Margaret W. Leigh, M.D.
Affiliations: | University of North Carolina, Chapel Hill, Chapel Hill, NC |
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"Margaret Leigh"Children
Sign in to add traineeCarlos Perez | fellowship/program director | 1990 | UNC Chapel Hill |
Terry L. Noah | fellowship/program director | 1991 | UNC Chapel Hill |
Gary Albers | fellowship/program director | 1992 | UNC Chapel Hill |
Christopher Harris | fellowship/program director | 1990-1993 | UNC Chapel Hill |
William Ashe | fellowship/program director | 1994 | UNC Chapel Hill |
Pierre Barker | fellowship/program director | 1994 | UNC Chapel Hill |
Giovanni Piedimonte | fellowship/program director | 1995 | UNC Chapel Hill |
David E. Thomas | fellowship/program director | 1995 | UNC Chapel Hill |
Peter H. Michelson | fellowship/program director | 1992-1995 | UNC Chapel Hill |
Michael Schechter | fellowship/program director | 1996 | UNC Chapel Hill |
Hugh R. Black | fellowship/program director | 1997 | UNC Chapel Hill |
Drew Barber | research mentor | University of North Carlina at Chapel Hill |
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Publications
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Crowley S, Azevedo I, Boon M, et al. (2020) Access to medicines for rare diseases: beating the drum for primary ciliary dyskinesia. Erj Open Research. 6 |
Kinghorn B, McNamara S, Genatossio A, et al. (2020) Comparison of Multiple Breath Washout and Spirometry in Children with Primary Ciliary Dyskinesia and Cystic Fibrosis and Healthy Controls. Annals of the American Thoracic Society |
Pappa AK, Sullivan KM, Lopez EM, et al. (2020) Sinus Development and Pneumatization in a Primary Ciliary Dyskinesia Cohort. American Journal of Rhinology & Allergy. 1945892420933175 |
Shoemark A, Boon M, Brochhausen C, et al. (2020) International consensus guideline for reporting transmission electron microscopy results in the diagnosis of Primary Ciliary Dyskinesia (BEAT PCD TEM Criteria). The European Respiratory Journal |
Shapiro AJ, Dell SD, Gaston B, et al. (2019) Nasal Nitric Oxide Measurement in Primary Ciliary Dyskinesia: A Technical Paper on Standardized Testing Protocols. Annals of the American Thoracic Society |
Bustamante-Marin XM, Shapiro A, Sears PR, et al. (2019) Identification of genetic variants in CFAP221 as a cause of primary ciliary dyskinesia. Journal of Human Genetics |
Wallmeier J, Frank D, Shoemark A, et al. (2019) De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry. American Journal of Human Genetics |
Vece TJ, Sagel SD, Zariwala MA, et al. (2019) Cytoplasmic "ciliary inclusions" in isolation are not sufficient for the diagnosis of primary ciliary dyskinesia. Pediatric Pulmonology |
Morimoto K, Hijikata M, Zariwala MA, et al. (2019) Recurring large deletion in DRC1 (CCDC164) identified as causing primary ciliary dyskinesia in two Asian patients. Molecular Genetics & Genomic Medicine. e838 |
Shoemark A, Boon M, Brochhausen C, et al. (2019) International consensus guideline for reporting transmission electron microscopy results in the diagnosis of Primary Ciliary Dyskinesia European Respiratory Journal. 54 |