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Differential
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abdominal distention

accomodation, abnormal

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, infants and children

acquired immunodeficiency syndrome-related complex

acute ataxia of childhood

acute ataxic sensory neuropathy

acute cerebellar ataxia

acute disseminated encephalomyelitis

Addison's disease

adolescent medicine

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

alexia without agraphia

alien hand syndrome

alternating rapid movement

alternating rapid movement, impaired

aminoacidopathies

amphiphysin antibodies

anemia, hemolytic

anemia, megaloblastic

Angelman syndrome

ankle reflex, absent

ankle, swelling of

anterior tibial muscle weakness

anti citrullinated antibody

anti MAG antibodies

anticonvulsants

anticonvulsants, untoward effects of

antiviral agents

aphasia, progressive, primary

apraxia of eye movements

apraxia, constructional

arm swing, reduced

arrhythmia, cardiac

ascending paralysis

aspartate aminotransferase

ataxia telangiectasia

ataxia, acute onset

ataxia, cerebellar

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

ataxia, sensory

ataxia, truncal

ataxia, truncal, associated with ocular oscillations

ataxic-dystonia syndromes

athetosis, causes of

atrial fibrillation

attention deficit disorder with hyperactivity

autoimmune disease

automobile accidents

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal degeneration

axonal spheroid

azidodeoxythymidine

B 12 deficiency

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basophilic stippling of red blood cells

behavior, combative

behavioral disorder

benign essential tremor

beta adrenergic blocker

biologic markers

biopterin deficiency

bladder dysfunction

blinking, reduced

bone marrow suppression

botulinum toxin

botulinum toxin, complications of

brain biopsy, stereotaxic

brainstem, atrophy

brainstem, dysfunction

brainstem, infarction of

brainstem, lesion of

Brueghel's syndrome

bulbar dysfunction

burning paresthesia

calcification, intracranial

carcinoma of breast

carcinoma of lung

carcinoma of ovary

CAT scan, abnormal

CAT scan, emission, abnormal

CAT scan, pelvis

CAT scan, ring sign

cauda equina, enhancement

central cord syndrome

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar infarction

cerebellar lesion

cerebellar vermis

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral infarction

cerebral palsy, associated problems with

cerebral peduncle

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, complications with

ceruloplasmin, serum

cervical myelopathy

Charcot-Marie-Tooth

chelation therapy

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chorea, causes of

choreoathetosis

chromosomal abnormality

chronic progressive external ophthalmoplegia

cirrhosis, causes of childhood

Clinical Pathologic Conference(C.P.C.)

Cockayne's syndrome

cogwheel rigidty

cold hands sign

concentration, impaired

conduction block

contractures, joint

convergence, impaired

conversion reaction

copper metabolism, abnormal

cornea, abnormal

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical-basal ganglionic degeneration

cranial nerve enhancement

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

cryptococcal meningitis

cultured skin fibroblasts

cytomegalovirus infection

decerebrate posture

deep gray nuclei

degenerative cervical myelopathy

degenerative diseases of CNS

delay in diagnosis

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei, lesion of

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diagnostic criteria

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

dilantin, toxicity

disability rating scale, neurological

disability, neurological

distal muscle atrophy

distal muscle weakness

diurnal variation

dopa responsive dystonia

dopamine antagonist

down-beat nystagmus

down-beat nystagmus, primary position of gaze

drug abuse, inhalation

drug induced neurologic disorders

dysarthria-clumsy hand syndrome

dysdiadochokinesia

dysferlinopathy

dyskinesia, buccal lingual facial

dyskinesia, causes of

dyskinesia, drug induced

dyskinesia, facial

dystonia musculorum deformens

dystonia, cervical

dystonia, children

dystonia, classification

dystonia, delayed onset

dystonia, drug induced

dystonia, etiology of

dystonia, evaluation of

dystonia, focal

dystonia, focal lesion causing

dystonia, focal task specific

dystonia, laryngeal

dystonia, post traumatic

dystonia, psychogenic

dystonia, symptomatic

dystonia, treatment of

dystonic reaction, acute

dystonic tremor

eating disorder

electrical sensation

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electrophoretic pattern, CSF

