I Hausmanowa-Pétrusewicz

Polish Academy of Sciences

36H指数

393论文数

6.3K被引数

收录论文 37

发表时间

Correlating motor unit morphology with bioelectrical activity - A simulation study

CLINICAL NEUROPHYSIOLOGY

IF3.6

2018-01-01

PREAI

Zalewska, Ewa; Hausmanowa-Petrusewicz, Irena

Cardiac pacing in 21 patients with Emery-Dreifuss muscular dystrophy: a single-centre study with a 39-year follow-up

KARDIOLOGIA POLSKA

IF3.7

2016-06-15

OAAI

Steckiewicz, Roman; Stolarz, Przemyslaw; Swieton, Elzbieta; Madej-Pilarczyk, Agnieszka; Grabowski, Marcin; Marchel, Michal; Pieniak, Marian; Filipiak, Krzysztof J.; Hausmanowa-Petrusewicz, Irena; Opolski, Grzegorz

Low symptomatic malignant cardiac arrhythmia in a patient with lamin-related congenital muscular dystrophy

KARDIOLOGIA POLSKA

IF3.7

2015-10-28

OAAI

Madej-Pilarczyk, Agnieszka; Marchel, Michal; Fidzianska, Anna; Opolski, Grzegorz; Hausmanowa-Petrusewicz, Irena

Tissue inhibitors of matrix metalloproteinases in serum are cardiac biomarkers in Emery-Dreifuss muscular dystrophy 血清中基质金属蛋白酶的组织抑制剂是Emery-Dreifuss肌营养不良症的心脏生物标志物

KARDIOLOGIA POLSKA

IF3.7

2015-05-20

OAAI

Niebroj-Dobosz, Irena Maria; Sokolowska, Beata; Madej-Pilarczyk, Agnieszka; Marchel, Michal; Hausmanowa-Petrusewicz, Irena

Truncating and Missense Mutations in IGHMBP2 Cause Charcot-Marie Tooth Disease Type 2

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2014-11-01

OAAI

Cottenie, Ellen; Kochanski, Andrzej; Jordanova, Albena; Bansagi, Boglarka; Zimon, Magdalena; Horga, Alejandro; Jaunmuktane, Zane; Saveri, Paola; Rasic, Vedrana Milic; Baets, Jonathan; Bartsakoulia, Marina; Ploski, Rafal; Teterycz, Pawel; Nikolic, Milos; Quinlivan, Ros; Laura, Matilde; Sweeney, Mary G.; Taroni, Franco; Lunn, Michael P.; Moroni, Isabella; Gonzalez, Michael; Hanna, Michael G.; Bettencourt, Conceicao; Chabrol, Elodie; Franke, Andre; von Au, Katja; Schilhabel, Markus; Kabzinska, Dagmara; Hausmanowa-Petrusewicz, Irena; Brandner, Sebastian; Lim, Siew Choo; Song, Haiwei; Choi, Byung-Ok; Horvath, Rita; Chung, Ki-Wha; Zuchner, Stephan; Pareyson, Davide; Harms, Matthew; Reilly, Mary M.; Houlden, Henry

Cardiovascular risk markers in dilated cardiomyopathy in Emery-Dreifuss muscular dystrophy (EDMD)Emery-Dreifuss肌营养不良症 (EDMD) 的扩张型心肌病的心血管风险标志物

INTERNATIONAL JOURNAL OF CARDIOLOGY

IF3.2

2014-05-01

PREAI

Niebroj-Dobosz, Irena; Sokolowska, Beata; Madej-Pilarczyk, Agnieszka; Marchel, Michal; Hausmanowa-Petrusewicz, Irena

Amyotrophic lateral sclerosis: a dying motor unit?

FRONTIERS IN AGING NEUROSCIENCE

IF4.5

2013-01-01

OAAI

Piotrkiewicz, Maria; Hausmanowa-Petrusewicz, Irena

Dominant GDAP1 mutations cause predominantly mild CMT phenotypes

NEUROLOGY

IF8.5

2011-08-09

OAAI

Zimon, M.; Baets, J.; Fabrizi, G. M.; Jaakkola, E.; Kabzinska, D.; Pilch, J.; Schindler, A. B.; Cornblath, D. R.; Fischbeck, K. H.; Auer-Grumbach, M.; Guelly, C.; Huber, N.; De Vriendt, E.; Timmerman, V.; Suter, U.; Hausmanowa-Petrusewicz, I.; Niemann, A.; Kochanski, A.; De Jonghe, P.; Jordanova, A.

