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

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1948 1
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1971 3
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1973 1
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1976 2
1977 1
1978 1
1980 5
1981 4
1982 3
1983 1
1984 1
1985 8
1987 3
1988 2
1989 5
1990 5
1991 4
1992 5
1993 4
1994 5
1995 1
1996 2
1997 3
1998 6
1999 7
2000 7
2001 8
2002 10
2003 12
2004 5
2005 7
2006 4
2007 4
2008 9
2009 14
2010 7
2011 17
2012 15
2013 14
2014 19
2015 15
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365 results

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Page 1
May-Hegglin Anomaly.
Untanu RV, Vajpayee N. Untanu RV, et al. 2023 Jul 17. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. 2023 Jul 17. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. PMID: 28722981 Free Books & Documents.
The May-Hegglin anomaly (MHA) is a rare autosomal dominant disease due to MYH9 gene mutation characterized by neutrophils with abnormal cytoplasmic inclusions, large platelets, and variable thrombocytopenia. ...
The May-Hegglin anomaly (MHA) is a rare autosomal dominant disease due to MYH9 gene mutation characterized by neutrophi …
May-Hegglin Anomaly.
Wang HT, Chiu CF, Bai LY. Wang HT, et al. Am J Med Sci. 2021 Mar;361(3):e23-e24. doi: 10.1016/j.amjms.2020.08.009. Epub 2020 Aug 10. Am J Med Sci. 2021. PMID: 32958165 No abstract available.
Anesthetic considerations for May-Hegglin anomaly.
Koyama Y. Koyama Y. Minerva Anestesiol. 2023 Nov;89(11):1057-1058. doi: 10.23736/S0375-9393.23.17444-X. Epub 2023 Jul 11. Minerva Anestesiol. 2023. PMID: 37432314 Free article. No abstract available.
May-Hegglin anomaly.
Hsia CC, Xenocostas A. Hsia CC, et al. Blood. 2012 Jan 12;119(2):328. doi: 10.1182/blood-2010-12-325431. Blood. 2012. PMID: 22351964 Free article. No abstract available.
May-Hegglin anomaly.
So CC, Wong KF. So CC, et al. Br J Haematol. 2003 Feb;120(3):373. doi: 10.1046/j.1365-2141.2003.03950.x. Br J Haematol. 2003. PMID: 12580949 No abstract available.
May-Hegglin anomaly and pregnancy: a systematic review.
Hussein BA, Gomez K, Kadir RA. Hussein BA, et al. Blood Coagul Fibrinolysis. 2013 Jul;24(5):554-61. doi: 10.1097/MBC.0b013e32835fad03. Blood Coagul Fibrinolysis. 2013. PMID: 23811802
May-Hegglin anomaly (MHA) is an autosomal dominant disorder, characterized by a variable degree of thrombocytopaenia, large platelets and inclusion bodies in white blood cells. ...
May-Hegglin anomaly (MHA) is an autosomal dominant disorder, characterized by a variable degree of thrombocytopaenia, l …
May-Hegglin anomaly associated nephropathy: Case series.
Nguyen MD, Dileep G, Quizon M, Nguyen V, Demerci A, Hanna R. Nguyen MD, et al. SAGE Open Med Case Rep. 2024 Nov 25;12:2050313X241302013. doi: 10.1177/2050313X241302013. eCollection 2024. SAGE Open Med Case Rep. 2024. PMID: 39588168 Free PMC article.
May-Hegglin anomaly (MHA) is a rare autosomal dominant disease associated with a mutation in the MYH-9 gene. ...
May-Hegglin anomaly (MHA) is a rare autosomal dominant disease associated with a mutation in the MYH-9 gene. ...
The May-Hegglin anomaly.
Filanovsky K, Shvidel L, Vorst E, Berrebi A, Shtalrid M. Filanovsky K, et al. Eur J Haematol. 2009 Oct;83(4):390. doi: 10.1111/j.1600-0609.2009.01286.x. Epub 2009 Jun 2. Eur J Haematol. 2009. PMID: 19500132 No abstract available.
May-Hegglin anomaly.
Rosenberg T, Arad E, Pillar T, Gidron E. Rosenberg T, et al. Isr J Med Sci. 1971 Sep;7(9):1073-8. Isr J Med Sci. 1971. PMID: 5151273 No abstract available.
[May-hegglin anomaly].
Lesesve J, Latger-Cannard V, Briquel M, André E, Maistre ED, Lecompte T. Lesesve J, et al. Ann Biol Clin (Paris). 2000 Mar-Apr;58(2):204-7. Ann Biol Clin (Paris). 2000. PMID: 10760708 Free article. French. No abstract available.
365 results