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I. Hausmanowa‐Petrusewicz, Poland
40
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1
EFNS task force on molecular diagnosis of neurologic disord..:
Members of the task force on molecular diagnosis of neurologic disorders: T. Gasser, Germany
;
M. Dichgans, Germany
;
J. Finsterer, Austria
;
I. Hausmanowa‐Petrusewicz, Poland
;
K. Jurkat‐Rott, Germany
;
T. Klopstock, Germany
;
E. Leguern, France
;
A.‐E. Lehesjoki, Finland
;
F. Lehmann‐Horn, Germany
;
T. Lynch, UK
;
H. Morris, UK
;
M. Rossor, UK
;
O.K. Steinlein, Germany
;
N. Wood, UK
;
J. Zaremba, Poland
;
M. Zeviani, Italy
;
A. Zoharn, Israel
European Journal of Neurology. 8 (2001) 5 - p. 407-424 , 2001
Link:
https://doi.org/10.1046/..
?
2
Age‐related change in duration of afterhyperpolarization of..:
Piotrkiewicz, M.
;
Kudina, L.
;
Mierzejewska, J.
..
The Journal of Physiology. 585 (2007) 2 - p. 483-490 , 2007
Link:
https://doi.org/10.1113/..
?
3
1111 Assessment of left ventricular systolic dysfunction by..:
MARCHEL, M
;
MADEJ, A
;
STEPIEN, V
...
European Journal of Echocardiography. 7 (2006) - p. S194-S194 , 2006
Link:
https://doi.org/10.1016/..
?
4
Atypical motor unit potentials in Emery–Dreifuss muscular d..:
ROWINSKAMARCINSKA, K
;
SZMIDTSALKOWSKA, E
;
FIDZIANSKA, A
...
Clinical Neurophysiology. 116 (2005) 11 - p. 2520-2527 , 2005
Link:
https://doi.org/10.1016/..
?
5
Focally folded myelin in Charcot–Marie–Tooth type 1B diseas..:
Kochański, A.
;
Drac, H.
;
Jędrzejowska, H.
.
European Journal of Neurology. 10 (2003) 5 - p. 547-549 , 2003
Link:
https://doi.org/10.1046/..
?
6
Genetic Refinement And Physical Mapping Of The CMT4B Gene O..:
Bolino, A.
;
Levy, E.R.
;
Muglia, M.
...
Journal of the Peripheral Nervous System. 5 (2000) 2 - p. 116-116 , 2000
Link:
https://doi.org/10.1046/..
?
7
Mutation Screening of Charcot‐Marie‐Tooth Patients in Polan:
KOCHAŃSKI, A.
;
TIMMERMAN, V.
;
JEDRZEJOWSKA, H.
...
Annals of the New York Academy of Sciences. 883 (1999) 1 - p. 493-496 , 1999
Link:
https://doi.org/10.1111/..
?
8
Calpain III mutation analysis of a heterogeneous limb–girdl..:
Chou, F.-L.
;
Angelini, C.
;
Daentl, D.
...
Neurology. 52 (1999) 5 - p. 1015-1015 , 1999
Link:
https://doi.org/10.1212/..
?
9
Detection of deletions within the dystrophin gene in Polish..:
Zimowski, J. G.
;
Bisko, M. U.
;
Fidziańska, E. J.
...
European Journal of Neurology. 4 (1997) 2 - p. 138-142 , 1997
Link:
https://doi.org/10.1111/..
?
10
Proteins of muscle subcellular fractions in Duchenne progre..:
Niebroj‐Dobosz, I.
;
Kornguth, S.
;
Schutta, H.
..
Muscle & Nerve. 12 (1989) 4 - p. 273-280 , 1989
Link:
https://doi.org/10.1002/..
?
11
Is Kugelberg‐Welander spinal muscular atrophy a fetal defec..:
Hausmanowa‐Petrusewicz, I.
;
Fidziańska, A.
;
Niebróaj‐Doposz, I.
.
Muscle & Nerve. 3 (1980) 5 - p. 389-402 , 1980
Link:
https://doi.org/10.1002/..
?
12
G.P.96 The point mutations spectrum of survival motor neuro..:
Jedrzejowska, M.
;
Gos, M.
;
Zimowski, J.
...
Neuromuscular Disorders. 22 (2012) 9-10 - p. 871 , 2012
Link:
https://doi.org/10.1016/..
?
13
DominantGDAP1mutations cause predominantly mild CMT phenoty..:
Zimoń, M.
;
Baets, J.
;
Fabrizi, G.M.
...
Neurology. 77 (2011) 6 - p. 540-548 , 2011
Link:
https://doi.org/10.1212/..
?
14
S45-1 The diagnostic yield of atypical motor unit potential:
Zalewska, E.
;
Hausmanowa-Petrusewicz, I.
Clinical Neurophysiology. 121 (2010) - p. S64 , 2010
Link:
https://doi.org/10.1016/..
?
15
JS2-1 Using motor unit potentials analysis to get an insigh..:
Zalewska, E.
;
Hausmanowa-Petrusewicz, I.
Clinical Neurophysiology. 121 (2010) - p. S99 , 2010
Link:
https://doi.org/10.1016/..
1-15