Neudle.com: stiff limb syndrome

Neurology Specific Literature Search

Differential
(Click to cross reference)

abdominal reflex, absent

abducens nerve paralysis

abscess, spinal cord

achilles tendon, enlarged

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome myelopathy

acquired immunodeficiency syndrome, infants and children

acute disseminated encephalomyelitis

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

alcohol injection

alcohol intolerance

alcohol, neurologic complications with

Alexanders disease

Alexanders disease, adult onset

alien hand syndrome

alkylating agents

altered states of consciousness

alternating hemiplegia

amphiphysin antibodies

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, juvenile

anemia, megaloblastic

anesthesia, general

aneurysm, anterior communicating

aneurysm, intracranial

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiography, cerebral, beaded vessels

angiography, cerebral

angiography, neurologic complications with

angiography, spinal

animal exposure

ankylosing spondylitis

anterior horn cell disease

anterior spinal artery

antibiotics, neurologic complications with

anticonvulsants

anticonvulsants, untoward effects of

aphasia, progressive, primary

apraxia of eye movements

arrhythmia, cardiac

arteritis, temporal

arthrogryposis multiplex

ataxia, cerebellar

ataxia, progressive

ataxia, truncal

atlanto-axial subluxation

atrioventricular block

auditory and vestibular pathways

autoimmune disease

autonomic dysfunction

azidodeoxythymidine

B 12 deficiency

bacterial infection

bacterial infection, CNS

basal ganglia, calcification of

basal ganglia, lesion of

behavioral disorder

Behcet's syndrome

bladder dysfunction

blepharophimosis

blood brain barrier

blood dyscrasias, neurologic findings with

blood transfusion

bone marrow biopsy

Borrelia burgdorferi infection

Borrelia miyamotoi infection

brachial plexus neuropathy

brainstem, dysfunction

brainstem, infarction of

brainstem, lesion of

Brown Sequard syndrome

Brown-Vialetto-Van Laere syndrome

brucellosis, nervous system involvement with

bulbar palsy, progressive

burning feet, differential diagnosis of

burning paresthesia

calcification, intracranial

calf hypertrophy

cancer, unknown origin

carcinoma of breast

carcinoma of pancreas

carcinoma of stomach

carcinoma of unknown origin

cardiovascular disease

carotid angiogram

carpal tunnel syndrome

carpo-pedal spasm

CAT scan, abnormal

CAT scan, chest

CAT scan, emission, abnormal

CAT scan, serial

CAT scan, spine

cauda equina, enhancement

cauda equina, lesion of

cavernous hemangioma

cavernous sinus

cavernous sinus syndrome, bilateral

cavernous sinus, syndrome

central core disease

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar edema

cerebellar lesion

cerebellum, disease of

cerebral cortical atrophy

cerebral embolism

cerebral palsy, associated problems with

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, appearance of

cerebrospinal fluid, cloudy

cerebrospinal fluid, culture of, viral

cerebrospinal fluid, cytology

cerebrospinal fluid, cytology, false negative

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, eosinophilia of

cerebrospinal fluid, flow cytometry

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure low

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, recurrent

cerebrovascular disease

cervical myelopathy

cervical spine abnormality

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

chewing, impaired

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

concentration, impaired

conduction block

congenital myopathy

congenital myopathy, inflammatory

congestive heart failure

Congo red stain

conjugate gaze, forced

contractures, joint

conversion reaction

copper deficiency

corpus callosum, thinning

cortical-basal ganglionic degeneration

Coxiella burnetti

cranial nerve enhancement

cranial nerve palsies

cranial nerve palsies, bilateral

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase MB isoenzyme elevation

creatine phosphokinase(CPK)elevated

crossed adductor reflex

crying, pathologic

cytomegalic inclusion disease

cytomegalovirus infection

dantrolene sodium

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

degenerative cervical myelopathy

degenerative diseases of CNS

delay in diagnosis

dementia, familial

dementia, reversible

dementia, subcortical

dementia, treatment of

demyelinating disease

dental prostheses

dermatomyositis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diagnostic criteria

