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Differential
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abdominal muscle paralysis
abducens nerve paralysis
abducens nerve paralysis, bilateral
abortion, spontaneous
acanthocytosis
acid maltase deficiency
acid maltase deficiency, adult
acromicria
agenesis of aqueduct of Sylvius
aggression
alien hand syndrome
alpha glucosidase
amniocentesis
amyloidosis
amyotrophic chorea-acanthocytosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, juvenile
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, sensory symptoms in
amyotrophic lateral sclerosis, treatment of
anemia
anemia, megaloblastic
Angelman syndrome
angiography, posterior fossa
anorexia
anterior horn cell disease
aphonia
apraxia
apraxia of eye movements
aqueduct of Sylvius, stenosis
aqueductal stenosis
areflexia
arterial dissection, carotid
arthralgia
arthritis
arylsulfatase B
aspartate aminotransferase
aspiration
ataxia
ataxia, cerebellar
ataxic gait
attention span
autoimmune disease
automobile accidents
B 12 deficiency
Babinski sign
Babinski-Nageotte syndrome
basal ganglia
basal ganglia, degeneration
behavior, combative
behavioral disorder
Behcet's syndrome
blue tongue virus
bone marrow biopsy
brachial plexus
brachial plexus injury
brachial plexus, lesion of
brachycephaly
bradykinesia
brain atrophy
brain biopsy
brainstem, infarction of
brainstem, lesion of
brainstem, metastasis to
bright tongue sign
bulbar palsy
bulbar palsy, progressive
burning hands
burning paresthesia
C0ORF72
CAG repeats
carcinoma
cardiomyopathy
carotid angiogram
carpal tunnel syndrome
CAT scan
CAT scan, abnormal
CAT scan, base of skull
CAT scan, false negative
caudate nucleus, atrophy
celiac disease, adult
celiac disease, childhood
central nervous system, infection of
cerebellar atrophy, primary
cerebellar lesion
cerebral cortical atrophy
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cervical osteophyte
cervical spine
cervical spine abnormality
cervical spine disease
chewing, impaired
children
chorea
chorein
chromosomal abnormality
chromosome 15
chromosome 5
Clinical Pathologic Conference(C.P.C.)
cognition
conduction block
congenital bilateral perisylvian syndrome
congenital heart disease
congestive heart failure
cornea, opacity of
corpus callosum, lesion of
cortical-basal ganglionic degeneration
cranial nerve palsies
cranial nerve palsies, unilateral
cranial nerve tumor
cranial neuropathy
cranial neuropathy, multiple
cranio-cervical junction
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, weak
crying, pathologic
cultured skin fibroblasts
cyst, porencephalic
deafness
degenerative diseases of CNS
dementia
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
denervation of muscle
denervation potentials
dermatitis herpetiformis
developmental retardation
dexterity, impaired
diarrhea
differential diagnosis
diplegia, brachial
diplopia
dissociated sensory loss
distal muscle atrophy
distal muscle weakness
drooling
dysarthria
dyskinesia, buccal lingual facial
dysmorphic
dysphagia
dysphonia
dyspnea
dyspraxia
dystonia
eating disorder
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electromyogram
electromyogram, decremental response
electron microscopy
embryogenesis
emotional lability
encephalomalacia
entrapment neuropathy
enzyme treatment
enzyme, defect
epidemiology of neurology
face, inexpressive
facial appearance, abnormal
facial expression abnormality
facial weakness
facial weakness, bilateral
failure to thrive
falling
familial
fasciculation
fatigable chewing
fatigue
feeding disorder
fever
fibrillations
fish
flail arm syndrome
fluorescene in situ hybridization
foot drop
foramen magnum, lesion of
frontal lobe, atrophy
frontotemporal dementia, behavioral variant
gadolinium
gag reflex, depressed
gait disorder
gait, spastic
gait, waddling
gammaglobulin therapy, intravenous
gastrointestinal disease, neurologic complications
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
genital ulcerations
glomus jugulare tumor
gluten ataxia
gluten sensitivity
gluten-free diet
glycogen storage disease
GM1 ganglioside antibodies
grasp reflex
growth hormone deficiency
growth retardation
Guillain Barre syndrome
gunshot wounds
gynecomastia
hallucination
hand flapping
hand weakness
head injury
headache
headache, intermittent
headache, severe
headache, unilateral
hearing loss
hemiparesis
hepatitis
hepatomegaly
herpes simplex virus
HLA
hoarseness
hydranencephally
hydrocephalus
hyperactivity
hypercalcemia
hyperparathyroidism
hyperphagia
hyperreflexia
hypersegmented polys
hypogeusia
hypoglossal nerve
hypoglossal nerve paralysis
hypogonadism
hypopigmentation of skin
hyporeflexia
hypotonia
hypotonia, infants
imbalance
immunosuppression
infectious mononucleosis, neurologic findings with
