Supratentorial astrocytoma associated with arteriovenous malformation. Case report.

abstract：:Glioblastoma, the most malignant astrocytic tumour, is associated with limited survival and thus rare metastases. We analysed a particularly interesting case - a 51-year-old male diagnosed within 2 years with primary and recurrent glioblastoma, isocitrate dehydrogenase (IDH)-wild type, as well as with numerous extra-c...

journal_title：Folia neuropathologica

authors： Janik K,Och W,Popeda M,Rosiak K,Peciak J,Rieske P,Kulbacki K,Szostak B,Parda A,Stoczynska-Fidelus E

更新日期：2019-01-01 00:00:00

abstract：:The aim of our study was to present six cases with cystic changes within the white matter in infant brains and discuss the variants of this type of neuropathological lesions of the developing brain. Two of them exhibited the changes characteristic for cystic leucoencephalopathy. To the others with moderate involvement...

journal_title：Folia neuropathologica

authors： Dambska M,Kuchna I,Nowicki K

更新日期：1994-01-01 00:00:00

abstract：:Human T lymphotropic virus type I (HTLV-I)-associated myelopathy/tropical spastic paraparesis (HAM/TSP) is a chronic progressive myelopathy characterized by bilateral pyramidal tract involvement with sphincteric disturbances. The primary neuropathological feature of HAM/TSP is chronic myelitis characterized by perivas...

journal_title：Folia neuropathologica

authors： Nakamura T

更新日期：2009-01-01 00:00:00

abstract：:Prion-like transmission of protein aggregates or amyloid in several neurodegenerative diseases, such as Parkinson's disease, Huntington's disease and Alzheimer's disease, in addition to the transmissible spongiform encephalopathies (or prion diseases), has been proposed recently. This is a controversial idea and, in t...

journal_title：Folia neuropathologica

authors： Hope J,Kirby L

更新日期：2012-01-01 00:00:00

abstract：:Morphometric analysis of the cerebellar cortex capillary cross-section area performed in experimental valproate encephalopathy using transmission electron microscopy showed that prolongation of VPA application resulted in more enhanced lumen narrowing manifested in gradual reduction in the mean value of the coefficien...

journal_title：Folia neuropathologica

authors： Sobaniec-Lotowska M,Sobaniec W,Augustynowicz A

更新日期：2001-01-01 00:00:00

abstract：:Chordoid glioma is a rare benign neoplasm of uncertain histogenesis occurring in the third ventricle/ /suprasellar region. Recently, data have emerged suggesting that chordoid glioma is a variant of ependymoma related to a specialised ependyma of the subcommisural organ or the lamina terminalis area. In this study, we...

journal_title：Folia neuropathologica

authors： Taraszewska A,Bogucki J,Andrychowski J,Koszewski W,Czernicki Z

更新日期：2003-01-01 00:00:00

abstract：:Globoid cell leukodystrophy (GLD, also known as Krabbe disease), whose pathophysiology is still not completely elucidated, is an inherited, metabolic, and neurodegenerative disease, caused by the deficiency of β-galactocerebrosidase (GALC) or in very rare cases by lack of active saposin A. We describe two patients, i...

journal_title：Folia neuropathologica

authors： Szymańska K,Ługowska A,Laure-Kamionowska M,Bekiesińska-Figatowska M,Gieruszczak-Białek D,Musielak M,Eichler S,Giese AK,Rolfs A

更新日期：2012-01-01 00:00:00

abstract：:The inflammatory process is a nonspecific complex, stereotype, coordinated response of tissues to injury. This process involves vascular permeability, active migration of blood cells, and passage of plasma constituents into the injurious tissue. The molecules that mediate the initial events of inflammation are the adh...

journal_title：Folia neuropathologica

authors： Maślińska D,Gajewski M

更新日期：1998-01-01 00:00:00

abstract：:The Warburg micro syndrome (WARBM) is a genetically heterogeneous syndrome linked to at least 4 loci. At the clinical level, WARBM is characterized by microcephaly, microphthalmia, microcornea, congenital cataracts, corpus callosum hypoplasia, severe mental retardation, and hypogonadism. In some families additional cl...

journal_title：Folia neuropathologica

authors： Kabzińska D,Mierzewska H,Senderek J,Kochański A

更新日期：2016-01-01 00:00:00

abstract：:We describe here a variety of autophagous forms encountered in the terminal stages of two models of scrapie in hamsters. We also show that the number of autophagic vacuoles increased through the incubation period in the 263K strain scrapie model. In addition, we demonstrated for the first time the presence of aggresom...

journal_title：Folia neuropathologica

authors： Sikorska B,Liberski PP,Brown P

更新日期：2007-01-01 00:00:00

abstract：BACKGROUND:The efficacy of tempol and its acyl derivative tempol-C8 as retinoprotective agents was compared in a rat model of NMDA-induced retinal ganglion cell (RGC) damage. MATERIAL AND METHODS:Tempol or tempol-C8 in different doses was administered intraperitoneally to 6 weeks old (pre-adolescent) and 9-10 weeks ol...

journal_title：Folia neuropathologica

authors： Fiedorowicz M,Rejdak R,Schuettauf F,Wozniak M,Grieb P,Thaler S

更新日期：2014-01-01 00:00:00

abstract：:Granular osmiophilic material (GOM) is a pathognomonic feature of CADASIL that may be a consequence of pathological processes triggered by Notch3 mutations. Since knowledge of the effects of CADASIL-associated GOM deposits is important to understand the molecular pathogenesis of this disorder, we performed a thorough ...

