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Published: 26 July 2024
Last updated: 26 July 2024

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1

Tanner, Stuart. "Wilson Disease." Journal of Pediatric Gastroenterology and Nutrition 54, no. 1 (January 2012): 6–7. http://dx.doi.org/10.1097/mpg.0b013e3182301328.

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2

Iorio, Raffaele, and Giusy Ranucci. "Wilson Disease." Journal of Pediatric Gastroenterology and Nutrition 60, no. 4 (April 2015): 423–24. http://dx.doi.org/10.1097/mpg.0000000000000725.

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3

Thiel, Markus. "«Ich mag coole CHARAKTERE»." Opernwelt 63, no. 8 (2022): 34–37. http://dx.doi.org/10.5771/0030-3690-2022-8-034.

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Zwischen ihr und Puccinis Manon Lescaut gibt es einen wesentlichen Unterschied: RACHAEL WILSON hat die Wüste verlassen. Und eine große Karriere noch vor sich. Ein Gespräch über Kulturschocks, inneren und äußeren Druck sowie den großen Vorteil, Mezzosopranistin zu sein VON MARKUS THIEL
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4

Wiernicka, Anna, Maciej Dądalski, Wojciech Jańczyk, Diana Kamińska, Magdalena Naorniakowska, Anna Hüsing-Kabar, Hartmut Schmidt, and Piotr Socha. "Early Onset of Wilson Disease." Journal of Pediatric Gastroenterology and Nutrition 65, no. 5 (November 2017): 555–60. http://dx.doi.org/10.1097/mpg.0000000000001700.

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5

Horslen, Simon, and Si Houn Hahn. "Genotype-Phenotype Correlation in Wilson Disease." Journal of Clinical Gastroenterology 44, no. 6 (July 2010): 387–88. http://dx.doi.org/10.1097/mcg.0b013e3181d96ac4.

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6

Sheffer, Jolie A. "Melting Pot Modernism by Sarah Wilson." MFS Modern Fiction Studies 60, no. 2 (2014): 413–16. http://dx.doi.org/10.1353/mfs.2014.0032.

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7

Kämpfer, Ingrid, Anita Seese, Angelika Schäfer, M. Reuter, J. Lößner, J. Dietrich, A. Wagner, W. H. Knapp, and Simone Bettin. "Striatale Aufnahme von 1-123-ß-CIT und I-123-IBZM bei Patienten mit extrapyramidaler Symptomatik." Nuklearmedizin 36, no. 05 (1997): 167–72. http://dx.doi.org/10.1055/s-0038-1629787.

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Zusammenfassung Ziel: In der vorliegenden Pilotstudie wurde untersucht, ob charakteristische Veränderungen der Dopamintransportfunktion und der D2-Bin-dungskapazität bei Patienten mit der klinischen Diagnose eines idiopathischen Parkinson-Syndroms (IPS) mit der SPET nachgewiesen werden können und ob sich diese Veränderungen von jenen unterscheiden, die mit sekundärem Parkinson-Syndrom (SPS) einhergehen. Methode: Bei 16 Patienten wurden SPET-Studien (Doppelkopfkamera) sowohl mit I-123-ß-CIT als auch mit I-123-IBZM 20-24 h p.i. bzw. 2 h p.i. durchgeführt (darunter 6 Pt. mit IPS, 6 Pt. mit SPS außer M. Wilson und 4 Pt. mit M. Wilson). Die Auswertung der ß-CIT-Studien erfolgte auf der Grundlage der Aktivitätsrelationen zwischen Basalganglien (BG) und Cerebellum (CER), die der IBZM-Studien unter Verwendung von BG und medialem frontalen Kortex (MFC). Ergebnisse: Die Relation BG/CER für 1-123-ß-CIT betrug 3,04 ± 0,83 bei IPS und 7,73 ± 3,28 bei SPS ohne Morbus Wilson (p< 0,05). Die Relation BG/MFC für I-123-IBZM war bei IPS jeweils kontralateral zur Symptomatik erhöht (MW = 1,75 ± 0,12 gegenüber 1,61 ± 0,16). Die entsprechenden Werte bei SPS waren gegenüber denen bei IPS nur mäßig, aber signifikant vermindert (1,58 ± 0,24 vs. 1,68 ± 0,16). Bei den Patienten mit M. Wilson war die Relation BG/MFC für IBZM zum Teil erheblich vermindert (bis 1,29), während die I-123-ß-CIT-Aufnahme mit BG/CER-Relationen von 8,00 ± 2,90 gegenüber der von Patienten mit SPS (p < 0,01) nur gering reduziert war. Schlußfolgerung: Es wird gefolgert, daß die beiden verwendeten Radiopharmaka zwar tendenziell die bei den untersuchten Krankheitsbildern erwarteten neurochemischen Veränderungen darzustellen in der Lage sind, daß aber eine Differenzierung zwischen IPS und SPS eher mit I-123-ß-CIT gelingt als mit I-123-IBZM.
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8

