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Items: 1 to 50 of 261

1.

Rhinovirus (RV) is the most common virus and RV-C the most common RV species in paediatric intensive care respiratory admissions.

Cox DW, Khoo SK, Zhang G, Lindsay K, Keil AD, Knight G, Gern JE, Laing IA, Bizzintino J, Le Souëf PN.

Eur Respir J. 2018 Jul 5. pii: 1800207. doi: 10.1183/13993003.00207-2018. [Epub ahead of print]

PMID:
29976655
2.

Attachment avoidance, alexithymia, and gender: Examining their associations with distress disclosure tendencies and event-specific disclosure.

O'Loughlin JI, Cox DW, Kahn JH, Wu AD.

J Couns Psychol. 2018 Jan;65(1):65-73. doi: 10.1037/cou0000245.

PMID:
29355345
3.

Emotion Dysregulation and Social Support in PTSD and Depression: A Study of Trauma-Exposed Veterans.

Cox DW, Bakker AM, Naifeh JA.

J Trauma Stress. 2017 Oct;30(5):545-549. doi: 10.1002/jts.22226. Epub 2017 Oct 12.

PMID:
29024028
4.

Laps or lengths? The effects of different exercise programs on asthma control in children.

Carew C, Cox DW.

J Asthma. 2017 Sep 5:1-5. doi: 10.1080/02770903.2017.1373806. [Epub ahead of print]

PMID:
28872938
5.

Group Psychotherapeutic Factors and Perceived Social Support Among Veterans With PTSD Symptoms.

Cox DW, Owen JJ, Ogrodniczuk JS.

J Nerv Ment Dis. 2017 Feb;205(2):127-132. doi: 10.1097/NMD.0000000000000635.

PMID:
27918323
6.

Pulmonary arteriovenous malformations: an uncharacterised phenotype of dyskeratosis congenita and related telomere biology disorders.

Khincha PP, Bertuch AA, Agarwal S, Townsley DM, Young NS, Keel S, Shimamura A, Boulad F, Simoneau T, Justino H, Kuo C, Artandi S, McCaslin C, Cox DW, Chaffee S, Collins BF, Giri N, Alter BP, Raghu G, Savage SA.

Eur Respir J. 2017 Jan 25;49(1). pii: 1601640. doi: 10.1183/13993003.01640-2016. Print 2017 Jan. No abstract available.

7.

Longitudinal assessment of airway responsiveness from 1 month to 18 years in the PIAF birth cohort.

Cox DW, Mullane D, Zhang GC, Turner SW, Hayden CM, Goldblatt J, Landau LI, Le Souëf PN.

Eur Respir J. 2015 Dec;46(6):1654-61. doi: 10.1183/13993003.00397-2015. Epub 2015 Oct 22.

8.

How Parental Reactions Change in Response to Adolescent Suicide Attempt.

Greene-Palmer FN, Wagner BM, Neely LL, Cox DW, Kochanski KM, Perera KU, Ghahramanlou-Holloway M.

Arch Suicide Res. 2015;19(4):414-21. doi: 10.1080/13811118.2015.1094367. Epub 2015 Oct 9.

PMID:
26452767
9.

Recurrent rhinovirus detections in children following a rhinovirus-induced wheezing exacerbation: A retrospective study.

Halmø Hürdum S, Zhang G, Khoo SK, Bizzintino J, Franks KM, Lindsay K, Keil AD, Cox DW, Goldblatt J, Bochkov YA, Gern J, Ulrik CS, Souëf PN, Laing IA.

Int J Pediatr Child Health. 2015 Aug;3(1):10-18. doi: 10.12974/2311-8687.2015.03.01.2.

10.

Diagnosis and treatment of sleep related breathing disorders in children: 2007 to 2011.

Walsh A, Phelan F, Phelan M, Ryan M, Healy F, Slattery DM, Elnazir B, Greally P, Linnane B, Ní Chróinín M, Mullane D, Herzig M, Cox DW, Javadpour S, McNally P.

Ir Med J. 2015 Mar;108(3):71-3.

PMID:
25876296
11.

Evaluation of a group intervention for veterans who experienced military-related trauma.

Cox DW, Westwood MJ, Hoover SM, Chan EK, Kivari CA, Dadson MR, Zumbo BD.

Int J Group Psychother. 2014 Jul;64(3):367-80. doi: 10.1521/ijgp.2014.64.3.367.

