Zeitschriftenartikel: „Shonens“

1

Détrez, Christine. „Des shonens pour les garçons, des shojos pour les filles ?“ Réseaux 168-169, Nr. 4 (2011): 165. http://dx.doi.org/10.3917/res.168.0165.

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2

Dalton, Tyler J., William K. Johnson, Evelyn M. Kuhn, Benjamin H. Goot, Ronald K. Woods, Michael E. Mitchell und Viktor Hraska. „Outcomes Following Surgery to Address Shone Syndrome in Children“. World Journal for Pediatric and Congenital Heart Surgery 12, Nr. 3 (Mai 2021): 360–66. http://dx.doi.org/10.1177/2150135121994083.

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Background: Shone syndrome is characterized by coincident mitral valve stenosis and left ventricular outflow tract obstruction. Although first described in 1963, little research has expounded surgical outcomes. We sought to evaluate our experience with this cohort, emphasizing outcomes including mortality, morbidity, and cardiac function. Methods: A retrospective chart review of 46 patients who underwent operation for Shone syndrome between 1990 and May 2018 was conducted. Index operations included 32 repairs of the left ventricular outflow tract, four mitral valve repair/replacements, nine combined repairs, and one non-Shone’s repair. Median age at index procedure was 22 days (2 days-10 years). Mean follow-up was 9.1 years (2 months-21 years), and 70 additional operations (51 reoperations) were required. Three patients were lost to follow-up. Results: Overall survival was 95.7% with two late deaths. Freedom from death or transplant was 93.5%. Thirteen (28.3%) patients remained free from reoperation. Thirty-three patients required 51 reoperations of the left ventricle outflow tract (n = 12), mitral valve (n = 16), combined repairs (n = 21), and transplant (n = 1). At most recent follow-up, patients exhibited mitral stenosis (n = 21), aortic stenosis (n = 7), and diminished LV function (n = 2). Conclusion: Surgical correction of Shone’s offers excellent survival benefit, but reoperation burden is high, with >70% of patients requiring reintervention in the follow-up period. A total of 65% of patients developed recurrent obstruction of left ventricular inflow or outflow, however, ventricular function is preserved in the majority of patients. All but one patient had no functional deficits, classified as New York Heart Association I with > 60% requiring no medication.

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3

Ayhan, Hüseyin. „Atypical Shone's Complex“. Kosuyolu Heart Journal 18, Nr. 3 (07.12.2015): 158. http://dx.doi.org/10.5578/khj.9944.

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4

Morel, Geneviève. „Shonen (Le petit garçon)“. Savoirs et clinique 20, Nr. 1 (2016): 107. http://dx.doi.org/10.3917/sc.020.0107.

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5

Zhang, Xin, Guiqin Ma, Lin Zheng, Hongju Zhang, Yan Sun, Jingya Li und Ning Ma. „Echocardiographic diagnosis of Shone’s syndrome“. Echocardiography 37, Nr. 12 (18.10.2020): 2139–43. http://dx.doi.org/10.1111/echo.14899.

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6

Rauch, Ralf, Lars Grosse-Wortmann, Judy Jones, Elizabeth Burrill, Eva Welisch, Herschel C. Rosenberg und Kambiz Norozi. „Shone's Complex and Levoatriocardinal Vein“. Journal of the American College of Cardiology 59, Nr. 7 (Februar 2012): 698. http://dx.doi.org/10.1016/j.jacc.2011.06.081.

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7

Yachi, Teruo. „English Articles in SHONEN BUNSHU“. Historical English Studies in Japan, Nr. 18 (1986): 51–58. http://dx.doi.org/10.5024/jeigakushi.1986.51.

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8

Jin, Justin B., Mary Kay Haynes, Abdelrahman Masri, Razleen Brar und Rukmini Komarlu. „AN EVEN MORE COMPLEX SHONE'S COMPLEX“. Journal of the American College of Cardiology 79, Nr. 9 (März 2022): 3137. http://dx.doi.org/10.1016/s0735-1097(22)04128-6.

