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Wyszukujesz frazę ""Dorobek, Małgorzata"" wg kryterium: Autor


Tytuł :
Analiza heterogenności genetycznej i klinicznej dystrofii typu obręczowo-kończynowegoAnaliza heterogenności genetycznej i klinicznej dystrofii typu obręczowo-kończynowego
Autorzy :
Hausmanowa-Petrusewicz, Irena (1917- ) (Prom.)
Hausmanowa-Petrusewicz, Irena (1917- ) (Prom.)
Dorobek, Małgorzata
Dorobek, Małgorzata
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Dostęp URL :
https://www.europeana.eu/item/0940431/_nnbZXkr?utm_source=api&utm_medium=api&utm_campaign=YuvuWBeCa
Tytuł :
The usefulness of diffusion-weighted/fluid-attenuated inversion recovery imaging in the diagnostics and timing of lacunar and nonlacunar stroke
Autorzy :
Witkowski, Grzegorz
Piliszek, Agnieszka
Sienkiewicz-Jarosz, Halina
Skierczyńska, Agnieszka
Poniatowska, Renata
Dorobek, Małgorzata
Filipek-Gliszczynska, Anna
Ryglewicz, Danuta
Walecki, Jerzy
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Źródło :
Neuroradiology: A Journal Dedicated to Neuroimagingand Interventional Neuroradiology. October 2014 56(10):825-831
Czasopismo naukowe
Tytuł :
MMP-9 and/or TIMP as predictors of ischaemic stroke in patients with symptomatic and asymptomatic atherosclerotic stenosis of carotid artery treated by stenting or endarterectomy – A review
Autorzy :
Zielinska-Turek, Justyna
Dorobek, Małgorzata
Turek, Grzegorz
Barcikowska-Kotowicz, Maria
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Źródło :
Neurologia I Neurochirurgia Polska / Polish Journal of Neurology and Neurosurgery; September-October 2018, Vol. 52 Issue: 5 p555-561, 7p
Periodyk
Tytuł :
Early-Onset Facioscapulohumeral Muscular Dystrophy Type 1 With Some Atypical Features.
Autorzy :
Dorobek, Małgorzata
van der Maarel, Silvère M.
Lemmers, Richard J. L. F.
Ryniewicz, Barbara
Kabzińska, Dagmara
Frants, Rune R.
Gawel, Malgorzata
Walecki, Jerzy
Hausmanowa-Petrusewicz, Irena
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Temat :
MUSCULAR dystrophy
RESPIRATORY insufficiency
CARDIOMYOPATHIES
LUNG diseases
PHENOTYPES
Źródło :
Journal of Child Neurology; Apr2015, Vol. 30 Issue 5, p580-587, 8p
Czasopismo naukowe
Tytuł :
Creutzfeldt-Jakob disease mimicking Lewy body dementia - a case report.
Autorzy :
Nesteruk M; Klinika Neurologii, Centralny Szpital Kliniczny Ministerstwa Spraw Wewnętrznych i Administracji, Warszawa.
Nesteruk T; Zakład Radiologii, Centralny Szpital Kliniczny Ministerstwa Spraw Wewnętrznych i Administracji, Warszawa.
Ułamek-Kozioł M; I Klinika Neurologii, Instytut Psychiatrii i Neurologii, Warszawa.
Holak-Puczyńska A; Zakład Radiologii, Centralny Szpital Kliniczny Ministerstwa Spraw Wewnętrznych i Administracji, Warszawa.
Dorobek M; Klinika Neurologii, Centralny Szpital Kliniczny Ministerstwa Spraw Wewnętrznych i Administracji, Warszawa.
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Transliterated Title :
Choroba Creutzfeldta-Jakoba o początkowym przebiegu naśladującym otępienie z ciałami Lewy’ego – opis przypadku.
Źródło :
Psychiatria polska [Psychiatr Pol] 2021 Jun 30; Vol. 55 (3), pp. 621-627. Date of Electronic Publication: 2021 Jun 30.
Typ publikacji :
Case Reports
Raport
Tytuł :
Real-world effectiveness of fingolimod in Polish group of patients with relapsing-remitting multiple sclerosis.
Autorzy :
Walczak A; Department of Neurology, Medical University of Lodz, Lodz, Poland. Electronic address: .
Kurkowska-Jastrzebska I; 2nd Department of Neurology, Institute of Psychiatry and Neurology in Warsaw, Poland.
Zakrzewska-Pniewska B; Department of Neurology, Medical University of Warsaw, Poland.
Dorobek M; Department of Neurology, Central Clinical Hospital of the Ministry of Interior, Warsaw, Poland.
Brola W; Department of Neurology, Specialist Hospital in Konskie, Poland.
Zajdel R; Chair of Informatics in Business, University of Lodz, Poland.