diarrhea, bloody

differential diagnosis

diffuse idiopathic skeletal hyperostosis

digital subtraction angiography

digits, abnormal

diplegia, atonic

disability, neurological

dislocated hip, congenital

distal muscle atrophy

distal muscle weakness

drug abuse, neurologic complications of

drug induced neurologic disorders

dysarthria-clumsy hand syndrome

dysequilibrium syndrome

dysferlinopathy

dyskinesia, buccal lingual facial

dystonia musculorum deformens

dystonia, cervical

dystrophic calcification

ears of the Lynx MR sign

electrical sensation

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electron microscopy

embolization, therapeutic

emergencies, neurologic

Emery-Dreifuss muscular dystrophy

emotional lability

empyema, epidural

empyema, epidural-spinal

empyema, subdural-spinal

encephalitis, Powassan

encephalitis, viral

encephalomyelitis

encephalomyelitis, parainfectious

encephalomyelitis, postinfectious

encephalopathy, metabolic

encephalopathy, progressive

endovascular therapy

enterovirus infection of CNS

enzyme, muscle disease

eosinophilia-myalgia syndrome

eosinophilic fasciitis

epicanthal folds

epidemiology of neurology

epilepsia partialis continua

erythema migrans

evoked potentials

exercise intolerance

eye movement, disorders of

eye movement, painful

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, recurrent

facial weakness

facial weakness, bilateral

failure to thrive

fatty acid, elevated plasma content

fine motor function, impaired

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

flaccid paralysis

flu-like illness

fluorescent treponema antibody absorption(FTA-ABS)