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9

Rodrigues, Ricardo C., André Correia, Gomes Serrão, Paula Faria, Susana Gomes und Décio Pereira. „Incomplete Shone’s complex: adult age diagnosis“. Acta Cardiologica 72, Nr. 1 (02.01.2017): 85–86. http://dx.doi.org/10.1080/00015385.2017.1281529.

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10

Ma, Xiao-jing, Guo-ying Huang, Xue-cun Liang, Xiao-qin Liu und Bing Jia. „Atypical Shone’s Complex Diagnosed by Echocardiography“. Pediatric Cardiology 32, Nr. 4 (29.01.2011): 442–48. http://dx.doi.org/10.1007/s00246-011-9886-y.

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11

Shalev, Y., und A. Caspi. „Complete atrioventricular block in shone's syndrome“. Clinical Cardiology 10, Nr. 1 (Januar 1987): 65–67. http://dx.doi.org/10.1002/clc.4960100116.

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12

Diah Padmawati, Made, und I. G. A. G. Sosiowati. „The Violation of Cooperative Principle In the Kindaichi Shonen No Jikenbo 20’th Anniversary Series Comic Vol.1“. Linguistika: Buletin Ilmiah Program Magister Linguistik Universitas Udayana 28, Nr. 1 (31.03.2021): 82. http://dx.doi.org/10.24843/ling.2021.v28.i01.p08.

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The purpose of this research was to determine the violation types of cooperative principle in the utterance between characters in the dialogue of Kindaichi Shonen No Jikenzbo 20th Series Comic Vol.1. This research used descriptive qualitative method. The data of this research are in the form of utterances between characters in the dialogue of Kindaichi Shonen No Jikenbo 20th Series Comic Vol.1. The method used to collect the data is observation method which refers to the tapping and note-taking techniques. The method used to analyze the data is pragmatic analysis method with heuristic technique. The result showed that there were four violation types of cooperative principle including: maxim of quantity, maxim of quality, maxim of relevance or relation and maxim of manner in the Kindaichi Shonen No Jikenbo 20th Series Comic Vol.1. The most frequently flouted maxim in the utterance between characters in the dialogue of Kindaichi Shonen No Jikenbo 20th Series Comic Vol.1 was maxim of quality. This indicates that the characters in the Kindaichi Shonen No Jikenbo 20th Series Comic Vol.1 often say something that is still doubtful. On the other hand, related to the three violations of maxims, it was found that the same number of violations occurred between maxim of quality, maxim of relation and maxim of manner.

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13

Elmahrouk, Ahmed F., Mohamed F. Ismail, Amr A. Arafat, Ahmed M. Dohain, Abdelmonem M. Helal, Tamer E. Hamouda, Mohamed Galal, Azzahra M. Edrees, Osman O. Al‐Radi und Ahmed A. Jamjoom. „Outcomes of biventricular repair for shone's complex“. Journal of Cardiac Surgery 36, Nr. 1 (08.10.2020): 12–20. http://dx.doi.org/10.1111/jocs.15090.

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14

Vivas, Martín F., María T. Politi, Laura M. Riznyk, María F. Castro, Gustavo Avegliano und Ricardo Ronderos. „Shone's syndrome: Insights from three-dimensional echocardiography“. Echocardiography 35, Nr. 3 (22.12.2017): 417–19. http://dx.doi.org/10.1111/echo.13787.

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15

Ochirjav, Enkhee, M. Tsetsegdelger, B. Tuul und D. Batbaatar. „Congenital heart defect: Shone’s complex (case report)“. Pathology 48 (Februar 2016): S147. http://dx.doi.org/10.1016/j.pathol.2015.12.400.

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16

Bolling, Steven F., Mark D. Iannettoni, Macdonald Dick, Amnon Rosenthal und Edward L. Bove. „Shone's anomaly: Operative results and late outcome“. Annals of Thoracic Surgery 49, Nr. 6 (Juni 1990): 887–93. http://dx.doi.org/10.1016/0003-4975(90)90861-y.

