Zobrazeno 1 - 10 of 25 pro vyhledávání: '"P M Frossard"'
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Akademický článek
Factors associated with adherence to anti-hypertensive treatment in Pakistan.
Autor: Saman K Hashmi, Maria B Afridi, Kanza Abbas, Rubina A Sajwani, Danish Saleheen, Philippe M Frossard, Mohammad Ishaq, Aisha Ambreen, Usman Ahmad
Publikováno v: PLoS ONE, Vol 2, Iss 3, p e280 (2007)
OBJECTIVES: Poor adherence is one of the biggest obstacles in therapeutic control of high blood pressure. The objectives of this study were (i) to measure adherence to antihypertensive therapy in a representative sample of the hypertensive Pakistani
Externí odkaz: https://doaj.org/article/8c6c0818d6af46298ff7971d19bf26e5
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2
Disease severity associated with cystic fibrosis mutations delta F508 and S549R [T-G]
Autor: B Al-Awar, K. P. Dawson, P M Frossard
Publikováno v: Eastern Mediterranean Health Journal. 7:975-980
We compared the clinical severity associated with the two cystic fibrosis [CF] mutations S549R [T [R] G] and deltaF508. Clinical and biochemical variables of CF were compared in two age- and sex-matched groups of CF children in the United Arab Emirat
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::646c93949785dd058a09108202fc0ab7
https://doi.org/10.26719/2001.7.6.975
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3
X-linked dyskeratosis congenita: restrictive pulmonary disease and a novel mutation
Autor: W F Safa, G G Lestringant, P M Frossard
Publikováno v: Thorax. 56:891-894
Dyskeratosis congenita (DC) is a rare inherited multisystem disorder characterised by lesions of the skin and appendages. Bone marrow failure occurs in 80% of patients. The gene for the X-linked form of DC has been identified on Xq28 and designated a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8645f63987486b27c8c9baeabcfd57bf
https://doi.org/10.1136/thorax.56.11.891
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4
Radiological analysis of children with cystic fibrosis who are homozygous for cystic fibrosis transmembrane conductance regulator mutation S549R (T->G)
Autor: K P Dawson, J Hertecant, P M Frossard, Y Bossaert, D Bakalinova
Publikováno v: Journal of Tropical Pediatrics. 45:158-160
Genotype-phenotype analyses in cystic fibrosis (CF) have shown that cystic fibrosis transmembrane conductance regulator (CFTR) genotypes can predict pancreatic status but that correlations with pulmonary status remain elusive. We investigated the ext
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bab5760d0b490a4a97a56f6788dea60d
https://doi.org/10.1093/tropej/45.3.158
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5
Disease severity associated with cystic fibrosis mutations deltaF508 and S549R(T--G)
Autor: K P, Dawson, P M, Frossard, B, Al-Awar
Publikováno v: Eastern Mediterranean health journal = La revue de sante de la Mediterranee orientale = al-Majallah al-sihhiyah li-sharq al-mutawassit. 7(6)
We compared the clinical severity associated with the two cystic fibrosis (CF) mutations S549R(T--G) and deltaF508. Clinical and biochemical variables of CF were compared in two age- and sex-matched groups of CF children in the United Arab Emirates (
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::842657e18c8dedf4cef737ebf43067e7
https://pubmed.ncbi.nlm.nih.gov/15332739
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7
Etiology of toe-web disease in Al-Ain, United Arab Emirates: bacteriological and mycological studies
Autor: G G, Lestringant, K A, Saarinen, P M, Frossard, A, Bener, A M, Ameen
Publikováno v: Eastern Mediterranean health journal = La revue de sante de la Mediterranee orientale = al-Majallah al-sihhiyah li-sharq al-mutawassit. 7(1-2)
We examined and sampled 45 patients with toe-web intertrigo for bacteriological and mycological studies. Prominent isolated pathogens were the genus Candida (57.7%), genus Aspergillus (28.8%), Pseudomonas aeruginosa (26.7%) and coliforms (24.4%). Der
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::42b92a3a283bd4a4eadb9a314ec2d6b9
https://pubmed.ncbi.nlm.nih.gov/12596950
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9
The geographic distribution of cystic fibrosis mutations gives clues about population origins
Autor: P M Frossard, K P Dawson
Publikováno v: European journal of pediatrics. 159(7)
Information regarding three of the more common cystic fibrosis mutations is presented (delta F508, G542X, N13031K) to support the concept of a geography associated with cystic fibrosis mutations. We present the hypothesis that a knowledge of the geog
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15cecc53895dd14d3f446d3a1ebf40f8
https://pubmed.ncbi.nlm.nih.gov/10923221
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10
Genotype-phenotype correlations in cystic fibrosis: clinical severity of mutation S549R(T--G)
Autor: P M Frossard, Y Bossaert, J Hertecant, K P Dawson
Publikováno v: The European respiratory journal. 13(1)
With a view to assessing genotype-to-phenotype correlations in cystic fibrosis (CF), the clinical presentation of CF children from the United Arab Emirates (UAE) who were homozygous for cystic fibrosis transmembrane conductance regulator (CFTR) mutat
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63c811f598205e3cc6f3dffa37258f8f
https://pubmed.ncbi.nlm.nih.gov/10836331
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