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...

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...

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...

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...

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,...

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...

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....

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...

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...

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...