Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Susan L. Minnix"'
Autor:
Susan L. Minnix, Maimoona A. Zariwala, Michael R. Knowles, Peadar G. Noone, Paul L. Molina, Margaret W. Leigh, Marcus P. Kennedy
Publikováno v:
American Journal of Roentgenology. 188:1232-1238
High-resolution CT is an important tool in the detection and management of bronchiectasis, but there is little information about high-resolution CT findings in primary ciliary dyskinesia (PCD). We analyzed all high-resolution CT studies of the chest
Autor:
Michael R. Knowles, Peadar G. Noone, Marcus P. Kennedy, Paul L. Molina, Andrew J. Ghio, Susan L. Minnix, Johnny L. Carson, Maimoona B Zariwala
Publikováno v:
Respiratory Medicine. 101:76-83
Summary Background An association between lithoptysis and primary ciliary dyskinesia (PCD) has not been previously reported. However, reports of lithoptysis from 2 older patients (>60yr) prompted a study of this association. Methods We performed a pr
Autor:
Maimoona B Zariwala, Susan L. Minnix, Milan J. Hazucha, Margaret W. Leigh, Peadar G. Noone, Michael R. Knowles, Johnny L. Carson, Aruna Sannuti
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 169:459-467
Primary ciliary dyskinesia (PCD) is a genetic disease characterized by abnormalities in ciliary structure/function. We hypothesized that the major clinical and biologic phenotypic markers of the disease could be evaluated by studying a cohort of subj
Autor:
Maimoona A. Zariwala, Susan L. Minnix, Johnny L. Carson, Michael R. Knowles, Zhaoqing Zhou, Milan J. Hazucha, Peadar G. Noone, Margaret W. Leigh, Aruna Sannuti
Publikováno v:
American Journal of Respiratory Cell and Molecular Biology. 25:577-583
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous, autosomal recessive disorder caused by abnormal ciliary ultrastructure and function, characterized clinically by oto-sino-pulmonary disease. Mutations in an intermediate chain dynein (D
Autor:
Scott D. Sagel, Kenneth N. Olivier, Susan L. Minnix, Johnny L. Carson, Miriam Schmidts, Heike Olbrich, Maimoona A. Zariwala, Milan J. Hazucha, Michael C. Armstrong, Margaret W. Leigh, Sharon D. Dell, Niki Tomas Loges, Kimberlie A. Burns, Adriana Lori, Stephanie D. Davis, Anita Becker-Heck, Margaret Rosenfeld, Thomas W. Ferkol, Heymut Omran, Claudius Werner, Michael R. Knowles
Publikováno v:
Thorax. 67(5)
Rationale Primary ciliary dyskinesia (PCD) is an autosomal recessive, genetically heterogeneous disorder characterised by oto-sino-pulmonary disease and situs abnormalities (Kartagener syndrome) due to abnormal structure and/or function of cilia. Mos
Autor:
Stephanie D. Davis, Scott D. Sagel, Susan L. Minnix, Carlos Milla, Michael R. Knowles, Johnny L. Carson, Margaret Rosenfeld, Thomas W. Ferkol, Kenneth N. Olivier, Brock R. Baker, Margaret W. Leigh, Mary Leigh Anne Daniels, Sharon D. Dell
Publikováno v:
A28. CILIA IN HEALTH AND DISEASE: PRIMARY CILIARY DYSKINESIA AND BRONCHIECTASIS.
Autor:
Adam J. Shapiro, Knowles, Milan J. Hazucha, Jessica E. Pittman, David E. Brown, Susan L. Minnix, Kunal K. Chawla, Margaret W. Leigh
Publikováno v:
B96. NEW DATA REGARDING UNCOMMON PEDIATRIC LUNG DISEASES.
Rationale: Nasal nitric oxide (nNO) is a promising non−invasive screening test for Primary Ciliary Dyskinesia (PCD) in people over 6 years of age. Little is known about how nNO production changes between birth and 6 years. Methods: Using an IRB app
Autor:
Scott D. Sagel, Heike Olbrich, M Armstrong, Susan L. Minnix, Maimoona A. Zariwala, Margaret W. Leigh, Margaret Rosenfeld, Milan J. Hazucha, A Becker, Heymut Omran, Michael R. Knowles, Niki T. Loges, Sharon D. Dell, A Lori, Thomas W. Ferkol, Kenneth N. Olivier, Miriam Schmidts
Publikováno v:
A27. GENETIC AND ACQUIRED CILIA DISEASE.
Autor:
Peadar G. Noone, Lars Lange, Michael R. Knowles, Heymut Omran, Margaret W. Leigh, Maimoona A. Zariwala, Blair V. Robinson, Hilda N. Morillas, Lucy Morgan, Thomas Severin, Marcus P. Kennedy, Susan L. Minnix, Paul L. Molina, Heike Olbrich, Sharon D. Dell, Peter Ahrens
Publikováno v:
Circulation. 115(22)
Background—Primary ciliary dyskinesia (PCD) is a recessive genetic disorder that is characterized by sinopulmonary disease and reflects abnormal ciliary structure and function. Situs inversus totalis occurs in ≈50% of PCD patients (Kartagener’s
Autor:
Marcus P. Kennedy, John L. Carson, Michael R. Knowles, Maimoona A. Zariwala, Peadar G. Noone, Paul L. Molina, Susan L. Minnix, Andy J. Ghio
Publikováno v:
Chest. 128:153S