Margaret W. Leigh, M.D.

Affiliations: 
University of North Carolina, Chapel Hill, Chapel Hill, NC 
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"Margaret Leigh"

Parents

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Robert E. Wood fellowship/program director 1982-1985 UNC Chapel Hill

Children

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Carlos 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
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