209,377 research outputs found
Kurtzer und Warhafftiger Bericht/ Mit was Christlichen Ceremonien ein Erbar Wolweiser Rath der alten löblichen Stadt Eimbeck/ die new erbawete Schul auff der newen Stadt in S. Marien Magdalenen Kloster eingeweihet/ eingeführet und eröffnet hat/ den 19. Tag des Monats Novembris Anno Christi 1611. / Beschrieben durch den alten M. Johan. Velium Predigern daselbst bey S. Jacob
No full textSchlüsselseiten aus dem Exemplar der ULB Halle: AB 152944 (9)Vorlageform des Erscheinungsvermerks: Gedruckt in der Keyserfreyen Reichstadt Goßlar durch Johan Vogt/ im Jahr 1612
Commentatio Philologica, Ethico-Historica De Avaritia Saepivs Clericis Temere Exprobrata Qvod Illvstratvr Exemplo D. Joannis Bvgenhagii Pommerani Primi Svperint. Evang. Witteb. / Avtore M. Henric. Christoph. Vogt ..
No full textCOMMENTATIO PHILOLOGICA, ETHICO-HISTORICA DE AVARITIA SAEPIVS CLERICIS TEMERE EXPROBRATA QVOD ILLVSTRATVR EXEMPLO D. JOANNIS BVGENHAGII POMMERANI PRIMI SVPERINT. EVANG. WITTEB. / AVTORE M. HENRIC. CHRISTOPH. VOGT ..
Commentatio Philologica, Ethico-Historica De Avaritia Saepivs Clericis Temere Exprobrata Qvod Illvstratvr Exemplo D. Joannis Bvgenhagii Pommerani Primi Svperint. Evang. Witteb. / Avtore M. Henric. Christoph. Vogt .. (1)
Titelblatt (1)
Widmung (3)
Sectio I. De Avaritia In Se Spectata (7)
Sectio II. De Avaritia Clericorum (26)
Sectio III. De Avaritia Bugenhagii (35)
Addenda Ad §. XL. & XLI. (95
Uveo-Meningeal Syndromes: Vogt-Koyanagi-Harada (VKH) Disease
No full textOcular inflammatory symptoms with concurrent neuro-ophthalmologic manifestations can be diagnostically challenging. We provide a general overview of uveo-meningeal syndromes, which comprises a heterogeneous group of disorders that involve inflammation of the uveal tract, retina, and meninges. The presentation focuses on the uveomeningeal syndrome of Vogt-Koyanagi-Harada (VKH) Disease by providing a comprehensive overview of diagnostic criteria, pathogenesis, clinical course, and management. To demonstrate the heterogeneous clinical presentations and possible neuro-ophthalmological manifestations that can challenge diagnosis, we chronicle three cases of VKH seen at our institution and highlight the diagnostic work-up, management, and outcomes. This presentation summarizes a practical strategy for approaching the clinical heterogeneity of VKH.[1] Brazis PW, Stewart M, Lee A. The Uveo-Meningeal Syndromes. The Neurologist 2004, 10(4):171-184; [2] Tsuboyama M, Chandler JV, Scharf E, et al. Neurologic Complications of Acute Posterior Multifocal Placoid Pigment Epitheliopathy: A Case Series of 4 Patients. Neurohospitalist 2018; 8(3):146-151.; [3] Allegri P, Risotto R, Herbort CP, Murialdo U. CNS Disease and Uveitis. J Ophthalmic Vis Res. 2011; 6(4): 284-308.; [4] Lavezzo MM, Sakata VM, et al. Vogt-Koyanagi-Harada disease: review of a rare autoimmune disease targeting antigens of melanocytes. Ophanet Journal of Rare Diseases. 2016; 11: 29; [5] Read RW, Rao NA: Utility of existing Vogt-Koyanagi-Harada syndrome diagnostic criteria at initial evaluation of the individual patient: a retrospective analysis. Ocul Immunol Inflamm 2000; 8: pp. 227-234.; [6] Read RW, Rao NA, Cunningham ET. Vogt-Koyanagi-Harada Disease. Curr Opin Ophthal. 2000; 11(6):437-442; [7] Read RW, Holland GN, Rao NA, et. al.: Revised diagnostic criteria for Vogt-Koyanagi-Harada disease: report of an international committee on nomenclature. Am J Ophthalmol 2001; 131: pp. 647-652.; [8] Goto, Rao, and Rao. Ryan\u27s Retina 7th Edition 2022; 76, 1577-1589; [9] Feldman BH, O\u27Keefe GD, Salcedo HR, et al. Vogt-Koyanagi-Harada Disease. Eyewiki 2023. https://eyewiki.aao.org/Vogt-Koyanagi-Harada_Disease; [10] Dogan B, Erol MK, Cengiz A. Vogt-Koyanagi-Harada disease following BCG vaccination and tuberculosis. Springerplus. 