Nancy H Augustine
Overview
Explore the profile of Nancy H Augustine including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
15
Citations
300
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Buchbinder D, Baker R, Lee Y, Ravell J, Zhang Y, McElwee J, et al.
J Clin Immunol
. 2014 Dec;
35(2):119-24.
PMID: 25516070
Purpose: Combined immunodeficiency (CID) presents a unique challenge to clinicians. Two patients presented with the prior clinical diagnosis of common variable immunodeficiency (CVID) disorder marked by an early age of...
2.
Caron J, La Pine T, Augustine N, Martins T, Kumanovics A, Hill H
Pediatr Res
. 2014 Sep;
76(6):522-7.
PMID: 25192396
Background: The role of T-helper 17 cells (Th17) in neonatal host defense remains to be fully elucidated. Interleukin (IL)-17 plays an important role in the immune response to bacterial and...
3.
Chen K, Coonrod E, Kumanovics A, Franks Z, Durtschi J, Margraf R, et al.
Am J Hum Genet
. 2013 Oct;
93(5):812-24.
PMID: 24140114
Common variable immunodeficiency (CVID) is a heterogeneous disorder characterized by antibody deficiency, poor humoral response to antigens, and recurrent infections. To investigate the molecular cause of CVID, we carried out...
4.
Margraf R, Coonrod E, Durtschi J, Augustine N, Voelkerding K, Hill H, et al.
Clin Immunol
. 2012 Nov;
146(1):10-2.
PMID: 23165285
No abstract available.
5.
Stasia M, van Leeuwen K, de Boer M, Martel C, Mollin M, Thuret I, et al.
J Clin Immunol
. 2012 Mar;
32(4):653-62.
PMID: 22382877
Chronic granulomatous disease (CGD) is a rare congenital disorder in which phagocytes cannot generate superoxide (O(2)(-)) and other microbicidal oxidants due to mutations in one of the five components of...
6.
Kumanovics A, Perkins S, Gilbert H, Cessna M, Augustine N, Hill H
J Clin Immunol
. 2010 Sep;
30(6):886-93.
PMID: 20859667
The Job or hyper-immunoglobulinemia E syndrome is a primary immunodeficiency that is usually inherited in an autosomal dominant fashion. With the discovery of mutations in the STAT3 gene in the...
7.
Hill H, Augustine N, Pryor R, Reed G, Bagnato J, Tebo A, et al.
J Mol Diagn
. 2010 Mar;
12(3):368-76.
PMID: 20228266
High-resolution melting analysis was applied to X-linked chronic granulomatous disease, a rare disorder resulting from mutations in CYBB. Melting curves of the 13 PCR products bracketing CYBB exons were predicted...
8.
Kumanovics A, Wittwer C, Pryor R, Augustine N, Leppert M, Carey J, et al.
J Mol Diagn
. 2010 Jan;
12(2):213-9.
PMID: 20093388
With the recent discovery of mutations in the STAT3 gene in the majority of patients with classic Hyper-IgE syndrome, it is now possible to make a molecular diagnosis in most...
9.
Caron J, La Pine T, Augustine N, Martins T, Hill H
Neonatology
. 2009 Dec;
97(3):266-73.
PMID: 19955831
Background: The human neonate's increased susceptibility to bacterial infections is not completely understood. Toll-like receptors (TLRs) have been recognized as pattern-recognition receptors critical to the innate immune response. TLR function...
10.
Bender J, Rand T, Ampofo K, Pavia A, Schober M, Tebo A, et al.
Pediatr Infect Dis J
. 2009 Jun;
28(6):529-33.
PMID: 19483518
Chronic granulomatous disease (CGD) is a rare inherited immunodeficiency disorder. The clinical presentation is varied depending on the degree of involvement of the NADPH oxidase system responsible for the oxidative...