Zobrazeno 1 - 10 of 528 pro vyhledávání: '"Sheppard, Mn"'
1
Vascular histopathology and connective tissue ultrastructure in spontaneous coronary artery dissection: pathophysiological and clinical implications
Autor: Margaritis, M, Saini, F, Baranowska-Clarke, AA, Parsons, S, Vink, A, Budgeon, C, Allcock, N, Wagner, BE, Samani, NJ, von der Thüsen, J, Robertus, JL, Sheppard, MN, Adlam, D
AIMS : Spontaneous coronary artery dissection (SCAD) is a cause of acute coronary syndromes and in rare cases sudden cardiac death (SCD). Connective tissue abnormalities, coronary inflammation, increased coronary vasa vasorum (VV) density, and corona
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::4f013bd3fa24b83c0d20569b025e2f24
https://openaccess.sgul.ac.uk/id/eprint/113320/6/cvab183.pdf
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2
Autopsy in adults with congenital heart disease (ACHD)
Autor: Angelini, A, di Gioia, C, Doran, H, Fedrigo, M, Henriques de Gouveia, R, Ho, SY, Leone, O, Sheppard, MN, Thiene, G, Dimopoulos, K, Mulder, B, Padalino, M, van der Wal, AC, Association for European Cardiovascular Pathology (AECVP)
Publikováno v: Virchows Archiv
The adult congenital heart diseases (ACHD) population is exceeding the pediatric congenital heart diseases (CHD) population and is progressively expanding each year, representing more than 90% of patients with CHD. Of these, about 75% have undergone
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8eb00040b37f2cf8cf96acfbf384e54
https://doi.org/10.1007/s00428-020-02779-8
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3
Cardiac hypertrophy at autopsy
Autor: Basso, C, Michaud, K, d'Amati, G, Banner, J, Lucena, J, Cunningham, K, Leone, O, Vink, A, van der Wal, AC, Sheppard, MN, Association for European Cardiovascular Pathology
Since cardiac hypertrophy may be considered a cause of death at autopsy, its assessment requires a uniform approach. Common terminology and methodology to measure the heart weight, size, and thickness as well as a systematic use of cut off values for
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::b1cdeb9c20e4d2f4b1f26d513dce345a
https://openaccess.sgul.ac.uk/id/eprint/113101/1/Basso2021_Article_CardiacHypertrophyAtAutopsy.pdf
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4
Sudden Death and Left Ventricular Involvement in Arrhythmogenic Cardiomyopathy
Autor: Miles, C, Finocchiaro, G, Papadakis, M, Gray, B, Westaby, J, Ensam, B, Basu, J, Parry-Williams, G, Papatheodorou, E, Paterson, C, Malhotra, A, Robertus, JL, Ware, JS, Cook, SA, Asimaki, A, Witney, A, Chis Ster, I, Tome, M, Sharma, S, Behr, ER, Sheppard, MN
Publikováno v: Circulation
Miles, C, Finocchiaro, G, Papadakis, M, Gray, B, Westaby, J, Ensam, B, Basu, J, Parry-Williams, G, Papatheodorou, E, Paterson, C, Malhotra, A, Robertus, J L, Ware, J S, Cook, S A, Asimaki, A, Witney, A, Ster, I C, Tome, M, Sharma, S, Behr, E R & Sheppard, M N 2019, ' Sudden Death and Left Ventricular Involvement in Arrhythmogenic Cardiomyopathy ', Circulation, vol. 139, no. 15, pp. 1786-1797 . https://doi.org/10.1161/CIRCULATIONAHA.118.037230
Supplemental Digital Content is available in the text.
Background: Arrhythmogenic cardiomyopathy (ACM) is an inherited heart muscle disorder characterized by myocardial fibrofatty replacement and an increased risk of sudden cardiac death (SCD).