Bartosik-Psujek H; Department of Neurology, Clinical Regional Hospital No. 2 in Rzeszow, Rzeszow, Poland.
Stasiolek M; Department of Neurology, Medical University of Lodz, Lodz, Poland.
Kulakowska A; Department of Neurology, Medical University of Bialystok, Bialystok, Poland.
Rusek S; Department of Neurology, Specialist Hospital Ludwika Rydygiera in Krakow, Krakow, Poland.
Tutaj A; Department of Neurology, Voivodeship Specialist Hospital in Olsztyn, Olsztyn, Poland.
Glabinski A; Department of Neurology and Stroke, Medical University of Lodz, Lodz, Poland.
Wlodek A; Department of Neurology, Masovian Voivodeship Hospital in Siedlce, Siedlce, Poland.
Kochanowski J; Bielanski Hospital, Warsaw, Poland.
Ciach A; Department of Neurology, Medical University of Lodz, Lodz, Poland.
Siger M; Department of Neurology, Medical University of Lodz, Lodz, Poland.
Kurowska K; 2nd Department of Neurology, Institute of Psychiatry and Neurology in Warsaw, Poland.
Wicha W; 2nd Department of Neurology, Institute of Psychiatry and Neurology in Warsaw, Poland.
Nojszewska M; Department of Neurology, Medical University of Warsaw, Poland.
Podlecka-Pietowska A; Department of Neurology, Medical University of Warsaw, Poland.
Czajka A; Department of Neurology, Central Clinical Hospital of the Ministry of Interior, Warsaw, Poland.
Kapica-Topczewska K; Department of Neurology, Medical University of Bialystok, Bialystok, Poland.
Bielecki B; Department of Neurology and Stroke, Medical University of Lodz, Lodz, Poland.
Maciagowska-Terela M; Department of Neurology, Military Institute of Medicine in Warsaw, Poland.
Stepien A; Department of Neurology, Military Institute of Medicine in Warsaw, Poland.
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Źródło :
Clinical neurology and neurosurgery [Clin Neurol Neurosurg] 2019 Sep; Vol. 184, pp. 105453. Date of Electronic Publication: 2019 Jul 23.
Typ publikacji :
Journal Article
MeSH Terms :
Fingolimod Hydrochloride/*therapeutic use
Immunosuppressive Agents/*therapeutic use
Multiple Sclerosis, Relapsing-Remitting/*drug therapy
Adult ; Disabled Persons/rehabilitation ; Disease Progression ; Female ; Humans ; Male ; Middle Aged ; Poland ; Recurrence
Czasopismo naukowe
Tytuł :
The frequency of mitochondrial polymerase gamma related disorders in a large Polish population cohort.
Autorzy :
Piekutowska-Abramczuk D; Department of Medical Genetics, The Children's Memorial Health Institute, Al. Dzieci Polskich 20, 04-730 Warsaw, Poland. Electronic address: .
Kaliszewska M; Institute of Genetics and Biotechnology, Faculty of Biology, University of Warsaw, Pawinskiego 5a, 02-106 Warsaw, Poland.
Sułek A; Department of Genetics, Institute of Psychiatry and Neurology, Sobieskiego 9, 02-957 Warsaw, Poland.
Jurkowska N; Department of Medical Genetics, The Children's Memorial Health Institute, Al. Dzieci Polskich 20, 04-730 Warsaw, Poland.
Ołtarzewski M; Screening Tests Department, Institute of Mother and Child, Kasprzaka 17a, 01-211 Warsaw, Poland.
Jabłońska E; Screening Tests Department, Institute of Mother and Child, Kasprzaka 17a, 01-211 Warsaw, Poland.
Trubicka J; Department of Medical Genetics, The Children's Memorial Health Institute, Al. Dzieci Polskich 20, 04-730 Warsaw, Poland.
Głowacka A; Department of Medical Genetics, The Children's Memorial Health Institute, Al. Dzieci Polskich 20, 04-730 Warsaw, Poland.
Ciara E; Department of Medical Genetics, The Children's Memorial Health Institute, Al. Dzieci Polskich 20, 04-730 Warsaw, Poland.
Kowalski P; Department of Medical Genetics, The Children's Memorial Health Institute, Al. Dzieci Polskich 20, 04-730 Warsaw, Poland.
Langiewicz-Wojciechowska K; Institute of Genetics and Biotechnology, Faculty of Biology, University of Warsaw, Pawinskiego 5a, 02-106 Warsaw, Poland.
Tesarova M; Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University and General University Hospital in Prague, Ke Karlovu 455/2, 128 08 Prague 2, Czech Republic.
Zeman J; Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University and General University Hospital in Prague, Ke Karlovu 455/2, 128 08 Prague 2, Czech Republic.