influenza A virus
insular cortex
intellectual deficit
intellectual deterioration
intrinsic hand muscles, wasting of
jaundice
jaw closure weakness
jaw jerk, abnormal
jugular foramen syndrome
lactic dehydrogenase(LDH)
language disorders in children
laughing, pathologic
leg weakness, bilateral
leg weakness, unilateral
levitation
lip, biting
lobar atrophy
lymphoma
lymphoma involving CNS
lysosomal storage disease
lysosomes, abnoral
macrognathia
malabsorption
malformation, CNS, congenital
masseter muscle wasting
masseter muscle weakness
mastectomy, radical
medial medullary syndrome
medulla oblongata, infarction of
medulla oblongata, lesion of
medulla oblongata, neoplasm of
meningioma
mental retardation
mental status, abnormal
methylmalonic acid, serum
microcephaly
misdiagnosis
misdirection
molecular genetics
monoclonal gammopathy
mononeuropathy
mortality
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, skull bone changes
MRI, spinal cord
mucopolysaccharidoses
multiple sclerosis
mumps virus
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle stiffness
muscle twitching
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
myelopathy
myeloschisis
myoclonic jerks
myopathy
myopathy, amyloid
myopathy, vacuolar
nasal speech
nasopharyngeal carcinoma
neck pain
neck weakness
neonatal infection, viral
nerve conduction studies
nerve conduction studies, motor
neuroendocrinology
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neuroma
neuromuscular disease, electrodiagnosis of
neuronopathy
neuropathology
neuropathy
neuropathy, motor
neuropathy, motor, multifocal
neuropathy, multifocal
neuropathy, sensory
nonverbal
nusinersen
nystagmus
obesity
occipital condyle fracture
occipital condyle syndrome
occipital pain
opened mouth
operculum syndrome
operculum syndrome, bilateral
ophthalmoplegia
optic nerve
oral ulcerations
osteomalacia
osteoporosis
pain
pain, abdominal
palate, paralysis-unilateral
papilledema
paranoia
paraparesis, spastic
paraspinal muscle
paraspinal muscle weakness
parathyroid adenoma
paresthesias
paresthesias, hands
parvovirus
peripheral blood smear, abnormal
peripheral nerve, lesion of
pernicious anemia
plasma cell dyscrasia
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
polyneuropathy, chronic inflammatory demyelinating
Pompe's disease of glycogen storage
posterior inferior cerebellar artery syndrome
postural abnormality
Prader-Labhart-Willi syndrome
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
primary lateral sclerosis
prognathism
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
pseudobulbar palsy
pseudohypertrophy
pseudomyotonia
psychiatric problems in neurologic disorders
puberty
puberty, delayed
quadriparesis
radiation therapy, CNS treatment and complications with
recurrent laryngeal nerve paralysis
renal stones
repetitive nerve stimulation
respiratory failure
review article
rheumatoid arthritis
rheumatoid arthritis, neurologic complications of
rheumatoid pachymeningitis
rigidity
risk factors
Romberg's sign
rubella virus
scleritis
scoliosis
scoliosis, neurologic association with
screening
seizure
seizure, recurrent
sensory loss
sensory loss, cortical
sensory nerve action potentials
sensory symptoms
serologic testing
short stature
Sicard-Collet syndrome
skin, biopsy
skin, lesions in neurologic disorders
skull fracture, basal
smiling
SMN1 gene
spasticity
speech disorder
speech disorder, childhood
speech, delayed development of
spinal cord, compression of
spinal muscular atrophy
spinal muscular atrophy, classification
standing difficulty
sternocleidomastoid wasting
sternocleidomastoid weakness
strabismus
suck, poor
symmetric brain lesions
systemic illness
tandem gait, ataxic
Tapia's syndrome
taste
teeth, wide-spaced
temper tantrums
temporal lobe, atrophy
temporal lobe, lesion
temporal lobe, lesion, bilateral
temporalis muscle wasting
teratogenesis
teratogenesis, viral
third nerve palsy
tinnitus
tinnitus, pulsatile
tongue deviation
tongue, atrophy
tongue, biting
tongue, enlarged
tongue, fasciculations of
tongue, hemiatrophy of
tongue, impaired movements of
tongue, protrusion of
tongue, smooth
tongue, swelling
tongue, ulcer
tongue, weakness
transient ischemic attack
trapezius weakness
trauma
treatment of neurologic disorder
tremor
tremor, postural
tremulousness
urine, dark
vagal neuropathy
vagus nerve, lesion of
vasculitides
viral infection
viral infection, CNS
visual acuity, decreased
visual field defect
vocal cord paralysis
vocalizations
Waldenstrom's macroglobulinemia
walking, difficulty with
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
wheelchair
wide based gait
winging of scapula
word-finding difficulty
writing
X-linked bulbospinal neuronopathy
Showing articles 100 to 150 of 2394 << Previous Next >>

