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I Cordeiro

Explore the profile of I Cordeiro including associated specialties, affiliations and a list of published articles. Areas
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Articles 23
Citations 192
Followers 0
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Recent Articles
1.
Cordeiro I, Duarte A, Ferreira J, Goncalves M, Meirinhos T, Rocha T, et al.
Acta Reumatol Port . 2016 Sep; 41(2):112-30. PMID: 27606471
Background: Serious infections are a major cause of morbidity and mortality in systemic inflammatory rheumatic disease (SIRD) patients. Although vaccination may prevent numerous infections, vaccination uptake rates are low in...
2.
Araujo F, Cordeiro I, Teixeira F, Rovisco J, Ramiro S, Mourao A, et al.
Acta Reumatol Port . 2014 May; 39(2):158-71. PMID: 24850289
Objective: To develop Portuguese evidence-based recommendations for the Diagnosis and Management of Gout. Methods: As part of the 3e Initiative (Evidence, Expertise and Exchange), a panel of 78 international rheumatologists...
3.
Araujo F, Cordeiro I, Teixeira F, Goncalves J, Fonseca J
Acta Reumatol Port . 2014 May; 39(1):19-26. PMID: 24811458
Objective: To review current evidence concerning pharmacology of biosimilar candidates to be used in rheumatology. Methods: A PubMed search up to August 2013 was performed using relevant search terms to...
4.
Makrythanasis P, van Bon B, Steehouwer M, Rodriguez-Santiago B, Simpson M, Dias P, et al.
Clin Genet . 2013 Jan; 84(6):539-45. PMID: 23320472
Recently, pathogenic variants in the MLL2 gene were identified as the most common cause of Kabuki (Niikawa-Kuroki) syndrome (MIM#147920). To further elucidate the genotype-phenotype correlation, we studied a large cohort...
5.
Roque R, Vinagre F, Cordeiro I, Goncalves P, Bartolo E, Canas da Silva J, et al.
Acta Reumatol Port . 2012 Nov; 37(2):175-9. PMID: 23149640
Syphilis is a disease caused by Treponema pallidum infection with protean clinical manifestations. Musculoskeletal complaints are however uncommon and most of the time mild. Occasionally they can dominate the clinical...
6.
Almeida M, Campos-Xavier A, Medeira A, Cordeiro I, Sousa A, Lima M, et al.
Clin Genet . 2009 Feb; 75(2):150-6. PMID: 19215249
Mutations in the gene that encodes Fibroblast Growth Factor Receptor 3 (FGFR3) are associated with Achondroplasia (MIM 100800), Hypochondroplasia (MIM 146000), Muenke Syndrome (MIM 602849), Thanatophoric Dysplasia (MIM 187600, MIM...
7.
Janeiro P, Cunha M, Cordeiro I, Santos H, Antunes N
Rev Neurol . 2008 Mar; 46(6):347-50. PMID: 18368679
Introduction: Neurofibromatosis type 1 and tuberous sclerosis are two distinct neurocutaneous syndromes that result of a mutation of tumoral suppressor genes, increasing the risk of tumorigenesis. They both have dominant...
8.
Cardoso M, Balreira A, Martins E, Nunes L, Cabral A, Marques M, et al.
Mol Genet Metab . 2005 Jun; 85(3):228-35. PMID: 15979035
Smith-Lemli-Opitz syndrome (SLO) is an autosomal recessive disorder characterised by craniofacial dysmorphism, mental retardation, multiple congenital anomalies, and increased levels of 7-dehydrocholesterol (7-DHC) in body tissues and fluids. SLO is...
9.
Darc Felicio J, Rossi M, Park H, Goncalez E, Braggio M, David J, et al.
Fitoterapia . 2001 Jun; 72(4):453-5. PMID: 11395278
A new flavone dimer, 3-hydroxy-4',5,7-trimethoxyflavone-(6-->8")-3"-hydroxy-3"',4"', 5",7"-tetramethoxyflavone, together with amenthoflavone, have been isolated from the leaves of Ouratea multiflora. Its structure was established by spectroscopic methods, including two-dimensional NMR spectroscopy.
10.
Vassal H, Medeira A, Cordeiro I, Santos H, Castedo S, Saraiva C, et al.
Am J Med Genet . 2001 Mar; 99(4):331-4. PMID: 11252003
No abstract available.