353 related articles for article (PubMed ID: 14578966)
1. 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]
2. [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]
3. 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. PubMed ID: 9439064
[TBL] [Abstract][Full Text] [Related]
4. Correlation of SMNt and SMNc gene copy number with age of onset and survival in spinal muscular atrophy.
Taylor JE; Thomas NH; Lewis CM; Abbs SJ; Rodrigues NR; Davies KE; Mathew CG
Eur J Hum Genet; 1998; 6(5):467-74. PubMed ID: 9801871
[TBL] [Abstract][Full Text] [Related]
5. [Detection of SMN gene deletions in spinal muscular atrophy].
Yang T; Yuan L; Liu T; Zhou W; Wu H; Zhao S; Shun L; Huo L; Ma S; Lin Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Apr; 15(2):95-7. PubMed ID: 9531649
[TBL] [Abstract][Full Text] [Related]
6. An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA).
Wirth B
Hum Mutat; 2000; 15(3):228-37. PubMed ID: 10679938
[TBL] [Abstract][Full Text] [Related]
7. Clinical application of the molecular diagnosis of spinal muscular atrophy: deletions of neuronal apoptosis inhibitor protein and survival motor neuron genes.
Somerville MJ; Hunter AG; Aubry HL; Korneluk RG; MacKenzie AE; Surh LC
Am J Med Genet; 1997 Mar; 69(2):159-65. PubMed ID: 9056553
[TBL] [Abstract][Full Text] [Related]
8. [Molecular basis of spinal muscular atrophy: th SMN gene].
Tizzano E; Baiget M
Neurologia; 2000 Nov; 15(9):393-400. PubMed ID: 11195146
[TBL] [Abstract][Full Text] [Related]
9. Deletion analysis of Bulgarian SMA families.
Jordanova A; Stoyanova V; Uzunova M; Litvinenko I; Kremensky I
Hum Mutat; 1998; 12(1):33-8. PubMed ID: 9633817
[TBL] [Abstract][Full Text] [Related]
10. Spinal muscular atrophy due to an isolated deletion of exon 8 of the telomeric survival motor neuron gene.
Gambardella A; Mazzei R; Toscano A; Annesi G; Pasqua A; Annesi F; Quattrone F; Oliveri RL; Valentino P; Bono F; Aguglia U; Zappia M; Vita G; Quattrone A
Ann Neurol; 1998 Nov; 44(5):836-9. PubMed ID: 9818944
[TBL] [Abstract][Full Text] [Related]
11. [Molecular genetic diagnosis and deletion analysis in Type I-III spinal muscular atrophy].
Spiegel R; Hagmann A; Boltshauser E; Moser H
Schweiz Med Wochenschr; 1996 May; 126(21):907-14. PubMed ID: 8693311
[TBL] [Abstract][Full Text] [Related]
12. [A study of survival motor neuron and neuronal apoptosis inhibitory protein gene in spinal muscular atrophy].
Zhang L; Yang X; Xiao B
Zhonghua Nei Ke Za Zhi; 2001 Jun; 40(6):401-4. PubMed ID: 11798607
[TBL] [Abstract][Full Text] [Related]
13. Sequence of a 131-kb region of 5q13.1 containing the spinal muscular atrophy candidate genes SMN and NAIP.
Chen Q; Baird SD; Mahadevan M; Besner-Johnston A; Farahani R; Xuan J; Kang X; Lefebvre C; Ikeda JE; Korneluk RG; MacKenzie AE
Genomics; 1998 Feb; 48(1):121-7. PubMed ID: 9503025
[TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis of spinal muscular atrophy in Turkish families.
Erdem H; Dayangaç D; Pehlivan S; Topaloglu H
Cent Eur J Public Health; 2001 Feb; 9(1):35-7. PubMed ID: 11243588
[TBL] [Abstract][Full Text] [Related]
15. Gene deletion patterns in spinal muscular atrophy patients with different clinical phenotypes.
Haider MZ; Moosa A; Dalal H; Habib Y; Reynold L
J Biomed Sci; 2001; 8(2):191-6. PubMed ID: 11287750
[TBL] [Abstract][Full Text] [Related]
16. Molecular analysis of the SMN and NAIP genes in Saudi spinal muscular atrophy patients.
Al Rajeh S; Majumdar R; Awada A; Adeyokunnu A; Al Jumah M; Al Bunyan M; Snellen A
J Neurol Sci; 1998 Jun; 158(1):43-6. PubMed ID: 9667776
[TBL] [Abstract][Full Text] [Related]
17. SMA type 2 unrelated to chromosome 5q13.
Nevo Y; Kramer U; Legum C; Shomrat R; Fatal A; Soffer D; Harel S; Shapira Y
Am J Med Genet; 1998 Jan; 75(2):193-5. PubMed ID: 9450884
[TBL] [Abstract][Full Text] [Related]
18. SMN oligomerization defect correlates with spinal muscular atrophy severity.
Lorson CL; Strasswimmer J; Yao JM; Baleja JD; Hahnen E; Wirth B; Le T; Burghes AH; Androphy EJ
Nat Genet; 1998 May; 19(1):63-6. PubMed ID: 9590291
[TBL] [Abstract][Full Text] [Related]
19. Screening of deletions in SMN, NAIP and BTF2p44 genes in Turkish spinal muscular atrophy patients.
Savas S; Gokgoz N; Kayserili H; Ozkinay F; Yuksel-Apak M; Kirdar B
Hum Hered; 2000; 50(3):162-5. PubMed ID: 10686493
[TBL] [Abstract][Full Text] [Related]
20. Spinal Muscular Atrophies: An Ongoing Diagnostic Dilemma?
Biros I; Forshaw K; Sheffield LJ; Kornberg AJ; Forrest S
Mol Diagn; 1997 Dec; 2(4):241-249. PubMed ID: 10462616
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]