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  • Molecular Mechanisms of Ataxia Telangiectasiaby Shamim I. Ahmad

    Landes Bioscience 2009; US$ 129.00

    Ataxia telangiectasia (AT) is an incurable, rare autosomal recessive genetic disorder which affects approximately one in 40,000-100,000 and the carrier frequency is estimated to be 1:100-200. In the United Kingdom it affects 1 in 300,000 live births amounting to about 5 or 6 cases per year. Although the medial survival rate of affected persons is between... more...

  • Molecular Mechanisms of Cockayne Syndromeby Shamim I. Ahmad

    Landes Bioscience 2009; US$ 129.00

    Cockayne syndrome (CS) is a rare autosomal genetic disorder that was first identified almost 62 years ago by Alfred Cockayne and was named after him. The earliest publication record (PubMed) available is a paper by Marie et al in 1958. Since then 815 research papers including excellent reviews have been published (PubMed, December 2008), yet we are... more...

  • Diabetesby Shamim I. Ahmad

    Springer 2012; US$ 239.00

     Diabetes is a complex disease and is also one of the most common.  It is very difficult to reach an accurate estimate for the global prevalence of diabetes since the standards and methods of data collection vary widely in different parts of the world. In addition, many potential sufferers are not included in the count because according to... more...

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