Neudle.com: neuronal loss

Differential
(Click to cross reference)

abdominal cramps

abducens nerve paralysis

abducens nerve paralysis, bilateral

abiotrophy

abortion, spontaneous

acid maltase deficiency

acid maltase deficiency, adult

acoustic nerve

acral sensory symptoms

acute disseminated encephalomyelitis

adenylate kinase 5 autoantibodies

Adies pupil

adrenoleukodystrophy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

altered states of consciousness

alternating rapid movement

alveolar hypoventilation

AMPA receptor antibodies

AMPA receptors

amphiphysin antibodies

amygdala

amyotrophic lateral sclerosis, differential diagnosis

angiotensin-converting enzyme

anterior horn cell disease

anterior tibial muscle weakness

anti GQ1b IgG antibody

anti signal recognition particle antibody

antibodies to voltage-gated calcium channels

anticoagulant, treatment

antidepressant

antiendomysial antibodies

antiganglioside antibodies

antiphospholipid antibodies

antiphospholipid antibody syndrome

antiretinal antibodies

anti-sulfatide antibodies

antithyroid antibodies

antiviral agents

anxiety

aphasia

aphasia, progressive, primary

apnea

apnea, primary central

applause sign

apraxia

apraxia of eye movements

area postrema

area postrema syndrome

arthropathy, neuropathic

arylsulfatase A

aspartate aminotransferase

ataxia telangiectasia

attention deficit disorder with hyperactivity

autoimmune basal ganglia encephalitis

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

autoimmune epilepsy

autoimmune GFAP astrocytopathy

automatic behavior

automobile accidents

autonomic dysfunction

Barkhof MR criteria for MS

basal ganglia

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

bat bite

behavior, combative

behavioral disorder

behavioral disorder, acute

Bickerstaff's brainstem encephalitis

bilateral periventricular nodular heterotopia

bone marrow transplantation

botulinum toxin

bovine spongiform encephalopathy

bradykinesia

brain atrophy

brain biopsy

brain natriuretic peptide

brain transplantation

brainstem

brainstem, atrophy

brainstem, dysfunction

brainstem, infarction of

bulbar palsy, childhood

bulbar palsy, progressive

burning feet

burning feet, differential diagnosis of

campylobacter infection

Canavan's disease

cancer, unknown origin

carcinoma of pancreas

carcinoma of testis

carcinoma of unknown origin

CAT scan, emission, abnormal

celiac disease, adult

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellitis

cerebellitis, autoimmune

cerebellum, disease of

cerebral cortex

cerebral cortical atrophy

cerebral cortical encephaliis

cerebral edema

cerebral edema, vasogenic

cerebral folate deficiency syndrome

cerebral infarction

cerebral palsy

cerebral vasculature

cerebral venous thrombosis

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal bands, absent

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, mimics

cerebrovascular accident, young adult

cerebrovascular disease, cardiovascular disease with

chairbound

channelopathy

chemosis

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

children

chloride channel dysfunction

chromosomal abnormality

chromosome 20

chromosome 5

Clinical Pathologic Conference(C.P.C.)

collapsin response mediator protein 5 IgG

Collier's sign

color vision

color vision, impaired

colpocephaly

coma

coma, episodic

coma, medically induced

comorbidities

complications

compulsivity

concentration, impaired

confabulation

confusion

confusional state, acute

congenital malformation

congestive heart failure

conjunctival biopsy

conjunctival injection

conjunctivitis

consanguinity

constipation

contactin associated protein like 2 antibodies

contractures, joint

controversies in neurology

conus medullaris, lesion of

conversion reaction

Coombs test, positive

cornea, opacity of

corneal dystrophy

corneal reflex, abnormal

corneal ulceration

corpus callosum

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical-basal ganglionic degeneration