Valentino, Pamela L., Eve A. Roberts, Stacey Beer, Tamir Miloh, Ronen Arnon, Jennifer M. Vittorio, and Michael L. Schilsky. "Management of Wilson Disease Diagnosed in Infancy." Journal of Pediatric Gastroenterology and Nutrition 70, no. 5 (May 2020): 547–54. http://dx.doi.org/10.1097/mpg.0000000000002608.

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9

Manolaki, Nina, Georgia Nikolopoulou, George L. Daikos, Eleni Panagiotakaki, Maria Tzetis, Eleftheria Roma, Emmanouel Kanavakis, and Vassiliki P. Syriopoulou. "Wilson Disease in Children: Analysis of 57 Cases." Journal of Pediatric Gastroenterology and Nutrition 48, no. 1 (January 2009): 72–77. http://dx.doi.org/10.1097/mpg.0b013e31817d80b8.

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10

Ranucci, Giusy, Fabiola Di Dato, Federica Leone, Pietro Vajro, Maria Immacolata Spagnuolo, and Raffaele Iorio. "Penicillamine-induced Elastosis Perforans Serpiginosa in Wilson Disease." Journal of Pediatric Gastroenterology and Nutrition 64, no. 3 (March 2017): e72-e73. http://dx.doi.org/10.1097/mpg.0000000000000613.

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11

Selimoglu, Mukadder Ayse, Vildan Ertekin, Hakan Doneray, and Mustafa Yildirim. "Bone Mineral Density of Children With Wilson Disease." Journal of Clinical Gastroenterology 42, no. 2 (February 2008): 194–98. http://dx.doi.org/10.1097/mcg.0b013e318032388d.

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12

Azcoiti, V., G. Di Carlo, A. Galante, A. F. Grillo, and V. Laliena. "The Schwinger model with Wilson fermions in the MFA approach." Nuclear Physics B - Proceedings Supplements 47, no. 1-3 (March 1996): 687–90. http://dx.doi.org/10.1016/0920-5632(96)00151-x.

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13

Medici, Valentina, Carlo Pietro Trevisan, Renata D??Inc??, Michela Barollo, Lucia Zancan, Stefano Fagiuoli, Diego Martines, Paola Irato, and Giacomo Carlo Sturniolo. "Diagnosis and Management of Wilson??s Disease." Journal of Clinical Gastroenterology 40, no. 10 (November 2006): 936–41. http://dx.doi.org/10.1097/01.mcg.0000225670.91722.59.

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14

Van Biervliet, Stephanie, Sébastien Küry, Ruth De Bruyne, Olivier M. Vanakker, Sébastien Schmitt, Saskia Vande Velde, Eric Blouin, and Stéphane Bézieau. "Clinical Zinc Deficiency as Early Presentation of Wilson Disease." Journal of Pediatric Gastroenterology and Nutrition 60, no. 4 (April 2015): 457–59. http://dx.doi.org/10.1097/mpg.0000000000000628.

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15

Juhász, Lilla. "Civil társadalom, modernizáció, IKT." Információs Társadalom 5, no. 1 (March 1, 2005): 61. http://dx.doi.org/10.22503/inftars.v.2005.1.4.

