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003 | OSt | ||
005 | 20240305192611.0 | ||
008 | 220901b |||||||| |||| 00| 0 eng d | ||
020 | _a1455748129 | ||
020 | _a 9781455748129 | ||
040 | _cDLC | ||
082 | _a618.928 PIN | ||
100 |
_aJ. Eric Piña-Garza _927691 |
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222 | _aabnormal absence acid activity acute adults affected appear artery associated ataxia attacks autosomal become begins birth blood brain cause cerebral Chapter child childhood chronic Clinical Features common complete concentration congenital cord course cranial nerve decreased defect deficiency develop Diagnosis disease disorders disturbances dose drugs early encephalopathy epilepsy et al examination facial focal function gene genetic glucose head headache hearing hearing impairment hemorrhage impairment increased indicates infantile infants infection inheritance initial injury intracranial intracranial pressure involvement Last later legs less limbs loss malformations Management Medical meningitis migraine months motor movements muscle mutation myoclonic myopathy nerve neurological neuropathy newborns normal occur onset optic pain palsy patients present pressure produce progressive rare recessive reduce reflexes require response seizures severe shows sometimes spinal studies suggests symptoms syndrome testing therapy tion treatment tumors usually visual weakness weeks | ||
245 |
_aFenichel's Clinical Pediatric Neurology _b A Signs and Symptoms Approach |
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250 | _a7th edition | ||
260 |
_aLondon: _bElsevier Health Sciences, _cc2013 |
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300 | _a 412 pages | ||
505 | _aContents: Paroxysmal disorders -- Altered states of consciousness -- Headache -- Increased intracranial pressure -- Psychomotor retardation and regression -- The hypotonic infant -- Flaccid limb weakness in childhood -- Cramps, muscles stiffness, and exercise intolerance -- Sensory and autonomic disturbances -- Ataxia -- Hemiplegia -- Paraplegia and quadriplegia -- Monoplegia -- Movement disorders -- Disorders of ocular motility -- Disorders of the visual system -- Lower brainstem and cranial nerve dysfunction -- Disorders of cranial volume and shape. | ||
520 | _aConfidently diagnose and manage primary neurologic disorders of childhood with actionable, step-by-step assistance from Fenichel’s Clinical Pediatric Neurology! A signs-and-symptoms-based approach - with consideration of each presenting symptom in terms of differential diagnosis and treatment - mirrors the way you would typically evaluate and manage a patient. A practical and well-organized introduction to pediatric neurology, this is an ideal resource for board exam preparation, office use, and reference during residency.Quickly identify the progression of each neurological disease. Extensive coverage clearly defines age at onset, course of illness, clinical features, and treatment options.Evaluate and manage even the most difficult neurodegenerative disorders—including those caused by inborn errors of metabolism – with the aid of differential diagnosis tables and treatment algorithms.Search crucial information at a glance. An organization by neurological signs and symptoms, together with a user-friendly, highly templated format allows for quick and easy reference.Rely on it anytime, anywhere! | ||
600 |
_xPediatric neurology _933679 |
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600 |
_x Pediatric neurology -- Diagnosis _943823 |
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_x Health & Fitness -- Children's Health _931257 |
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_xMedical -- Pediatrics _926838 |
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_xPediatric neurology _933679 |
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_xPediatric neurology -- Diagnosis _943824 |
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_x Nervous System Diseases -- diagnosis _936873 |
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_x Nervous System Diseases -- therapy _943038 |
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_x Infant _928528 |
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_x Medical / Pediatrics _926838 |
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_xMedical / Neurology _926948 |
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_xMedical / Clinical Medicine _926816 |
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_x Medical › Neurology _927053 |
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700 |
_aGerald M Fenichel _931976 |
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_2ddc _cBK |
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_c9237 _d9237 |