| Year |
Citation |
Score |
| Low-probability matches (unlikely to be authored by this person) |
| 2021 |
Thiryayi SA, Ettler H, Goebel EA, Prefontaine M, Paton TA, Wong A, Yee D, Agro E, Mayers J, Lerner-Ellis J, Turashvili G. BCOR Internal Tandem Duplication Associated Uterine Sarcoma: Expanding the Clinicopathologic Spectrum. International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists. PMID 34456278 DOI: 10.1097/PGP.0000000000000822 |
0.01 |
|
| 2021 |
Cohn I, Manshaei R, Liston E, Okello JBA, Khan R, Curtis MR, Krupski AJ, Jobling RK, Kalbfleisch K, Paton TA, Reuter MS, Hayeems RZ, Verstegen RHJ, Goldman A, Kim RH, et al. Assessment of the Implementation of Pharmacogenomic Testing in a Pediatric Tertiary Care Setting. Jama Network Open. 4: e2110446. PMID 34037732 DOI: 10.1001/jamanetworkopen.2021.10446 |
0.01 |
|
| 2019 |
Zarrei M, Burton CL, Engchuan W, Young EJ, Higginbotham EJ, MacDonald JR, Trost B, Chan AJS, Walker S, Lamoureux S, Heung T, Mojarad BA, Kellam B, Paton T, Faheem M, et al. A large data resource of genomic copy number variation across neurodevelopmental disorders. Npj Genomic Medicine. 4: 26. PMID 31602316 DOI: 10.1038/S41525-019-0098-3 |
0.01 |
|
| 2019 |
Sullivan K, Isabel S, Khodai-Booran N, Paton TA, Abdulnoor M, Dipchand AI, Hébert D, Ng VL, Allen UD. Epstein-Barr VIRUS latent gene EBNA-1 genetic diversity among transplant patients compared with patients with infectious mononucleosis. Clinical Transplantation. e13504. PMID 30790353 DOI: 10.1111/Ctr.13504 |
0.01 |
|
| 2019 |
Baribeau DA, Dupuis A, Paton TA, Hammill C, Scherer SW, Schachar RJ, Arnold PD, Szatmari P, Nicolson R, Georgiades S, Crosbie J, Brian J, Iaboni A, Kushki A, Lerch JP, et al. Structural neuroimaging correlates of social deficits are similar in autism spectrum disorder and attention-deficit/hyperactivity disorder: analysis from the POND Network. Translational Psychiatry. 9: 72. PMID 30718456 DOI: 10.1038/S41398-019-0382-0 |
0.01 |
|
| 2019 |
Abdulnoor M, Khodai-Booran N, Schechter T, Paton T, Casallo G, Allen UD. 1778. Epstein–Barr Virus Genetic Diversity: Evaluation of BZLF1 Variants among Bone Marrow Transplant Patients and Individuals with Infectious Mononucleosis Open Forum Infectious Diseases. 6: S655-S655. DOI: 10.1093/Ofid/Ofz360.1641 |
0.01 |
|
| 2018 |
Reuter MS, Walker S, Thiruvahindrapuram B, Whitney J, Cohn I, Sondheimer N, Yuen RKC, Trost B, Paton TA, Pereira SL, Herbrick JA, Wintle RF, Merico D, Howe J, MacDonald JR, et al. The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants. Cmaj : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne. 190: E126-E136. PMID 29431110 DOI: 10.1503/Cmaj.171151 |
0.01 |
|
| 2018 |
Abdulnoor M, Khodai-Booran N, Pietrzyk J, Paton T, Casallo G, Allen U. 657. Epstein–Barr Virus Genetic Diversity in Blood vs. Saliva Samples From Patients with Infectious Mononucleosis Open Forum Infectious Diseases. 5: S238-S238. DOI: 10.1093/Ofid/Ofy210.664 |
0.01 |
|
| 2017 |
Cohn I, Paton TA, Marshall CR, Basran R, Stavropoulos DJ, Ray PN, Monfared N, Hayeems RZ, Meyn MS, Bowdin S, Scherer SW, Cohn RD, Ito S. Genome sequencing as a platform for pharmacogenetic genotyping: a pediatric cohort study. Npj Genomic Medicine. 2: 19. PMID 29263831 DOI: 10.1038/S41525-017-0021-8 |
0.01 |
|
| 2017 |
