Zobrazeno 1 - 10 of 97 pro vyhledávání: '"B Graziani"'
1
Akademický článek
Aquecimento em forno de microondas / desenvolvimento de alguns conceitos fundamentais Heating in microwave ovens/ developing of basic concepts
Autor: Ana Claudia R. N. Barboza, Camila V. M. S. Cruz, Marcelo B. Graziani, Myrian C. F. Lorenzetti, Edvaldo Sabadini
Publikováno v: Química Nova, Vol 24, Iss 6, Pp 901-904 (2001)
The microwave oven became a common domestic equipment, due mainly to the short time spent to heat foods. One of the most interesting characteristics of the microwave oven is the selective heating. Different from the conventional oven, where the heati
Externí odkaz: https://doaj.org/article/0d038f3f679e49af8f9c0dd265e623b3
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2
Aquecimento em forno de microondas / desenvolvimento de alguns conceitos fundamentais
Autor: Myrian Cristina de Freitas Lorenzetti, Marcelo B. Graziani, Ana Claudia Rueda Nery Barboza, Camila V. M. S. Cruz, Edvaldo Sabadini
Publikováno v: Química Nova, Volume: 24, Issue: 6, Pages: 901-904, Published: DEC 2001
Química Nova v.24 n.6 2001
Química Nova
Sociedade Brasileira de Química (SBQ)
instacron:SBQ
The microwave oven became a common domestic equipment, due mainly to the short time spent to heat foods. One of the most interesting characteristics of the microwave oven is the selective heating. Different from the conventional oven, where the heati
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c89528806b12b07ac13c7b81c858e2e
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422001000600030&lng=en&tlng=en
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3
Serum levels of erythropoietin and soluble transferrin receptor in the course of pregnancy in non beta thalassemic and beta thalassemic women
Autor: I, Bianco, F, Mastropietro, C, D'Asero, B, Graziani, P, Piergrossi, M, Mezzabotta, G, Modiano
Publikováno v: Haematologica. 85(9)
In non-thalassaemic women serum erythropoietin (Epo) level increases during pregnancy, whereas that of soluble transferrin receptor (STFR) drops slightly in the first two trimesters to attain the original values in the third trimester. In this study
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ba0f083f4ca5aac192afde8a7a95e709
https://pubmed.ncbi.nlm.nih.gov/10980626
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4
Phenotypes of individuals with a beta thal classical allele associated either with a beta thal silent allele or with alpha globin gene triplication
Autor: I, Bianco, M, Lerone, E, Foglietta, G, Deidda, M P, Cappabianca, L, Morlupi, D, Ponzini, P, Grisanti, P, Di Biagio, A, Amato, M, Mezzabotta, B, Graziani
Publikováno v: Haematologica. 82(5)
beta thalassemia intermedia has its origins in compound heterozygosity for many different beta thal defects or in an interaction of a beta thal defect with altered alpha cluster. Two specific genetic associations (beta thal/beta(+) -101 C--T and beta
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::8f14e375e9aad608ccca78ae5b32e353
https://pubmed.ncbi.nlm.nih.gov/9407714
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5
Silent thalassemias: genotypes and phenotypes
Autor: I, Bianco, M P, Cappabianca, E, Foglietta, M, Lerone, G, Deidda, L, Morlupi, P, Grisanti, D, Ponzini, S, Rinaldi, B, Graziani
Publikováno v: Haematologica. 82(3)
Current application of molecular biology techniques to the study of the DNA of globin genes has confirmed the existence of silent alpha and beta thalassemias; which had already been reported on the basis of red blood cell parameters and family studie
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::badf8733931b0320d0d4ae703ef12710
https://pubmed.ncbi.nlm.nih.gov/9234568
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7
Akademický článek
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8
Screening of thalassaemia carriers in intermediate school of Latium: results of four years' work
Autor: Lerone M, Valente M, I Bianco, B Graziani, S U D'Arca, Silvestroni E, Carboni C
Publikováno v: Journal of Medical Genetics. 17:161-164
From 1975 to 1979 the Rome Microcythaemia Centre carried out four health education campaigns and thalassaemia screenings among students of the intermediate schools throughout Latium, under the auspices and with the financial support of the Health Aut
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a443de290503418a0dbc82f7d392018a
https://doi.org/10.1136/jmg.17.3.161
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10
Heterozygous β-Thalassaemia with Normal Haemoglobin Pattern
Autor: I Bianco, E. Silvestroni, B Graziani, Claudio Carboni
Publikováno v: Acta Haematologica. 59:332-340
Thalassaemia with normal levels of Hb A, and Hb F and with an α/β ratio higher than 1 is described in 4 families. 3 of these families show direct or indirect signs of the presence of the δ-thalassaemia gene along with the β-thalassaemia gene. The
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::dc6c919e68720abf0d96c1cbd3635d28
https://doi.org/10.1159/000207784
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