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Journal articles on the topic 'Wegener'

Author: Grafiati

Published: 4 June 2021

Last updated: 27 January 2023

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1

Nithyanandham Masilamani and Dhanraj Ganapathy. "Awareness About Wegeners Granulomatosis Disease Among Dental Students." International Journal of Research in Pharmaceutical Sciences 11, SPL3 (October 7, 2020): 1081–84. http://dx.doi.org/10.26452/ijrps.v11ispl3.3339.

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Wegener’s granulomatosis (WG) is a systemic disease characterized by necrotizing granulomatous inflammation of the upper and lower respiratory tract, glomerulonephritis, and vasculitis. The clinical manifestations and laboratory findings suggest an autoimmune disease resulting from a hypersensitivity reaction to some environmental agent. The purpose of the survey is for assessing the awareness about wegeners granulomatosis disease amongst dental students. A cross-sectional survey was done with questionnaire comprising a total of ten multiple-choice questions which were distributed to 100 undergraduate dental students. The questions elicited awareness about the etiology, clinical features, diagnostic tests, treatment methods and complications of wegeners granulomatosis. The responses were collected and analysed. 7% were aware of etiology of Wegeners granulomatosis, 9% were aware of clinical features of Wegeners granulomatosis, 5% were aware of diagnostic tests of Wegeners granulomatosis, 5% were aware of the treatment of Wegeners granulomatosis, and 4% were aware of complications of Wegeners granulomatosis. The awareness of Wegener's granulomatosis among dental students is inadequate. Granulomatosis of Wegener is a relatively uncommon, autoimmune condition of unknown origin. Without medication, thus many patients would then inevitably die of those same illness. Therefore, awareness and education initiatives must be pursued to enlighten students about this illness.

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2

Socias, R., D. G. James, and A. Pozniak. "Wegener and Wegener's granulomatosis." Thorax 42, no. 12 (December 1, 1987): 920–21. http://dx.doi.org/10.1136/thx.42.12.920.

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3

Kolyvanos Naumann, Urania, Käser, and Vetter. "Wegener Granulomatose (Morbus Wegener)." Praxis 92, no. 46 (November 1, 2003): 1943–47. http://dx.doi.org/10.1024/0369-8394.92.46.1943.

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4

Bachmeyer, Claude, and Bruno Halioua. "“Granulomatosis With Polyangiitis (Wegener's)” for “Wegener Granulomatosis”." JAMA Dermatology 149, no. 5 (May 1, 2013): 526. http://dx.doi.org/10.1001/jamadermatol.2013.2060.

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5

Greene, Mott. "Alfred Wegener and the Origin of Lunar Craters." Earth Sciences History 17, no. 2 (January 1, 1998): 111–38. http://dx.doi.org/10.17704/eshi.17.2.b342311n1w401vv7.

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Alfred Wegener is universally known for his work on continental drift, but Wegener also made an interesting contribution, just after the First World War, to the study of lunar craters. Wegener reviewed the various hypotheses for lunar cratering, evaluated them from the standpoint of physics, and then performed a series of simple but ingenious experiments from which he concluded that the craters were impact phenomena, occasionally accompanied by secondary melting. This work was probably more important for the theory of scale models in geophysical experiments than it was to the history of selenology, but Wegener's view that lunar craters were impact phenomena and (perhaps more significantly) the reasoning on which he based this conclusion are now generally accepted, along with his once-scorned ideas on continental mobility.

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6

Barzilay, Willemjan. "Vening Meinesz and the theory of Wegener." Earth Sciences History 29, no. 2 (December 1, 2010): 213–31. http://dx.doi.org/10.17704/eshi.29.2.j767410043u34111.

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The Dutch geophysicist Felix Vening Meinesz is a familiar name in the history of plate tectonics, because of his discovery of the so-called Meinesz zone, a large-scale gravity anomaly in Indonesia. However, what is not familiar is how he himself viewed the theory of Wegener. This article traces how Vening Meinesz thought about Wegener's theory, how it related to his scientific work and how his view of it changed during his career. Vening Meinesz influenced how Dutch geologists thought about Wegener's theory.

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7

Greenbaum, Larry. "Wegener Granulomatosis." Annals of Internal Medicine 117, no. 7 (October 1, 1992): 619. http://dx.doi.org/10.7326/0003-4819-117-7-619_2.

