Neudle.com: "sensory ataxia"

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Differential
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abducens nerve paralysis

acral sensory symptoms

Addison's disease

adrenoleukodystrophy

adrenomyeloneuropathy

adult polyglucosan body disease

adverse drug reaction

alcohol intolerance

alien hand syndrome

alkylating agents

altered states of consciousness

alternating rapid movement

amaurosis fugax

amphiphysin antibodies

anemia, megaloblastic

angiography, spinal

antecedent illness

anterior choroidal artery

anti GQ1b IgG antibody

anti Hu antibody

anti Ri antibody

anti Yo antibody

antiamphiphysin

antibiotics, neurologic complications with

antiganglioside antibodies

arrhythmia, cardiac

arterial dissection, vertebral

ascending paralysis

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

ataxic hemiparesis

auditory evoked brainstem potentials

autoimmune disease

autonomic dysfunction

autonomic neuropathy

axonal degeneration

axonopathy, distal

B 12 deficiency

basal ganglia, lesion of

Bassen-Kornzweig syndrome

behavioral disorder

Bell's phenomenon

bladder dysfunction

blood dyscrasias, neurologic findings with

bovine spongiform encephalopathy

brainstem, hematoma

brainstem, hemorrhage, primary

brainstem, infarction of

brainstem, lesion of

brainstem, syndrome

burning paresthesia

carcinoma of breast

carcinoma of cervix

carcinoma of lung

carcinoma of ovary

carcinoma of uterus

carpal tunnel syndrome

CAT scan, abnormal

CAT scan, chest

CAT scan, false negative

caudate nucleus, atrophy

cavernous hemangioma

central nervous system, infection of

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemorrhage

cerebellar infarction

cerebellar lesion

cerebellar peduncle

cerebellar vermis

cerebellum, disease of

cerebral cortical atrophy

cerebral infarction

cerebro hepato renal syndrome

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure low

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, vascular territory involved

cervical myelopathy

Charcot-Marie-Tooth

Cheiro-oral syndrome

chemotherapy, CNS treatment and complications with

choreoathetosis

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

Cockayne's syndrome

collagen vascular disease

collapsin response mediator protein 5 IgG

concentration, impaired

conduction block

congestive heart failure

contactin associated protein like 2 antibodies

conus medullaris, lesion of

convergence, impaired

conversion reaction

copper deficiency

cortical-basal ganglionic degeneration

cranial nerve palsies

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

deafness, unilateral

deep gray nuclei

delay in diagnosis

demyelinating disease

dermatomyositis

dexterity, impaired

diagnostic criteria

differential diagnosis

difficulty climbing stairs

disability, neurological

dissociated sensory loss

distal muscle weakness

down-beat nystagmus

drug induced neurologic disorders

dural arteriovenous malformation

dysarthria-clumsy hand syndrome

dysdiadochokinesia

dyskinesia, buccal lingual facial

dystrophic calcification

ejection fraction, abnormal

electrical sensation

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electronystagmography

electroretinograph

emotional lability

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

encephalomyelitis

encephalomyelitis, paraneoplastic

enzyme, muscle disease

epidemiology of neurology

erythema migrans

evoked potentials

exercise-induced leg numbness

exercise-induced vascular symptoms

eye movement, disorders of

face, numbness of

facial nerve palsy

facial nerve palsy, bilateral

facial weakness

facial weakness, bilateral

family planning

fine motor function, impaired

Fisher's syndrome

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

flaccid paralysis

flu-like illness

fluorescent treponema antibody absorption(FTA-ABS)

food-borne infection

Friedreich's ataxia

Friedreich's ataxia, late onset

fundus, abnormality of

gammaglobulin therapy, intravenous

gasserian ganglia

gastrectomy, neurologic complications following

gastric partitioning

gastroenteritis

gaze palsy, horizontal

genetic counselling

genetic linkage

genetic neurologic disorders

genetic testing

girdle sensation

gluten sensitivity

Guillain Barre syndrome

Guillain Barre syndrome, ataxic form

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, ophthalmoplegia in

Guillain Barre syndrome, prognosis of

Guillain Barre syndrome, sensory

Guillain Barre syndrome, variant forms of

Hallervorden Spatz disease

hallucination, visual

headache, severe

headache, sudden onset of

heel-knee-shin test

hemianopia, homonymous

hemisensory loss

hemisensory syndrome

hemorrhage, thalamic

herpes simplex virus

herpes virus infection

herpes, genital

Hodgkin's disease

homocysteine, serum

Horner's syndrome

hot cross bun sign

human immunodeficiency virus type 1

hyperhomocysteinemia

hypersegmented polys

hypophosphatemia

iatrogenic neurologic disorders

immune checkpoint inhibitors

immunologic disease

immunology and the nervous system

immunosuppressive agents

inappropriate antidiuretic(A.D.H.)hormone

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inclusion bodies

incontinence, fecal

intellectual deficit

internal capsule

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intracerebral hemorrhage

intracerebral hemorrhage, small

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

Kearns-Sayre syndrome

Korsakoff's psychosis

kyphoscoliosis, neurologic causes of

lactic dehydrogenase(LDH)

