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Items: 1 to 50 of 127

1.

WITHDRAWN: Evidence for a relatively high proportion of DM2 mutations in a large group of Polish patients.

Sulek A, Lusakowska A, Krysa W, Rajkiewicz M, Kaminska A, Nojszewska M, Kostera-Pruszczyk A, Zdzienicka E, Kubalska J, Rakowicz M, Szirkowiec W, Kwiecinski H, Zaremba J.

Neurol Neurochir Pol. 2018 May 17. pii: S0028-3843(18)30152-X. doi: 10.1016/j.pjnns.2018.04.004. [Epub ahead of print]

2.

Evidence for a relatively high proportion of DM2 mutations in a large group of Polish patients.

Sulek A, Lusakowska A, Krysa W, Rajkiewicz M, Kaminska A, Nojszewska M, Kostera-Pruszczyk A, Zdzienicka E, Kubalska J, Rakowicz M, Szirkowiec W, Kwiecinski H, Zaremba J.

Neurol Neurochir Pol. 2018 Nov - Dec;52(6):736-742. doi: 10.1016/j.pjnns.2018.02.008. Epub 2018 Mar 7.

PMID:
29588063
3.

Changing phenotypic expression in a patient with a mitochondrial encephalopathy due to 13042G>A de novo mutation--a 5 year follow up.

Schinwelski M, Kierdaszuk B, Dulski J, Tońska K, Kodroń A, Sitek EJ, Bartnik E, Kamińska A, Kwieciński H, Sławek J.

Metab Brain Dis. 2015 Aug;30(4):1083-5. doi: 10.1007/s11011-014-9645-x. Epub 2014 Dec 31.

4.

The N-terminal pro-brain natriuretic peptide as a marker of mitoxantrone-induced cardiotoxicity in multiple sclerosis patients.

Podlecka-Piętowska A, Kochanowski J, Zakrzewska-Pniewska B, Opolski G, Kwieciński H, Kamińska AM.

Neurol Neurochir Pol. 2014;48(2):111-5. doi: 10.1016/j.pjnns.2013.12.005. Epub 2014 Jan 23.

PMID:
24821636
5.

Mitochondrial encephalomyopathy: towards diagnosis. A case report.

Gaweł M, Kierdaszuk B, Tońska K, Kaliszewska M, Kubiszewska J, Jamrozik Z, Bartnik E, Kwieciński H, Kamińska AM.

Neurol Neurochir Pol. 2014 Jan-Feb;48(1):76-80. doi: 10.1016/j.pjnns.2013.09.003. Epub 2014 Jan 23.

PMID:
24636775
6.

Recurrent K3E mutation in Cu/Zn superoxide dismutase gene associated with amyotrophic lateral sclerosis.

Kuźma-Kozakiewicz M, Berdyński M, Morita M, Takahashi Y, Kawata A, Kaida K, Kaźmierczak B, Lusakowska A, Goto J, Tsuji S, Zekanowski C, Kwieciński H.

Amyotroph Lateral Scler Frontotemporal Degener. 2013 Dec;14(7-8):608-14. doi: 10.3109/21678421.2013.812119. Epub 2013 Jul 30.

PMID:
23898858
7.

Analysis of PITX3 gene in patients with multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration.

Jamrozik Z, Berdynski M, Zekanowski C, Baranczyk-Kuzma A, Sławek J, Kuzma-Kozakiewicz M, Maruszak A, Kwiecinski H.

Ann Clin Lab Sci. 2013 Spring;43(2):151-3. Erratum in: Ann Clin Lab Sci. 2014 Winter;44(1):110.

PMID:
23694789
8.

ALS Untangled No. 20: the Deanna protocol.

