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Journal articles on the topic 'Nemoc'

Author: Grafiati

Published: 4 June 2021

Last updated: 18 February 2022

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1

Rusina, Robert, and Eva Bolceková. "Wilsonova nemoc." Neurologie pro praxi 17, no. 3 (2016): 79–86. http://dx.doi.org/10.36290/neu.2016.030.

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2

Magner, Martin, and Jitka Jirečková. "Pompe disease." Neurologie pro praxi 19, no. 3 (2018): 200–204. http://dx.doi.org/10.36290/neu.2018.037.

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3

Bártlová, Sylva. "Disease as a stigma." Kontakt 8, no. 2 (2006): 265–71. http://dx.doi.org/10.32725/kont.2006.044.

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4

Mildnerová, Kateřina. "Local Conceptualisation of Health, Illness and Body in Lusaka, Zambia." Anthropologia integra 1, no. 1 (2010): 13–23. http://dx.doi.org/10.5817/ai2010-1-13.

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Zdraví/nemoc je sociálně a kulturně konstruovaná kategorie. V Zambii je nemoc chápána komplexně, v jejím kosmologickém a sociálním rozměru. Nemoc není konceptualizována pouze jako narušení fyzické a psychické integrity člověka, ale představuje v nejširším slova smyslu neštěstí nebo smůlu, jehož příčina má externí povahu a je spojována s konkrétní agresí a záměrem démonů, mstivých duchů nebo zlých čarodějů/nic. Místní věří, že tyto neviditelné síly prostupují celým jejich životem a významně ovlivňují zdraví, plodnost, bohatství a mezilidské vztahy. Na rozdíl od biomedicíny založené na kartezián

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5

Kotolová, Hana, and Tomáš Hammer. "Chronic obstructive pulmonary disease." Praktické lékárenství 14, no. 4 (2018): 156–60. http://dx.doi.org/10.36290/lek.2018.030.

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6

Janoušek, Hynek. "Nemoc mladého Huma a filosofická krize." REFLEXE 2020, no. 59 (2021): 81–104. http://dx.doi.org/10.14712/25337637.2021.3.

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7

Ridzoň, Petr. "Kennedy's disease (bulbar and spinal muscular atrophy)." Neurologie pro praxi 17, no. 6 (2016): 359–61. http://dx.doi.org/10.36290/neu.2016.075.

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8

Nytrová, Petra, Jana Kopecká, and Dana Horáková. "Neuromyelitis optica (Devic's disease) - a rare demyelinating disease." Medicína pro praxi 13, no. 1 (2016): 43–46. http://dx.doi.org/10.36290/med.2016.009.

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9

Eckhardt, Tomáš, and Michal Pazderník. "(Cardiac allograft vasculopathy nowadays)." Cor et Vasa 63, no. 1 (2021): 73–78. http://dx.doi.org/10.33678/cor.2020.105.

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10

Sova, Milan. "Chronic pulmonary disease and metabolic syndrome." Interní medicína pro praxi 20, no. 3 (2018): 118–20. http://dx.doi.org/10.36290/int.2018.022.

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11

Chrudimský, Leoš. "Whipple disease - systemic disease with gastrointestinal manifestations." Vnitřní lékařství 67, no. 5 (2021): e03-e08. http://dx.doi.org/10.36290/vnl.2021.080.

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12

Kubánek, Miloš, Milan Elleder, Jakub Sikora, et al. "Danon disease - a disorder of autophagy as a cause of hypertrophic cardiomyopathy." Cor et Vasa 52, no. 11-12 (2010): 706–12. http://dx.doi.org/10.33678/cor.2010.176.

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13

Bártů, Václava. "Chronic obstructive pulmonary disease - benefit of dual bronchodilator therapy." Interní medicína pro praxi 18, no. 4 (2016): 198–202. http://dx.doi.org/10.36290/int.2016.045.

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14

Urbánek, Robin, Lukáš Tichý, and Tomáš Freiberger. "Tangier disease in family with the phenotype of familial hypercholesterolemia." Vnitřní lékařství 66, no. 7 (2020): 443–46. http://dx.doi.org/10.36290/vnl.2020.125.

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15

Kohoutová, Jarmila. "Highly infectious disease - exercise at the University hospital Olomouc 2017." Hygiena 63, no. 2 (2018): 69. http://dx.doi.org/10.21101/hygiena.b0018.

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16

Želízko, Michael. "STEMI and multivessel disease: How should we treat?" Cor et Vasa 56, no. 6 (2014): e527-e528. http://dx.doi.org/10.1016/j.crvasa.2014.06.003.

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17

Ryba, Luděk, and Pavel Rozsíval. "Kawasaki disease associated with Covid-19 - two cases." Pediatrie pro praxi 22, no. 1 (2021): 54–58. http://dx.doi.org/10.36290/ped.2021.009.

