Search Results - "Hahn, Katalin"
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Improving Outcomes Achieved by a New Stroke Program in Hungary
Published in Cerebrovascular diseases extra (30-10-2015)“…Background: Stroke is a devastating disease with increasing incidence and prevalence due to population aging. Even with the best care, a proportion of patients…”
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In memoriam Prof. Dr. Ferenc Garzuly (1937-2021)
Published in Ideggyógyászati szemle (30-07-2021)“…Ferenc Garzuly passed away after a long and productive life at the age of 84. He worked for almost 60 years at the Markusovszky University Teaching Hospital,…”
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In memoriam prof. dr. Garzuly Ferenc (1937–2021)
Published in Ideggyógyászati szemle (2021)“…Garzuly Ferenc címzetes egyetemi tanár hosszú, aktív élet után hunyt el 84 évesen. Közel 60 éven át dolgozott a szombathelyi Markusovszky Egyetemi…”
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Life threatening rare lymphomas presenting as longitudinally extensive transverse myelitis: a diagnostic challenge
Published in Ideggyógyászati szemle (30-07-2020)Get full text
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Utilization of acute vascular imaging and neurointervention for acute ischaemic stroke patients in 20 Hungarian stroke centers
Published in Ideggyógyászati szemle (30-11-2019)“…Acute mortality rate of stroke in Hungary is significantly higher than in Western Europe, which is likely to be partially attributable to suboptimal treatment…”
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ASSOCIATION OF TEMPORAL LOBE INFLAMMATORY LEUKOENCEPHALOPATHY WITH TWO B CELL MALIGNANCIES
Published in Ideggyógyászati szemle (30-03-2014)“…Identification of etiological connections among virtually distinct diseases in a patient may be sometimes challenging. We report a unique case with two B cell…”
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Botulinum toxin therapy for focal dystonia
Published in Orvosi hetilap (19-07-2009)“…Dystonia is a syndrome characterized by sustained muscle contraction. It is frequently causing twisting and repetitive movements, or leading to development…”
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Novel sequence variants of the α-galactosidase A gene in patients with Fabry disease
Published in Molecular genetics and metabolism (01-12-2008)“…We carried out molecular studies of 15 unrelated Hungarian families diagnosed with Fabry disease (FD). Genetic analysis of the α-galactosidase A gene was…”
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Az akut vascularis képalkotás és a neurointervenció igénybevétele akut ischaemiás stroke betegeknél Magyarországon
Published in Ideggyógyászati szemle (2019)Get full text
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Molecular pathology and clinical manifestations of Fabry disease
Published in Orvosi hetilap (10-06-2007)“…Fabry disease is a rare, progressive lysosomal storage disorder caused by mutation in the GAL gene and an impaired function of the alpha-galactosidase A…”
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