ALSUntangled Group, Fournier C, Bedlack B, Hardiman O, Heiman-Patterson T, Gutmann L, Bromberg M, Ostrow L, Carter G, Kabashi E, Bertorini T, Mozaffar T, Andersen P, Dietz J, Gamez J, Dimachkie M, Wang Y, Wicks P, Heywood J, Novella S, Rowland LP, Pioro E, Kinsley L, Mitchell K, Glass J, Sathornsumetee S, Kwiecinski H, Baker J, Atassi N, Forshew D, Ravits J, Conwit R, Jackson C, Sherman A, Dalton K, Tindall K, Gonzalez G, Robertson J, Phillips L, Benatar M, Sorenson E, Shoesmith C, Nash S, Maragakis N, Moore D, Caress J, Boylan K, Armon C, Grosso M, Gerecke B, Wymer J, Oskarsson B, Bowser R, Drory V, Shefner J, Lechtzin N, Leitner M, Miller R, Mitsumoto H, Levine T, Russell J, Sharma K, Saperstein D, McClusky L, MacGowan D, Licht J, Verma A, Strong M, Lomen-Hoerth C, Tandan R, Rivner M, Kolb S, Polak M, Rudnicki S, Kittrell P, Quereshi M, Sachs G, Pattee G, Weiss M, Kissel J, Goldstein J, Rothstein J, Pastula D, Gleb L, Ogino M, Rosenfeld J, Carmi E, Oster C, Barkhaus P, Valor E.

Amyotroph Lateral Scler Frontotemporal Degener. 2013 May;14(4):319-23. doi: 10.3109/21678421.2013.788405. Epub 2013 May 2. Review. No abstract available.

PMID:
23638638
9.

A case report of 'variant' biochemical phenotype of Niemann-Pick C disease and a discussion of therapeutic options.

Jamrozik Z, Szczudlik P, Lugowska A, Weiß S, Rolfs A, Czartoryska B, Kwieciński H.

Neurol Neurochir Pol. 2013 Jan-Feb;47(1):86-9.

PMID:
23487299
10.

[Psychotic symptoms and cognitive impairment in neurosarcoidosis. Case report and review of literature].

Gaweł M, Domitrz I, Dziewulska D, Dabrowski A, Przyjałkowski W, Gołebiowski M, Kwieciński H.

Psychiatr Pol. 2012 Nov-Dec;46(6):1099-108. Review. Polish.

PMID:
23479950
11.

Mitochondrial encephalopathy in a patient with a 13042G>A de novo mutation.

Slawek J, Kierdaszuk B, Tonska K, Kodron A, Schinwelski M, Sitek EJ, Bartnik E, Kaminska A, Kwiecinski H.

J Clin Pathol. 2012 Dec;65(12):1147-9. doi: 10.1136/jclinpath-2012-200778. Epub 2012 Aug 10. No abstract available.

PMID:
22888120
12.

A single-fibre electromyography study of neuromuscular transmission in patients with cluster headache.

Domitrz I, Gaweł M, Domitrz W, Kostera-Pruszczyk A, Kwieciński H.

Neurol Neurochir Pol. 2012 Mar-Apr;46(2):140-4.

PMID:
22581595
13.

[Expert opinion on use of intravenous immunoglobulins in the management of neurological disorders].

Stępień A, Korsak J, Kozubski W, Ryglewicz D, Losy J, Drozdowski W, Kotowicz J, Nyka W, Kwieciński H.

Neurol Neurochir Pol. 2011 Nov-Dec;45(6):525-35. Polish. No abstract available.

PMID:
22212982
14.

Recurrent G41S mutation in Cu/Zn superoxide dismutase gene (SOD1) causing familial amyotrophic lateral sclerosis in a large Polish family.

Berdyński M, Kuźma-Kozakiewicz M, Ricci C, Kubiszewska J, Millecamps S, Salachas F, Łusakowska A, Carrera P, Meininger V, Battistini S, Kwieciński H, Zekanowski C.

Amyotroph Lateral Scler. 2012 Jan;13(1):132-6. doi: 10.3109/17482968.2011.600316. Epub 2011 Aug 30. Erratum in: Amyotroph Lateral Scler. 2012 Jun;13(4):405.

PMID:
21877919
15.

Muscle pathology in myotonic dystrophy: light and electron microscopic investigation in eighteen patients.

Nadaj-Pakleza A, Lusakowska A, Sułek-Piątkowska A, Krysa W, Rajkiewicz M, Kwieciński H, Kamińska A.

Folia Morphol (Warsz). 2011 May;70(2):121-9.

PMID:
21630234
16.

Professor Kazimierz Orzechowski - initiator of the first university department of neurology in Warsaw.

