Search Results - "Dziewulska, Dorota"

Diplomyelia in a patient with a clinical suspicion of autosomal recessive spastic ataxia of Charlevoix-Saguenay type (ARSACS) by Dziewulska, Dorota

“…Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a form of cerebellar ataxia related to mutations in the SACS gene on chromosome 13q12.12…”
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Pericytes as a new target for pathological processes in CADASIL by Dziewulska, Dorota, Lewandowska, Eliza

“…CADASIL is a generalized angiopathy caused by mutations in NOTCH 3 gene leading to degeneration and loss of vascular smooth muscle cells (VSMC) in small…”
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Technical aspects and current clinical applications of the skin and skeletal muscle biopsy in neurological diagnostics: an overview by Dziewulska, Dorota, Kierdaszuk, Biruta, Gogol, Paweł

“…This short overview recalls the basic principles and technical aspects of skin and skeletal muscle biopsies in humans with paying special attention to the…”
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The spectrum of microvascular ultrastructural changes in the subpopulation of patients with migraine and cerebral white matter hyperintensities on MRI by Dziewulska, Dorota, Lewandowska, Eliza, Domitrz, Izabela, Acewicz, Albert

“…Migraine is considered not only as a separate clinical entity but also as a symptom of various brain disorders, including cerebral small vessel diseases. Since…”
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Disturbed integrin expression in the vascular media in CADASIL by Dziewulska, Dorota, Nycz, Ewelina

“…CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy) is an inherited angiopathy characterized by degeneration…”
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Nuclear abnormalities in vascular myocytes in cerebral autosomal‐dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) by Dziewulska, Dorota, Nycz, Ewelina, Rajczewska‐Oleszkiewicz, Cecylia, Bojakowski, Jacek, Sulejczak, Dorota

“…Cerebral autosomal‐dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a stroke and dementia syndrome with degeneration and…”
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What factors determine phenotype of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)? Considerations in the context of a novel pathogenic R110C mutation in the NOTCH3 gene by Dziewulska, Dorota, Sulejczak, Dorota, Wężyk, Michalina

“…We report patients from a Polish family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) who possess a…”
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In memoriam: Professor Janina Rafałowska by Dziewulska, Dorota, Matyja, Ewa, Laure-Kamionowska, Milena

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Clinical presentation of Y189C mutation of the NOTCH3 gene in the Polish family with CADASIL by Dorszewska, Jolanta, Kowalska, Marta, Grzegorski, Tomasz, Dziewulska, Dorota, Karmelita-Katulska, Katarzyna, Barciszewska, Anna-Maria, Prendecki, Michał, Gorczyński, Wojciech, Kozubski, Wojciech

“…Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary, progressive ischemic disease of small…”
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Diverse expression of selected SMN complex proteins in humans with sporadic amyotrophic lateral sclerosis and in a transgenic rat model of familial form of the disease by Rafałowska, Janina, Sulejczak, Dorota, Chrapusta, Stanisław J, Gadamski, Roman, Dziewulska, Dorota

“…There is circumstantial evidence linking sporadic amyotrophic lateral sclerosis (ALS) cases to a malfunction or deficit of a multimeric SMN complex that…”
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Sporadic amyotrophic lateral sclerosis: is SMN-Gemins protein complex of importance for the relative resistance of oculomotor nucleus motoneurons to degeneration? by Sulejczak, Dorota, Chrapusta, Stanisław J., Dziewulska, Dorota, Rafałowska, Janina

“…Lower motoneurons (MNs) show varied vulnerability in amyotrophic lateral sclerosis (ALS): those of non-ocular brainstem nuclei and most of those of the spinal…”
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ELISA reveals a difference in the structure of substantia nigra ferritin in Parkinson's disease and incidental Lewy body compared to control by Koziorowski, Dariusz, Friedman, Andrzej, Arosio, Paolo, Santambrogio, Paolo, Dziewulska, Dorota

“…Abstract Iron released from ferritin may trigger oxidative stress leading to progressive neurodegeneration of substantia nigra resulting in Parkinson's disease…”
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Nanofiber mat spinal cord dressing-released glutamate impairs blood-spinal cord barrier by Sulejczak, Dorota, Taraszewska, Anna, Chrapusta, Stanisław J, Dziewulska, Dorota, Nakielski, Paweł, Rafałowska, Janina

“…An excessive glutamate level can result in excitotoxic damage and death of central nervous system (CNS) cells, and is involved in the pathogenesis of many CNS…”
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CADASIL – obraz kliniczny, diagnostyka i leczenie by Dorota Dziewulska

“…Mózgowa autosomalna dominująca arteriopatia z zawałami podkorowymi i zwyrodnieniem istoty białej (CADASIL) wbrew swojej nazwie jest uogólnioną arteriopatią…”
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CADASIL – obraz zmian morfologicznych i ich patomechanizm by Dorota Dziewulska

“…CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy) jest uogólnioną chorobą naczyń związaną z obecnością…”
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CADASIL – rola systemu sygnałowego Notch 3 w patomechanizmie choroby by Dorota Dziewulska

“…System sygnałowy Notch jest bardzo konserwatywnym systemem komunikacji międzykomórkowej, odgrywającym istotną rolę zarówno w rozwoju naczyń, jak i w…”
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Role of endoglin and transforming growth factor-beta in progressive white matter damage after an ischemic stroke by Dziewulska, Dorota, Rafałowska, Janina

“…We morphologically examined human brains several years after a territorial ischemic stroke to assess the development of progressing white matter damage and its…”
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Intraosseous Lipoma of the Sphenoid : A Case Study by Jamrozik, Zygmunt, Rosiak, Grzegorz, Kierdaszuk, Biruta, Milczarek, Krzysztof, Kamińska, Anna, Dziewulska, Dorota, Krzeski, Antoni

“…Intraosseous lipoma is very rare, usually benign tumor of flat bones. However, the localization in skull bones is described in sporadic cases. The differential…”
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Ultrastructural changes in microvessels in familial hemiplegic migraine with CACNA1A mutation by Dziewulska, Dorota, Kierdaszuk, Biruta

“…Familial hemiplegic migraine type 1 (FHM1) due to mutations in the gene is known as functional vascular disorder with cerebellar atrophy. We describe a case of…”
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CADASIL or CADVaSIL? by Rafalowska, Janina, Fidzianska, Anna, Dziewulska, Dorota, Podlecka, Aleksandra, Szpak, Grazyna Maria, Kwiecinski, Hubert

“…In the present study, morphological examination of patients from two unrelated Polish families with CADASIL was performed. Using light microscopy, there were…”
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