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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...

  • Diseases of DNA Repairby Shamim I. Ahmad

    Springer New York 2011; US$ 210.23

    This book presents an updated detailed account of some important additional diseases of DNA repair. It provides brief accounts of the basics of DNA damage, repair, mutagenesis and cancer.  more...

  • Reactive Oxygen Species in Biology and Human Healthby Shamim I. Ahmad

    CRC Press 2016; US$ 179.95

    Unlike other narrowly focused books, Reactive Oxygen Species in Biology and Human Health provides a comprehensive overview of ROS. It covers the current status of research and provides pointers to future research goals. Additionally, it authoritatively reviews the impact of reactive oxygen species with respect to various human diseases and discusses... more...

  • Molecular Mechanisms of Fanconi Anemiaby Shamim I. Ahmad; Sandra Kirk

    Springer US 2007; US$ 147.89

    Molecular Mechanisms of Fanconi Anemia will give research students a platform for further investigation, and act as a source of information regarding experimental design. Clinicians will find this title useful for its comprehensive description of Fanconi Anemia and information on the latest molecular theories underlying its causes. more...

  • Molecular Mechanisms of Xeroderma Pigmentosumby Shamim I. Ahmad; Fumio Hanaoka

    Springer New York 2008; US$ 210.23

    Xeroderma pigmentosum (XP), meaning parchment skin and pigmentary dist- bance, is a rare and mostly autosomal recessive genetic disorder that was originally named by two dermatologists, the Austrian Ferdinand Ritter von Hebra and his H- garian son in law Moritz Kaposi in 1874i and 1883. 2 The earliest published record (PubMed) available on the internet... more...

  • Obesityby Shamim I. Ahmad; Syed Khalid Imam

    Springer International Publishing 2015; US$ 179.58

    This book brings a comprehensive treatise about obesity, examining the measures that can be taken to stop and even reduce obesity if these right measures are taken in time. Recent studies show that obesity is on the increase at an alarming rate, especially in the industrialized and affluent countries. A number of reasons have been put forward for... more...

  • Thyroid Disordersby Syed Khalid Imam; Shamim I. Ahmad

    Springer International Publishing 2016; US$ 137.32

    This book provides comprehensive knowledge about thyroid gland and highlights the recent trends in the management of thyroid dysfunctions. Thyroid disorders are amongst the most prevalent of medical conditions possibly after diabetes. The prevalence of thyroid dysfunction in adults in the general population ranges from 1 to 10 percent, and is... more...

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