsera

Jezela-Stanek, Aleksandra, Pelc, Magdalena, Krajewska-Walasek, Małgorzata

Journal:

Pediatria Polska

Year:

2014

Language:

polish

File:

PDF, 379 KB

polish, 2014

44

Zespoły subtelomerowych mikrodelecji w praktyce pediatrycznej: zespół delecji 22q13

Krajewska-Walasek, Małgorzata, Jezela-Stanek, Aleksandra, Grabowska, Ewa

Journal:

Pediatria Polska

Year:

2008

Language:

polish

File:

PDF, 227 KB

polish, 2008

45

Table of Contents

Krajewska-Walasek, Małgorzata, Jezela-Stanek, Aleksandra, Grabowska, Ewa

Journal:

Regional Anesthesia and Pain Medicine

Year:

2006

Language:

english

File:

PDF, 27 KB

english, 2006

46

Contents

Krajewska-Walasek, Małgorzata, Jezela-Stanek, Aleksandra, Grabowska, Ewa

Journal:

La Revue de Médecine Interne

Year:

1993

Language:

english

File:

PDF, 66 KB

english, 1993

47

Zespół Costello jako przykład rzadkich zaburzeń funkcji szlaku sygnalnego Ras-MAPK: obraz kliniczny i diagnostyka molekularna choroby

Pelc, Magdalena, Ciara, Elżbieta, Krajewska-Walasek, Małgorzata

Journal:

Pediatria Polska

Year:

2012

Language:

polish

File:

PDF, 476 KB

polish, 2012

48

Dziecko z dysmorfią: wczoraj i dziś

Krajewska-Walasek, Małgorzata

Journal:

Pediatria Polska

Year:

2008

Language:

polish

File:

PDF, 226 KB

polish, 2008

49

N-acetyl-β-hexosaminidase in chronic tonsillitis and tonsillar hypertrophy

Zagor, Mariola, Minarowska, Alina, Knaś, Małgorzata, Krajewska, Katarzyna, Niemcunowicz-Janica, Anna, Marciniak, Justyna, Bierć, Marcin, Zaniewska, Agnieszka, Minarowski, Łukasz, Jackowska, Anna, Jack

Journal:

Otolaryngologia Polska

Year:

2013

Language:

english

File:

PDF, 473 KB

english, 2013

50

Rola genu SURF1 w patogenezie zespołu Leigha sprzężonego z deficytem aktywności oksydazy cytochromu c

Piekutowska-Abramczuk, Dorota, Pronicka, Ewa, Krajewska-Walasek, Małgorzata

Journal:

Pediatria Polska

Year:

2008

Language:

polish

File:

PDF, 194 KB

polish, 2008