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17

Labrada, L., J. Mazurek, C. Haeffele, A. Weingarten, T. Gupta und J. Menachem. „Shone's Complex: Not So ‘Simple’ after All“. Journal of Heart and Lung Transplantation 42, Nr. 4 (April 2023): S214—S215. http://dx.doi.org/10.1016/j.healun.2023.02.482.

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18

Ganju, NeerajK, Arvind Kandoria, Suresh Thakur und SuniteA Ganju. „A constellation of cardiac anomalies: Beyond shone's complex“. Heart Views 17, Nr. 1 (2016): 23. http://dx.doi.org/10.4103/1995-705x.182643.

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19

Setty, Huliyurdurga Srinivasasetty Natraj, Veeresh Patil Hebbal, Shivanand S. Patil, Beeresh B, Ishwarappa Balekundri Vijayalakshmi, Bhanuprakash B, Banandur Nanjundappa Krishnamurthy und Cholenahalli Nanjappa Manjunath. „Shone’s complex and Cortriatriatum Sinister: A Rare Combination.“ Journal of Cardiovascular Disease Research 7, Nr. 3 (01.10.2016): 128–29. http://dx.doi.org/10.5530/jcdr.2016.3.8.

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20

Tian, Zhuang, Ligang Fang und Ruiyi Xu. „Infective Endocarditis in a Patient with Incomplete Shone's Anomaly“. Internal Medicine 51, Nr. 19 (2012): 2835–36. http://dx.doi.org/10.2169/internalmedicine.51.8478.

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21

Musaad, Walaa, Aisling Lyons, Nicholas Allen und Johannes Letshwiti. „Mowat-Wilson syndrome presenting with Shone’s complex cardiac anomaly“. BMJ Case Reports 15, Nr. 2 (Februar 2022): e246913. http://dx.doi.org/10.1136/bcr-2021-246913.

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A female infant, who was diagnosed antenatally with complex heart disease, confirmed to be Shone’s complex postnatally, underwent bilateral pulmonary artery banding, patent ductus arteriosus stent insertion and balloon aortic valvuloplasty soon after birth. She was found to have bilateral megaureters, left hydronephrosis and asplenia. She was on lifelong prophylactic antibiotics and extra vaccines. She had two episodes of pseudo-obstruction of the small bowel, but barium follow-through was normal. She also had a large bowel obstruction and work-up for Hirschsprung disease confirmed the diagnosis. It was noticed that she had developmental delay and hypotonia, together with subtle dysmorphism. She also had failure to thrive and difficulty feeding. Exome sequencing revealed a diagnosis of Mowat-Wilson syndrome (MWS). This case shows a previously undescribed association of Shone’s complex, a complex left-sided obstructive heart defect, and MWS. It also highlights the usefulness of trio-exome sequencing in detecting such rare mutations.

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22

Akgullu, Cagdas, und Ercan Erdogan. „Adult Patient with Shone's Syndrome and Patent Ductus Arteriosus“. Turk Kardiyoloji Dernegi Arsivi-Archives of the Turkish Society of Cardiology 40, Nr. 4 (2012): 350–53. http://dx.doi.org/10.5543/tkda.2012.27003.

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23

Popescu, Bogdan A., Ruxandra Jurcut, Marinela Serban, Liliana Parascan und Carmen Ginghina. „Shone's syndrome diagnosed with echocardiography and confirmed at pathology“. European Heart Journal - Cardiovascular Imaging 9, Nr. 6 (11.07.2008): 865–67. http://dx.doi.org/10.1093/ejechocard/jen200.

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24

Rehfeldt, Kent H., William J. Mauermann, Rakesh M. Suri und Martha Grogan. „The Diagnosis of Shone's Anomaly by Intraoperative Transesophageal Echocardiography“. Journal of Cardiothoracic and Vascular Anesthesia 23, Nr. 1 (Februar 2009): 75–76. http://dx.doi.org/10.1053/j.jvca.2007.11.008.