PMID:
24911228
12.

A longitudinal study of lung function from 1 month to 18 years of age.

Turner S, Fielding S, Mullane D, Cox DW, Goldblatt J, Landau L, le Souef P.

Thorax. 2014 Nov;69(11):1015-20. doi: 10.1136/thoraxjnl-2013-204931. Epub 2014 Jun 2.

PMID:
24891326
13.

Comparison of rhinovirus antibody titers in children with asthma exacerbations and species-specific rhinovirus infection.

Iwasaki J, Smith WA, Khoo SK, Bizzintino J, Zhang G, Cox DW, Laing IA, Le Souëf PN, Thomas WR, Hales BJ.

J Allergy Clin Immunol. 2014 Jul;134(1):25-32. doi: 10.1016/j.jaci.2014.03.014. Epub 2014 Apr 24.

PMID:
24767874
14.

Rhinovirus and the developing lung.

Cox DW, Le Souëf PN.

Paediatr Respir Rev. 2014 Sep;15(3):268-74. doi: 10.1016/j.prrv.2014.03.002. Epub 2014 Mar 27. Review.

PMID:
24767866
15.

The retinoblastoma tumor suppressor pathway modulates the invasiveness of ErbB2-positive breast cancer.

Witkiewicz AK, Cox DW, Rivadeneira D, Ertel AE, Fortina P, Schwartz GF, Knudsen ES.

Oncogene. 2014 Jul 24;33(30):3980-91. doi: 10.1038/onc.2013.367. Epub 2013 Oct 14.

16.

Human rhinovirus species C infection in young children with acute wheeze is associated with increased acute respiratory hospital admissions.

Cox DW, Bizzintino J, Ferrari G, Khoo SK, Zhang G, Whelan S, Lee WM, Bochkov YA, Geelhoed GC, Goldblatt J, Gern JE, Laing IA, Le Souëf PN.

Am J Respir Crit Care Med. 2013 Dec 1;188(11):1358-64. doi: 10.1164/rccm.201303-0498OC.

17.

Reduced infant lung function, active smoking, and wheeze in 18-year-old individuals.

Mullane D, Turner SW, Cox DW, Goldblatt J, Landau LI, le Souëf PN.

JAMA Pediatr. 2013 Apr;167(4):368-73. doi: 10.1001/jamapediatrics.2013.633. Erratum in: JAMA Pediatr. 2013 Sep;167(9):873. Cox, Des [corrected to Cox, Des W].

PMID:
23420147
18.

Characterization of maximal respiratory pressures in healthy children.

Cox DW, Verheggen MM, Stick SM, Hall GL.

Respiration. 2012;84(6):485-91. doi: 10.1159/000342298. Epub 2012 Sep 13.

19.

The impact of MRSA infection in the airways of children with cystic fibrosis; a case-control study.

Cox DW, Kelly C, Rush R, O'Sullivan N, Canny G, Linnane B.

Ir Med J. 2011 Nov-Dec;104(10):305-8.

PMID:
22256443
20.

A guide for the assessment and treatment of suicidal patients with traumatic brain injuries.

Dennis JP, Ghahramanlou-Holloway M, Cox DW, Brown GK.

J Head Trauma Rehabil. 2011 Jul-Aug;26(4):244-56. doi: 10.1097/HTR.0b013e3182225528. Review.

PMID:
21734508
21.

Suicide in the United States Air Force: Risk factors communicated before and at death.

Cox DW, Ghahramanlou-Holloway M, Greene FN, Bakalar JL, Schendel CL, Nademin ME, Jobes DA, Englert DR, Kindt M.

J Affect Disord. 2011 Oct;133(3):398-405. doi: 10.1016/j.jad.2011.05.011. Epub 2011 Jun 8.

PMID:
21652080
22.

Call for participation in the neurogenetics consortium within the Human Variome Project.

Haworth A, Bertram L, Carrera P, Elson JL, Braastad CD, Cox DW, Cruts M, den Dunnen JT, Farrer MJ, Fink JK, Hamed SA, Houlden H, Johnson DR, Nuytemans K, Palau F, Rayan DL, Robinson PN, Salas A, Schüle B, Sweeney MG, Woods MO, Amigo J, Cotton RG, Sobrido MJ.