lacunar infarction

lacunar infarction, differential diagnosis of

lateral medullary syndrome

Laurence-Moon-Bardet-Biedl syndrome

leg weakness, bilateral

Leigh's disease

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

leukoencephalopathy

Lhermitte's sign

limbic encephalitis

listeria monocytogenes

listeriosis, CNS

lymph node biopsy

lymphadenopathy

lymphadenopathy, hilar

macular degeneration

malformation, vascular

malignancy screen

malignancy, occult

medial medullary syndrome

mediastinum, mass of

medulla oblongata, infarction of

memory, impairment of

meningitis, aseptic

meningitis, chronic

meningoencephalopathy

meningomyelitis

mental retardation

mental status, abnormal

methylhydrazine derivatives

methylmalonic acid, serum

methylmalonic acidemia

midbrain, atrophy

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

Minamata disease

mitochondrial disease

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

molecular genetics

monoamine oxidase inhibitors

monoclonal gammopathy

monoclonal gammopathy of uncertain significance

mononeuritis multiplex

mononeuropathy multiplex

motor dysfunction

movement disorder

movement disorder, psychogenic

MRI, angiography

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, contrast enhanced, subependymal

MRI, disappearing lesion on

MRI, flow void, blood

MRI, mass effect on

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

mucopolysaccharidoses

multiple sclerosis

muscle atrophy, progressive

muscle weakness

muscle weakness, proximal

muscular dystrophy

myasthenia gravis, paraneoplastic

myasthenic syndrome

myelitis, longitudinal

myeloneuropathy

myelopathy, ascending

myelopathy, chronic progressive

myopathy, mitochondrial

myopathy, proximal

nasal septum, perforation of

nausea and vomiting

nerve conduction studies

nerve conduction studies, sensory

nerve growth factor

nerve root enhancement

neurofibromatosis 1

neurogenic bladder

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic examination

neurologic signs

neurologic symptoms

neuromuscular junction

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronopathy, sensory

neuroophthalmology

neuropathology, brain

neuropathy, amyloid

neuropathy, ataxic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, motor, multifocal

neuropathy, onion bulb

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, recurrent

neuropathy, sensory

neuropathy, small-fiber

neuropathy, small-fiber, painful sensory

neuropathy, toxic

neuropathy, vasculitic, systemic

next-generation sequencing

night blindness

nitrogen mustard

NMDA antagonists

non-dominant hemisphere

numbness, ascending

numbness, extremity

numbness, generalized

nystagmus, dissociated

nystagmus, gaze-evoked

nystagmus, upbeating on upgaze

nystagmus, vertical

old age, neurology of

onconeural antibodies

one and a half syndrome

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, progressive external

ophthalmoplegia, recurrent

ophthalmoplegia, total

opsoclonus-myoclonus syndrome

optic neuropathy

orthostatic hypotension

otitis, neurologic complications with

overlap syndrome

pain, abdominal

pain, neuropathic

pain, testicular

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paraneoplastic ganglionopathy

paraparesis, spastic

parenteral alimentation

paresthesias, feet

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinsonism syndrome

pathologic reflex

periarteritis nodosa

perineum, numbness of

perioral numbness

peripheral blood smear

peripheral blood smear, abnormal

peripheral nerve, lesion of

pernicious anemia

peroxisomal disease

personality change

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

poison, mercury

polyclonal gammopathy

polyglucosan body

polyglucosan body disease

polyneuritis, acute sensory

polyneuropathy, acute sensory

polyneuropathy, chronic idiopathic

polyneuropathy, chronic idiopathic, ataxic

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic inflammatory demyelinating, variant form

