Neudle.com: brisk reflexes

Neurology Specific Literature Search

Differential
(Click to cross reference)

abdominal distention

abdominal reflex, absent

achilles tendon, enlarged

acute respiratory distress syndrome

Addison's disease

adrenoleukodystrophy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

alcohol intolerance

Alexanders disease

Alexanders disease, adult onset

alien hand syndrome

altered states of consciousness

alternating rapid movement

alternating rapid movement, impaired

Alzheimer's disease

Alzheimer's disease, early onset

Alzheimer's disease, familial

amphiphysin antibodies

amyloid angiopathy, cerebral

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, juvenile

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

anemia, megaloblastic

anesthesia, general

animal exposure

antecedent illness

anterior horn cell disease

anterior tibial muscle weakness

anti GQ1b IgG antibody

antibiotics, neurologic complications with

anticholinergic drugs

anticonvulsants

anticonvulsants, untoward effects of

antiviral agents

aphasia, progressive

apraxia of eye movements

arm swing, reduced

Arnold Chiari malformation

aspartate aminotransferase

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

atherosclerosis, premature

atlanto-axial subluxation

atrial fibrillation

attention deficit disorder with hyperactivity

autoimmune disease

autonomic dysfunction

autosomal dominant leukodystrophy

B 12 deficiency

basal ganglia, lesion of

basilar impression

baylisascariasis

behavior, combative

behavioral disorder

Bickerstaff's brainstem encephalitis

bladder dysfunction

bone marrow transplantation

brain biopsy, false negative

brainstem, atrophy

brainstem, dysfunction

brainstem, ischemia

brainstem, lesion of

bulbar palsy, acute

bulbar palsy, acute-causes of

bulbar palsy, progressive

calcification, intracranial

campylobacter infection

cancer, unknown origin

carbamazepine, toxicity

carbon monoxide poisoning

carcinoma of breast

carcinoma of unknown origin

carpal tunnel syndrome

CAT scan, abnormal

CAT scan, chest

CAT scan, emission, abnormal

CAT scan, metrizamide

CAT scan, myelogram with

CAT scan, spine

caudate nucleus, atrophy

central pontine myelinolysis

cerebellar atrophy, primary

cerebellar lesion

cerebellar plaques, amyloid

cerebral cortical atrophy

cerebral infarction

cerebral venous thrombosis

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, proteincytologic dissociation

