154 related articles for article (PubMed ID: 38388850)
1. NAIP Gene Deletion and SMN2 Copy Number as Molecular Tools in Predicting the Severity of Spinal Muscular Atrophy.
Abd El Mutaleb ANH; Ibrahim FAR; Megahed FAK; Atta A; Ali BA; Omar TEI; Rashad MM
Biochem Genet; 2024 Feb; ():. PubMed ID: 38388850
[TBL] [Abstract][Full Text] [Related]
2. 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. PubMed ID: 18842367
[TBL] [Abstract][Full Text] [Related]
3. The analysis of the association between the copy numbers of survival motor neuron gene 2 and neuronal apoptosis inhibitory protein genes and the clinical phenotypes in 40 patients with spinal muscular atrophy: Observational study.
Zhang Y; He J; Zhang Y; Li L; Tang X; Wang L; Guo J; Jin C; Tighe S; Zhang Y; Zhu Y; Zhu B
Medicine (Baltimore); 2020 Jan; 99(3):e18809. PubMed ID: 32011487
[TBL] [Abstract][Full Text] [Related]
4. 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 Singap; 2007 Nov; 36(11):937-41. PubMed ID: 18071605
[TBL] [Abstract][Full Text] [Related]
5. 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. PubMed ID: 16936383
[TBL] [Abstract][Full Text] [Related]
6. 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. PubMed ID: 14578966
[TBL] [Abstract][Full Text] [Related]
7. [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. PubMed ID: 24711022
[TBL] [Abstract][Full Text] [Related]
8. [Molecular Features of SMA-related Genes in Spinal Muscular Atrophy Patients of Han Nationality in Southwest China.].
Wang MJ; Wang J; Bai MG; Zhou WJ; Wu LJ; Tang SS; Lu XJ; Ying BW
Sichuan Da Xue Xue Bao Yi Xue Ban; 2016 Nov; 47(6):936-940. PubMed ID: 28598128
[TBL] [Abstract][Full Text] [Related]
9. A comprehensive overview of SMN and NAIP copy numbers in Iranian SMA patients.
Savad S; Ashrafi MR; Samadaian N; Heidari M; Modarressi MH; Zamani G; Amidi S; Younesi S; Amin MMT; Saadati P; Ronagh A; Ardakani HS; Eslami S; Ghafouri-Fard S
Sci Rep; 2023 Feb; 13(1):3202. PubMed ID: 36828874
[TBL] [Abstract][Full Text] [Related]
10. 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. PubMed ID: 18533950
[TBL] [Abstract][Full Text] [Related]
11. 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; 518(2):325-9. PubMed ID: 23352792
[TBL] [Abstract][Full Text] [Related]
12. Clinical and Genetic Study of Algerian Patients with Spinal Muscular Atrophy.
Sifi Y; Sifi K; Boulefkhad A; Abadi N; Bouderda Z; Cheriet R; Magen M; Bonnefont JP; Munnich A; Benlatreche C; Hamri A
J Neurodegener Dis; 2013; 2013():903875. PubMed ID: 26317002
[TBL] [Abstract][Full Text] [Related]
13. 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. PubMed ID: 19198020
[TBL] [Abstract][Full Text] [Related]
14. 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; 16(1):11. PubMed ID: 25888055
[TBL] [Abstract][Full Text] [Related]
15. 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 Nov; 225(3):153-9. PubMed ID: 21971302
[TBL] [Abstract][Full Text] [Related]
16. Genotype-phenotype correlation of survival motor neuron and neuronal apoptosis inhibitory protein genes in spinal muscular atrophy patients from Iran.
Sedghi M; Behnam M; Fazel E; Salehi M; Ganji H; Meamar R; Hosseinzadeh M; Nouri N
Adv Biomed Res; 2014; 3():74. PubMed ID: 24627882
[TBL] [Abstract][Full Text] [Related]
17. 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. PubMed ID: 17250498
[TBL] [Abstract][Full Text] [Related]
18. Deletion analysis of SMN and NAIP genes in Tunisian patients with spinal muscular atrophy.
Rekik I; Boukhris A; Ketata S; Amri M; Essid N; Feki I; Mhiri C
Ann Indian Acad Neurol; 2013 Jan; 16(1):57-61. PubMed ID: 23661964
[TBL] [Abstract][Full Text] [Related]
19. Molecular analysis of the SMN and NAIP genes in Iranian spinal muscular atrophy patients.
Omrani O; Bonyadi M; Barzgar M
Pediatr Int; 2009 Apr; 51(2):193-6. PubMed ID: 19405914
[TBL] [Abstract][Full Text] [Related]
20. Intragenic and structural variation in the
Wadman RI; Jansen MD; Stam M; Wijngaarde CA; Curial CAD; Medic J; Sodaar P; Schouten J; Vijzelaar R; Lemmink HH; van den Berg LH; Groen EJN; van der Pol WL
Brain Commun; 2020; 2(2):fcaa075. PubMed ID: 32954327
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