Clinicopathologic Conference, Systemic Immunoglobulin Light-Chain (AL) Amyloidosis
NEJM 389:166-175, Case 21-2023, 2023

Primary Diffuse Leptomeningeal Melanocytosis, A Diagnoatic Conundrum
Neurol 101:e576-3580, Selvarajan,J.M.P.,et al, 2023

Multidisciplinary End-of-Life Care for a Patient with Amyotrophic Lateral Sclerosis Requesting Euthanasia
Lancet 402:484, Kruithof,W.J.,et al, 2023

A 67-YEar-Old Man with Multiple Intracranial Lesions
Neurol 101:e845-e851, Ngo,A.,et al, 2023

A 17-Year-Old Girl with Progressive Cognitive Impairment
Neurol 101:e1466-e1472, Zhao,B.,et al, 2023

A Young Woman with Rapidly Progressive Weakness and Paresthesia
Neurol 101:676-681, Alwakeel,S.S.,et al, 2023

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

Clinicopathologic Conference, Antiphospholipid Syndrome due to SLE with Hypocomplimentemia
NEJM 389: 2277-2285, Case 38-2023, 2023

Spectrum of Neuroradiologic Findings Associated with Monogenic Interferonopathies
AJNR 43:2-10, Benjamin, P.,et al, 2022

A 31-Year-Old Man with Sequential Vision Loss
Neurol 98:163-169, Fortes, B.,et al, 2022

Confused About Confusion
NEJM 386:80-87, Spanjaart, A.M.,et al, 2022

Rare Cause of Hemiparesis and Ataxia in a 36-Year-Old Man
Neurol 98:251-255, Decker, J. & Singh, M., 2022

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

Leber Hereditary Optic Neuropathy with Longitudinal Spinal Cord Lesion Mimicking Spinal Cord Infarction
Neurol 98:468-469, Zhao, B.,et al, 2022

A 37-Year-Old Man with Involuntary Movements, Gait Disturbance, and Hyperasthesia
Neurol 98:851-853, Meng, D.,et al, 2022

Amyotrophic Lateral Sclerosis
Lancet 400:1363-1380, Feldman, E.L.,et al, 2022

An 80-Year-Old Woman with a Homonymous Hemianopsia
Neurol 99:713-717, Tajfirouz, D.,et al, 2022

Epidemiology, Survival, and Clinical Characteristics of Inclusion Body Myositis
Ann Neurol 92:201-212, Lindgren, U.,et al, 2022

Clinicopathological Conference, Chronic Candida Albicans Meningitis
NEJM 387:641-650, Case 25-2022, 2022

Reversible Parkinsonism Caused by Lumboperitoneal Shunt Overdrainage
Neurol 99:486-488, Takeuchi, H.,et al, 2022

Spontaneous Subarachnoid Haemorrhage
Lancet 400:846-862, Claassen, J. & Park, S., 2022

