Search Results - "weber"

The case of severe form of Weber-Christchen’s disease in 31 year old man is described. The difficulty of diagnosis for the fist half a year is stressed - until characteristic nodes in subcutaneous layer appears. The diagnosis is confirmed by the data of biopsy of the node which revealed typical mult...

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We investigate coherent and incoherent nonparaxial Weber beams both theoretically and numerically. We clarify the understanding of coherence properties of Weber beams. We show that the superposition of coherent self-accelerating Weber beams with transverse displacement cannot display the nonparaxial...

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In his essay on Max Weber, Toni Negri reconstructs with extreme precision and punctuality the debate that removed him from the hitherto dominant exclusively methodological reading. Weber’s political problematics, his relationship with Nietzsche, the complicated modern dialectic between the rationali...

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Introduction: The Klippel-Trénaunay-Weber syndrome (KTWS) is characterized by several signs, including capillary malformations and venous malformations with or without lymphatic malformations associated with limb overgrowth. In most cases, only one extremity is involved with arteriovenous malformati...

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El síndrome de Rendu-Osler-Weber (SROW) se caracteriza por el desarrollo de estructuras vasculares aberrantes, tales como microvasos dilatados y malformaciones arteriovenosas (MAV) en la piel, el tracto gastrointestinal (GI), los pulmones, el hígado, el cerebro y, en menor frecuencia, en el riñón y...

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Weber-Christian disease (WCD), or idiopathic panniculitis, refers to rare diseases from a group of systemic connective tissue diseases. To verify the diagnosis of WCD is a difficult task, for there are no precise diagnostic tests for this disease.Objective: to study the clinical features and additio...

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Der vorliegende Beitrag widmet sich den Cuentos de la oficina des argentinischen Schriftstellers Roberto Mariani aus dem Jahr 1925. Ausgehend von Überlegungen Max Webers zur bürokratischen Effizienz und Michel Foucaults zur Disziplin, werden daraus ausgewählte Texte – Balada de la oficina, Rillo un...

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Purpose: to describe surgical treatment of glaucoma of a patient with Sturge — Weber — Krabbe syndrome. We present a clinical case of a patient with Sturge — Weber — Krabbe syndrome who sought assistance with us due to secondary stage III glaucoma with moderately elevated intraocular pressure. The e...

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The paper addresses the relatively rare inherited neurodermal disorder – Sturge-Weber syndrome that can manifest in epileptic seizures. We describe updated concepts, epidemiology, etiology, pathogenesis, clinical manifestations, and surgical treatment of the disease. We examined medical records of 2...

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Weber-Christian disease (WCD), also known as idiopathic lobular panniculitis, is a rare disease belonging to the group of diffuse connective tissue diseases. No therapy for WCD has been developed; empirical treatment is typically used. The first description of the use of tumor necrosis factor α inhi...

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Introduction. The multi-vector strengthening of China leads to a lively international expert discussion. This article examines the possibilities of applying the methodology developed by M. Weber to the analysis of modern Chinese foreign policy. Despite the fact that M. Weber's studies were publ...

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Christian–Weber disease refers to the group of panniculitis, which present an inflammation of the subcutaneous adipose tissue with the involvement of neutrophils, white blood cells and histiocytics, which leads to fibrosis in adipose tissue and sometimes to granulomatous changes. Clinically this pat...

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Sturge–Weber syndrome (SWS) is a rare, nonhereditary developmental condition characterized by a hamartomatous vascular proliferation involving the tissues of the brain and face. We reported a case of an 11-year-old boy with features of facial port-wine stains over the left side with unilateral advan...

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The publication presents a clinical case of hereditary hemorrhagic telangiectasia in a woman of 75 years. In the first part of the article, literature data on the incidence and features of Rundu-Osler-Weber disease are presented, modern diagnostic principles based on the Curaçao criteria(1999) are r...

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Purpose: This study aimed to report the efficiency and safety of using intensity-modulated radiation therapy (IMRT) in treating diffuse choroidal hemangioma (DCH) in patients with Sturge- Weber syndrome (SWS). Methods: IMRT planning was carried out for each case after patient fixation, CT simulatio...

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Objective: The purpose of this study was to assess the antioxidant capability and bioactive chemical profile of Taraxacum officinale roots, a medicinal plant with potential therapeutic uses.Methods: 70% methanol was used to extract the roots, and the solvent was then evaporated. Both the total flavo...

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Parkes-Weber Syndrome is a rare congenital vascular abnormality characterized by aneurismatic illness of blood arteries in the afflicted limb, as well as hypertrophy, ulceration, ischemia, and high-output heart failure. Imaging investigations are required to provide a diagnosis, with contrast arteri...

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El síndrome de Sturge-Weber es un trastorno neurocutáneo congénito, esporádico, que se manifiesta con malformación capilar facial, angiomatosis leptomeníngea y angiomas coroideos que predisponen a glaucoma. Para el manejo de la malformación capilar facial, el láser de colorante pulsado es el que ha...

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