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Items: 1 to 20 of 180

1.

[Analysis and carrier screening for copy numbers of SMN and NAIP genes in children with spinal muscular atrophy].

Zeng G, Zheng H, Cheng J, Chen R, Lin H, Yang J, Zhang D.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Apr;31(2):152-5. doi: 10.3760/cma.j.issn.1003-9406.2014.02.006. Chinese.

PMID:
24711022
2.

Correlation of SMN2, NAIP, p44, H4F5 and Occludin genes copy number with spinal muscular atrophy phenotype in Tunisian patients.

Amara A, Adala L, Ben Charfeddine I, Mamaï O, Mili A, Lazreg TB, H'mida D, Amri F, Salem N, Boughammura L, Saad A, Gribaa M.

Eur J Paediatr Neurol. 2012 Mar;16(2):167-74. doi: 10.1016/j.ejpn.2011.07.007.

PMID:
21821450
3.

Molecular analysis of SMN1, SMN2, NAIP, GTF2H2, and H4F5 genes in 157 Chinese patients with spinal muscular atrophy.

He J, Zhang QJ, Lin QF, Chen YF, Lin XZ, Lin MT, Murong SX, Wang N, Chen WJ.

Gene. 2013 Apr 15;518(2):325-9. doi: 10.1016/j.gene.2012.12.109.

PMID:
23352792
4.

Deletion analysis of SMN1 and NAIP genes in Southern Chinese children with spinal muscular atrophy.

Liang YH, Chen XL, Yu ZS, Chen CY, Bi S, Mao LG, Zhou BL, Zhang XN.

J Zhejiang Univ Sci B. 2009 Jan;10(1):29-34. doi: 10.1631/jzus.B0820125.

5.

Combination of SMN2 copy number and NAIP deletion predicts disease severity in spinal muscular atrophy.

Watihayati MS, Fatemeh H, Marini M, Atif AB, Zahiruddin WM, Sasongko TH, Tang TH, Zabidi-Hussin ZA, Nishio H, Zilfalil BA.

Brain Dev. 2009 Jan;31(1):42-5. doi: 10.1016/j.braindev.2008.08.012.

PMID:
18842367
6.

Molecular analysis of the SMN1 and NAIP genes in Iranian patients with spinal muscular atrophy.

Derakhshandeh-Peykar P, Esmaili M, Ousati-Ashtiani Z, Rahmani M, Babrzadeh F, Farshidi S, Attaran E, Sajedifar MM, Farhud DD.

Ann Acad Med Singapore. 2007 Nov;36(11):937-41.

7.

Molecular characterization and copy number of SMN1, SMN2 and NAIP in Chinese patients with spinal muscular atrophy and unrelated healthy controls.

Fang P, Li L, Zeng J, Zhou WJ, Wu WQ, Zhong ZY, Yan TZ, Xie JS, Huang J, Lin L, Zhao Y, Xu XM.

BMC Musculoskelet Disord. 2015 Feb 7;16:11. doi: 10.1186/s12891-015-0457-x.

8.

[Molecular analysis of survival motor neuron gene in 338 suspicious children patients with spinal muscular atrophy].

Song F, Qu YJ, Zou LP, Wang LW, Long MJ, Wang X, Yang YL, Chen Q, Wang H, Jin YW.

Zhonghua Er Ke Za Zhi. 2008 Dec;46(12):919-23. Chinese.

PMID:
19134255
9.

Correlation between deletion patterns of SMN and NAIP genes and the clinical features of spinal muscular atrophy in Indian patients.

Dastur RS, Gaitonde PS, Khadilkar SV, Udani VP, Nadkarni JJ.

Neurol India. 2006 Sep;54(3):255-9.

10.

[Quantitative analysis of SMN1 and SMN2 genes based on DHPLC: a reliable method for detection of non-homozygous patients with spinal muscular atrophy].

Long MJ, Song F, Qu YJ, Meng Y, Wang H, Jin YW, Huang SZ.