Baribeau DA, Dupuis A, Paton TA, Scherer SW, Schachar RJ, Arnold PD, Szatmari P, Nicolson R, Georgiades S, Crosbie J, Brian J, Iaboni A, Lerch J, Anagnostou E. Oxytocin Receptor Polymorphisms are Differentially Associated with Social Abilities across Neurodevelopmental Disorders. Scientific Reports. 7: 11618. PMID 28912494 DOI: 10.1038/S41598-017-10821-0 |
0.01 |
|
| 2017 |
Farrell SA, Sodhi S, Marshall CR, Guerin A, Slavotinek A, Paton T, Chong K, Sirkin WL, Scherer SW, Bérubé-Simard FA, Pilon N. HLX is a candidate gene for a pattern of anomalies associated with congenital diaphragmatic hernia, short bowel, and asplenia. American Journal of Medical Genetics. Part A. PMID 28898547 DOI: 10.1002/Ajmg.A.38354 |
0.01 |
|
| 2017 |
Evans DR, Green JS, Johnson GJ, Schwartzentruber J, Majewski J, Beaulieu CL, Qin W, Marshall CR, Paton TA, Roslin NM, Paterson AD, Fahiminiya S, French J, Boycott KM, Woods MO, et al. Novel 25 kb Deletion of MERTK Causes Retinitis Pigmentosa With Severe Progression. Investigative Ophthalmology & Visual Science. 58: 1736-1742. PMID 28324114 DOI: 10.1167/Iovs.16-20864 |
0.01 |
|
| 2017 |
C Yuen RK, Merico D, Bookman M, L Howe J, Thiruvahindrapuram B, Patel RV, Whitney J, Deflaux N, Bingham J, Wang Z, Pellecchia G, Buchanan JA, Walker S, Marshall CR, Uddin M, ... Paton T, et al. Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder. Nature Neuroscience. PMID 28263302 DOI: 10.1038/Nn.4524 |
0.01 |
|
| 2017 |
Lok S, Paton TA, Wang Z, Kaur G, Walker S, Yuen RK, Sung WW, Whitney J, Buchanan JA, Trost B, Singh N, Apresto B, Chen N, Coole M, Dawson TJ, et al. De novo genome and transcriptome assembly of the Canadian beaver (Castor canadensis). G3 (Bethesda, Md.). PMID 28087693 DOI: 10.1534/G3.116.038208 |
0.01 |
|
| 2017 |
Allen U, Abdulnoor M, Khodai-Booran N, Paton T, Dipchand A, Hebert D, Ng V, Solomon M. Genetic Diversity of Epstein–Barr Virus Lytic Gene BZLF-1 among Patients with and Without Post-transplant Lymphoproliferative Disorder Open Forum Infectious Diseases. 4: S733-S733. DOI: 10.1093/Ofid/Ofx163.1976 |
0.01 |
|
| 2016 |
Samuel N, Wilson G, Said BI, Pan A, Deblois G, Fischer NW, Alexandrova R, Casallo G, Paton T, Lupien M, Gariepy J, Merico D, Hudson TJ, Malkin D. Transcriptome-wide characterization of the endogenous miR-34A-p53 tumor suppressor network. Oncotarget. PMID 27391063 DOI: 10.18632/Oncotarget.10417 |
0.01 |
|
| 2016 |
Yoon G, Malam Z, Paton T, Marshall CR, Hyatt E, Ivakine Z, Scherer SW, Lee KS, Hawkins C, Cohn RD. Lethal Disorder of Mitochondrial Fission Caused by Mutations in DNM1L. The Journal of Pediatrics. PMID 26825290 DOI: 10.1016/J.Jpeds.2015.12.060 |
0.01 |
|
| 2015 |
Allen UD, Hu P, Pereira SL, Robinson JL, Paton TA, Beyene J, Khodai-Booran N, Dipchand A, Hébert D, Ng V, Nalpathamkalam T, Read S. The genetic diversity of Epstein-Barr virus in the setting of transplantation relative to non-transplant settings: A feasibility study. Pediatric Transplantation. PMID 26578436 DOI: 10.1111/Petr.12610 |
0.01 |
|
| 2015 |
Day GS, Prüss H, Benseler SM, Paton TA, Paterson AD, Andrade DM. GRIN1 polymorphisms do not affect susceptibility or phenotype in NMDA receptor encephalitis. Neurology® Neuroimmunology & Neuroinflammation. 2: e153. PMID 26443875 DOI: 10.1212/Nxi.0000000000000153 |
0.01 |
|
| 2015 |
