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suma/fever

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Participants will receive Herceptin in addition to chemotherapy with Taxol and FEC. 'FEC' is Fluorouracil, Cyclophosphamide and Epirubicin. During the first course of therapy Herceptin will be given on day 1 through a needle in a vein over 90 minutes. Participants will then be observed for 1 hour
Dengue fever has various levels of severity, from mild disease to severe hemorrhagic complications and shock. Dengue is endemic world-wide and has been found in the United States. The mortality from dengue fever can be as high as 15-20%, with nearly 22,000 deaths annually, most of them children

Observational Study With PASCALLERG ® in Patients With Hay Fever

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There are documented male and female patients over the age of one year who suffer from hay fever. The traetment time is about a period of 4 weeks with PASCALLERG® tablets.

Whole-body Hyperthermia for Moderate to Severe Depressive Disorder

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Fever and Neutropenia in Pediatric Oncology Patients

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Outpatient management of patients considered to be at low risk for serious bacterial infection has been explored using risk stratification schema based on clinical parameters. First, patients will be stratified based on a clinical risk stratification schema. Patients stratified to the low risk group

The Brain on Whole Body Hyperthermia: A Neuroimaging Study

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The Investigators have observed in an open trial that a single session of whole body hyperthermia (WBH) induced rapid antidepressant effects that persisted for at least a week in patients with major depression (MDD) severe enough to warrant inpatient hospitalization. In addition to reducing

Whole Body Hyperthermia (WBH) as a Rapid Treatment for Fibromyalgia

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We will direct a clinical trial of Whole Body Hyperthermia (WBH) for the treatment Fibromyalgia. Although we have not yet studied WBH for Fibromyalgia we have data indicating that WBH is effective for the acute treatment of major depression (MDD). Given the high overlap of symptoms between
Totally, 33 children (age range: 5 - 17 years; 15 male and 18 female) were enrolled to the study who were diagnosed as ARF at the Pediatric Cardiology Department, Medical Faculty, Eskişehir Osmangazi University. The study protocol was approved by Ethics Committee of Medical Faculty, Eskişehir

Chronic Q-fever in Patients With an Abdominal Aortic Disease (QAAD-study)

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Study design: Prospective observational survey Domain: Patients with an abdominal aneurysm or central vascular reconstruction in an endemic area after an outbreak of acute Q-fever. Data collection: In Jeroen Bosch Hospital and Bernhoven Hospital all patients with an aneurysm or central vascular

A Diagnostic Test for Familial Mediterranean Fever

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Optimal Application Dose of Superficial Hyperthermia

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This is a phase III, multicenter, randomized, open-label study. One center in the United Arab Emirates and 1 center in Turkey will participate in this trial and approximately 50 patients will be recruited. Patients will be adults with hematological malignancies undergoing chemotherapy for leukemia
Objectives: To study the incidence etiological spectrum of febrile illness occurring during a travel to the tropics, as well as clinical course, care, treatment and outcome of these febrile illness episodes. Design: Prospective cohort study of febrile illness in international travelers Population:
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