encephalitis, acanthamoeba

encephalitis, amebic

encephalitis, autoimmune

encephalitis, episodic

encephalitis, focal

encephalitis, human immunodeficiency virus type 1

encephalitis, St.Louis

encephalitis, viral

encephalomyelitis, paraneoplastic

encephalopathy, parainfectious

encephalopathy, progressive

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

erectile dysfunction

esophageal varices

executive dysfunction

exome sequencing

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

failure to thrive

feeding disorder

fetal movements, reduced

fine motor function, impaired

finger nose finger test

finger numbness

fingernails, abnormal

fingerprint bodies

flu-like illness

foot drop, bilateral

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

Friedreich's ataxia

frontal behavioral spatial syndrome

frontal lobe, pathologic signs of

F-wave response

gait, festinating

gammaglobulin therapy, intravenous

gastrocnemius muscle weakness

gastroenteritis

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

genu of corpus callosum

gests antagoniste

Gilles de la Tourette syndrome

globus pallidus

globus pallidus, lesion of

glycogen storage disease

granular osmiphilic material

growth hormone deficiency

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Hallervorden Spatz disease

hallucination, visual

heavy metal intoxication

hemianopia, homonymous

hemifacial spasm

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatosplenomegaly

heralding manifestation

herniated disc, central

herniated disc, cervical

herniation syndromes, intracranial

high arched feet

highly active antiretroviral therapy

hip flexor weakness

histochemistry of muscle

HIV CSF viral escape syndrome

homocysteine, serum

Horner's syndrome

human immunodeficiency virus type 1

human immunodeficiency virus type 1, asymptomatic

human immunodeficiency virus type 1, pathogenesis

Huntington's chorea

hyperamylasemia

hyperhomocysteinemia

hyperosmolality

hyperphosphatasia

hypersegmented polys

hypoalbuminemia

hypogonadism, hypogonadotropic

hypopigmentation of skin

hypotension, systemic

hypotonia, infants

iatrogenic neurologic disorders

ideomotor apraxia

imbalance, postural

immunohistochemistry

immunomodulation

immunosuppression

immunosuppressive agents

inability to stand on tiptoes

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

industrial neurologic disorders

influenza A virus

influenza B virus

intellectual deficit

intellectual deterioration

intelligence quotient

intracerebral hemorrhage

intracranial pressure, increased

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

jaw jerk, abnormal

Kayser-Fleischer ring

kinesia paradoxica

Krabbe's disease

lactic acidemia

lacunar infarction, differential diagnosis of

laminectomy, cervical

laminectomy, lumbar

language disorder in adults

laughing, pathologic

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leukocyte enzyme abnormality

leukoencephalopathy

leukoencephalopathy, adult onset, sporadic

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

Lhermitte's sign

limb immobilization

lipid storage disorder of CNS

liver function enzymes

liver transplantation

lymph node biopsy

lymphadenopathy

lymphadenopathy, hilar

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

marche a petits pas

Marcus Gunn pupil

meconium staining

medical-legal aspects of neurology

memory, defect of recent

memory, impairment of

meningeal enhancement

meningoencephalitis

meningoencephalitis, amoebic

mental retardation

mental status, abnormal

metabolic disorder, primary-screening tests

methylmalonic acid, serum

methylmalonic acidemia

midbrain, atrophy

midbrain, infarction of

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

molecular genetics

monoclonal gammopathy

mononeuritis multiplex

mononeuropathy multiplex

motor dysfunction

motor neuron disease

motor neuron disease, misdiagnosis

movement disorder

movement disorder, delayed onset

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, psychogenic

movement disorder, treatment of

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, hypointense signal foci on

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

multinucleated giant cell

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle stiffness

muscle tenderness

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, limb-girdle

musician's dystonia

myelinolysis, extrapontine

myelitis, longitudinal

myeloneuropathy

myelopathy, chronic progressive

myelopathy, tract-specific

myelopathy, vacuolar

myoclonic jerks

myoclonus, epilepsy

myoclonus, segmental

myositis, acute of childhood

myositis, post infectious

nausea and vomiting

neoplasm, intracranial

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-recurrent

neoplasm, primary of CNS-survival

neoplasm, primary of CNS-treatment of

neoplastic angioendotheliosis

nerve conduction studies

nerve conduction studies, sensory

nerve root biopsy

neuritis, heavy metals causing

neuroaxonal dystrophy

neuroaxonal leukodystrophy

neuroendocrinology

neurofibrillary degeneration

neurogenic bladder

neuroleptic malignant syndrome

neurologic complications of, surgery

neurologic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic evaluation

neurologic examination

neurologic signs

neurologic symptoms

neurologic symptoms, unexplained

neuromuscular disease, electrodiagnosis of

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronopathy, sensory

neuroophthalmology

neuropathology, brain

neuropathy, acute

neuropathy, ataxic

neuropathy, chronic

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, immune

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, toxic

neuropathy, vasculitic, systemic

next-generation sequencing

Niemann-Pick disease

night blindness

numb clumsy hands syndrome

numbness, extremity

numbness, generalized

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, vertical

occupational neurologic disorders

ocular motility, disorders of

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

opportunistic infection

opportunistic infection, CNS

opsoclonus, differential diagnosis of

opsoclonus-myoclonus syndrome

optic chiasm, enlarged

optic nerve, enlarged

optic neuropathy

ornithine transcarbamylase deficiency

orthostatic hypotension

osmotic demyelination syndrome

ovarian dysgenesis

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, spastic

paraproteinemia

parasitic infection

parasitic infection, CNS

paresthesias, feet

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinson disease, asymmetric onset

Parkinson disease, axial symptoms

Parkinson disease, dementia with

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, etiology of

Parkinson disease, fluctuations in

Parkinson disease, freezing phenomena in

Parkinson disease, heterogeneity of

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, mode of onset

Parkinson disease, prognosis of

Parkinson disease, psychogenic

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinson disease, unilateral

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal neurologic deficits

paroxysmal nonkinesigenic dyskinesia

PAS positive material in the brain

patient information and support

penguin silhouette sign

pericardial effusion

peripheral blood smear

peripheral blood smear, abnormal

pernicious anemia

Perrault syndrome

personality change

personality disorder

phenylketonuria

photosensitivity, skin

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pleural effusion

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

polyradiculoneuropathy

pons, lesion of

position sensation

position sensation, abnormal

posterior cerebral artery

posterior cerebral artery embolism

posterior cerebral artery territory infarction

posterior column disease

postoperative neurologic complications

postural abnormality

Prader-Labhart-Willi syndrome

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

primary episodic ataxia

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive supranuclear palsy

prolactin, elevated

proprioception, abnormal

protozoan infection

pseudoathetosis

pseudobulbar palsy

psoriatic arthritis

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

ptosis, bilateral

pupil, dilated and fixed, bilateral

pure sensory stroke

pursuit eye movements, abnormal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quality of life

radiation therapy, CNS treatment and complications with

rapid onset dystonia parkinsonism

rapidly fatal neurologic illness

rapidly progressing neurologic illness

real-time quaking-induced conversion

reflex sympathetic dystrophy

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

respiratory failure

retinal degeneration

retinitis pigmentosa

Rett's syndrome

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

rheumatoid arthritis, neurologic complications of

rheumatoid vasculitis

rigidity, axial

rubella encephalitis

rubella encephalitis, progressive

saccadic eye movements, abnormal

salivation, excessive

scoliosis, neurologic association with

sea-blue histiocytes

sedimentation rate, elevated

seizure, adult onset

seizure, children

seizure, psychomotor-temporal lobe

sensorineural hearing loss

sensory loss, asymmetric

sensory loss, cortical

sensory nerve action potentials

sequencing difficulty

serologic testing

serologic testing of cerebrospinal fluid

serum alanine aminotransferase

Sjogren's syndrome

skin, lesions in neurologic disorders

sleep pathology and physiology

slit lamp examination

sodium valproate

sodium valproate, toxicity

spastic dysphonia

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, loss of

spinal cord, compression of

spinal cord, lesion of

spinocerebellar ataxia

spinocerebellar ataxia type 28

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

spontaneous remission

sprain, cervical

square wave jerks

startle reaction

status epilepticus

stem cell rescue

stem cell transplantation

stereotaxic surgery

stereotyped behavior

stimulation, deep brain

stimulation, deep brain, bilateral

stooped posture

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

strokelike episodes

subarachnoid hemorrhage

substantia nigra

superior cerebellar artery infarction

superior cerebellar artery syndrome

swallow evaluation

sweating, abnormality of

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, neurologic complications with

