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Merritt's neurology (Record no. 38539)

MARC details
000 -LEADER
fixed length control field	06617cam a2200253 4500
001 - CONTROL NUMBER
control field	u33250
003 - CONTROL NUMBER IDENTIFIER
control field	SIRSI
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field	000000n2016 000 0 eng u
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number	9781451193367
050 #4 - LIBRARY OF CONGRESS CALL NUMBER
Classification number	HUR
082 #4 - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number	616.8
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name	Louis, Elan D.
9 (RLIN)	63660
245 10 - TITLE STATEMENT
Title	Merritt's neurology
Statement of responsibility, etc.	Elan D. Louis, Stephan A. Mayer, Lewis. P Rowland
250 ## - EDITION STATEMENT
Edition statement	13th ed.
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc.	Philadelphia, Pa.
--	London
Name of publisher, distributor, etc.	Lippincott Williams & Wilkins
Date of publication, distribution, etc.	2016.
300 ## - PHYSICAL DESCRIPTION
Extent	xxvii, 1402 p.
Other physical details	ill.
Dimensions	29 cm.
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc. note	Includes bibliographical references and index
505 0# - FORMATTED CONTENTS NOTE
Formatted contents note	Signs and symptoms in neurologic diagnosis: approach to the patient -- Delirium and confusion -- Memory loss, behavioral changes and dementia -- Aphasia, apraxia, and agnosia -- Syncope, seizures and their mimics -- Coma -- Headache -- Diagnosis of pain and paresthesias -- Dizziness, vertigo, and hearing loss -- Impaired vision -- Involuntary movements -- Syndromes caused by weak muscles -- Gait disorders -- CT and MRI -- Electroencephalography and evoked potentials -- Electromyography, nerve conduction studies, and and magnetic stimulation -- Autonomic testing -- Neurovascular imaging -- Endovascular neuroradiology -- Lumbar puncture and cerebrospinal fluid examination -- Muscle and nerve biopsy -- Neuropsychological evaluation -- DNA diagnosis -- Bacterial infections -- Focal infections -- Viral infections and postviral syndromes -- Human immunodeficiency virus (HIV) and acquired immunodeficiency syndrome (AIDS) -- Fungal infections -- Neurosarcoidosis -- Neurosyphilis -- Leptospirosis -- Lyme disease -- Parasitic infections -- Bacterial toxins -- Prion diseases -- Whipple disease -- Pathogenesis, classification, and epidemiology of cerebrovascular disease -- Examination of the patient with cerebrovascular disease -- Transient ischemic attack -- Cerebral infarction -- Intracerebral hemorrhage -- Genetics of stroke -- Other cerebrovascular syndromes -- Differential diagnosis of stroke -- Stroke in children -- Treatment and prevention of stroke -- Subarachnoid hemorrhage -- Cerebral venous and sinus thrombosis -- Vascular disease of the spinal cord -- Vasculitis -- Susac syndrome -- Vascular tumors and malformations -- Hydrocephalus -- Normal pressure hydrocephalus (NPH) -- Brain edema and disorders of intracranial pressure -- Superficial siderosis and intracerebral hypotension -- Hyperosmolar syndromes -- General considerations -- Tumors of the skull and cranial nerves -- Tumors of the meninges -- Gliomas -- Lymphomas -- Pineal region tumors -- Tumors of the pituitary gland -- Congenital and childhood tumors -- Metastatic tumors -- Spinal tumors -- Paraneoplastic syndromes -- Complications of cancer chemotherapy -- Head injury -- Spine injury -- Cranial and peripheral nerve lesions -- Complex regional pain syndrome -- Radiation injury -- Electrical and lightning injury -- Decompression sickness -- Intervertebral dics and radiculopathy -- Cervical spondylotic myelopathy -- Thoracic outlet syndrome -- Hereditary and acquired spastic paraplegia -- Syringomyelia -- Neonatal neurology -- Floppy infant syndrome -- Disorders of motor and mental development -- Autism spectrum disorders -- Laurence-Moon-Biedl syndrome -- Cerebral and spinal malformations -- Chromosomal diseases -- Marcus Gunn -- Mo*bius syndrome -- Disorders of amino acid metabolism -- Disorders of purine and pyrimidine metabolism -- Lysosomal and other storage diseases -- Disorders of carbohydrate metabolism -- Glucose transporter type 1 deficiency syndrome -- Disorders of DNA maintenance, transcription, and translation -- Hyperammonemia -- Peroxisomal diseases: adrenoleukodystrophy, zellweger syndrome, and refsum disease -- Organic acidurias -- Disorders of metal metabolism -- Acute intermittent porphyria -- Neurologic syndromes with acanthocytes -- Cerebral degenerations of childhood -- Diffuse sclerosis and vanishing white matter disease -- Mitochondrial encephalomyopathies: diseases of mitochondrial DNA -- Leber hereditary optic neuropathy -- Mitochondrial diseases with mutations of nuclear DNA -- Neurofibromatosis -- Tuberous sclerosis complex -- Encephalotrigeminal angiomatosis -- Incontinentia pigmenti -- General considerations -- Alzheimer disease -- Frontotemporal dementia -- Lewy body dementias -- Huntington disease -- Choreas -- Myoclonus -- Gilles de la tourette syndrome -- Dystonia -- Essential tremor -- Parkinson disease -- Parkinson-plus syndromes -- Paroxysmal dyskinesias -- Tradive dyskinesia and other neuroleptic-induced syndromes -- Autosomal recessive ataxias -- Autosomal dominant ataxias -- Amyotrophic lateral sclerosis, progressive muscular atrophy, and primary lateral sclerosis -- Kennedy disease -- Spinal muscular atrophies of childhood -- Monomelic muscular atrophy -- General considerations -- The inherited peripheral neuropathies -- Acquired neuropathies -- Neuropathic pain -- Myasthenia gravis -- Lambert-Eaton syndrome -- Botulism and antibiotic-induced neuromuscular disorders -- Critical illness myopathy and neuropathy -- Identifying disorders of the motor unit -- Progressive muscular dystrophies -- Familial periodic paralysis -- Congenital disorders of muslce -- Myoglobinuria -- Muscle cramps and stiffness -- Dermatomyositis -- Polymyositis, inclusion body myositis, and related myopathies -- Myositis ossificans -- Multiple sclerosis -- Neuromyelitis optica -- Marchiafava-Bignami disease -- Central pontine myelinolysis -- Epilepsy -- Febrile seizures -- Primary and secondary headaches -- Transient global amnesia -- Meńie`re syndrome -- Sleep disorders -- Neurogenic orthostatic hypotension, autonomic failure, and autonomic neuropathy -- Familial dysautonomia -- Endocrine diseases -- Hematologic and related diseases -- Hepatic disease -- Cerebral complications of cardiac surgery -- Bone disease -- Renal disease -- Respiratory support for neurologic diseases -- Nutritional disorders: malnutrition, malabsorption, and B12 and other vitamin deficiency -- Hypertrophic pachymeningitis -- Neurologic disease during pregnancy -- Hashimoto encephalopathy -- Schizophrenia -- Mood disorders -- Anxiety disorders -- Somatoform disorders -- Alcoholism -- Drug dependence -- Iatrogenic disease -- Occupational and environmental neurotoxicology -- HIV, fetal alcohol and drug effects, and the battered child -- Falls in the elderly -- Neurologic rehabilitation -- End-of-life issues in neurology.
596 ## -
--	1 2
650 #4 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element	Neurology
9 (RLIN)	68141
650 12 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element	Nervous System Diseases
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name	Mayer, Stephan A.
9 (RLIN)	63661
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name	Rowland, Lewis P.
9 (RLIN)	73347

Holdings
Withdrawn status	Lost status	Source of classification or shelving scheme	Damaged status	Not for loan	Home library	Current library	Shelving location	Total Checkouts	Full call number	Barcode	Date last seen	Copy number	Price effective from	Koha item type
Not Withdrawn	Not Lost	Dewey Decimal Classification	Not Damaged	Available for Loan	St. Luke's General Hospital Kilkenny	St. Luke's General Hospital Kilkenny	Open Shelves		616.8	036947	18/07/2018	1	18/07/2018	4 Week Loan