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A tanulmány Ernest J. Wilson elméletét felhasználva mutatja be a modern társadalmak ipari társadalomból információs társadalommá történő fejődésének útját, különös hangsúlyt helyezve a struktúrák működésének vizsgálatára, melyben a rendszer egészének működését az egyének és az egyes társadalmi alrendszerek mindent átszövő kapcsolati hálói határozzák meg. A modell ismertetése után a szerző vázolja a civil társadalom működési lehetőségeit a virtuális térben.
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16

Durand, Fran??ois. "Wilson??s disease: an old disease keeps its old secrets." European Journal of Gastroenterology & Hepatology 19, no. 2 (February 2007): 97–99. http://dx.doi.org/10.1097/meg.0b013e32800fef34.

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17

Schaefer, Mark, Daniel N. Gotthardt, Christian Didion, Wolfgang Stremmel, and Karl H. Weiss. "Increased Prevalence of Subcutaneous Lipomas in Patients With Wilson Disease." Journal of Clinical Gastroenterology 49, no. 7 (August 2015): e61-e63. http://dx.doi.org/10.1097/mcg.0000000000000248.

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18

Johnson, Kerry L. "Translations of Gender, Pain and Space: Wilson Harris's The Carnival Trilogy." MFS Modern Fiction Studies 44, no. 1 (1998): 123–43. http://dx.doi.org/10.1353/mfs.1998.0005.

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19

Mosca, Antonella, Francesco Nicita, Alessandro Capuano, and Valerio Nobili. "Wilson Disease in a Child With Mild Neuropsychiatric and Hepatic Involvement." Journal of Pediatric Gastroenterology & Nutrition 69, no. 4 (October 2019): e118-e119. http://dx.doi.org/10.1097/mpg.0000000000002433.

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20

Proost, Renee, David Cassiman, Elena Levtchenko, Eva Morava-Kozicz, Jef Neirynck, and Peter Witters. "Fulminant Wilson Disease in Children: Recovery After Plasma Exchange Without Transplantation." Journal of Pediatric Gastroenterology & Nutrition 71, no. 6 (August 12, 2020): 720–25. http://dx.doi.org/10.1097/mpg.0000000000002894.

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21

Santiago, Raoul, Frédéric Gottrand, Dominique Debray, Laure Bridoux, Alain Lachaux, Alain Morali, Delphine Lapeyre, and Thierry Lamireau. "Zinc Therapy for Wilson Disease in Children in French Pediatric Centers." Journal of Pediatric Gastroenterology and Nutrition 61, no. 6 (December 2015): 613–18. http://dx.doi.org/10.1097/mpg.0000000000000926.

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22

Sintusek, Palittiya, and Anil Dhawan. "Aberrance of Serum Zinc and Free Copper Level in Wilson Disease." Journal of Pediatric Gastroenterology and Nutrition 62, no. 5 (May 2016): e46. http://dx.doi.org/10.1097/mpg.0000000000001084.

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23

Sturm, Ekkehard, Femke E. Piersma, Malcolm S. Tanner, Piotr Socha, Eve A. Roberts, and Benjamin L. Shneider. "Controversies and Variation in Diagnosing and Treating Children With Wilson Disease." Journal of Pediatric Gastroenterology & Nutrition 63, no. 1 (July 2016): 82–87. http://dx.doi.org/10.1097/mpg.0000000000001102.

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24

Iorio, Raffaele, and Giusy Ranucci. "Aberrance of Serum Zinc and Free Copper Level in Wilson Disease." Journal of Pediatric Gastroenterology and Nutrition 62, no. 5 (May 2016): e46. http://dx.doi.org/10.1097/mpg.0000000000001159.

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25

Lévai, Dániel. "Roosevelt és Truman: a második világháborús amerikai külpolitikai tervezés és valóság Kelet-Ázsia kontextusában." Külügyi Szemle 22, no. 4 (2023): 7–27. http://dx.doi.org/10.47707/kulugyi_szemle.2023.4.2.