polyneuropathy, chronic inflammatory demyelinating-pure motor syn

polyneuropathy, chronic inflammatory demyelinating-sens atax var

polyneuropathy, chronic inflammatory demyelinating-variant forms

polyneuropathy, chronic relapsing

polyradiculoneuropathy

pons, infarction of

pons, lesion of

pontine hemorrhage

position sensation

position sensation, abnormal

positional head-hanging test

posterior column disease

posterior inferior cerebellar artery syndrome

postoperative neurologic complications

progressive neurologic disorder

proprioception, abnormal

pseudoathetosis

psychiatric problems in neurologic disorders

psychological testing

ptosis, bilateral

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, dilated, bilateral

pupil, light reflex, abnormal

pure motor hemiplegia

pure sensory stroke

pyramidal tract

pyramidal tract dysfunction

Raynaud's phenomenon

reading disorder, acquired

real-time quaking-induced conversion

rectal sphincter tone, decreased

reflex, cutaneous

refractive errors

Refsum's disease

remote effect of cancer on the nervous system

respiratory failure

respiratory tract infection

retinal artery occlusion

retinal degeneration

retinitis pigmentosa

reversible neurologic disorder

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

Riley-Day syndrome

saccadic eye movements, abnormal

sarcoidosis, CNS

scleroderma, neurologic involvement with

sedimentation rate, elevated

seizure, hysterical

sensorimotor stroke

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory loss, asymmetric

sensory loss, band distribution

sensory loss, cortical

sensory loss, crossed pattern

sensory loss, cutaneous

sensory loss, leg

sensory loss, patchy

sensory loss, truncal

sensory nerve action potentials

sensory polyneuropathy

sensory symptoms

serologic testing

shell fish poisoning

Shy-Drager syndrome

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

small vessel disease

somatosensory evoked potentials

speech disorder

speech disorder, non aphasic

spinal cord, biopsy

spinal cord, cervical

spinal cord, compression of

spinal cord, dorsal subpial enhancement

spinal cord, enlargement

spinal cord, lesion of

spinal cord, neoplasm, intramedullary

spinal cord, vascular malformation of

spinocerebellar ataxia

spinocerebellar ataxia type 6

spinocerebellar degeneration

spongy degeneration of brain

starvation, therapeutic

steroid therapy, CNS treatment and complications with

stiff man syndrome

strokelike episodes

superior cerebellar artery syndrome

suspended sensory loss

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

systemic illness

tandem gait, ataxic

tapetoretinal degeneration

testicular biopsy

thalamic ataxia syndrome

thalamic syndrome

thalamus, infarction of

thalamus, lesion of

thalamus, lesion of-bilateral

third nerve palsy

tongue, numbness of

tongue, swelling

tongue, weakness

toxic encephalopathy

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

tremor, thalamic

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

ulcers, fingertip

upgaze, paralysis of

urinary frequency

urinary incontinence

urinary retention

urinary urgency

Usher's syndrome

vertebral artery occlusion

vertebral artery stenosis

vibratory sensation

vibratory sensation, abnormal

vincristine neurotoxicity

viral infection

vision, blurred

visual evoked response

visual field defect

visual fields, constricted

vitamin deficiency

vitamin E deficiency

vitamin, multiple

vocal cord paralysis

voice, abnormality of

walking, difficulty with

weakness, functional

weakness, generalized

weakness, progressive

white matter disease

wide based gait

Showing articles 0 to 50 of 1760 Next >>

Expanding Clinical Spectrum an Anti-GQ1b Antibody Syndrome, A Review
JAMA Neurol 81:762-770, Lee,S-U.,et al, 2024

Clinicopathologic Conference, Functional Vitamin B12 Deficiency from Use of Nitrous Oxide
NEJM 388:1893-1900, Case 15-2023, 2023

A 48-Year-Old Man With Spasticity and Progressive Ataxia
Neurol 101:e1747-e1752, Vizcarra,J.A.,et al, 2023

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

Functional Neurological Disorders
Neurologist 27:276-289, Mishra, A. & Pandey, S., 2022

Miller Fisher Syndrome and Acute Motor and Sensory Axonal Neuropathy (AMSAN) Variant Guillain-Barre Overlap Syndrome (MFS/AMSAN-GBS) After Upper Respiratory Tract Infection (URTI)
Acta Sci Clin Case Reports 3:19-24, Chau,T.C. & Muhamad,N.A.N., 2022

Paraneoplastic Myeloneuropathies
Neurol 96:e632-e639, Shah, S.,et al, 2021

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

A 49-Year-OLD Woman with Progressive Numbness and Gait Instability
Neurol 97:342-347, Zahid, A.,et al, 2021

Pernicious Anaemia
BMJ 369:m1319, Mohamed, M.,et al, 2020

A 57-Year-Old Woman with Progressive Ataxia and Falls
Neurol 95:650-656, Badahdah, A., 2020

Sensory Ganglionopathy
NEJM 383:1657-1662, Amato, A.A. & Ropper, A.H., 2020

Orofacial Dyskinesia in a Young Man
JAMA Neurol 76:1517-1518, Tian, X.,et al, 2019

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019

A 78-year-old Man with a Gait Disorder
Neurol 93:223-227, Saucedo, M.,et al, 2019

A 55-Year-Old Woman Presenting with Ataxia and Numbness 1 Year After Ileum Resection
Neurol 93:675-679, Cassano, V.,et al, 2019

A 58-year-old Woman with Systemic Scleroderma and Progressive Cervical Cord Compression
Neurol 91:e1262-e1264, Karschnia, P.,et al, 2018

