نتایج جستجو برای: weil syndrome

تعداد نتایج: 625361  

Journal: :archives of clinical infectious diseases 0
narges najafi antimicrobial resistance research center, department of infectious diseases, mazandaran university of medical sciences, sari, ir iran ali reza davoudi antimicrobial resistance research center, department of infectious diseases, mazandaran university of medical sciences, sari, ir iran; antimicrobial resistance research center, department of infectious diseases, mazandaran university of medical sciences, sari, ir iran. tel/fax: +98-1142316319 shahriar alian antimicrobial resistance research center, department of infectious diseases, mazandaran university of medical sciences, sari, ir iran fatemeh ahangarkani antimicrobial resistance research center, department of infectious diseases, mazandaran university of medical sciences, sari, ir iran elham asghari antimicrobial resistance research center, department of infectious diseases, mazandaran university of medical sciences, sari, ir iran

results; out of 634 patients, 61 subjects (9.62%) had significant complications including: acute renal failure, alveolar hemorrhage, ards, clotting disorders, pancreatitis, gastrointestinal bleeding and intracranial bleeding; age, jaundice, renal and pulmonary involvement (oliguria and anuria), hypotension, leukocytosis, thrombocytopenia, hyponatremia, elevated bilirubin, alanine aminotransfera...

Journal: :Archivos de bronconeumologia 2006
E Márquez-Martín B Valera-Bestard R Luque-Márquez A Alarcón-González

We reviewed a series of 5 cases of leptospirosis treated in our hospital between 1998 and 2004 and found that lung involvement was observed in 3 of the 5 cases. All patients met the criteria for the diagnosis of leptospirosis. Weil syndrome was diagnosed in 4 patients and anicteric leptospirosis in 1 patient. The 3 patients with lung sequelae were admitted into the intensive care unit because o...

2005
JOHN GOODFELLOW

This paper describes and seeks to explain a clinical syndrome which occurs characteristically, but not exclusively, as a complication of haemophilia. The main features of the syndrome are the sudden onset of severe pain in the groin accompanied by marked flexion deformity at the hip, followed by a mass in the iliac fossa and femoral nerve palsy. Episodes of this sort have been reported in the l...

Journal: :Indian Journal of Critical Care Medicine 2011

Journal: :Hong Kong medical journal = Xianggang yi xue za zhi 2005
F W T Cheng T F Leung N Lee F Yap J Hui T F Fok P C Ng

Leptospirosis is rarely reported in children. It is easily treated with antibiotics but can be fatal if treatment is delayed. A 12-year-old girl was diagnosed with Weil syndrome, a severe form of leptospirosis, 10 days after returning from Mainland China. She presented with fever, hypotension, jaundice, and acute renal failure. She had used well water for bathing and swum in freshwater.

2011
Elena Forouhar Dimitra Mitsani

Severe leptospirosis (Weil Syndrome) was diagnosed in an otherwise healthy environmental worker in Baltimore alleys in late November 2010. He developed multiple organ failure but responded to antibiotic therapy and experienced a full recovery within 4 weeks. His diagnosis was confirmed by a rise in indirect hemagglutinin titer (acute 0, convalescent 400). The subject had close contact with Balt...

Journal: :The Journal of the Association of Physicians of India 2014
A G Diwan Rahul Shewale Shivakumar Iyer Amit Nisal Prakhar Agrawa

Macrophage activation syndrome is a potentially life threatening phenomenon characterised by aggressive proliferation of macrophages and T lymphocytes leading to haemophagocytosis of other blood cells and multi organ failure. Here we present a very unusual combination of leptospirosis and scrub typhus infection leading to macrophage activation syndrome. Scrub typhus associated with macrophage a...

Journal: :IACR Cryptology ePrint Archive 2005
Bo Gyeong Kang Je Hong Park

In this paper, we investigate the relationship between the squared Weil/Tate pairing and the plain Weil/Tate pairing. Along these lines, we first show that the squared pairing for arbitrary chosen point can be transformed into a plain pairing for the trace zero point which has a special form to compute them more efficiently. This transformation requires only a cost of some Frobenius actions. Ad...

Journal: :Advances in experimental medicine and biology 2003
Uwe Wolfrum

Defects in myosin VIIa are responsible for Usher Syndrome 1B (Weil et al., 1995). Human Usher syndrome (USH), named after the British ophthalmologist Charles Usher (Usher, 1914), is the most common hereditary form of combined blindand deafness (≈ 50 % of cases in the developed countries). USH designates a group of clinically and genetically heterogeneous disorders with hearing loss and retiniti...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید