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Differential
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abdominal distention
abdominal protrusion
abducens nerve paralysis, bilateral
abscess, brainstem
abscess, intracerebral
abscess, lung
acute ataxia of childhood
acute cerebellar ataxia
adult polyglucosan body disease
advances in neurology
Alexanders disease
Alexanders disease, adult onset
alternating hemiplegia
alternating hemiplegia of childhood
AMPA receptor antibodies
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, differential diagnosis
aneurysm, abdominal aortic
aneurysm, aortic arch
angiography, cerebral
angiography, posterior fossa
animal exposure
anti GQ1b IgG antibody
anticonvulsants
anticonvulsants, effectiveness
aorta, abdominal
aorta, abnormal
aortitis
apnea
areflexia
arm weakness
arterial dissection
arterial dissection, carotid
arterial dissection, intracranial
arterial dissection, multiple
arterial dissection, ruptured
arterial dissection, vertebral
arthralgia
arthritis
ascending paralysis
astrogliopathy
ataxia
ataxia, acute onset
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
ATP1A3 gene
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
autonomic dysfunction
axonal degeneration
Babinski sign
bacterial infection
bacterial infection, CNS
basal ganglia, lesion of
basilar artery migraine
Bassen-Kornzweig syndrome
BCG treatment
behavior, combative
behavioral disorder
bladder dysfunction
blindness
blindness, monocular
blindness, transient
blood cultures
bone marrow biopsy
brachial plexus neuropathy
bradykinesia
brain atrophy
brainstem, infarction of
brainstem, lesion of
Brown-Vialetto-Van Laere syndrome
bulbar palsy
bulbar palsy, progressive
C9orf72
cachexia
carcinoma
carcinoma of bladder
carotid artery disease
CAT scan
CAT scan, abdomen
CAT scan, abnormal
catalepsy
cataplexy
cat-scratch disease
cauda equina, enhancement
CD4 counts
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar cognitive affective syndrome
cerebellar degeneration
cerebellar infarction
cerebellar lesion
cerebellitis
cerebral cortex
cerebral cortical atrophy
cerebral palsy
cerebral venous thrombosis
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, genetic
cerebrovascular accident, prognosis in
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cerebrovascular disease
cerebrovascular disease, risk factors in
cerebrovascular disease, surgical treatment of
chickenpox
children
chorea
choreoathetosis
chorioretinitis
chromosomal abnormality
chromosome 2
Clinical Pathologic Conference(C.P.C.)
cognition
coma
conduction block
confusion
consanguinity
contractures, joint
counterimmunoelectrophoresis
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
Creutzfeldt-Jakob disease, genetic
cyanide poison
deafness
degenerative diseases of CNS
delirium
dementia
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
demyelinating disease
dermatitis
dermatomyositis
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
diagnostic criteria
diarrhea
diarrhea, bloody
differential diagnosis
difficulty climbing stairs
dilantin
disability, neurological
disease modifying agents
distal muscle atrophy
doll's head maneuver
Dravet syndrome
drug induced neurologic disorders in children
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dyspnea
dystonia
ear, pain in
electroencephalogram, abnormalities of
electromyogram
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, episodic
encephalitis, paraneoplastic
encephalitis, viral
encephalomyelitis
encephalomyelitis, postinfectious
encephalopathy
enterovirus
enterovirus infection of CNS
epidemic
epileptic encephalopathy
Epstein-Barr virus
executive dysfunction
exome sequencing
extraocular muscle lesion
eye movement, disorders of
face, numbness of
facial nerve palsy
facial nerve palsy, recurrent
failure to thrive
falling
familial
FARS2 deficiency
fasciculation
fatigue
fever
fibrillations
fine motor function, impaired
Fisher's syndrome
flaccid paralysis
food-borne infection
foot drop
frontal lobe, atrophy
frontotemporal dementia, behavioral variant
gait disorder
gait, spastic
gait, waddling
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gastroenteritis
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
GFAP gene
glutamic acid decarboxylase, antibody
glycogen storage disease
gram negative rod
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
Guillain Barre syndrome, etiology of
Guillain Barre syndrome, variant forms of
gynecomastia
hand deformity
hand-foot-mouth disease
Hartnup's disease
headache
headache, occipital
headache, severe
headache, sudden onset of
headache, throbbing
hearing loss
hemiparesis
hepatomegaly
hepatosplenomegaly
heralding manifestation
herpes simplex virus
herpes virus
herpes virus infection
herpes, genital
heterophile antibody test
hiccoughs
histochemistry of muscle
Hodgkin's disease
hypercalcemia
hyperosmolality
hyperreflexia
hypertension
hypertension, cerebrovascular disease with
hyperthyroidism
hypoglycemia
hypokalemia
hypokalemic periodic paralysis
hyponatremia
hyporeflexia
hypotension, systemic
hypotonia
hypoxia
iatrogenic neurologic disorders
imbalance
immunization, neurologic complications with
immunotherapy
inappropriate antidiuretic(A.D.H.)hormone
inborn errors of metabolism
inclusion bodies
inclusion bodies, intranuclear
incoordination
infection
infectious mononucleosis
infectious mononucleosis, neurologic findings with
intellectual deficit
intellectual deterioration
intestinal pseudoobstruction
intrinsic hand muscles, wasting of
Jakob-Creutzfeldt disease
jaundice
Jewish
lactic acidemia
laughing
laughing, pathologic
learning disability
learning disability, in children
leg numbness
leg weakness, bilateral
Leigh's disease
lethargy
leucine rich glioma inactivated 1 antibodies
leukodystrophy
leukoencephalopathy
life expectancy
limbic encephalitis
linear lesion
lipid storage disorder of CNS
listeria monocytogenes
listeriosis, CNS
liver disease
lobar atrophy
lymphadenopathy
lymphadenopathy, paraaortic
lysosomal storage disease
macrocephaly
Melkersson's syndrome
memory, defect of recent
memory, impairment of
meningismus
meningitis
meningitis, aseptic
meningitis, carcinomatous
meningitis, CSF cell count-normal
meningitis, recurrent
meningoencephalitis
meningoencephalitis, mumps
mental status, abnormal
microcephaly
miglustat
migraine
migraine, children
migraine, visual symptoms in
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
monoclonal antibodies
monoclonal gammopathy
mononeuritis multiplex
monoparesis
mortality
motor cortex
motor neuron disease
movement disorder
movement disorder, extrapyramidal
movement disorder, hyperkinetic
MRI
MRI, abnormal
MRI, brachial plexus
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, negative
MRI, spinal cord
MRI, susceptibility weighted
multiple sclerosis
mumps virus
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle pain
muscle stiffness
muscle weakness
muscle weakness, proximal
myasthenia gravis
mycobacterial infection
mycobacterium bovis
mycoplasma
mycoplasma pneumoniae
mycotic aneurysm
myelinolysis, extrapontine
myelomalacia
myeloneuropathy
myelopathy
myelopathy, chronic progressive
myoclonic jerks
myoclonus
myoclonus, cortical
myoclonus, epilepsy
myoclonus, stimulus sensitive
myopathy
myopathy, vacuolar
myositis
myositis, ocular
nausea and vomiting
nemaline rod myopathy
nemaline rod myopathy, adult onset
nerve conduction studies
nerve conduction studies, motor
neurogenic bladder
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic disease, tempo
neuromuscular disease, electrodiagnosis of
neuronal intranuclear inclusion disease
neuropathy
neuropathy, acute
neuropathy, motor
neuropathy, motor, multifocal
neurotoxin
Niemann-Pick disease
NMDA antagonists
nystagmus
nystagmus, monocular
nystagmus, rotary
old age, neurology of
ophelia syndrome
ophthalmoplegia
optic atrophy
optic neuritis
oral ulcerations
organomegaly
osmotic demyelination syndrome
otitis, neurologic complications with
pain, abdominal
pain, leg
palatal myoclonus
pancytopenia
paralysis, acute
paralysis, acute areflexic
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paraspinal muscle
paraspinal muscle weakness
paresthesias
Parkinson disease, dystonia with
Parkinsonism syndrome
parotitis
paroxysmal hemiplegia
paroxysmal neurologic deficits
pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection
periodic paralysis
periodic paralysis, thyrotoxic
pleocytosis of cerebrospinal fluid
poison, mercury
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polymyositis
polyneuritis
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
pons, lesion of
post infectious cerebellar ataxia
postinfectious
potassium
potassium channel antibodies
practice guidelines
precipitating factors
prion disease
prognosis
progressive neurologic disorder
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychotic behavior
ptosis
ptosis, bilateral
pulmonary nodules
pyramidal tract
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
quadriparesis, progressive
quadriplegia, transient
radiculopathy
ragged-red fibers
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
real-time quaking-induced conversion
recurrent
Refsum's disease
regional enteritis
renal tubular acidosis
respiratory failure
respiratory tract infection
retina, abnormal
retinal lesion
review article
riboflavin transporter deficiency
risk factors
rituximab
Romberg's sign
salivation, excessive
schizophrenia
SCN1A gene
screening
sedimentation rate, elevated
seizure
seizure, children
seizure, familial
seizure, febrile
seizure, intractable
seizure, laughing as manifestation
seizure, neonatal
seizure, paradoxical
seizure, photosensitive
seizure, tonic-clonic
seizure, treatment of
sensorineural hearing loss
sensory loss, band distribution
serologic testing
serologic testing, false negative
seronegative
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
sleep pathology and physiology
slurred speech
sodium channel dysfunction
solitary scerlosis
spastic diplegia
spasticity
speech, loss of
spinal cord, cervical
splenomegaly
standing difficulty
status epilepticus
stem cell transplantation
steroid
steroid therapy, CNS treatment and complications with
stooped posture
striatal encephalitis
striatonigral degeneration
striatonigral degeneration, infantile
subarachnoid hemorrhage
subarachnoid hemorrhage, recurrent
suspended sensory loss
systemic illness
tandem gait, ataxic
temporal lobe, atrophy
thrush
thyrotoxicosis
tick bite
tick paralysis
titubation
toe walking
tongue, fasciculations of
topiramate
toxins, nervous system
transient ischemic attack
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
ulcerative colitis
urinary incontinence
urinary retention
urticaria
vasculitides
vertebral-basilar insufficiency
vertigo
viral infection
viral infection, CNS
visual acuity, decreased
visual impairment
visual loss
visual loss, sudden-unilateral
visual loss, transient
walking, difficulty with
weakness
weakness, acute
weakness, episodic
weakness, focal
weakness, generalized
weakness, progressive
weakness, proximal
weaning from respirator, failure to
weight loss
wheelchair
white matter disease
whole genome sequencing
wide based gait
workup
wrist drop
Showing articles 850 to 900 of 8215 << Previous Next >>

Pseudointernuclear Ophthalmoplegia in Acute Idiopathic Polyneuritis (Fisher's Syndrome)
Am J Ophthalmol 77:725, Swick,H.M., 1974

Ataxia, Vertigo, & Hearing Loss
Arch Otolarygn l00:l30, Healy,G.B.,et al, 1974

Neurotoxicity of Commonly Used Antineoplastic Agents
NEJM 291:75, 1271974., Weiss,H.,et al, 1974

Infiltration of the Leptomeninges by Systemic Cancer:a Clinical & Pathologic Study
Arch Neurol 30:122, Olson,M.E.,et al, 1974

Neuro Complica of Coeliac Disease & Trop Sprue, Neurology of GI Disease
1974, Major Problems in Neurology V-3, W. B. Saunders Co, Ltd., Pallis,C.A.&Lewis,P.D., 1974

Ataxia-Telangiectasia-Clonal Growth of Translocation Lymphocytes
NEJM 289:286, Hecht,F.,et al, 1973

Organic Disease Presenting as a Psychiatric Syndrome
Postgrad Med 54:78, , 1973

Psychiatric Aspects of Normal Pressure Hydrocephalus
JAMA 223:409, Rice,E.,et al, 1973

Neurologic Complications of Heroin Addiction
Bull NY Acad Sci 49:4, Ritcher,R.W.,et al, 1973

Clinical Neuropathological Conference
Dis Nerv Syst 34:263, Aronson,S.,et al, 1973

Case Records of MGH-NEJM 286:1047
1972 Progressive Multifocal Leukoencephalopathy., , 1972

Genetic Counseling in Retinitis Pigmentosa
MCV Quart 8:283, Noah,V., 1972

Sudden Blindness with Pituitary Tumors
J Neurosurg 36:83, Robinson,J., 1972

Neurological Problems in Endocrine Diseases
Med Clin North Am 56:1029, Dale,A., 1972

Hypokalemic Periodic Paralysis withArrhythmia
NEJM 286:253, Levitt,L.,et al, 1972

Mollaret's Meningitis & Differential Diagnosis of Recurrent Meningitis
Am J Med 52:128, Hermans,P.,et al, 1972

Pituitary Apoplexy in Five Patients with Pituitary Tumors
BMJ 2:267, Epstein,S.,et al, 1971

Peperazine Neurotoxicity:"Worm Wobble"
BMJ 792, 1971 Dec., Parsons,A.C., 1971

Pituitary Apoplexy
J Oslo City Hosp 20:17, Lopez,I., 1970

Complains of Muscle Weakness
Patient Care Clinical Concepts, 21, 1970 Jan., , 1970

Newer Concepts of Cerebral Vascular Disease
Med Clin North Am 54:1970., Meyer,J., 1970

Brain Stem Tumors of Childhood & Adolescence
Am J Dis Child 119:465-472, Panitch,H.S.,et al, 1970

Atherosclerotic CVD-Its Nature & Management
Am J Med 46:763, Heyden,S.,et al, 1969

The Neuropathy of Acute Intermittent Porphyria
Quart J Med 38:307, 1969 July., Ridley,A., 1969

Huntington's Chorea
Bruyn, G. W. In Vinken & Bruyn, Handbk of Clin Neurol, North-Holland Publ Co, Amsterdam, 6:298, , 1968

The Uveomeningoencephalitic Syndrome
Neurol 16, 6031966., Riehl,J.L.,et al, 1966

Epilepsy in Children
Current Therapy, 1966, p. 574., Scholl,M.L., 1966

Neuro CPC of MGH
Acute Multiple Sclerosis, NEJM 273:760-7671965., , 1965

Central Nervous System Manifestations of Periarteritis Nodosa
Neurol 15:114, Ford,R.G.,et al, 1965

The Ataxic Form of Polyradiculoneuritis (Landry-Guillain-Barre Syndrome) Clinical & Pathologic Observations
J Neuropath Exper Neurol 21:171, Richter,R.B., 1962

The Diagnosis & Treatment of Seizures
Pediatr Clin North Am 9:353, Scholl,M.L., 1962

Dilantin Toxicity
Neurol 11:912-922, Roseman,E., 1961

An Unusual Variant of Acute Idiopathic Polyneuritis (Syndrome of Ophthalmoplegia, Ataxia, & Areflexia)
NEJM 255:57, Fisher,C.M., 1956

Cerebellar Ataxia in Children
Handout & References., Gilbert,J.J., 1850

Investigating suspected subarachnoid hemorrhage in adults
, Brown, S.C., et al,

Increased Prevalence of Nitrous Oxide-Induced Subacute Combined Degeneration of the Spinal Cord: Clinical and Imaging Findings
AJNR 47:513-520, Bruen,R.,et al, 2026

Tenecteplase for Acute Non-Large Vessel Occlusion 4.5 to 24 Hours After IschemicStroke, The OPTION Randomized Clinical Trial
JAMA doi:10.1001/JAMA.2026.0210, Ma,G.,et al, 2026

A Randomized Trial of Tenecteplase in Acute Central Retinal Artery Occlusion
NEJM 394:442-450, Ryan,S.J.,et al, 2026

Turning Slowly Predicts Future Diagnosis of Parkinsons Disease:A Decade-Long Longitudinal Analysis
Ann Neurol 99:114-123, Elshehabi,M.,, 2026

Clinicopathologic Conference, Disseminated Infection with Hypervirulent Klebsiella Pneumoniae
NEJM 394:282-294, Case 202026, 2026

Progressive Quadriparesis and Falls in a 66-Year-Old Man With Longstanding Human Immunodeficiency Virus
Neurol 106:e214621, Ong,B.A. & Carlson,A.K., 2026

Congenital Zika Syndrome
NEJM 394:e2, Bacin,F. & Montenegro,M.A., 2026

Systematic Genetic Assessment in Young Patients with Cryptogenic Stroke: The ES-EASY Project
Stroke 57:148-156, Mania-Paris,L.,et al, 2026

A 41-Year-Old Man with Steroid-Responsive Hemiparesis
Neurol 106:e214088, Obaidi,Z.A.,et al, 2026

Safety and Outcomes of Dibigatran Reversal with Idarucizumab Before IV Thrombolysis in Patients with Acute Ischemic Stroke
Neurol 106:e218012, Saflund,M.,et al, 2026

Late-Onset Seizures, Etiology and Demographics in US Tertiary Care Epilepsy Centers
Neurol 106:e214948, Blank,L.J.,et al, 2026

Zorevunersen in Children and Adolescents with Dravet Syndrome
NEJM 394:969-982, Laux,L.,et al, 2026

Using Susceptibility-Based Imaging in highly ctive Late-Onset Multiple Sclerosis
Neurol 106:e214794, Sosa,S.M.,et al, 2026

Myelitis-Predominant Agressive Phenotype:Unveiling Unique Paterns of Late-Onset Neuromyelitis Optica Spectrum Disorders
Ann Neurol 99:1139-1151, Pu,Y-L.,et al, 2026

Status Epilepticus After Carotid Endarterectomy:An Illustrative Case of Cerebral Hyperfusion Syndrome
Stroke 57:e188-191, Reuter,P.,et al, 2026



Showing articles 850 to 900 of 8215 << Previous Next >>