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

Year Number of Results
1887 1
1896 1
1903 2
1906 1
1910 1
1914 1
1915 1
1916 3
1918 1
1929 1
1930 2
1935 1
1939 1
1944 1
1945 3
1946 2
1947 9
1948 9
1949 13
1950 18
1951 19
1952 18
1953 12
1954 13
1955 30
1956 19
1957 21
1958 19
1959 28
1960 24
1961 24
1962 27
1963 31
1964 56
1965 43
1966 35
1967 45
1968 42
1969 49
1970 35
1971 37
1972 48
1973 61
1974 50
1975 42
1976 32
1977 36
1978 36
1979 48
1980 40
1981 37
1982 36
1983 45
1984 31
1985 47
1986 52
1987 55
1988 36
1989 69
1990 69
1991 56
1992 82
1993 82
1994 89
1995 76
1996 67
1997 71
1998 40
1999 65
2000 67
2001 78
2002 83
2003 82
2004 68
2005 64
2006 73
2007 80
2008 83
2009 75
2010 98
2011 122
2012 168
2013 124
2014 150
2015 171
2016 151
2017 170
2018 172
2019 145
2020 162
2021 178
2022 173
2023 183
2024 70

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4,863 results

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Page 1
Paroxysmal nocturnal hemoglobinuria (PNH) and primary p.Cys89Tyr mutation in CD59: Differences and similarities.
Mevorach D. Mevorach D. Mol Immunol. 2015 Sep;67(1):51-5. doi: 10.1016/j.molimm.2015.03.005. Epub 2015 Mar 26. Mol Immunol. 2015. PMID: 25818314 Review.
CD59 deficiency is a common finding in adult patients with paroxysmal nocturnal hemoglobinuria (PNH). In this condition, there is a clonal expansion of hematopoietic stem cells that have acquired a mutation in the PIGA gene (phosphatidylinositol glycan anchor biosyn …
CD59 deficiency is a common finding in adult patients with paroxysmal nocturnal hemoglobinuria (PNH). In this condition, there …
How we('ll) treat paroxysmal nocturnal haemoglobinuria: diving into the future.
Risitano AM, Peffault de Latour R. Risitano AM, et al. Br J Haematol. 2022 Jan;196(2):288-303. doi: 10.1111/bjh.17753. Epub 2021 Aug 5. Br J Haematol. 2022. PMID: 34355382 Free PMC article. Review.
Paroxysmal nocturnal haemoglobinuria (PNH) is characterized by complement-mediated intravascular haemolysis, severe thrombophilia and bone marrow failure. ...
Paroxysmal nocturnal haemoglobinuria (PNH) is characterized by complement-mediated intravascular haemolysis, severe thrombophi
Paroxysmal cold hemoglobinuria.
Djaldetti M. Djaldetti M. CRC Crit Rev Clin Lab Sci. 1978;9(1):49-83. doi: 10.3109/10408367809150915. CRC Crit Rev Clin Lab Sci. 1978. PMID: 401365 Review.
Evolutionary dynamics of paroxysmal nocturnal hemoglobinuria.
Mon Père N, Lenaerts T, Pacheco JM, Dingli D. Mon Père N, et al. PLoS Comput Biol. 2018 Jun 18;14(6):e1006133. doi: 10.1371/journal.pcbi.1006133. eCollection 2018 Jun. PLoS Comput Biol. 2018. PMID: 29912864 Free PMC article.
Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal blood disorder characterized by hemolysis and a high risk of thrombosis, that is due to a deficiency in several cell surface proteins that prevent complement activation. ...
Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal blood disorder characterized by hemolysis and a high risk of t
PAROXYSMAL nocturnal hemoglobinuria.
[No authors listed] [No authors listed] J Am Med Assoc. 1960 May 21;173:260-1. doi: 10.1001/jama.1960.03020210040011. J Am Med Assoc. 1960. PMID: 13857330 No abstract available.
Congenital CD59 Deficiency.
Höchsmann B, Schrezenmeier H. Höchsmann B, et al. Hematol Oncol Clin North Am. 2015 Jun;29(3):495-507. doi: 10.1016/j.hoc.2015.01.006. Epub 2015 Apr 4. Hematol Oncol Clin North Am. 2015. PMID: 26043388 Review.
Hemoglobinuria.
HAM TH. HAM TH. Am J Med. 1955 Jun;18(6):990-1006. doi: 10.1016/0002-9343(55)90177-7. Am J Med. 1955. PMID: 14376416 No abstract available.
4,863 results