Kierdaszuk B; Department of Neurology, Medical University of Warsaw, Banacha 1a, 02-097 Warsaw, Poland.
Kuczyński D; Department of Neurology and Epileptology, The Children's Memorial Health Institute, Al. Dzieci Polskich 20, 04-730 Warsaw, Poland.
Chmielewski D; Department of Neurology and Epileptology, The Children's Memorial Health Institute, Al. Dzieci Polskich 20, 04-730 Warsaw, Poland.
Szymańska E; Department of Pediatrics, Nutrition and Metabolic Disorders, The Children's Memorial Health Institute, Al. Dzieci Polskich 20, 04-730 Warsaw, Poland.
Bakuła A; Department of Gastroenterology, Hepatology, Feeding Disorders and Pediatrics, The Children's Memorial Health Institute, Al. Dzieci Polskich 20, 04-730 Warsaw, Poland.
Łusakowska A; Department of Neurology, Medical University of Warsaw, Banacha 1a, 02-097 Warsaw, Poland.
Lipowska M; Department of Neurology, Medical University of Warsaw, Banacha 1a, 02-097 Warsaw, Poland.
Brodacki B; Clinic of Neurology, Military Institute of Medicine, Szaserow 128, 04-349 Warsaw, Poland.
Pera J; Department of Neurology, Jagiellonian University Medical College, Botaniczna 3, 31-503 Krakow, Poland.
Dorobek M; Department of Neurology, Central Clinical Hospital of the Ministry of Interior in Warsaw, Woloska 137, 02-507 Warsaw, Poland.
Rydzanicz M; Department of Medical Genetics, Warsaw Medical University, Pawinskiego 3c, 02-106 Warsaw, Poland.
Płoski R; Department of Medical Genetics, Warsaw Medical University, Pawinskiego 3c, 02-106 Warsaw, Poland.
Chrzanowska KH; Department of Medical Genetics, The Children's Memorial Health Institute, Al. Dzieci Polskich 20, 04-730 Warsaw, Poland.
Bartnik E; Institute of Genetics and Biotechnology, Faculty of Biology, University of Warsaw, Pawinskiego 5a, 02-106 Warsaw, Poland; Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Pawinskiego 5a, 02-106 Warsaw, Poland.
Placha G; Department of Internal Medicine, Hypertension, and Vascular Diseases, Medical University of Warsaw, Banacha 1a, 02-097 Warsaw, Poland.
Kamińska A; Department of Neurology, Medical University of Warsaw, Banacha 1a, 02-097 Warsaw, Poland.
Kostera-Pruszczyk A; Department of Neurology, Medical University of Warsaw, Banacha 1a, 02-097 Warsaw, Poland.
Krajewska-Walasek M; Department of Medical Genetics, The Children's Memorial Health Institute, Al. Dzieci Polskich 20, 04-730 Warsaw, Poland.
Tońska K; Institute of Genetics and Biotechnology, Faculty of Biology, University of Warsaw, Pawinskiego 5a, 02-106 Warsaw, Poland.
Pronicka E; Department of Medical Genetics, The Children's Memorial Health Institute, Al. Dzieci Polskich 20, 04-730 Warsaw, Poland; Department of Pediatrics, Nutrition and Metabolic Disorders, The Children's Memorial Health Institute, Al. Dzieci Polskich 20, 04-730 Warsaw, Poland.
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Źródło :
Mitochondrion [Mitochondrion] 2019 Jul; Vol. 47, pp. 179-187. Date of Electronic Publication: 2018 Nov 10.
Typ publikacji :
Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Genes, Recessive*
Mutation, Missense*
Ataxia/*genetics
DNA Polymerase gamma/*genetics
Diffuse Cerebral Sclerosis of Schilder/*genetics
Mitochondrial Diseases/*genetics
Adolescent ; Adult ; Amino Acid Substitution ; Ataxia/enzymology ; Child ; Child, Preschool ; Diffuse Cerebral Sclerosis of Schilder/enzymology ; Female ; Humans ; Infant ; Infant, Newborn ; Male ; Middle Aged ; Mitochondrial Diseases/enzymology ; Poland
Czasopismo naukowe
Tytuł :
Early onset facioscapulohumeral dystrophy - a systematic review using individual patient data.
Autorzy :
Goselink RJM; Department of Neurology, Donders Centre for Medical Neuroscience, Radboud University Medical Centre, Nijmegen, The Netherlands. Electronic address: .
Voermans NC; Department of Neurology, Donders Centre for Medical Neuroscience, Radboud University Medical Centre, Nijmegen, The Netherlands.
Okkersen K; Department of Neurology, Donders Centre for Medical Neuroscience, Radboud University Medical Centre, Nijmegen, The Netherlands.