cerebrotendinous xanthomatosis

cerebrovascular accident

cervical myelopathy

cervical spine abnormality

cervical spondylosis

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chenodeoxycholic acid

choreoathetosis

chromosomal abnormality

chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids

claudication, intermittent of cauda equina

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cobalamin C deficiency

cogwheel rigidty

cold temperature

compression fracture

conduction block

cone-rod dystrophy

congenital deformities

congenital malformation

congenital malformation, non CNS

congestive heart failure

contractures, joint

conversion reaction

copper deficiency

corpus callosum, atrophy of

corpus callosum, lesion of

cortical-basal ganglionic degeneration

cranial nerve palsies

cranial neuropathy

C-reactive protein, elevated

critical care unit

crossed adductor reflex

crying, pathologic

cyst, parenchymal

deep tendon reflexes

degenerative cervical myelopathy

degenerative diseases of CNS

dementia, familial

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dental prostheses

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diaphragmatic paralysis

diaphragmatic paralysis, causes of

diastematomyelia

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

disability, neurological

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

drug induced neurologic disorders

drug interactions

drug overdose, management of

drug withdrawal

dysdiadochokinesia

dyskinesia, buccal lingual facial

dysostosis multiplex

dystonia musculorum deformens

dystonia, focal

dystonia, treatment of

eclampsia, postpartum

electrical sensation

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, triphasic delta waves

electroretinograph

emergencies, neurologic

emotional lability

encephalitis, brainstem

encephalopathy, delayed

encephalopathy, Hashimoto's

encephalopathy, progressive

entrapment neuropathy

epileptic encephalopathy

Epstein-Barr virus

exome sequencing

extrapyramidal movement disorder, progressive

eye movement, disorders of

facial appearance, abnormal

facial nerve palsy, bilateral

facial weakness

facial weakness, bilateral

failure to thrive

FARS2 deficiency

fatty acid, elevated plasma content

fine motor function, impaired

finger nose finger test

finger numbness

Fisher's syndrome

flaccid paralysis

flail arm syndrome

fontanel, bulging

foot drop, bilateral

Friedreich's ataxia

fundus, abnormality of

gag reflex, depressed

gammaglobulin therapy, intravenous

gastric partitioning

Gaucher's disease

gaze palsy, supranuclear

genetic counselling

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

geographic location

globus pallidus

globus pallidus, lesion of

glucocerebrosidase

glutamic acid decarboxylase, antibody

GM1 ganglioside antibodies

granular osmiphilic material

granulomatous disease

Graves ophthalmopathy

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, variant forms of

hairline, abnormal

Hallervorden Spatz disease

hallucination, auditory

hallucination, visual

head circumference

head retraction reflex

headache, cough

heat intolerance

heel-knee-shin test

helminthic infection of CNS

hepatic failure

hepatosplenomegaly

heralding manifestation

herniated disc, cervical

high arched feet

highly active antiretroviral therapy

homocysteine, serum

human immunodeficiency virus type 1

human T-lymphotropic virus type I(HTLV-I)

Huntington's chorea

Huntington's disease, children

hyperhomocysteinemia

hyperparathyroidism

hyperphosphatasia

hyperpigmentation of skin

hyperthyroidism

hypothalamus, disturbance of

hypotonia, infants

iatrogenic neurologic disorders

imbalance, postural

immunomodulation

immunosuppression

immunosuppressive agents

inability to stand on tiptoes

inappropriate behavior

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intranuclear

incontinence, fecal

incontinentia pigmenti

infection, recurrent

intellectual deficit

intellectual deterioration

internuclear ophthalmoplegia

intrinsic hand muscles, wasting of

jaw jerk, abnormal

klippel feil syndrome

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactic acidemia

laminectomy, cervical

laminectomy, lumbar

laughing, pathologic

leg spasms, painful

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leukemia, neurologic findings assoc.with

leukoencephalopathy

leukoencephalopathy with calcification and cysts

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

Lhermitte's sign

life expectancy

limbic encephalitis

liver function enzymes

locked-in syndrome

lymph node biopsy

lymphadenopathy

lymphadenopathy, axillary

lymphadenopathy, hilar

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

malabsorption syndrome

malformation, CNS, congenital

marche a petits pas

Marcus Gunn pupil

meconium staining

mediastinum, lymph-node biopsy

mediastinum, mass of

medulla oblongata, lesion of

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, CSF cell count-normal

meningitis, eosinophilic

meningoencephalitis

mental retardation

mental status, abnormal

metastasis to bone

methylmalonic acid, serum

methylmalonic acidemia

microangiopathy, brain

middle cerebellar peduncle, lesion, bilateral

Mini Mental Status Examination

mitochondrial disease

molecular genetics

monoamine oxidase inhibitors

motor neuron disease

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, treatment of

MRI, contrast enhanced

MRI, contrast enhanced, high dose

MRI, contrast enhanced, subependymal

MRI, disappearing lesion on

MRI, linear enhancement

MRI, nodular enhancement

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, progressive

muscle stiffness

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

myasthenia gravis

mycobacterium kansasii

myelinolysis, extrapontine

myelitis, longitudinal

myelitis, transverse

myelogram, complications of

myelogram, metrizamide

myeloneuropathy

myelopathy, chronic progressive

myelopathy, tract-specific

myeloradiculopathy

myoclonic jerks

myoclonus, epilepsy

myoclonus, stimulus sensitive

myopathy, distal

myopathy, distal, vacuolar

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, thyroid disease causing

myopathy, vacuolar

nausea and vomiting

nemaline rod myopathy

nemaline rod myopathy, adult onset

neonatal abstinence syndrome

neoplasm, intracranial, congenital

neoplasm, intracranial, infants

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplastic angioendotheliosis

nerve conduction studies

nerve root hypertrophy

neuritis, causes of

neuroaxonal dystrophy

neuroendocrinology

neurogenic bladder

neurologic complications of, chronic pulmonary disease

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic disease

neurologic disease, burden

neurologic disease, diagnoses of

neurologic examination

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuronal ceroid-lipofuscinosis