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Franklin Delano Rooseveltet és Harry Spencer Trumant az amerikai globális szerepvállalás történetében az alapító atyákként tartják számon. A két elnök a második világháború során az Amerikai Egyesült Államokat a szuperhatalmi pozícióba vezette. Néhány ciklussal előttük a hivatalt Thomas Woodrow Wilson töltötte be, aki 1918-ban fektette le az ország külpolitikai alapvetését: a világ biztonságosabbá tételét a demokrácia számára. Roosevelt az ő örökségét fejlesztette tovább és valósította meg. A világégés idején, a realitásokat figyelembe véve dolgozta ki a háború utáni világrend koncepcióját, amelynek a gyakorlati megvalósítását azonban már nem élhette meg. Az utódja, Harry S. Truman 143 nap alatt képes volt elérni a roosevelti célkitűzéseket, mégpedig egy rohamosan romló szövetségesi együttműködés keretében. A jelen tanulmány a kelet-ázsiai kontextuson keresztül, a korabeli amerikai külpolitikai stratégia akkori kulcsterületének számító régió helyzetének az elemző bemutatásával vizsgálja meg Roosevelt és Truman második világháború alatti külpolitikáját.
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26

Irmer, Thomas. "The History of Dance as Hypertext." Maska 33, no. 189 (June 1, 2018): 116–17. http://dx.doi.org/10.1386/maska.33.189-190.116_5.

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This review presents Transforming Acts, a theatrical installation conceived by Penelope Wehrli and Detlev Schneider in 2014, which brings more than a hundred hours of documentary footage of performances and interviews with their authors, Pina Bausch, Laurent Chétouan, Joe Fabian, Jan Fabre, Johann Kresnik, Thomas Lehmen, Heiner Müller, Einar Schleef, Meg Stuart, Robert Wilson and others. The arrangement enabling their simultaneous screenings on five screens establishes numerous new connections between their works and thoughts.
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27

Lorente-Arencibia, Pascual, Luis García-Villarreal, Rafaela González-Montelongo, Luis A. Rubio-Rodríguez, Carlos Flores, Paloma Garay-Sánchez, Tanausú delaCruz, et al. "Wilson Disease Prevalence: Discrepancy Between Clinical Records, Registries and Mutation Carrier Frequency." Journal of Pediatric Gastroenterology & Nutrition 74, no. 2 (October 5, 2021): 192–99. http://dx.doi.org/10.1097/mpg.0000000000003322.

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28

Wong, Robert J., Robert Gish, Michael Schilsky, and Catherine Frenette. "A Clinical Assessment of Wilson Disease in Patients With Concurrent Liver Disease." Journal of Clinical Gastroenterology 45, no. 3 (March 2011): 267–73. http://dx.doi.org/10.1097/mcg.0b013e3181dffaa5.

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29

Yu, Zizi, Johanna Sheu Song, Birgitta Schmidt, Kristen Corey, and Elena B. Hawryluk. "Pediatric Pseudo-pseudoxanthoma Elasticum Resulting From D-Penicillamine Treatment for Wilson Disease." Journal of Pediatric Gastroenterology & Nutrition 71, no. 6 (August 7, 2020): 731–33. http://dx.doi.org/10.1097/mpg.0000000000002888.

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30

Fischer, Ryan T., Kyle A. Soltys, Robert H. Squires, Ronald Jaffe, George V. Mazariegos, and Benjamin L. Shneider. "Prognostic Scoring Indices in Wilson Disease: A Case Series and Cautionary Tale." Journal of Pediatric Gastroenterology and Nutrition 52, no. 4 (April 2011): 466–69. http://dx.doi.org/10.1097/mpg.0b013e31820b0211.

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31

Loudianos, Georgios, Antonietta Zappu, Maria B. Lepori, Valentina Dessì, Eva Mameli, Sandra Orrù, Rosa A. Podda, and Stefano De Virgiliis. "Acute Liver Failure Because of Wilson Disease With Overlapping Autoimmune Hepatitis Features." Journal of Pediatric Gastroenterology and Nutrition 63, no. 2 (August 2016): e23-e24. http://dx.doi.org/10.1097/mpg.0000000000000557.