Neuroimaging Findings in CHANTER Syndrome
AJNR 43:1136-1141, Mallikarjun, K.S.,et al, 2022

A 65-Year-Old Woman with Cancer History and Wrist Drop
Neurol 99:570-576, Merrill, R.,et al, 2022

Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
Lancet 400:1144, Sabino de Oliveira, D.,et al, 2022

Disabling Jaw Clonus in a Patient with Bulbar-Onset Amyotrophic Lateral Sclerosis Successfully Treated with Botulinum Toxin
Neurol 99:671, Santos, M.O.,et al, 2022

Neuroimaging Biomarkers in a Patient with Probable Psychiatric-Onset Prodromal Dementia with Lewy Bodies
Neurol 99:654-657, Urso, D.,et al, 2022

Sweet Syndrome
Stat Pearls www.ncbi.nlm.gov, Sept, Goyal,V.P. & Holmes,H, 2022

Cases with IgG4-related Ophthalmic Disease with Mass Lesions Surrounding the Optic Nerve
Am J Ophthalmol 25:101324, Hamaoka, S.,t al, 2022

Infantile and Childhood Hydrocephalus
NEJM 387:2067-2073, Whitehead,W.E.&Weiner,J.L., 2022

A 36-Year-Old Man With Asymmetric Muscle Weakness
Neurol 99"1057-1061, Harada,Y.,et al, 2022

Sturge-Weber Syndrome
www.UptoDate.com,Dec, Patterson,M.C., 2022

The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022

Congenital Cytomegalovirus Infection
BMJ 373:m1212, Pesch, M.H.,et al, 2021

A Case of Primary Leptomeningeal Lymphoma Presenting with Hydrocephalus Characterized by Disproportionately Large Fourth Vehicle
NMCCRJ 8:399-404, Nohira, S.,et al, 2021

A Middle-Aged Man with a History of Muscle Pain Presenting with Progressive Leukoencephalopathy and Subsequent Coma
Neurol 97:910-915, Jakobsson, A.S.,et al, 2021

The First Examination of Diagnostic Performance of Automated Measurement of the Callosal Angle in 1856 Elderly Patients and Volunteers Indicates that 12.4% of Exams Met the Criteria for Possible Normal Pressure Hydrocephalus
AJNR 42:1942-1948, Morzage, M.,et al, 2021

A 59-Year-Old Man with Progressive Proximal Weakness Since Childhood
Neurol 97:958-963, Davalos, L.,et al, 2021

Transocular Sonography in Acute Arterial Occlusions of the Eye in Elderly Patients
PlusOne doi.org/10.1371/journal.pone.0247072, Czihal, M.,et al, 2021

A Middle-Aged Man with Progressive Gait Abnormalities
Neurol 97:e2423-e2428, Lin, J.,et al, 2021

Clinicopathologic Conference, Lympohplasmic Lymphoma of the CNS (Bing-Neel Syndrome)
NEJM 384:745-753, Case 6-2021, 2021

Clinicopathologic Conference, Normal Pressure Hydrocephalus
NEJM 384:1350-1358, Case 10-2021, 2021

Natural History of "Pure" Primary Lateral Sclerosis
Neurol 96:e2231-e2238, Hassan, A.,et al, 2021

A Teenager with Shortness of Breath and Difficulty Walking
Neurol 96:e2346-e2350, Liu, S.C.,et al, 2021

Teaching Video NeuroImages: Jaw Clonus in Amyotrophic Lateral Sclerosis
Neurol 96:e2563, Goel, A.,et al, 2021

Complete Evaluation of Dementia: PET and MRI Correlation and Diagnosis for the Neuroradiologist
AJNR 42:998-1007, Oldan, J.D.,et al, 2021

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

Vitamin B12 Deficiency in a 29-Year-Old Woman
Neurol 97:e643-e646, Huddar, A.,et al, 2021

Chronic Meningitis
NEJM 385:930-936, Aksamit, A.J., 2021

A 79-Year-Old Woman with Subacute Bilateral Visual Loss
Neurol 97:e1159-e1165, Rossi, S.,et al, 2021

Nitromethane-Induced Acute Reversible Encephalopathy
Neurol 97:e1361-e1362, Palumbo, G.,et al, 2021



Showing articles 100 to 150 of 2394 << Previous Next >>