syphilis, ocular

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tandem gait, ataxic

tardive dyskinesia

tardive dystonia

temper tantrums

thalamic dystonia

thalamic tumors

thalamus, infarction of

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytopenia

tongue, protrusion of

tonic foot response

torticollis, post traumatic

toxoplasmosis, CNS

transcutaneous electrical nerve stimulation

transient ischemic attack

transient neurologic deficit

transient neurologic deficit, benign syndrome in young adults

treatment failure

treatment of neurologic disorder

treatment, empirical

tremor, cerebellar

tremor, intention

tremor, orthostatic

tremor, post traumatic

tremor, postural

tremor, psychogenic

tremor, resting

tremor, thalamic

tremor, treatment of

tremor, writing

trientine dihydrochloride

trinucleotide repeats

tyrosine hydroxylase deficiency

uncal herniation

unconsciousness

unconsciousness, episodic

unconsciousness, transient

upgaze, paralysis of

urea-cycle enzymopathies

urinary incontinence

urine test for metabolic disorders

urine test in toxic screen

vascular endothelial growth factor

ventricular enlargement

vertigo, positional

vibratory sensation

vibratory sensation, abnormal

viral infection

viral infection, CNS

vision, blurred

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss, progressive

visual symptoms

visuospatial disturbance

vitamin deficiency

vitamin E deficiency

voice, abnormality of

walking, delayed

walking, difficulty with

weakness, congenital

weakness, generalized

weakness, progressive

Wernekinck commissure syndrome

Whipple's disease

white matter disease

wide based gait

word-finding difficulty

Showing articles 150 to 200 of 1481 << Previous Next >>

The Serological Diagnosis of St. Louis Encephalitis in Patient with Syndr. of Opsoclonia, Body Tremulousness, & Benign Encephalitis
Ann Neurol 1:596, Estrin,W., 1977

Blepharospasm-oromandibular Dystonia Dyndrome (Brueghel's syndrome) :A Variant of Adult-onset Torsion Dystonia
JNNP 39:1204, Marsden,C.D., 1976

Dystonia & Choreoathetosis in Multiple Sclerosis
Arch Neurol 33:590, Bachman,D.S.,et al, 1976

Progressive Rubella Panencephalitis
Arch Neurol 33:722, Wolinsky,J.S.,et al, 1976

Anticonvulsant-induced Dyskinesias:A Comparison with Dyskinesias Induced by Neuroleptics
JNNP 39:1210, Chadwick,D.,et al, 1976

Clinical Diagnosis of the Dyskinesias
Med Clin of North Am 56:1321, Duvoisin,R., 1972

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

Parkinson's Disease
In Handbk of Clinical Neurology, Vinken, P. J. & Bruyn, G. W. , Ed, North-Holland Publ Co, Amsterdam, 6:173, 1968. Selby, G., 1968

Neurological & Psychiatric Signs Associated with SLE
JAMA l60:455, Clark,E.,et al, 1956

Progressive Quadriparesis and Falls in a 66-Year-Old Man With Longstanding Human Immunodeficiency Virus
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Complex Regional Pain Syndrome
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A 19-Year-Old Woman with Progressive Weakness and Numbness in Her Arms and Legs
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Neuropathologic Changes in People with Essential Tremor With Dementia
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A 30-Year-Old Female Patient with Multiple Sclerosis Presenting with Rapidly Progressive Cranial Neuropathies, Weakness, and Ataxia
Neurol 105:e214429, Trentadue,T.,et al, 2025