coumarin

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cry, abnormal

cultured skin fibroblasts

degenerative diseases of CNS

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, treatment of

demyelinating disease

denervation of muscle

denervation potentials

dentatorubral-pallidoluysian atrophy

depression

dermatomyositis

developmental abnormality of brain

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

diplopia

disability, neurological

disorientation

distal muscle atrophy

distal muscle weakness

DPPX, antibodies, encephalitis

drooling

dropped head syndrome

drowsiness

drug induced neurologic disorders

dyskinesia, buccal lingual facial

dysthyroid ocularmyopathy

electroencephalogram, abnormalities of

electroencephalogram, triphasic delta waves

electromyogram

electromyogram, decremental response

electromyogram, incremental response

electron microscopy

electronystagmography

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, clinical picture and treatment of

encephalitis, episodic

encephalitis, etiology

encephalitis, paraneoplastic

encephalitis, recurrent

encephalitis, unknown etiology

encephalitis, viral

encephalomyelitis

encephalomyelitis, paraneoplastic

encephalopathy

encephalopathy, Hashimoto's

endocarditis, marantic

enteritis

enzyme treatment

enzyme, defect

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

erectile dysfunction

ethics in neurology

evoked potentials

executive dysfunction

exercise intolerance

exome sequencing

extralimbic encephalitis

eye movement, disorders of

eye movement, painful

eye, pain in

Fabry's disease

face, numbness of

facial appearance, abnormal

facial weakness, bilateral

faciobrachial dystonic seizure

fine motor function, impaired

fingerprint bodies

Fisher's syndrome

Fisher's syndrome, atypical

folic acid deficiency

fourth ventricle, floor

Fragile-X associated tremor/ataxia-syndrome

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontotemporal dementia, behavioral variant

fucosidosis

fundus, abnormality of

gamma amino butyric acid

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastrointestinal disease, neurologic complications

gaze palsy

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamic acid decarboxylase, antibody

gluten sensitivity

gluten-free diet

glycine receptor antibodies

glycogen storage disease

glycoprotein

GM1 ganglioside antibodies

granular osmiphilic material

granulomatosis with polyangiitis

grasp reflex

Graves ophthalmopathy

grimacing

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, complications

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, ophthalmoplegia in

Guillain Barre syndrome, prognosis of

Guillain Barre syndrome, variant forms of

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination

hallucination, olfactory

hallucination, visual

hearing loss, bilateral

heat intolerance

heavy metal intoxication

heel-knee-shin test

hemimyoclonic jerks

hemiparesis

hemorrhagic diathesis

heparin

heparin, low-molecular-weight

heralding manifestation

herpes simplex encephalitis

herpes simplex virus

heterotopia

hexosaminidase-A

hexosaminidase-A and B

hippocampus, hyperintense

HLA

HMGcoA reductase inhibitors

hoarseness

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

hot cross bun sign

H-reflex testing

H-sign, spinal cord

human immunodeficiency virus type 1

Huntington's chorea

Huntington's chorea, genetic counselling

hydrocephalus

hyperekplexia

hyperesthesia

hypergammaglobulinemia

hyponatremia with cerebral disorders

hypophonia

hypopigmentation of skin

hyporeflexia

hyposmia

hypotension, systemic

hypothalamus

hypothalamus, damage to

hypothalamus, lesion of

iatrogenic neurologic disorders

immunology and the nervous system

immunomodulation

immunosuppressive agents

immunotherapy

impulsivity

inappropriate antidiuretic(A.D.H.)hormone

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

inattention

inborn errors of metabolism

incidence

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

incoordination

infantile neuronal degeneration

intellectual deterioration

intelligence quotient

internet

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intestinal biopsy

intrauterine

intrauterine infection

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

Kearns-Sayre syndrome

kelch-like protein 11 antibodies

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactic acidemia

language disorder in adults

lateropulsion

laughing

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

L-dopa

L-dopa, drug interactions with and side effects of

leg spasms, painful

leg weakness, bilateral

Leigh's disease

lethargy

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

leukopenia

level of consciousness

level of consciousness, decreased

limbic-predominant age-related TDP-43 encephalopathy

linear lesion

lip biopsy

lipid storage disorder of CNS

lissencephaly

livedo reticularis

liver disease

liver function enzymes

lobar atrophy

locus ceruleus, lesion of

lymphadenopathy, axillary

lymphadenopathy, hilar

lymphocyte fingerprint profiles

lymphoma

lymphoma involving CNS

lysosomal storage disease

malformation, CNS, congenital

masseter muscle wasting

medial longitudinal fasciculus(MLF)

