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acral sensory symptoms

Addison's disease

adrenomyeloneuropathy

adult polyglucosan body disease

adverse drug reaction

alternating rapid movement

alternating rapid movement, impaired

amyotrophic lateral sclerosis, differential diagnosis

angiography, cerebral, beaded vessels

angiography, cerebral

ankle reflex, absent

anorexia nervosa

anti citrullinated antibody

anti MAG antibodies

anticonvulsants

anticonvulsants, untoward effects of

arrhythmia, cardiac

ascending paralysis

ataxia telangiectasia

ataxia, cerebellar

ataxia, progressive

ataxia, sensory

ataxia, truncal

atrophy, muscle

auditory evoked brainstem potentials

autonomic dysfunction

axonal degeneration

axonopathy, distal

B 12 deficiency

basal ganglia, lesion of

basophilic stippling of red blood cells

biologic markers

bladder dysfunction

bone marrow suppression

brainstem, infarction of

burning paresthesia

cardiac arrest and resuscitation

CAT scan, abdomen

CAT scan, abnormal

CAT scan, emission, abnormal

cauda equina, enhancement

cauda equina, lesion of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar lesion

cerebellum, disease of

cerebrospinal fluid, abnormal

cerebrospinal fluid, drainage of

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, mimics

Charcot-Marie-Tooth

chest x-ray, abnormal

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

compression neuropathy

conduction block

congenital myopathy

congestive heart failure

corneal reflex, abnormal

corneal reflex, absent

cranial nerve enhancement

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

deep gray nuclei

demyelinating disease

denervation potentials

descending paralysis

dexterity, impaired

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic mononeuropathy

differential diagnosis

difficulty climbing stairs

digital health, wearable technology

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

dysdiadochokinesia

edema, periorbital

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electroencephalogram, inflammatory disease

electromyogram, decremental response

electron microscopy

entrapment neuropathy

enzyme, muscle disease

evoked potentials

exome sequencing

eye movement, disorders of

face, numbness of

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failed medical management

fall prevention

fine motor function, impaired

fingernails, abnormal

flaccid paralysis

Friedreich's ataxia

F-wave response

gammaglobulin therapy, intravenous

gastroenteritis

genetic counselling

genetic neurologic disorders

genetic testing

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, infantile and childhood form

Guillain Barre syndrome, sensory

headache, severe

heavy metal intoxication

heel-knee-shin test

hepatosplenomegaly

heralding manifestation

herpes simplex virus

herpes virus infection

herpes, genital

high arched feet

hip flexor weakness

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

hot cross bun sign

hydrocephalus, normal pressure

hydrocephalus, treatment of

hyperamylasemia

hypophosphatemia

hypopigmentation of skin

imbalance, postural

immunoelectrophoresis, serum

immunohistochemistry

immunomodulation

immunosuppression

immunosuppressive agents

inappropriate antidiuretic(A.D.H.)hormone

inclusion bodies

industrial neurologic disorders

intellectual deficit

intellectual deterioration

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

lactic dehydrogenase(LDH)