Brouwer OF; Department of Neurology, University Medical Centre Groningen, University of Groningen, Groningen, The Netherlands.
Padberg GW; Department of Neurology, Donders Centre for Medical Neuroscience, Radboud University Medical Centre, Nijmegen, The Netherlands.
Nikolic A; Department of Life Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Tupler R; Department of Life Sciences, University of Modena and Reggio Emilia, Modena, Italy; Department of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, USA.
Dorobek M; Department of Neurology, Central Clinical Hospital of the Ministry of Interior in Warsaw, Warsaw, Poland.
Mah JK; Department of Paediatrics, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
van Engelen BGM; Department of Neurology, Donders Centre for Medical Neuroscience, Radboud University Medical Centre, Nijmegen, The Netherlands.
Schreuder THA; Department of Neurology, Donders Centre for Medical Neuroscience, Radboud University Medical Centre, Nijmegen, The Netherlands.
Erasmus CE; Department of Neurology, Donders Centre for Medical Neuroscience, Radboud University Medical Centre, Nijmegen, The Netherlands.
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Źródło :
Neuromuscular disorders : NMD [Neuromuscul Disord] 2017 Dec; Vol. 27 (12), pp. 1077-1083. Date of Electronic Publication: 2017 Sep 21.
Typ publikacji :
Journal Article; Review; Systematic Review
MeSH Terms :
Age of Onset*
Muscular Dystrophy, Facioscapulohumeral/*physiopathology
Adult ; Child ; Humans ; Infant ; Muscular Dystrophy, Facioscapulohumeral/genetics ; Muscular Dystrophy, Facioscapulohumeral/therapy
SCR Disease Name :
Facioscapulohumeral muscular dystrophy 1a
Czasopismo naukowe
Tytuł :
Posterior reversible encephalopathy syndrome with neurological sequelae - a case report.
Autorzy :
Nesteruk M; Central Clinical Hospital of the Ministry of Interior, Warsaw, Poland: Department of Neurology.
Kurdyła A; Central Clinical Hospital of the Ministry of Interior, Warsaw, Poland: Department of Neurology.
Nesteruk T; Central Clinical Hospital of the Ministry of Interior, Warsaw, Poland: Department of Radiology.
Dorobek M; Central Clinical Hospital of the Ministry of Interior, Warsaw, Poland: Department of Neurology.
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Źródło :
Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego [Pol Merkur Lekarski] 2016 Apr; Vol. 40 (238), pp. 252-4.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Brain/*pathology
Posterior Leukoencephalopathy Syndrome/*diagnosis
Cognition Disorders/etiology ; Diagnosis, Differential ; Female ; Humans ; Magnetic Resonance Imaging ; Middle Aged ; Posterior Leukoencephalopathy Syndrome/complications ; Posterior Leukoencephalopathy Syndrome/pathology
Czasopismo naukowe
Tytuł :
The Frequency of c.550delA Mutation of the CANP3 Gene in the Polish LGMD2A Population.
Autorzy :
Dorobek M; 1 Department of Neurology, Central Clinical Hospital of the Ministry of Interior in Warsaw , Warsaw, Poland .
Ryniewicz B; 2 Department of Neurology, Warsaw Medical University , Poland .
Kabzińska D; 3 Neuromuscular Unit, Mossakowski Medical Research Centre, Polish Academy of Sciences , Warsaw, Poland .
Fidziańska A; 3 Neuromuscular Unit, Mossakowski Medical Research Centre, Polish Academy of Sciences , Warsaw, Poland .
Styczyńska M; 1 Department of Neurology, Central Clinical Hospital of the Ministry of Interior in Warsaw , Warsaw, Poland .; 4 Department of Neurodegenerative Disorders, Mossakowski Medical Research Centre, Polish Academy of Sciences , Warsaw, Poland .
Hausmanowa-Petrusewicz I; 3 Neuromuscular Unit, Mossakowski Medical Research Centre, Polish Academy of Sciences , Warsaw, Poland .
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Źródło :
Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2015 Nov; Vol. 19 (11), pp. 637-40. Date of Electronic Publication: 2015 Oct 20.
Typ publikacji :
Journal Article
MeSH Terms :
Mutation*
Calpain/*genetics
Muscle Proteins/*genetics
Muscular Dystrophies, Limb-Girdle/*genetics
Dysferlin ; Female ; Genetic Association Studies ; Heterozygote ; Humans ; Male ; Membrane Proteins/genetics ; Muscular Dystrophies, Limb-Girdle/epidemiology ; Muscular Dystrophies, Limb-Girdle/metabolism ; Poland/epidemiology ; Polymerase Chain Reaction ; Prevalence ; Sarcoglycans/metabolism
SCR Disease Name :
Limb-girdle muscular dystrophy type 2A
Czasopismo naukowe

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