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Differential
(Click to cross reference)
abdominal distention
abducens nerve paralysis
acanthocytosis
acetazolamide
achondroplasia
acromicria
adverse drug reaction
alcohol
alcohol, neurologic complications with
algorithm
alopecia
alpha-fetoprotein
alveolar hypoventilation
amenorrhea
aminoacidopathies
aminoacidurias
ammonia
amniocentesis
amphetamines
anatomy of
anemia
Angelman syndrome
angiokeratoma
anorexia nervosa
anticonvulsants
aphasia
apraxia of eye movements
aqueduct of Sylvius, stenosis
aqueductal stenosis
areflexia
arthralgia
arthritis
arylsulfatase B
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
atlanto-axial subluxation
attention deficit disorder with hyperactivity
autism
autoimmune disease
basal ganglia, calcification of
basal ganglia, lesion, bilateral
basilar impression
Bassen-Kornzweig syndrome
battered child syndrome
behavior modification
behavior, combative
behavioral disorder
biologic markers
bitemporal visual field defect
blepharophimosis
blepharospasm
blind spot, enlarged
blindness
blindness, sudden
bone age
bone biopsy
bone marrow transplantation
brachial plexus neuropathy
brachial plexus neuropathy, familial
brain atrophy
brain biopsy
brainstem, atrophy
breech delivery
bruxism
cachexia
calcification, gyral
calcification, intracranial
carbonic anhydrase II deficiency
carcinoembryonic antigen
carcinoma
cardiomyopathy
caries
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataracts
cavernous sinus
cavernous sinus, metastasis to
celiac disease, adult
celiac disease, childhood
central hypoventilation, congenital
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebral cortex
cerebral cortical atrophy
cerebral palsy
cerebral vasculature
cerebrospinal fluid, biochemical markers of CNS tumors
cerebrospinal fluid, cytology
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, pressure increased
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, mimics
cerebrovascular accident, multiple
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
chemotherapy, CNS treatment and complications with
child abuse
children
chorea
choreoathetosis
chorionic gonadotropin
chorioretinitis
chromosomal abnormality
chromosome 11
chromosome 14
chromosome 15
chromosome 8
chronic graft versus host disease
chronic progressive external ophthalmoplegia
cisterna magna, enlarged
cisternogram, radionuclide
cleft palate
Clinical Pathologic Conference(C.P.C.)
clinodactyly
Cockayne's syndrome
codfish vertebrae
cold hands sign
collagen vascular disease
coma
complications
compression fracture
congenital heart disease
congenital heart disease, CNS complications with
congenital malformation
congenital malformation, non CNS
conjunctivitis
consanguinity
contractures, joint
cornea, abnormal
cornea, opacity of
Cornelia de Lange syndrome
corpus callosotomy
corpus callosum, atrophy of
corpus callosum, thinning
cortical blindness
cranial nerve palsies
craniopharyngioma
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, weak
cryopyrin-associated periodic syndrome
cryptorchidism
cultured skin fibroblasts
cystinosis
cystinuria
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafmute
deafness
degenerative diseases of CNS
dementia
dementia, childhood
dementia, rapidly progressive
dentate nuclei, lesion of
dermatitis herpetiformis
developmental evaluation
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
diagnostic criteria
diarrhea
differential diagnosis
difficulty climbing stairs
digits, abnormal
diplopia
dislocated hip, congenital
dissociated sensory loss
distal muscle atrophy
distal muscle weakness
dopa responsive dystonia
drooling
dural sinus thrombosis
dwarfism
dysarthria
dyslexia
dysmorphic
dysostosis multiplex
dysphagia
dyspraxia
dystonia
ear, abnormal
eating disorder
echocardiogram
ectopic pinealoma
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
empty sella
encephalopathy
encephalopathy, progressive
endovascular therapy
enophthalmous
enzyme treatment
enzyme, defect
enzyme, muscle disease
enzyme, serum
epicanthal folds
epidemiology of neurology
episodic disorders
evoked potentials
exercise
exercise intolerance
exostosis
eye movement, disorders of
eyebrows, abnormal
eyes, sunken
facial anomalies
facial appearance, abnormal
facial hypoplasia
facial nerve palsy
failure to thrive
false negative
familial
fatigue
feeding disorder
fetal alcohol syndrome
fetus
fever
fever, recurrent
fibrillations
finger tapping