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32

Favre, Emilie, Laurence Lion-François, Marie Canton, Claire Vanlemmens, Marjorie Bonneton, Lise Bouillet, Anne-Sophie Brunet, and Alain Lachaux. "Cognitive Abilities of Children With Neurological and Liver Forms of Wilson Disease." Journal of Pediatric Gastroenterology and Nutrition 64, no. 3 (March 2017): 436–39. http://dx.doi.org/10.1097/mpg.0000000000001346.

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33

Haftu, Hansa, Mohammed Mustefa, and Teklu Gebrehiwot. "Zinc Monotherapy as an Alternative Treatment Option for Decompensated Liver Disease due to Wilson Disease?" Case Reports in Hepatology 2020 (January 14, 2020): 1–5. http://dx.doi.org/10.1155/2020/1275940.

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Background. Wilson disease is a rare metabolic disorder involving copper metabolism, and patients may present with a variable degree of hepatic, neurologic, and psychiatric manifestations. In the case of hepatic presentation, treatment is usually initiated with potentially toxic copper chelators (D-penicillamine or Trenton). Although zinc is of low toxicity and low cost for treatment of Wilson disease, it has been limited to the adjunctive as a single maintenance drug or for asymptomatic patients. The use of zinc monotherapy in patients suffering from a severe liver disease was not well studied. In our case report, we describe a pediatric patient who presented with liver failure and the use of zinc monotherapy in patients with severe hepatic manifestations. Case presentation. A 15-year-old male patient from Ethiopia presented with generalized body swelling (edema and ascites) with yellowish discoloration of his eyes and easy fatigability. He had hyperbilirubinemia, coagulopathy, hypoalbuminemia, and deranged liver enzymes. He had a Keyser–Fleischer ring visible with the naked eye, which was confirmed by slit-lamp examination. He had very low serum ceruloplasmin (<8 mg/L) and high 24-hour urine copper (150 mcg/dl). In accordance with the scoring system proposed by the 8th International Meeting on Wilson Disease and Menkes Disease, a diagnosis of Wilson disease was made. Zinc monotherapy with low copper diet was initiated for decompensated liver disease due to Wilson disease because of the inaccessibility of chelators (D-penicillamine or Trientine). After months of treatment with zinc, the patient experienced normalization of hepatic synthetic function and resolution of hypoalbuminemia and coagulopathy. The patient had also clinically stabilized (ascites, lower extremity swelling, edema, and jaundice were improved. Currently, the patient is on follow-up almost for the last four years in the gastrointestinal clinic. Conclusion. Our case shows that zinc has the potential for treatment in improving liver function. Though zinc has its own side effects, it is important and maybe an alternative treatment option in those with limited resources (not able to access chelators). This example hopefully will encourage future investigations and researches on zinc monotherapy for treating symptomatic decompensated hepatic Wilson disease.
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34

Barada, Kassem, Mazen El-Atrache, Ihab I. El-Hajj, Khaled Rida, Jida El-Hajjar, Ziyad Mahfoud, and Julnar Usta. "Homozygous Mutations in the Conserved ATP Hinge Region of the Wilson Disease Gene." Journal of Clinical Gastroenterology 44, no. 6 (July 2010): 432–39. http://dx.doi.org/10.1097/mcg.0b013e3181ce5138.

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35

Peña-Quintana, Luis, María R. García-Luzardo, Luis García-Villarreal, María D. Arias-Santos, Paloma Garay-Sánchez, Alfredo Santana, Daniel González-Santana, Juan C. Ramos-Varela, Ramiro Rial-González, and Antonio Tugores. "Manifestations and Evolution of Wilson Disease in Pediatric Patients Carrying ATP7B Mutation L708P." Journal of Pediatric Gastroenterology and Nutrition 54, no. 1 (January 2012): 48–54. http://dx.doi.org/10.1097/mpg.0b013e318230130c.