Reversible Gait Ataxia
Neurol 88:e145-e149, Abkur, T.M. & Bede, P., 2017

A 58-year-old man with Progressive Ptosis and Walking Difficulty
Neurol 89:e1-e5, Kuo, P.,et al, 2017

The Useless Hand of Oppenheim
Pract Neurol 17:464-468, Wiblin, L. & Guadagno, J., 2017

Copper Deficiency
BMJ 348:g3691, Chhetri, S.K.,et al, 2014

Diseases of the Nervous System Caused by Nutritional Deficiency, Vitamin B12 (Cobalamin) Deficiency (Subacute Combined Degeneration)
Adams & Victors Principles of Neurology Chp 41, pg 1172, Ropper, A.H.,et al, 2014

Paraneoplastic Neurological Syndromes
Clin Exp Immunol 175:336-348, Leypoldt, F. & Wandinger, K.-P., 2014

A Man with Tingling Fingers
BMJ 346:f1443, Larkman, M.,et al, 2013

Clinical Reasoning: A Middle-Aged Woman with Progressive Symmetric Weakness and a CSF Pleocytosis
Neurol 78:e88-e92, Marks,D.,et al, 2012

Clinicalpathologic Conference, Vitamin B12 Deficiency due to Pernicious Anemia
NEJM 366:1626-1633, Case 13-2012, 2012

Exercise-Associated Numbness and Tingling in the Legs
Arch Neurol 68:1599-1602, Sharp, L.,et al, 2011

Clinicopathologic Conference, Sjogrens syndrome with dorsal-root ganglionitis
NEJM 364:1856-1865, Case 14-2011, 2011

A Strange Case of Waitress Headache
Lancet 378:1824, Libera, D.D.,et al, 2011

Copper Deficiency as a Treatable Cause of Poor Balance
BMJ 340:864-866, Khaleeli,Z., et al, 2010

Sensory Ganglionopathy Due to Gluten Sensitivity
Neurol 75:1003-1008, Hadjivassiliou,M.,et al, 2010

A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia
Neurol 72:1262-1276, DiMauro,S.,et al, 2009

A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
Neurol 72:1607-1613, Lossos,A.,et al, 2009

Neuro-Ophthalmologic Manifestations of Paraneoplastic Syndromes
J Neuro-Ophthalmol 28:58-68, Ko,M.W.,et al, 2008

Ataxic vs Painful Form of Paraneoplastic Neuropathy
Neurol 69:564-572, Oki,Y.,et al, 2007

Spinal dural arteriovenous fistulas: a congestive myelopathy that initially mimics a peripheral nerve disorder
Brain 129:3150-3164, Jellema, K., et al, 2006

Five New Cases of a Recently Described Leukoencephalopathy with High Brain Lactate
Neurol 63:688-692, Linnankivi,T.,et al, 2004

Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders
Arch Neurol 61:875-880, Smith,C.O.,et al, 2004

Spectrum of Paraneoplastic Neurologic Disorders in Women with Breast and Gynecologic Cancer
Medicine 82:216-223, Rojas-Marcos,I.,et al, 2003

Spinal Dural Arteriovenous Fistulas: Clinical Features in 80 Patients
JNNP 74:1438-1440, Jellema,K.,et al, 2003

Clinicopath Conf, Lymphocytic Meningitis and Lymphocytic Encephalomyelitis, Sensory Neuronopathy, Gangliositis, Small-Cell Carcinoma of Lung
NEJM 345:1758-1765, Case 38-2001, 2001

Paraneoplastic Syndromes
Arch Neurol 56:405-408, Dalmau,J.O.&Posner,J.B., 1999

Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
Arch Neurol 55:957-961, Kompoliti,K.,et al, 1998

Ataxic Hemiparesis,Critical Appraisal of a Lacunar Syndrome
Stroke 29:2549-2555, Gorman,M. J.,et al, 1998

Lateral Medullary Infarction
Stroke, Pathophysiology, Diagnosis and management, Churchhill Livingstone, NY 3rd Ed, Ch 22, p. 534, Amarenco,P.,et al, 1998

Hypophosphatemia-Induced Neuropathy: Clinical and Electrophysiologic Findings
Muscle Nerve 21:650-652, Siddiqui,M.F. &Bertorini,T.E., 1998

Pain After Thalamic Stroke:Right Diencephalic Predominance and Clinical Features in 180 Patients
Neurol 48:1196-1199, Nasreddine,Z.S.&Saver,J.L., 1997

New Variant Creutzfeldt-Jakob Disease:Neurological Features and Diagnostic Tests
Lancet 350:903-907, Zeidler,M.,et al, 1997

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997

Showing articles 0 to 50 of 1760 Next >>