floppy infant
foam cells
follicle stimulating hormone
foot drop
foot drop, bilateral
fracture, pathologic
Friedreich's ataxia
frontal bossing
fucosidosis
gadolinium
gait disorder
gait, apraxic
gait, spastic
gangliosidosis GM1
gangliosidosis GM2
gargoylism
gastrointestinal disease, neurologic complications
gastrointestinal motility
gender
gene
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
genital hypoplasia
genu valgum
glaucoma
glucose tolerance test, abnormal
gluten ataxia
gluten sensitivity
gluten-free diet
glycogen debranching enzyme deficiency
glycogen storage disease
glycoprotein
Gowers maneuver
gray hair
growth hormone
growth hormone deficiency
growth retardation
hair, darkening of
hair, loss
Hallgren's syndrome
hamartoma
hand flapping
hand weakness
head circumference
head injury
head injury, hypothalamic and pituitary damage
head injury, pediatric
headache
hearing loss
heart block
heart murmur
hemiparesis
hemoglobin abnormality, neurologic complications of
hemorrhage, intracranial, newborn
hemorrhagic diathesis
hepatitis
hepatomegaly
hepatosplenomegaly
heralding manifestation
hereditary multiple exostoses
herpes simplex virus
herpes simplex virus infection, newborn
herpes simplex virus, human nervous system and
high arched palate
hip dysplasia
Hirschprung's disease
hirsutism
HLA
homocystinuria
Hunter's syndrome
Hurler's syndrome
hydrocephalus
hydrocephalus, normal pressure
hydrocephalus, normal pressure in children
hypercapnia
hyperhomocysteinemia
hyperphagia
hyperpigmentation of skin
hyperreflexia
hypertelorism
hypertonia
hypertrophic cardiomyopathy
hypertrophic intracranial pachymeningitis
hypodontia
hypoglycemia
hypogonadism
hypomagnesemia
hypomyelination
hypoparathyroidism
hypopigmentation of skin
hypopituitarism
hyporeflexia
hypotelorism
hypothalamus
hypothalamus, disturbance of
hypothalamus, lesion of
hypothalamus, neoplasm of
hypothermia
hypothermia, causes of
hypothyroidism
hypotonia
hypotonia, infants
hypoxia
iatrogenic neurologic disorders
imbalance
immunodeficiency
immunosuppression
imperforate anus
impulsivity
inability to stand on tiptoes
inclusion bodies, intranuclear
infection, recurrent
insulin resistance
intellectual deficit
intellectual deterioration
intelligence quotient
intestinal biopsy
intestinal pseudoobstruction
intracranial hemorrhage
intracranial hypertension, benign
intracranial hypertension, benign, differential diagnosis
intracranial hypertension, benign, pathogenesis of
intracranial pressure, increased
intrauterine
intrauterine infection
intrauterine infection, viral
joint hypermobility
Kearns-Sayre syndrome
keratoconus
Klinefelter's syndrome
Krabbe's disease
kyphoscoliosis, neurologic causes of
lactate
lactic acidemia
laminar necrosis, cortical
language disorders in children
Laurence-Moon-Bardet-Biedl syndrome
L-dopa
learning disability, in children
Leber's hereditary optic neuropathy
leg weakness, bilateral
Leigh's disease
lens, dislocation of
lens, ectopic
leukemia
leuko-araiosis
leukodystrophy
leukodystrophy, 4H
leukoencephalopathy
level of consciousness, decreased
life expectancy
lip, abnormal
lipid storage disorder of CNS
livedo reticularis
low birth weight
Lowe's syndrome
lumbar puncture
luteinizing hormone
lymphoma
lysosomal storage disease
macrocephaly
malabsorption
malabsorption syndrome
malformation, CNS, congenital
megalencephaly
melanomatosis, primary malignant
MELAS syndrome
meningitis, aseptic
menses
mental retardation
mental status, abnormal
MERRF syndrome
metabolic acidosis
metabolic disorder, primary
metachromatic leukodystrophy
microcephaly
micrognathia
micromelia
microspherophakia
migraine
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
Morquio syndrome
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRS
mucopolysaccharidoses
multiple system atrophy
muscle biopsy
muscle cramp
muscle spasm
muscle stiffness
muscle weakness
muscle weakness, proximal
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myelination of nervous system
myelopathy
myoclonus
myoclonus, epilepsy
myopathy
myopathy, distal
myopathy, distal, vacuolar
myopathy, inclusion body
myopathy, inclusion body, hereditary
myopathy, mitochondrial
myopathy, vacuolar
myopia
myotonia
nasal bridge, wide
nausea and vomiting
neck, webbed
negative
neoplasm, intracranial with metastasis extracranially
neoplasm, pituitary
neoplasm, primary intracranial-treatment of
neoplasm, primary of CNS
neoplasm, primary of CNS-children
neoplasm, primary of CNS-incidence of