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36

Mizuochi, Tatsuki, Akihiko Kimura, Norikazu Shimizu, Hiroshi Nishiura, Masami Matsushita, and Makoto Yoshino. "Zinc Monotherapy From Time of Diagnosis for Young Pediatric Patients With Presymptomatic Wilson Disease." Journal of Pediatric Gastroenterology and Nutrition 53, no. 4 (October 2011): 365–67. http://dx.doi.org/10.1097/mpg.0b013e31821d5abe.

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37

Eckstein, Barbara J. "Postcolonial Narrative and the Work of Mourning: J.M. Coetzee, Wilson Harris, and Toni Morrison (review)." MFS Modern Fiction Studies 51, no. 3 (2005): 714–17. http://dx.doi.org/10.1353/mfs.2005.0057.

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38

Arnon, Ronen, Judith Flores Calderon, Michael Schilsky, Sukru Emre, and Benjamin L. Shneider. "Wilson Disease in Children: Serum Aminotransferases and Urinary Copper on Triethylene Tetramine Dihydrochloride (Trientine) Treatment." Journal of Pediatric Gastroenterology and Nutrition 44, no. 5 (May 2007): 596–602. http://dx.doi.org/10.1097/mpg.0b013e3180467715.

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39

Abdelaziz, A. E., Y. H. M. Hendy, A. Shokry, S. M. Saad, F. Y. Kamal, and K. A. Edris. "AN ASTROMETRIC AND PHOTOMETRIC STUDY OF THE INTERMEDIATE-AGE OPEN CLUSTER NGC 2158 AND ITS ECLIPSING BINARY [NBN2015]78." Revista Mexicana de Astronomía y Astrofísica 56, no. 2 (October 1, 2020): 245–57. http://dx.doi.org/10.22201/ia.01851101p.2020.56.02.07.

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We present a photometric and astrometric analysis of the NGC 2158 cluster using Gaia DR2 and 2MASS data. The cluster age, color excess, intrinsic distance modulus and distance are calculated to be t = 2.240 ± 0.260 Gyr, E(B − V) = 0.420 ± 0.050 mag, (m − M)⨀ = 12.540 ± 0.130 mag and d⨀ = 3224 ± 200 pc respectively. The photometric analysis and light curve modelling of the proposed eclipsing binary member [NBN2015]78 is performed using the latest version of the Wilson-Devinney (W-D) code. The solutions show that the system is an over-contact binary with a secondary component filling its Roche lobe, with a mass ratio q = 0.262. The primary and the secondary components of the system consist of two late spectral types K1 and K2 respectively. The membership of [NBN2015]78 is discussed using two independent methods, and we find that [NBN2015]78 is an interloper and not a member of NGC 2158.
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40

Zimmerman, Marc. "Myth and History in Caribbean Fiction: Alejo Carpentier, Wilson Harris and Edouard Glissant (review)." MFS Modern Fiction Studies 40, no. 1 (1994): 168–69. http://dx.doi.org/10.1353/mfs.0.0994.

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41

Akyldz, Basak Nur, Songul Yldrm, Meda Kondolot, and Duran Arslan. "Is Plasma Exchange Effective in Prevention of Hepatic Transplantation in Fulminant Wilson Disease With Hepatic Failure?" Journal of Pediatric Gastroenterology and Nutrition 52, no. 6 (June 2011): 778–80. http://dx.doi.org/10.1097/mpg.0b013e318208d0a3.

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42

Rustom, Najla, Muriel Bost, Fleur Cour-Andlauer, Alain Lachaux, Anne-Sophie Brunet, Olivier Boillot, Fabienne Bordet, Frederic Valla, Nathalie Richard, and Etienne Javouhey. "Effect of Molecular Adsorbents Recirculating System Treatment in Children With Acute Liver Failure Caused by Wilson Disease." Journal of Pediatric Gastroenterology and Nutrition 58, no. 2 (February 2014): 160–64. http://dx.doi.org/10.1097/mpg.0b013e3182a853a3.

