Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Gail Deutsch"'
Autor:
Przemyslaw Szafranski, Rijutha P. Garimella, Haresh Mani, Ryan Hartman, Gail Deutsch, Alan Silk, Alan Benheim, Paweł Stankiewicz
Publikováno v:
Clinical Epigenetics, Vol 15, Iss 1, Pp 1-6 (2023)
Abstract Heterozygous SNVs or CNV deletions involving the FOXF1 gene, or its distant enhancer, are causative for 80–90% of cases of alveolar capillary dysplasia with misalignment of pulmonary veins. Recently, we proposed bimodal structure and paren
Externí odkaz:
https://doaj.org/article/f586cec64f4549ceaf3bf3d1ae46ce56
Autor:
Zuzanna Kozłowska, Zuzanna Owsiańska, Joanna P. Wroblewska, Apolonia Kałużna, Andrzej Marszałek, Yogen Singh, Bartłomiej Mroziński, Qian Liu, Justyna A. Karolak, Paweł Stankiewicz, Gail Deutsch, Marta Szymankiewicz-Bręborowicz, Tomasz Szczapa
Publikováno v:
BMC Pediatrics, Vol 20, Iss 1, Pp 1-7 (2020)
Abstract Background Alveolar capillary dysplasia (ACD) is a rare cause of severe pulmonary hypertension and respiratory failure in neonates. The onset of ACD is usually preceded by a short asymptomatic period. The condition is refractory to all avail
Externí odkaz:
https://doaj.org/article/76cc8384c7354543b6c9647b65fc9007
Autor:
Robin Deterding, Matthias Griese, Gail Deutsch, David Warburton, Emily M. DeBoer, Steven Cunningham, Annick Clement, Nicolaus Schwerk, Kevin R. Flaherty, Kevin K. Brown, Florian Voss, Ulrike Schmid, Rozsa Schlenker-Herceg, Daniela Verri, Mihaela Dumistracel, Marilisa Schiwek, Susanne Stowasser, Kay Tetzlaff, Emmanuelle Clerisme-Beaty, Lisa R. Young
Publikováno v:
ERJ Open Research, Vol 7, Iss 2 (2021)
Childhood interstitial lung disease (chILD) comprises >200 rare respiratory disorders, with no currently approved therapies and variable prognosis. Nintedanib reduces the rate of forced vital capacity (FVC) decline in adults with progressive fibrosin
Externí odkaz:
https://doaj.org/article/44d5db22b39344b2a8349a04d7f20b85
Autor:
Robert M. DiBlasi, RRT-NPS, FAARC, Masaki Kajimoto, MD, PhD, Jonathan A. Poli, MS, Gail Deutsch, MD, Juergen Pfeiffer, MS, Joseph Zimmerman, RRT-NPS, David N. Crotwell, MHL, RRT-NPS, Patrik Malone, RRT, James B. Fink, RRT-NPS, PhD, Coral Ringer, RN, Rajesh Uthamanthil, DVM, PhD, Dolena Ledee, PhD, Michael A. Portman, MD
Publikováno v:
Critical Care Explorations, Vol 3, Iss 2, p e0338 (2021)
Objectives:. Effective treatment options for surfactant therapy in acute respiratory distress syndrome and coronavirus disease 2019 have not been established. To conduct preclinical studies in vitro and in vivo to evaluate efficiency, particle size,
Externí odkaz:
https://doaj.org/article/40c5820562d444c88bba89d3ddc037a5
Autor:
Justyna A. Karolak, Gail Deutsch, Tomasz Gambin, Przemyslaw Szafranski, Edwina Popek, Paweł Stankiewicz
Publikováno v:
Am J Respir Cell Mol Biol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b30170f165dc090da7a7e015d1f47521
https://doi.org/10.1165/rcmb.2021-0470le
https://doi.org/10.1165/rcmb.2021-0470le
Autor:
Andrew Frauenpreis, Antony Hoarau, Soumyaroop Bhattacharya, Ian Glass, Gail Deutsch, Thomas Mariani, Denise Al Alam, Soula Danopoulos
Publikováno v:
A54. PEDIATRIC PULMONARY VASCULAR DISEASE.
