FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Anna Fidzianska

Research Profile

Physiology

Concepts & Ideas

Disorders

Chemicals & Drugs

Anatomy

Co-author Network

Publications

TOP 3
Pallavi Gupta; Zofia T Bilinska; Nicolas Sylvius; Emilie Boudreau; John P Veinot; Sarah Labib; Pierrette M Bolongo; Akil Hamza; Tracy Jackson; Rafal Ploski; Michal Walski; Jacek Grzybowski; Ewa Walczak; Grzegorz Religa; Anna Fidzianska; Frédérique Tesson
Genetic and ultrastructural studies in dilated cardiomyopathy patients: a large deletion in the lamin A/C gene is associated with cardiomyocyte nuclear envelope disruption.
Monica Ohlsson; Anna Fidzianska; Homa Tajsharghi; Anders Oldfors
TPM3 mutation in one of the original cases of cap disease.
Dorota Piotrowska-Kownacka; Lukasz Kownacki; Marek Kuch; Ewa Walczak; Agnieszka Kosieradzka; Anna Fidzianska; Leszek Krolicki
Cardiovascular magnetic resonance findings in a case of Danon disease.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Anna Fidzianska (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2010: Pallavi Gupta; Zofia T Bilinska; Nicolas Sylvius; Emilie Boudreau; John P Veinot; Sarah Labib; Pierrette M Bolongo; Akil Hamza; Tracy Jackson; Rafal Ploski; Michal Walski; Jacek Grzybowski; Ewa Walczak; Grzegorz Religa; Anna Fidzianska; Frédérique Tesson
Genetic and ultrastructural studies in dilated cardiomyopathy patients: a large deletion in the lamin A/C gene is associated with cardiomyocyte nuclear envelope disruption.
Basic research in cardiology 2010;105(3):365-77.
2009: Monica Ohlsson; Anna Fidzianska; Homa Tajsharghi; Anders Oldfors
TPM3 mutation in one of the original cases of cap disease.
Neurology 2009;72(22):1961-3.
2009: Dorota Piotrowska-Kownacka; Lukasz Kownacki; Marek Kuch; Ewa Walczak; Agnieszka Kosieradzka; Anna Fidzianska; Leszek Krolicki
Cardiovascular magnetic resonance findings in a case of Danon disease.
Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance 2009;11():12.
2008: Anna Fidzianska; Z Glinka; Anna Kaminska; Irena Niebroj-Dobosz
Altered distribution of lamin and emerin in muscle nuclei of sIBM patients.
Clinical neuropathology 2008;27(6):424-9.
2006: Anna Kostera-Pruszczyk; Bertrand Goudeau; Ana Ferreiro; Pascal Richard; Stéphanie Simon; Patrick Vicart; Anna Fidzianska
Myofibrillar myopathy with congenital cataract and skeletal anomalies without mutations in the desmin, alphaB-crystallin, myotilin, LMNA or SEPN1 genes.
Neuromuscular disorders : NMD 2006;16(11):759-62.
2006: Dagmara Kabzinska; Hanna Drac; Katarzyna Rowinska-Marcinska; Anna Fidzianska; Andrzej Kochanski; Irena Hausmanowa-Petrusewicz
Early onset Charcot-Marie-Tooth disease caused by a homozygous Leu239Phe mutation in the GDAP1 gene.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases 2006;25(1):34-7.
2005: Anna Fidzianska; Barbara Ryniewicz; Xing-Ming Shen; Andrew G Engel
IBM-type inclusions in a patient with slow-channel syndrome caused by a mutation in the AChR epsilon subunit.
Neuromuscular disorders : NMD 2005;15(11):753-9.
2005: Nicolas Sylvius; Zofia T Bilinska; John P Veinot; Anna Fidzianska; P M Bolongo; S Poon; P McKeown; R A Davies; K-L Chan; Anthony S L Tang; S Dyack; Jacek Grzybowski; Witold Ruzyllo; Heidi McBride; Frédérique Tesson