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43

Sintusek, Palittiya, Eirini Kyrana, and Anil Dhawan. "Value of Serum Zinc in Diagnosing and Assessing Severity of Liver Disease in Children With Wilson Disease." Journal of Pediatric Gastroenterology and Nutrition 67, no. 3 (September 2018): 377–82. http://dx.doi.org/10.1097/mpg.0000000000002007.

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44

Folhoffer, Aniko, Peter Ferenci, Timea Csak, Andrea Horvath, Dalma Hegedus, Gabor Firneisz, Janos Osztovits, et al. "Novel mutations of the ATP7B gene among 109 Hungarian patients with Wilson??s disease." European Journal of Gastroenterology & Hepatology 19, no. 2 (February 2007): 105–11. http://dx.doi.org/10.1097/01.meg.0000223904.70492.0b.

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45

Balogh, Beatrix. "Puritán apokaliptika: amerikai küldetéstudat és történelemszemlélet." Axis 4, no. 1 (July 7, 2023): 129–43. http://dx.doi.org/10.61176/axis.2023.4.1.11.

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Az amerikai nemzeti önmeghatározás szerves része a küldetéstudat, az Isten kiválasztott népeként feladatot kapott nemzet történelmi fejlődésútja, mely először a puritán kivándorlásban nyilvánul meg. A különlegességtudat, a vallásos háttér és az óhaza hibáinak meghaladása mellett leginkább a forradalomban kikristályosodott és alkotmányba foglalt szabadság- és demokráciaeszményekből és azok terjesztéséből táplálkozik. Ezek szorosan összeforrottak az idők folyamán, Woodrow Wilson a küldetést már úgy definiálta, hogy Amerikának „a világot biztonságossá kell tennie a demokrácia számára”. Azonban a puritánokról és szerepükről alkotott véleménykülönbségek mellett abban konszenzus van, hogy a John Winthrop által 1630-ban meghirdetett politikai-társadalmi rendszer és erkölcsi normák az amerikai történelmi fejlődés meghatározó alapkövei, a winthropi „város a hegyen” pedig az amerikai különlegességtudat, az „excepcionalizmus” elsődleges kifejeződése.
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46

Niethammer, Barbara. "Book review: “Analytic Methods for Coagulation-Fragmentation Models, Volumes I + II” by Jacek Banasiak, Wilson Lamb and Philippe Laurençot." European Mathematical Society Magazine, no. 123 (February 25, 2022): 54–56. http://dx.doi.org/10.4171/mag/77.

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47

Niethammer, Barbara. "Book review: “Analytic Methods for Coagulation-Fragmentation Models, Volumes I + II” by Jacek Banasiak, Wilson Lamb and Philippe Laurençot." European Mathematical Society Magazine, no. 123 (February 25, 2022): 54–56. http://dx.doi.org/10.4171/mag-77.

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48

Antonietta, Zappu, Magli Olympia, Maria Barbara Lepori, Dessì Valentina, Diana Stefania, Incollu Simona, Kanavakis Emmanuel, et al. "High Incidence and Allelic Homogeneity of Wilson Disease in 2 Isolated Populations: A Prerequisite for Efficient Disease Prevention Programs." Journal of Pediatric Gastroenterology and Nutrition 47, no. 3 (September 2008): 334–38. http://dx.doi.org/10.1097/mpg.0b013e31817094f6.

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49

Tampaki, Maria, Nikolaos K. Gatselis, Spyridon Savvanis, Emmanouil Koullias, Asterios Saitis, Stella Gabeta, Melanie Deutsch, Emmanouil Manesis, Georgios N. Dalekos, and John Koskinas. "Wilson disease: 30-year data on epidemiology, clinical presentation, treatment modalities and disease outcomes from two tertiary Greek centers." European Journal of Gastroenterology & Hepatology 32, no. 12 (February 27, 2020): 1545–52. http://dx.doi.org/10.1097/meg.0000000000001670.

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50

Pilon, Juliana Geran. "Meg Wilson, Health Behaviors of Homeless Women: Using a Cross-selectional, Descriptive, and Non Experimental Design." Gender Issues 25, no. 3 (September 2008): 210–13. http://dx.doi.org/10.1007/s12147-008-9059-3.

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