Neudle.com: Romberg s sign

Neurology Specific Literature Search

Differential
(Click to cross reference)

abdominal reflex, absent

acute disseminated encephalomyelitis

Addison's disease

adult polyglucosan body disease

alcohol, neurologic complications with

alternating rapid movement

alternating rapid movement, impaired

amphiphysin antibodies

anemia, megaloblastic

anesthesia, general

aneurysm, cavernous sinus

aneurysm, internal carotid artery

ankle reflex, absent

antiviral agents

Argyll Robertson pupil

arrhythmia, cardiac

arterial dissection, aorta

arteriovenous malformation

arteriovenous malformation, cerebral

ataxia, cerebellar

ataxia, progressive

ataxia, sensory

ataxia, truncal

autonomic dysfunction

axonal degeneration

B 12 deficiency

bacterial endocarditis, neurologic manifestations of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

behavioral disorder, acute

benign positional vertigo

bladder dysfunction

brain biopsy, stereotaxic

brainstem, atrophy

Brudzinski's sign

burning paresthesia

calcification, intracranial

caloric testing

carcinoma of breast

carcinoma of lung

CAT scan, abnormal

CAT scan, chest

CAT scan, delta sign, empty

CAT scan, emission, abnormal

CAT scan, ring sign

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

cavernous sinus, syndrome

central nervous system, infection of

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar atrophy, secondary

cerebellar hemangioma

cerebellar hemorrhage

cerebellar vermis

cerebral cortex

cerebral embolism

cerebral venous thrombosis

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, infancy and childhood

Chaddock's sign

Charcot-Marie-Tooth

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cogwheel rigidty

conduction block

cone-rod dystrophy

congenital heart disease, CNS complications with

congestive heart failure

copper deficiency

corkscrew hairs

cranial nerve palsies

Creutzfeldt-Jakob disease, genetic

deafness, unilateral

deep gray nuclei

Dejerine's sign

delay in diagnosis

dementia, rapidly progressive

dementia, subcortical

dental procedure, neurologic complications with

dexterity, impaired

diabetes mellitus

differential diagnosis

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

down-beat nystagmus

drug abuse, inhalation

drug abuse, neurologic complications of

drug induced neurologic disorders

dural sinus thrombosis

dysdiadochokinesia

electrical sensation

electroretinograph

emotional lability

encephalomyelitis, paraneoplastic

encephalopathy, anoxic

encephalopathy, delayed

encephalopathy, post anoxic

endocarditis, neurologic manifestations with

erectile dysfunction

evoked potentials

executive dysfunction

exome sequencing

extrapyramidal movement disorder, progressive

eye movement, disorders of

face, numbness of

fine motor function, impaired

finger nose finger test

finger numbness

fistula, perilymphatic

fluorescent treponema antibody absorption(FTA-ABS)

fluorescent treponema antibody absorption/false positive

foot drop, bilateral

Friedreich's ataxia

Fukuda step test

fundus, abnormality of

F-wave response

gastric partitioning

general paresis of the insane

genetic counselling

genetic neurologic disorders

genetic testing

hearing loss, bilateral

hearing loss, sudden, bilateral

hearing loss, unilateral

heel-knee-shin test

hemangioma, brainstem

hemianopia, homonymous

hemifacial atrophy

herpes simplex virus

herpes simplex virus, human nervous system and

heterochromia iridis

high arched feet

hip flexor weakness

Hoffmann's sign

homocysteine, serum

Horner's syndrome

Horner's syndrome, etiologies of

hot cross bun sign

human immunodeficiency virus type 1

hyperhomocysteinemia

hypersegmented polys

hyperviscosity fundus

hypoxic encephalopathy

imbalance, postural

immune checkpoint inhibitors

immunohistochemistry

immunosuppressive agents

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

incontinence, fecal

intellectual deterioration

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, Heidenhain variant

Jakob-Creutzfeldt disease, variant

labyrinth, disorder of

labyrinthitis, acute

lactic dehydrogenase(LDH)

