Zobrazeno 1 - 10
of 2 113
pro vyhledávání: '"A. H. Jacobs"'
Autor:
José H. Jacobs, Maciej Strak, Guus J․M. Velders, Jelle Zorn, Lenny Hogerwerf, Mariana Simões, Suzanne Mijnen-Visser, Joost Wesseling, Miriam E. Gerlofs-Nijland, Lidwien A․M. Smit, Roel Vermeulen, Saskia van der Zee, Lapo Mughini-Gras, Massimo Stafoggia
Publikováno v:
Environmental Advances, Vol 17, Iss , Pp 100592- (2024)
This study aimed to examine acute effects of exposure to ambient air pollution on COVID-19 hospital admissions and mortality in the Netherlands. We hypothesized that exposure to increased air pollution in the preceding week might trigger an exacerbat
Externí odkaz:
https://doaj.org/article/bc49193f3bdf4e2e8662598c7be6fa5f
Autor:
Jennifer Kudelka, Malte Ollenschläger, Richard Dodel, Bjoern M. Eskofier, Markus A. Hobert, Klaus Jahn, Jochen Klucken, Bendix Labeit, M. Cristina Polidori, Tino Prell, Tobias Warnecke, Christine A. F. von Arnim, Walter Maetzler, Andreas H. Jacobs, for the DGG working group Neurology
Publikováno v:
BMC Geriatrics, Vol 24, Iss 1, Pp 1-19 (2024)
Abstract Background The Comprehensive Geriatric Assessment (CGA) records geriatric syndromes in a standardized manner, allowing individualized treatment tailored to the patient’s needs and resources. Its use has shown a beneficial effect on the fun
Externí odkaz:
https://doaj.org/article/527af05bf2624a8e91e58b533806d719
Autor:
Elizabeth H. Jacobs, Jacquelyn Schatzman Raposo, Annarita Scardamaglia, Fowzan S. Alkuraya, Shahriar Nafissi, Henry Houlden, Stephan Zuchner, Mario A. Saporta
Publikováno v:
Stem Cell Research, Vol 81, Iss , Pp 103599- (2024)
Myotubularin-Related Protein 5 (MTMR5) is an inactive, poorly characterized D3-phosphatidylinositol phosphatase. Mutations in MTMR5 have been linked to Charcot-Marie-Tooth Disease Type 4B3 (CMT4B3), a rare, early-onset, recessive peripheral neuropath
Externí odkaz:
https://doaj.org/article/bbedd8f413e748e1972a41db4fc7773a
Autor:
Scott A. Langenecker, Mindy Westlund Schreiner, Katie L. Bessette, Henrietta Roberts, Leah Thomas, Alina Dillahunt, Stephanie L. Pocius, Daniel A. Feldman, Dave Jago, Brian Farstead, Myah Pazdera, Erin Kaufman, Jennica A. Galloway, Patricia K. Kerig, Amanda Bakian, Robert C. Welsh, Rachel H. Jacobs, Sheila E. Crowell, Edward R. Watkins
Publikováno v:
Biological Psychiatry Global Open Science, Vol 4, Iss 1, Pp 1-10 (2024)
Background: Rumination-focused cognitive behavioral therapy (RF-CBT) is designed to reduce depressive rumination or the habitual tendency to dwell on experiences in a repetitive, negative, passive, and global manner. RF-CBT uses functional analysis,
Externí odkaz:
https://doaj.org/article/6873e1a4b11148018245415079f3c2b8
Autor:
Richard J. Nowak, Ari Breiner, Vera Bril, Jeffrey A. Allen, Shaida Khan, Todd Levine, Daniel H. Jacobs, Gregory Sahagian, Zaeem A. Siddiqi, Jing Xu, William L. Macias, Michael Benatar, ASCEND MG Study Group
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 11, Iss 1, Pp 194-206 (2024)
Abstract Objectives To assess the safety, tolerability, and key pharmacodynamic effects of subcutaneous batoclimab, a fully human anti‐neonatal Fc receptor monoclonal antibody, in patients with generalized myasthenia gravis and anti‐acetylcholine
Externí odkaz:
https://doaj.org/article/88f6f869acee42ffae3f50c106820b47
Autor:
Henrietta Roberts, Mindy Westlund Schreiner, Stephanie Pocius, Alina K. Dillahunt, Brian Farstead, Daniel Feldman, Katie L. Bessette, Erin A. Kaufman, Will Slattery, Rachel H. Jacobs, David Jago, Sheila E. Crowell, Edward R Watkins, Scott A. Langenecker
Publikováno v:
Journal of Affective Disorders Reports, Vol 16, Iss , Pp 100729- (2024)
Background: Trait rumination is a habitual response to negative experiences that can emerge during adolescence, increasing risk of depression. Trait rumination is correlated with poor inhibitory control (IC) and altered default mode network (DMN) and
Externí odkaz:
https://doaj.org/article/3a07def517c943089f70be2d5d7a3ab8
Publikováno v:
Molecular Imaging, Vol 1 (2002)
Gliomas are the most common types of brain tumors. Although sophisticated regimens of conventional therapies are being carried out to treat patients with gliomas, the disease invariably leads to death over months or years. Before new and potentially
Externí odkaz:
https://doaj.org/article/b27bb2e1906f4995bc831af7c5a80822
Autor:
Imke Ortland, Monique Mendel Ott, Michael Kowar, Christoph Sippel, Yon-Dschun Ko, Andreas H. Jacobs, Ulrich Jaehde
Publikováno v:
BMC Geriatrics, Vol 22, Iss 1, Pp 1-10 (2022)
Abstract Background To evaluate medication-related risks in older patients with cancer and their association with severe toxicity during antineoplastic therapy. Methods This is a secondary analysis of two prospective, single-center observational stud
Externí odkaz:
https://doaj.org/article/e9af0fc72864439c866367e3968fd8f0
Autor:
Harmke A. van Kooten, Imke A. M. Ditters, Marianne Hoogeveen-Westerveld, Edwin H. Jacobs, Johanna M. P. van den Hout, Pieter A. van Doorn, W. W. M. Pim Pijnappel, Ans T. van der Ploeg, Nadine A. M. E. van der Beek
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-13 (2022)
Abstract Background Enzyme replacement therapy (ERT) with recombinant human alpha-glucosidase (rhGAA, alglucosidase alfa) has improved survival, motor outcomes, daily life activity and quality of life in Pompe patients. However, ERT in Pompe disease
Externí odkaz:
https://doaj.org/article/cdbdc84961404c50b4089ea2e7a833db
Autor:
Merel Stok, Helen de Boer, Marshall W. Huston, Edwin H. Jacobs, Onno Roovers, Trudi P. Visser, Holger Jahr, Dirk J. Duncker, Elza D. van Deel, Arnold J.J. Reuser, Niek P. van Til, Gerard Wagemaker
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 17, Iss , Pp 1014-1025 (2020)
Pompe disease is an autosomal recessive lysosomal storage disorder characterized by progressive muscle weakness. The disease is caused by mutations in the acid α-glucosidase (GAA) gene. Despite the currently available enzyme replacement therapy (ERT
Externí odkaz:
https://doaj.org/article/81835f573420466a90338ee21c4f9707