Emeryk-Szajewska B, Kwieciński H.

Neurol Neurochir Pol. 2011 Mar-Apr;45(2):188-94. English, Polish. No abstract available.

PMID:
21574125
17.

New therapeutic targets for amyotrophic lateral sclerosis.

Kuzma-Kozakiewicz M, Kwiecinski H.

Expert Opin Ther Targets. 2011 Feb;15(2):127-43. doi: 10.1517/14728222.2011.542152. Epub 2010 Dec 7. Review.

PMID:
21133819
18.

Familial partial lipodystrophy associated with the heterozygous LMNA mutation 1445G>A (Arg482Gln) in a Polish family.

Drac H, Madej-Pilarczyk A, Gospodarczyk-Szot K, Gaweł M, Kwieciński H, Hausmanowa-Petrusewicz I.

Neurol Neurochir Pol. 2010 May-Jun;44(3):291-6.

PMID:
20625965
19.

The analysis of selected neurotransmitter concentrations in serum of patients with Tourette syndrome.

Janik P, Kalbarczyk A, Gutowicz M, Barańczyk-Kuźma A, Kwieciński H.

Neurol Neurochir Pol. 2010 May-Jun;44(3):251-9.

PMID:
20625961
20.

[Ischaemic stroke in people with migraine: is everything clear?].

Domitrz I, Kwieciński H.

Neurol Neurochir Pol. 2010 Mar-Apr;44(2):115-7. Polish. No abstract available.

PMID:
20496280
21.

Polymorphisms in the factor VII gene and ischemic stroke in young adults.

Lopaciuk S, Windyga J, Watala CW, Bykowska K, Pietrucha T, Kwiecinski H, Czlonkowska A, Kuczynska-Zardzewialy A, Jackson AA, Carew JA, Bauer KA.

Blood Coagul Fibrinolysis. 2010 Jul;21(5):442-7. doi: 10.1097/MBC.0b013e3283389513.

PMID:
20453637
22.

Evaluation of matrix metalloproteinases in serum of patients with amyotrophic lateral sclerosis with pattern recognition methods.

Sokolowska B, Jozwik A, Niebroj-Dobosz I, Janik P, Kwiecinski H.

J Physiol Pharmacol. 2009 Nov;60 Suppl 5:117-20.

PMID:
20134051
23.

Neurology training around the world: asking the trainees.

Rejdak K, Petzold A, Ng K, Afra J, Dujmovic I, Stelmasiak Z, Ryglewicz D, Kwiecinski H, Grisold W, Vecsei L.

Lancet Neurol. 2010 Jan;9(1):32-3. doi: 10.1016/S1474-4422(09)70352-7. No abstract available.

PMID:
20083035
24.

The genetics of amyotrophic lateral sclerosis.

Kuźma-Kozakiewicz M, Kwieciński H.

Neurol Neurochir Pol. 2009 Nov-Dec;43(6):538-49. Review.

PMID:
20054757
25.

Erythropoietin concentration in serum and cerebrospinal fluid of patients with amyotrophic lateral sclerosis.

Janik P, Kwiecinski H, Sokolowska B, Niebroj-Dobosz I.

J Neural Transm (Vienna). 2010 Mar;117(3):343-7. doi: 10.1007/s00702-009-0354-2. Epub 2009 Dec 12.

PMID:
20012656
26.

Glucocerebrosidase mutations p.L444P and p.N370S are not associated with multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration in Polish patients.

Jamrozik Z, Lugowska A, Slawek J, Kwiecinski H.

J Neurol. 2010 Mar;257(3):459-60. doi: 10.1007/s00415-009-5363-4. Epub 2009 Nov 1. No abstract available.

PMID:
19882201
27.

Matrix metalloproteinases and their tissue inhibitors in serum and cerebrospinal fluid of patients with amyotrophic lateral sclerosis.

Niebroj-Dobosz I, Janik P, Sokołowska B, Kwiecinski H.

Eur J Neurol. 2010 Feb;17(2):226-31. doi: 10.1111/j.1468-1331.2009.02775.x. Epub 2009 Oct 1.

PMID:
19796283
28.

Mitochondrial cytopathies: clinical, morphological and genetic characteristics.