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25

Ikemba, Catherine M., Benjamin W. Eidem, J. Kennard Fraley, Reenu S. Eapen, Ricardo Pignatelli, Nancy A. Ayres und Louis I. Bezold. „Mitral valve morphology and morbidity/mortality in Shone's complex“. American Journal of Cardiology 95, Nr. 4 (Februar 2005): 541–43. http://dx.doi.org/10.1016/j.amjcard.2004.10.030.

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26

Escárcega, Ricardo O., Hector I. Michelena und Alfred A. Bove. „Bicuspid Aortic Valve: A Neglected Feature of Shone’s Complex?“ Pediatric Cardiology 35, Nr. 1 (29.09.2013): 186–87. http://dx.doi.org/10.1007/s00246-013-0804-3.

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27

Joffe, Denise, Michelle Gurvitz und Donald Oxorn. „An Unusual Presentation in a Patient with Shone’s Anomaly“. Anesthesia & Analgesia 107, Nr. 6 (Dezember 2008): 1825–27. http://dx.doi.org/10.1213/ane.0b013e318185ccd3.

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28

Liegise, Avitso, Gopal Chandra Ghosh, Lijo Varghese, Anoop George Alex und Oommen K. George. „Shone’s plus complex: an interesting combination of cardiac defects“. Indian Heart Journal 70 (November 2018): S129. http://dx.doi.org/10.1016/j.ihj.2018.10.393.

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29

Turkoz, Rıza, Canan Ayabakan, Can Vuran, Oğuz Omay, Selman Vefa Yildirim und N. Kurşad Tokel. „Duplicate Mitral Valve in an Infant With Shone's Anomaly“. Annals of Thoracic Surgery 88, Nr. 5 (November 2009): 1683–85. http://dx.doi.org/10.1016/j.athoracsur.2009.03.097.

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30

Brown, John W., Mark Ruzmetov, Palaniswamy Vijay, Mark H. Hoyer, Donald Girod, Mark D. Rodefeld und Mark W. Turrentine. „Operative Results and Outcomes in Children With Shone's Anomaly“. Annals of Thoracic Surgery 79, Nr. 4 (April 2005): 1358–65. http://dx.doi.org/10.1016/j.athoracsur.2004.09.013.

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31

Jeong, Sun Young, Naing Moore und Daniel R. Sanchez. „MITRAL STENOSIS, NOT ALWAYS RHEUMATIC - UNRAVELING THE SHONE'S VARIANT“. Journal of the American College of Cardiology 83, Nr. 13 (April 2024): 3122. http://dx.doi.org/10.1016/s0735-1097(24)05112-x.

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32

LEE, Yeon-suk. „Myoe Shonin's Understanding of “Ichinen”“. JOURNAL OF INDIAN AND BUDDHIST STUDIES (INDOGAKU BUKKYOGAKU KENKYU) 51, Nr. 2 (2003): 661–63. http://dx.doi.org/10.4259/ibk.51.661.

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33

Nicholson, George T., Michael S. Kelleman, Caridad M. De la Uz, Ricardo H. Pignatelli, Nancy A. Ayres und Christopher J. Petit. „Late outcomes in children with Shone’s complex: a single-centre, 20-year experience“. Cardiology in the Young 27, Nr. 4 (26.07.2016): 697–705. http://dx.doi.org/10.1017/s1047951116001104.