mediastinum, mass of

medulla oblongata

medulla oblongata, lesion of

memory

memory, defect of recent

memory, impairment of

meningeal enhancement

meningismus

meningoencephalitis

meningoencephalomyelitis

mental retardation

mental status, abnormal

mesial temporal lobe

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

mGlu R5 antibodies

microangiopathy, brain

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mild cognitive impairment

mimics

miosis

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

modafinil

molecular genetics

monoclonal antibodies

monoclonal gammopathy

mononeuritis multiplex

mononeuropathy

Montreal cognitive assessment

mood change

mortality

Morvan's fibrillary chorea

motor neuron disease

motor neuron disease, misdiagnosis

movement disorder

movement disorder, extrapyramidal

MRI

MRI pattern

MRI, abnormal

MRI, contrast enhanced

MRI, contrast enhanced, cloud-like

MRI, cortical enhancement

MRI, cranial nerves

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, FLAIR

MRI, hypointense signal foci on

MRI, muscle

MRI, negative

MRI, optic nerve

MRI, paramagnetic effect

MRI, spinal cord, increased intramedullary cord signal

MRS

mucopolysaccharidoses

multiple organ failure

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sleep latency test

multiple system atrophy

muscle atrophy, progressive

muscle strength, testing

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

mutism

myasthenia gravis, paraneoplastic

myasthenic syndrome

myelination of nervous system

myelitis

myelitis, longitudinal

myelitis, transverse

myelitis, transverse, recurrent

myelomalacia

myeloneuropathy

myelopathy

myelopathy, chronic progressive

myocardial infarction

myopathy, drug-induced

myopathy, mitochondrial

myopathy, necrotizing, autoimmune

nerve conduction studies

nerve conduction studies, motor

nerve root enhancement

neuraminidase deficiency

neurexin-3 alpha antibodies

neuroaxonal leukodystrophy

neuroblastoma

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurogenic bladder

neuroinfectious diseases

neurolipidosis IV

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic disease, multiple

neurologic examination, focal

neurologic signs

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuromyelitis optica (Devic's disease)

neuromyelitis optica (Devic's disease), screening

neuromyelitis optica spectrum disorder

neuromyelitis optica, IgG

neuromyotonia

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal intranuclear inclusion disease

neuronal loss

neuronal migration disorder

neuronopathy

neuronopathy, sensory

neurons

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, asymmetric

neuropathy, ataxic

neuropathy, autoimmune

neuropathy, chronic

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, small-fiber

neuropathy, small-fiber, painful sensory

neurotoxic

neutropenia

next-generation sequencing

Niemann-Pick disease

night blindness

night sweats

nigrostriatal pathway

nucleus basalis of Meynert

numbness, ascending

numbness, extremity

nystagmus

nystagmus, dissociated

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, vertical

obsessive-compulsive disorder

obstetric complications

ocular dipping

ocular motility, disorders of

oculocephalic reflex

old age, neurology of

olivary degeneration, hypertrophic

onconeural antibodies

one and a half syndrome

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, postinfectious

ophthalmoplegia, progressive external

ophthalmoplegia, total

opisthotonus

opsoclonus

opsoclonus-myoclonus syndrome

optic atrophy

optic chiasm

optic chiasm, lesion of

optic disc edema

optic nerve

optic nerve sheath enhancement

optic nerve, compression of

optic nerve, decompression of

optic nerve, enhancement

optic nerve, enlarged

optic nerve, lesion of

optic neuritis

optic neuritis, alternating

optic neuritis, bilateral

optic neuritis, recurrent

optic neuropathy

optic neuropathy, ischemic

optical coherence tomography

orthostatic hypotension

oscillopsia

ovarian tumor

overlap syndrome

pachymeningitis, cranial

paralysis, acute areflexic

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paranoia

paraparesis, familial spastic

paraparesis, familial spastic, classification

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinson disease, axial symptoms