In vivo and in vitro examination of the functional significances of novel lamin gene mutations in heart failure patients.
Journal of medical genetics 2005;42(8):639-47.
2004: Janina Rafalowska; Dorota Dziewulska; Anna Fidzianska
CADASIL: what component of the vessel wall is really a target for Notch 3 gene mutations?
Neurological research 2004;26(5):558-62.
2004: Janina Rafalowska; Anna Fidzianska; Dorota Dziewulska; Aleksandra Podlecka; Grazyna M Szpak; Hubert Kwiecinski
CADASIL or CADVaSIL?
Neuropathology : official journal of the Japanese Society of Neuropathology 2004;24(1):16-20.
2004: Anna Kaminska; Sergei V Strelkov; Bertrand Goudeau; Montse Olivé; Ayush Dagvadorj; Anna Fidzianska; Monique Simon-Casteras; Alexey Shatunov; Marinos C Dalakas; Isidro Ferrer; Hubert Kwiecinski; Patrick Vicart; Lev G Goldfarb
Small deletions disturb desmin architecture leading to breakdown of muscle cells and development of skeletal or cardioskeletal myopathy.
Human genetics 2004;114(3):306-13.
2003: Irena Niebroj-Dobosz; Anna Fidzianska; Irena Hausmanowa-Petrusewicz
Expression of emerin and lamins in muscle of patients with different forms of Emery-Dreifuss muscular dystrophy.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases 2003;22(2):52-7.
2002: Martin Tristani-Firouzi; Judy L Jensen; Matthew R Donaldson; Valeria Sansone; Giovanni Meola; Angelika Hahn; Saïd Bendahhou; Hubert Kwiecinski; Anna Fidzianska; Nikki Plaster; Ying-Hui Fu; Louis J Ptacek; Rabi Tawil
Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome).
The Journal of clinical investigation 2002;110(3):381-8.
1999: F L Chou; Corrado Angelini; D Daentl; C Garcia; C Greco; Irena Hausmanowa-Petrusewicz; Anna Fidzianska; Howard Wessel; Eric Hoffman
Calpain III mutation analysis of a heterogeneous limb-girdle muscular dystrophy population.
Neurology 1999;52(5):1015-20.
1998: L R Goldberg; Irena Hausmanowa-Petrusewicz; Anna Fidzianska; DJ Duggan; L S Steinberg; Eric Hoffman
A dystrophin missense mutation showing persistence of dystrophin and dystrophin-associated proteins yet a severe phenotype.
Annals of neurology 1998;44(6):971-6.
1995: Anna Fidzianska; A Morrone; Elena Pegoraro; Barbara Ryniewicz; A Ilnicka; Enrico Zammarchi; Eric Hoffman
An X:autosome translocation stabilizes truncated dystrophin: implications for lack of truncated dystrophins in Duchenne muscular dystrophy.
Neuropediatrics 1995;26(3):163-7.
1993: J Wang; J Zhou; S M Todorovic; William G. Feero; F Barany; R Conwit; Irena Hausmanowa-Petrusewicz; Anna Fidzianska; K Arahata; H B Wessel
Molecular genetic and genetic correlations in sodium channelopathies: lack of founder effect and evidence for a second gene.
American journal of human genetics 1993;52(6):1074-84.
1993: William G. Feero; J Wang; F Barany; J Zhou; S M Todorovic; R Conwit; G Galloway; Irena Hausmanowa-Petrusewicz; Anna Fidzianska; K Arahata
Hyperkalemic periodic paralysis: rapid molecular diagnosis and relationship of genotype to phenotype in 12 families.
Neurology 1993;43(4):668-73.
1992: Anna Fidzianska; H H Goebel
Phagocytic capacity of human muscle fibers.
Human pathology 1992;23(9):1044-7.
1981: Anna Fidzianska; B Badurska; Barbara Ryniewicz; I Dembek
"Cap disease": new congenital myopathy.
Neurology 1981;31(9):1113-20.