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8

QURESHI, NAUSHEEN. "WEGENER GRANULOMATOSIS." Professional Medical Journal 15, no. 01 (March 10, 2008): 13–19. http://dx.doi.org/10.29309/tpmj/2008.15.01.2690.

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Objective: To highlight the different clinical features, parameters of diagnosis and to see the effectof chemotherapy and steroids on this disease. Setting: Department of Otolaryngology Head & Neck Surgery JinnahHospital Lahore. Period: From Dec 1998 to July 2001.Methods: Five cases of Wegener Granulomatosis were studiedduring the study period. Three patients had limited disease while two patients had generalized disease with renalinvolvement. All patients were started on azathiopurine (2mg/Kg/day) or cyclophoshamide (1-2mg/km/day) along withsteroids. After a months time the dose of steroid was reduced to alternate day. Weekly monitoring of white blood cellcount with urine examination for RBCs or protein casts was done. Any patient with haematuria or TLC reduced to lessthan 3500 were immediately taken off from cyclophoshamide and azathiopurine was started. Patients having classicdisease , dose of cyclophoshamide had to be increased from two to four milligram / per Kilogram per day to achievea good response. The response to treatment was measured by noticing the resolution of pulmonary infiltrates reducedESR and negative C-ANCA. Results: We found nasal symptoms like nasal obstruction and epistaxis to be the mostcommon symptom followed by fever, cough and deafness. Crusting, granulations and occasional perforation wereusually found on nasal examination. Conductive deafness wasmost common ear finding. History, clinical examination,ESR, C-ANCA and a representative biopsy were all essential in diagnosing this condition. Azathiopurine andcyclophosphamidewere the main chemotherapeutic agents used with prednisone to cause remission in all our patientsexcept one who died two weeks after having been admitted in our institution. Surprisingly in contrast to the normalcause of high mortality reported in international literature in this disease to be renal failure, our patient died due torespiratory failure. Four out of five patients went into remission a year after regular treatment with this regime. Themajor complications occurring during hospital stay and their treatment were nausea, vomiting, sudden fall of TLC, andoral thrush. Conclusion: The common presentation of patient with Wegner’s Granulomatosis is of upper respiratorytract symptoms like nasal obstruction and epistaxis followed by lower respiratory symptoms like cough, fever andHaemoptysis. A representative biopsy with positive C-ANCA and high ESR are hallmarks of diagnosing this condition.The most effective medical regime till today is cyclophosphamide and azathiopurine with alternate day prednisone forinducing remission.

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9

Kuhlman, Janet E., Ralph H. Hruban, and Elliot K. Fishman. "Wegener Granulomatosis." Journal of Computer Assisted Tomography 15, no. 6 (November 1991): 948–52. http://dx.doi.org/10.1097/00004728-199111000-00008.

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10

Girdler, R. "Wegener revisited." Eos, Transactions American Geophysical Union 79, no. 5 (1998): 59. http://dx.doi.org/10.1029/98eo00039.

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11

Graves, Nichole. "Wegener Granulomatosis." Baylor University Medical Center Proceedings 19, no. 4 (October 2006): 342–44. http://dx.doi.org/10.1080/08998280.2006.11928198.

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12

Jansen, Thomas, Melanie Schmidt, Dirk Sudholt, Carsten Witt, and Christine Zarges. "Ingo Wegener." Evolutionary Computation 17, no. 1 (March 2009): 1–2. http://dx.doi.org/10.1162/evco.2009.17.1.1.

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13

Koneth and Kronauer. "Wegener Granulomatose." Praxis 92, no. 37 (September 1, 2003): 1523–32. http://dx.doi.org/10.1024/0369-8394.92.37.1523.

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Nous décrivons six patients, dont quatre femmes et deux hommes, agés de 61 à 83 ans, qui ont été traités pour une Granulomatose de Wegener. Nous soulignons les symptômes et la radiologie et, en respect de notre specialité médicale, nous soulignons les aspects pulmonaires de cette vasculite. Se référant aux descriptions des cas nous discutons la présentation clinique et les aspects diagnostiques de la Granulomatose de Wegener chez une population âgée.

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14

Barra Quílez, F., P. Gutiérrez Ibañes, M. Lafuente Mateo, and M. Jiménez Ríos. "¡Era Wegener!" Medicina Intensiva 34, no. 9 (December 2010): 633–34. http://dx.doi.org/10.1016/j.medin.2010.03.006.