Zhonghua Yi Xue Za Zhi. 2008 May 13;88(18):1259-63. Chinese.

PMID:
18844099
11.

Deletion analyses of SMN1 and NAIP genes in Malaysian spinal muscular atrophy patients.

Watihayati MS, Zabidi-Hussin AM, Tang TH, Matsuo M, Nishio H, Zilfalil BA.

Pediatr Int. 2007 Feb;49(1):11-4. Erratum in: Pediatr Int. 2007 Apr;49(2):303. Zilfalil, Bin Alwi [added].

PMID:
17250498
12.

Association between the SMN2 gene copy number and clinical characteristics of patients with spinal muscular atrophy with homozygous deletion of exon 7 of the SMN1 gene.

Zarkov M, Stojadinović A, Sekulić S, Barjaktarović I, Perić S, Keković G, Drasković B, Stević Z.

Vojnosanit Pregl. 2015 Oct;72(10):859-63.

PMID:
26665550
13.

[Quantitative analysis of the genes determining spinal muscular atrophy].

Nagymihály M, Herczegfalvi A, Tímár L, Karcagi V.

Ideggyogy Sz. 2009 Nov 30;62(11-12):390-7. Hungarian.

PMID:
20025129
14.

Lower incidence of deletions in the survival of motor neuron gene and the neuronal apoptosis inhibitory protein gene in children with spinal muscular atrophy from Serbia.

Miskovic M, Lalic T, Radivojevic D, Cirkovic S, Vlahovic G, Zamurovic D, Guc-Scekic M.

Tohoku J Exp Med. 2011;225(3):153-9.

15.

Spinal muscular atrophy type III: Molecular genetic characterization of Turkish patients.

Bora-Tatar G, Yesbek-Kaymaz A, Bekircan-Kurt CE, Erdem-Özdamar S, Erdem-Yurter H.

Eur J Med Genet. 2015 Dec;58(12):654-8. doi: 10.1016/j.ejmg.2015.11.002.

PMID:
26548498
16.

Deletions in the SMN and NAIP genes in patients with spinal muscular atrophy in Croatia.

Sertić J, Barisić N, Sostarko M, Bosnjak N, Culić V, Cvitanović L, Ferencak G, Brzović Z, Stavljenić-Rukavina A.

Coll Antropol. 1997 Dec;21(2):487-92.

PMID:
9439064
17.

Genetic and expression studies of SMN2 gene in Russian patients with spinal muscular atrophy type II and III.

Zheleznyakova GY, Kiselev AV, Vakharlovsky VG, Rask-Andersen M, Chavan R, Egorova AA, Schiöth HB, Baranov VS.

BMC Med Genet. 2011 Jul 15;12:96. doi: 10.1186/1471-2350-12-96.

18.

Molecular analysis of the spinal muscular atrophy and neuronal apoptosis inhibitory protein genes in Saudi patients with spinal muscular atrophy.

Al-Jumah M, Majumdar R, Al-Rajeh S, Awada A, Chaves-Carbello E, Salih M, Al-Shahwan S, Al-Subiey K, Al-Uthaim S.

Saudi Med J. 2003 Oct;24(10):1052-4.

PMID:
14578966
19.

SMN2 and NAIP gene dosages in Vietnamese patients with spinal muscular atrophy.

Tran VK, Sasongko TH, Hong DD, Hoan NT, Dung VC, Lee MJ, Gunadi, Takeshima Y, Matsuo M, Nishio H.

Pediatr Int. 2008 Jun;50(3):346-51. doi: 10.1111/j.1442-200X.2008.02590.x.

PMID:
18533950
20.

Molecular analysis of SMN, NAIP and P44 genes of SMA patients and their families.

Tsai CH, Jong YJ, Hu CJ, Chen CM, Shih MC, Chang CP, Chang JG.

J Neurol Sci. 2001 Sep 15;190(1-2):35-40.

PMID:
11574104
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