333 related articles for article (PubMed ID: 12654964)
1. Classical infantile spinal muscular atrophy with SMN deficiency causes sensory neuronopathy.
Rudnik-Schöneborn S; Goebel HH; Schlote W; Molaian S; Omran H; Ketelsen U; Korinthenberg R; Wenzel D; Lauffer H; Kreiss-Nachtsheim M; Wirth B; Zerres K
Neurology; 2003 Mar; 60(6):983-7. PubMed ID: 12654964
[TBL] [Abstract][Full Text] [Related]
2. Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individuals.
Hahnen E; Forkert R; Marke C; Rudnik-Schöneborn S; Schönling J; Zerres K; Wirth B
Hum Mol Genet; 1995 Oct; 4(10):1927-33. PubMed ID: 8595417
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Axonal neuropathy and predominance of type II myofibers in infantile spinal muscular atrophy.
Omran H; Ketelsen UP; Heinen F; Sauer M; Rudnik-Schöneborn S; Wirth B; Zerres K; Kratzer W; Korinthenberg R
J Child Neurol; 1998 Jul; 13(7):327-31. PubMed ID: 9701481
[TBL] [Abstract][Full Text] [Related]
5. 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; 190(1-2):35-40. PubMed ID: 11574104
[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. 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]
8. 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]
9. Congenital axonal neuropathy caused by deletions in the spinal muscular atrophy region.
Korinthenberg R; Sauer M; Ketelsen UP; Hanemann CO; Stoll G; Graf M; Baborie A; Volk B; Wirth B; Rudnik-Schöneborn S; Zerres K
Ann Neurol; 1997 Sep; 42(3):364-8. PubMed ID: 9307259
[TBL] [Abstract][Full Text] [Related]
10. Neonatal spinal muscular atrophy with multiple contractures, bone fractures, respiratory insufficiency and 5q13 deletion.
García-Cabezas MA; García-Alix A; Martín Y; Gutiérrez M; Hernández C; Rodríguez JI; Morales C
Acta Neuropathol; 2004 May; 107(5):475-8. PubMed ID: 14968368
[TBL] [Abstract][Full Text] [Related]
11. SMN(T) and NAIP mutations in Canadian families with spinal muscular atrophy (SMA): genotype/phenotype correlations with disease severity.
Simard LR; Rochette C; Semionov A; Morgan K; Vanasse M
Am J Med Genet; 1997 Oct; 72(1):51-8. PubMed ID: 9295075
[TBL] [Abstract][Full Text] [Related]
12. Molecular analysis of survival motor neuron (SMN) and neuronal apoptosis inhibitory protein (NAIP) genes of spinal muscular atrophy patients and their parents.
Chang JG; Jong YJ; Lin SP; Soong BW; Tsai CH; Yang TY; Chang CP; Wang WS
Hum Genet; 1997 Oct; 100(5-6):577-81. PubMed ID: 9341874
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. SMN1 deletions among singaporean patients with spinal muscular atrophy.
Lai AH; Tan ES; Law HY; Yoon CS; Ng IS
Ann Acad Med Singap; 2005 Jan; 34(1):73-7. PubMed ID: 15726222
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. [Spinal muscular atrophy: SMN protein deficiency].
Jedrzejowska M
Neurol Neurochir Pol; 2001; 35(2):289-97. PubMed ID: 11599226
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Molecular diagnosis of spinal muscular atrophy.
Stewart H; Wallace A; McGaughran J; Mountford R; Kingston H
Arch Dis Child; 1998 Jun; 78(6):531-5. PubMed ID: 9713008
[TBL] [Abstract][Full Text] [Related]
19. Correlation between genotype and phenotype in Korean patients with spinal muscular atrophy.
Cho K; Ryu K; Lee E; Won S; Kim J; Yoo OJ; Hahn S
Mol Cells; 2001 Feb; 11(1):21-7. PubMed ID: 11266116
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