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15

Katsanis, Emmanuel, and Peter N. McLaine. "Wegener granulomatosis." Journal of Pediatrics 108, no. 5 (May 1986): 792. http://dx.doi.org/10.1016/s0022-3476(86)81075-7.

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16

Goerttler, K. "Kurt Wegener." Der Pathologe 29, S2 (September 28, 2008): 389–90. http://dx.doi.org/10.1007/s00292-008-1082-3.

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17

Lefrak, Stephen S., and Eric L. Matteson. "Freidrich Wegener." Chest 132, no. 6 (December 2007): 2065. http://dx.doi.org/10.1378/chest.07-2353.

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18

Lehmann, H., K. Andrassy, N. Rasmussen, and F. v. d. Woude. "Friedrich Wegener." DMW - Deutsche Medizinische Wochenschrift 116, no. 03 (August 20, 2009): 113–14. http://dx.doi.org/10.1055/s-0029-1235429.

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19

Wegener, Matt. "Matt Wegener." Fisheries 42, no. 8 (August 3, 2017): 415. http://dx.doi.org/10.1080/03632415.2017.1346997.

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20

Tompson, Lester D. R. "Wegener Granulomatosis." Ear, Nose & Throat Journal 92, no. 1 (January 2013): 18–22. http://dx.doi.org/10.1177/014556131309200107.

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21

Langford, Carol A. "Wegener Granulomatosis." American Journal of the Medical Sciences 321, no. 1 (January 2001): 76–82. http://dx.doi.org/10.1097/00000441-200101000-00011.

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22

Antonescu, Bogdan, Hugo M. A. M. Ricketts, and David M. Schultz. "100 Years Later: Reflecting on Alfred Wegener’s Contributions to Tornado Research in Europe." Bulletin of the American Meteorological Society 100, no. 4 (April 1, 2019): 567–78. http://dx.doi.org/10.1175/bams-d-17-0316.1.

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Abstract Alfred Wegener (1880–1930) was a leading geophysicist, atmospheric scientist, and an Arctic explorer who is mainly remembered today for his contributions to the theory of continental drift. Less well known are his contributions to research on tornadoes in Europe. Published 100 years ago, Wegener’s 1917 book Wind- und Wasserhosen in Europa (Tornadoes and Waterspouts in Europe) is an impressive synthesis of knowledge on tornadoes and is considered the first modern pan-European tornado climatology, with 258 reports from 1456 to 1913. Unfortunately, Wegener’s book was overlooked after the 1950s amid declining interest in tornadoes by European researchers and meteorologists. The recent revival of tornado studies in Europe invites a reflection on Wegener’s book. Using a relatively small dataset, Wegener was able to describe characteristics of tornadoes (e.g., direction of movement, speed, rotation, formation mechanism), as well as their frequency of occurrence and climatology, comparable with the results from modern tornado climatologies. Wegener’s lasting scientific contributions to tornado research are presented in the context of European research on this topic. Specifically, his book showed the utility of reports from citizen scientists and inspired other researchers, namely, Johannes Letzmann, who continued to study European tornadoes after Wegener’s death.

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23

Herrera Ariza, Jorge Luis Alfredo, and Perla Villamor Rojas. "Enfoque otorrinolaringológico de la granulomatosis con poliangeítis (de Wegener) Otolaryngologic approach to granulomatosis with polyangitis (Wegener’s)." ACTA DE OTORRINOLARINGOLOGÍA & CIRUGÍA DE CABEZA Y CUELLO 42, no. 4 (August 14, 2018): 254–62. http://dx.doi.org/10.37076/acorl.v42i4.150.

