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Results: 1-25 | 26-28
Results: 1-25/28
Cutaneous nocardiosis of the chest wall and pleura - 10-year consequences of a hand actinomycetoma
Authors: Saarinen, KA Lestringant, GG Czechowski, J Frossard, PM
Citation: Ka. Saarinen et al., Cutaneous nocardiosis of the chest wall and pleura - 10-year consequences of a hand actinomycetoma, DERMATOLOGY, 202(2), 2001, pp. 131-133
Haplotypes of the human renin gene associated with essential hypertension and stroke
Authors: Frossard, PM Malloy, MJ Lestringant, GG Kane, JP
Citation: Pm. Frossard et al., Haplotypes of the human renin gene associated with essential hypertension and stroke, J HUM HYPER, 15(1), 2001, pp. 49-55
Congenital insensitivity to pain with anhidrosis
Authors: Sztriha, L Lestringant, GG Hertecant, J Frossard, PM Masouye, I
Citation: L. Sztriha et al., Congenital insensitivity to pain with anhidrosis, PED NEUROL, 25(1), 2001, pp. 63-66
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
X-linked dyskeratosis congenita: restrictive pulmonary disease and a novelmutation
Authors: Safa, WF Lestringant, GG Frossard, PM
Citation: Wf. Safa et al., X-linked dyskeratosis congenita: restrictive pulmonary disease and a novelmutation, THORAX, 56(11), 2001, pp. 891-894
Genetic and clinical heterogeneity in transgressive palmoplantar keratoderma
Authors: Lestringant, GG Frossard, PM Eckl, KM Reis, A Hennies, HC
Citation: Gg. Lestringant et al., Genetic and clinical heterogeneity in transgressive palmoplantar keratoderma, J INVES DER, 116(5), 2001, pp. 825-827
Identification, by homozygosity mapping, of a novel locus for autosomal recessive congenital ichthyosis on chromosome 17p, and evidence for further genetic heterogeneity
Authors: Krebsova, A Kuster, W Lestringant, GG Schulze, B Hinz, B Frossard, PM Reis, A Hennies, HC
Citation: A. Krebsova et al., Identification, by homozygosity mapping, of a novel locus for autosomal recessive congenital ichthyosis on chromosome 17p, and evidence for further genetic heterogeneity, AM J HU GEN, 69(1), 2001, pp. 216-222
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
Diffuse calcinosis cutis in a patient with congenital leukemia and leukemia cutis
Authors: Lestringant, GG Masouye, I El-Hayek, M Girardet, C Revesz, T Frossard, PM
Citation: Gg. Lestringant et al., Diffuse calcinosis cutis in a patient with congenital leukemia and leukemia cutis, DERMATOLOGY, 200(2), 2000, pp. 147-150
Lack of association between human TGF-beta 1 gene variants and primary hypertension
Authors: Frossard, PM Pravica, V Perrey, C Hutchinson, IV Lukic, ML
Citation: Pm. Frossard et al., Lack of association between human TGF-beta 1 gene variants and primary hypertension, AM J HYPERT, 13(8), 2000, pp. 944-945
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
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
Settling the score on hairless - Reply
Authors: Sprecher, E Lestringant, GG Szargel, R Bergman, R Labay, V Frossard, PM Friedman-Birnbaum, R Cohen, N
Citation: E. Sprecher et al., Settling the score on hairless - Reply, J INVES DER, 115(4), 2000, pp. 762-763
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
Actinic damage and squamous cell carcinoma in sun-exposed skin affected byvitiligo
Authors: Saarinen, KA Lestringant, GG Masouye, I Frossard, PM
Citation: Ka. Saarinen et al., Actinic damage and squamous cell carcinoma in sun-exposed skin affected byvitiligo, BR J DERM, 143(1), 2000, pp. 219-221
Renin gene MboI dimorphism is a discriminator for hypertension in hyperlipidaemic subjects
Authors: Frossard, PM Kane, JP Malloy, MJ Bener, A
Citation: Pm. Frossard et al., Renin gene MboI dimorphism is a discriminator for hypertension in hyperlipidaemic subjects, HYPERTENS R, 22(4), 1999, pp. 285-289
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
Analysis of the apolipoprotein B gene 3 ' hypervariable region among nationals of the Abu Dhabi Emirate and comparisons with other populations
Authors: Frossard, PM Lestringant, GG
Citation: Pm. Frossard et Gg. Lestringant, Analysis of the apolipoprotein B gene 3 ' hypervariable region among nationals of the Abu Dhabi Emirate and comparisons with other populations, ANN SAUDI M, 19(6), 1999, pp. 490-494
Association of an apolipoprotein B gene marker with essential hypertension
Authors: Frossard, PM Obineche, EN Lestringant, GG
Citation: Pm. Frossard et al., Association of an apolipoprotein B gene marker with essential hypertension, HYPERTENSIO, 33(4), 1999, pp. 1052-1056
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
Atrichia with papular lesions resulting from a nonsense mutation within the human hairless gene
Authors: Sprecher, E Lestringant, GG Szargel, R Bergman, R Labay, V Frossard, PM Friedman-Birnbaum, R Cohen, N
Citation: E. Sprecher et al., Atrichia with papular lesions resulting from a nonsense mutation within the human hairless gene, J INVES DER, 113(4), 1999, pp. 687-690
Allergic contact dermatitis in the United Arab Emirates
Authors: Lestringant, GG Bener, A Sawaya, M Galadari, IH Frossard, PM
Citation: Gg. Lestringant et al., Allergic contact dermatitis in the United Arab Emirates, INT J DERM, 38(3), 1999, pp. 181-186
Human renin gene BglI dimorphism associated with hypertension in two independent populations
Authors: Frossard, PM Lestringant, GG Malloy, MJ Kane, JP
Citation: Pm. Frossard et al., Human renin gene BglI dimorphism associated with hypertension in two independent populations, CLIN GENET, 56(6), 1999, pp. 428-433
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: 1-25 | 26-28