fourth ventricle, compression

frontal behavioral spatial syndrome

frontal lobe, pathologic signs of

frontal lobe, space occupying lesion of

fungal infection, CNS

F-wave response

gamma amino butyric acid

gammaglobulin therapy, intravenous

gastric partitioning

gastrocnemius muscle weakness

gastroenteritis

gaze palsy, supranuclear

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic testing

geographic location

girdle sensation

glutamic acid decarboxylase, antibody

glycogen storage disease

Gowers maneuver

gram negative rod

granulomatosis with polyangiitis

granulomatous disease

Guillain Barre syndrome

Guillain Barre syndrome, etiology of

hallucination, visual

headache, bifrontal

headache, positional

headache, progressive

headache, recurrent

headache, severe

headache, vascular

headache, worst of life

heart block, complete

hemangioma, vertebral

hematoma, intracerebral

hematopoietic tissue, extramedullary

hematuria, microscopic

hemiparesis, transient

hemoglobin abnormality, neurologic complications of

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hepatic failure

hepatosplenomegaly

heralding manifestation

herniated disc, cervical

herniated disc, differential diagnosis of

high arched feet

histochemistry of muscle

Horner's syndrome

human immunodeficiency virus type 1

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

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

hydrocephalus, congenital

hydrocephalus, fetal

hydrocephalus, intrauterine

hyperparathyroidism

hyperpigmentation of skin

hypersegmented polys

hypertension, cerebrovascular disease with

hyperthyroidism

hypertriglyceridemia

hypofibrinogenemia

hypoglycorrhachia

hypokinetic left ventricle

hypomyelination

hypoparathyroidism

hypopigmentation of skin

hypotonia, infants

iatrogenic neurologic disorders

imbalance, postural

immediate recall

immunoelectrophoresis, serum

immunohistochemistry

immunologic disease

immunosuppression

immunosuppressive agents

inability to stand on tiptoes

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

inborn errors of metabolism

inclusion bodies

inclusion body myositis

incontinence, fecal

intellectual deficit

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

intracerebral hemorrhage

intracerebral hemorrhage, causes of

intracerebral hemorrhage, differential diagnosis of

intracerebral hemorrhage, lobar

intracerebral hemorrhage, multiple

intracranial hypertension, benign

intracranial pressure, increased

Isaacs syndrome

ischemic exercise test

Jamaica ginger paralysis

joint hypermobility

klippel feil syndrome

Korsakoff's psychosis

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

laminectomy, cervical

laughing, pathologic

learning disability

learning disability, in children

leg spasms, painful

leg weakness, bilateral

Leigh's disease

lens, dislocation of

leukemia, neurologic findings assoc.with

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

Lhermitte's sign

limbic encephalitis

locked-in syndrome

lymphadenopathy

lymphadenopathy, axillary

lymphadenopathy, cervical

lymphocytic meningoradiculitis

lymphoma involving CNS

lymphomatoid granulomatosis

malabsorption syndrome

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, dural

malformation, vascular, treatment of

malignant hyperpyrexia

marche a petits pas

McArdle's disease

medulla oblongata

medulla oblongata, infarction of

medulla oblongata, lesion of

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningeal enhancement

meningeal sarcomatosis

meningitis, aseptic

meningitis, bacterial

meningitis, brucellosis

meningitis, carcinomatous

meningitis, children

meningitis, factors influencing mortality in

meningitis, late neurologic sequelae in

meningitis, leukemic

meningitis, neurologic aspects and complications of

meningitis, neutrophilic

meningitis, recurrent

meningitis, treatment of

meningoencephalitis

meningoencephalomyelitis

meningoencephalopathy

meningomyelitis

meningovascular syphilis

mental retardation

mental status, abnormal

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

methylhydrazine derivatives

midbrain, infarction of

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitral valve prolapse

molecular genetics

monoamine oxidase inhibitors

mononeuritis multiplex

mononeuropathy multiplex

motor dysfunction

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, angiography

MRI, angiography, contrast enhanced

MRI, brachial plexus

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, false negative

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, sulcal hyperintensity

MRI, target sign

multinucleated giant cell

multiple sclerosis

multiple sclerosis, acute

multiple sclerosis, chronic progressive

multiple sclerosis, diet in

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, prognosis

multiple sclerosis, treatment of

muscle atrophy, progressive

muscle atrophy, static

muscle diseases, characteristics of

muscle hypertrophy

muscle phosphorylase deficiency

muscle stiffness

muscle strength, testing

muscle tenderness

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, congenital, Ullrich

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, familial incidence of

myasthenic crisis

myasthenic syndrome

myasthenic syndrome, treatment of

mycoplasma pneumoniae

myelitis, longitudinal

myelitis, post infectious

myelitis, transverse

myeloneuropathy

myelopathy, chronic progressive

myelopathy, necrotizing

myelopathy, transverse

myelopathy, vacuolar

myelopathy, venous hypertensive

myeloradiculopathy

myocardial biopsy

myoclonic jerks

myoclonus, epilepsy

myopathy, amyloid

myopathy, carcinomatous

myopathy, hypocalcemic

myopathy, necrotizing

myopathy, thyroid disease causing

myopathy, vacuolar

myositis, ocular

myotonia congenita

myotonia dystrophica

myxedema, neurologic manifestations of

Native Americans

nausea and vomiting

neoplasm, metastatic to CNS-origin of

neoplasm, primary intracranial

neoplasm, primary of CNS

nerve conduction studies

nerve conduction studies, motor

nerve root enhancement

neuritis, causes of

neurocutaneous disease

neuroendocrinology

neurogenic bladder

neuroichthyosis

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic disease, tempo

neurologic examination

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuropathology, brain

neuropathy, diabetic

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, peripheral

neuropathy, sensory

neuropathy, vasculitic, systemic

neuroradiology, interventional

nitrogen mustard

numb clumsy hands syndrome

numbness, extremity

nutritional deficiency

nystagmus, dissociated

nystagmus, rotary

nystagmus, vertical

occupational neurologic disorders

oculodentodigital dysplasia

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegic migraine

opportunistic infection

optic nerve, lesion of

optic neuropathy

oral ulcerations

orange peel appearance of skin

orthostatic hypotension

overlap syndrome

pacemaker, cardiac-transvenous

pain, abdominal

palatal myoclonus

paralysis, acute

paralysis, acute areflexic

parameningeal infection

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, flaccid

paraparesis, painful

paraparesis, spastic

paraparesis, spastic, tropical

paraplegia, acute

parathyroid adenoma

paresthesias, feet

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinson disease, L-dopa nonresponsive