leg weakness, bilateral

Leigh's disease

leukoencephalopathy

leukoencephalopathy, differential diagnosis

Lhermitte's sign

lymph node biopsy

lymphadenopathy

lymphadenopathy, hilar

lymphoma involving CNS

lymphoma, primary of CNS

malformation, vascular

marche a petits pas

mediastinum, lymph-node biopsy

mediastinum, mass of

memory, defect of recent

memory, impairment of

Meniere's disease

meningitis, aseptic

meningitis, neutrophilic

meningitis, syphilitic

meningovascular syphilis

mental status, abnormal

methylmalonic acid, serum

methylmalonic acidemia

Mini Mental Status Examination

mitochondrial disease

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

molecular genetics

monoclonal antibodies

monoclonal gammopathy

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, contrast enhanced

MRI, contrast enhanced, subependymal

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, high signal foci on

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple system atrophy

mycotic aneurysm

myelitis, longitudinal

myeloneuropathy

myelopathy, tract-specific

myoclonic jerks

myoclonus, action

myoclonus, cortical

myoclonus, post anoxic

myoclonus, stimulus sensitive

nausea and vomiting

nerve conduction studies

nerve conduction studies, sensory

neuroendocrinology

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination

neurologic signs

neurologic symptoms

neuronal intranuclear inclusion disease

neuronopathy, sensory

neuropathology, brain

neuropathy, hereditary peripheral

neuropathy, sensory

neuropathy, toxic

night blindness

numbness, ascending

numbness, extremity

nutritional deficiency

nystagmus, direction fixed

nystagmus, rotary

nystagmus, spontaneous

nystagmus, vertical

occipital cortex

occipital lobe, lesion of

optical coherence tomography

orthostatic hypotension

otitis, neurologic complications with

pain, abdominal

palmomental response

papilledema, differential diagnosis of

paraneoplastic ganglionopathy

paratrigeminal syndrome

paresthesias, feet

paresthesias, generalized

paresthesias, hands

Parkinson disease, L-dopa nonresponsive

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal neurologic deficits

perifollicular hemorrhage

peripheral blood smear, abnormal

pernicious anemia

personality change

pleocytosis of cerebrospinal fluid

polyglucosan body disease

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, familial

position sensation

position sensation, abnormal

posterior column disease

posterior fossa, arteriovenous malformation

posterior fossa, lesion of

posterior inferior cerebellar artery syndrome

postural abnormality

progressive hemifacial atrophy

progressive neurologic disorder

proprioception, abnormal

protein 14-3-3, cerebrospinal fluid, false negative

protein S deficiency

pseudoathetosis

psychiatric disorder

psychiatric problems in neurologic disorders

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pursuit eye movements, abnormal

rapidly progressing neurologic illness

real-time quaking-induced conversion

remote effect of cancer on the nervous system

respiratory failure

retina, abnormal

retinal degeneration

reversible neurologic disorder

rheumatoid arthritis factor(R.A.factor)

saccadic eye movements, abnormal

sarcoidosis, CNS

scleroderma, neurologic involvement with

sedimentation rate, elevated

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory loss, asymmetric

sensory loss, leg

sensory loss, patchy

sensory loss, truncal

sensory nerve action potentials

serologic testing

Sjogren's syndrome

skin, lesions in neurologic disorders

sleep pathology and physiology

spinal cord, dorsal subpial enhancement

spinal cord, lesion of

spinocerebellar ataxia

spinocerebellar ataxia type 7

spirochete infection

spontaneous remission

square wave jerks

startle myoclonus

stem cell transplantation

steroid therapy, CNS treatment and complications with

subarachnoid hemorrhage

subcortical U fibers

superior sagittal sinus thrombosis

symmetric brain lesions

synucleinopathy

syphilis, asymptomatic

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

syphilis, ocular

systemic illness

systemic lupus erythematosus

tandem gait, ataxic

thalamus, lesion of-bilateral

tongue, swelling

transposition of the great vessels

treatment of neurologic disorder

tremor, postural

trinucleotide repeats

urinary frequency

urinary incontinence

valsalva maneuver

vascular endothelial growth factor

Venereal Disease Research Laboratory test

vertigo, episodic

vestibular areflexia

vestibular neuritis

vibratory sensation

vibratory sensation, abnormal

viral infection

vision, blurred

visual evoked response

visual loss, progressive

visual loss, slow

vitamin deficiency

walking, difficulty with

walking, difficulty with in dark

weakness, acute

weakness, focal

weakness, progressive

Wernicke's encephalopathy

white matter disease

wide based gait

word-finding difficulty

Showing articles 2150 to 2200 of 2417 << Previous Next >>

Spinocerebellar Degeneration Secondary to Chronic Intestinal Malabsorption:A Vitamin E Deficiency Syndrome
Ann Neurol 12:419-424, Harding,A.E.,et al, 1982

Neurologic Complications of Primary Sjogren's Syndrome
Medicine 61:247-257, Alexander,E.L.,et al, 1982

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

Lhermitte's Sign in Behcet's Disease
BMJ 284:704-705, , 1982

Clinical & Electrophysiological Studies in Primary Lateral Sclerosis
Jr. , Arch Neurol 39:662-664982., Russo,L.S., 1982

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

Auscultatory Percussion of the Head
BMJ 284:1075-1077, Guarino,J.R., 1982

Truncal Ataxia in Terminal Bronchial Carcinoma
Arch Neurol 39:787-788, Puvanendran,K., 1982

Neuroaxonal Dystrophy in Young Adults:A Clinicopathological Study of Two Unrelated Cases
Ann Neurol 11:335-343, Williamson,K.,et al, 1982

CT Abnormalities of the Pituitary in Hyperprolactinaemic Women with Normal or Equivocal Sellae Radiologically
BMJ 285:1078-1081, Jung,R.T.,et al, 1982

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

Peripheral Neuropathy & Starvation After Gastric Partitioning for Morbid Obesity
Ann Int Med 96:453-455, Feit,H.,et al, 1982