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::53209902499421b9ecbc932e0e81bc7c
http://europepmc.org/articles/PMC6467560
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5
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
Autor: Walsh R, Lahrouchi N, Tadros R, Kyndt F, Glinge C, Postema PG, Amin AS, Nannenberg EA, Ware JS, Whiffin N, Mazzarotto F, Škoric-Milosavljevic D, Krijger C, Arbelo E, Babuty D, Barajas-Martinez H, Beckmann BM, Bézieau S, Bos JM, Breckpot J, Campuzano O, Castelletti S, Celen C, Clauss S, Corveleyn A, Crotti L, Dagradi F, de Asmundis C, Denjoy I, Dittmann S, Ellinor PT, Ortuño CG, Giustetto C, Gourraud JB, Hazeki D, Horie M, Ishikawa T, Itoh H, Kaneko Y, Kanters JK, Kimoto H, Kotta MC, Krapels IPC, Kurabayashi M, Lazarte J, Leenhardt A, Loeys BL, Lundin C, Makiyama T, Mansourati J, Martins RP, Mazzanti A, Mörner S, Napolitano C, Ohkubo K, Papadakis M, Rudic B, Molina MS, Sacher F, Sahin H, Sarquella-Brugada G, Sebastiano R, Sharma S, Sheppard MN, Shimamoto K, Shoemaker MB, Stallmeyer B, Steinfurt J, Tanaka Y, Tester DJ, Usuda K, van der Zwaag PA, Van Dooren S, Van Laer L, Winbo A, Winkel BG, Yamagata K, Zumhagen S, Volders PGA, Lubitz SA, Antzelevitch C, Platonov PG, Odening KE, Roden DM, Roberts JD, Skinner JR, Tfelt-Hansen J, van den Berg MP, Olesen MS, Lambiase PD, Borggrefe M, Hayashi K, Rydberg A, Nakajima T, Yoshinaga M, Saenen JB, Kääb S, Brugada P, Robyns T, Giachino DF, Ackerman MJ, Brugada R, Brugada-Terradellas J, Gimeno JR, Hasdemir C, Guicheney P, Priori SG, Schulze-Bahr E, Makita N, Schwartz PJ, Shimizu W, Aiba T, Schott JJ, Redon R, Ohno S, Probst V, Behr ER, Barc J, Bezzina CR, Nantes Referral Center for inherited cardiac arrhythmia
Publikováno v: GENETICS IN MEDICINE
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
PURPOSE: Stringent variant interpretation guidelines can lead to high rates of variants of uncertain significance (VUS) for genetically heterogeneous disease like long QT syndrome (LQTS) and Brugada syndrome (BrS). Quantitative and disease-specific c
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e87c9928a8521edcd91c04ed927a7b68
https://openaccess.sgul.ac.uk/id/eprint/112371/3/s41436-020-00946-5.pdf
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7
The Role of Endocarditis in Sudden Cardiac Death: Highlighting the value of the autopsy, pathological features and cardiac complications
Autor: Cooper, ST, Westaby, DJD, Griffin, DKJ, Sheppard, MN
OBJECTIVE: Endocarditis is increasing in incidence due to growing numbers of cardiac interventions, valve replacements and immunosuppressants. It can be difficult to diagnose clinically, has high mortality and can present as sudden cardiac death (SCD
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::44a9e2a821c9ee8ba7ef3ebc404be3e1
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9
Diagnosis of myocardial infarction at autopsy: AECVP reappraisal in the light of the current clinical classification
Autor: Michaud, K., Basso, C., d'Amati, G., Giordano, C., Kholová, I., Preston, SD, Rizzo, S., Sabatasso, S., Sheppard, MN, Vink, A., van der Wal, AC
Publikováno v: Virchows Archiv, vol. 476, no. 2, pp. 179-194
Ischemic heart disease is one of the leading causes of morbidity and death worldwide. Consequently, myocardial infarctions are often encountered in clinical and forensic autopsies, and diagnosis can be challenging, especially in the absence of an acu
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______1900::0132ae721933c153660ab7721acbb2d1
https://serval.unil.ch/notice/serval:BIB_67A450A64E99
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