A Randomized Trial of Shunting for Idiopathic Normal-Pressure Hydrocephalus
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A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,et al, 2025

Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency
Neurol 104:e213636, Chanda,G.,et al, 2025

A 59-Year-Old Man with Progressive Dysarthria and Gait Instability
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The Spectrum of Fragile X Disorders
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A 63-Year-Old Female Patient Presenting with Orthostatic Hypotension and Ataxia
Neurol 105:e213993, Shen,F.,et al, 2025

A 72-Year-Old Man with Progressive Pan-Dysautonomia
Neurol 105:e213994, Zelikovich,A.S.,et al, 2025

A 73-Year-Old Man With Progressive Proximal Muscle Weakness and Binocular Diplopia
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Gait Analysis in Neurologic Disorders, Methodology, Applications and Clinical Considerations
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A Woman with Subacute Progression of Distal Upper Extremity Weakness
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A 58-Year-Old Man With Resting tremor, Bradykinesia, and Distal Numbness
Neurol 105:e214183, Costa,R., et al, 2025

A 10-Year-Old Boy with Progressive Tremor, Insomnia and Autonomic Dysfunction
Neurol 105:e214297, Chen,Z., et al, 2025

A 38-Year-Old Man With Involuntary Jerk-Like Movements and Ataxia
Neurol 105:e214381, Gomez,A.C.et al, 2025

A 24-Year-Old Man With Persistent Spontaneous Dizziness
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Acromegaly
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Efficacy and Safety of Sodium Oxybate in Isolated Focal Laryngeal Dystonia:A Phase IIb Double-Blind Placebo-Controlled Cross-Over Randomized Clinical Trial
Ann Neurol 97:329-343, Simonyan,K.,et al, 2025

A 67 YEar-Old Woman with Progressive Headache, Visual Hallucinations, and Seizures
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Reversible Cerebral Atrophy and Substantia Nigra Changes after Vitamin B12 Treatment in Infantile Tremor Syndrome
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Clinicopathologic Conference, Thyrotoxic Periodic Paralysis Associated with Graves Disease
NEJM 390:1514-1522, Case 13-2024, 2024

Risk Assessment and Prevention of Falls In Older Community-Dwelling Adults
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Rabbit Syndrome
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A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
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Neurologic Manifestations of Hyperthyroidism and Graves Disease
www.UptoDate.com, Oct 28, Rubin,D.I., 2024

Clinicopathological Conference, Glutamic Acid Decarborylase 65 Autoantibody-Associated Stiff-Person Syndrome
NEJM 390:1712-1719, Case 14-2024, 2024

A 55-Year -Old Woman with Painless Hand Weakness and Atrophy
Neurol 103:e209561, Ticku,H. & Katirji,B.,, 2024

Congenital and Acquired Chiari Syndrome
NEJM 390:2191-2198, Friedlander,R.M., 2024

Vitamin B12 Deficiency:NICE Guideline Summary
BMJ 385:q1019, q1262, Sands,T.,et al, 2024

Parkinsons Disease
NEJM 391:442-452, Tanner,C.M. & Ostrem,J.L., 2024

A 26-Year-Old Woman with Chronic Progressive Gait Dysfunction
Neurol 103:e2098-e2030, Jones,F.J.S. & Orthmann-Murphy,J., 2024

Neuroleptic Malignant Syndrome
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Clinical Features, Diagnosis and Management of Klinefelter Syndrome
www.UptoDaate.com, Matsumoto,A.M. & Anawals,B.D., 2024

Neurologic Complications of Babesiosis, United States, 2011-2021
Emerg Inf Dis 29:1127-1135, Locke,S.,et al, 2023

Clinicopathologic Conference, Noncirrhotic hyperammonemia after Roux-en-Y Gastric Bypass
NEJM 389:1221-1230, Case 30-2023, 2023

Clinicopathologic Conference,Limb-Shaking Transient Ischemia Attacks
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Polymyalgia Rheumatica
Lancet 402:1459-1472, Espigol-Frigole,G.,et al, 2023

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

Showing articles 150 to 200 of 1481 << Previous Next >>