journal_title：Folia neuropathologica

authors： Lewandowska E,Dziewulska D,Parys M,Pasennik E

更新日期：2011-01-01 00:00:00

abstract：:This paper presents ultrastructural changes in neuronal and glial cells with special reference to intranuclear inclusion bodies in subacute sclerosing panencephalitis (SSPE) with different duration (from several weeks to seven years). Brain autopsy at ultrastructural level revealed the nucleocapsids of paramyxovirus i...

journal_title：Folia neuropathologica

authors： Lewandowska E,Szpak GM,Lechowicz W,Pasennik E,Sobczyk W

更新日期：2001-01-01 00:00:00

abstract：:Paralytic tremor (pt), a hereditary neurological disorder of rabbits, is a recessive, X-linked point mutation in exon 2 of the plp gene, responsible for substitution of 38 His by Glu in the PLP molecule. Pt genotype is expressed in a range of phenotypes, distinguished by the severity of neurological symptoms. Variable...

journal_title：Folia neuropathologica

authors： Sypecka J,Domańska-Janik K

更新日期：2006-01-01 00:00:00

abstract：:A fetal, cryopreserved ventral mesencephalic rat tissue was transplanted into striatum of healthy adult rats. A stereotactic apparatus was used for transplantation of solid tissue blocks. The survival of transplanted dopaminergic cells in rat striatum was evaluated by means of histological and immunocytochemical metho...

journal_title：Folia neuropathologica

authors： Kosno-Kruszewska E,Wierzba-Bobrowicz T,Ilnicki K,Lechowicz W,Dymecki J

更新日期：1996-01-01 00:00:00

abstract：INTRODUCTION:To investigate the effects of crocin on proliferation and migration of endogenous neural stem cells and the Notch1 signalling pathway in rats after cerebral ischemia reperfusion. MATERIAL AND METHODS:SD rats were randomly divided into the sham operation group, model group and administration group (crocin)...

journal_title：Folia neuropathologica

authors： An B,Ma Y,Xu Y,Liu X,Zhang X,Zhang J,Yang C

更新日期：2020-01-01 00:00:00

abstract：:Chemokines play an important role in pathogenesis of multiple sclerosis (MS), mediating migration of leukocytes into the central nervous system. CCL2 (MCP-1) chemokine is expressed in astrocytes in MS lesions. The aim of the study was to evaluate the effect of a two-year treatment with IFN-beta 1a on serum CCL2 level ...

journal_title：Folia neuropathologica

authors： Szczuciński A,Losy J

更新日期：2004-01-01 00:00:00

abstract：:The investigations were based on 3 cases with Leigh, 5 cases with Krabbe's, 4 cases of Alpers, 2 cases with Sandhoff, 1 case with Alexander's disease and 1 case with metachromatic leukodystrophy. In 1 case included into the study we have diagnosed nonketotic hyperglycinemia II. All the diseases under examination are r...

journal_title：Folia neuropathologica

authors： Kałuza J,Marszał E,Jamroz E,Pietruszewski J

更新日期：1999-01-01 00:00:00

abstract：:Autopsy material of 18 patients, who died between 66-86 years of age and of 4 ones, who died between 20 and 38 years of age was investigated. The white matter of frontal lobe, corpus callosum and cerebellum was studied using histological and biochemical methods. According to the results of neuropathological studies, t...

journal_title：Folia neuropathologica

authors： Wender M,Adamczewska-Goncerzewicz Z,Szczech J

更新日期：1994-01-01 00:00:00

abstract：:Early reviews identified over 20 risk factors associated with Alzheimer's disease (AD) including age, familial inheritance, exposure to aluminium, traumatic brain injury (TBI), and associated co-morbidities such as vascular disease and infection. In the light of recent evidence, this review reconsiders these risk fact...

journal_title：Folia neuropathologica

authors： A Armstrong R

更新日期：2019-01-01 00:00:00

abstract：:Since the earliest descriptions of the disease, senile plaques (SP) and neurofibrillary tangles (NFT) have been regarded as the pathological 'hallmarks' of Alzheimer's disease (AD). Whether or not SP and NFT are sufficient cause to explain the neurodegeneration of AD is controversial. The major molecular constituents ...

journal_title：Folia neuropathologica

authors： Armstrong RA

更新日期：2009-01-01 00:00:00

abstract：:Idiopathic hypertrophic pachymeningitis (IHPM) is a rare pathological state, with still unclear aetiopathogenesis. We present a case of a 63-year-old woman with cranial variety of that disease. The manifestations of the disease included headaches, paresis of VI, IX, X nerves and cerebellar ataxia. The disease was diag...

journal_title：Folia neuropathologica

authors： Rudnik A,Larysz D,Gamrot J,Rudnik A,Skorupa A,Bierzyńska-Macyszyn G,Bazowski P

更新日期：2007-01-01 00:00:00

abstract：:Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) is an autosomal dominant neurodegenerative disorder caused by mutations in the MAPT gene which encodes the microtubule-associated protein tau. This hereditary tauopathy is a rare clinical syndrome, affecting approximately two hundred kindreds a...

journal_title：Folia neuropathologica

authors： Wszołek ZK,Słowiński J,Golan M,Dickson DW

更新日期：2005-01-01 00:00:00

abstract：:Myositis specific autoantibodies (MSA) are the most specific markers of idiopathic inflammatory myopathies (IIM). There is no evidence of presence MSA in patients with other neuromuscular or connective tissue diseases. We compared the frequency of MSA in two groups of IIM patients, one from Poland and one from North A...

journal_title：Folia neuropathologica

authors： Kowalska-Oledzka E,Stern LZ

更新日期：2000-01-01 00:00:00

abstract：:Inherited neurodegenerative disorders are debilitating diseases that occur across different species, such as the domestic dog (Canis lupus familiaris), and many are caused by mutations in the same genes as corresponding human conditions. In the present study, we report an inherited neurodegenerative condition, term...