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18

Adamczyk, Roman. "Philosophical-Anthropological Contribution by Viktor Frankl - the Human, Meaning, Illness and Health." E-LOGOS 26, no. 2 (2019): 4–13. http://dx.doi.org/10.18267/j.e-logos.464.

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19

Petráková, Katarína. "Residual disease after neoadjuvant systemic anti-HER2 therapy: the KATHERINE trial." Onkologie 14, no. 2 (2020): 93–95. http://dx.doi.org/10.36290/xon.2020.017.

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20

Hanulík, Vojtěch, Kateřina Kybicová, Světlana Brychtová, Viktor Palla, Jan Šternberský, and Martin Tichý. "Cat‑scratch disease with atypical trajectory and manifestation." Dermatologie pro praxi 14, no. 3 (2020): 152–54. http://dx.doi.org/10.36290/der.2020.028.

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21

Dusilová Sulková, Sylvie, Anita Pokorná, Roman Šafránek, Ladislava Pavlíková, and Vladimír Palička. "Bone disesase in end-stage kidney disease - renal and non-renal components." Vnitřní lékařství 67, no. 5 (2021): 258–63. http://dx.doi.org/10.36290/vnl.2021.072.

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22

Vosečková, Alena, and Zuzana Truhlářová. "ASSESSMENT OF SELECTED HEALTH MODERATORS WITHIN CONTEXT OF PHYSICAL ACTIVITY." Military Medical Science Letters 87, no. 4 (2018): 148–57. http://dx.doi.org/10.31482/mmsl.2018.035.

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23

Kocík, Miroslav, Jaroslav Hubáček, Ivan Málek, et al. "Oxide synthase donor gene polymorphisms and cardiac graft coronary artery disease." Cor et Vasa 51, no. 3 (2009): 202–9. http://dx.doi.org/10.33678/cor.2009.046.

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24

Halenka Jan Schovánek, Milan, and Zdeněk Fryšák David Karásek. "Subacute (de Quervain) thyroiditis, "the forgotten disease" - part I." Interní medicína pro praxi 21, no. 3 (2019): 162–66. http://dx.doi.org/10.36290/int.2019.024.

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25

Halenka Ph. Jan Schovánek Zdeněk Fryšák David, Milan D., and Karásek Charlotte Mlčochová. "Subacute (de Quervain) thyroiditis, the forgotten disease - part II: clinical study." Interní medicína pro praxi 21, no. 4 (2019): 233–37. http://dx.doi.org/10.36290/int.2019.036.

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26

Fialová, Daniela, Veronika Příhodová, Jovana Brkič, et al. "Evaluation of geriatric drug‑disease interactions in seniors in log‑term care in the Czech Republic." Klinická farmakologie a farmacie 34, no. 3 (2020): 99–107. http://dx.doi.org/10.36290/far.2020.019.

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27

Koblížek, Vladimír, Jaromír Zatloukal, Jan Chlumský, and Karel Hejduk. "An 2018 update of personalised Czech COPD guidelines; a country specificconsensus of The Czech Pneumological and Phthiseological Society." Medicína pro praxi 15, no. 3 (2018): 127–33. http://dx.doi.org/10.36290/med.2018.027.

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28

Sheardová, Kateřina, Daniel Hudeček, Olga Hromková, Rafal Marciniak, and Jakub Hort. "Alzheimer's disease as a neuropathological continuum in clinical practice." Neurologie pro praxi 17, no. 5 (2016): 305–9. http://dx.doi.org/10.36290/neu.2016.063.

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29

Brat, Kristián, Jaromír Zatloukal, Kateřina Neumannová, et al. "Chronic obstructive pulmonary disease: diagnosis and treatment of stable phase of disease; personalized treatment approach using phenotype features of the disease." Vnitřní lékařství 67, no. 4 (2021): 230–39. http://dx.doi.org/10.36290/vnl.2021.058.

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30

FELTKAMP, Régine, and Gerrit HENDRIKX. "Market Coupling and the Capacity Allocation and Congestion Management Regulation." European Journal of Risk Regulation 9, no. 2 (2018): 208–26. http://dx.doi.org/10.1017/err.2018.16.

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AbstractThis article assesses the manner in which Commission Regulation (EU) 2015/1222 of 24 July 2015 establishing a guideline on capacity allocation and congestion management (“CACM”) alters the legal context within which power exchanges (“PXs”) perform their activities related to market coupling. By submitting the cooperation among the newly-introduced NEMO-entities, and between these NEMOs and TSOs, regarding market coupling to a new set of rules, CACM affects the market coupling activities of PXs in different ways. This article in particular examines from the power exchanges’ perspective

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31

Bartoníková, Tereza, Kateřina Menšíková, Vladimír Janout, and Petr Kaňovský. "Epidemiology of Parkinson's disease." Neurologie pro praxi 21, no. 5 (2020): 390–94. http://dx.doi.org/10.36290/neu.2020.016.

