M W Kilpatrick
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Explore the profile of M W Kilpatrick including associated specialties, affiliations and a list of published articles.
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51
Citations
950
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Recent Articles
1.
Mitchell S, Phylactou L, Fox J, Kilpatrick M, Murray P
Ocul Immunol Inflamm
. 2012 Jul;
4(1):33-8.
PMID: 22827331
Members of the herpesvirus family have been found in association with a variety of intraocular inflammatory conditions. The aetiology and pathogenic mechanisms underlying the specific uveitis entity Fuchs' heterochromic cyclitis...
2.
Ntouroupi T, Ashraf S, McGregor S, Turney B, Seppo A, Kim Y, et al.
Br J Cancer
. 2008 Aug;
99(5):789-95.
PMID: 18682708
We have developed an automated, highly sensitive and specific method for identifying and enumerating circulating tumour cells (CTCs) in the blood. Blood samples from 10 prostate, 25 colorectal and 4...
3.
Phylactou L, Kilpatrick M
Expert Opin Investig Drugs
. 2005 Jul;
8(7):983-93.
PMID: 15992100
Marfan syndrome is the most common genetic disorder of the connective tissue with an estimated prevalence of 1:10,000. The disease is characterised by manifestations in the cardiovascular, skeletal and ocular...
4.
Smicun Y, Kilpatrick M, Florer J, Toudjarska I, Wu G, Wenstrup R, et al.
Gene Ther
. 2003 Oct;
10(24):2005-12.
PMID: 14566359
Antisense hammerhead ribozymes have the capability to cleave complementary RNA in a sequence-dependent manner. In osteogenesis imperfecta, a genetic disorder of connective tissue, mutant collagen type I has been shown...
5.
Basel D, DePaepe A, Kilpatrick M, Tsipouras P
Clin Genet
. 2003 Sep;
64(4):350-4.
PMID: 12974740
Split hand foot malformation (SHFM) is a congenital limb malformation presenting with a median cleft of the hand and/or foot, syndactyly and polydactyly. SHFM is genetically heterogeneous with four loci...
6.
Toudjarska I, Kilpatrick M, Niu J, Wenstrup R, Tsipouras P
Antisense Nucleic Acid Drug Dev
. 2002 Jan;
11(5):341-6.
PMID: 11763351
Osteogenesis imperfecta (OI) is a systemic heritable disorder of connective tissue, caused by a mutation in one of the genes for type I collagen, whose cardinal manifestation is bone fragility....
7.
Toudjarska I, Kilpatrick M, Lembessis P, Carra S, Harton G, Sisson M, et al.
Am J Med Genet
. 2001 Mar;
99(4):294-302.
PMID: 11251996
Marfan syndrome is an autosomal dominant disorder affecting the skeletal, ocular, and cardiovascular systems. Defects in the gene that encodes fibrillin-1 (FBN1), the main structural component of the elastin-associated microfibrils,...
8.
Ianakiev P, van Baren MJ , Daly M, Toledo S, Cavalcanti M, Neto J, et al.
Am J Hum Genet
. 2000 Nov;
68(1):38-45.
PMID: 11090342
Acheiropodia is an autosomal recessive developmental disorder presenting with bilateral congenital amputations of the upper and lower extremities and aplasia of the hands and feet. This severely handicapping condition appears...
9.
Ianakiev P, Kilpatrick M, Daly M, Zolindaki A, Bagley D, Beighton G, et al.
Clin Genet
. 2000 Jun;
57(4):278-83.
PMID: 10845568
The acromesomelic dysplasias (AMDs) are a group of genetic disorders that primarily affect the middle and distal segments of the extremities. A form of AMD is present on the isolated...
10.
Ianakiev P, Kilpatrick M, Toudjarska I, Basel D, Beighton P, Tsipouras P
Am J Hum Genet
. 2000 Jun;
67(1):59-66.
PMID: 10839977
Split-hand/split-foot malformation (SHFM), a limb malformation involving the central rays of the autopod and presenting with syndactyly, median clefts of the hands and feet, and aplasia and/or hypoplasia of the...