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Alpha-Thalassemia Myelodysplasia Syndrome

Known as: ATMDS, Hemoglobin H Disease, Acquired 
 
National Institutes of Health

Related topics

Related topics

3 relations

Broader (3)

Genetic Diseases, X-LinkedMYELODYSPLASTIC SYNDROMEalpha-Thalassemia

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Active Tuned Mass Damper
The objective of this paper is to demonstrate the design and implementation of an Active Tuned Mass Damper (ATMD) and to… Expand
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2013
2013
Active Tuned Mass Damper Control of Wind Turbine Nacelle/Tower Vibrations with Damaged Foundations
The aim of this paper is to develop an active structural control scheme to control wind turbine nacelle/tower out-of-plane… Expand
Highly Cited
2012
Highly Cited
2012
Modal identification of Shanghai World Financial Center both from free and ambient vibration response
Abstract The Shanghai World Financial Center (SWFC), a currently built super high-rise building, is located in Lujiazui area. The… Expand
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2012
2012
α-Thalassemia, mental retardation, and myelodysplastic syndrome.
  • R. Gibbons
  • Cold Spring Harbor perspectives in medicine
  • 2012
    • Corpus ID: 42266336
This article describes three rare syndromes in which the presence of α-thalassemia provided an important clue to the molecular… Expand
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2006
2006
Patient Decision Making
A 73-year-old man requests a prostate-specific antigen (PSA) test from his primary care physician, but the physician does not… Expand
Highly Cited
2005
Highly Cited
2005
Somatic point mutations in RUNX1/CBFA2/AML1 are common in high‐risk myelodysplastic syndrome, but not in myelofibrosis with myeloid metaplasia
Objective: Acquired somatic point mutations in RUNX1/CBFA2/AML1 have recently been described in a subset of patients with… Expand
Highly Cited
2004
Highly Cited
2004
Acquired somatic ATRX mutations in myelodysplastic syndrome associated with alpha thalassemia (ATMDS) convey a more severe hematologic phenotype than germline ATRX mutations.
Acquired somatic mutations in ATRX, an X-linked gene encoding a chromatin-associated protein, were recently identified in 4… Expand
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2004
2004
Attenuation of an amino-terminal premature stop codon mutation in the ATRX gene by an alternative mode of translational initiation
Nonsense mutations located in the 5′ end of the coding sequence of a gene are commonly considered to be null alleles. Not only do… Expand
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2004
2004
Deletion of the α-globin gene cluster as a cause of acquired α-thalassemia in myelodysplastic syndrome
Rarely, myelodysplastic syndrome (MDS) is complicated by an acquired form of α-thalassemia (α-thalassemia in myelodysplastic… Expand
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2004
2004
Deletion of the alpha-globin gene cluster as a cause of acquired alpha-thalassemia in myelodysplastic syndrome.
Rarely, myelodysplastic syndrome (MDS) is complicated by an acquired form of alpha-thalassemia (alpha-thalassemia in… Expand
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