neuropathology, peripheral nerves

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, peripheral

neuroprotective agents

next-generation sequencing

night blindness

numbness, ascending

numbness, extremity

nutritional deficiency

nystagmus, gaze-evoked

nystagmus, rotary

nystagmus, upbeating on upgaze

ocular dysmetria

odontoid process

ophthalmoplegia

ophthalmoplegia, total

optic nerve, lesion of

optic neuropathy

optical coherence tomography

organ transplantation

orthostatic hypotension

osmotic demyelination syndrome

pain, interscapular

palatal myoclonus

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, spastic

paraparesis, spastic, tropical

parathyroid adenoma

paresthesias, feet

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinson disease, hemiparesis in

Parkinson disease, L-dopa nonresponsive

Parkinson disease, unilateral

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal neurologic deficits

paroxysmal neurologic disorder

periodic paralysis

periodic paralysis, thyrotoxic

perivascular enhancement

pernicious anemia

personality change

phenothiazine, dyskinesia associated with

phenylketonuria

pituitary stalk

pituitary stalk, lesion of

pleocytosis of cerebrospinal fluid

polyglucosan body disease

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, familial

polyradiculoneuropathy

pons, lesion of

position sensation

positive sharp waves

post transplant lymphoproliferative disease

posterior column disease

posterior leukoencephalopathy syndrome

postural abnormality

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

primary lateral sclerosis

primitive neuroectodermal tumors

progressive encephalomyelitis with rigidity syndrome

progressive myoclonic epilepsy

progressive neurologic disorder

pseudoathetosis

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis, acute

pulmonary embolism

pupil, dilated, bilateral

pupil, dilated, episodic

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

release phenomena

remote effect of cancer on the nervous system

renal transplantation

respiratory failure

respiratory tract infection

reticulum cell sarcoma

retina, abnormal

retinal degeneration

retinitis pigmentosa

reversible neurologic disorder

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

Rosenthal fibers

saccadic eye movements, abnormal

sarcoidosis, CNS

scoliosis, neurologic association with

sea-blue histiocytes

sedimentation rate, elevated

seizure, children

seizure, withdrawal

selective serotonin reuptake inhibitors

sensory loss, cortical

serotonin agonist

serotonin syndrome

serum alanine aminotransferase

serum gamma glutamyl transferase

severe acute respiratory syndrome

skin, darkening of

skin, lesions in neurologic disorders

sleep pathology and physiology

sodium valproate

somatosensory evoked potentials

spastic diplegia

speech disorder

speech disorder, childhood

speech, loss of

spinal cord, compression of

spinal cord, dorsal subpial enhancement

spinal cord, injury of

spinal cord, lesion of

spinal stenosis

spinal stenosis, familial

spine, metastasis to

spinocerebellar ataxia

spinocerebellar ataxia type 12

spinocerebellar ataxia type 7

spontaneous remission

standing difficulty

startle reaction

status epilepticus

stem cell rescue

stem cell transplantation

steroid therapy, CNS treatment and complications with

stiff man syndrome

striatonigral degeneration

striatonigral degeneration, infantile

subcortical U fibers

substantia nigra

superior cerebellar peduncle

synucleinopathy

tandem gait, ataxic

teeth, abnormal

teeth, number of in infants