leg weakness, bilateral

leg weakness, unilateral

leukoencephalopathy

lid closure, weakness of

liver function enzymes

long bone lesion

lumbosacral plexopathy

lymphadenopathy

McLeod syndrome

mediastinum, mass of

memory, impairment of

meningeal enhancement

mental status, abnormal

midbrain, atrophy

midbrain, infarction of

molecular genetics

monoclonal gammopathy

mononeuritis multiplex

mononeuropathy chronic inflammatory demyelinating

mononeuropathy, children

movement disorder

MRI, contrast enhanced

MRI, lumbosacral plexus

MRI, peripheral nerve

MRI, spinal cord

multiple myeloma

muscle atrophy, progressive

muscle hypertrophy

muscle hypertrophy, congenital

muscle stiffness

muscle tenderness

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, facioscapulohumeral

myasthenia gravis

myasthenia gravis, late-onset

myasthenia gravis, misdiagnosis of

myasthenia gravis, presenting manifestations

myelin protein zero gene

myeloma, osteosclerotic

myeloneuropathy

myoclonic jerks

myopathy, focal

myopathy, monomelic

nausea and vomiting

neoplasm, primary intracerebral

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve enlargement

nerve hypertrophy

nerve root biopsy

nerve root enhancement

nerve root hypertrophy

neuritis, heavy metals causing

neuroendocrinology

neurogenic bladder

neurologic complications of, surgery

neurologic disease

neurologic disease, diagnoses of

neuromuscular disease, electrodiagnosis of

neuronopathy, sensory

neuronopathy, sensory and motor

neuropathology, brain

neuropathy, chronic

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, toxic

neuropathy, vasculitic, systemic

night blindness

numbness, extremity

numbness, generalized

occupational neuropathies

old age, neurology of

opportunistic infection

ornithine transcarbamylase deficiency

orthostatic hypotension

pain, abdominal

pain, total body

paraneoplastic ganglionopathy

paraparesis, spastic

paraproteinemia

parenteral alimentation

paresthesias, feet

paresthesias, hands

Parkinson disease

Parkinson disease, diagnosis

Parkinson disease, early symptoms

Parkinson disease, presymptomatic detection

periarteritis nodosa

pericardial effusion

perioral numbness

peripheral blood smear

peripheral blood smear, abnormal

peroneal nerve palsy

peroneal nerve palsy, bilateral

peroneal nerve, lesion of

pleocytosis of cerebrospinal fluid

pleural effusion

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic inflammatory demyelinating, childhood

polyradiculoneuropathy

position sensation, abnormal

positional head-hanging test

posterior column disease

postoperative neurologic complications

prevention of neurologic disorders

progressive neurologic disorder

proprioception, abnormal

pseudohypertrophy

psychological testing

pulmonary infiltrates

pupil, dilated and fixed, bilateral

pyramidal tract dysfunction

quadriceps atrophy

reading disorder, acquired

real-time quaking-induced conversion

remote effect of cancer on the nervous system

renal cell carcinoma

repetitive nerve stimulation

respiratory failure

retroperitoneal mass

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

rheumatoid arthritis, neurologic complications of

rheumatoid vasculitis

Sabin-Feldman dye test

saccadic eye movements, abnormal

sciatic neuropathy

sclerosis, bone

sedimentation rate

sedimentation rate, elevated

sensory ganglia

sensory ganglia, abnormal

sensory loss, asymmetric

sensory loss, band distribution

sensory polyneuropathy

serum glutamic oxaloacetic transaminase

shoulder-girdle wasting

shunt procedure, ventricular

Sjogren's syndrome

skin, lesions in neurologic disorders

sodium valproate

sodium valproate, toxicity

somatosensory evoked potentials

speech disorder

speech disorder, non aphasic

steroid therapy, CNS treatment and complications with

suspended sensory loss

sweating, abnormality of

systemic illness

tandem gait, ataxic

temporalis muscle wasting

thiamine deficiency

thrombocytopenia

tongue, fasciculations of

toxoplasma complement fixation test

toxoplasmosis, acquired

toxoplasmosis, CNS

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

tremor, postural

trigeminal nerve, abnormality of

urea-cycle enzymopathies

urinary incontinence

urine test in toxic screen

varicella zoster virus

vascular endothelial growth factor

vestibular migraine

vibratory sensation

vibratory sensation, abnormal

viral infection

viral infection, CNS

visual impairment

vitamin deficiency

vitamin E deficiency

voice, abnormality of

walking, difficulty with

weakness, fatiguable

weakness, generalized

weakness, progressive

whistle, inability to

white matter disease

wide based gait

winging of scapula

zoster sine herpete

Showing articles 1400 to 1450 of 2661 << Previous Next >>

Mycoplasma Pneumoniae Infection Associated with an Acute Brainstem Syndrome
Acta Neurol Scand 93:203-206, OBrien, P.M.,et al, 1996

