Zobrazeno 1 - 10
of 166
pro vyhledávání: '"A G Wasserman"'
Autor:
Margaret Irwin, Veeraya K. Tanawattanacharoen, Amy Turner, Mary Beth F. Son, Rebecca C. Hale, Craig D. Platt, Juan Putra, Birgitta A.R. Schmidt, Mollie G. Wasserman
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 21, Iss 1, Pp 1-5 (2023)
Abstract Background Sweet syndrome (SS), also known as acute febrile neutrophilic dermatosis, is an immunologic syndrome characterized by widespread neutrophilic infiltration. Histiocytoid Sweet syndrome (H-SS) is a histopathologic variant of SS. Whi
Externí odkaz:
https://doaj.org/article/dd0cf0f729d34e20b4b04ea44e1763df
Publikováno v:
Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies. 23(10)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7cb6a7b38c94486a042c24b8ddd1249a
https://pubmed.ncbi.nlm.nih.gov/35767569
https://pubmed.ncbi.nlm.nih.gov/35767569
Autor:
James L. Januzzi, Shweta R. Motiwala, Nasrien E. Ibrahim, Javed Butler, J. Herbert Patterson, Thomas M. Maddox, Alan G. Wasserman, Gregg C. Fonarow, JoAnn Lindenfeld, Leslie L. Davis, Quentin R. Youmans, Frederick A. Masoudi, Clyde W. Yancy, Khadijah Breathett, Mary Norine Walsh, Larry A. Allen, Estefania Oliveros
Publikováno v:
Journal of the American College of Cardiology. 77:772-810
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1113f380100deee17cf2b51dfda55d2
https://doi.org/10.1016/j.jacc.2020.11.022
https://doi.org/10.1016/j.jacc.2020.11.022
Publikováno v:
Transformation Groups.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a5ed51b93006525278bd97b82c0c1f4
https://doi.org/10.1007/s00031-022-09728-6
https://doi.org/10.1007/s00031-022-09728-6
Publikováno v:
Academic medicine : journal of the Association of American Medical CollegesReference. 97(7)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6a1557d1597fa967766ab7a8b31dc55
https://pubmed.ncbi.nlm.nih.gov/34554951
https://pubmed.ncbi.nlm.nih.gov/34554951
Publikováno v:
The Journal of Physical Chemistry A. 123:10406-10417
An analysis of the 1:1 complex of thiophene and water is presented. In this study, computation and matrix isolation Fourier transform infrared spectroscopy (FTIR) were used to determine stable complexes of thiophene and water. Computational studies f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f4c64c52ef4d73425fe8b1b9f9255e2
https://doi.org/10.1021/acs.jpca.9b07355
https://doi.org/10.1021/acs.jpca.9b07355
Publikováno v:
Transformation Groups. 25:483-515
Suppose G is a cyclic group and M a closed smooth G-manifold with exactly one isotropy type. We will show that there is a nonsingular real algebraic G-variety X such that X is equivariantly diffeomorphic to M and all G-vector bundles over X are stron
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e93e50627d0960c72c11a5b9f8c008bc
https://doi.org/10.1007/s00031-019-09519-6
https://doi.org/10.1007/s00031-019-09519-6
Publikováno v:
Case Reports in Pathology, Vol 2014 (2014)
Langerhan’s cell histiocytosis (LCH) results from the proliferation of immunophenotypically and functionally immature, morphologically rounded Langerhan’s cells along with eosinophils, macrophages, lymphocytes, and, commonly, multinucleated giant
Externí odkaz:
https://doaj.org/article/da78bc1c46794fdaaf2cd349330eaf55
CCDC65 mutation causes primary ciliary dyskinesia with normal ultrastructure and hyperkinetic cilia.
Autor:
Amjad Horani, Steven L Brody, Thomas W Ferkol, David Shoseyov, Mollie G Wasserman, Asaf Ta-shma, Kate S Wilson, Philip V Bayly, Israel Amirav, Malena Cohen-Cymberknoh, Susan K Dutcher, Orly Elpeleg, Eitan Kerem
Publikováno v:
PLoS ONE, Vol 8, Iss 8, p e72299 (2013)
Primary ciliary dyskinesia (PCD) is a genetic disorder characterized by impaired ciliary function, leading to chronic sinopulmonary disease. The genetic causes of PCD are still evolving, while the diagnosis is often dependent on finding a ciliary ult
Externí odkaz:
https://doaj.org/article/7fdb448575d6472db50f26d20a7fe4a0
Autor:
Amjad Horani, Thomas W Ferkol, David Shoseyov, Mollie G Wasserman, Yifat S Oren, Batsheva Kerem, Israel Amirav, Malena Cohen-Cymberknoh, Susan K Dutcher, Steven L Brody, Orly Elpeleg, Eitan Kerem
Publikováno v:
PLoS ONE, Vol 8, Iss 3, p e59436 (2013)
Despite recent progress in defining the ciliome, the genetic basis for many cases of primary ciliary dyskinesia (PCD) remains elusive. We evaluated five children from two unrelated, consanguineous Palestinian families who had PCD with typical clinica
Externí odkaz:
https://doaj.org/article/30c757d765204d78b98ccfadea311c95