Marshall CR, Scherer SW, Zariwala MA, Lau L, Paton TA, Stockley T, Jobling RK, Ray PN, Knowles MR, Hall DA, Dell SD, Kim RH. Whole Exome Sequencing and Targeted Copy Number Analysis in Primary Ciliary Dyskinesia. G3 (Bethesda, Md.). PMID 26139845 DOI: 10.1534/G3.115.019851 |
0.01 |
|
| 2015 |
Marshall CR, Farrell SA, Cushing D, Paton T, Stockley TL, Stavropoulos DJ, Ray PN, Szego M, Lau L, Pereira SL, Cohn RD, Wintle RF, Abuzenadah AM, Abu-Elmagd M, Scherer SW. Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome. Bmc Genomics. 16: S12. PMID 25923536 DOI: 10.1186/1471-2164-16-S1-S12 |
0.01 |
|
| 2015 |
Ammar R, Paton TA, Torti D, Shlien A, Bader GD. Long read nanopore sequencing for detection of HLA and CYP2D6 variants and haplotypes. F1000research. 4: 17. PMID 25901276 DOI: 10.12688/F1000Research.6037.1 |
0.01 |
|
| 2015 |
Jobling RK, Assoum M, Gakh O, Blaser S, Raiman JA, Mignot C, Roze E, Dürr A, Brice A, Lévy N, Prasad C, Paton T, Paterson AD, Roslin NM, Marshall CR, et al. PMPCA mutations cause abnormal mitochondrial protein processing in patients with non-progressive cerebellar ataxia. Brain : a Journal of Neurology. 138: 1505-17. PMID 25808372 DOI: 10.1093/Brain/Awv057 |
0.01 |
|
| 2015 |
Al-Maawali A, Dupuis L, Blaser S, Heon E, Tarnopolsky M, Al-Murshedi F, Marshall CR, Paton T, Scherer SW, Roelofsen J, van Kuilenburg AB, Mendoza-Londono R. Prenatal growth restriction, retinal dystrophy, diabetes insipidus and white matter disease: expanding the spectrum of PRPS1-related disorders. European Journal of Human Genetics : Ejhg. 23: 310-6. PMID 24961627 DOI: 10.1038/Ejhg.2014.112 |
0.01 |
|
| 2015 |
Roifman M, Marcelis CL, Paton T, Marshall C, Silver R, Lohr JL, Yntema HG, Venselaar H, Kayserili H, van Bon B, Seaward G, Brunner HG, Chitayat D. De novo WNT5A-associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotype. Clinical Genetics. 87: 34-41. PMID 24716670 DOI: 10.1111/Cge.12401 |
0.01 |
|
| 2015 |
Sullivan K, Isabel S, Edilova M, Paton T, Yeung S, Booran N, Ng V, Allen U. 125: Genetic Diversity of Epstein-Barr Virus Latent Gene EBNA-1 Among Transplant Patients and Patients with Infectious Mononucleosis. Paediatrics & Child Health. 20: e79-e79. DOI: 10.1093/pch/20.5.e79a |
0.01 |
|
| 2014 |
Mowjoodi A, Paton TA, Scherer SW. Discrimination of SNPs in GC-rich regions using a modified hydrolysis probe chemistry protocol. Biotechniques. 57: 313-6. PMID 25495732 DOI: 10.2144/000114240 |
0.01 |
|
| 2014 |
Vincent A, Forster N, Maynes JT, Paton TA, Billingsley G, Roslin NM, Ali A, Sutherland J, Wright T, Westall CA, Paterson AD, Marshall CR, Héon E. OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epithelium. Journal of Medical Genetics. 51: 797-805. PMID 25293953 DOI: 10.1136/Jmedgenet-2014-102620 |
0.01 |
|
| 2014 |
Aïssi D, Dennis J, Ladouceur M, Truong V, Zwingerman N, Rocanin-Arjo A, Germain M, Paton TA, Morange PE, Gagnon F, Trégouët DA. Genome-wide investigation of DNA methylation marks associated with FV Leiden mutation. Plos One. 9: e108087. PMID 25265411 DOI: 10.1371/Journal.Pone.0108087 |
0.01 |
|
| 2013 |
Kim S, Medvedev P, Paton TA, Bafna V. Reprever: resolving low-copy duplicated sequences using template driven assembly. Nucleic Acids Research. 41: e128. PMID 23658221 DOI: 10.1093/Nar/Gkt339 |
0.01 |
|
| 2012 |