2016; 5: 603; [11] Ferriera FT, Araujo DC, et al. Possible Association between Vogt-Koyanagi-Harada Disease and Coronavirus Disease Vaccine: A report for Four Cases. Ocul Immunol Inflamm. 2022; 1-7; [12] Rao NA, Gupta A, Dustin L, et al. Frequency of distinguishing clinical features in Vogt-Koyanagi-Harada disease. Ophthalmology 2010;117:591-9; [13] Weisz JM, Holland GN, Roer LN, et. al.: Association between Vogt-Koyanagi-Harada syndrome and HLA-DR1 and DR4 in Hispanic patients living in Southern California. Ophthalmology 1995; 102: pp. 1012-1015.; [14] Shi T, Lv W, Zhang L, Chen J, Chen H. Association of HLA-DR4/HLA-DRB1*04 with Vogt-Koyanagi-Harada disease: a systematic review and meta-analysis. Sci Rep. 2014 Nov 10;4:6887
M. l'Abbé Albert Vogt († 4 octobre 1942)
No full textGuilland Rodolphe. M. l'Abbé Albert Vogt († 4 octobre 1942). In: Études byzantines, tome 3, 1945. pp. 268-272
Editorial
No full textGötz M, Vogt M. Editorial. In: Götz M, Vogt M, eds. Schulwissen für und über Kinder. Beiträge zur historischen Primarschulforschung. 1st ed. Bad Heilbrunn: Julius Klinkhardt; 2016: 7-18
Kongruenzen und Inkongruenzen im Schulwissen über Unterstufenschüler in der DDR
No full textVogt M. Kongruenzen und Inkongruenzen im Schulwissen über Unterstufenschüler in der DDR. In: Götz M, Vogt M, eds. Schulwissen für und über Kinder. Beiträge zur historischen Primarschulforschung. 1st ed. Bad Heilbrunn: Julius Klinkhardt; 2016: 98-124
A propos des fouilles de M. Baxter. Une hypothèse
No full textVogt Albert. A propos des fouilles de M. Baxter. Une hypothèse. In: Échos d'Orient, tome 35, n°184, 1936. pp. 436-441
Rapport sur le mémoire de M. Vogt, sur les microcéphales
No full textLetourneau Ch. Rapport sur le mémoire de M. Vogt, sur les microcéphales. In: Bulletins de la Société d'anthropologie de Paris, II° Série. Tome 2, 1867. pp. 477-491
Vogt-Koyanagi-Harada disease and HLA type in Italian patients
No full textPURPOSE: To study the frequencies of human leukocyte antigen (HLA) specificities in Italian patients with Vogt-Koyanagi-Harada disease and to correlate the presence of each specificity to the clinical features. METHODS: Human leukocyte antigen specificities were determined by standard microlymphocyto-toxicity assay in 16 patients with Vogt-Koyanagi-Harada disease and compared with HLA specificities of 116 healthy controls, RESULTS: HLA-DR4 was statistically related to Vogt-Koyanagi-Harada disease (P = .0063), whereas only a trend toward a significant association between the disease and HLA-B41 was found (P = .06). HLA-DQ1 was detected in a disproportionate number of controls (68.9%) compared with patients (31.5%). CONCLUSIONS: HLA-DR4 was significantly related to Vogt-Koyanagi-Harada disease in Caucasian European patients, specifically in Italian patients, as it was described in other racial groups. No clear relation was found between the ophthalmologic and systemic manifestations of Vogt-Koyanagi-Harada disease and the presence of HLA specificities
Perrot (E. M.) et Vogt (E. M.). Poisons de flèches et poisons d'épreuve.
No full textPoutrin . Perrot (E. M.) et Vogt (E. M.). Poisons de flèches et poisons d'épreuve.. In: Journal de la Société des Américanistes. Tome 10 n°2, 1913. pp. 601-602
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