Search Results - "Lyons, J. D. M."

Non-bronchoscopic sampling and culture of bronchial epithelial cells in children by Doherty, G. M., Christie, S. N., Skibinski, G., Puddicombe, S. M., Warke, T. J., De Courcey, F., Cross, A. L., Lyons, J. D. M., Ennis, M., Shields, M. D., Heaney, L. G.

“…Background The bronchial epithelium is likely to play a vital role in airway diseases in children, such as asthma and viral‐associated wheeze. In adults,…”
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Exhaled nitric oxide correlates with airway eosinophils in childhood asthma by Warke, T J, Fitch, P S, Brown, V, Taylor, R, Lyons, J D M, Ennis, M, Shields, M D

“…Background: Exhaled nitric oxide has been proposed as a marker for airway inflammation in asthma. The aim of this study was to compare exhaled nitric oxide…”
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Outgrown asthma does not mean no airways inflammation by Warke, T.J, Fitch, P.S, Brown, V, Taylor, R, Lyons, J.D.M, Ennis, M, Shields, M.D

“…Although some asthmatic children seem to recover from their asthma, 30-80% develop asthma again in later life. The underlying risk factors are unknown. The…”
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Role responsibilities in mechanical ventilation and weaning in pediatric intensive care units: a national survey by Blackwood, Bronagh, Junk, Carol, Lyons, Jeremy David Morrell, McAuley, Danny F, Rose, Louise

“…Organizational processes affect the duration of mechanical ventilation in adult and pediatric intensive care units, but surprisingly little is known about role…”
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Autosomal recessive phosphoglucomutase 3 ( PGM3 ) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment by Zhang, Yu, PhD, Yu, Xiaomin, PhD, Ichikawa, Mie, BSc, Lyons, Jonathan J., MD, Datta, Shrimati, PhD, Lamborn, Ian T., BSc, Jing, Huie, PhD, Kim, Emily S., BSc, Biancalana, Matthew, BSc, Wolfe, Lynne A., CRNP, DiMaggio, Thomas, ADN, Matthews, Helen F., BSN, Kranick, Sarah M., MD, Stone, Kelly D., MD, PhD, Holland, Steven M., MD, Reich, Daniel S., MD, PhD, Hughes, Jason D., PhD, Mehmet, Huseyin, PhD, McElwee, Joshua, PhD, Freeman, Alexandra F., MD, Freeze, Hudson H., PhD, Su, Helen C., MD, PhD, Milner, Joshua D., MD

“…Background Identifying genetic syndromes that lead to significant atopic disease can open new pathways for investigation and intervention in allergy. Objective…”
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Hereditary Alpha Tryptasemia by Lyons, Jonathan J., MD

“…Hereditary alpha tryptasemia is an autosomal dominant genetic trait caused by increased germline copies of TPSAB1 encoding alpha-tryptase. Individuals with…”
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Mendelian inheritance of elevated serum tryptase associated with atopy and connective tissue abnormalities by Lyons, Jonathan J., MD, Sun, Guangping, MD, Stone, Kelly D., MD, PhD, Nelson, Celeste, CRNP, Wisch, Laura, MSN, O'Brien, Michelle, RN, BSN, Jones, Nina, RN, BSN, Lindsley, Andrew, MD, PhD, Komarow, Hirsh D., MD, Bai, Yun, MS, Scott, Linda M., MS, CRNP, Cantave, Daly, MSN, Maric, Irina, MD, Abonia, J. Pablo, MD, Rothenberg, Marc E., MD, PhD, Schwartz, Lawrence B., MD, PhD, Milner, Joshua D., MD, Wilson, Todd M., DO

“…Genome-wide association studies and candidate gene approaches have produced an array of allelic variants that impart risk for allergic diatheses.E1 Although…”
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Diminution of signal transducer and activator of transcription 3 signaling inhibits vascular permeability and anaphylaxis by Hox, Valerie, MD, PhD, O'Connell, Michael P., PhD, Lyons, Jonathan J., MD, Sackstein, Paul, BS, Dimaggio, Thomas, ADN, RN, Jones, Nina, BSN, RN, Nelson, Celeste, MS CRNP, Boehm, Manfred, MD, Holland, Steven M., MD, Freeman, Alexandra F., MD, Tweardy, David J., MD, Olivera, Ana, PhD, Metcalfe, Dean D., MD, Milner, Joshua D., MD

“…Background During IgE-mediated immediate hypersensitivity reactions, vascular endothelial cells permeabilize in response to mast cell mediators. We have…”
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Food allergies can persist after myeloablative hematopoietic stem cell transplantation in dedicator of cytokinesis 8–deficient patients by Happel, Corinne S., MD, Stone, Kelly D., MD, PhD, Freeman, Alexandra F., MD, Shah, Nirali N., MD, Wang, Angela, BSN, Lyons, Jonathan J., MD, Guerrerio, Pamela A., MD, PhD, Hickstein, Dennis D., MD, Su, Helen C., MD, PhD

“…Patient 7 also had a history of anaphylaxis to walnut as recently as 3 years before HSCT. Because of persisting positive skin prick tests, he continued to…”
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Detection of phosphoglucomutase-3 (PGM3) deficiency by lectin-based flow cytometry by Carlson, Ryan J., BS, Bond, Michelle R., PhD, Hutchins, Shermaine, BS, Brown, Yishai, Wolfe, Lynne A., CRNP, Lam, Christina, MD, Nelson, Celeste, CRNP, DiMaggio, Thomas, ADN, Jones, Nina, RN, BSN, Rosenzweig, Sergio D., MD, PhD, Stone, Kelly D., MD, PhD, Freeman, Alexandra F., MD, Holland, Steven M., MD, Hanover, John A., PhD, Milner, Joshua D., MD, Lyons, Jonathan J., MD

