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Results: 1-13 |
Results: 13
Diet, clothing, sunshine exposure and micronutrient status of Arab infantsand young children
Authors: Dawodu, A Dawson, KP Amirlak, I Kochiyil, J Agarwal, M Badrinath, P
Citation: A. Dawodu et al., Diet, clothing, sunshine exposure and micronutrient status of Arab infantsand young children, ANN TROP PA, 21(1), 2001, pp. 39-44
The S549R (T -> G) cystic fibrosis gene mutation
Authors: Dawson, KP Frossard, PM
Citation: Kp. Dawson et Pm. Frossard, The S549R (T -> G) cystic fibrosis gene mutation, J TROP PEDI, 47(4), 2001, pp. 196-198
A hypothesis regarding the origin and spread of the cystic fibrosis mutation Delta F508
Authors: Dawson, KP Frossard, PM
Citation: Kp. Dawson et Pm. Frossard, A hypothesis regarding the origin and spread of the cystic fibrosis mutation Delta F508, QJM-MON J A, 93(5), 2000, pp. 313-315
Bartter syndrome: an overview
Authors: Amirlak, I Dawson, KP
Citation: I. Amirlak et Kp. Dawson, Bartter syndrome: an overview, QJM-MON J A, 93(4), 2000, pp. 207-215
The geographic distribution of cystic fibrosis mutations gives clues aboutpopulation origins
Authors: Dawson, KP Frossard, PM
Citation: Kp. Dawson et Pm. Frossard, The geographic distribution of cystic fibrosis mutations gives clues aboutpopulation origins, EUR J PED, 159(7), 2000, pp. 496-499
Group A streptococcal throat colonization is a dynamic phenomenon
Authors: Dawson, KP Nsanze, H Ameen, AS Mustafa, N
Citation: Kp. Dawson et al., Group A streptococcal throat colonization is a dynamic phenomenon, ANN TROP PA, 20(1), 2000, pp. 16-21
Cystic fibrosis in the Middle East: The historical perspective
Authors: Dawson, KP Frossard, PM
Citation: Kp. Dawson et Pm. Frossard, Cystic fibrosis in the Middle East: The historical perspective, ANN SAUDI M, 20(1), 2000, pp. 20-23
Mild clinical phenotype associated with R1158X/S549R(T -> G) CFTR genotype
Authors: Frossard, PM Abdelaziz, SA Hertecant, J Girodon, E Goossens, M Dawson, KP
Citation: Pm. Frossard et al., Mild clinical phenotype associated with R1158X/S549R(T -> G) CFTR genotype, CLIN GENET, 58(2), 2000, pp. 147-149
Identification of cystic fibrosis mutations in Oman
Authors: Frossard, PM Dawson, KP Das, SJ Alexander, PC Girodon, E Goossens, M
Citation: Pm. Frossard et al., Identification of cystic fibrosis mutations in Oman, CLIN GENET, 57(3), 2000, pp. 235-236
Genotype-phenotype correlations in cystic fibrosis: clinical severity of mutation S549R(T -> G)
Authors: Frossard, PM Hertecant, J Bossaert, Y Dawson, KP
Citation: Pm. Frossard et al., Genotype-phenotype correlations in cystic fibrosis: clinical severity of mutation S549R(T -> G), EUR RESP J, 13(1), 1999, pp. 100-102
Complex allele [-102T > A+S549R(T > G)] is associated with milder forms ofcystic fibrosis than allele S549R[T > G) alone
Authors: Romey, MC Guittard, C Chazalette, JP Frossard, P Dawson, KP Patton, MA Casals, T Bazarbachi, T Girodon, E Rault, G Bozon, D Seguret, F Demaille, J Claustres, M
Citation: Mc. Romey et al., Complex allele [-102T > A+S549R(T > G)] is associated with milder forms ofcystic fibrosis than allele S549R[T > G) alone, HUM GENET, 105(1-2), 1999, pp. 145-150
Radiological analysis of children with cystic fibrosis who are homozygous for cystic fibrosis transmembrane conductance regulator mutation S549R (T -> G)
Authors: Frossard, PM Bakalinova, D Hertecant, J Bossaert, Y Dawson, KP
Citation: Pm. Frossard et al., Radiological analysis of children with cystic fibrosis who are homozygous for cystic fibrosis transmembrane conductance regulator mutation S549R (T -> G), J TROP PEDI, 45(3), 1999, pp. 158-160
Determination of the prevalence of cystic fibrosis in the United Arab Emirates by genetic carrier screening
Authors: Frossard, PM Lestringant, G Girodon, E Goossens, M Dawson, KP
Citation: Pm. Frossard et al., Determination of the prevalence of cystic fibrosis in the United Arab Emirates by genetic carrier screening, CLIN GENET, 55(6), 1999, pp. 496-497
Risultati: 1-13 |