Parkinson disease, pathogenesis of

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Parkinsonism, freezing phenomena in

paroxysmal neurologic deficits

paroxysmal neurologic disorder

PAS positive

PAS positive material in the brain

pathognomonic

pathologic reflex

patient information and support

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

pediatric neurology

penguin silhouette sign

periaqueductal lesion

perineuritis

perineuritis, optic

perioral numbness

peripheral blood smear

peripheral nerve, lesion of

perivascular enhancement

photosensitivity, eye

Pick bodies

Pick's disease

pigmentary retinopathy

pitfalls

plasmapheresis

platelet inhibiting drugs

PLEDs

PLEDs, bilateral independent

PLEDs, etiology of

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pneumonia

poison, mercury

poison, neurologic problems with

polyglucosan body

polyglucosan body disease

polyneuropathy

polyneuropathy, carcinomatous

polyradiculoneuropathy

polysomnogram

Pompe's disease of glycogen storage

pontocerebellar atrophy

positional head-hanging test

posterior leukoencephalopathy syndrome

postinfectious

postpartum

postural abnormality

potassium channel antibodies

potassium channel dysfunction

practice guidelines

pramipexole

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

pretectal syndrome

prevention of neurologic disorders

prion disease

prognosis

progressive myoclonic epilepsy

progressive neurologic disorder

progressive supranuclear palsy

proptosis

proptosis, unilateral

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

pupil, abnormality in neurologic disorders

pupil, dilated, unilateral

pupil, light reflex, abnormal

pupil, tonic

purkinje cell cytoplastic autoantibody

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

quadriplegia

rabies, nervous system involvement with

radiation therapy, CNS treatment and complications with

radiation, ionizing

radiation, ionizing, intrauterine

radiculopathy

ragged-red fibers

rapidly progressing neurologic illness

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal failure

renal infarct

renal vein thrombosis

repetitive nerve stimulation

respirator

respiratory failure

respiratory tract infection

retina, abnormal

retinal arteriole attenuation

reversal of sleep wake cycle

reversible neurologic disorder

review article

rhabdomyolysis

rheumatoid arthritis factor(R.A.factor)

