151 related articles for article (PubMed ID: 24840836)
1. Carrier screening for spinal muscular atrophy in Italian population.
Calì F; Ruggeri G; Chiavetta V; Scuderi C; Bianca S; Barone C; Ragalmuto A; Schinocca P; Vitello GA; Romano V; Musumeci S
J Genet; 2014 Apr; 93(1):179-81. PubMed ID: 24840836
[No Abstract] [Full Text] [Related]
2. Large-scale population screening for spinal muscular atrophy: clinical implications.
Ben-Shachar S; Orr-Urtreger A; Bardugo E; Shomrat R; Yaron Y
Genet Med; 2011 Feb; 13(2):110-4. PubMed ID: 21233719
[TBL] [Abstract][Full Text] [Related]
3. New approaches in molecular diagnosis and population carrier screening for spinal muscular atrophy.
Gonçalves-Rocha M; Oliveira J; Rodrigues L; Santos R
Genet Test Mol Biomarkers; 2011 May; 15(5):319-26. PubMed ID: 21329463
[TBL] [Abstract][Full Text] [Related]
4. Spinal muscular atrophy carrier frequency and estimated prevalence of the disease in Moroccan newborns.
Lyahyai J; Sbiti A; Barkat A; Ratbi I; Sefiani A
Genet Test Mol Biomarkers; 2012 Mar; 16(3):215-8. PubMed ID: 21950724
[TBL] [Abstract][Full Text] [Related]
5. False Negative Carrier Screening in Spinal Muscular Atrophy.
Butcher S; Smith M; Woodcock IR; Delatycki M; Ryan MM; Forbes R
J Child Neurol; 2020 Mar; 35(4):274-277. PubMed ID: 31858866
[TBL] [Abstract][Full Text] [Related]
6. Incidence of spinal muscular atrophy in Poland--more frequent than predicted?
Jedrzejowska M; Milewski M; Zimowski J; Zagozdzon P; Kostera-Pruszczyk A; Borkowska J; Sielska D; Jurek M; Hausmanowa-Petrusewicz I
Neuroepidemiology; 2010; 34(3):152-7. PubMed ID: 20090376
[TBL] [Abstract][Full Text] [Related]
7. Carrier frequency of spinal muscular atrophy in Thailand.
Dejsuphong D; Taweewongsounton A; Khemthong P; Chitphuk S; Stitchantrakul W; Sritara P; Tunteeratum A; Sura T
Neurol Sci; 2019 Aug; 40(8):1729-1732. PubMed ID: 31004230
[TBL] [Abstract][Full Text] [Related]
8. [Spinal muscular atrophy carrier frequency in Ukraine].
Solov'ev AA; Grishchenko NV; Livshits LA
Genetika; 2013 Sep; 49(9):1126-8. PubMed ID: 25486782
[TBL] [Abstract][Full Text] [Related]
9. Evaluation and characterization of a high-resolution melting analysis kit for rapid carrier-screening test of spinal muscular atrophy.
Wang KC; Chang CC; Chang YF; Wang SH; Chiang CK; Tsai CP
J Neurogenet; 2015; 29(2-3):113-6. PubMed ID: 25895942
[TBL] [Abstract][Full Text] [Related]
10. Diagnostic Testing for Patients with Spinal Muscular Atrophy.
Brandsema JF; Gross BN; Matesanz SE
Clin Lab Med; 2020 Sep; 40(3):357-367. PubMed ID: 32718505
[TBL] [Abstract][Full Text] [Related]
11. Spinal muscular atrophy: newborn and carrier screening.
Prior TW
Obstet Gynecol Clin North Am; 2010 Mar; 37(1):23-36, Table of Contents. PubMed ID: 20494255
[TBL] [Abstract][Full Text] [Related]
12. 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. PubMed ID: 21338334
[TBL] [Abstract][Full Text] [Related]
13. Carrier screening for spinal muscular atrophy (SMA) in 107,611 pregnant women during the period 2005-2009: a prospective population-based cohort study.
Su YN; Hung CC; Lin SY; Chen FY; Chern JP; Tsai C; Chang TS; Yang CC; Li H; Ho HN; Lee CN
PLoS One; 2011 Feb; 6(2):e17067. PubMed ID: 21364876
[TBL] [Abstract][Full Text] [Related]
14. 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 Singap; 2009 Feb; 38(2):139-41. PubMed ID: 19271042
[TBL] [Abstract][Full Text] [Related]
15. Carrier Screening and Prenatal Diagnosis for Spinal Muscular Atrophy in 13,069 Chinese Pregnant Women.
Zhang J; Wang Y; Ma D; Sun Y; Li Y; Yang P; Luo C; Jiang T; Hu P; Xu Z
J Mol Diagn; 2020 Jun; 22(6):817-822. PubMed ID: 32205292
[TBL] [Abstract][Full Text] [Related]
16. Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72,400 specimens.
Sugarman EA; Nagan N; Zhu H; Akmaev VR; Zhou Z; Rohlfs EM; Flynn K; Hendrickson BC; Scholl T; Sirko-Osadsa DA; Allitto BA
Eur J Hum Genet; 2012 Jan; 20(1):27-32. PubMed ID: 21811307
[TBL] [Abstract][Full Text] [Related]
17. [A pilot study on spinal muscular atrophy carrier screening in Shanghai region using real-time PCR].
Qu XX; Xiao B; Ji X; Jiang WT; Yang ZJ; Tao J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):1-4. PubMed ID: 23450468
[TBL] [Abstract][Full Text] [Related]
18. [Point mutation analysis of SMN1 gene in patients with spinal muscular atrophy].
QU YJ; DU J; LI EZ; YANG YL; ZOU LP; BAI JL; WANG H; JIN YW; SONG F
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Apr; 28(2):121-6. PubMed ID: 21462119
[TBL] [Abstract][Full Text] [Related]
19. [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]
20. Detection of spinal muscular atrophy carriers in a sample of the Brazilian population.
Bueno KC; Gouvea SP; Genari AB; Funayama CA; Zanette DL; Silva WA; Oliveira AB; Scola RH; Werneck LC; Marques W
Neuroepidemiology; 2011; 36(2):105-8. PubMed ID: 21335981
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