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32

Plagge, Mark, Christopher D. Carothers, Elsa Gonsiorowski, and Neil Mcglohon. "NeMo." ACM Transactions on Modeling and Computer Simulation 28, no. 4 (2018): 1–25. http://dx.doi.org/10.1145/3186317.

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33

Corn, A. "Nemo." Literary Imagination 9, no. 3 (2007): 273. http://dx.doi.org/10.1093/litimag/imm006.

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34

Mazanec -editor hlavního tématu, Radim. "Nemoci motorických neuronů." Neurologie pro praxi 17, no. 6 (2016): 348. http://dx.doi.org/10.36290/neu.2016.072.

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35

Claréus, Ingrid, and Per Olov Enquist. "Kapten Nemos bibliotek." World Literature Today 67, no. 1 (1993): 198. http://dx.doi.org/10.2307/40148973.

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36

Medunjanin, Senad, Maximilian Putzier, Till Nöthen та ін. "DNA-PK: gatekeeper for IKKγ/NEMO nucleocytoplasmic shuttling in genotoxic stress-induced NF-kappaB activation". Cellular and Molecular Life Sciences 77, № 20 (2020): 4133–42. http://dx.doi.org/10.1007/s00018-019-03411-y.

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Abstract The transcription factors of the nuclear factor κB (NF-κB) family play a pivotal role in the cellular response to DNA damage. Genotoxic stress-induced activation of NF-κB differs from the classical canonical pathway by shuttling of the NF-κB Essential Modifier (IKKγ/NEMO) subunit through the nucleus. Here, we show that DNA-dependent protein kinase (DNA-PK), an enzyme involved in DNA double-strand break (DSB) repair, triggers the phosphorylation of NEMO by genotoxic stress, thereby enabling shuttling of NEMO through the nucleus with subsequent NF-κB activation. We identified serine 43

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37

Bates, Jane. "Nemo complex." Nursing Standard 21, no. 19 (2007): 27. http://dx.doi.org/10.7748/ns.21.19.27.s35.

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38

Renouard, Jean-Philippe. "merci nemo." Vacarme 24, no. 3 (2003): 72. http://dx.doi.org/10.3917/vaca.024.0072.

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39

Hay, Ronald T. "Modifiying NEMO." Nature Cell Biology 6, no. 2 (2004): 89–91. http://dx.doi.org/10.1038/ncb0204-89.

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40

Smallridge, Rachel. "Understanding NEMO." Nature Reviews Molecular Cell Biology 7, no. 6 (2006): 384–85. http://dx.doi.org/10.1038/nrm1944.

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41

Goláň, Lubor. "Cardiologic evaluation in Fabry disease." Intervenční a akutní kardiologie 17, no. 2 (2018): 67–70. http://dx.doi.org/10.36290/kar.2018.039.

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42

Ludka, Ondřej. "Antithrombotic therapy of thromboembolic disease." Interní medicína pro praxi 18, no. 5 (2016): 222–25. http://dx.doi.org/10.36290/int.2016.051.

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43

Novák, František. "Nutrition in the acute phase of illness." Vnitřní lékařství 65, no. 3 (2019): 219–26. http://dx.doi.org/10.36290/vnl.2019.039.

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44

Hubeau, Marjorie, Flora Ngadjeua, Anne Puel, et al. "New mechanism of X-linked anhidrotic ectodermal dysplasia with immunodeficiency: impairment of ubiquitin binding despite normal folding of NEMO protein." Blood 118, no. 4 (2011): 926–35. http://dx.doi.org/10.1182/blood-2010-10-315234.

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Abstract Nuclear factor-κB essential modulator (NEMO), the regulatory subunit of the IκB kinase complex, is a critical component of the NF-κB pathway. Hypomorphic mutations in the X-linked human NEMO gene cause various forms of anhidrotic ectodermal dysplasia with immunodeficiency (EDA-ID). All known X-linked EDA-ID–causing mutations impair NEMO protein expression, folding, or both. We describe here 2 EDA-ID–causing missense mutations that affect the same residue in the CC2-LZ domain (D311N and D311G) that do not impair NEMO production or folding. Structural studies based on pull-down experime

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45

Zilberman-Rudenko, Jevgenia, Linda Monaco Shawver, Alex W. Wessel та ін. "Recruitment of A20 by the C-terminal domain of NEMO suppresses NF-κB activation and autoinflammatory disease". Proceedings of the National Academy of Sciences 113, № 6 (2016): 1612–17. http://dx.doi.org/10.1073/pnas.1518163113.