Kierdaszuk B, Jamrozik Z, Tońska K, Bartnik E, Kaliszewska M, Kamińska A, Kwieciński H.

Neurol Neurochir Pol. 2009 May-Jun;43(3):216-27.

PMID:
19618304
29.

[Intravenous thrombolysis in the treatment of acute ischaemic stroke: 3, 4.5, or 6 hours?].

Kwieciński H.

Neurol Neurochir Pol. 2009 May-Jun;43(3):213-5. Polish. No abstract available.

PMID:
19618303
30.

Juvenile seropositive myasthenia gravis with anti-MuSK antibody after thymectomy.

Kostera-Pruszczyk A, Kwiecinski H.

J Neurol. 2009 Oct;256(10):1780-1. doi: 10.1007/s00415-009-5215-2. Epub 2009 Jun 23.

PMID:
19548060
31.

Oculopharyngeal muscular dystrophy: phenotypic and genotypic characteristics of 9 Polish patients.

Nadaj-Pakleza A, Richard P, Lusakowska A, Gajewska J, Jamrozik Z, Kostera-Pruszczyk A, Kwieciński H, Kamińska A.

Neurol Neurochir Pol. 2009 Mar-Apr;43(2):113-20.

PMID:
19484687
32.

Paroxysmal non-kinesigenic dyskinesia caused by the mutation of MR-1 in a large Polish kindred.

Friedman A, Zakrzewska-Pniewska B, Domitrz I, Lee HY, Ptacek L, Kwiecinski H.

Eur Neurol. 2009;61(1):39-41. doi: 10.1159/000165348. Epub 2008 Oct 24.

PMID:
18948699
33.

[CADASIL syndrome - cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy].

Dziewulska D, Kwieciński H.

Neurol Neurochir Pol. 2008 Mar-Apr;42(2):123-30. Review. Polish.

PMID:
18512169
34.

MuSK-positive myasthenia gravis is rare in the Polish population.

Kostera-Pruszczyk A, Kamińska A, Dutkiewicz M, Emeryk-Szajewska B, Strugalska-Cynowska MH, Vincent A, Kwieciński H.

Eur J Neurol. 2008 Jul;15(7):720-4. doi: 10.1111/j.1468-1331.2008.02176.x. Epub 2008 May 20.

PMID:
18494794
35.

Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia.

Watts GD, Thomasova D, Ramdeen SK, Fulchiero EC, Mehta SG, Drachman DA, Weihl CC, Jamrozik Z, Kwiecinski H, Kaminska A, Kimonis VE.

Clin Genet. 2007 Nov;72(5):420-6.

PMID:
17935506
36.

Elevated levels of anti-Chlamydia pneumoniae IgA and IgG antibodies in young adults with ischemic stroke.

Piechowski-Jóźwiak B, Mickielewicz A, Gaciong Z, Berent H, Kwieciński H.

Acta Neurol Scand. 2007 Sep;116(3):144-9.

PMID:
17714326
37.

Multi-minicore myopathy: a clinical and histopathological study of 17 cases.

Nadaj-Pakleza A, Fidziańska A, Ryniewicz B, Kostera-Pruszczyk A, Ferreiro A, Kwieciński H, Kamińska A.

Folia Neuropathol. 2007;45(2):56-65.

38.

Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesia.

Bruno MK, Lee HY, Auburger GW, Friedman A, Nielsen JE, Lang AE, Bertini E, Van Bogaert P, Averyanov Y, Hallett M, Gwinn-Hardy K, Sorenson B, Pandolfo M, Kwiecinski H, Servidei S, Fu YH, Ptácek L.

Neurology. 2007 May 22;68(21):1782-9.

PMID:
17515540
39.

[Neurological disorders in patients with obstructive sleep apnea (OSA)].

Zakrzewska-Pniewska B, Kwieciński H.

Pneumonol Alergol Pol. 2007;75 Suppl 1:62-4. Polish. No abstract available.

PMID:
17440895
40.

Ischaemic stroke in patients with patent foramen ovale.

Piechowski-Jóźwiak B, Kwieciński H.

Neurol Neurochir Pol. 2007 Jan-Feb;41(1):55-63. Review.

PMID:
17330181
41.

