Zobrazeno 1 - 10
of 60
pro vyhledávání: '"T, Rozov"'
Autor:
T Rozov, MTN Silva, N Damascene, MA Santana, PJC Marâstica, RCNC Melloti, VC Martins, CA Riedi, El Souza, N Ludwig Neto, RA Athanazio, G Ferrari, Mago Ribeiro, A Quittner, AF Ribeiro
Publikováno v:
Brasília Médica. 60
Publikováno v:
Allergologia et Immunopathologia. 39:284-290
Background The objectives of this study were to determine the prevalence of asthma and allergies in 13- to 14-year-old adolescents in the city of Taubate, Sao Paulo, Brazil using the INTERNATIONAL STUDY OF ASTHMA AND ALLERGIES IN CHILDHOOD (ISAAC) qu
Autor:
S, Raskin, J A, Phillips, G, Kaplan, M, McClure, C, Vnencak-Jones, T, Rozov, J M, Cardieri, P, Marostica, F, Abreu, R, Giugliani, F, Reis, N A, Rosario, N, Ludwig, L, Pereira, F, Faucz, J, Gabardo, L, Culpi
Publikováno v:
Human biology. 71(1)
Cystic fibrosis (CF) is an autosomal recessive disease caused by at least 750 different mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. The frequency of the most common mutation (DF508) in Brazilian patients of Europ
Publikováno v:
Revista do Hospital das Clinicas. 53(2)
Fifty nine asthmatic children and adolescents, clinically stable, aged 6 to 15 years, 37 boys and 22 girls, from Instituto da Criança do Hospital das Clínicas da FMUSP, were studied from September to November, 1994. The patients were classified by
Autor:
S, Raskin, J A, Phillips, M R, Krishnamani, C, Vnencak-Jones, R A, Parker, T, Rozov, J M, Cardieri, P, Marostica, F, Abreu, R, Giugliani, F, Reis, N A, Rosario, N, Ludwig, L, Culpi
Publikováno v:
Human biology. 69(4)
We have used PCR amplification of DNA obtained from Guthrie cards to identify the DF508 mutation and correlate it with the allele frequencies at two polymorphic loci (XV-2C and KM-19) closely linked to the cystic fibrosis gene. The DNA came from 193
Autor:
S, Raskin, J A, Philips, M R, Krishnamani, C, Vnencak-Jones, R A, Parker, E, Dawson, T, Rozov, J M, Cardieri, P, Marostica, F, Abreu, R, Giugliani, F, Reis, N A, Rosario, N, Ludwig, L, Culpi
Publikováno v:
Human biology. 69(1)
The restriction fragment length polymorphism (RFLP) haplotypes of cystic fibrosis (CF) alleles vary between populations. To determine the distribution of two RFLPs (XV-2C and KM-19) that are tightly linked to the CF locus, we analyzed a white sample
Autor:
Cma Nakaie, M T Margarido, Ceres Concilio Romaldini, T Rozov, F R Carraza, Ary Lopes Cardoso, Msf Souza
Publikováno v:
Pediatric Research. 44:816-816
Pulmonary complications of obesity have been extensively investigated in adults. However, few studies have evaluated the pulmonary function in obese children. The aim of this study was to perform a pulmonary function test in 29 obese children (15 fem
Autor:
R Liberatori, C Lma Nakaie, A Tg Silva, J Cardieri, M Zullo, T Rozov, A Shinobe, R Liberatore
Publikováno v:
Pediatric Research. 36:825-825
The prevalence and treatment of glucose intolerance were evaluated in 18 cystic fibrosis patients.
Akademický článek
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Publikováno v:
Revista paulista de medicina. 97(4-6)