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Results: 1 to 20 of 108

Similar articles for PubMed (Select 22661569)

1.

Spinal muscular atrophy: manifestations and management.

Mesfin A, Sponseller PD, Leet AI.

J Am Acad Orthop Surg. 2012 Jun;20(6):393-401. doi: 10.5435/JAAOS-20-06-393. Review.

PMID:
22661569
2.

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;225(3):153-9.

3.

Spinal muscular atrophy: newborn and carrier screening.

Prior TW.

Obstet Gynecol Clin North Am. 2010 Mar;37(1):23-36, Table of Contents. doi: 10.1016/j.ogc.2010.03.001.

PMID:
20494255
4.

[Clinical, electrophysiological and molecular study of 26 chilean patients with spinal muscular atrophy].

Castiglioni C, Levicán J, Rodillo E, Garmendia MA, Díaz A, Pizarro L, Contreras L.

Rev Med Chil. 2011 Feb;139(2):197-204. doi: /S0034-98872011000200009. Epub 2011 Jul 11. Spanish.

5.

High incidence of SMN1 gene deletion in Moroccan adult-onset spinal muscular atrophy patients.

Bouhouche A, Benomar A, Birouk N, Bouslam N, Ouazzani R, Yahyaoui M, Chkili T.

J Neurol. 2003 Oct;250(10):1209-13.

PMID:
14586604
7.
8.

Transmission ratio distortion in the spinal muscular atrophy locus: data from 314 prenatal tests.

Botta A, Tacconelli A, Bagni I, Giardina E, Bonifazi E, Pietropolli A, Clementi M, Novelli G.

Neurology. 2005 Nov 22;65(10):1631-5.

PMID:
16301493
9.

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. doi: 10.1016/j.braindev.2008.08.012. Epub 2008 Oct 7.

PMID:
18842367
10.

Spinal muscular atrophy: mechanisms and therapeutic strategies.

Lorson CL, Rindt H, Shababi M.

Hum Mol Genet. 2010 Apr 15;19(R1):R111-8. doi: 10.1093/hmg/ddq147. Epub 2010 Apr 13. Review.

11.

Recurrent hip dislocation in intermediate spinal atrophy.

Thompson CE, Larsen LJ.

J Pediatr Orthop. 1990 Sep-Oct;10(5):638-41.

PMID:
2394817
12.

Deletions in the survival motor neuron gene in Iranian patients with spinal muscular atrophy.

Hasanzad M, Golkar Z, Kariminejad R, Hadavi V, Almadani N, Afroozan F, Salahshurifar I, Shafeghati Y, Kahrizi K, Najmabadi H.

Ann Acad Med Singapore. 2009 Feb;38(2):139-41.

13.

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.

PMID:
14578966
14.

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.

15.

[Quantitative analysis of the genes determining spinal muscular atrophy].

Nagymihály M, Herczegfalvi A, Tímár L, Karcagi V.

Ideggyogy Sz. 2009 Nov 30;62(11-12):390-7. Hungarian.

PMID:
20025129
16.

Spinal muscular atrophy: from animal model to clinical trial.

Zanoteli E, Maximino JR, Conti Reed U, Chadi G.

Funct Neurol. 2010 Apr-Jun;25(2):73-9. Review.

PMID:
20923604
17.

Deletion analysis of SMN1 exon 7 alone may be necessary and sufficient for the diagnosis of spinal muscular atrophy.

Sasongko TH, Gunadi, Zilfalil BA, Zabidi-Hussin Z.

J Neurogenet. 2011 Mar;25(1-2):15-6. doi: 10.3109/01677063.2011.559561. Epub 2011 Feb 22.

PMID:
21338334
18.

[Mutation analysis of SMN1 gene in patients with spinal muscular atrophy].

DU J, Qu YJ, Xiong H, Li EZ, Jin YW, Bai JL, Wang H, Song F.

Zhonghua Er Ke Za Zhi. 2011 Jun;49(6):411-5. Chinese.

PMID:
21924051
19.

[Genetic tests and clinical re-evaluation of 85 children with suspected spinal muscular atrophy].

Ji X, Liu XQ, Shen JW, Li XH, Tao J.

Zhonghua Er Ke Za Zhi. 2010 Jun;48(6):425-30. Chinese.

PMID:
21055263
20.

Correlation between SMN2 copy number and clinical phenotype of spinal muscular atrophy: three SMN2 copies fail to rescue some patients from the disease severity.

Harada Y, Sutomo R, Sadewa AH, Akutsu T, Takeshima Y, Wada H, Matsuo M, Nishio H.

J Neurol. 2002 Sep;249(9):1211-9.

PMID:
12242541
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