Merritt's neurology handbook/ (Record no. 10713)

MARC details
000 -LEADER
fixed length control field 03033nam a2200193Ia 4500
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 210804s2006||||xx |||||||||||||| ||und||
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
ISBN 9788189836344
041 ## - LANGUAGE CODE
Language code of text/sound track or separate title eng
082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 616.8
Item number MAZ/ME
100 ## - MAIN ENTRY--AUTHOR NAME
Personal name Mazzoni Pietro
245 #0 - TITLE STATEMENT
Title Merritt's neurology handbook/
250 ## - EDITION STATEMENT
Edition statement 2
260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT)
Place of publication Philadelphia:
Name of publisher Lippincott williams & wilkins,
Year of publication 2006.
300 ## - PHYSICAL DESCRIPTION
Number of Pages 708p.
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical Term delirium and dementia,aphasia,apraxia,agnosia,syncope,seizures,coma,diagnosis of pain and paresthesias,dizziness and hearing loss,impaired vision,involuntary movements and related syndromes,syndroms caused by weak muscles,gait disorders,signs and symptoms in neurologic diagnosis,ct and mri,eeg and evoked potentials,nerve conduction studies,electromyography and magnetic stimulation,neurovascular imaging,endovascular surgical neurocardiology,lumbar puncture and csf examination,nerve biopsy,neuropsychological evaluation,dna diagnosis,bacterial infections and aseptic meningitis,focal infections,viral infections,neurosarcoidosis,lyme disease,prion disease,whipple disease,epidemiology of cerebrovascula disease, transient ischemic attack,cerebral infarction,genetics of stroke,hydrocephalus,disorders of intracranial pressure,hyperglycemic nonketotic syndrome,gliomas,metastatic tumors,intervertebral discs and radiculopathy,lumbar spondylosis, radiation injury,decompression sickness,neonatal neurology,floppy infant syndrome, laurence-moon-biedl syndrome,marcus gunn and mobius syndromes, chromosomal diseases,disorders of aminoacid metabolism,lysosomal and other storage diseases,hyperammonemia,organic acidurias,leber hereditary optic neuropathy, neurofibromatosis,encephalotrigeminal angiomatosis,hereditary ataxias,huntington disease,sydenham and other forms of chorea,myoclonus,dystonia,progressive supranuclear palsy,tardive dyskinesia,spastic paraplegia,syringomyelia,myasthenia gravis,lambert-eaton myasthenic syndrome,acute quadriplegic myopathy,progressive muscular dystrophies,familial periodic paralysis,congenital myopathies,myoglobinuria,dermatomyositis,myositis ossificans,multiple sclerosis,marchiafava-bignami disease,central pontine myelinolysis,neurogenic orthostatic hypotension ,acute autonomic neuropathy,familial dysautonomia,epilepsy,febrile seizures,transient global amnesia,meniere syndrome,hematologic and related disease,hepatic disease,paraneoplastic syndromes,malabsorption,malnutrition,vitamin deficinecies,vasculitis syndromes,hypertrophic pachymeningitis,hashimoto encephalopathy,anxiety disorders,schizophrenia,somatoform disorders,alcoholism,latrogenic disease,cancer chemotherapy,occupational and environmental neurotoxicology,falls in elderly,neurologic rehabilitation, bone disease,renal disease,hashimoto encephalopathy,disorders of carbohydrate metabolism,acute intermittent porphyria,diffuse sclerosis,differential diagnosis,leber hereditary optic neuropathy,mitochondrial diseases with mutations of nuclear dna
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Pearson Toni Shih
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Rowland Lewis P
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type Books
Holdings
Withdrawn status Home library Current library Date acquired Full call number Accession Number Koha item type
  VPSVAC Central Library VPSVAC Central Library 02/04/2011 616.8 MAZ/ME 17756 Books
  VPSVAC Central Library VPSVAC Central Library 02/04/2011 616.8 MAZ/ME 17757 Books
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