temporal lobe, lesion

temporal lobe, lesion, bilateral

thrombocytopenia

thrombophlebitis

tongue, atrophy

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

tonic foot response

tonsillar herniation of cerebellum

treatment of neurologic disorder

tremor, intention

tricyclic antidepressant

trigeminal nerve

trigeminal nerve, abnormality of

trinucleotide repeats

unconsciousness

unconsciousness, transient

upgaze, paralysis of

urinary frequency

urinary incontinence

urinary retention

urinary urgency

venous thrombosis, non-cerebral

vertebral artery

vertebral artery occlusion

vertebral-basilar insufficiency

vertigo, episodic

vibratory sensation, abnormal

violent behavior

viral infection

viral infection, CNS

vision, blurred

visual acuity, decreased

visual evoked response

visual loss, progressive

visual loss, slow

vitamin deficiency

walking, delayed

walking, difficulty with

weakness, generalized

weakness, progressive

weaning from respirator, failure to

white matter disease

whole body imaging

wide based gait

xanthoma, tendon

x-ray, cervical spine

Showing articles 400 to 450 of 486 << Previous Next >>

Gerstmann-Straussler-Scheinker Disease with Coincidental Familial Onset
Ann Neurol 14:670-678, Hudson,A.J.,et al, 1983

Sexual Automatisms in Complex Partial Seizures
Neurol 33:527-533, Spencer,S.S.,et al, 1983

Classical"Parietal"Neglect Syndrome after Subcortical Right Frontal Lobe Infarction
Neurol 33:797-799, Stein,S.,et al, 1983

Sclerosteosis:Neurogenetic & Pathophysiologic Analysis of an American Kinship
Neurol 33:267-277, Stein,S.A.,et al, 1983

Self-Grasping:A Focal Neurological Sign
Ann Neurol 12:575-577, Ropper,A.H., 1982

Undiagnosed Syncope:Search for an Arrhythmic Etiology
Stroke 13:746-749, Klein,G.J.,et al, 1982

Diagnosis & Management of Diabetic Autonomic Neuropathy
BMJ 285:916-918, Ewing,D.J.,et al, 1982

Ross Syndrome & Skin Changes
Neurol 32:1041-1042, Heath,P.D.,et al, 1982

Cardiomyopathy Associated with the Syndrome of Amyotrophic Chorea & Acanthocytosis
Ann Int Med 96:616-617, Faillace,R.T.,et al, 1982

Primitive Reflexes & Cognitive Function in the Elderly
Ann Neurol 12:302-304, Koller,W.C.,et al, 1982

Spinal Automatism In Cerebral Death
NEJM 307:501, Mandel,S.,et al, 1982

Brainstem Encephalitis & The Syndrome Of Miller Fisher
Brain 105:481-495, Al-Din,A.N.,et al, 1982

Clinical Significance of the Corneomandibular Reflex
Arch Neurol 39:578-580, Guberman,A., 1982

Transient Areflexia & Quadriplegia Following Metrizamide Myelography
Ann Neurol 12:406-407, Peroutka,S.J.,et al, 1982

Significance of Cortical Disinhibition Signs
Neurol 32:169-173, Tweedy,J.,et al, 1982

Clin. Path. Conference
Adrenoleukodystrophy, with Peripheral Neuropathy, Case Record 5-1982, NEJM 306:286-29382., , 1982

Fibrodysplasia Ossificans Progressiva, The Clinical Features & Natural Hx of 34 Pts
J Bone Joint Surg 64B:76-83, Connor,J.M.&Evans,D.A.P., 1982

Neurologic Signs In Uncomplicated Aging (Senscence)
Seminars In Neurology, Thieme-Stratton Inc. , New York, N. Y. pp. 21-30, Jenkyn,L.R.&Reeves,A.G., 1981

Neurological Manifestation of Accidental Hypothermia
Ann Neurol 10:384-387, Fischbeck,K.H.,et al, 1981

Guidelines for the Determination of Death
JAMA 246:2184-2186, , 1981

Neurologic Prognosis After Cardiopulmonary Arrest:IV. Brainstem Reflexes
Neurol 31:1092-1097, Snyder,B.D.,et al, 1981

Depression-Induced Neurologic Dysfunction
NEJM 305:642, Brumback,R.A.,et al, 1981

Intracardiac Electrophysiologic Techniques in Recurrent Syncope of Unknown Cause
Ann Int Med 95:542-548, DiMarco,J.P.,et al, 1981