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Introducción: La granulomatosis con poliangeítis (de Wegener) es una enfermedad poco frecuente, sin embargo, el 80 a 90% de los casos tienen manifestaciones otorrinolaringológicas, muchas como único síntoma inicial de la enfermedad. Objetivos: El propósito de este artículo es revisar la literatura disponible actualizada sobre granulomatosis con poliangeítis: manifestaciones clínicas, estándares de enfoque, diagnóstico y tratamiento en otorrinolaringología. Diseño: Revisión narrativa de la literatura. Materiales y métodos: Revisión de la literatura mediante búsqueda selectiva por términos MeSH: Otorhinolaryngologic Diseases, Granulomatosis with polyangiitis, Wegener Granulomatosis, de las bases de datos:MEDLINE, Current Contents, Cochrane, Pubmed y Scielo, entre los años 2000 y 2014. Resultados: Se revisaron 39 artículos según los requerimientos de los objetivos. La evidencia científica actual reconoce la importancia del conocimiento sobre granulomatosis con poliangeítis (de Wegener) en otorrinolaringología, para obtener diagnósticos tempranos y ofrecer manejos oportunos. Conclusiones: El diagnóstico y tratamiento tempranos de la granulomatosis con poliangeítis (de Wegener) son las únicas herramientas para mejorar el pronóstico y calidad de vida de los pacientes con esta enfermedad.Introduction: Granulomatosis with polyangiitis (Wegener’s) is a rare disease,however 80% to 90% of the cases have otolaryngologic manifestations, many as initial symptoms of the disease. Objectives: The purpose of this article is to review the current literature about granulomatosis with polyangiitis: Clinic manifestations, approach standards, diagnosis and treatment in otolaryngology. Design: Narrative review. Materials and methods: Literature review by selective search for MeSH terms: Otorhinolaryngologic Diseases, granulomatosis with polyangiitis, Wegenergranulomatosis, in the databases: MEDLINE, Current Contents, Cochrane, PubMed and SciELO, between 2000 and 2014. Results: 39 articles were reviewed according to the requirements of the objectives. Current scientific evidence recognizes the importance of the knowledge about granulomatosis with polyangiitis (Wegener’s) in otolaryngology, in order to give an early diagnosis and to provide an opportune treatment. Conclusions: Early diagnosis and treatment of granulomatosis with polyangiitis (Wegener’s) are the only tools to change the prognosis as well as quality of life of patients with this disease.

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24

CAVADAS, BENTO. "FROM THE CONTRACTING EARTH TO CONTINENTAL DRIFT: WEGENER'S INFLUENCE ON PORTUGUESE AND SPANISH SCIENCE TEXTBOOKS THROUGH THE TWENTIETH CENTURY." Earth Sciences History 38, no. 1 (April 1, 2019): 74–93. http://dx.doi.org/10.17704/1944-6178-38.1.74.

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ABSTRACT Alfred Wegener's work on continental drift profoundly influenced the development of geology during the twentieth century. The main objective of this historical research is to explore how Wegener's hypothesis about the origin of continents and oceans influenced Portuguese and Spanish science textbooks published in the twentieth century. For this purpose, a qualitative method based on the Chevallard's concept of didactic transposition was used. The didactic transposition of the fundamentals of continental drift, including displacements forces and geographical, geophysical, geological, paleontological, biological, and paleoclimatic arguments used by Wegener to support this hypothesis, was studied in a comprehensive sample of twenty science textbooks published after the publication of Die Entstehung der Kontinente und Ozeane (Wegener 1915). The analysis of textbooks shows that the didactic transposition of continental drift was commonly present in Portuguese and Spanish textbooks beginning in the 1930s, although, with different degrees of development. Science textbooks since the 1950s presented the displacement forces of sial continental blocks proposed by Wegener, namely the centrifugal force of Earth's rotation and the attractive gravitational force that results from the interaction of the earth with the moon and sun. The geographical, geological, paleontological and biological arguments supporting continental drift were commonly addressed in many science textbooks, followed by the paleoclimatic arguments. The geophysical arguments were briefly addressed in only two textbooks. Many Portuguese and Spanish textbooks also presented critiques of Wegener's work, mainly focused on the lack of explanation for the origin and nature of forces that could move continents at the Earth's surface.

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25

Pearce, J. "Death of Wegener." Journal of Neurology, Neurosurgery & Psychiatry 55, no. 12 (December 1, 1992): 1149. http://dx.doi.org/10.1136/jnnp.55.12.1149.

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26

Pagnoux, C. "Maladie de Wegener." La Revue de Médecine Interne 28 (December 2007): S261—S262. http://dx.doi.org/10.1016/j.revmed.2007.09.019.

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27

Lê Thi Huong, D. "Granulomatose de Wegener." EMC - Traité de médecine AKOS 6, no. 2 (January 2011): 1–3. http://dx.doi.org/10.1016/s1634-6939(11)49772-6.

