Clinical Neuroscience - 2009;62(11-12)

Clinical Neuroscience

NOVEMBER 30, 2009

Clinical Neuroscience

NOVEMBER 30, 2009

[New vistas and views in the concept of generalized epilepsies]

HALÁSZ Péter, KELEMEN Anna

[The aim of this work is to show explicitly why the “idiopathic generalized epilepsy” concept becomes outfashioned and untenable. As the concept of “generalized epilepsies” is from long ago closely related to the thalamo-cortical system, we briefly summarize the functional anatomy, the double working mode of the thalamo-cortical system in different vigilance states and it’s role in development of the spike - wave pattern. The next part shows weaknesses of this concept from the EEG, seizure... tovább »

Clinical Neuroscience

NOVEMBER 30, 2009

[Role of zonisamid in treating epilepsy, Parkinson disorders and other neurological diseases]

JANSZKY József

[On the basis of six randomized controlled trials, zonisamide (ZNS) can be prescribed as add-on treatment in focal adulthood epilepsy in USA and Europe. In Japan, it can be prescribed as first-line monotherapy drug - independent of age. ZNS may also be effective in idiopathic generalized epilepsy and some difficult-to-treat epilepsies including West, Lennox-Gastaut, or Dravet syndromes. The most frequent side effects of ZNS are related to central nervous system occurring in 19%. Kidney stones... tovább »

Clinical Neuroscience

NOVEMBER 30, 2009

[Quantitative analysis of the genes determining spinal muscular atrophy]

NAGYMIHÁLY Mariann, HERCZEGFALVI Ágnes, TÍMÁR László, KARCAGI Veronika

[Spinal muscular atrophy (SMA) is one of the most common autosomal recessive diseases, affecting approximately one in 10.000 live births and with a carrier frequency of approximately one in 35. The disease is caused by a deficiency of the ubiquitous protein survival of motor neuron (SMN), which is encoded by the SMN1 and SMN2 genes. Due to a single nucleotide polymorphism in exon 7, SMN2 produces less full-length transcript than SMN1 and cannot prevent neuronal cell death at physiologic gene... tovább »

Clinical Neuroscience

NOVEMBER 30, 2009

[Guillain–Barré syndrome in childhood]

KOLLÁR Katalin, LIPTAI Zoltán, ROSDY Beáta, MÓSER Judit

[Background - Guillain-Barré syndrome (GBS) is clinically well known since 1916. It can occur at any age. Its main characteristic is acute rapidly ascending flaccid paresis. It is a neuro-immunologic disorder with heterogeneous background. In Hungary we could not find reports about big paediatric population with GBS. Patient and method - We analysed retrospectively the data of 38 children diagnosed and treated with GBS at the Neurological Department of Paul Heim Children’s Hospital or at the... tovább »

Clinical Neuroscience

NOVEMBER 30, 2009

[Myelination disturbance in a patient with hyperuricemia and hyperserotoninemia combined with 18q deletion syndrome]

LÁSZLÓ Aranka, VÖRÖS Erika, BUGA Klára, HORVÁTH Katalin, MAYER Péter, OSZTOVICS Magda†, PÁVICS László, SVEKUS András, PATTERSON C. Marc

[We previously reported a male patient with an 18q21.3 deletion, hyperuricemia and typical symptoms of the Lesch- Nyhan syndrome who lacked hypoxanthine-guanine-phosphoribosyl- transferase (HGPRT) deficiency. The patient developed progressive peripheral neuropathy in additon to his profound mental retardation and self-injurious behavior. At the age of 23 years MR imaging revealed globally delayed myelination with relative sparing of the corpus callosum and frontal lobes. They were focal... tovább »

Clinical Neuroscience

NOVEMBER 30, 2009

[Application of robots at patients with paresis of the upper limb as a consequence of central motor neuron lesion for supporting physiotherapy during rehabilitation]

FAZEKAS Gábor

[Application of robots at patients with paresis of the upper limb as a consequence of central motor neuron lesion for supporting physiotherapy during rehabilitation 2009;62(11-12)]

Clinical Neuroscience

NOVEMBER 30, 2009

[Darwin anniversaries and the neurology]

KATONA Ferenc, BERÉNYI Marianne

[Darwin anniversaries and the neurology 2009;62(11-12)]

Clinical Neuroscience

NOVEMBER 30, 2009

Clinical Neuroscience

NOVEMBER 30, 2009