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Permissibility of prenatal diagnosis and abortion for fetuses with severe genetic disorder: type 1 spinal muscular atrophy

автор

Teguh Haryo Sasongko

Bin Alwi Zilfalil

опубліковано в: Annals of Saudi Medicine

дата публікації: 2010-11-01

основна тема: аборт, cпінальна м'язова атрофія, muscular atrophy

Cites articles 25

Дата

Заголовок

Автори

2008-10-07

Combination of SMN2 copy number and NAIP deletion predicts disease severity in spinal muscular atrophy

Teguh Haryo Sasongko, Bin Alwi Zilfalil
2008-06-01

Spinal muscular atrophy.

Mitchell R. Lunn
2008-02-01

The use of invasive ventilation is appropriate in children with genetically proven spinal muscular atrophy type 1: the motion against

Monique Ryan
2008-02-01

The use of mechanical ventilation is appropriate in children with genetically proven spinal muscular atrophy type 1: the motion for.
2008-06-01

SMN2 and NAIP gene dosages in Vietnamese patients with spinal muscular atrophy.

Teguh Haryo Sasongko
2007-11-01

Molecular analysis of the SMN1 and NAIP genes in Iranian patients with spinal muscular atrophy
2007-02-01

Deletion analyses of SMN1 and NAIP genes in Malaysian spinal muscular atrophy patients

Bin Alwi Zilfalil
2006-08-01

Molecular analysis of the SMN1 and NAIP genes in 60 Tunisian spinal muscular atrophy patients
2005-08-01

Prenatal diagnosis of spinal muscular atrophy: Indian scenario

Akanchha Kesari, Balraj Mittal
2004-10-18

Spinal muscular atrophy: survival pattern and functional status
2004-10-01

Homozygous SMN1 deletions in unaffected family members and modification of the phenotype by SMN2.

Kathryn J Swoboda
2003-02-01

Spinal muscular atrophy type 1 quality of life
2003-10-01

Molecular analysis of the spinal muscular atrophy and neuronal apoptosis inhibitory protein genes in Saudi patients with spinal muscular atrophy
2003-02-01

Genetic diagnosis of Werdnig-Hoffmann disease: a problem for application to prenatal diagnosis.

Hideo Orimo
2002-01-01

Assessment of pain and health-related quality of life in slowly progressive neuromuscular disease

Gregory Carter, Richard T Abresch
2002-01-01

Molecular analysis of spinal muscular atrophy and modification of the phenotype by SMN2

Arthur Burghes
2002-08-01

Prenatal prediction of childhood-onset spinal muscular atrophy (SMA) in Turkish families

Sevtap Savas, Serpil Eraslan
2002-09-01

Correlation between SMN2 copy number and clinical phenotype of spinal muscular atrophy: three SMN2 copies fail to rescue some patients from the disease severity
2001-09-01

Induced abortion from an islamic perspective: is it criminal or just elective?
2001-12-21

Quantitative analyses of SMN1 and SMN2 based on real-time lightCycler PCR: fast and highly reliable carrier testing and prediction of severity of spinal muscular atrophy
1999-01-01

Prenatal onset spinal muscular atrophy
1999-05-25

A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy
1999-01-01

Very severe spinal muscular atrophy (SMA type 0): an expanding clinical phenotype
1997-07-01

Extensive DNA deletion associated with severe disease alleles on spinal muscular atrophy homologues
1995-01-13

Identification and characterization of a spinal muscular atrophy-determining gene

Стаття - wd:Q34363145

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