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Results of search for 'au:"Parfrey, N A"', page 2 of 2
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Authors
Byrne, P C
Cockfield, S M
Colle, E
Collum, L M
Darden, A G
FitzSimon, J S
Fitzgerald, B
Forbes, R D
Gomersall, M
Guttmann, R D
Halloran, P F
Hand, C K
Hutchins, G M
Hutchinson, M
Kennedy, S M
Leahy, D T
O'Donoghue, D P
Parfrey, N A
Prud'homme, G J
Webb, S
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Genetic Linkage
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Interferon-gamma
Kidney Transplantation
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analysis
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Your search returned 33 results.
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21.
The decreased incidence of aseptic necrosis in renal transplant recipients--a case control study.
[electronic resource]
by
Parfrey, P S
Farge, D
Parfrey, N A
Hanley, J A
Guttman, R D
Producer:
19860314
In:
Transplantation
vol. 41
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22.
Phenotype of AD-HSP due to mutations in the SPAST gene: comparison with AD-HSP without mutations.
[electronic resource]
by
McMonagle, P
Byrne, P C
Fitzgerald, B
Webb, S
Parfrey, N A
Hutchinson, M
Producer:
20010201
In:
Neurology
vol. 55
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23.
Linkage of AD HSP and cognitive impairment to chromosome 2p: haplotype and phenotype analysis indicates variable expression and low or delayed penetrance.
[electronic resource]
by
Byrne, P C
Webb, S
McSweeney, F
Burke, T
Hutchinson, M
Parfrey, N A
Producer:
19981104
In:
European journal of human genetics : EJHG
vol. 6
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24.
Age-related cognitive decline in hereditary spastic paraparesis linked to chromosome 2p.
[electronic resource]
by
Byrne, P C
Mc Monagle, P
Webb, S
Fitzgerald, B
Parfrey, N A
Hutchinson, M
Producer:
20000504
In:
Neurology
vol. 54
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25.
Prognostic significance of p53 abnormalities in colorectal carcinoma detected by PCR-SSCP and immunohistochemical analysis.
[electronic resource]
by
Leahy, D T
Salman, R
Mulcahy, H
Sheahan, K
O'Donoghue, D P
Parfrey, N A
Producer:
19970220
In:
The Journal of pathology
vol. 180
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26.
Expansion of peripheral blood CD5+ B cells is associated with mild disease in chronic hepatitis C virus infection.
[electronic resource]
by
Curry, M P
Golden-Mason, L
Nolan, N
Parfrey, N A
Hegarty, J E
O'Farrelly, C
Producer:
20000224
In:
Journal of hepatology
vol. 32
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27.
SPG15, a new locus for autosomal recessive complicated HSP on chromosome 14q.
[electronic resource]
by
Hughes, C A
Byrne, P C
Webb, S
McMonagle, P
Patterson, V
Hutchinson, M
Parfrey, N A
Producer:
20010628
In:
Neurology
vol. 56
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28.
Homozygosity mapping and linkage analysis demonstrate that autosomal recessive congenital hereditary endothelial dystrophy (CHED) and autosomal dominant CHED are genetically distinct.
[electronic resource]
by
Callaghan, M
Hand, C K
Kennedy, S M
FitzSimon, J S
Collum, L M
Parfrey, N A
Producer:
19990427
In:
The British journal of ophthalmology
vol. 83
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29.
Interferon-gamma gene expression during acute graft-versus-host disease: relationship to MHC induction and tissue injury.
[electronic resource]
by
Parfrey, N A
El-Sheikh, A
Monckton, E A
Cockfield, S M
Halloran, P F
Linetsky, E
Producer:
20000306
In:
The Journal of pathology
vol. 189
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30.
Localization of the gene for autosomal recessive congenital hereditary endothelial dystrophy (CHED2) to chromosome 20 by homozygosity mapping.
[electronic resource]
by
Hand, C K
Harmon, D L
Kennedy, S M
FitzSimon, J S
Collum, L M
Parfrey, N A
Producer:
19991109
In:
Genomics
vol. 61
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31.
Urokinase-type plasminogen activator and outcome in Dukes' B colorectal cancer.
[electronic resource]
by
Mulcahy, H E
Duffy, M J
Gibbons, D
McCarthy, P
Parfrey, N A
O'Donoghue, D P
Sheahan, K
Producer:
19940922
In:
Lancet (London, England)
vol. 344
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32.
Immunologic and genetic studies of diabetes in the BB rat.
[electronic resource]
by
Parfrey, N A
Prud'homme, G J
Colle, E
Fuks, A
Seemayer, T A
Guttmann, R D
Ono, S J
Producer:
19890526
In:
Critical reviews in immunology
vol. 9
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33.
Laser induced fluorescence identification of sinoatrial and atrioventricular nodal conduction tissue.
[electronic resource]
by
Perk, M
Flynn, G J
Gulamhusein, S
Wen, Y
Smith, C
Bathgate, B
Tulip, J
Parfrey, N A
Lucas, A
Producer:
19931021
In:
Pacing and clinical electrophysiology : PACE
vol. 16
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