Zobrazeno 1 - 10
of 311
pro vyhledávání: '"A J, Barbier"'
Publikováno v:
Quarterly Journal of the Royal Meteorological Society
Quarterly Journal of the Royal Meteorological Society, 2022, ⟨10.1002/qj.4365⟩
Quarterly Journal of the Royal Meteorological Society, 2022, ⟨10.1002/qj.4365⟩
International audience; A severe heatwave occurred in April 2010 over West Africa. It was characterisedby a particularly high daily minimum temperature reaching more than 35◦ Clocally and a high water vapour content. In this study we analyse the ab
Autor:
Christian J. Hendriksz, Joseph Muenzer, Adeline Vanderver, Jonathan M. Davis, Barbara K. Burton, Nancy J. Mendelsohn, Nan Wang, Luying Pan, Arian Pano, Ann J. Barbier
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 5, Iss C, Pp 103-106 (2015)
In mucopolysaccharidoses (MPS), glycosaminoglycans (GAG) accumulate in tissues. In MPS II, approximately two-thirds of patients are cognitively impaired. We investigated levels of GAG in cerebrospinal fluid (CSF) in different populations from four cl
Externí odkaz:
https://doaj.org/article/88b22d02839a4098a411f02b7d972091
Autor:
Christian J. Hendriksz MD, Joseph Muenzer MD, PhD, Barbara K. Burton MD, Luying Pan PhD, Nan Wang MS, Hicham Naimy PhD, Arian Pano MD, MPH, Ann J. Barbier MD, PhD
Publikováno v:
Journal of Inborn Errors of Metabolism and Screening, Vol 3 (2015)
Hunter syndrome (mucopolysaccharidosis II [MPS II]) is characterized by lysosomal glycosaminoglycan (GAG) accumulation. Although a majority of patients with MPS II experience neurocognitive involvement, few data are available on cerebrospinal fluid (
Externí odkaz:
https://doaj.org/article/44f864c277834cba9dd735f119dfda5b
Autor:
Catharina Landström, J. Barbier
Publikováno v:
Technikfolgenabschätzung – Theorie und Praxis, Vol 21, Iss 3 (2012)
Externí odkaz:
https://doaj.org/article/3049b1544c1643bdaf7a35b90d4fe298
Publikováno v:
Nature biotechnology. 40(6)
The emergency use authorizations (EUAs) of two mRNA-based severe acute respiratory syndrome coronavirus (SARS-CoV)-2 vaccines approximately 11 months after publication of the viral sequence highlights the transformative potential of this nucleic acid
Autor:
Bruce Silver, Susan Bodie, Janet L. Kwiatkowski, Chris Bowden, Bertil Glader, Kevin H.M. Kuo, Eduard J. van Beers, Frédéric Galactéros, Peter Hawkins, Christian Rose, Yaddanapudi Ravindranath, Marie Hélène Jouvin, Sujit Sheth, Lei Hua, D. Mark Layton, Charles Kung, Wilma Barcellini, Hassan M. Yaish, D. Holmes Morton, Ann J Barbier, Rachael F. Grace
Publikováno v:
The New England journal of medicine, 381(10), 933. Massachussetts Medical Society
BACKGROUND: Pyruvate kinase deficiency is caused by mutations in PKLR and leads to congenital hemolytic anemia. Mitapivat is an oral, small-molecule allosteric activator of pyruvate kinase in red cells. METHODS: In this uncontrolled, phase 2 study, w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76495ae23af100463de397dc069f99ed
https://dspace.library.uu.nl/handle/1874/387483
https://dspace.library.uu.nl/handle/1874/387483
Autor:
Hicham Naimy, Barbara K. Burton, Nan Wang, Luying Pan, Arian Pano, Ann J. Barbier, Christian J. Hendriksz, Joseph Muenzer
Publikováno v:
Journal of Inborn Errors of Metabolism and Screening, Volume: 3, Article number: e150002, Published: 19 JUN 2019
Journal of Inborn Errors of Metabolism and Screening, Vol 3 (2015)
Journal of Inborn Errors of Metabolism and Screening v.3 2015
Journal of Inborn Errors of Metabolism and Screening
Instituto Genética para Todos (IGPT)
instacron:IGPT
Journal of Inborn Errors of Metabolism and Screening, Vol 3 (2015)
Journal of Inborn Errors of Metabolism and Screening v.3 2015
Journal of Inborn Errors of Metabolism and Screening
Instituto Genética para Todos (IGPT)
instacron:IGPT
Hunter syndrome (mucopolysaccharidosis II [MPS II]) is characterized by lysosomal glycosaminoglycan (GAG) accumulation. Although a majority of patients with MPS II experience neurocognitive involvement, few data are available on cerebrospinal fluid (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59c4674d9cb4b6a7c5966e73a2069bbd
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2326-45942015000100601&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2326-45942015000100601&lng=en&tlng=en
Autor:
Maria G. González, Esther N. Ponzi, Osmar A. Ferretti, Claudia E. Quincoces, P. Marecot, J. Barbier
Publikováno v:
Adsorption Science & Technology, Vol 18 (2000)
The influence of molybdenum on the CO 2 reforming of methane, simultaneous sulphur poisoning and carbon formation over alumina-supported Ni catalysts was studied. A series of Ni/Al 2 O 3 catalysts modified by Mo was prepared to enable the effect of m
Externí odkaz:
https://doaj.org/article/50fdc3a926cd4ab29d6678537de5e259
Autor:
Ann J. Barbier, Suresh Vijayaraghavan, Mary Ann Mascelli, Nan Wang, Joseph Muenzer, Christian J. Hendriksz, Saikat Santra, Victor Perry, Kenneth Sciarappa, Zheng Fan, Guirish A. Solanki, Luying Pan
Publikováno v:
Genetics in Medicine. 18:73-81
Approximately two-thirds of patients with the lysosomal storage disease mucopolysaccharidosis II have progressive cognitive impairment. Intravenous (i.v.) enzyme replacement therapy does not affect cognitive impairment because recombinant iduronate-2
Autor:
Ann J. Barbier, Adeline Vanderver, Jonathan M. Davis, Nan Wang, Barbara K. Burton, Luying Pan, Christian J. Hendriksz, Joseph Muenzer, Arian Pano, Nancy J. Mendelsohn
Publikováno v:
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 5, Iss C, Pp 103-106 (2015)
Molecular Genetics and Metabolism Reports, Vol 5, Iss C, Pp 103-106 (2015)
In mucopolysaccharidoses (MPS), glycosaminoglycans (GAG) accumulate in tissues. In MPS II, approximately two-thirds of patients are cognitively impaired. We investigated levels of GAG in cerebrospinal fluid (CSF) in different populations from four cl