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

Year Number of Results
1920 1
1945 4
1946 9
1947 1
1948 7
1949 7
1950 12
1951 17
1952 19
1953 27
1954 17
1955 12
1956 15
1957 13
1958 14
1959 12
1960 5
1961 13
1962 12
1963 19
1964 20
1965 19
1966 7
1967 14
1968 19
1969 13
1970 12
1971 17
1972 18
1973 10
1974 17
1975 23
1976 18
1977 14
1978 13
1979 20
1980 28
1981 18
1982 28
1983 22
1984 20
1985 34
1986 32
1987 46
1988 34
1989 40
1990 33
1991 21
1992 39
1993 33
1994 31
1995 40
1996 51
1997 43
1998 38
1999 55
2000 46
2001 39
2002 33
2003 37
2004 36
2005 52
2006 57
2007 64
2008 66
2009 88
2010 79
2011 75
2012 84
2013 83
2014 105
2015 122
2016 113
2017 114
2018 115
2019 116
2020 146
2021 158
2022 119
2023 119
2024 118
2025 6

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3,101 results

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Page 1
Persistent pseudo-Pelger-Huet anomaly.
Savaşan S, Buck S, Gadgeel M, Poulik J. Savaşan S, et al. Ann Hematol. 2021 Oct;100(10):2661-2663. doi: 10.1007/s00277-020-04242-9. Epub 2020 Aug 29. Ann Hematol. 2021. PMID: 32862285 No abstract available.
Pelger-Huet anomaly and T-cell lymphoma.
Schroers R, Mika T. Schroers R, et al. EJHaem. 2021 Mar 21;2(2):315-316. doi: 10.1002/jha2.184. eCollection 2021 May. EJHaem. 2021. PMID: 35845275 Free PMC article. No abstract available.
Pelger-Huet anomaly: a critical review of the literature.
Speeckaert MM, Verhelst C, Koch A, Speeckaert R, Lacquet F. Speeckaert MM, et al. Acta Haematol. 2009;121(4):202-6. doi: 10.1159/000220333. Epub 2009 May 26. Acta Haematol. 2009. PMID: 19468205 Review.
Pelger-Huet anomaly (PHA), an autosomal dominant haematological trait is characterised by neutrophil nuclear hypolobulation and modified chromatin distribution. ...
Pelger-Huet anomaly (PHA), an autosomal dominant haematological trait is characterised by neutrophil nuclear hypolobulation and modif …
Acquired Pelger-Huet: what does it really mean?
Dusse LM, Moreira AM, Vieira LM, Rios DR, Silva RM, Carvalho Md. Dusse LM, et al. Clin Chim Acta. 2010 Nov 11;411(21-22):1587-90. doi: 10.1016/j.cca.2010.07.011. Epub 2010 Aug 5. Clin Chim Acta. 2010. PMID: 20691170 Free article. Review.
Pelger-Huet anomaly (PHA) is a benign inherited condition characterized by hyposegmentation of the neutrophil's nucleus and excessive chromatin clumping. ...
Pelger-Huet anomaly (PHA) is a benign inherited condition characterized by hyposegmentation of the neutrophil's nucleus and excessive …
[Pelger-Huet anomaly].
Shinjo K, Ohno R. Shinjo K, et al. Ryoikibetsu Shokogun Shirizu. 2000;(32):139-41. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11212667 Review. Japanese. No abstract available.
Familial Pelger-Huet Anomaly.
Shah SS, Parikh RS, Vaswani LP, Divkar R. Shah SS, et al. Indian J Hematol Blood Transfus. 2016 Jun;32(Suppl 1):347-50. doi: 10.1007/s12288-015-0508-3. Epub 2015 Jan 25. Indian J Hematol Blood Transfus. 2016. PMID: 27408433 Free PMC article.
Pelger-Huet anomaly is usually autosomal dominant, although it is likely that new mutations are common. ...As these changes were evident in granulocytic leucocytes of the patient as well as her mother, both her sisters and her son, with exception of her brother, the diagno …
Pelger-Huet anomaly is usually autosomal dominant, although it is likely that new mutations are common. ...As these changes were evid …
[Pseudo Pelger-Huet anomaly].
Kurokawa Y, Komiyama A. Kurokawa Y, et al. Ryoikibetsu Shokogun Shirizu. 1998;(21 Pt 2):94-5. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9833440 Review. Japanese. No abstract available.
Understanding and recognizing the Pelger-Huet anomaly.
Colella R, Hollensead SC. Colella R, et al. Am J Clin Pathol. 2012 Mar;137(3):358-66. doi: 10.1309/AJCP3G8MDUXYSCID. Am J Clin Pathol. 2012. PMID: 22338047 Review.
The Pelger-Huet anomaly (PHA) is a recognized morphologic variant affecting all granulocytes but is most evident in polymorphonuclear neutrophils (PMNs). ...
The Pelger-Huet anomaly (PHA) is a recognized morphologic variant affecting all granulocytes but is most evident in polymorphonuclear …
A family with congenital Pelger-Huet anomaly.
Mitsuhashi K, Hatanaka S, Hoshino S. Mitsuhashi K, et al. Int J Hematol. 2019 Jun;109(6):631-632. doi: 10.1007/s12185-019-02654-6. Epub 2019 Apr 30. Int J Hematol. 2019. PMID: 31041635 No abstract available.
3,101 results