Neurogenetics. 2011 Aug;12(3):169-73. doi: 10.1007/s10048-011-0287-4. Epub 2011 Jun 1.

PMID:
21630033
23.

Gender differences on documented trauma histories: inpatients admitted to a military psychiatric unit for suicide-related thoughts or behaviors.

Cox DW, Ghahramanlou-Holloway M, Szeto EH, Greene FN, Engel C, Wynn GH, Bradley J, Grammer G.

J Nerv Ment Dis. 2011 Mar;199(3):183-90. doi: 10.1097/NMD.0b013e31820c71c9.

PMID:
21346489
24.

Association between human rhinovirus C and severity of acute asthma in children.

Bizzintino J, Lee WM, Laing IA, Vang F, Pappas T, Zhang G, Martin AC, Khoo SK, Cox DW, Geelhoed GC, McMinn PC, Goldblatt J, Gern JE, Le Souëf PN.

Eur Respir J. 2011 May;37(5):1037-42. doi: 10.1183/09031936.00092410. Epub 2010 Aug 6.

25.

Association of NPAS3 exonic variation with schizophrenia.

Macintyre G, Alford T, Xiong L, Rouleau GA, Tibbo PG, Cox DW.

Schizophr Res. 2010 Jul;120(1-3):143-9. doi: 10.1016/j.schres.2010.04.002. Epub 2010 May 14.

PMID:
20466522
26.

Functional analysis of mutations in the ATP loop of the Wilson disease copper transporter, ATP7B.

Luoma LM, Deeb TM, Macintyre G, Cox DW.

Hum Mutat. 2010 May;31(5):569-77. doi: 10.1002/humu.21228.

PMID:
20333758
27.

A minigene approach for analysis of ATP7B splice variants in patients with Wilson disease.

Wilson AM, Schlade-Bartusiak K, Tison JL, Macintyre G, Cox DW.

Biochimie. 2009 Oct;91(10):1342-5. doi: 10.1016/j.biochi.2009.06.008. Epub 2009 Jun 21.

PMID:
19540904
28.

A child with terminal 14q deletion syndrome: consideration of genotype-phenotype correlations.

Schlade-Bartusiak K, Ardinger H, Cox DW.

Am J Med Genet A. 2009 May;149A(5):1012-8. doi: 10.1002/ajmg.a.32752.

PMID:
19365838
29.

New mutations in the Wilson disease gene, ATP7B: implications for molecular testing.

Davies LP, Macintyre G, Cox DW.

Genet Test. 2008 Mar;12(1):139-45. doi: 10.1089/gte.2007.0072.

PMID:
18373411
30.

Loss of taste with clopidogrel.

Cave AJ, Cox DW, Vicaruddin O.

Can Fam Physician. 2008 Feb;54(2):195-6. No abstract available.

31.

Sequence variation in the ATP-binding domain of the Wilson disease transporter, ATP7B, affects copper transport in a yeast model system.

Hsi G, Cullen LM, Macintyre G, Chen MM, Glerum DM, Cox DW.

Hum Mutat. 2008 Apr;29(4):491-501. doi: 10.1002/humu.20674.

PMID:
18203200
32.

Recommendations for locus-specific databases and their curation.

Cotton RG, Auerbach AD, Beckmann JS, Blumenfeld OO, Brookes AJ, Brown AF, Carrera P, Cox DW, Gottlieb B, Greenblatt MS, Hilbert P, Lehvaslaiho H, Liang P, Marsh S, Nebert DW, Povey S, Rossetti S, Scriver CR, Summar M, Tolan DR, Verma IC, Vihinen M, den Dunnen JT.

Hum Mutat. 2008 Jan;29(1):2-5.

33.

A child with deletion (14)(q24.3q32.13) and auditory neuropathy.

Schlade-Bartusiak K, Macintyre G, Zunich J, Cox DW.

Am J Med Genet A. 2008 Jan 1;146A(1):117-23.

PMID:
18074379
34.

A structured simple form for ordering genetic tests is needed to ensure coupling of clinical detail (phenotype) with DNA variants (genotype) to ensure utility in publication and databases.

Cotton RG, Auerbach AD, Brown AF, Carrera P, Christodoulou J, Claustres M, Compton J, Cox DW, De Baere E, den Dunnen JT, Greenblatt M, Fujiwara M, Hilbert P, Jani A, Lehvaslaiho H, Nebert DW, Verma I, Vihinen M; Members of the Human Genome Variation Society; Human Variome Project Diagnostic Laboratory Working Group.

