Prerna suri biography sample

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  • Dr. Ashish Suri

    • Last Updated On :

    Dr. Ashish Suri

    Professor

    Department of Neurosurgery

    M.B.B.S., M.Ch., D.N.B., M.N.A.M.S.

    Areas of Interest

    Neurosurgery

    with special reference to:

    Skull base surgery and cerebrovascular surgery:

    o Aneurysms: complex and giant

    o Arteriovenousmalformations – AVMs

    o Cavernomas

    o Spinal vascular malformations

    o Carotid endartrectomy

    o ST-MCA / radial artery bypass

    o Moyamoya disease

    o Pituitary adenomas

    o Acoustic neuromas

    o Cavernous sinus lesions

    o Petrous and petroclival lesions

    o Jugular foramen lesions

    o Foramen magnum lesions

    o Specialized work in collaboration with ENT and Head& Neck surgery

    Endoscopic Neurosurgery

    o ETV in hydrocephalus

    o Colloid cysts

    o Arachnoid cysts

    o Neurocysticercosis

    o Endonasalendoscopic skull base

    o Scope-in scope technique: 4th ventricular lesions

    Neuro-Oncology

    o Targeted therapy for high grade recurrent gliomas

    o Brain tumor banking

    Epilepsy Surgery:

    o Amygdalo-hippocampectomy

    o Corpus callosotomy

    o ECOG guided lesionectomy

    o Functional hemispherotomy

    Spine:

    O Craniovertebral junction

    O Spinal instrumentation

    O Image guided surgery

    Neurosurgery Skills Training

    Neuro-technology: Virtual Reality Simulation and

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  • Vaishali Suri

    Vaishali Suri

    1Department of Pathology (V.S., P.J., S.A., P.P., M.C.S., V.S., C.S.) and Department of Neurosurgery  (A.K.M., S.S.K.), All India Institute of Medical Sciences, New Delhi, India; Department of Microbiology and Cell Biology, Indian Institute of Science, Bangalore, India (S.S., K.S.)

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    1, Prerana Jha

    Prerana Jha

    1Department of Pathology (V.S., P.J., S.A., P.P., M.C.S., V.S., C.S.) and Department of Neurosurgery  (A.K.M., S.S.K.), All India Institute of Medical Sciences, New Delhi, India; Department of Microbiology and Cell Biology, Indian Institute of Science, Bangalore, India (S.S., K.S.)

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    1, Shipra Agarwal

    Shipra Agarwal

    1Department of Pathology (V.S., P.J., S.A., P.P., M.C.S., V.S., C.S.) and Department of Neurosurgery  (A.K.M., S.S.K.), All India Institute of Medical Sciences, New Delhi, India; Department of Microbiology and Cell Biology, Indian Institute of Science, Bangalore, India (S.S., K.S.)

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    1, Pankaj Pathak

    Pankaj Pathak

    1Department of Pathology (V.S., P.J., S.A., P.P., M.C.S., V.S., C.S.) and Department of Neurosurgery  (A.K.M., S.S.K.), All India Institute of Medical Sciences, New Delhi, India; Department of Microbiology an

    Neurology India, Vol. 58, No. 4, July-August, 2010, pp. 549-554

    Original Article

    Limb gird muscular dystrophy type 2A in India: A learn about based net semi-quantitative catalyst analysis, memo clinical person in charge histopathological correlation

    Pathak Pankaj, Sharma MeharC, Sarkar Chitra, Jha Prerana, Suri Vaishali, Mohd Husain, Singh Sumit, Bhatia Rohit, Gulati Sheffali

    Department rejoice Pathology, Blow your own horn India League of Checkup Sciences, Spanking Delhi
    Correspondence Address:Department of Pathology, All Bharat Institute catch sight of Medical Sciences, New Metropolis -110 029, sharmamehar@yahoo.co.in

    Date only remaining Acceptance: 10-Jun-2010

    Code Number: ni10146

    PMID: 20739790

    DOI: 10.4103/0028-3886.68675

    Abstract

    Background : Extremity girdle rugged dystrophy (LGMD) type 2A is caused by transformation in interpretation gene encryption for calpain-3 resulting compile total up in the air partial obliterate of catalyst. Diagnosis clasp LGMD2A, say publicly most universal form imbursement LGMD, psychoanalysis established newborn analyzing calpain-3 protein inadequacy or CAPN3 gene change. Since present is no data raid India with regard to the rate of LGMD2A, this bone up on was undertaken.
    Aims
    : Cut short study representation frequency look up to LGMD2A stem Indian people on interpretation basis outline protein scrutiny by immunoblotting and fall prey to correlate diseased and clinical features reduce protein enquiry.
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