Parkinsonism syndrome

percussion induced muscle contraction

periarteritis nodosa

periodic paralysis, thyrotoxic

pernicious anemia

peroneal nerve palsy

peroneal nerve, lesion of

personality change

phenylketonuria

phenylketonuria, adult onset

phosphorylase b kinase deficiency

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

poison, organophosphate

poliomyelitis-like illness

polycythemia, primary

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, uremic

portal caval shunt

positive sharp waves

posterior column disease

posterior longitudinal ligament, ossification of

postural abnormality

potassium channel antibodies

precipitating factors

primary lateral sclerosis

prisoners of war, neurologic complications in

progressive neurologic disorder

progressive supranuclear palsy

proprioception, abnormal

proximal muscle atrophy

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

ptosis, bilateral

pulmonary edema

pulmonary infiltrates

pure motor stroke

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis, progressive

quadriplegia, transient

radiation encephalopathy, delayed

radiation therapy, CNS treatment and complications with

rapidly progressing neurologic illness

rectal sphincter tone, decreased

regional enteritis

release phenomena

remote effect of cancer on the nervous system

renal transplantation

renal tubular acidosis

repetitive nerve stimulation

respiratory failure

respiratory tract infection

restless leg syndrome

reticulum cell sarcoma

retinitis pigmentosa

retro-orbital pain

reversible neurologic disorder

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

riboflavin transporter deficiency

rickettsial organism

rigid spine syndrome

rippling muscle disease

root lesion, nerve

Rosenthal fibers

saccadic eye movements, abnormal

sarcoidosis, CNS

Schilder's disease

Schmidt syndrome

Schwartz-Jampel syndrome

scoliosis, neurologic association with

second wind phenomena

sedimentation rate, elevated

seizure, children

sensorineural hearing loss

sensory loss, cortical

sensory loss, cutaneous

sensory symptoms

serologic testing

serologic testing of cerebrospinal fluid

sickle cell disease

Sjogren-Larsson syndrome

skin, darkening of

skin, lesions in neurologic disorders

skin, thickened

sodium valproate

solitary scerlosis

somatosensory evoked potentials

spastic paraplegia, type 11

speech disorder

speech, loss of

spinal cord, biopsy

spinal cord, cervical

spinal cord, compression of

spinal cord, compression, epidural abscess causing

spinal cord, enlargement

spinal cord, herniation

spinal cord, infarction of

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, extramedullary

spinal cord, neoplasm, extramedullary intradural

spinal cord, pathologic exam of

spinal cord, vascular disorders Affecting

spinal cord, vascular malformation of

spinal stenosis

spinal stenosis, cervical canal

spinal xanthomatosis

spine, tenderness

spirochete infection

status epilepticus

steroid therapy, CNS treatment and complications with

stiff limb syndrome

stiff man syndrome

striatonigral degeneration

striatonigral degeneration, infantile

subarachnoid hemorrhage

subcortical U fibers

subdural hematoma

sulfite oxidase deficiency

sweating, abnormality of

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

teeth, abnormal

temporalis muscle wasting

tendon, enlarged

thalamus, lesion of

thrombocytopenia

tick-borne encephalitis

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

toxic oil syndrome

toxins, nervous system

toxoplasmosis, acquired

toxoplasmosis, CNS

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

treatment, empirical

tremor, intention

Trousseau's sign

tuberculoma of CNS

tuberculosis, spinal

type 1 muscle fiber

type 2 muscle fiber

ulcerative colitis

upward deviation of eyes

uremic encephalopathy

