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Anna Fidziańska

Polish Academy of Sciences

30H指数
175论文数
3.3K被引数
收录论文 22
发表时间
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Low symptomatic malignant cardiac arrhythmia in a patient with lamin-related congenital muscular dystrophy
errKARDIOLOGIA POLSKA
IF3.7
err2015-10-28
err4
errOAAI
errMadej-Pilarczyk, Agnieszka; Marchel, Michal; Fidzianska, Anna; Opolski, Grzegorz; Hausmanowa-Petrusewicz, Irena
err分享
err收藏
Cardiac involvement in neuronal ceroid lipofuscinosis
errKARDIOLOGIA POLSKA
IF3.7
err2013-08-20
err0
errOAAI
errSzwoch, Malgorzata; Wojtowicz, Dagmara; Dorniak, Karolina; Walczak, Ewa; Raczak, Grzegorz; Fidzianska, Anna
err分享
err收藏
Late form of Pompe disease with glycogen storage in peripheral nerves axons
errJOURNAL OF THE NEUROLOGICAL SCIENCES
IF3.2
err2011-02-01
err10
PREAI
errFidzianska, Anna; Lugowska, Agnieszka; Tylki-Szymanska, Anna
err分享
err收藏
Genetic and ultrastructural studies in dilated cardiomyopathy patients: a large deletion in the lamin A/C gene is associated with cardiomyocyte nuclear envelope disruption
errBASIC RESEARCH IN CARDIOLOGY
IF8
err2010-02-03
err80
errOAAI
errGupta, Pallavi; Bilinska, Zofia T.; Sylvius, Nicolas; Boudreau, Emilie; Veinot, John P.; Labib, Sarah; Bolongo, Pierrette M.; Hamza, Akil; Jackson, Tracy; Ploski, Rafal; Walski, Michal; Grzybowski, Jacek; Walczak, Ewa; Religa, Grzegorz; Fidzianska, Anna; Tesson, Frederique
err分享
err收藏
TPM3 MUTATION IN ONE OF THE ORIGINAL CASES OF CAP DISEASE
errNEUROLOGY
IF8.5
err2009-06-02
err33
PREAI
errOhlsson, Monica; Fidzianska, Anna; Tajsharghi, Homa; Oldfors, Anders
err分享
err收藏
Cardiovascular magnetic resonance findings in a case of Danon disease
errJOURNAL OF CARDIOVASCULAR MAGNETIC RESONANCE
IF6.1
err2009-01-01
err37
errOAAI
errPiotrowska-Kownacka, Dorota; Kownacki, Lukasz; Kuch, Marek; Walczak, Ewa; Kosieradzka, Agnieszka; Fidzianska, Anna; Krolicki, Leszek
err分享
err收藏
Obliteration of cardiomyocyte nuclear architecture in a patient with LMNA gene mutation
errJOURNAL OF THE NEUROLOGICAL SCIENCES
IF3.2
err2008-08-01
err26
PREAI
errFidzianska, Anna; Bilinska, Zofia T.; Tesson, Frederique; Wagner, Terresa; Walski, Michal; Grzybowski, Jacek; Ruzyllo, Witold; Hausmanowa-Petrusewicz, Irena
err分享
err收藏
Atypical motor unit potentials in Emery-Dreifuss muscular dystrophy (EDMD)
errCLINICAL NEUROPHYSIOLOGY
IF3.6
err2005-11-01
err22
PREAI
errRowinska-Marcinska, K; Szmidt-Salkowska, E; Fidzianska, A; Zalewska, E; Dorobek, M; Karwanska, A; Hausmanowa-Petrusewicz, I
err分享
err收藏
In vivo and in vitro examination of the functional significances of novel lamin gene mutations in heart failure patients
errJOURNAL OF MEDICAL GENETICS
IF3.7
err2005-08-01
err88
errOAAI
errSylvius, N; Bilinska, ZT; Veinot, JP; Fidzianska, A; Bolongo, PM; Poon, S; McKeown, P; Davies, RA; Chan, KL; Tang, ASL; Dyack, S; Grzybowski, J; Ruzyllo, W; McBride, H; Tesson, F
err分享
err收藏
A dystrophin missense mutation showing persistence of dystrophin and dystrophin-associated proteins yet a severe phenotype