Andrade DM, Paton T, Turnbull J, Marshall CR, Scherer SW, Minassian BA. Mutation of the CLN6 gene in teenage-onset progressive myoclonus epilepsy. Pediatric Neurology. 47: 205-8. PMID 22883287 DOI: 10.1016/J.Pediatrneurol.2012.05.004 |
0.01 |
|
| 2012 |
Anney R, Klei L, Pinto D, Almeida J, Bacchelli E, Baird G, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Casey J, Conroy J, Correia C, ... Paton T, et al. Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Human Molecular Genetics. 21: 4781-92. PMID 22843504 DOI: 10.1093/Hmg/Dds301 |
0.01 |
|
| 2011 |
Lazar NL, Singh S, Paton T, Clapcote SJ, Gondo Y, Fukumura R, Roder JC, Cain DP. Missense mutation of the reticulon-4 receptor alters spatial memory and social interaction in mice. Behavioural Brain Research. 224: 73-9. PMID 21645550 DOI: 10.1016/J.Bbr.2011.05.020 |
0.01 |
|
| 2010 |
Anney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Sykes N, Pagnamenta AT, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, ... Paton T, et al. A genome-wide scan for common alleles affecting risk for autism. Human Molecular Genetics. 19: 4072-82. PMID 20663923 DOI: 10.1093/Hmg/Ddq307 |
0.01 |
|
| 2010 |
Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Almeida J, Bacchelli E, Bader GD, Bailey AJ, Baird G, ... Paton T, et al. Functional impact of global rare copy number variation in autism spectrum disorders. Nature. 466: 368-72. PMID 20531469 DOI: 10.1038/Nature09146 |
0.01 |
|
| 2008 |
Baker AJ, Pereira SL, Paton TA. Phylogenetic relationships and divergence times of Charadriiformes genera: multigene evidence for the Cretaceous origin of at least 14 clades of shorebirds: Biol. Lett. 3, 205–209 (2007) Biology Letters. 4: 762-763. DOI: 10.1098/Rsbl.2006.0606Erratum |
0.01 |
|
| 2007 |
Mastronardi FG, Noor A, Wood DD, Paton T, Moscarello MA. Peptidyl argininedeiminase 2 CpG island in multiple sclerosis white matter is hypomethylated. Journal of Neuroscience Research. 85: 2006-16. PMID 17469138 DOI: 10.1002/Jnr.21329 |
0.01 |
|
| 2007 |
Baker AJ, Pereira SL, Paton TA. Phylogenetic relationships and divergence times of Charadriiformes genera: multigene evidence for the Cretaceous origin of at least 14 clades of shorebirds. Biology Letters. 3: 205-9. PMID 17284401 DOI: 10.1098/Rsbl.2006.0606 |
0.01 |
|
| 2006 |
Paton TA, Baker AJ. Sequences from 14 mitochondrial genes provide a well-supported phylogeny of the Charadriiform birds congruent with the nuclear RAG-1 tree. Molecular Phylogenetics and Evolution. 39: 657-67. PMID 16531074 DOI: 10.1016/J.Ympev.2006.01.011 |
0.01 |
|
| 2005 |
Hughes S, Colantonio A, Santaguida PL, Paton T. Amantadine to enhance readiness for rehabilitation following severe traumatic brain injury. Brain Injury. 19: 1197-206. PMID 16286335 DOI: 10.1080/02699050500309296 |
0.01 |
|
| 2004 |
Dranitsaris G, Kahn SR, Stumpo C, Paton TW, Martineau J, Smith R, Ginsberg JS. Pharmacoeconomic analysis of fondaparinux versus enoxaparin for the prevention of thromboembolic events in orthopedic surgery patients American Journal of Cardiovascular Drugs. 4: 325-333. PMID 15449974 DOI: 10.2165/00129784-200404050-00005 |
0.01 |
|
| 2004 |
Nakabayashi K, Makino S, Minagawa S, Smith AC, Bamforth JS, Stanier P, Preece M, Parker-Katiraee L, Paton T, Oshimura M, Mill P, Yoshikawa Y, Hui CC, Monk D, Moore GE, et al. Genomic imprinting of PPP1R9A encoding neurabin I in skeletal muscle and extra-embryonic tissues. Journal of Medical Genetics. 41: 601-8. PMID 15286155 DOI: 10.1136/Jmg.2003.014142 |
