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1983
2025

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

Year Number of Results
1983 2
1988 1
1991 3
1992 2
1993 3
1994 2
1995 3
1996 7
1997 7
1998 3
1999 2
2000 3
2001 7
2002 9
2003 10
2004 4
2005 3
2006 8
2007 14
2008 5
2009 5
2010 8
2011 9
2012 9
2013 17
2014 7
2015 9
2016 7
2017 12
2018 6
2019 9
2020 7
2021 8
2022 5
2023 8
2024 6
2025 1

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201 results

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Page 1
Severe congenital neutropenias.
Skokowa J, Dale DC, Touw IP, Zeidler C, Welte K. Skokowa J, et al. Nat Rev Dis Primers. 2017 Jun 8;3:17032. doi: 10.1038/nrdp.2017.32. Nat Rev Dis Primers. 2017. PMID: 28593997 Free PMC article. Review.
Severe congenital neutropenias are a heterogeneous group of rare haematological diseases characterized by impaired maturation of neutrophil granulocytes. Patients with severe congenital neutropenia are prone to recurrent, often life-threa
Severe congenital neutropenias are a heterogeneous group of rare haematological diseases characterized by impaired matu
Congenital neutropenia and primary immunodeficiency diseases.
Spoor J, Farajifard H, Rezaei N. Spoor J, et al. Crit Rev Oncol Hematol. 2019 Jan;133:149-162. doi: 10.1016/j.critrevonc.2018.10.003. Epub 2018 Oct 13. Crit Rev Oncol Hematol. 2019. PMID: 30661651 Review.
Apart from these isolated forms, congenital neutropenia is associated with a multiplicity of syndromic diseases that includes among others: oculocutaneous albinism, metabolic diseases and bone marrow failure syndromes. Congenital neutropenia is a prima …
Apart from these isolated forms, congenital neutropenia is associated with a multiplicity of syndromic diseases that includes …
Neutropenia: etiology and pathogenesis.
Schwartzberg LS. Schwartzberg LS. Clin Cornerstone. 2006;8 Suppl 5:S5-11. doi: 10.1016/s1098-3597(06)80053-0. Clin Cornerstone. 2006. PMID: 17379162 Review.
Neutropenia is defined as an absolute neutrophil count <1500 cells/mm(3) and can be graded as mild (1000-1500 cells/mm(3)), moderate (500-1000 cells/mm(3)), or severe (<500 cells/mm(3)). ...This risk is directly proportional to the severity and duration
Neutropenia is defined as an absolute neutrophil count <1500 cells/mm(3) and can be graded as mild (1000-1500 cells/mm(3)), modera
How I manage children with neutropenia.
Dale DC. Dale DC. Br J Haematol. 2017 Aug;178(3):351-363. doi: 10.1111/bjh.14677. Epub 2017 Apr 17. Br J Haematol. 2017. PMID: 28419427 Free article. Review.
At birth and for the first few months of life, neutropenia is often attributable to isoimmune or alloimmune mechanisms and predisposes to the risk of severe bacterial infections. ...The congenital neutropenia syndromes are usually recognized when there …
At birth and for the first few months of life, neutropenia is often attributable to isoimmune or alloimmune mechanisms and predispose …
WHIM Syndrome: from Pathogenesis Towards Personalized Medicine and Cure.
Heusinkveld LE, Majumdar S, Gao JL, McDermott DH, Murphy PM. Heusinkveld LE, et al. J Clin Immunol. 2019 Aug;39(6):532-556. doi: 10.1007/s10875-019-00665-w. Epub 2019 Jul 16. J Clin Immunol. 2019. PMID: 31313072 Free PMC article. Review.
Myelokathexis is a unique form of non-cyclic severe congenital neutropenia caused by accumulation of mature and degenerating neutrophils in the bone marrow; monocytopenia and lymphopenia, especially B lymphopenia, also commonly occur. ...
Myelokathexis is a unique form of non-cyclic severe congenital neutropenia caused by accumulation of mature and degener …
Diagnostic guidance for hereditary neutropenia in children: Narrative literature review.
Kasmi Z, El Bakkouri J, Ailal F, Oukkache B, Donadieu J, Bousfiha AA. Kasmi Z, et al. Tunis Med. 2023 Jul 5;101(7):591-596. Tunis Med. 2023. PMID: 38445418 Free PMC article. Review. French.
The thirty responsible genes now explain 60% of congenital neutropenia. These are rare since they are only found in 1 of all congenital neutropenia, estimated at 1% of the population. ...The objective of this narrative literature review is to provide a …
The thirty responsible genes now explain 60% of congenital neutropenia. These are rare since they are only found in 1 of all …
Dapagliflozin and Empagliflozin in Paediatric Indications: A Systematic Review.
Lava SAG, Laurence C, Di Deo A, Sekarski N, Burch M, Della Pasqua O. Lava SAG, et al. Paediatr Drugs. 2024 May;26(3):229-243. doi: 10.1007/s40272-024-00623-z. Epub 2024 Apr 18. Paediatr Drugs. 2024. PMID: 38635113
RESULTS: Thirty-five articles (nine case reports, ten case series, one prospective non-controlled trial, four controlled randomised trials, two surveys, six pharmacokinetic studies, and three pharmacovigilance studies) were selected, in which 415 children were exposed to either d …
RESULTS: Thirty-five articles (nine case reports, ten case series, one prospective non-controlled trial, four controlled randomised trials, …
Congenital neutropenia.
Ancliff PJ. Ancliff PJ. Blood Rev. 2003 Dec;17(4):209-16. doi: 10.1016/s0268-960x(03)00019-5. Blood Rev. 2003. PMID: 14556775 Review.
Congenital neutropenia is strictly defined as neutropenia present at birth. However, it is more generally used to describe neutropenia secondary to inherited genetic mutations. This review will discuss the presentation of such children and the various
Congenital neutropenia is strictly defined as neutropenia present at birth. However, it is more generally used to descr
Severe congenital neutropenia.
Welte K, Zeidler C, Dale DC. Welte K, et al. Semin Hematol. 2006 Jul;43(3):189-95. doi: 10.1053/j.seminhematol.2006.04.004. Semin Hematol. 2006. PMID: 16822461 Review.
Severe congenital neutropenia (CN) includes a variety of hematologic disorders characterized by severe neutropenia, with absolute neutrophil counts (ANC) below 0.5 x 10(9)/L, and associated with severe systemic bacterial infections from e
Severe congenital neutropenia (CN) includes a variety of hematologic disorders characterized by severe neutro
Hereditary myeloid malignancies.
Rafei H, DiNardo CD. Rafei H, et al. Best Pract Res Clin Haematol. 2019 Jun;32(2):163-176. doi: 10.1016/j.beha.2019.05.001. Epub 2019 May 3. Best Pract Res Clin Haematol. 2019. PMID: 31203998 Free PMC article. Review.
Genetic predispositions to myeloid malignancies can be classified into three categories: familial cancer syndromes associated with increased risk of various malignancies including myelodysplasia and acute myeloid leukemia such as Li-Fraumeni syndrome and constitutional mismatch r …
Genetic predispositions to myeloid malignancies can be classified into three categories: familial cancer syndromes associated with increased …
201 results