Similar articles for PMID: 20721470

Year	Number of Results
1986	1
1994	12
1995	10
1996	10
1997	8
1998	9
1999	3
2000	14
2001	13
2002	7
2003	5
2004	8
2005	4
2006	8
2007	10
2008	17
2009	9
2010	9
2011	7
2012	4
2013	7
2014	13
2015	7
2016	8
2017	4
2018	9
2019	15
2020	15
2021	21
2022	12
2023	3
2024	0

1

Mutations of Bruton's tyrosine kinase gene in Brazilian patients with X-linked agammaglobulinemia.

Ramalho VD, Oliveira Júnior EB, Tani SM, Roxo Júnior P, Vilela MM. Ramalho VD, et al. Braz J Med Biol Res. 2010 Sep;43(9):910-3. doi: 10.1590/s0100-879x2010007500079. Epub 2010 Aug 16. Braz J Med Biol Res. 2010. PMID: 20721470 Free article.

2

Identification of mutations of Bruton's tyrosine kinase gene (BTK) in Brazilian patients with X-linked agammaglobulinemia.

Tani SM, Wang Y, Kanegane H, Futatani T, Pinto J, Vilela MM, Miyawaki T. Tani SM, et al. Hum Mutat. 2002 Sep;20(3):235-6. doi: 10.1002/humu.9060. Hum Mutat. 2002. PMID: 12204007

3

Clinical characteristics and prenatal diagnosis for 22 families in Henan Province of China with X-linked agammaglobulinemia (XLA) related to Bruton's tyrosine kinase (BTK) gene mutations.

Gao S, Hu S, Duan H, Wang L, Kong X. Gao S, et al. BMC Med Genet. 2020 Jun 17;21(1):131. doi: 10.1186/s12881-020-01063-5. BMC Med Genet. 2020. PMID: 32552675 Free PMC article.

4

Identification of novel Bruton's tyrosine kinase mutations in 10 unrelated subjects with X linked agammaglobulinaemia.

Brooimans RA, van den Berg AJ, Rijkers GT, Sanders LA, van Amstel JK, Tilanus MG, Grubben MJ, Zegers BJ. Brooimans RA, et al. J Med Genet. 1997 Jun;34(6):484-8. doi: 10.1136/jmg.34.6.484. J Med Genet. 1997. PMID: 9192269 Free PMC article.

5

Mutation screening of the BTK gene in 56 families with X-linked agammaglobulinemia (XLA): 47 unique mutations without correlation to clinical course.

Holinski-Feder E, Weiss M, Brandau O, Jedele KB, Nore B, Bäckesjö CM, Vihinen M, Hubbard SR, Belohradsky BH, Smith CI, Meindl A. Holinski-Feder E, et al. Pediatrics. 1998 Feb;101(2):276-84. doi: 10.1542/peds.101.2.276. Pediatrics. 1998. PMID: 9445504

6

Molecular and structural characterization of five novel mutations in the Bruton's tyrosine kinase gene from patients with X-linked agammaglobulinemia.

Saha BK, Curtis SK, Vogler LB, Vihinen M. Saha BK, et al. Mol Med. 1997 Jul;3(7):477-85. Mol Med. 1997. PMID: 9260159 Free PMC article.

7

Identification of Bruton's tyrosine kinase (Btk) gene mutations and characterization of the derived proteins in 35 X-linked agammaglobulinemia families: a nationwide study of Btk deficiency in Japan.

Hashimoto S, Tsukada S, Matsushita M, Miyawaki T, Niida Y, Yachie A, Kobayashi S, Iwata T, Hayakawa H, Matsuoka H, Tsuge I, Yamadori T, Kunikata T, Arai S, Yoshizaki K, Taniguchi N, Kishimoto T. Hashimoto S, et al. Blood. 1996 Jul 15;88(2):561-73. Blood. 1996. PMID: 8695804 Free article.

8

BTK: 22 novel and 25 recurrent mutations in European patients with X-linked agammaglobulinemia.

Fiorini M, Franceschini R, Soresina A, Schumacher RF, Ugazio AG, Rossi P, Plebani A, Notarangelo LD. Fiorini M, et al. Hum Mutat. 2004 Mar;23(3):286. doi: 10.1002/humu.9219. Hum Mutat. 2004. PMID: 14974089

9

[Detection of Bruton's tyrosine kinase gene mutations and clinical analysis of 6 patients with X-linked agammaglobulinemia].

Zhang X, Li H, Li Q, Gao J, Shi X. Zhang X, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Feb;31(1):29-33. doi: 10.3760/cma.j.issn.1003-9406.2014.01.007. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 24510558 Chinese.

10

X-chromosome inactivation and mutation pattern in the Bruton's tyrosine kinase gene in patients with X-linked agammaglobulinemia. Italian XLA Collaborative Group.

Moschese V, Orlandi P, Plebani A, Arvanitidis K, Fiorini M, Speletas M, Mella P, Ritis K, Sideras P, Finocchi A, Livadiotti S, Rossi P. Moschese V, et al. Mol Med. 2000 Feb;6(2):104-13. Mol Med. 2000. PMID: 10859027 Free PMC article.

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