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AbstractObjectiveShone’s syndrome is a complex consisting of mitral valve stenosis in addition to left ventricle outflow obstruction. There are a few studies evaluating the long-term outcomes in this population. We sought to determine the long-term outcomes in our paediatric population with Shone’s syndrome and the factors associated with left heart growth.MethodsAll patients diagnosed with Shone’s syndrome with biventricular circulation treated between 1978 and 2010 were reviewed. Baseline echocardiograms and data from catheterisations were also reviewed. Number of interventions (surgical+transcatheter), incidence of mitral valve replacement, and incidence of heart transplantation were tracked. Survival of the population and left heart structural growth were also reviewed.ResultsA total of 121 patients with Shone’s syndrome presented at a median age of 28 days (0–17.3 years) and were followed-up for 7.2 years (0.01–35.5 years). These patients underwent 258 interventions during the study period, and the presence of coarctation was associated with repeat left heart interventions. The 10-year, transplant-free survival was 86%. Presence of pulmonary hypertension was associated with mortality. Left heart structural growth was seen for mitral and aortic valve annuli and left ventricular end-diastolic dimension over time.ConclusionsShone’s syndrome patients undergo a number of left heart interventions. Coarctation of the aorta is associated with an increased likelihood for repeat interventions. Survival appears to be more favourable than expected. Significant left heart growth will occur in the population. Pulmonary hypertension is associated with an increased risk of mortality.

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34

Wasserman, Evan, Asma Syeda, Naga Vaishnavi Gadela und Nikola Perosevic. „SEVERE PULMONARY HYPERTENSION IN AN ADULT PATIENT WITH SHONE’S COMPLEX“. Journal of the American College of Cardiology 77, Nr. 18 (Mai 2021): 2212. http://dx.doi.org/10.1016/s0735-1097(21)03567-1.

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35

PATEL, JANMEJAY J., JOHN J. ROSS und KRISHNASWAMY CHANDRASEKARAN. „A Form Fruste of Shone's Complex Diagnosed by Transesophageal Echocardiography“. Echocardiography 13, Nr. 2 (März 1996): 147–50. http://dx.doi.org/10.1111/j.1540-8175.1996.tb00882.x.

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36

Roche, K. J., Nancy B. Genieser, Michael M. Ambrosino und Gillian L. Henry. „MR findings in Shone's complex of left heart obstructive lesions“. Pediatric Radiology 28, Nr. 11 (03.11.1998): 841–45. http://dx.doi.org/10.1007/s002470050478.

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37

Zucker, N., A. Levitas und E. Zalzstein. „Prenatal diagnosis of Shone's syndrome: parental counseling and clinical outcome“. Ultrasound in Obstetrics and Gynecology 24, Nr. 6 (2004): 629–32. http://dx.doi.org/10.1002/uog.1753.

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38

Derrer, F., S. Gisin, A. Linka und C. H. Kindler. „Shone-Anomalie“. Der Anaesthesist 54, Nr. 1 (Januar 2005): 29–34. http://dx.doi.org/10.1007/s00101-004-0781-2.

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39

Chandra, Sharad, Rajiv Bharat Kharwar und Ajeya Mundhekar. „Shone Complex“. Journal of Cardiovascular Ultrasound 23, Nr. 1 (2015): 54. http://dx.doi.org/10.4250/jcu.2015.23.1.54.

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40

KOBAYASHI, Shoei. „Honen Shonin's Conception of a Ojo“. Journal of Research Society of Buddhism and Cultural Heritage, Nr. 10 (2001): 108–35. http://dx.doi.org/10.5845/bukkyobunka.2001.108.

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41

OKAMOTO, Sadao. „Ippen Shonin's Marital Status: A Reexamination“. JOURNAL OF INDIAN AND BUDDHIST STUDIES (INDOGAKU BUKKYOGAKU KENKYU) 55, Nr. 1 (2006): 174–77. http://dx.doi.org/10.4259/ibk.55.174.

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42

Risteski, Petar, Oana Bartos, Aleksandra Miskovic und Thomas Walther. „An Incomplete Form of Shone’s Complex With Double Orifice Mitral Valve“. Heart Surgery Forum 24, Nr. 1 (02.02.2021): E079—E081. http://dx.doi.org/10.1532/hsf.3239.

