E-LIB Suche - Ergebnisse für: I. Hausmanowa‐Petrusewicz, Poland

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

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/..

15

Charcot-Marie-Tooth type 1A disease caused by a novel Ser11..:

Kabzińska, D. ; Sinkiewicz-Darol, E. ; Hausmanowa-Petrusewicz, I..
Journal of Applied Genetics. 51 (2010) 2 - p. 203-209 , 2010

Link: https://doi.org/10.1007/..