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Results by year

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

Year Number of Results
1970 1
1973 1
1974 3
1975 5
1976 9
1977 10
1978 10
1979 10
1980 7
1981 8
1982 9
1983 17
1984 12
1985 14
1986 14
1987 12
1988 15
1989 17
1990 18
1991 19
1992 24
1993 23
1994 28
1995 26
1996 24
1997 29
1998 40
1999 36
2000 28
2001 43
2002 45
2003 33
2004 31
2005 30
2006 29
2007 31
2008 30
2009 29
2010 41
2011 43
2012 48
2013 55
2014 58
2015 49
2016 49
2017 44
2018 37
2019 41
2020 39
2021 45
2022 34
2023 34
2024 7

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1,308 results

Results by year

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Page 1
Primary myelofibrosis: 2021 update on diagnosis, risk-stratification and management.
Tefferi A. Tefferi A. Am J Hematol. 2021 Jan;96(1):145-162. doi: 10.1002/ajh.26050. Epub 2020 Dec 2. Am J Hematol. 2021. PMID: 33197049 Free article. Review.
Furthermore, approximately 15% of patients with ET or PV might progress into a PMF-like phenotype (post-ET/PV MF) during their clinical course. ADVERSE MUTATIONS: SRSF2, ASXL1, and U2AF1-Q157 mutations predict inferior survival in PMF, independent of each other and …
Furthermore, approximately 15% of patients with ET or PV might progress into a PMF-like phenotype (post-ET/PV MF) during their clinical c …
Disease manifestations and burden of illness in patients with acid sphingomyelinase deficiency (ASMD).
McGovern MM, Avetisyan R, Sanson BJ, Lidove O. McGovern MM, et al. Orphanet J Rare Dis. 2017 Feb 23;12(1):41. doi: 10.1186/s13023-017-0572-x. Orphanet J Rare Dis. 2017. PMID: 28228103 Free PMC article. Review.
Historically, ASMD has been classified as Niemann-Pick disease (NPD) types A (NPD A) and B (NPD B). NPD A is associated with a uniformly devastating disease course, with rapidly progressing psychomotor degeneration, leading to death typically by the age of 3 years, most of …
Historically, ASMD has been classified as Niemann-Pick disease (NPD) types A (NPD A) and B (NPD B). NPD A is associated with a uniformly dev …
Histoplasmosis in transplant recipients.
Gajurel K, Dhakal R, Deresinski S. Gajurel K, et al. Clin Transplant. 2017 Oct;31(10). doi: 10.1111/ctr.13087. Epub 2017 Sep 5. Clin Transplant. 2017. PMID: 28805270 Review.
Other features, including pancytopenia and hepatosplenomegaly, may not be prominent early in the course of illness. Contemporary histoplasma antigen assays are the most sensitive tests but cross-reactivity with antigens of other fungi, including with Aspergillus galactoman …
Other features, including pancytopenia and hepatosplenomegaly, may not be prominent early in the course of illness. Contemporary hist …
Malignant Infantile osteopetrosis.
Vomero A, Tapie A, Arroyo C, Raggio V, Peluffo G, Dufort G. Vomero A, et al. Rev Chil Pediatr. 2019 Aug;90(4):443-447. doi: 10.32641/rchped.v90i4.987. Rev Chil Pediatr. 2019. PMID: 31859718 Free article. English, Spanish.
Griscelli syndrome.
Malhotra AK, Bhaskar G, Nanda M, Kabra M, Singh MK, Ramam M. Malhotra AK, et al. J Am Acad Dermatol. 2006 Aug;55(2):337-40. doi: 10.1016/j.jaad.2005.11.1056. J Am Acad Dermatol. 2006. PMID: 16844525
Pulmonary toxoplasmosis: a review.
Pomeroy C, Filice GA. Pomeroy C, et al. Clin Infect Dis. 1992 Apr;14(4):863-70. doi: 10.1093/clinids/14.4.863. Clin Infect Dis. 1992. PMID: 1576281 Review.
Clinical Symptoms, Laboratory Parameters and Long-Term Follow-up in a National DADA2 Cohort.
Andriessen MVE, Legger GE, Bredius RGM, van Gijn ME, Hak AE, Muller PCEH, Kamphuis S, Klouwer FCC, Kuijpers TW, Leavis HL, Nierkens S, Rutgers A, van der Veken LT, van Well GTJ, Mulders-Manders CM, van Montfrans JM. Andriessen MVE, et al. J Clin Immunol. 2023 Oct;43(7):1581-1596. doi: 10.1007/s10875-023-01521-8. Epub 2023 Jun 5. J Clin Immunol. 2023. PMID: 37277582 Free PMC article. Review.
Lysosomal storage disorders: A review of the musculoskeletal features.
James RA, Singh-Grewal D, Lee SJ, McGill J, Adib N; Australian Paediatric Rheumatology Group. James RA, et al. J Paediatr Child Health. 2016 Mar;52(3):262-71. doi: 10.1111/jpc.13122. J Paediatr Child Health. 2016. PMID: 27124840 Review.
Musculoskeletal manifestations often occur early in the disease course, hence are useful as diagnostics clues. Non-inflammatory joint stiffness or pain, carpal tunnel syndrome, trigger fingers, unexplained pain crises and short stature should all prompt consideration of a …
Musculoskeletal manifestations often occur early in the disease course, hence are useful as diagnostics clues. Non-inflammatory joint …
An ACE diagnosis.
Nasher O, Gupta A. Nasher O, et al. BMJ Case Rep. 2013 Feb 14;2013:bcr2012008185. doi: 10.1136/bcr-2012-008185. BMJ Case Rep. 2013. PMID: 23417380 Free PMC article.
1,308 results