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28

Pagnoux, Christian, and Luis Teixeira. "Granulomatose de Wegener." La Presse Médicale 36, no. 5 (May 2007): 860–74. http://dx.doi.org/10.1016/j.lpm.2007.02.015.

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29

Ahmed, Hamza El Shafaai, and Fred H. Linthicum. "Wegener??s Granuloma." Otology & Neurotology 26, no. 3 (May 2005): 548–49. http://dx.doi.org/10.1097/01.mao.0000169759.76140.03.

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30

Antunes, Telma, and Carmen Sílvia Valente Barbas. "Granulomatose de Wegener." Jornal Brasileiro de Pneumologia 31, suppl 1 (July 2005): s21—s26. http://dx.doi.org/10.1590/s1806-37132005000700007.

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A granulomatose de Wegener caracteriza-se por vasculite necrosante granulomatosa que acomete preferencialmente vias aéreas superiores, inferiores e rins. Seu diagnóstico é feito associando-se as manifestações clínicas, radiológicas (multiplos nódulos escavados) e os achados anatomopatológicos e o anticorpo anticitoplasma de neutrófilos positivo. O tratamento com corticosteróides e ciclofosfamida leva a 90% de remissão da doença em 1 ano.

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31

Harris, Michael S., and Michael G. Moore. "Seronegative Wegener Granulomatosis." Otolaryngology–Head and Neck Surgery 142, no. 1 (January 2010): 142–43. http://dx.doi.org/10.1016/j.otohns.2009.08.015.

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32

Abraham-Inpijn, L. "Ziekte van Wegener." TandartsPraktijk 28, no. 1 (January 2007): 33–36. http://dx.doi.org/10.1007/bf03073025.

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33

Lamprecht, Peter, and Wolfgang L. Gross. "Wegener?s Granulomatosis." Herz 29, no. 1 (February 1, 2004): 47–56. http://dx.doi.org/10.1007/s00059-004-2525-0.

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34

Achmad Satya Negara, Harijono Kariosentono, and Endra Yustin Elistasari. "Granulomatosis Wegener dengan Antineutrophil Cytoplasmic Antibodies (ANCA) Negatif pada Laki-laki Usia 38 Tahun." MEDICINUS 34, no. 2 (August 1, 2021): 51–62. http://dx.doi.org/10.56951/medicinus.v34i2.72.

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Latar belakang : Granulomatosis Wegener atau granulomatosis dengan poliangiitis adalah vaskulitis nekrotikan sistemik yang menyerang pembuluh darah berukuran kecil dan sedang. Penyakit ini sering berkaitan dengan antineutrophil cytoplasmic antibodies (ANCA). Faktor pencetus terjadinya granulomatosis Wegener antara lain faktor lingkungan, infeksi, obat-obatan dan genetik. Manifestasi klinis granulomatosis Wegener dapat berupa gejala tidak spesifik seperti nyeri otot, artralgia, demam, anoreksia dan penurunan berat badan. Ujud kelainan kulit granulomatosis Wegener dapat berupa vaskulitis leukositoklastik, purpura, ulkus dan nodul subkutan. Granulomatosis Wegener juga dapat menyerang berbagai organ. Kasus : Seorang laki-laki berusia 38 tahun datang dengan keluhan muncul bercak kemerahan dan kaku pada wajah, tangan dan kaki. Status dermatologi pada regio fasialis tampak adanya saddle nose dan pada ekstremitas superior dan inferior tampak purpura multipel diskret. Pada pemeriksaan ANCA pasien didapatkan hasil negatif. Pemeriksaan gambaran histopatologi pada lapisan epidermis menunjukkan proliferasi padat sel-sel limfosit, perivaskular infiltrat dan sedikit sel neutrofil. Pada lapisan dermis didapatkan granuloma-granuloma yang terdiri atas banyak histiosit epiteloid dan makrofag berbuih serta pembuluh darah yang rusak dengan infiltrasi neutrofil pada dinding serta ekstravasasi eritrosit. Diskusi : Granulomatosis Wegener merupakan penyakit autoimun langka berupa inflamasi granulomatosis pada saluran pernapasan atas dan bawah serta vaskulitis sistemik yang berhubungan dengan ANCA. Gejala yang timbul pada granulomatosis Wegener berupa gejala ringan, namun dapat berkembang progresif dengan gambaran klinis yang lebih berat. Hasil pemeriksaan ANCA negatif tidak dapat langsung menyingkirkan diagnosis granulomatosis Wegener. Terapi awal granulomatosis Wegener berupa cyclophosphamide dan glucocorticoid yang diberikan selama 3-6 bulan. Pasien menunjukkan perbaikan klinis yang cukup bermakna dengan berkurangnya purpura pada seluruh tubuh setelah pemberian terapi selama lima minggu.

