نتایج جستجو برای: cosenza

تعداد نتایج: 244  

2007
M. Minniti M. Commisso A. Sindona E. Sicilia A. Bonanno P. Barone R. A. Baragiola P. Riccardi

M. Minniti,1 M. Commisso,1 A. Sindona,1 E. Sicilia,2 A. Bonanno,1 P. Barone,1 R. A. Baragiola,3 and P. Riccardi1,* 1Laboratorio IIS, Università della Calabria and INFN-Gruppo Collegato di Cosenza-87036 Rende, Cosenza, Italy 2Dipartimeto di Chimica, Università della Calabria-87036 Rende, Cosenza, Italy 3Laboratory for Atomic and Surface Physics, Department of Engineering Physics, University of V...

Journal: :iranian journal of medical sciences 0
seyed reza kazemi nezhad department of genetics, faculty of science, shahid chamran university of ahvaz, ahvaz, iran fatemeh fahmi department of genetics, faculty of science, shahid chamran university of ahvaz, ahvaz, iran saeid reza khatami department of genetics, faculty of science, shahid chamran university of ahvaz, ahvaz, iran mohsen musaviun department of genetics, faculty of science, shahid chamran university of ahvaz, ahvaz, iran

glucose-6-phosphate dehydrogenase (g6pd) deficiency is one of the most common hereditary enzymatic disorders in human, increases the vulnerability of erythrocytes to oxidative stress. it is also characterized by remarkable molecular and biochemical heterogeneity. according to previous investigations, g6pd cosenza (g1376c) is a common g6pd mutation in some parts of iran. therefore in the present...

Fatemeh Fahmi Mohsen Musaviun Saeid Reza Khatami Seyed Reza Kazemi Nezhad,

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is one of the most common hereditary enzymatic disorders in human, increases the vulnerability of erythrocytes to oxidative stress. It is also characterized by remarkable molecular and biochemical heterogeneity. According to previous investigations, G6PD Cosenza (G1376C) is a common G6PD mutation in some parts of Iran. Therefore in the present...

2011
Seyed Reza Kazemi Nezhad Fatemeh Fahmi Saeid Reza Khatami Mohsen Musaviun

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is one of the most common hereditary enzymatic disorders in human, increases the vulnerability of erythrocytes to oxidative stress. It is also characterized by remarkable molecular and biochemical heterogeneity. According to previous investigations, G6PD Cosenza (G1376C) is a common G6PD mutation in some parts of . Therefore in the present stu...

2010
S. Servidio W. H. Matthaeus M. A. Shay P. Dmitruk P. A. Cassak M. Wan

magnetohydrodynamic turbulence S. Servidio, W. H. Matthaeus, M. A. Shay, P. Dmitruk, P. A. Cassak, and M. Wan Department of Physics and Astronomy and Bartol Research Institute, University of Delaware, Newark, Delaware 19716, USA Dipartimento di Fisica, Università della Calabria, Cosenza I-87036, Italy Departamento de Física, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires,...

Journal: :international journal of molecular and cellular medicine 0
yadollah zahedpasha non-communicable pediatric diseases research center, babol university of medical sciences, babol, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی بابل (babol university of medical sciences) mousa ahmadpour kachouri non-communicable pediatric diseases research center, babol university of medical sciences, babol, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی بابل (babol university of medical sciences) haleh akhavan niaki cellular and molecular biology research center (cmbrc), babol university of medical sciences, babol, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی بابل (babol university of medical sciences) roya farhadi non-communicable pediatric diseases research center, babol university of medical sciences, babol, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی بابل (babol university of medical sciences)

background and aim: jaundice is a common disorder in neonates and one of the provable causes of glucose-6-phosphate dehydrogenase (g6pd) deficiency, some mutation types of which may be associated with severe neonatal icter. in this line, the present study has been conducted to compare g6pd mutations in incteric and non icteric neonates. materials and methods: this case-control study was impleme...

2010
Sashi K. Kunnath YeongAe Heo Jon F. Mohle Edoardo Cosenza Fiorenzo De Cicco Andrea Prota

Edoardo Cosenza; Fiorenzo De Cicco, Ph.D.; and Andrea Prota Full Professor, Dept. of Structural Engineering, Univ. of Naples “Federico II”, Via Claudio 21, 80125 Naples, Italy. E-mail: cosenza@ unina.it Dept. of Structural Engineering, Univ. of Naples “Federico II”, Via Claudio 21, 80125 Naples, Italy. E-mail: [email protected] Assistant Professor, Dept. of Structural Engineering, Univ....

2012
M. L. CASTELLANI M. FELACO F. PANDOLFI V. SALINI D. DE AMICIS C. ORSO J. VECCHIET S. TETÈ C. CIAMPOLI F. CONTI G. CERULLI A. CARAFFA P. ANTINOLFI C. CUCCURULLO P. FELACO D. KEMPURAJ P. BOSCOLO G. SABATINO Y. B. SHAIK

1Pediatrics, University Department of Medical and Surgical Specialty and Public Health, Perugia; 2Medical and Scientific Department, Stallergenes, Milan; 3Marketing Department, Stallergenes, Milan; 4Pediatrics, General Hospital, Empoli; 5Pediatric National Health Service, Garlasco; 6Allergy Unit, General Hospital, Cosenza; 7ENT Department, Santobono Hospital, Naples; 8Clinical Immunology, Miull...

2013
Yadollah Zahedpasha Mousa Ahmadpour Kachouri Haleh Akhavan Niaki Roya Farhadi

Jaundice is a common disorder in neonates and one of the provable causes of glucose-6-phosphate dehydrogenase (G6PD) deficiency, some mutation types of which may be associated with severe neonatal icter. The present study has been conducted to compare G6PD mutations in incteric and non icteric neonates. This case-control study was implemented in the NICU and Newborn Ward of Amirkola Children Ho...

Journal: :journal of chemical health risks 0
omolbanin javadi genetics department, ahar branch, islamic azad university, ahar, iran habib onsori cell and molecular biology department, marand branch, islamic azad university, marand, iran

glucose-6-phosphate dehydrogenase (g6pd) is a greatly polymorphic enzyme encoded by human x-linked gene. g6pd deficit is the most public enzymopathy in human with about 400 million people affected globally. it is the main controlling enzyme in the hexose monophosphate shunt catalase the oxidation of glucose-6-phosphate  to 6-phosphogluconolacton and the creation of reducing equals in the form o...

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