Merritt's neurology handbook/

By:

Mazzoni Pietro

Contributor(s):

Material type: Text

TextLanguage: English Publication details: Philadelphia: Lippincott williams & wilkins, 2006.Edition: 2Description: 708pISBN:

9788189836344

Subject(s):

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

DDC classification:

616.8 MAZ/ME

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Holdings
Item type	Current library	Call number	Status	Date due	Barcode
Books	VPSVAC Central Library	616.8 MAZ/ME (Browse shelf(Opens below))	Available		17756
Books	VPSVAC Central Library	616.8 MAZ/ME (Browse shelf(Opens below))	Available		17757

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