neoplasm, primary of CNS-survival
neoplasm, primary of CNS-treatment of
nerve biopsy
neuritis
neurocutaneous disease
neuroendocrinology
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, peripheral
Niemann-Pick disease
Noonan Syndrome
normal
nose, abnormal
nystagmus
nystagmus, see-saw
obesity
ocular motility, disorders of
ocular myopathy
oligodactyly
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
optic atrophy, bilateral
optic foramina
optic foramina, abnormal
optic nerve sheath fenestration
optic nerve, decompression of
optic neuropathy
oral ulcerations
osteogenesis imperfecta
osteopetrosis
osteoporosis
otosclerosis
P300
Pallister-Hall syndrome
palpebral fissure, short
pancytopenia
papilledema
paraparesis
paraparesis, spastic
Parkinson disease, differential diagnosis of
Parkinsonism syndrome
PAS positive
patent ductus arteriosus
pathology
pectus carinatum
pectus excavatum
perceptual-motor dysfunction
personality change
philtrum, hypoplastic
phocomelia
photophobia
photosensitivity, skin
pigmentary retinopathy
pinched face
pituitary
pituitary stalk
pituitary, adenoma
pituitary, dysfunction
pituitary, enlargement
pituitary, hyppoplasia
pituitary, lesion of
PLEDs
PLEDs, bilateral independent
PLEDs, etiology of
pleocytosis of cerebrospinal fluid
polydactyly
polyhydramnios
polyps, gastrointestinal tract
posterior pituitary ectopia
postural abnormality
Prader-Labhart-Willi syndrome
precocious puberty
pregnancy, neurologic complications in
premature infant
prenatal diagnosis by amniocentesis
pretectal syndrome
progeria
prognathism
prognosis
progressive neurologic disorder
proteinuria
pseudoretinitis pigmentosa
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychomotor retardation
psychosis
psychosocial aspects
ptosis
puberty
puberty, delayed
pulmonary stenosis
pupil, abnormality in neurologic disorders
pupil, ectopic-congenital
putamen, lesion of
putamen, lesion of, bilateral
quadriparesis
quadriplegia
radiation hypersensitivity
radiation therapy, CNS treatment and complications with
ragged-red fibers
rapidly progressing neurologic illness
rash
reading problem, causes of
recurrent
red eye
renal failure
renal tubular acidosis
respirations in CNS disease
respirator
respiratory failure
respiratory tract infection
retinal degeneration
retinitis pigmentosa
retinopathy
Rett's syndrome
review article
rickets
risk factors
ritalin
rocking
root lesion, nerve
saddle nose
Sanfilippo syndrome
schizophrenia
Schwartz-Jampel syndrome
sclerae, blue
scoliosis
scoliosis, neurologic association with
seizure
seizure, children
seizure, drug resistance
seizure, focal
seizure, injury following
sella turcica, enlargement of
sella turcica, hypoplasia of
sensorineural hearing loss
serologic testing
short neck
short stature
shunt procedure, lumboperitoneal
sickle cell trait
simian crease
skin, biopsy
skin, darkening of
skin, lesions in neurologic disorders
skull bone, thickening
skull x-ray, abnormal
skull x-ray, bony defect on
sleep
sleep pathology and physiology
small vessel disease
somatosensory evoked potentials
spasticity
speech disorder
speech disorder, childhood
speech, delayed development of
Spielmeyer Vogt syndrome
spinal cord, compression of
spinal cord, lesion of
spinal muscular atrophy
splenomegaly
spongy degeneration of brain
standing difficulty
stem cell transplantation
stent, venous sinus
steppage gait
stereotyped behavior
stimulant drugs
stooped posture
strabismus
strokelike episodes
subarachnoid hemorrhage
subdural hematoma
subdural hematoma, neonates and infants
suck, poor
suprasellar lesion
syndactyly
synophrys
systemic illness
teeth, abnormal
telangiectases
temper tantrums
temporal lobe, lesion
teratoma
third ventricle, mass of
thyroid function tests
toe walking
tongue, enlarged
tongue, protrusion of
treatment of neurologic disorder
tremor
tremor, postural
tremulousness
trichopoliodystrophy
upgaze, paralysis of
urea-cycle enzymopathies
urinary 17 hydroxycorticosteroids
urinary 17 ketosteroids
Usher's syndrome
valvulopathy
viral infection, CNS
visual acuity, decreased
visual field defect
visual field testing
visual fields, constricted
visual impairment
visual loss
vomiting, recurrent
walking, difficulty with
weakness
weakness, generalized
weight gain
weight loss
Werner's syndrome
wheelchair
white matter disease
wide based gait
xeroderma pigmentosa
x-linked mental retardation
x-ray, cervical spine
Showing articles 100 to 150 of 888 << Previous Next >>