Hum Mutat. 2007 Oct;28(10):931-2.

PMID:
17726697
35.

Sequence variation database for the Wilson disease copper transporter, ATP7B.

Kenney SM, Cox DW.

Hum Mutat. 2007 Dec;28(12):1171-7.

PMID:
17680703
36.

Three atypical cases of Wilson disease: assessment of the Leipzig scoring system in making a diagnosis.

Xuan A, Bookman I, Cox DW, Heathcote J.

J Hepatol. 2007 Sep;47(3):428-33. Epub 2007 Jun 25.

PMID:
17629589
37.

Polymorphisms in canine ATP7B: candidate modifier of copper toxicosis in the Bedlington terrier.

Coronado VA, O'Neill B, Nanji M, Cox DW.

Vet J. 2008 Aug;177(2):293-6. Epub 2007 Jun 14.

PMID:
17572118
38.

COMMD1 (MURR1) as a candidate in patients with copper storage disease of undefined etiology.

Coronado VA, Bonneville JA, Nazer H, Roberts EA, Cox DW.

Clin Genet. 2005 Dec;68(6):548-51. No abstract available.

PMID:
16283886
39.

FISH-mapping of telomeric 14q32 deletions: search for the cause of seizures.

Schlade-Bartusiak K, Costa T, Summers AM, Nowaczyk MJ, Cox DW.

Am J Med Genet A. 2005 Oct 15;138A(3):218-24.

PMID:
16152642
40.

Twenty-four novel mutations in Wilson disease patients of predominantly European ancestry.

Cox DW, Prat L, Walshe JM, Heathcote J, Gaffney D.

Hum Mutat. 2005 Sep;26(3):280.

PMID:
16088907
41.

Defining a holoprosencephaly locus on human chromosome 14q13 and characterization of potential candidate genes.

Kamnasaran D, Chen CP, Devriendt K, Mehta L, Cox DW.

Genomics. 2005 May;85(5):608-21.

PMID:
15820313
42.

Value of an enzymatic assay for the determination of serum ceruloplasmin.

Macintyre G, Gutfreund KS, Martin WR, Camicioli R, Cox DW.

J Lab Clin Med. 2004 Dec;144(6):294-301.

PMID:
15614251
43.

Prenatal diagnosis for alpha1-antitrypsin deficiency.

Cox DW.

Prenat Diagn. 2004 Jun;24(6):468-70. Review. No abstract available.

PMID:
15229848
44.

Functional assessment of the carboxy-terminus of the Wilson disease copper-transporting ATPase, ATP7B.

Hsi G, Cullen LM, Moira Glerum D, Cox DW.

Genomics. 2004 Mar;83(3):473-81.

PMID:
14962673
45.

In vivo reduction of amyloid-beta by a mutant copper transporter.

Phinney AL, Drisaldi B, Schmidt SD, Lugowski S, Coronado V, Liang Y, Horne P, Yang J, Sekoulidis J, Coomaraswamy J, Chishti MA, Cox DW, Mathews PM, Nixon RA, Carlson GA, St George-Hyslop P, Westaway D.

Proc Natl Acad Sci U S A. 2003 Nov 25;100(24):14193-8. Epub 2003 Nov 14.

46.
47.

A comparison of the mutation spectra of Menkes disease and Wilson disease.

Hsi G, Cox DW.

Hum Genet. 2004 Jan;114(2):165-72. Epub 2003 Oct 25.

PMID:
14579150
48.

New haplotypes in the Bedlington terrier indicate complexity in copper toxicosis.

Coronado VA, Damaraju D, Kohijoki R, Cox DW.

Mamm Genome. 2003 Jul;14(7):483-91.

PMID:
12925897
49.

Disruption of the neuronal PAS3 gene in a family affected with schizophrenia.

Kamnasaran D, Muir WJ, Ferguson-Smith MA, Cox DW.

J Med Genet. 2003 May;40(5):325-32.

50.

Rearrangement in the PITX2 and MIPOL1 genes in a patient with a t(4;14) chromosome.

Kamnasaran D, O'Brien PC, Zackai EH, Muenke M, Ferguson-Smith MA, Cox DW.

Eur J Hum Genet. 2003 Apr;11(4):315-24.

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