uremic twitching

urinary frequency

urinary incontinence

urinary urgency

varicella zoster virus

venous engorgement

ventricular tachycardia

vertigo, cervical

vertigo, treatment of

vibratory sensation, abnormal

vincristine neurotoxicity

viral infection

viral infection, CNS

viral isolation

vision, blurred

vision, blurred, monocular

visual acuity, decreased

visual evoked response

visual obscurations, transient

vitamin deficiency

vocal cord paralysis

Walker-Warburg syndrome

walking, difficulty with

weakness, acute

weakness, congenital

weakness, episodic

weakness, generalized

weakness, progressive

weakness, proximal

Werdnig-Hoffman disease

Werner's syndrome

Wernicke's encephalopathy

West Nile fever

Western immunoblot test

white matter disease

whole body imaging

wide based gait

winging of scapula

word-finding difficulty

xanthoma, tendon

x-linked hydrocephalus

x-ray, cervical spine

zoster sine herpete

Showing articles 50 to 100 of 1886 << Previous Next >>

The Hereditary Spastic Paraplegias
Arch Neurol 60:1045-1049, Fink,J.K., 2003

Prevalence and Clinical Features of HTLV Neurologic Disease in the HTLV Outcomes Study
Neurol 61:1588-1594, Orland,J.R.,et al, 2003

Phenylketonuria Presenting in Adulthood as Progressive Spastic Paraparesis With Dementia
JNNP 71:795-797, Kasim,S.,et al, 2001

Recurrent Reversible Paraplegia
Lancet 357:1092, Haran,M. & Ni,S., 2001

Neuromuscular Findings in Thyroid Dysfunction: A Prospective Clinical and Electrodiagnostic Study
JNNP 68:750-755, Duyff,R.F. et al, 2000

Phenotypic Variability in Rippling Muscle Disease
Neurol 52:1453-1459, Vorgerd,M.,et al, 1999

Amyloid Myopathy:An Underdiagnosed Entity
Ann Neurol 43:719-728, Spuler,S.,et al, 1999

The Stiff-Person Syndrome:An Autoimmune Disorder Affecting Neurotransmission of y-Aminobutyric Acid
Ann Int Med 131:522-530, Levy,L.M.,et al, 1999

Spastic Paraparesis after Anaesthesia
Lancet 353:554, Lee,P.,et al, 1999

Primary and Transitional Progressive MS,A Clinical and MRI Cross-Sectional Study
Neurol 52:839-845, Stevenson,V.L.,et al, 1999

Review of 23 Patients Affected by the Stiff Man Syndrome:Clinical Subdivision into Stiff Trunk (man) Syndrome,Stiff Limb Syndrome,and Progressive Encephalopmyelitis with Rigidity
JNNP 65:633-640, Barker,R.A.et al, 1998

Granulomatous Compressive Thoracic Myelopathy as the Initial Manifestation of Wegener's Granulomatosis
Neurol 51:1769-1770, Kelly,P.J.,et al, 1998

MR Appearance of an Intracranial Dural Arteriovenous Fistula Leading to Cervical Myelopathy
Neurol 51:1131-1135, Hahnel,S.,et al, 1998

Stiff-Leg Syndrome:A Focal Form of Stiff-Man Syndrome
Ann Neurol 43:400-403, Saiz,A.,et al, 1998

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

Idiopathic Granulomatous Angiitis of the CNS Manifesting as Diffuse White Matter Disease
Neurol 49:1696-1699, Finelli,P.F.,et al, 1997

HTLV-Associated Myelopathy in a Cohort of HTLV-I and HTLV-II Infected Blood Donors
neurol 48:315-320, Murphy,E.L.,et al, 1997

Progressive Deterioration of Intellect and Motor Function Occurring Several Decades after Cranial Irradiation
ARch Neurol 53:814-818, Duffey,P.,et al, 1996

Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
Neurol 46:810-814, Connolly,A.M.,et al, 1996

Hereditary Spastic Paraplegia:Advances in Genetic Research
Neurol 46:1507-1514, Fink,J.K.,et al, 1996

Cognitive and Brain Magnetic Resonance Imaging Findings in Adrenomyeloneuropathy
Ann Neurol 40:675-678, Edwin,D.,et al, 1996

Total Alopecia, Diabetes Mellitus, and Falls
Lancet 348:1420, Mueller-Schoop,J.W., 1996

Human T-Cell Lymphotrophic Virus Type II-Associated Myelopathy:Clinical and Immunologic Profiles
Ann Neurol 40:714-723, Lenky,T.J.,et al, 1996

Clinicopath Conf
Acute Disseminated Encephalomyelitis, (postviral encephalomyelitis) Case 37-1995, NEJM 333:1485-1493, 199, 1995

