نتایج جستجو برای: pierson test
تعداد نتایج: 812396 فیلتر نتایج به سال:
background: anxiety is a basic human emotion. however, when taken to extremes it may produce unwarranted results. one of the most threatening events that cause anxiety in students today is testing. this study investigated the relationship between test anxiety and academic performance of midwifery students in islamic azad university, najaf abad branch. methods: in this descriptive-sectional stud...
28 Background: LAMB2 mutations cause Pierson syndrome (OMIM 609049), an 29 autosomal recessive genetic disease typically characterized by congenital nephrotic 30 syndrome (CNS) and early onset renal failure, as well as bilateral microcoria. 31 NPHP1 mutations cause familial juvenile nephronophthisis type 1 (NPHP1, OMIM 32 256100), another autosomal recessive renal disease that usually occurs ye...
Cerebellum is the region of the brain that is related to motor control, physical coordination and balance. Recent studies have also established that it is also associated with cognition and learning (Bauer et al., 2009). Cerebellum regulates motor activity and muscle tonus and prompts cognitive behavior. In addition, it plays a key role in memory and learning in the cerebellar thalamic cortical...
Ian T Paulsen1,*, Caroline M Press2, Jacques Ravel1, Donald Y Kobayashi3, Garry S A Myers1, Dmitri V Mavrodi4, Robert T DeBoy1, Rekha Seshadri1, Qinghu Ren1, Ramana Madupu1, Robert J Dodson1, A Scott Durkin1, Lauren M Brinkac1, Sean C Daugherty1, Stephen A Sullivan1, Mary J Rosovitz1, Michelle L Gwinn1, Liwei Zhou1, Davd J Schneider5, Samuel W Cartinhour5, William C Nelson1, Janice Weidman1, Ki...
Advisory Board Thomas B. Ferguson, USA Nobuo Hashimoto, Japan Laurence Klotz, Canada Nora Noni MacDonald, Canada Anand Malaviya, India Ana Marusic, Croatia V. Mohan, India Dan J. Ncayiyana, South Africa G. B. Parulkar, India David J. Pierson, USA Andrew P. Schachat, USA Shirish S. Sheth, India Michael Swash, UK P. N. Tandon, India Jim Thornton, UK Jean-Louis Vincent, Belgium Print ISSN 0022-385...
BACKGROUND LAMB2 mutations cause Pierson syndrome (OMIM 609049), an autosomal recessive genetic disease typically characterized by congenital nephrotic syndrome (CNS) and early onset renal failure, as well as bilateral microcoria. NPHP1 mutations cause familial juvenile nephronophthisis type 1 (NPHP1, OMIM 256100), another autosomal recessive renal disease that usually occurs years after birth....
Mary C. Mandni, MD Si M. Pham, MD Richard Norris Pierson Robert S. Poston, Jr., Monica RobotinAndrew J. Sherman, Louisiana State University of III, MD MD Johnson, MD MD University Pittsburgh Vanderbik University Stanford University Hospital Marie Northwestern Medical Center TSFRE Research Medical Center Medical Center Lannelongue University Medical Nina Braun~ald Grant John Alexander TSFRE Rese...
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