Clin Electrophy & Molec Correl in 13 Families with Hered Neurop with Liabil to Press Palsies & Chromosome 17p11. 2 Deletion
Neurol 45:2018-2023, Gouider,R.,et al, 1995

Autonomic and Peripheral Neuropathies in Patients with Chronic Alcoholism
Arch Neurol 52:45-51, Monforte,R.,et al, 1995

Effect of Intensive Diabetes Treatment on Nerve Conduction
Diabetes Control and Complication Trial (DCCT) Reserach Group, Ann Neurol 38:869-88095., , 1995

The Effect of Deprenyl and Levodopa on the Progression of Parkinson's Disease
Ann Neurol 38:771-777, Olanow,C.W.,et al, 1995

Complementary Positron Emission Tomographic Studies of the Striatal Dopaminergic System in Parkinson's Disease
Arch Neurol 52:1183-1190, Antonini,A.,et al, 1995

MRI In Patients with Suspected Vascular Parkinsonism
Neurol 45:2183-2188, Jijlmans,J.C.M.,et al, 1995

Early Differential Diagnosis of Parkinson's Disease with F-flurodeoxyglucose and Positron Emission Tomography
Neurol 45:1995-2004, Eidelberg,D.,et al, 1995

Effect of GPi Pallidotomy on Motor Function in Parkinson's Disease
Lancet 346:1383-1387, Lozano,A.M.,et al, 1995

Clinical and[18F]dopa PET Findings in Early Parkinson's Disease
JNNP 59:597-600, Morrish,P.K.,et al, 1995

Generalized Mitochondrial Dysfunction in Parkinson's Disease Detected by Magnetic Resonance Spectroscopy of Muscle
Neurol 45:2097-2099, Penn,A.M.W.,et al, 1995

Decreased SPECT[123I]B-CIT Striatal Uptake Correlates with Symptom Severity in Parkinson's Disease
Ann Neurol 38:589-598, Seibyl,J.P.,et al, 1995

Esophageal Carcinoma Metastatic to the Brain:Clin Value & Cost-Effect of Enhanced Head CT Before Esophagectomy
AJNR 16:1915-1921, Gabrielsen,T.O.,et al, 1995

Comparison of Therapeutic Effects & Mortality Data of Levodopa & Levodopa with Selegiline in Pts with Early, Mild Parkinson's
BMJ 311:1602-1607, 15831995., Lee,A.J.,et al, 1995

Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
Lancet 1458-1463, Barrett,T.G.,et al, 1995

Neurological Sequelae of Cyanide Intoxication-The Patterns of Clinical MRI & Pet Findings
Ann Neurol 38:825-828, Rosenow,F.,et al, 1995

Investigations of Disorders of Balance
JNNP 59:568-578, Rudge,P.&Bronstein,A.M., 1995

Clinical and Topographical Range of Callosal Infarction:A Clinical and Radiological Correlation Study
JNNP 59:238-242, Giroud,M.&Duman,R., 1995

Medial Medullary Syndrome:Report of 18 New Patients and a Review of the Literature
Stroke 26:1548-1552, Kim,J.S.,et al, 1995

Levorotatory Form of 5-Hydroxytryptophan in Friedreich's Ataxia
Arch Neurol 52:456-460, Trouillas,P.,et al, 1995

Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
Arch Neurol 52:451-455, 4401995., Wessel,K.,et al, 1995

Kayser-Fleischer Ring:Hepatolenticular Degeneration (Wilson's Disease)
Neurol 45:1261-1262, Finelli,P.F., 1995

Neuroleptic Drug Exposure and Treatment of Parkinsonism in the Elderly:A Case-Control Study
Am J Med 99:48-54, Avorn,J.,et al, 1995