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Receptor-induced NF-κB activation is controlled by NEMO, the NF-κB essential modulator. Hypomorphic NEMO mutations result in X-linked ectodermal dysplasia with anhidrosis and immunodeficiency, also referred to as NEMO syndrome. Here we describe a distinct group of patients with NEMO C-terminal deletion (ΔCT-NEMO) mutations. Individuals harboring these mutations develop inflammatory skin and intestinal disease in addition to ectodermal dysplasia with anhidrosis and immunodeficiency. Both primary cells from these patients, as well as reconstituted cell lines with this deletion, exhibited increas

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46

Nishikomori, Ryuta, Hiroshi Akutagawa, Kyoko Maruyama, et al. "X-linked ectodermal dysplasia and immunodeficiency caused by reversion mosaicism of NEMO reveals a critical role for NEMO in human T-cell development and/or survival." Blood 103, no. 12 (2004): 4565–72. http://dx.doi.org/10.1182/blood-2003-10-3655.

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Abstract X-linked ectodermal dysplasia and immunodeficiency (XL-EDA-ID) is an X-linked recessive disease caused by a mutation in the nuclear factor-κB (NF-κB) essential modulator (NEMO). Here we report an XL-EDA-ID patient with atypical features of very few naive-phenotype T cells and defective mitogen-induced proliferation of peripheral blood mononuclear cells (PBMCs). The patient's NEMO defect was diagnosed by flow cytometric analysis of intracellular NEMO staining. Specific cell lineages (monocytes and neutrophils) expressed reduced levels of NEMO, but 2 populations of T, B, and NK cells we

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47

Sakowicz, Agata, Michalina Lisowska, Lidia Biesiada, et al. "Placental Expression of NEMO Protein in Normal Pregnancy and Preeclampsia." Disease Markers 2019 (January 2, 2019): 1–12. http://dx.doi.org/10.1155/2019/8418379.

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Background. Preeclamptic pregnancies often present an intensified inflammatory state associated with the nuclear activity of NFκB. NEMO is an essential regulator of nuclear factor kappa B (NFκB) in cytoplasmic and nuclear cellular compartments. The aim of the present study is to examine the level and localization of the NEMO protein in preeclamptic and nonpreeclamptic placentas. Methods. The study includes 97 preeclamptic cases and 88 controls. NEMO distribution was analyzed immunohistochemically. Its localization in the nuclear and cytoplasmic fractions, as well as in total homogenates of pla

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48

Rappoport, Nimrod, and Ron Shamir. "NEMO: cancer subtyping by integration of partial multi-omic data." Bioinformatics 35, no. 18 (2019): 3348–56. http://dx.doi.org/10.1093/bioinformatics/btz058.

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Abstract Motivation Cancer subtypes were usually defined based on molecular characterization of single omic data. Increasingly, measurements of multiple omic profiles for the same cohort are available. Defining cancer subtypes using multi-omic data may improve our understanding of cancer, and suggest more precise treatment for patients. Results We present NEMO (NEighborhood based Multi-Omics clustering), a novel algorithm for multi-omics clustering. Importantly, NEMO can be applied to partial datasets in which some patients have data for only a subset of the omics, without performing data impu

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49

Kawai, Tomoki, Ryuta Nishikomori, Kazushi Izawa, et al. "Frequent somatic mosaicism of NEMO in T cells of patients with X-linked anhidrotic ectodermal dysplasia with immunodeficiency." Blood 119, no. 23 (2012): 5458–66. http://dx.doi.org/10.1182/blood-2011-05-354167.

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Abstract Somatic mosaicism has been described in several primary immunodeficiency diseases and causes modified phenotypes in affected patients. X-linked anhidrotic ectodermal dysplasia with immunodeficiency (XL-EDA-ID) is caused by hypomorphic mutations in the NF-κB essential modulator (NEMO) gene and manifests clinically in various ways. We have previously reported a case of XL-EDA-ID with somatic mosaicism caused by a duplication mutation of the NEMO gene, but the frequency of somatic mosaicism of NEMO and its clinical impact on XL-EDA-ID is not fully understood. In this study, somatic mosai

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50

Fernández, Gael, Vasiliki Stratigaki, and Peter Troch. "Irregular Wave Validation of a Coupling Methodology for Numerical Modelling of Near and Far Field Effects of Wave Energy Converter Arrays." Energies 12, no. 3 (2019): 538. http://dx.doi.org/10.3390/en12030538.

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Between the Wave Energy Converters (WECs) of a farm, hydrodynamic interactions occur and have an impact on the surrounding wave field, both close to the WECs (“near field” effects) and at large distances from their location (“far field” effects). To simulate this “far field” impact in a fast and accurate way, a generic coupling methodology between hydrodynamic models has been developed by the Coastal Engineering Research Group of Ghent University in Belgium. This coupling methodology has been widely used for regular waves. However, it has not been developed yet for realistic irregular sea stat

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