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E C Lawrence

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Articles 72
Citations 1701
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Recent Articles
1.
Mohammed A, Ulukpo O, Lawrence E, Fernandez F, Pickens A, Gal A, et al.
Transplant Proc . 2011 Dec; 43(10):3892-8. PMID: 22172867
Outcomes following lung transplant remain suboptimal. This is attributable to variable posttransplant recovery of lung function, and inconsistent degrees of lung function loss after peak function is reached. Granzyme B...
2.
Neujahr D, Perez S, Mohammed A, Ulukpo O, Lawrence E, Fernandez F, et al.
Am J Transplant . 2011 Dec; 12(2):438-46. PMID: 22151926
Outcomes following lung transplant are suboptimal owing to chronic allograft failure termed bronchiolitis obliterans syndrome (BOS). Prior work in both mice and humans has shown that interferon gamma (IFNG)-induced chemokines,...
3.
Shah N, Force S, Mitchell P, Lin E, Lawrence E, Easley K, et al.
Transplant Proc . 2010 Sep; 42(7):2702-6. PMID: 20832573
Purpose: Gastric fundoplication (GF) for gastroesophageal reflux disease (GERD) may protect against the progression of chronic rejection in lung transplant (LT) recipients. However, the association of GERD with acute rejection...
4.
Pelaez A, Force S, Gal A, Neujahr D, Ramirez A, Naik P, et al.
Am J Transplant . 2010 Feb; 10(4):900-907. PMID: 20121754
Development of primary graft dysfunction (PGD) is associated with poor outcomes after transplantation. We hypothesized that Receptor for Advanced Glycation End-products (RAGE) levels in donor lungs is associated with the...
5.
Vega J, Kanter K, Lawrence E
J Med Assoc Ga . 2005 Nov; 87(2):105-7. PMID: 16259253
Lung transplantation is a viable therapeutic option for patients with end-stage lung disease. Quality of life and survival are improved for most recipients. Donor availability remains an impediment to widespread...
6.
Schneider A, Lawrence E, Barmada M, Norris J, Hamman R, Marshall J, et al.
Diabet Med . 2005 May; 22(6):744-8. PMID: 15910626
Aims: Mutations in the serine protease inhibitor (SPINK1) gene have been associated with all forms of chronic pancreatitis. Recently, an association of SPINK1 mutations with early-onset Type 2 diabetes mellitus...
7.
Baysal B, Willett-Brozick J, Filho P, Lawrence E, Myers E, Ferrell R
J Med Genet . 2004 Sep; 41(9):703-9. PMID: 15342702
No abstract available.
8.
Baysal B, Willett-Brozick J, Lawrence E, Drovdlic C, Savul S, McLeod D, et al.
J Med Genet . 2002 Mar; 39(3):178-83. PMID: 11897817
Background: Paragangliomas are rare and highly heritable tumours of neuroectodermal origin that often develop in the head and neck region. Germline mutations in the mitochondrial complex II genes, SDHB, SDHC,...
9.
Karkkainen M, Saaristo A, Jussila L, Karila K, Lawrence E, Pajusola K, et al.
Proc Natl Acad Sci U S A . 2001 Oct; 98(22):12677-82. PMID: 11592985
Primary human lymphedema (Milroy's disease), characterized by a chronic and disfiguring swelling of the extremities, is associated with heterozygous inactivating missense mutations of the gene encoding vascular endothelial growth factor...
10.
Finegold D, Kimak M, Lawrence E, Levinson K, Cherniske E, Pober B, et al.
Hum Mol Genet . 2001 May; 10(11):1185-9. PMID: 11371511
Hereditary lymphedemas are developmental disorders of the lymphatics resulting in edema of the extremities due to altered lymphatic flow. One such disorder, the lymphedema-distichiasis syndrome, has been reported to be...