Circulating tenascin-C levels in patients with dilated cardiomyopathy in the course of Emery-Dreifuss muscular dystrophy 扩张型心肌病患者在Emery-Dreifuss肌营养不良过程中的循环tenascin-C水平

CLINICA CHIMICA ACTA

IF2.9

2011-08-01

PREAI

Niebroj-Dobosz, Irena; Madej-Pilarczyk, Agnieszka; Marchel, Michal; Sokolowska, Beata; Hausmanowa-Petrusewicz, Irena

Incidence of Spinal Muscular Atrophy in Poland - More Frequent than Predicted?波兰脊髓性肌萎缩症的发病率-比预期的更频繁？

NEUROEPIDEMIOLOGY

IF4

2010-01-15

PREAI

Jedrzejowska, Maria; Milewski, Michal; Zimowski, Janusz; Zagozdzon, Pawel; Kostera-Pruszczyk, Anna; Borkowska, Janina; Sielska, Danuta; Jurek, Marta; Hausmanowa-Petrusewicz, Irena

Approximation of motor unit structure from the analysis of motor unit potential

CLINICAL NEUROPHYSIOLOGY

IF3.6

2008-11-01

PREAI

Zalewska, Ewa; Hausmanowa-Petrusewicz, Irena

Obliteration of cardiomyocyte nuclear architecture in a patient with LMNA gene mutation

JOURNAL OF THE NEUROLOGICAL SCIENCES

IF3.2

2008-08-01

PREAI

Fidzianska, Anna; Bilinska, Zofia T.; Tesson, Frederique; Wagner, Terresa; Walski, Michal; Grzybowski, Jacek; Ruzyllo, Witold; Hausmanowa-Petrusewicz, Irena

Unaffected patients with a homozygous absence of the SMN1 gene SMN1基因纯合缺失的未受影响的患者

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2008-03-12

OAAI

Jedrzejowska, Maria; Borkowska, Janina; Zimowski, Janusz; Kostera-Pruszczyk, Anna; Milewski, Michal; Jurek, Marta; Sielska, Danuta; Kostyk, Ewa; Nyka, Walenty; Zaremba, Jacek; Hausmanowa-Petrusewicz, Irena

Cardiomyopathy associated with Emery-Dreifuss muscular dystrophy, echocardiographic and biomarker study

EUROPEAN JOURNAL OF HEART FAILURE

IF10.8

2007-06-01

PREAI

Marchel, M.; Stepien, V.; Madej, A.; Steckiewicz, R.; Kochanowski, J.; Filipiak, K. J.; Hausmanowa-Petrusewicz, I.; Opolski, G.

Is a novel I214M substitution in the NEFL gene a cause of Charcot-Marie-Tooth disease?: Functional analysis using cell culture models

JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM

IF3.2

2006-08-24

PREAI

Kabzinska, Dagmara; Perez-Olle, Raul; Goryunov, Dmitry; Drac, Hanna; Ryniewicz, Barbara; Hausmanowa-Petrusewicz, Irena; Kochanski, Andrzej; Liem, Ronald K. H.

The inner nuclear membrane protein Emerin regulates β-catenin activity by restricting its accumulation in the nucleus

EMBO JOURNAL

IF8.3

2006-07-20

226

OAAI

Markiewicz, Ewa; Tilgner, Katarzyna; Barker, Nick; van de Wetering, Mark; Clevers, Hans; Dorobek, Margareth; Hausmanowa-Petrusewicz, Irena; Ramaekers, Frans C. S.; Broers, Jos L. V.; Blankesteijn, W. Matthijs; Salpingidou, Georgia; Wilson, Robert G.; Ellis, Juliet A.; Hutchison, Christopher J.

Charcot-Marie-Tooth type 4F disease caused by S399fsx410 mutation in the PRX gene

NEUROLOGY

IF8.5

2006-03-14

PREAI

Kabzinska, D; Drac, H; Sherman, DL; Kostera-Pruszczyk, A; Brophy, PJ; Kochanski, A; Hausmanowa-Petrusewicz, I

Mutation screening of Charcot-Marie-Tooth patients in Poland

CHARCOT-MARIE-TOOTH DISORDERS

IF0

2006-02-06

PREAI

Kochanski, A; Timmerman, V; Jedrzejowska, H; Ryniewicz, B; Löfgren, A; De Vriendt, E; Van Broeckhoven, C; Latos-Bielenska, A; Hausmanowa-Petrusewicz, I

A novel Met116Thr mutation in the GDAP1 gene in a Polish family with the axonal recessive Charcot-Marie-Tooth type 4 disease 波兰轴突隐性charcot-marie-tooth 4型疾病家族中GDAP1基因的新型Met116Thr突变

JOURNAL OF THE NEUROLOGICAL SCIENCES

IF3.2

2006-02-01

PREAI

Kabzinska, D; Kochanski, A; Drac, H; Rowinska-Marcinska, K; Ryniewicz, B; Pedrola, L; Palau, F; Hausmanowa-Petrusewiez, I

Atypical motor unit potentials in Emery-Dreifuss muscular dystrophy (EDMD)

CLINICAL NEUROPHYSIOLOGY

IF3.6

2005-11-01

PREAI

Rowinska-Marcinska, K; Szmidt-Salkowska, E; Fidzianska, A; Zalewska, E; Dorobek, M; Karwanska, A; Hausmanowa-Petrusewicz, I

研究方向