“…Lectin-based flow cytometry using L-PHA provides a method to screen for PGM3 deficiency…”
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Lysosomal Acid Lipase Deficiency in all Siblings of the Same Parents by Maciejko, James J., PhD, FACC, Anne, Premchand, MD, FACC, Raza, Saleem, MD, Lyons, Hernando J., MD

“…Abstract We present four normal-weight sibling children with lysosomal acid lipase deficiency (LAL-D). LAL-D was considered in the differential diagnosis based…”
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GATA3 haploinsufficiency does not block allergic sensitization or atopic disease by Lawrence, Monica G., MD, Leiding, Jennifer W., MD, Lyons, Jonathan J., MD, Hsu, Amy P., BS, Nelson, Celeste C., CRNP, Jones, Nina, RN, Fitzgerald, Alan, RN, Chien, Wade W., MD, Workman, Lisa, BA, Platts-Mills, Thomas A., MD, Brewer, Carmen, PhD, Gafni, Rachel I., MD, Stone, Kelly D., MD, PhD, Milner, Joshua D., MD, Holland, Steven M., MD

“…Analysis of cytokine production by CD3+CD4+CD27-CD45RO+ effector memory T cells following stimulation with phorbol 12-myristate 13-acetate (PMA)/ionomycin…”
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Atopic Dermatitis in Children by Lyons, Jonathan J., MD, Milner, Joshua D., MD, Stone, Kelly D., MD, PhD

“…Atopic dermatitis (AD) is a chronic, relapsing, highly pruritic skin condition resulting from disruption of the epithelial barrier and associated immune…”
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Acquired Microcephaly in Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome Because of an Interstitial 3q22.3q23 Deletion by Dean, Sarah J., MD, Holden, Kenton R., MD, Dwivedi, Alka, PhD, Dupont, Barbara R., PhD, Lyons, Michael J., MD

“…Abstract Background Blepharophimosis-ptosis-epicanthus inversus syndrome is an autosomal dominant condition because of mutations or deletions of the FOXL2…”
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Presentation of the Southern Society for Clinical Investigation Founders’ Medal for 2011 to Michael S. Bronze, MD by Lyons, Timothy J., MD

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Convergence of Clinical and Cellular Phenotypes Among Patients with STAT3 and ERBB2IP Mutations by Lyons, Jonathan J., MD, Yu, Xiaomin, PhD, Karpe, Kendal A., BS, Treadwell, Shirin M., MS, Ma, Chi A., PhD, O'Connell, Michael P., PhD, Sun, Guangping, MD, Hughes, Jason D., PhD, Mehmet, Huseyin, PhD, McElwee, Joshua, PhD, Holland, Steven M., MD, Freeman, Alexandra F., MD, Milner, Joshua D., MD

“…Rationale A number of congenital syndromes with connective tissue abnormalities are also associated with allergic disease, some of which are caused by altered…”
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Novel CLCN1 Mutation in Carbamazepine-Responsive Myotonia Congenita by Lyons, Michael J., MD, Duron, Reyna, MD, Molinero, Isaac, BA, Sangiuolo, Federica, PhD, Holden, Kenton R., MD

“…Myotonia congenita is a nondystrophic muscle disorder characterized by muscle stiffness and muscle hypertrophy. The disorder can be inherited in…”
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Andrew Q. McCormick, MD, FRCSC by Lyons, Christopher J., MD, FRCSC

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Royal academy of medicine in Ireland section of biomedical sciences: Proceedings of winter meeting held in Trinity College Dublin, 1996 by Sharma, S., Sharma, S. C., Byrne, P. D., Lyons, J. B., Boylan, J. F., McShane, A. J., Galligan, E. S., Sweetman, S. F., Clements, B. A., Lowe, A. S., McCormack, K. J. M., Walsh, D. M., Baxter, G. D., Allen, J. M., Kelleher, S., Keenan, A. K., Burns, D. M., Brown, J. C. W., Ruddock, M. W., Kennovin, G. D., Dykes, E. L., Flitney, F. W., Hirst, D. G., Winter, D. C., Cuffe, J., O’Sullivan, G. C., Harvey, B. J., Thompson, G. H., Murray, J. M., Brehony, F., Kelly, J. P., Leonard, B. E., Cotton, K. D., Hollywood, M. A., McHale, N. G., Thornbury, K. D., Stapleton, M. T., Allshire, A. P., Freeburn, J. C., Wallace, J. M. W., Sinnamon, D., Craig, B., Strain, J. J., Gilmore, W. S., Lyons, J. D. M, Murray, J., Trinick, T., Fee, J. P. H., Hennessy, L., Watson, A. W. S., Halley, W. L., Weir, M. A., Friery, O. P., Hejmadi, M. V., McIntyre, I. A., McALeer, J. J. A., Patterson, L. H., McKeown, S. R., Leckey, J. L., Nevin, G. B., Soppitt, D. S., Harkin, A. J., Wrynn, A. S., Earley, B., Dineen, T. M., Powell, R., Houghton, J. A., Cantillon, D., McDaid, J., O’Halloran, K. D., Bradford, A., Curran, A. K., Harmon, D., Sweeney, M., McLoughlin, P., O’Leary, D., O’Connor, J. J., Broderick, A. M., Keon, N., Martin, F.

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