181 related articles for article (PubMed ID: 22921322)
1. Molecular prenatal diagnosis of autosomal recessive childhood spinal muscular atrophies (SMAs).
Essawi ML; Al-Attribi GM; Gaber KR; El-Harouni AA
Gene; 2012 Nov; 509(1):120-3. PubMed ID: 22921322
[TBL] [Abstract][Full Text] [Related]
2. Prenatal prediction of childhood-onset spinal muscular atrophy (SMA) in Turkish families.
Savas S; Eraslan S; Kantarci S; Karaman B; Acarsoz D; Tükel T; Cogulu O; Ozkinay F; Basaran S; Aydinli K; Yuksel-Apak M; Kirdar B
Prenat Diagn; 2002 Aug; 22(8):703-9. PubMed ID: 12210580
[TBL] [Abstract][Full Text] [Related]
3. [Gene diagnosis for spinal muscular atrophy and its application study].
Cao DH; Ren MH; Lin CK; Cui WT; Ma HW; Wu YY; Jin CL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):306-9. PubMed ID: 19504445
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Molecular analysis of SMN1 and NAIP genes in Egyptian patients with spinal muscular atrophy.
Essawi ML; Effat LK; Shanab GM; Al-Ettribi GM; El-Haronui AA; Karim AM
Bratisl Lek Listy; 2007; 108(3):133-7. PubMed ID: 17682539
[TBL] [Abstract][Full Text] [Related]
7. [Quantitative analysis of the genes determining spinal muscular atrophy].
Nagymihály M; Herczegfalvi A; Tímár L; Karcagi V
Ideggyogy Sz; 2009 Nov; 62(11-12):390-7. PubMed ID: 20025129
[TBL] [Abstract][Full Text] [Related]
8. Isolated exon 8 deletion in type 1 spinal muscular atrophy with bilateral optic atrophy: unusual genetic mutation leading to unusual manifestation?
Maiti D; Bhattacharya M; Yadav S
J Postgrad Med; 2012; 58(4):294-5. PubMed ID: 23298926
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Rapid diagnosis of spinal muscular atrophy using tetra-primer ARMS PCR assay: simultaneous detection of SMN1 and SMN2 deletion.
Baris I; Etlik O; Koksal V; Arican-Baris ST
Mol Cell Probes; 2010 Jun; 24(3):138-41. PubMed ID: 20025960
[TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of spinal muscular atrophy in Chinese by genetic analysis of fetal cells.
Wu T; Ding XS; Li WL; Yao J; Deng XX
Chin Med J (Engl); 2005 Aug; 118(15):1274-7. PubMed ID: 16117881
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis of spinal muscular atrophy in Macedonian families.
Kocheva SA; Plaseska-Karanfilska D; Trivodalieva S; Kuturec M; Vlaski-Jekic S; Efremov GD
Genet Test; 2008 Sep; 12(3):391-3. PubMed ID: 18752447
[TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis for risk of spinal muscular atrophy.
Cuscó I; Barceló MJ; Soler C; Parra J; Baiget M; Tizzano E
BJOG; 2002 Nov; 109(11):1244-9. PubMed ID: 12452462
[TBL] [Abstract][Full Text] [Related]
14. Molecular analysis of the SMN1 and NAIP genes in 60 Tunisian spinal muscular atrophy patients.
Mrad R; Dorboz I; Ben Jemaa L; Maazoul F; Trabelsi M; Chaabouni M; Mlaiki B; Miladi N; Hentati F; Chaabouni H
Tunis Med; 2006 Aug; 84(8):465-9. PubMed ID: 17175684
[TBL] [Abstract][Full Text] [Related]
15. [Prenatal diagnosis of spinal muscular atrophy (SMA) -- indications, restrictions, interpretation of results].
Jedrzejowska M; Zimowski J; Wiszniewski W; Sielska D; Bal J; Mazurczak T; Hausmanowa-Petrusewicz I; Zaremba J
Med Wieku Rozwoj; 2004; 8(3 Pt 2):651-61. PubMed ID: 15858238
[TBL] [Abstract][Full Text] [Related]
16. [Analysis of deletional damage in SMN1, SMN2, and NAIP genes in patients with spinal muscular atrophy in the northwestern region of Russia].
Glotov AS; Kiselev AV; Ivashchenko TE; Baranov VS
Genetika; 2001 Aug; 37(8):1156-9. PubMed ID: 11642117
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. [Molecular diagnosis of spinal muscular atrophy by multiplex ligation-dependent probe amplification].
Zeng J; Ke LF; Deng XJ; Cai MY; Tu XD; Lan FH
Zhonghua Yi Xue Za Zhi; 2008 Dec; 88(46):3262-4. PubMed ID: 19159550
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of Werdnig-Hoffmann disease in China.
Feng J; Toshiyuki Y
Chin Med J (Engl); 2003 May; 116(5):673-5. PubMed ID: 12875676
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
