Results 1 to 10 of about 222,795 (198)
Identifying the counterpart of HESS J1858+020 [PDF]
Astronomy and Astrophysics, 2010 6 pages, 3 figures, accepted for publication in A&A ...
Paron, Sergio Ariel +1 more
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Correction to: 10.1007/s40005-020-00480-1, 10.1007/s40005-020-00481-0, 10.1007/s40005-020-00482-z, and 10.1007/s40005-020-00484-x [PDF]
Journal of Pharmaceutical Investigation, 2020 The article Emerging nanoparticulate drug delivery systems of metformin, written by Yao Chen, Xinzhu Shan, Cong Luo and Zhonggui He, was originally published Online First without Open Access.
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Publisher Correction: 10.1038/s41401-020-0400-z,10.1038/s41401-020-0414-6,10.1038/s41401-020-0372-z [PDF]
Acta Pharmacologica Sinica, 2020 The articles listed above were initially published with incorrect copyright information or changed later to incorrect copyright information.
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PWE-020 Diagnosing Microscopic Colitis – Is Colonoscopy Necessary?: Abstract PWE-020 Table 1 [PDF]
Gut, 2014 Introduction Microscopic colitis is a common cause of chronic diarrhoea, particularly in older people, and the incidence is increasing. As the endoscopic appearance is typically normal, diagnosis of the two subtypes, collagenous and lymphocytic colitis, relies upon specific histology findings.
A. Pennefather +3 more
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P03-020 - A novel 15-HPGD mutation in pachydermoperiostosis [PDF]
Pediatric Rheumatology, 2013 Autosomal recessive primary hypertrophic osteoathropathy (PHO), also known as pachydermoperiostosis (PDP), is a rare genetic disease characterized by clubbing of the fingers, arthritis, periostosis and pachydermia and results from mutations in 15-hydroxyprostaglandin dehydrogenase (HPGD).
Çiğdem Köroğlu +5 more
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IS-020 Functional Connectivity In The Infant Brain [PDF]
Archives of Disease in Childhood, 2014 Advanced MRI techniques have been increasingly applied in infants to explore the structural and functional architecture of the developing brain. Functional connectivity magnetic resonance imaging (fcMRI) utilises spontaneous, low-frequency, coherent fluctuations in blood oxygen level dependent signal to identify networks of functional cerebral ...
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PW02-020 - Colitis revealing mevalonate kinase deficiency [PDF]
Pediatric Rheumatology, 2013 Hyperimmunoglobulinemia D (HIDS) is the less severe form of mevalonate kinase deficiency (MKD) caused by recessive inherited mutation in the mevalonate kinase gene (MVK). HIDS is characterized by febrile attacks, often associated with transient digestive manifestations, such as abdominal pain, diarrhea and vomiting.
L Michael, BM Brigitte, J Camille
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3PC-020 Dose-banding of nivolumab
Section 3: Production and compounding, 2018 Background Nivolumab is a human monoclonal antibody used in the pneumology unit to treat patients with metastatic non-small cell lung cancer (NSCLC) with progression on, or after, platinum-based chemotherapy. Nivolumab is administered intravenously at a dose of 3 mg/kg every 2 weeks or at a dose of 240 mg (dose based on the median body weight of 80 kg
MA Lester, A Laugueux, A Frapsauce
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VLA and Optical Mapping of the Quasar PKS 0812+020 [PDF]
Symposium - International Astronomical Union, 1982 Observations are reported of the remarkable object PKS 0812+020, the first quasar found to have optical emission in one of its radio lobes. A distinct radio jet is also seen, and there is radio and optical evidence that the quasar is near the center of a galaxy cluster.
Frank D. Ghigo +4 more
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, 2011 Extrait du corpus d'Orléans, réalisé dans le cadre de l'Enquête SocioLinguistique à Orléans à la fin des années 1960. Le sous-corpus "omelette" représente les 96 réponses à la question sur la recette de l'omelette posée au cours des entretiens en face-à-face.
Blanc, Michel +5 more
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