Prerna suri biography sample

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  • Dr. Ashish Suri

    • Last Updated On :

    Dr. Ashish Suri

    Professor

    Section of Neurosurgery

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

    Areas remaining Interest

    Neurosurgery

    with special allusion to:

    Skull base surgical treatment and cerebrovascular surgery:

    o Aneurysms: complex queue giant

    o Arteriovenousmalformations – AVMs

    o Cavernomas

    o Spinal vascular malformations

    o Carotid endartrectomy

    o ST-MCA / radial arteria bypass

    o Moyamoya disease

    o Hypophysis adenomas

    o Cure neuromas

    o Expansive sinus lesions

    o Petrous deed petroclival lesions

    o Jugular opening lesions

    o Hiatus magnum lesions

    o Specialized exertion in association with Punishment and Head& Neck surgery

    Endoscopic Neurosurgery

    o ETV pry open hydrocephalus

    o Colloid cysts

    o Spiderlike cysts

    o Neurocysticercosis

    o Endonasalendoscopic skull base

    o Scope-in scope technique: 4th ventricular lesions

    Neuro-Oncology

    o Targeted treatment for towering grade recurring gliomas

    o Strong point tumor banking

    Epilepsy Surgery:

    o Amygdalo-hippocampectomy

    o Principal callosotomy

    o ECOG guided lesionectomy

    o Functional hemispherotomy

    Spine:

    O Craniovertebral junction

    O Spinal instrumentation

    O Stance guided surgery

    Neurosurgery Skills Training

    Neuro-technology: Virtual Aristotelianism entelechy Simulation existing

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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 girdle muscular dystrophy type 2A in India: A study based on semi-quantitative protein analysis, with clinical and histopathological correlation

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

    Department of Pathology, All India Institute of Medical Sciences, New Delhi
    Correspondence Address:Department of Pathology, All India Institute of Medical Sciences, New Delhi -110 029, sharmamehar@yahoo.co.in

    Date of Acceptance: 10-Jun-2010

    Code Number: ni10146

    PMID: 20739790

    DOI: 10.4103/0028-3886.68675

    Abstract

    Background : Limb girdle muscular dystrophy (LGMD) type 2A is caused by mutation in the gene encoding for calpain-3 resulting in total or partial loss of protein. Diagnosis of LGMD2A, the most prevalent form of LGMD, is established by analyzing calpain-3 protein deficiency or CAPN3 gene mutation. Since there is no data from India regarding the incidence of LGMD2A, this study was undertaken.
    Aims
    : To study the frequency of LGMD2A in Indian population on the basis of protein analysis by immunoblotting and to correlate pathological and clinical features with protein analysis.
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