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We present the case of an adult male patient with an incomplete form of Shone’s complex associated with bicuspid aortic valve and a double orifice mitral valve. Intraoperative inspection of the mitral valve showed double orifice configuration with a small, rudimentary left-sided mitral valve and a large, dominant, right-sided parachute mitral valve with Barlow-type of degeneration. The patient underwent reconstruction of both valves through a minimally invasive incision. At one year echocardiographic control both valves function normally.

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43

Gil, Katarzyna Elżbieta, Christine Jellis und Brian Griffin. „Unrecognized incomplete Shone’s complex. Awareness is key in congenital heart disease“. Kardiologia Polska 80, Nr. 7-8 (31.08.2022): 859–60. http://dx.doi.org/10.33963/kp.a2022.0136.

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44

Castro, L. Ferreira, A. R. Andrade, J. Portela Dias, M. Magalhães, J. Braga und L. Guedes Martins. „VP22.22: Prenatal diagnosis of Shone's syndrome: ultrasonographic findings and parental counselling“. Ultrasound in Obstetrics & Gynecology 58, S1 (Oktober 2021): 193. http://dx.doi.org/10.1002/uog.24366.

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45

Ekici, Berkay. „Shone’s complex with dextrocardia and situs inversus totalis: a case report“. Turk Kardiyoloji Dernegi Arsivi-Archives of the Turkish Society of Cardiology 40, Nr. 7 (2012): 612–14. http://dx.doi.org/10.5543/tkda.2012.70750.

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46

Koelble, Nicole, Branko M. Weiss, Joseph Wisser, Rolf Jenni, Juraj Turina, Albert Huch und Marco I. Turina. „Shone's anomaly complicated by ascending aortic aneurysm in a pregnant woman“. Journal of Cardiothoracic and Vascular Anesthesia 15, Nr. 1 (Februar 2001): 84–87. http://dx.doi.org/10.1053/jcan.2001.20281.

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47

Pizzuto, Matthew F., und Jeffrey D. Zampi. „Left main coronary artery atresia in an infant with Shone’s complex“. Cardiology in the Young 26, Nr. 5 (22.02.2016): 991–92. http://dx.doi.org/10.1017/s1047951116000019.

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AbstractA 6-month-old infant with Shone’s complex was found to have left main coronary artery atresia during evaluation for recurrent subaortic stenosis with depressed left ventricular function. The ventricular function improved after surgical subaortic resection without coronary re-vascularisation. This case demonstrates first the rare finding of left main coronary artery atresia and second that coronary re-vascularisation is not necessarily required in all cases of left main coronary artery atresia.

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48

Kohli, Utkarsh. „Shone’s complex in a patient with chromosome 9q34.3 deletion (Kleefstra syndrome)“. Cardiology in the Young 29, Nr. 2 (26.12.2018): 249–51. http://dx.doi.org/10.1017/s104795111800210x.

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AbstractKleefstra syndrome (chromosome 9q34.3 deletion) is a rare genetic disorder with less than 110 patients reported till date. We report a 4-month-old Caucasian girl with Kleefstra syndrome and Shone’s complex, an association which has not been previously reported. Surgical planning for patients with Kleefstra syndrome and complex CHD can pose challenges due to an uncertain natural history and a risk of post-operative pulmonary hypertension.

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49

Woleben, Chris, und Antonio E. Muñiz. „ped-3. Shoneʼs Complex Presenting as an Acute Life-threatening Event.“ Southern Medical Journal 96, Supplement (November 2003): S71. http://dx.doi.org/10.1097/00007611-200311001-00215.

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50

Tsiotou, A. G., P. Matsota, E. Kouptsova und M. Papageorgiou-Brousta. „Use of remifentanil in an infant with surgically repaired Shone's syndrome“. Pediatric Anesthesia 14, Nr. 3 (März 2004): 261–64. http://dx.doi.org/10.1046/j.1460-9592.2003.01135.x.

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Zeitschriftenartikel zum Thema „Shonens“

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