Rationale: Down syndrome (DS), resulting from Trisomy 21 (T21), is the most common chromosomal disorder worldwide. Cardiopulmonary complications are a leading cause of morbidity and mortality in DS. Pulmonary disorders include pulmonary hypertension
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1571400865e4128e53c065c4e285936b
https://doi.org/10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a1890
https://doi.org/10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a1890
Autor:
Randa Belgacemi, Caroline Cherry, Ian Glass, Gail Deutsch, Y.S Prakash, Christina Pabelick, Soula Danopoulos, Denise Al Alam
Publikováno v:
Physiology. 38
Rationale Human chromosomal anomalies, notably trisomies, induce several alterations in gene expression, leading to various disease phenotypes. Recent studies showed that dermal fibroblasts from patients with trisomy 13 (T13), T18 or T21 present feat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d8a880cb055c2bf3e3fbbb97dd77366
https://doi.org/10.1152/physiol.2023.38.s1.5732910
https://doi.org/10.1152/physiol.2023.38.s1.5732910
Publikováno v:
Physiology. 38
Rationale: Trisomy 21 (T21), resulting in Down Syndrome (DS), is the most prevalent chromosomal abnormality worldwide. Recent studies have indicated that individuals with DS present with ciliopathies, as well as impaired mucociliary clearance. Wherea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af050cca7e4bdadcc794b7153a791abe
https://doi.org/10.1152/physiol.2023.38.s1.5731849
https://doi.org/10.1152/physiol.2023.38.s1.5731849
Autor:
Rebekah Nevel, Gail Deutsch, Daniel Craven, Robin Deterding, Martha Fishman, Jennifer Wambach (Guest Editor), Alicia Casey, Katie Krone, Deborah R. Liptzin, Michael O'Connor, Geoffrey Kurland, Jane Taylor, William Gower, James Hagood, Carol Conrad, Jade Tam-Williams, Elizabeth Fiorino, Samuel Goldfarb, Sara Sadreameli, Lawrence Nogee, Gregory Montgomery, Aaron Hamvas, Terri Laguna, Manvi Bansal, Cheryl Lew, Maria Santiago, Antonia Popova, Aliva De, Marilynn Chan, Michael Powers, Maureen B Josephson, Devaney Camburn, Laura Voss, Yun Li, Lisa Young
Childhood interstitial and diffuse lung disease (chILD) encompasses a broad spectrum of rare disorders. The Children’s Interstitial and Diffuse Lung Disease Research Network (chILDRN) established a prospective registry to advance knowledge regardin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6a52590e774d4b51c11f680d953700f
https://doi.org/10.22541/au.167985552.21776673/v1
https://doi.org/10.22541/au.167985552.21776673/v1
Autor:
Vivian E, Saper, Michael J, Ombrello, Adriana H, Tremoulet, Gonzalo, Montero-Martin, Sampath, Prahalad, Scott, Canna, Chisato, Shimizu, Gail, Deutsch, Serena Y, Tan, Elaine F, Remmers, Dimitri, Monos, Timothy, Hahn, Omkar K, Phadke, Elaine, Cassidy, Ian, Ferguson, Vamsee, Mallajosyula, Jianpeng, Xu, Jaime S, Rosa Duque, Gilbert T, Chua, Debopam, Ghosh, Ann Marie, Szymanski, Danielle, Rubin, Jane C, Burns, Lu, Tian, Marcelo A, Fernandez-Vina, Elizabeth D, Mellins, Jill A, Hollenbach, Claudio, Len
Publikováno v:
Annals of the Rheumatic Diseases. 81:406-415
ObjectivesDrug reaction with eosinophilia and systemic symptoms (DRESS) is a severe, delayed hypersensitivity reaction (DHR). We observed DRESS to inhibitors of interleukin 1 (IL-1) or IL-6 in a small group of patients with Still’s disease with aty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a93ee2030ac0da2800956da32ec43822
https://doi.org/10.1136/annrheumdis-2021-220578
https://doi.org/10.1136/annrheumdis-2021-220578