PubMed for id: 284

Year	Number of Results
1965	1
1966	1
1968	1
1969	1
1971	2
1974	1
1975	14
1976	15
1977	22
1978	10
1979	13
1980	19
1981	8
1982	11
1983	8
1984	8
1985	9
1986	6
1987	6
1988	6
1989	5
1990	5
1991	3
1992	4
1993	7
1994	8
1995	16
1996	10
1997	10
1998	7
1999	3
2000	16
2001	10
2002	8
2003	4
2004	6
2005	5
2006	6
2007	8
2008	3
2009	5
2010	5
2011	5
2012	6
2013	8
2014	11
2015	10
2016	12
2017	10
2018	19
2019	17
2020	14
2021	18
2022	17
2023	18
2024	6

1

Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency.

Bianchi P, Fermo E, Glader B, Kanno H, Agarwal A, Barcellini W, Eber S, Hoyer JD, Kuter DJ, Maia TM, Mañu-Pereira MDM, Kalfa TA, Pissard S, Segovia JC, van Beers E, Gallagher PG, Rees DC, van Wijk R; with the endorsement of EuroBloodNet, the European Reference Network in Rare Hematological Diseases. Bianchi P, et al. Am J Hematol. 2019 Jan;94(1):149-161. doi: 10.1002/ajh.25325. Epub 2018 Nov 28. Am J Hematol. 2019. PMID: 30358897 Free PMC article.

2

Rare hereditary nonspherocytic hemolytic anemia caused by a novel homozygous mutation, c.301C > A, (Q101K), in the AK1 gene in an Indian family.

Dongerdiye R, Sampagar A, Devendra R, Warang P, Kedar P. Dongerdiye R, et al. BMC Med Genomics. 2021 Jul 28;14(1):191. doi: 10.1186/s12920-021-01038-2. BMC Med Genomics. 2021. PMID: 34321014 Free PMC article.

3

Congenital Nonspherocytic Hemolytic Anemia Caused by Krüppel-Like Factor 1 Gene Variants: Another Case Report.

Jiang H, Jiang F, Li J, Tang F, Li DZ. Jiang H, et al. Hemoglobin. 2019 Jul-Sep;43(4-5):292-295. doi: 10.1080/03630269.2019.1680384. Epub 2019 Oct 23. Hemoglobin. 2019. PMID: 31645145

4

Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular study.

Manco L, Bento C, Victor BL, Pereira J, Relvas L, Brito RM, Seabra C, Maia TM, Ribeiro ML. Manco L, et al. Blood Cells Mol Dis. 2016 Sep;60:18-23. doi: 10.1016/j.bcmd.2016.06.002. Epub 2016 Jun 11. Blood Cells Mol Dis. 2016. PMID: 27519939

5

Red cell glucose phosphate isomerase (GPI): a molecular study of three novel mutations associated with hereditary nonspherocytic hemolytic anemia.

Repiso A, Oliva B, Vives-Corrons JL, Beutler E, Carreras J, Climent F. Repiso A, et al. Hum Mutat. 2006 Nov;27(11):1159. doi: 10.1002/humu.9466. Hum Mutat. 2006. PMID: 17041899

6

Liver cirrhosis as a consequence of iron overload caused by hereditary nonspherocytic hemolytic anemia.

Hilgard P, Gerken G. Hilgard P, et al. World J Gastroenterol. 2005 Feb 28;11(8):1241-4. doi: 10.3748/wjg.v11.i8.1241. World J Gastroenterol. 2005. PMID: 15754414 Free PMC article.

7

Red cell adenylate kinase deficiency: molecular study of 3 new mutations (118G>A, 190G>A, and GAC deletion) associated with hereditary nonspherocytic hemolytic anemia.

Corrons JL, Garcia E, Tusell JJ, Varughese KI, West C, Beutler E. Corrons JL, et al. Blood. 2003 Jul 1;102(1):353-6. doi: 10.1182/blood-2002-07-2288. Epub 2003 Mar 20. Blood. 2003. PMID: 12649162 Free article.

8

Glucosephosphate isomerase (GPI) deficiency mutations associated with hereditary nonspherocytic hemolytic anemia (HNSHA).

Beutler E, West C, Britton HA, Harris J, Forman L. Beutler E, et al. Blood Cells Mol Dis. 1997 Dec;23(3):402-9. doi: 10.1006/bcmd.1997.0157. Blood Cells Mol Dis. 1997. PMID: 9446754

9

Three cases of hereditary nonspherocytic hemolytic anemia associated with red blood cell glutathione deficiency.

Hirono A, Iyori H, Sekine I, Ueyama J, Chiba H, Kanno H, Fujii H, Miwa S. Hirono A, et al. Blood. 1996 Mar 1;87(5):2071-4. Blood. 1996. PMID: 8634459 Free article. Review.

10

[Glucose phosphate isomerase deficiency with congenital nonspherocytic hemolytic anemia].

Shalev O, Leibowitz G, Brok-Simoni F. Shalev O, et al. Harefuah. 1994 Jun 15;126(12):699-702, 764, 763. Harefuah. 1994. PMID: 7927011 Hebrew.

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