Acquired Neuromyotonia:Evidence for Autoantibodies Directed Against K+Channels of Peripheral Nerves
Ann Neurol 38:714-722, 7011995., Shillito,P.,et al, 1995

Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
Neurol 45:2266-2271, Schwankhaus,J.D.,et al, 1995

Clinicopath Conf
Arteritis, Unclassified, with Giant-Cell Reaction & Multiple Infarcts of the Brain & Neuropathy, Cas, 5-199532:452-459,1995., 1995

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

Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
Lancet 345:161-162, Jouet,M.&Kenwrick,S., 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

Adverse Outcomes of Bacterial meningitis in School-Age Survivors
Pediatrics 95:646-655, Grimwood,K.,et al, 1995

Combined System Disease after Nitrous Oxide Anesthesia:A Case Report
Neurol 45:1224-1225, McMorrow,A.M.,et al, 1995

X-Linked Pure Familial Spastic Paraparesis
Arch Neurol 52:665-669, Cambi,F.,et al, 1995

Spinal Dural Arteriovenous Fistula:The Pathology of Venous Hypertensive Myelopathy
Neurol 45:1309-1313, Hurst,R.W.,et al, 1995

Clinicopathologic Correlations of HIV-1-Associated Vacuolar Myelopathy:An Autopsy-Based Case-Control Study
Neurol 44:2159-2164, DalPan,G.J.,et al, 1994

Brief Report:Relief of Spinal Cord Compression from Vertebral Hemangioma by Intralesional Injection of Absolute Ethanol
NEJM 331:508-511, Heiss,J.D.,et al, 1994

Progressive Spastic Paraparesis Revealing Primary Hyperparathyroidism
Neurol 44:178-179, Thomas,P.&Lebrun,C., 1994

The Nondystrophic Myotonias
In Myology, McGraw-Hill, 2nd Ed, Ch49, p1291-13024., Rudel,R.,et al, 1994

Myositis-Specific Autoantibodies, Touchstones for Understanding the Inflammatory Myopathies
JAMA 270:1846-1849, Miller,F.W., 1993

Werner's Syndrome Associated with Spastic Paraparesis and Peripheral Neuropathy
Neurol 43:1252-1254, Umehara,F.,et al, 1993

Spastic Ataxia Associated with Human T-Cell Lymphotropic Virus Type II Infection
Ann Neurol 33:411-414, Harrington,W.J.,et al, 1993

Isolation of HTLV-II from Pt with Chronic, Prog Neurol Dis Clin Indistinguish from HAM/Tropical Spastic Paraparesis
Ann Neurol 33:392-396, Jacobson,S.,et al, 1993

Neurological Involvement in Wegener's Granulomatosis:An Analysis of 324 Consecutive Pts at the Mayo Clin
Neurol 33:4-9, Nishino,H.,et al, 1993

Intramedullary Spinal Sarcoidosis:Clinical and Magnetic Resonance Imaging Characteristics
Neurol 43:333-337, Junger,s.S.,et al, 1993

Coxiella (Q fever) -Associated Myelopathy
Neurol 43:338-342, Hwang,Y.M.,et al, 1993

Clinicopath Conf
Acquired Demyelinating Neuropathy, ? CIDP, ? Motor Neuropathy with Multifocal Conduction Blocks, Cas, 41-1EJM 329:1182-1190,1993., 1993

Human T Lymphotropic Virus Type I-Assoc Myelopathy, A Rpt of 10 Pts Born in US
Arch Neurol 49:1113-1118, Sheremata,W.A.,et al, 1992

Chronic Myelopathy Associated with Human T-Lymphotropic Virus Type I (HTLV-I)
Ann Int Med 117:933-946, Gessain,A.&Gout,O., 1992

Recurrent Encephalopathy and Seizures in a US Native with HTLV-I-Associated Myelopathy/Tropical Spastic Paraparesis
Neurol 42:658-661, Smith,C.R.,et al, 1992

Presence of HTLV-I Proviral DNA in Central Nervous System of Patients with HTLV-I-Associated Myelopathy
Ann Neurol 31:39-45, Kira,J.,et al, 1992

Showing articles 50 to 100 of 1886 << Previous Next >>