0.01 |
|
| 2003 |
Paton TA, Baker AJ, Groth JG, Barrowclough GF. RAG-1 sequences resolve phylogenetic relationships within Charadriiform birds. Molecular Phylogenetics and Evolution. 29: 268-78. PMID 13678682 DOI: 10.1016/S1055-7903(03)00098-8 |
0.01 |
|
| 2003 |
van Tuinen M, Paton T, Haddrath O, Baker A. ‘Big bang’ for Tertiary birds? A reply Trends in Ecology & Evolution. 18: 442-443. DOI: 10.1016/S0169-5347(03)00212-X |
0.01 |
|
| 2002 |
Paton T, Haddrath O, Baker AJ. Complete mitochondrial DNA genome sequences show that modern birds are not descended from transitional shorebirds. Proceedings. Biological Sciences / the Royal Society. 269: 839-46. PMID 11958716 DOI: 10.1098/Rspb.2002.1961 |
0.01 |
|
| 2001 |
Juurlink DN, McGuigan MA, Paton TW, Redelmeier DA. Availability of antidotes at acute care hospitals in Ontario. Cmaj : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne. 165: 27-30. PMID 11468950 |
0.01 |
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| 2001 |
Fam AG, Dunne SM, Iazzetta J, Paton TW. Efficacy and safety of desensitization to allopurinol following cutaneous reactions. Arthritis and Rheumatism. 44: 231-8. PMID 11212165 DOI: 10.1002/1529-0131(200101)44:1<231::AID-ANR30>3.0.CO;2-7 |
0.01 |
|
| 1998 |
Paton TE, Renton KW. Cytokine-mediated down-regulation of CYP1A1 in Hepa1 cells. Biochemical Pharmacology. 55: 1791-6. PMID 9714297 |
0.01 |
|
| 1993 |
Wichman K, Hales B, O'Brodovich M, Paton T, Wielenga J. Management considerations to implementing pharmaceutical care. The Canadian Journal of Hospital Pharmacy. 46: 265-7. PMID 10131344 |
0.01 |
|
| 1992 |
Levine MA, Walker SE, Paton TW. The effect of food or sucralfate on the bioavailability of S(+) and R(-) enantiomers of ibuprofen. Journal of Clinical Pharmacology. 32: 1110-4. PMID 1487549 |
0.01 |
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| 1992 |
Fam AG, Lewtas J, Stein J, Paton TW. Desensitization to allopurinol in patients with gout and cutaneous reactions. The American Journal of Medicine. 93: 299-302. PMID 1388001 |
0.01 |
|
| 1991 |
Nikolaidis P, Walker SE, Dombros N, Tourkantonis A, Paton TW, Oreopoulos DG. Single-dose pefloxacin pharmacokinetics and metabolism in patients undergoing continuous ambulatory peritoneal dialysis (CAPD). Peritoneal Dialysis International : Journal of the International Society For Peritoneal Dialysis. 11: 59-63. PMID 2049424 |
0.01 |
|
| 1991 |
Paton TJ, Lee NJ, Yacoub WR, Angus B. A health centre survey of childhood injury in Edmonton Canadian Journal of Public Health. 82: 436-437. PMID 1790512 |
0.01 |
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| 1989 |
Rudinskas L, Paton TW, Walker SE, Dotten DA, Cowan DH. Poor clinical response to enteric-coated iron preparations. Cmaj : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne. 141: 565-6. PMID 2776097 |
0.01 |
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| 1989 |
Walker SE, Paton TW, Cowan DH, Manuel MA, Dranitsaris G. Bioavailability of iron in oral ferrous sulfate preparations in healthy volunteers. Cmaj : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne. 141: 543-7. PMID 2776093 |
0.01 |
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| 1989 |
