Neurodegenerative Diseases

Shamim I. Ahmad after obtaining his Master’s degree in Botany from Patna University, Bihar, India and his PhD in Molecular Genetics from Leicester University, England, joined Nottingham Polytechnic as Grade 1 lecturer and was subsequently promoted to SL post. Nottingham Polytechnic subsequently became Nottingham Trent University where, after serving for about 37 years, he took early retirement to spend the remaining time writing books and conducting full‑time research. For more than three decades he worked on different areas of biology including thymineless death in bacteria, genetic control of nucleotide catabolism, development of anti‑AIDS drugs, control of microbial infection of burns, phages of thermophilic bacteria and microbial flora of Chernobyl after the nuclear accident. But his primary interest, which started 27 years ago, is DNA damage and repair, particularly near UV photolysis of biological compounds, production of reactive oxygen species and their implications on human health including skin cancer and xeroderma pigmentosum. He is also investigating photolysis of non‑biological compounds such as 8‑methoxypsoralen+UVA, mitomycin C, and nitrogen mustard and their importance in psoriasis treatment and in Fanconi anemia. In 2003 he received a prestigious “Asian Jewel Award” in Britain for “Excellence in Education”. He is also the Editor of Molecular Mechanisms of Fanconi Anaemia, Molecular Mechanisms of Xeroderma Pigmentosum, Molecular Mechanisms of Fanconi Anaemia, Molecular Mechanisms of Xeroderma Pigmentosum, Molecular Mechanisms of Ataxia Telangiectasia, Molecular Mechanisms of Cockayne Syndrome and Diseases of DNA Repair published by Landes Bioscience.

Acute Disseminated Encephalomyelitis.- Age‑Related Macular Degeneration.- Arachnoid Cysts.- Autism Spectrum Disorders: Information for Pediatricians Supporting Families of Young Children on the Spectrum.- Autosomal Recessive Charcot‑Marie‑Tooth Neuropathy.- Creutzfeldt‑Jakob Disease.- Epigenetics in Autism and other Neurodevelopmental Diseases.- Epilepsy and Epileptic Syndrome.- Frontotemporal Lobar Degeneration.- Gerstmann‑ Sträussler ‑Scheinker Disease.- Juvenile Neuronal Ceroid Lipofuscinoses.- Kuru: The First Prion Disease.- Leukodystrophies.- Machado‑Joseph Disease and other Rare Autosomal Dominant Spinocerebellar Ataxias.- Neurodegenerations Induced by Organophosphorous Compounds.- Mitochondrial Importance in Alzheimer’s, Huntington’s and Parkinson’s Diseases.- Multiple Sclerosis.- Myotonic Dystrophy Type 1 or Steinert’s Disease.- Neurodegeneration in Diabetes Mellitus.- Neurofibromatoses.- Oxidative Stress in Developmental Brain Disorders.- Oxidative Stress and Mitochondrial Dysfunction in Down Syndrome.- Pick’s Disease.- Premature Aging Syndrome.- The Savant Syndrome and its Possible Relationship to Epilepsy.- Sjogren‑Larsson Syndrome.- The Spinocerebellar Ataxias: Clinical Aspects and Molecular Genetics.- Tourette Syndrome.