rhomboencephalopathy

rigidity

rigidity, axial

rippling muscle disease

risk factors

rituximab

Romberg's sign

saccadic eye movements, abnormal

salivation, excessive

scoliosis, neurologic association with

scotoma

scotoma, central

scotoma, paracentral-homonymous

screening

sea-blue histiocytes

sedimentation rate, elevated

segmental demyelination

seizure

seizure, adult onset

seizure, children

seizure, drug resistance

seizure, familial

seizure, focal

seizure, intractable

seizure, intractable, treatment of

seizure, psychomotor-temporal lobe

seizure, treatment of

seizure, unknown origin

semantic dementia

seminoma

senile plaques

sensorineural hearing loss

sensory loss

sensory loss, asymmetric

sequencing difficulty

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

seronegative

serum alanine aminotransferase

serum tumor markers

sex reassignment surgery

single photon emission computed tomography

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep offset paralysis

sleep onset paralysis

sleep paralysis

sleep pathology and physiology

speech disorder, childhood

speech, loss of

spinal cord

spinal cord degeneration

spinal cord, cervical

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinocerebellar ataxia

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

splenium of corpus callosum

splenomegaly

spongy degeneration of brain

sports medicine, neurology of

standing difficulty

staphylococcal protein A column therapy

stem cell transplantation

steroid

steroid responsive encephalopathy

steroid therapy, CNS treatment and complications with

storage disease of CNS

strabismus

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

stuttering

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

substantia nigra

suck reflex

suicide

survival motor neuron gene

sweating

sweating, abnormality of

sweet taste

symmetric brain lesions

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tandem gait, ataxic

tangential

tapetoretinal degeneration

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, lesion of-bilateral

third ventricle, wall

thrombocytopenia

thrombophlebitis

thrombotic microangiopathy

thymoma

thyroglobulin antibodies

thyroid function tests

thyroid peroxidase antibodies

tone, muscle, increased

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, impaired movements of

tongue, protrusion of

tonic spasms

transgender

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

triangle of Guillain and Mollaret

trichopoliodystrophy

trinucleotide repeats

unconsciousness, episodic

unconsciousness, transient

undiagnosed

upgaze, paralysis of

urinary incontinence

urinary sulfatidase excretion

urine test for metabolic disorders

varicella zoster virus

vasculitides

ventricular enlargement

vertigo

vestibular function, tests of

vestibulopathy

viral infection

viral infection, CNS

vision loss, sequential

vision, blurred

vision, failure of in childhood

visual acuity

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss

visual loss, progressive

visual loss, slow

visual loss, sudden

visual loss, transient

visual symptoms

vitiligo

vocalizations

vomiting, intractable

Waldenstrom's macroglobulinemia

walking, delayed

walking, difficulty with

water channel antibodies

weakness

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

weight gain

weight loss

Werdnig-Hoffman disease

West disease

wheelchair

white matter disease

white matter disease, periventricular

white matter disease, subcortical

whole body imaging

wide based gait

Wolfram syndrome

word-finding difficulty

Showing articles 200 to 250 of 4649 << Previous Next >>

Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
Neurol 42:1220-1224, 1992,, Rando,T.A.,et al, 1992

Causal Heterogeneity in Isolated Lissencephaly
Neurol 42:1375-1388, Dobyns,W.B.,et al, 1992

Wegener's Granulomatosis Mimicking Temporal Arteritis
Neurol 41:1694-1695, Palaic,M.,et al, 1991

Anti-Ri:An Antibody Associated with Paraneoplastic Opsoclonus and Breast Cancer
Ann Neurol 29:241-251, Luque,F.A.,et al, 1991

Neurodegenerative Diseases of Childhood:MR and CT Evaluation
J Comput Assist Tomogr 15:210-222, Mirowitz,S.A.,et al, 1991

Thyroid-Associated Eye Disease:Clinical Management
Lancet 338:29-32, Fells,P., 1991

The Diagnosis of Childhood Neurodegenerative Disorders Presenting as Dementia in Adults
Neurol 41:794-798, Coker,S.B., 1991

The Spectrum of Lissencephaly:Report of Ten Patients Analyzed by Magnetic Resonance Imaging
Ann Neurol 30:139-146, Barkovich,A.J.,et al, 1991

Fucosidosis Revisited:A Review of 77 Patients
Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991

Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
Neurol 40:1876-1882, Gascon,G.G.,et al, 1990

Perinatal Loss and Neurological Abnormalities Among Children of the Atomic Bomb
JAMA 264:605-609, 6221990., Yamazaki,J.N.&Schull,W.J., 1990

Anderson-Fabry Disease
Editorial, Lancet 336:24-251990., , 1990

A Clinical Triad to Diagnose Paraneoplastic Retinopathy
Ann Neurol 28:162-167, Jacobson,D.M.,et al, 1990

Cancer-Associated Retinopathy (Car Syndrome) with Antibodies Reacting with Retinal, Optic-Nerve, and Cancer Cells
NEJM 321:1589-1594, 1607-16081989., Thirkill,C.E.,et al, 1989

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

Paraneoplastic Syndromes Involving the Eyes
In Walsh & Hoyt's Clin Neuro-ophthal, 4th ed, Williams & Wilkins, Vol 3, p 1735-1746, Miller,N.R., 1988

Nervous System Involvement in Fabry's Disease:Clinicopath & Biochemical Correlation
Ann Neurol 23:505-509, Kaye,E.M.,et al, 1988

GM1 Gangliosidosis:Clinical and Laboratory Findings in Eight Families
Hum Genet 70:347-354, Giugliani,R.,et al, 1985

Clinicopathological Conference
Case 2-1984, Fabry's Disease, NEJM 310:106-114984., , 1984

A Progressive Neurologic Disorder with Supranuclear Vertical Gaze Paresis & Distinctive Bone Marrow Cells
Mayo Clin Proc 59:404-410, Yan-go,F.L.,et al, 1984

Neurodegenerative Disease of Infancy & Childhood
Ann Neurol 13:351-364, Dyken,P.,et al, 1983