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

Progressive Hemifacial Atrophy
Arch Neurol 39:44-46, Asher,S.W.,et al, 1982

Primary Cerebellopontine Progressive Multifocal Leukoencephalopathy Diagnosed Premortem by Cerebellar Biopsy
Ann Neurol 11:199-202, Jones,H.R.,et al, 1982

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

Lhermitte's Sign in Multiple Sclerosis:A Clinical Survey & Review of the Literature
JNNP 45:308-312, Kanchandani,R.,et al, 1982

Tethered Cord Syndrome in Adults
J Neurosurg 57:32-47, Pang,D.&Wilberger,J.E.Jr., 1982

Clin. Path. Conference
Fibrillary Astrocytoma of Medulla, with Invasion of Subarachnoid Space, Case Record 6-1981, NEJM 304, 3430,1981., 1981

Ataxia with Aniridia of Gillespie:A Case Report
Neurol 31:95-97, Lechtenberg,R.,et al, 1981

Post-encephalitic Parkinsonism:Current Experience
JNNP 44:670-676, Rail,D.,et al, 1981

Encephalopathy in Infants & Children With Chronic Renal Disease
Arch Neurol 38:656-658, Foley,C.M.,et al, 1981

Progressive Infantile Poliodystrophy, Assoc. With Disturbed Pyruvate Oxidation in Muscle & Liver
Arch Neurol 38:767-772, Prick,M.J.J.,et al, 1981

Multiple Sclerosis:Large Plaque Causing Mass Effect & Ring Sign
J Comput Assist Tomogr 5:892-894, Nelson,M.J.,et al, 1981

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

Pronounced Cerebellar Features in Legionnaires'Disease
BMJ 283:276, Maskill,M.R., 1981

Changes in the Basal Ganglia Following Cyanide Poisoning
J Comput Assist Tomogr 5:755-756, Finelli,P.F., 1981

Heredopathia Atactica Polyneuritiformis
Arch Neurol 38:605-606, Refsum,S., 1981

Biotin-Responsive Carboxylase Deficiency Associated With Subnormal Plasma & Urinary Biotin
NEJM 304:817-820, Thoene,J.,et al, 1981

Computed Tomography in Cerebrotendinous Xanthomatosis
Neurol 31:1463-1465, Berginer,V.M.,et al, 1981

Effect Of Thyrotropin-Releasing Hormone On Ataxia Of Spinocerebellar Degeneration
Lancet 1:418-419, Sobue,I.,et al, 1981

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

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

Cerebellar Atrophy Demonstrated by Computed Tomography
Neurol 31:405-412, Koller,W.C.,et al, 1981

Multiple Spontaneous Intracerebral Hematomas:Clinical & Computed Tomographic Correlations
Neurol 31:897-900, Weisberg,L., 1981

Double-blind, Triple-crossover Trial of Low Doses of Oral Physostigmine in Inherited Ataxias
Neurol 31:288-292, Kark,R.A.P.,et al, 1981

Lhermitte's Sign in Cobalamin (Vitamin B12) Deficiency
JAMA 245:1059, Butler,W.M.,et al, 1981

Tick Paralysis With Persistent Weakness & Electromyographic Abnormalities
Arch Neurol 38:59-61, Donat,J.R., 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

Neurologic Complications of Lymphomatoid Granulomatosis
Neurol 31:619-620, Hogan,P.J.,et al, 1981

Temporal Arteritis Presenting as Ataxia and Dementia
Post Grad Med 69:246-249, Shenberger,K.N.,et al, 1981

Nervous System Toxicity of Chemo Agents
Young, DF, in Vinken PJ, Bruyn GW, Handbook of Clin Neurol, North-Holland Publ Co, Amster, Vol 39, 1, 80, p 104, 1980

The False Falx Sign
Radiology 134:421-425, Osborn,A.G.,et al, 1980

A Family with Hereditary Ataxia:HLA Typing
Neurol 30:12-20, Nino,H.E.,et al, 1980

Clinical Criteria for Diagnosis of Machado-Joseph Disease:Report of a Non-Azorean Portuguese Family
Neurol 30:319-322, Lima,L.,et al, 1980

Progressive & Treatable Cerebellar Ataxia in Macroglobulinemia
Neurol 30:536-538, Spencer,S.S.,et al, 1980

Creutzfeldt-Jakob Disease in a 20-year-old Woman
Neurol 30:492-496, Packer,R.J.,et al, 1980

Acute Cerebellar Ataxia Associated With Epstein-Barr Virus Infection
JAMA 243:148-149, Cleary,T.G.,et al, 1980

Mycoplasma Antibody in Guillain-Barre Syndrome & Other Neurological Disorders
Ann Neurol 7:108-112, Goldschmidt,B.,et al, 1980

Cerebellar Involvement in Multifocal Eosinophilic Granuloma:Demonstration by CT Scan
Ann Neurol 7:125-129, Adornato,B.T.,et al, 1980

Showing articles 2150 to 2200 of 2417 << Previous Next >>