Bhim Singhal

Summary

Country: India

Publications

  1. ncbi request reprint Epidemiology and treatment of Parkinson's disease in India
    Bhim Singhal
    Medical Research Center, Bombay Hospital 12, Marine Lines, Mumbai 400 020, India
    Parkinsonism Relat Disord 9:S105-9. 2003
  2. ncbi request reprint Leukodystrophies: Indian scenario
    B S Singhal
    Department of Neurology, Bombay Hospital Institute of Medical Sciences, Mumbai, India
    Indian J Pediatr 72:315-8. 2005
  3. ncbi request reprint Megalencephalic leukoencephalopathy with subcortical cysts
    Bhim S Singhal
    Department of Neurology, Bombay Hospital Institute of Medical Sciences, Medical Research Center, Mumbai, India
    J Child Neurol 18:646-52. 2003

Collaborators

Detail Information

Publications3

  1. ncbi request reprint Epidemiology and treatment of Parkinson's disease in India
    Bhim Singhal
    Medical Research Center, Bombay Hospital 12, Marine Lines, Mumbai 400 020, India
    Parkinsonism Relat Disord 9:S105-9. 2003
    ..The present day management of PD in India is similar to that in the other countries. Unfortunately, lack of awareness, limitation of human resources and cost factors deny the benefits of therapy to many patients...
  2. ncbi request reprint Leukodystrophies: Indian scenario
    B S Singhal
    Department of Neurology, Bombay Hospital Institute of Medical Sciences, Mumbai, India
    Indian J Pediatr 72:315-8. 2005
    ..MRI studies show extensive white matter changes with temporal cysts. It is common in the Agarwal community in India. An identical mutation in exon 2 of the MLC 1 gene has been identified in this community suggesting a founder effect...
  3. ncbi request reprint Megalencephalic leukoencephalopathy with subcortical cysts
    Bhim S Singhal
    Department of Neurology, Bombay Hospital Institute of Medical Sciences, Medical Research Center, Mumbai, India
    J Child Neurol 18:646-52. 2003
    ..In India, megalencephalic leukoencephalopathy with subcortical cysts occurs predominantly in the Agarwal community. A common mutation in the MLC1 gene has been seen in 31 Agarwal patients, which suggests a founder effect...