Recommendations for the management of intracranial haemorrhage - part I: spontaneous intracerebral haemorrhage. The European Stroke Initiative Writing Committee and the Writing Committee for the EUSI Executive Committee.

Steiner T, Kaste M, Forsting M, Mendelow D, Kwiecinski H, Szikora I, Juvela S, Marchel A, Chapot R, Cognard C, Unterberg A, Hacke W.

Cerebrovasc Dis. 2006;22(4):294-316. Epub 2006 Jul 28. Erratum in: Cerebrovasc Dis. 2006;22(5-6):461. Katse, Markku [corrected to Kaste, Markku].

PMID:
16926557
42.

APOE epsilon variation in multiple sclerosis susceptibility and disease severity: some answers.

Burwick RM, Ramsay PP, Haines JL, Hauser SL, Oksenberg JR, Pericak-Vance MA, Schmidt S, Compston A, Sawcer S, Cittadella R, Savettieri G, Quattrone A, Polman CH, Uitdehaag BM, Zwemmer JN, Hawkins CP, Ollier WE, Weatherby S, Enzinger C, Fazekas F, Schmidt H, Schmidt R, Hillert J, Masterman T, Hogh P, Niino M, Kikuchi S, Maciel P, Santos M, Rio ME, Kwiecinski H, Zakrzewska-Pniewska B, Evangelou N, Palace J, Barcellos LF.

Neurology. 2006 May 9;66(9):1373-83.

PMID:
16682670
43.

[Is migraine a neuronal channelopothy?].

Kwieciński H.

Neurol Neurochir Pol. 2005;39(4 Suppl 1):S61-4. Review. Polish.

PMID:
16419572
44.

A single-fibre EMG study of neuromuscular transmission in migraine patients.

Domitrz I, Kostera-Pruszczyk A, Kwieciñski H.

Cephalalgia. 2005 Oct;25(10):817-21.

PMID:
16162259
45.

Frequency of a tau genotype in amyotrophic lateral sclerosis.

Münch C, Prechter F, Xu R, Linke P, Prudlo J, Kuzma M, Kwiecinski H, Ludolph AC, Meyer T.

J Neurol Sci. 2005 Sep 15;236(1-2):13-6.

PMID:
16005901
46.

Oxidative damage to proteins in the spinal cord in amyotrophic lateral sclerosis (ALS).

Niebrój-Dobosz I, Dziewulska D, Kwieciński H.

Folia Neuropathol. 2004;42(3):151-6.

PMID:
15535033
47.

Correlating phenotype and genotype in the periodic paralyses.

Miller TM, Dias da Silva MR, Miller HA, Kwiecinski H, Mendell JR, Tawil R, McManis P, Griggs RC, Angelini C, Servidei S, Petajan J, Dalakas MC, Ranum LP, Fu YH, Ptácek LJ.

Neurology. 2004 Nov 9;63(9):1647-55.

PMID:
15534250
48.

Mutations and polymorphisms of the CLCN2 gene in idiopathic epilepsy.

D'Agostino D, Bertelli M, Gallo S, Cecchin S, Albiero E, Garofalo PG, Gambardella A, St Hilaire JM, Kwiecinski H, Andermann E, Pandolfo M.

Neurology. 2004 Oct 26;63(8):1500-2.

PMID:
15505175
49.

The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathway.

Lee HY, Xu Y, Huang Y, Ahn AH, Auburger GW, Pandolfo M, Kwiecinski H, Grimes DA, Lang AE, Nielsen JE, Averyanov Y, Servidei S, Friedman A, Van Bogaert P, Abramowicz MJ, Bruno MK, Sorensen BF, Tang L, Fu YH, Ptácek LJ.

Hum Mol Genet. 2004 Dec 15;13(24):3161-70. Epub 2004 Oct 20.

PMID:
15496428
50.

Transcatheter closure of patent foramen ovale in patients with cryptogenic stroke.

Demkow M, Ruzyłło W, Kepka C, Pruszczyk P, Opuchlik A, Szyluk B, Konka M, Wilczyński J, Szulc M, Kwieciński H.

Kardiol Pol. 2004 Aug;61(8):101-9; discussion 109.

PMID:
15457276

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