145 related articles for article (PubMed ID: 36776076)
1. The First Report of Iranian Registry of Patients with Spinal Muscular Atrophy.
Mansouri V; Heidari M; Bemanalizadeh M; Azizimalamiri R; Nafissi S; Akbari MG; Barzegar M; Moayedi AR; Badv RS; Mohamadi M; Tavasoli AR; Amirsalari S; Khajeh A; Inaloo S; Fatehi F; Hosseinpour S; Babaei M; Hosseini SA; Mahdi Hosseiny SM; Fayyazi A; Hosseini F; Toosi MB; Khosroshahi N; Ghabeli H; Biglari HN; Kakhki SK; Mirlohi SH; Bidabadi E; Mohammadi B; Omrani A; Sedighi M; Vafaee-Shahi M; Rasulinezhad M; Hoseini SM; Movahedinia M; Rezaei Z; Karimi P; Farshadmoghadam H; Anvari S; Yaghini O; Nasiri J; Zamani G; Ashrafi MR
J Neuromuscul Dis; 2023; 10(2):211-225. PubMed ID: 36776076
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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. PubMed ID: 26665550
[TBL] [Abstract][Full Text] [Related]
6. One Year of Newborn Screening for SMA - Results of a German Pilot Project.
Vill K; Kölbel H; Schwartz O; Blaschek A; Olgemöller B; Harms E; Burggraf S; Röschinger W; Durner J; Gläser D; Nennstiel U; Wirth B; Schara U; Jensen B; Becker M; Hohenfellner K; Müller-Felber W
J Neuromuscul Dis; 2019; 6(4):503-515. PubMed ID: 31594245
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Observation of the natural course of type 3 spinal muscular atrophy: data from the polish registry of spinal muscular atrophy.
Lusakowska A; Jedrzejowska M; Kaminska A; Janiszewska K; Grochowski P; Zimowski J; Sierdzinski J; Kostera-Pruszczyk A
Orphanet J Rare Dis; 2021 Mar; 16(1):150. PubMed ID: 33761963
[TBL] [Abstract][Full Text] [Related]
9. Comprehensive Mutation Analysis and Report of 12 Novel Mutations in a Cohort of Patients with Spinal Muscular Atrophy in Iran.
Sharifi Z; Taheri M; Fallah MS; Abiri M; Golnabi F; Bagherian H; Zeinali R; Farahzadi H; Alborji M; Tehrani PG; Amini M; Asnavandi S; Hashemi M; Forouzesh F; Zeinali S
J Mol Neurosci; 2021 Nov; 71(11):2281-2298. PubMed ID: 33481221
[TBL] [Abstract][Full Text] [Related]
10. 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. PubMed ID: 26548498
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Genotype-phenotype correlation of SMN locus genes in spinal muscular atrophy children from Argentina.
Medrano S; Monges S; Gravina LP; Alías L; Mozzoni J; Aráoz HV; Bernal S; Moresco A; Chertkoff L; Tizzano E
Eur J Paediatr Neurol; 2016 Nov; 20(6):910-917. PubMed ID: 27510309
[TBL] [Abstract][Full Text] [Related]
13. RegistrAME: the Spanish self-reported patient registry of spinal muscular atrophy.
Cattinari MG; de Lemus M; Tizzano E
Orphanet J Rare Dis; 2024 Feb; 19(1):76. PubMed ID: 38373977
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. 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; 12():96. PubMed ID: 21762474
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. 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]
19. Simultaneous quantification of SMN1 and SMN2 copy numbers by MALDI-TOF mass spectrometry for spinal muscular atrophy genetic testing.
Jin W; Yang Z; Tang X; Wang X; Huang Y; Hui C; Yao J; Luan J; Tang S; Wu S; Jin S; Ding C
Clin Chim Acta; 2022 Jul; 532():45-52. PubMed ID: 35643151
[TBL] [Abstract][Full Text] [Related]
20. [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. PubMed ID: 19134255
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]