errANNALS OF NEUROLOGY
IF7.7
err2004-10-08
err38
PREAI
errGoldberg, LR; Hausmanowa-Petrusewicz, I; Fidzianska, A; Duggan, DJ; Steinberg, LS; Hoffman, EP
err分享
err收藏
Small deletions disturb desmin architecture leading to breakdown of muscle cells and development of skeletal or cardioskeletal myopathy
errHUMAN GENETICS
IF3.6
err2004-02-01
err52
PREAI
errKaminska, A; Strelkov, SV; Goudeau, B; Olivé, M; Dagvadorj, A; Fidzianska, A; Simon-Casteras, M; Shatunov, A; Dalakas, MC; Ferrer, I; Kwiecinski, H; Vicart, P; Goldfarb, LG
err分享
err收藏
CADASIL: new cases and new questions
errACTA NEUROPATHOLOGICA
IF9.3
err2003-12-01
err14
PREAI
errRafalowska, J; Fidzianska, A; Dziewulska, D; Podlecka, A; Szpak, GM; Kwiecinski, H
err分享
err收藏
Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)
errJOURNAL OF CLINICAL INVESTIGATION
IF13.6
err2002-08-01
err419
errOAAI
errTristani-Firouzi, M; Jensen, JL; Donaldson, MR; Sansone, V; Meola, G; Hahn, A; Bendahhou, S; Kwiecinski, H; Fidzianska, A; Plaster, N; Fu, YH; Ptacek, LJ; Tawil, R
err分享
err收藏
Familial inclusion body myopathy with desmin storage具有结蛋白储存的家族性包涵体肌病
errACTA NEUROPATHOLOGICA
IF9.3
err1999-05-09
err14
PREAI
errFidzianska, A; Drac, H; Kaminska, AM
err分享
err收藏
Calpain III mutation analysis of a heterogeneous limb-girdle muscular dystrophy population
errNEUROLOGY
IF8.5
err1999-03-01
err51
PREAI
errChou, FL; Angelini, C; Daentl, D; Garcia, C; Greco, C; Hausmanowa-Petrusewicz, I; Fidzianska, A; Wessel, H; Hoffman, EP
err分享
err收藏
Ultrastructural abnormality of sarcolemmal nuclei in Emery-Dreifuss muscular dystrophy (EDMD)
errJOURNAL OF THE NEUROLOGICAL SCIENCES
IF3.2
err1998-07-01
err102
PREAI
errFidzianska, A; Toniolo, D; Hausmanowa-Petrusewicz, I
err分享
err收藏
Mutations in the sarcoglycan genes in patients with myopathy
errNEW ENGLAND JOURNAL OF MEDICINE
IF78.5
err1997-02-27
err191
errOAAI
errDuggan, DJ; Gorospe, JR; Fanin, M; Hoffman, EP; Angelini, C; Pegoraro, E; Noguchi, S; Ozawa, E; Pendlebury, W; Waclawik, AJ; Duenas, DA; HausmanowaPetrusewicz, I; Fidzianska, A; Bean, SC; Haller, JS; Bodensteiner, J; Greco, CM; Pestronk, A; Berardinelli, A; Gelinas, DF; Abram, H; Kunel, RW
err分享
err收藏
HUMAN ONTOGENY .3. CELL-DEATH IN FETAL MUSCLE人类个体发育3.胎儿肌肉中的细胞死亡
errACTA NEUROPATHOLOGICA
IF9.3
err1991-04-01
err63
PREAI
errFIDZIANSKA, A; GOEBEL, HH
err分享
err收藏
TUBULORETICULAR STRUCTURES (TRS) AND CYLINDRIC CONFRONTING CISTERNAE (CCC) IN CHILDHOOD DERMATOMYOSITIS
errACTA NEUROPATHOLOGICA
IF9.3
err1989-12-01
err12
PREAI
errFIDZIANSKA, A; GOEBEL, HH
err分享
err收藏
ULTRASTRUCTURE OF THE ARTHUS PHENOMENON IN MUSCLE
errACTA NEUROPATHOLOGICA
IF9.3
err1984-06-01
err1
PREAI
errFIDZIANSKA, A; GOEBEL, HH; OSSE, G
err分享
err收藏

研究方向

暂时未获取到该数据
合作学者
合作期刊
I
Isidró Ferrer
H 指数: 119 · 论文数: 1.2K
E
Eric P. Hoffman
H 指数: 113 · 论文数: 1.3K
H
Hans H. Goebel
H 指数: 110 · 论文数: 1.6K
M
Marinos C. Dalakas
H 指数: 108 · 论文数: 596
C
C. Angelini
H 指数: 108 · 论文数: 1.8K
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