Clinicopathologic Conference, Myasthenia Gravis
NEJM 391:1441-1450, Case 32-2024, 2024

Rapidly Progressive Dementia in a Man With HIV Infection and Undetectable Plasma Viral Load
Neurol 100:344-348, Chishimba,L.C.,et al, 2023

Progressive Camptocormia with Head Drop and Dysphagia
JAMA Neurol 80:209-210, El-Wahsh,S., et al, 2023

Transient Global Amnesia
NEJM 388:635-640, Ropper,A.H., 2023

Lead Poisoning
NEJM 388:e63, Dhar,S. & Garg,D., 2023

Cognitive and Clinical Characteristics of Patients with Limbic-Predominant Age-Related TDP-43 Encephalopathy
Neurol 100:e2027-e2035, Pagnotti,R.M.B.,et al, 2023

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

Severe Vitamin B12 Deficiency Presenting as Pancytpenia, Hemolytic Anemia, and Parasthesia:Could Your B12 Be Any Lower?
Cureus doi:10.7759/cureus 29225, Pelling,M.M., et al, 2022

Clinicopathologic Conference, Diffuse Large B-Cell Lymphoma
NEJM 386:977-986, Case 7-2022, 2022

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

A 77-Year-Old Man with Involuntary Movements, Sleep Changes, Falls, Bulbar Symptoms, and Cognitive Complaints
Neurol 99:26-30, Cao, T.Q.,et al, 2022

Biopsy Negative Giant Cell Arteritis - Revised Diagnostic Criteria
J Stroke Cerebrovasc Dis 31:106660, Finelli, P.F., 2022

Dura Mater Thickening and Enhancement in Anti-NMDAR Encephalitis
Neurol 99:628-629, Xia, C. & Chen, H.S., 2022

Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022

A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance
Neurol 99:997-1003, Chaity,D.K.,et al, 2022

Clinicopathologic Conference, Mycobacterium Tuberculosis Meningitis
NEJM 384:166-176, Case 1-2021, 2021

Acute Flaccid Myelitis: Cause, Diagnosis, and Management
Lancet 394:334-397, Murphy, O.C.,et al, 2021

Rapidly Progressive Thalamic Dementia
Neurol 96:e809-e813, Rizzo, A.C.,et al, 2021

A 65-Year-Old Woman with Tremor
Neurol 97:e1257-e1261, Ye, J.,et al, 2021

Clinicopathologic Conference, Lead Poisoning
NEJM 385:2378-2388, Case 38-2021, 2021

Clinicopathologic Conference, Fat Embolism Syndrome
NEJM 385:2464-2474, Case 39-2021, 2021

