نتایج جستجو برای: inherited

تعداد نتایج: 31514  

Journal: :Clinical Medicine 2017

Journal: :Journal of Hospital Medicine 2016

2017
Nobuhiro Kodama Shuichi Matsumoto Sunao Matsubayashi

Cefmetazole occasionally prolongs the prothrombin time. The mechanism is considered to be because of (i) inhibition of vitamin K metabolism, (ii) a lack of vitamin K, and (iii) low vitamin K stores. We report the death of a 93-year-old woman who was administered cefmetazole and exhibited a prolonged prothrombin time. When using cefmetazole in elderly patients, PT-INR should be monitored every f...

Journal: :Antimicrobial agents and chemotherapy 1984
J J Lipsky J C Lewis W J Novick

To determine whether the hypoprothrombinemia associated with antibiotics containing a 1-methyl-5-thiotetrazole (MTT) group is a result of the presence of the MTT group, rats were maintained on a vitamin K-deficient diet for 10 days and then received either intravenous moxalactam or cefotaxime or oral MTT for two additional days. MTT and moxalactam, which contains the MTT group, prolonged prothr...

Journal: :Neuro-oncology 2010
Athanassios P Kyritsis Melissa L Bondy Jasti S Rao Chrissa Sioka

In gliomas, germline gene alterations play a significant role during malignant transformation of progenitor glial cells, at least for families with occurrence of multiple cancers or with specific hereditary cancer syndromes. Scientific evidence during the last few years has revealed several constitutive genetic abnormalities that may influence glioma formation. These germline abnormalities are ...

2008
Seshadri Balaji

Sinus node dysfunction has been described as an inherited (autosomal recessive form) problem by Benson et al1. The cause seems to be certain specific mutations on the SCN5A gene. Patients with long QT type 3 (SCN5A mutation) have sinus bradycardia as part of the spectrum of abnormalities in this disease2. Atrial standstill is a rare condition where the atrium is silent i.e. there is no electric...

Journal: :Thrombosis and haemostasis 1996
D A Lane P M Mannucci K A Bauer R M Bertina N P Bochkov V Boulyjenkov M Chandy B Dahlbäck E K Ginter J P Miletich F R Rosendaal U Seligsohn

From the 'Charing Cross and Westminster Medical School, London, UK; 1RCCS Maggiore Hospital, Milan, Italy; Beth Israel Hospital, Boston USA; Universitv Hospital Leiden, The Netherlands; Research Centre of Medical Genetics, Moscow, The Russian Federation; WHO, Switzerland; Christian Medical College Hospital, Vellore, India; University of Lund, Malmö, Sweden; 'Institute of Clinical Genetics, Mosc...

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