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35

NAKABAYASHI, Kimimasa. "Atypical Wegener''s Granulomatosis." Internal Medicine 38, no. 8 (1999): 619. http://dx.doi.org/10.2169/internalmedicine.38.619.

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36

GREMMEL, FRANZ. "Cyclosporin in Wegener Granulomatosis." Annals of Internal Medicine 108, no. 3 (March 1, 1988): 491. http://dx.doi.org/10.7326/0003-4819-108-3-491_1.

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37

White, Eric S., Carol A. Langford, Henry D. Tazelaar, and Joseph P. Lynch. "Management of Wegener Granulomatosis." Clinical Pulmonary Medicine 12, no. 4 (July 2005): 220–31. http://dx.doi.org/10.1097/01.cpm.0000171329.55658.88.

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Dörner, Dietrich, and Gerd Lüer. "Nachruf auf Hermann Wegener." Psychologische Rundschau 55, no. 1 (January 2004): 43–44. http://dx.doi.org/10.1026/0033-3042.55.1.43.

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39

Stern, D. "Why was wegener rejected?" Eos, Transactions American Geophysical Union 79, no. 14 (1998): 175. http://dx.doi.org/10.1029/98eo00132.

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40

Polus, M., J. Hamels, J. Dorzee, A. Henkinbrant, B. Carlier, and J. P. D’Odemont. "La Granulomatose De Wegener:." Acta Clinica Belgica 50, no. 5 (January 1995): 291–96. http://dx.doi.org/10.1080/17843286.1995.11718464.

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41

Mezni, Faouzi El, Essia Saiji, A. Ayadi-Kaddour, Olfa Ismail, Emna Braham, Hadhami Ben Turkia, and Agnès Hamzaoui. "La granulomatose de Wegener." Annales de Pathologie 25, no. 3 (June 2005): 255–56. http://dx.doi.org/10.1016/s0242-6498(05)80123-3.

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42

Wegener, Corine. "Remarks by Corine Wegener." Proceedings of the ASIL Annual Meeting 110 (2016): 98–100. http://dx.doi.org/10.1017/s0272503700102708.

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43

Puéchal, Xavier. "Granulomatose avec polyangéite (Wegener)." Revue du Rhumatisme 87, no. 5 (October 2020): 359–66. http://dx.doi.org/10.1016/j.rhum.2020.03.011.

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44

Saliba, S. "Wegener or Churg Strauss." La Presse Médicale 42, no. 4 (April 2013): 715. http://dx.doi.org/10.1016/j.lpm.2013.02.149.

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45

Dietzfelbinger, Martin. "Ingo Wegener: seine Bücher." Informatik-Spektrum 33, no. 5 (August 13, 2010): 489–98. http://dx.doi.org/10.1007/s00287-010-0463-1.

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46

Maurer, R., and R. Lesch. "Laudatio: Hans-Herbert Wegener." Der Pathologe 33, S2 (October 4, 2012): 198–99. http://dx.doi.org/10.1007/s00292-012-1631-7.

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47

Loscar, M., T. Hummel, M. Haller, J. Briegel, B. Wiebecke, W. Samtleben, H. Berger, P. Eichhorn, and G. Schelling. "ARDS und Wegener-Granulomatose." Der Anaesthesist 46, no. 11 (November 27, 1997): 969–73. http://dx.doi.org/10.1007/s001010050494.

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48

Langford, C. A. "Update on Wegener granulomatosis." Cleveland Clinic Journal of Medicine 72, no. 8 (August 1, 2005): 689–90. http://dx.doi.org/10.3949/ccjm.72.8.689.

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49

Lehmann, H. "Friedrich Wegener 75 Jahre." DMW - Deutsche Medizinische Wochenschrift 107, no. 13 (July 29, 2009): 512–13. http://dx.doi.org/10.1055/s-0029-1236733.

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