Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Claudia Thaler"'
Autor:
Hakan Cetin, Fritz Zimprich, Julia Jecel, Waltraud Kleindienst, Eva Lenzenweger, Marcus Erdler, Dierk Oel, Stefan Quasthoff, Karl Stieglbauer, Klaus Berek, Jakob Rath, Wolfgang Löscher, Susanne Grinzinger, Julia Wanschitz, Wolfgang Örtl, Michael Huemer, Eva-Maria Oberreiter, Isolde Hess, Norbert Embacher, Eva Laich, Raffi Topakian, Petra Müller, Claudia Thaler-Wolf, Valeriu Culea, Klaus Stadler, Corinne G. C. Horlings, Franz Stefan Höger
Publikováno v:
Journal of Neurology
Background and objectives Multifocal motor neuropathy (MMN) is a rare neuropathy and detailed descriptions of larger patient cohorts are scarce. The objective of this study was to evaluate epidemiological, clinical, and laboratory features of MMN pat
Publikováno v:
Muscle & Nerve. 28:760-763
We report on two cases of isolated damage to a muscle branch of the lateral pectoral nerve. Diagnosis was established by the clinical presentation and electromyographic examination. In the few reported cases of such injuries, the cause was trauma to
Autor:
Stephan Doering, Claudia Thaler, Ulrike Niedermüller, Gerhard Bauer, T. Moroder, Eugen Trinka, Gunther Ladurner
Publikováno v:
Seizure. 9(7):505-508
We report two adults who received gabapentin (GBP) and subsequently developed behavioural side effects. Indications for GBP treatment were newly diagnosed epilepsy in one and painful paraesthesiae in the other. Both had no past history of psychiatric
Autor:
Ursula Kohlendorfer, Michaela Jaksch, Johann Willeit, Stefan Kiechl, Daniela Skladal, B. Obermaier-Kusser, Claudia Thaler
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 67:364-368
OBJECTIVE—To characterise the main clinical phenotypes of debrancher deficiency myopathy and to increase awareness for this probably underdiagnosed disorder. METHODS—The diagnosis of debrancher deficiency was established by laboratory tests, EMG,
Autor:
Rita Horvath, Petri Luoma, Anu Suomalainen, Johann Willeit, Stefan Kiechl, Michaela Jaksch, Claudia Thaler, R Stucka, U. Kiechl-Kohlendorfer, B Wallacher-Scholz, Julia Wanschitz
Objectives: We report here the clinical and genetic features of two new families with autosomal dominant progressive external ophthalmoplegia (adPEO). Patients and methods: The examination of index patients included a detailed clinical characterisati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::137bde564dc9180222b420f176c0b442
https://europepmc.org/articles/PMC1739155/
https://europepmc.org/articles/PMC1739155/
Autor:
Claudia Thaler, Gerhard Luef, Erika Dilitz, Eugen Trinka, Gerhard Bauer, Florian Deisenhammer, Iris Unterberger, Ulrike Niedermüller
Publikováno v:
Journal of neurology. 249(10)
Purpose: Lamotrigine (LTG) and valproate (VPA) are widely used in the treatment of generalized epilepsies. Nevertheless seizure aggravation with LTG has been reported in juvenile myoclonic epilepsy and epilepsy with myoclonic absences. The aim of thi
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 73:205-205
Myasthenia gravis (MG) is an autoimmune disorder causing postsynaptic impairment of neuromuscular transmission.1–3 Ocular, bulbar, or proximal limb muscles are most frequently affected, and weakness worsens during exercise. Recently, variants of MG
Publikováno v:
Muscle & Nerve; Dec2003, Vol. 28 Issue 6, p760-763, 4p