The Publications (Eng.)

 

Petr Vondracek, M.D., Ph.D.

Associate Professor of Neurology

NEUROVON s.r.o.

 

Publication activity:

 

 

Principal publications:

  • Vondracek P, Hermanova M, Vodickova K, Fajkusova L, Brichtova E, Skotakova J. White Matter Involvement in Neuromuscular Disorders. In: Westland TB, Calton RN, editors. Handbook on White Matter: Structure, Function and Changes. 1st ed. New York: Nova Science Publishers; 2009. p. 89-109. ISBN: 978-1-60741-034-8.

 

  • Vondracek P, Fajkusova L, Hermanova M, Balintova Z, Seeman P, Mazanec R, Zapletalova E, Brabec P. New Perspectives in the Treatment of Inherited Neuromuscular Disorders: Innovative Ideas for the Third Millenium. In: Engels JV, editor. Focus on Birth Defects Research. 1st ed. New York: Nova Science Publishers; 2006. p.161-183. ISBN: 1-59454-959-1.

 

  • Rotthier A, Auer-Grumbach M, Janssens K, Baets J, Penno A, Almeida-Souza L, Van Hoof K, Jacobs A, De Vriendt E, Schlotter-Weigel B, Löscher W, Vondracek P, Seeman P, De Jonghe P, Van Dijck P, Jordanova A, Hornemann T, Timmerman V. Mutations in the SPTLC2 subunit of serine palmitoyltransferase cause hereditary sensory and autonomic neuropathy type I. Am J Hum Genet. 2010; 4: 513-522. IF=11,680.

 

 

  • Cirak S, Foley AR, Herrmann R, Willer T, Yau S, Stevens E, Torelli S, Brodd L, Kamynina A, Vondracek P, Roper H, Longman C, Korinthenberg R, Marrosu G, Nürnberg P; UK10K Consortium, Michele DE, Plagnol V, Hurles M, Moore SA, Sewry CA, Campbell KP, Voit T, Muntoni F. ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies. Brain. 2013; 1: 269–281. IF=9,457.

 

  • Brabec P, Vondracek P, Klimes D, Baumeister S, Lochmüller H, Pavlík T, Gregor J. Characterization of the DMD/BMD patient population in Czech Republic and Slovakia using an innovative registry approach. Neuromuscul Disord. 2009; 4: 250-254. (equal contribution of first 2 authors). IF=2,667.

 

  • Vondracek P, Oslejskova H, Kepak T, Mazanek P, Sterba J, Rysava M, Gal P. Efficacy of Pregabalin in Neuropathic Pain in Paediatric Oncological Patients. Eur J Paediatr Neurol. 2009; 4: 332-336. IF=2,01.

 

  • Vondracek P, Hermanova M, Sedlackova J, Fajkusova L, Stary D, Michenkova A, Gaillyova R, Seeman P, Mazanec R. Charcot-Marie-Tooth neuropathy type 1A combined with Duchenne muscular dystrophy. Eur J Neurol. 2007; 10: 1182-1185. IF=2,244.

 

  • Vondracek P, Hermanova M, Vodickova K, Fajkusova L, Blakely EL., He L, Turnbull DM, Taylor RW, Tajsharghi H. An unusual case of congenital muscular dystrophy with normal serum CK level, external ophtalmoplegia and white matter changes on brain MRI. Eur J Paediatr Neurol. 2007; 6: 381-384. IF=0,861.

 

  • Vondracek P, Bednarik J. Clinical and Electrophysiological Findings and Long-term Outcomes in Paediatric Patients with Critical Illness Polyneuromyopathy. Eur Paediatr Neurol. 2006; 4: 176-181. IF=1,364.

 

Kontakt

Doc. MUDr. Petr Vondráček, Ph.D.

U sokolovny 14
635 00 Brno

+42 734 455 719

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