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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1913 1
1915 1
1917 13
1919 1
1920 1
1933 1
1954 1
1955 3
1956 1
1957 1
1958 1
1959 1
1961 5
1962 3
1963 3
1964 1
1965 2
1966 6
1967 5
1968 4
1969 6
1970 7
1971 9
1972 6
1973 10
1974 7
1975 12
1976 11
1977 7
1978 9
1979 6
1980 9
1981 15
1982 7
1983 10
1984 11
1985 15
1986 19
1987 15
1988 8
1989 4
1990 9
1991 14
1992 9
1993 10
1994 13
1995 16
1996 12
1997 12
1998 17
1999 15
2000 19
2001 19
2002 20
2003 16
2004 20
2005 18
2006 14
2007 19
2008 20
2009 21
2010 15
2011 16
2012 23
2013 13
2014 22
2015 16
2016 19
2017 24
2018 26
2019 27
2020 39
2021 30
2022 18
Text availability
Article attribute
Article type
Publication date

Search Results

810 results
Results by year
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Page 1
Clinical guidelines for testing for heritable thrombophilia.
Baglin T, Gray E, Greaves M, Hunt BJ, Keeling D, Machin S, Mackie I, Makris M, Nokes T, Perry D, Tait RC, Walker I, Watson H; British Committee for Standards in Haematology. Baglin T, et al. Among authors: walker i. Br J Haematol. 2010 Apr;149(2):209-20. doi: 10.1111/j.1365-2141.2009.08022.x. Epub 2010 Jan 28. Br J Haematol. 2010. PMID: 20128794 No abstract available.
Treatment of Multiple Myeloma: ASCO and CCO Joint Clinical Practice Guideline.
Mikhael J, Ismaila N, Cheung MC, Costello C, Dhodapkar MV, Kumar S, Lacy M, Lipe B, Little RF, Nikonova A, Omel J, Peswani N, Prica A, Raje N, Seth R, Vesole DH, Walker I, Whitley A, Wildes TM, Wong SW, Martin T. Mikhael J, et al. Among authors: walker i. J Clin Oncol. 2019 May 10;37(14):1228-1263. doi: 10.1200/JCO.18.02096. Epub 2019 Apr 1. J Clin Oncol. 2019. PMID: 30932732
Integrative genomic analysis reveals cancer-associated mutations at diagnosis of CML in patients with high-risk disease.
Branford S, Wang P, Yeung DT, Thomson D, Purins A, Wadham C, Shahrin NH, Marum JE, Nataren N, Parker WT, Geoghegan J, Feng J, Shanmuganathan N, Mueller MC, Dietz C, Stangl D, Donaldson Z, Altamura H, Georgievski J, Braley J, Brown A, Hahn C, Walker I, Kim SH, Choi SY, Park SH, Kim DW, White DL, Yong ASM, Ross DM, Scott HS, Schreiber AW, Hughes TP. Branford S, et al. Among authors: walker i. Blood. 2018 Aug 30;132(9):948-961. doi: 10.1182/blood-2018-02-832253. Epub 2018 Jul 2. Blood. 2018. PMID: 29967129 Free article. Clinical Trial.
Genetics of haemostasis.
Goodeve AC, Perry DJ, Cumming T, Hill M, Jennings I, Kitchen S, Walker I, Gray E, Jayandharan GR, Tuddenham E. Goodeve AC, et al. Among authors: walker i. Haemophilia. 2012 Jul;18 Suppl 4:73-80. doi: 10.1111/j.1365-2516.2012.02832.x. Haemophilia. 2012. PMID: 22726087 Review.
Causality matters in medical imaging.
Castro DC, Walker I, Glocker B. Castro DC, et al. Among authors: walker i. Nat Commun. 2020 Jul 22;11(1):3673. doi: 10.1038/s41467-020-17478-w. Nat Commun. 2020. PMID: 32699250 Free PMC article. Review.
PPP2R5D Genetic Mutations and Early-Onset Parkinsonism.
Walker IM, Riboldi GM, Drummond P, Saade-Lemus S, Martin-Saavedra JS, Frucht S, Bardakjian TM, Gonzalez-Alegre P, Deik A. Walker IM, et al. Ann Neurol. 2021 Jan;89(1):194-195. doi: 10.1002/ana.25943. Epub 2020 Nov 5. Ann Neurol. 2021. PMID: 33098144 No abstract available.
Inherited thrombophilia.
Walker ID. Walker ID. Vasc Med. 2004 May;9(3):219-21. doi: 10.1191/1358863x04vm556xx. Vasc Med. 2004. PMID: 15675188 Review.
Amphibian therapeutics.
Walker ID, Whitaker BR. Walker ID, et al. Vet Clin North Am Exot Anim Pract. 2000 Jan;3(1):239-55, viii. doi: 10.1016/s1094-9194(17)30103-2. Vet Clin North Am Exot Anim Pract. 2000. PMID: 11228830 Review.
Response to letter from Dr Riegel and Mr James.
Carleton-Eagleton K, Walker I, Freene N, Gibson D, Semple S. Carleton-Eagleton K, et al. Among authors: walker i. Eur J Cardiovasc Nurs. 2021 Jun 29;20(5):514. doi: 10.1093/eurjcn/zvab039. Eur J Cardiovasc Nurs. 2021. PMID: 34115828 No abstract available.
810 results