Urinary Retention as a Sole Symptom of Intracranial Calcified Mass at the Rolandic Fissure
Ann Neurol 10:61-62, Kuroiwa,Y.,et al, 1981

A Progressive Neurologic Syndrome In Children With Chronic Liver Disease
NEJM 304:503-508, Rosenblum,J.L.,et al, 1981

Motor Neuropathy Associated with Cimetidine
BMJ 281:974-975, Walls,T.J.,et al, 1980

Abetalipoproteinemia, Report of Two Cases & Review of Therapy
Arch Neurol 37:659-662, Illingworth,D.R.,et al, 1980

Infantile Neuronal Degeneration Masquerading as Werdnig-Hoffmann Disease
Ann Neurol 8:317-324, Steiman,G.S.,et al, 1980

Fetal Hydantoin Syndrome, Neuroblastoma, & Hemorrhagic Disease in a Neonate
Jr. , et al, JAMA 244:1464-146580., Allen,R.W., 1980

Three Primitive Reflexes in Normal Adults
Neurol 30:184-188, Jacobs,L.,et al, 1980

The Acute Sensory Neuronopathy Syndrome:A Distinct Clinical Entity
Ann Neurol 7:354-358, Sterman,A.B.,et al, 1980

Jaw Reflex in Friedreich Ataxia
Neurol 29:1049-1050, Salisachs,P., 1979

Isaac Syndrome with Laryngeal Involvement:An Unusual Presentation of Myokymia
Neurol 29:1612-1615, Jackson,D.L.,et al, 1979

Familial Degeneration of the Basal Ganglia with Acanthocytosis:a Clinical Neuropathological, & Neurochemical Study
Ann Neurol 3:253, Bird,T.D.,et al, 1978

Dominant Spinopontine Atrophy
Arch Neurol 35:156, Pogacar,S.,et al, 1978

Polyneuropathy in Waldenstrom's Macroglobulinemia
Arch Neurol 35:423, Julien,J.,et al, 1978

Neuropathy Following Abuse of Nitrous Oxide
. et al, Neurol 28:504978., Layzer,R.B., 1978

The Third Alexia
Arch Neurol 34:327, Benson,D.F., 1977

Azorean Disease of the Nervous System
NEJM 296:1505, Romanul,F.C.A.,et al, 1977

Elevated Manganese Levels Associated with Dementia & Extrapyramidal Signs
Neurol 27:213, Banta,R.G.,et al, 1977

Fisher's Syndrome:A Pharmacological Study of the Pupils
Ann Neurol 2:63, Okajima,T.,et al, 1977

Lid Abnormalities Secondary to Cerebral Hemisphere Lesions
Ann Neurol 1:149, Nutt,J.G., 1977

Cervical Myelographic Changes in Hypertrophic Interstitial Polyneuropathy
Ann Neurol 2:83, Hammerschlag,S.B.,et al, 1977

Reversible Subacute Peripheral Neuropathy Induced by Phenytoin
Arch Neurol 34:189, Dobkin,B.H., 1977

Paroxysmal Choreoathetosis as a Presenting Symptom in Idiopathic Hypoparathyroidism
JNNP 40:692, Soffer,D.,et al, 1977

A Syndrome of Early Recognition of Occult Hydrocephalus & Cerebral Atrophy
Quart J Med 183:365, Botez,M.I.,et al, 1977

Clinical Pathologic Conference, Creutzfeldt-Jakob Disease, (Case record 43-1977)
NEJM 297:930, Scully,R.E.,et al, 1977

Guillain-Barre Syndrome with Hydrocephalus in Early Infancy
Arch Neurol 34:567, Gilmartin,R.C.,et al, 1977

Tonic Pupils with Acute Ophthalmoplegic Polyneuritis
Ann Neurol 2:393, Keane,J.R., 1977

Methyl Bromide Intoxication:Neurologic Features, Including Simulation of Reye Syndrome
Neurol 27:959, Shield,L.K.,et al, 1977

Showing articles 400 to 450 of 486 << Previous Next >>