Clin. Path. Conference
Multiple-System Atrophy with Parkinsonism, Case 28-13, NEJM 308:1406-1414983., , 1983

Hypomelanosis of Ito (incontinentia pigmenti achromians) :Macrocephaly & Gray Matter Heterotopias
Neurol 32:1013-1016, Ross,D.L.,et al, 1982

Santavuori Disease:Diagnosis by Leukocyte Ultrastructure
Neurol 32:1277-1281, Baumann,R.J.,et al, 1982

Progressive Pontobulbar Palsy With Deafness
Arch Neurol 38:186-190, Brucher,J.M.,et al, 1981

Fetal Methylmercury Poisoning:Clinical & Toxicological Data on 29 Cases
Ann Neurol 7:348-353, Marsh,D.O.,et al, 1980

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

Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
Ann Neurol 6:232-244, Miyatake,T.,et al, 1979

Clinical Pathological Conference
Neuronal Veroid-lipfuscinosis, Juvenile Variant, (Batten's disease) , NEJM 299:189., , 1978

Clinical & Extraneural Histologic Diagnosis of Neuronal Ceroidlipofuscinosis
Neurol 28:1008-1012, Miley,C.E.III.,et al, 1978

Juvenile Amaurotic Idiocy (Neuronal Ceroid Lipofuscinosis) & Lymphocyte Fingerprint Profiles
Ann Neurol 4:531-536, Baumann,R.J.,et al, 1978

Chronic Hexosaminidase A & B Deficiency
et al. , Ann Neurol 2:156977., Goldie,W.D., 1977

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

Corticodentatonigral Degeneration with Neuronal Achromasia
Arch Neurol 18:20-33, Rebeiz,J.J.,et al, 1968

Rocky Mountain Spotted Fever Encephalitis and "Starry Sky" Pattern on MRI, A Case Report
Neurologist 30:34-38, Mikhaiel,J.P.,et al, 2025

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

Clinicopathologic Conference, Posterior Reversible Encephalopathy Syndrome Due to Sickle Cell Disease
NEJM 392:268-276, Case 2-2025, 2025

Spontaneous Spinal Cord Infarction in a Young Patient: An Overview of Clinical Features and Management
Stroke 56:58-61, Chornay,C.,et al, 2025

A 68-YEar-Old Man with Progressive Numbness, Vertigo, and Cognitive Decline
Neurol 104:e213437, Regan,S.M. & Davalos,L.F., 2025

Black Turbinate Sign as an Early Clue of Rhino-Orbital-Cerebral Mucormycosis
Neurol 104:e210202, Xie,J.S.,et al, 2025

Bilateral Basal Ganglia Region Infarction after Trauma in a Patient With Bilateral Basal Ganglia Calcification
Stroke 56:e47-e48, Zhang,Q.,et al, 2025

Orbital Apex Syndrome Associated with Herpes Zoster Ophthalmicus
Neurol 104:e213387, Imamura,D.,et al, 2025

Clinicopathologic Conference, Metastatic Small-Cell Carcinoma of the Lung
NEJM 392:903-914, Case 7-2025, 2025

Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
Neurol 104:e213436, Paredes,N.C.,et al, 2025

A 56-Year-Old Woman with New-Onset Hoarsement and Dysphagia
Neurol 104:e213363, McAree,M. & Frontera, J.A., 2025

Next-Day Serum Glial Fibrillary Acidic Protein Levels to Aid Diagnosis of Sport-Related Concussion
Neurol 104:e210308, OBrien,W.T.,et al, 2025

A 26-Year-OldWoman with Headache and Eosinophilia
Neurol 104:e213434, Goh,W.G.W.,et al, 2025

A 19-Year-Old Woman with Progressive Weakness and Numbness in Her Arms and Legs
Neurol 104:e213495, Alsabah,A-A.,et al, 2025

Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
Ann Neurol 97:611-628, Coppens,S.,et al, 2025

A 67 YEar-Old Woman with Progressive Headache, Visual Hallucinations, and Seizures
Neurol 104:e213496, Gheihman,G.,et al, 2025

Showing articles 200 to 250 of 4649 << Previous Next >>