نتایج جستجو برای: rallison syndrome

تعداد نتایج: 621917  

Journal: :Family practice 2000
A A Verhoeven E J Boerma B Meyboom-de Jong

BACKGROUND Evidence-based medicine requires new skills of physicians, including literature searching. OBJECTIVE To determine which literature retrieving method is most effective for GPs: the printed Index Medicus; Medline through Grateful Med; or Medline on CD-ROM. METHODS The design was a randomized comparative study. In a continuing medical education course, three groups of health care pr...

Journal: :Zootaxa 2015
Vladimir Pešić Gustavo Cauê De Oliveira Piccoli Marcel Santos De Araújo José Marcos Rezende Ana Zangirolame Gonçalves

The rosette architecture of some bromeliad species traps water and organic matter from the canopy in leaf axils (forming phytotelmata) and harbors many species of invertebrate animals (Frank & Lounibos 2009). Some water mites are adapted to live in phytotelmata; typically recorded from water-filled tree holes, bromeliad tanks, and a range of plant axils. Karl Viets (1939) was the first acarolog...

Journal: :Clinical chemistry 2005
Fred S Apple Curtis A Parvin Kenneth F Buechler Robert H Christenson Alan H B Wu Allan S Jaffe

SCN5A gene encoding the cardiac sodium channel. Genomics 1996;34:9– 16. 13. Makielski JC, Ye B, Valdivia CR, Pagel MD, Pu J, Tester DJ, et al. A ubiquitous splice variant and a common polymorphism affect heterologous expression of recombinant human SCN5A heart sodium channels. Circ Res 2003;93:821–8. 14. Hiraoka M. Inherited arrhythmic disorders in Japan. J Cardiovasc Electrophysiol 2003;14:431...

Journal: :Indian journal of biochemistry & biophysics 2014
Vishwa Deepak Bharti Satya P Gupta Harish Kumar

QSAR study was performed on a series of 1,2-dihydro-4-quinazolinamines, 4,5-dialkylsubstituted-2-imino-1,3-thiazolidine derivatives and 4,5-disubstituted-1,3-oxazolidin-2-imine derivatives studied by Tinker et al. [J Med Chem (2003), 46, 913-916], Ueda et al. [Bioorg Med Chem (2004) 12, 4101-4116] and Ueda et al. [Bioorg Med Chem Lett (2004) 14, 313-316], respectively, as potent, highly selecti...

Journal: :American journal of human genetics 2011
Cathryn J Poulton Rachel Schot Sima Kheradmand Kia Marta Jones Frans W Verheijen Hanka Venselaar Marie-Claire Y de Wit Esther de Graaff Aida M Bertoli-Avella Grazia M S Mancini

We describe a syndrome of primary microcephaly with simplified gyral pattern in combination with severe infantile epileptic encephalopathy and early-onset permanent diabetes in two unrelated consanguineous families with at least three affected children. Linkage analysis revealed a region on chromosome 18 with a significant LOD score of 4.3. In this area, two homozygous nonconserved missense mut...

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