Walker SE, Paton TW, Churchill DN, Ojo B, Manuel MA, Wright N. Trimethoprim-sulfamethoxazole pharmacokinetics during continuous ambulatory peritoneal dialysis (CAPD). Peritoneal Dialysis International : Journal of the International Society For Peritoneal Dialysis. 9: 51-5. PMID 2488182 |
0.01 |
|
| 1988 |
McDonald J, Fam AG, Paton T, Senn J. Allopurinol hypersensitivity in a patient with coexistent systemic lupus erythematosus and tophaceous gout. The Journal of Rheumatology. 15: 865-8. PMID 3172103 |
0.01 |
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| 1985 |
Paton TW, Cornish WR, Manuel MA, Hardy BG. Drug therapy in patients undergoing peritoneal dialysis. Clinical pharmacokinetic considerations. Clinical Pharmacokinetics. 10: 404-25. PMID 3899455 |
0.01 |
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| 1984 |
Fam AG, Paton TW. Nail pigmentation after parenteral gold therapy for rheumatoid arthritis: "gold nails". Arthritis and Rheumatism. 27: 119-20. PMID 6691855 |
0.01 |
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| 1983 |
Paton TW, Walker SE, Leung FY, Little AH. Effect of cimetidine on bioavailability of enteric-coated aspirin tablets. Clinical Pharmacy. 2: 165-6. PMID 6883946 |
0.01 |
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| 1983 |
Walker SE, Paton TW, Iazzetta J. Single dose cross-over theophylline bioavailability study British Journal of Clinical Practice. 37: 23-27. PMID 6838753 |
0.01 |
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| 1982 |
Paton TJ, Cembrowski GS. Fluorometric assay of erythrocyte protoporphyrin: simple screening test for lead poisoning and iron deficiency. Canadian Medical Association Journal. 127: 860-2. PMID 7139505 |
0.01 |
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| 1982 |
Keystone EC, Paton TW, Littlejohn G, Verdejo A, Piper S, Wright LA, Goldsmith CH. Steady-state plasma levels of salicylate in patients with rheumatoid arthritis: effects of dosing interval and tablet strength. Canadian Medical Association Journal. 127: 283-6. PMID 7093867 |
0.01 |
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| 1981 |
Walker SE, Paton TW, Fabian TM, Liu CC, Coates PE. Stability and sterility of cimetidine admixtures frozen in minibags. American Journal of Hospital Pharmacy. 38: 881-3. PMID 7246565 |
0.01 |
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| 1981 |
Fam AG, Paton TW, Cowan DH. Herpes zoster during gold therapy. Annals of Internal Medicine. 94: 712-3. PMID 6786152 |
0.01 |
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| 1980 |
Fam AG, Paton TW, Shamess CJ, Lewis AJ. Fulminant colitis complicating gold therapy. The Journal of Rheumatology. 7: 479-85. PMID 6775079 |
0.01 |
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| 1980 |
Fam AG, Paton TW, Chaiton A. Reinstitution of allopurinol therapy for gouty arthritis after cutaneous reactions. Canadian Medical Association Journal. 123: 128-9. PMID 6455189 |
0.01 |
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| 1979 |
Bensen WG, Laskin CA, Paton TW, Little HA, Fam AG. Twice-daily dosing of enteric-coated aspirin in patients with rheumatic diseases. The Journal of Rheumatology. 6: 351-9. PMID 314982 |
0.01 |
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| Hide low-probability matches. |