CNS Demyelinating Attacks Requiring Ventilatory Support With Myelin Oligodendrocyte Glycoprotein or Aquaporin-4 Antibodies
Neurol 97:e1351-e1358, Zhao-Fleming,H.H.,et al, 2021

A Triad of Tremor, Ataxia, and Cognitive Impairment
Neurol 96:e1802-e1803, Au, L.W.C.,et al, 2021

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

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

Clinicopathologic Conference, Delayed Postthypoxic Leukoencephalopathy
NEJM 384:2438-2445, Case 19-2021, 2021

A Brewing Back Pain
NEJM 385:66-72, Pischel, L.,et al, 2021

Clinicopathologic Conference, Cerebral Amyloid Angiopatny-Related Inflammation
NEJM 385:358-368, Case 22-2021, 2021

Pneumorrhachis and Pneumothorax After Epidural Analgesia: A Case Report and Review
QMT doi.org/10.5339/qmj.2021.1, Shaikh,N.,et al, 2021

Pyogenic Brain Abscesses in a Patient with Digital Clubbing
JAMA Neurol 77:129-130, Paliwal, V.K.,et al, 2020

A Rare Presentation of Whipple Disease
Neurol 94:e758-e761, Koek, A.T.,et al, 2020

Homonymous Hemianopia with Normal Magnetic Resonance Imaging
JAMA Ophthalmol doi:10.1001/JAMAOphthalmol.2020.0447, Cai, S.,et al, 2020

Anti-NMDAR Encephalitis with Overlapping Demyelinating Syndrome
Neurol 94:e1866-e1869, Kim, H.W., et al, 2020

A Young Health Woman with Difficult-to-Wean Acute Ventilator Dependence
Neurol 94:e1340-e1343, Chandrashekhar, S.,et al, 2020

A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
Neurol 94:e1213-e1218, Lima, J.E.E.,et al, 2020

Pernicious Anaemia
BMJ 369:m1319, Mohamed, M.,et al, 2020

Coagulopathy and Antiphospholipid Antibodies in Patients with Covid-19
NEJM 382:e38, Zhang, Y.,et al, 2020

Severe Acute Respiratory Syndrome Coronavirus 2 Infection and Ischemic Stroke
Stroke 51:e124-e127, Valdes Valderrama, E.,et al, 2020

Arthralgia as an Initial Presentation of COVID-19
Rheumatol Int doi:10.1007/s00296-020-04561-0, Joob, B. & Wiwanitkit, V., 2020

A 57-Year-Old Woman with Progressive Ataxia and Falls
Neurol 95:650-656, Badahdah, A., 2020

Clinicopathologic Conference, Borrelia Miyamotoi Infection
NEJM 383:1578-1586, Case 32-2020, 2020

A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
Neurol 95:e2707-e2710, Lad, M. & Griffiths, T.D., 2020

Clinicopathologic conference, Frontotemporal Lobar Degeneration with tau-positive inclusions consistent with Picks disease
NEJM 383:2666-2675, Case 41-2020, 2020

Fat Embolism Syndrome in Sickle Cell Disease
J Clin Med 9:1-12, Tsitsikas, D.A.,et al, 2020

An Atypical Presentation of Creutzfeldt-Jakob Disease with a Heidenhain Variant and Balints Syndrome
Cureus DOI:10.7759/cureus,8608, Gupta,A. & Dhingra,A., 2020

Progressive Proximal Weakness in a 61-Year-Old Man
Neurol 98:122-127, Yu, M.,et al, 2020

Muscular Dystrophies
Lancet 394:2025-2038, Mercuri, E.,et al, 2019

Lyme Disease: What the Neuroradiologist Needs to Know
AJNR 40:1998-2000, Valand, H.A.,et al, 2019

Diagnostic Tools for Immune Causes of Encephalitis
Clin Microbiol Infect 25:431-436, Lascano, A.M.,et al, 2019

A 54-year-old man with Dyspnea and Muscle Weakness
Neurol 92:e1136-e1140, Chertcoff, A.,et al, 2019



Showing articles 100 to 150 of 888 << Previous Next >>