Low-Dose Clozapine in the Treatment of Levodopa-Induced Mental Disturbances in Parkinson's Disease
Neurol 45:432-434, Rabey,J.M.,et al, 1995

Clinicopath Conf
Granulomatous Angiitis of CNS, Case 33-1995, NEJM 333:1135-1143995., , 1995

Adult-Onset Spinocerebellar Dysfunction Caused by a Mutation in the Gene for the a-Tocopherol-Transfer Protein
NEJM 333:1313-1318, 13511995., Gotoda,T.,et al, 1995

Primary Orthostatic Tremor
BMJ 310:143-144, Britton,T.C.&Thompson,P.D., 1995

Effect on Parkinsonian Signs and Symptoms of Bilateral Subthalamic Nucleus Stimulation
Lancet 345:91-95, Limousin,P.,et al, 1995

Neurologic Aspects of Inflammatory Bowel Disease
Neurol 45:416-421, Lossos,A.,et al, 1995

Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
Muscle & Nerve 18:267-275995., Ionasecu,V.V., 1995

Comparative Study of Selegiline Plus L-Dopa-Carbidopa VS L-Dopa-Carbidopa Alone in Trtm of Parkinson's Disease
Ann Neurol 37:95-98, Brannan,T.&Yahr,M.D., 1995

Clinicopathological Study of 35 Cases of Multiple System Atrophy
JNNP 58:160-166, Wenning,G.K.,et al, 1995

Some Specific Clinical Features Differentiate Multiple System Atrophy (Striatonigral Variety) from Parkinson's Disease
Arch Neurol 52:294-298, Colosimo,C.,et al, 1995

Different of Multi Syst Atrophy from Idiopathic Parkinson's Disease Using Proton MR Spectroscopy
Ann Neurol 37:204-210, Davie,C.A.,et al, 1995

Drug Treatment of Parkinson's Disease
BMJ 310:575-579, Quinn,N., 1995

Parkinsonism-Recognition and Differential Diagnosis
BMJ 310:447-452, Quinn,N., 1995

Classic Neurogenic Thoracic Outlet Syndrome in a Competitive Swimmer:A True Scalenus Anticus Syndrome
Muscle & Nerve 18:229-233995., Katirji,B.&Hardy,R.W., 1995

Clinicopath Conf
Neurolymphomatosis, Case 8-1995, NEJM 332:730-737995., , 1995

Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,et al, 1995

Leukoencephalopathy with Swelling & A Discrepantly Mild Clinical Course in Eight Children
Ann Neurol 37:324-334, van der Knaap,M.S.,et al, 1995

A Novel Mutation in Exon 3 of the Proteolipid Protein Gene in Pelizaeus-Merzabacher Disease
Neurol 45:394-395, Pratt,V.M.,et al, 1995

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
Neurol 45:1-5, Rosenberg,R.N., 1995

Investigation of Peripheral Neuropathy
JNNP 58:274-283, McLeod,J.G., 1995

Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
Ann Neurol 37:769-775, Ikeuchi,T.,et al, 1995

Apolipoprotein E Genotype in Diverse Neurodegenerative Disorders
Ann Neurol 38:131-135, Schneider,J.A.,et al, 1995

Neurotox of Antimicrob & Antimalarial Agents
In Intox of Nervous System, Part II, Handbk Clin Neurol, Elsevier Science 21 (65) :471., Moorhouse,D.F.,et al, 1995

Prolonged Paralysis After Neuromuscular Blockage
Muscle & Nerve, 18:937-94295., Gooch,J., 1995

Exacerbation of Idiopathic Parkinson's Disease by Naproxen
BMJ 311:422, Shaunak,S.,et al, 1995

Encephalopathy with Parkinsonian Features in Children Following Bone Marrow Transplantations and High-Dose Amphotericin B
Ann Neurol 37:810-814, Mott,S.H.,et al, 1995

Showing articles 1400 to 1450 of 2661 << Previous Next >>