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Differential
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acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
acquired immunodeficiency syndrome, congenital
acquired immunodeficiency syndrome, infants and children
acromicria
advances in neurology
Aicardi-Goutieres syndrome
Alexanders disease
aneurysm
aneurysm, asymptomatic
aneurysm, intracranial
anorexia
apraxia of eye movements
aqueduct of Sylvius, stenosis
arm swing, reduced
arthritis
aspartocyclase
aspiration
ataxia
ataxia, truncal
ataxic gait
attention span
autoimmune epilepsy
B 12 deficiency
B 12 deficiency, infants
Babinski sign
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
biologic markers
blindness
blood transfusion
bone marrow biopsy
bradykinesia
brain atrophy
brain biopsy
breast feeding
Brown-Vialetto-Van Laere syndrome
cachexia
calcification, intracranial
Canavan's disease
CAT scan
CAT scan, abnormal
cataplexy
cerebellar lesion
cerebral cortical atrophy
cerebral palsy
cerebral vasculature
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular disease
cherry red spot
cherry red spot-myoclonus syndrome
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 3
Clinical Pathologic Conference(C.P.C.)
cold hands sign
complications
consanguinity
contractures, joint
controversies in neurology
corpus callosum, atrophy of
corpus callosum, thinning
cough
cranial nerve enhancement
cranial nerve enlargement
cranial neuropathy
cranial neuropathy, multiple
crawl regression
cry, abnormal
crying
cultured skin fibroblasts
cyst
cyst, parenchymal
D-dimer
decision analysis
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, childhood
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
developmental milestones
developmental milestones, loss of
developmental retardation
diagnostic criteria
differential diagnosis
difficulty climbing stairs
diplopia
dopa responsive dystonia
drooling
dropped head syndrome
dysarthria
dysmetria
dysphagia
dysphonia
dystonia
dystonia, children
electroencephalogram, abnormalities of
encephalitis
encephalitis, autoimmune
encephalopathy
encephalopathy, neonatal
encephalopathy, progressive
endoscopic surgery
endoscopy
enzyme, defect
epileptic encephalopathy
episodic disorders
evoked potentials
eye movement, disorders of
facial weakness
facial weakness, bilateral
failure to thrive
falling
familial
FARS2 deficiency
feeding disorder
fever
fine motor function, impaired
finger tapping
foam cells
fontanel, bulging
frontal bossing
fundus, abnormality of
gait disorder
galactorrhea
gangliosidosis GM2
Gaucher's disease
gaze palsy
gaze palsy, supranuclear
gender
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
globoid cells
glucocerebrosidase
glutamic acid decarboxylase, antibody
granular osmiphilic material
growth retardation
Hallervorden Spatz disease
hand deformity
hands, fisted
head circumference
head lag
headache
hearing loss
hepatic failure
hepatitis
hepatomegaly
hepatosplenomegaly
hexosaminidase-A
human immunodeficiency virus type 1
human immunodeficiency virus type 1, infants and children
hydrocephalus
hydrocephalus, complications with
hydrocephalus, etiology
hydrocephalus, fetal
hydrocephalus, non-communicating(obstructive)
hydrocephalus, treatment of
hyperreflexia
hypertonia
hypomyelination
hyporeflexia
hypothermia
hypotonia
hypotonia, infants
immunomodulation
inattention
inborn errors of metabolism
incoordination
intellectual deficit
intellectual deterioration
interferon alpha
intracranial pressure, increased
introverted
iron, brain
irritability
jaundice
Jewish
Krabbe's disease
lactic acidemia
L-dopa
Leigh's disease
lethargy
leukocyte enzyme abnormality
leukocytosis
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
life expectancy
lipid storage disorder of CNS
liver disease
liver function enzymes
lymphadenopathy
lymphadenopathy, axillary
lymphadenopathy, paraaortic
lysosomal storage disease
macrocephaly
masked facies
meconium staining
memory, impairment of
meningitis, CSF cell count-normal
mental retardation
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
metachromatic leukodystrophy, late-infantile
microcephaly
misdiagnosis
mitochondrial disease
monoclonal antibodies
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, angiography
MRI, contrast enhanced
MRI, hypointense signal foci on
MRI, paramagnetic effect
MRS
mucopolysaccharidoses
muscle biopsy
muscle spasm
myasthenia gravis
myasthenia gravis, infantile and juvenile
myelination of nervous system
myoclonus
myoclonus, epilepsy
nasal speech
nausea and vomiting
nerve conduction studies
neuroaxonal dystrophy
neurofibrillary degeneration
neurologic disease
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic examination
neurologic signs
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
Niemann-Pick disease
nystagmus
nystagmus, rotary
ophthalmoplegia
opisthotonus
opportunistic infection
opportunistic infection, CNS
optic atrophy
optic chiasm, enlarged
optic nerve
optic nerve, enlarged
pain
PANK2 mutation
papilledema
paraparesis, familial spastic
paraparesis, spastic
PAS positive material in the brain
pediatric neurology
pleocytosis of cerebrospinal fluid
postural abnormality
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
prolactin, elevated
psychological testing
psychomotor retardation
psychosis
ptosis
pulmonary infiltrates
pyramidal tract
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
rash
rectal biopsy
renal tubular acidosis
retinal degeneration
retinitis pigmentosa
retropulsion
Rett's syndrome
review article
riboflavin transporter deficiency
rigidity
rituximab
Rosenthal fibers
running
scoliosis
scoliosis, neurologic association with
screening
sedimentation rate, elevated
seizure
seizure, children
seizure, drug resistance
seizure, intractable
serositis
short stature
shunt procedure, ventricular
shunt procedure, ventricular-complications of
skin, lesions in neurologic disorders
slurred speech
somnolence
spastic diplegia
spasticity
speech disorder
speech disorder, childhood
speech, loss of
splenomegaly
spongy degeneration of brain
startle reaction
status epilepticus
stereotyped behavior
stiff joints
strabismus
striatonigral degeneration
striatonigral degeneration, infantile
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
suck, poor
symmetric brain lesions
systemic illness
systemic juvenile idiopathic arthritis
Tay-Sachs disease
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytosis
titubation
toe walking
tone, muscle, increased
toxoplasmosis, CNS
treatment of neurologic disorder
tremor
tremor, intention
trichopoliodystrophy
tuberous sclerosis
tumor necrosis factor
tyrosine hydroxylase deficiency
vegetarianism
ventricular enlargement
ventriculostomy
ventriculostomy, endoscopic
visual acuity, decreased
visual evoked response
visual fields, constricted
visual impairment
visual loss
vitamin deficiency
vomiting, episodic
vomiting, recurrent
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
Werdnig-Hoffman disease
West disease
wheelchair
white matter disease
wide based gait
workup
wrist drop
x-linked hydrocephalus
Showing articles 0 to 50 of 230 Next >>

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

A Middle-aged Woman with Severe Scoliosis and Encephalopathy
JAMA Neurol 78:251-252, Mohan, G.,et al, 2021

Clinicopathologic Conference, Systemic Juvenile Idiopathic Arthritis
NEJM 385:1220-1229, Case 29-2021, 2021

A Rare Case of Metachromatic Leukodystrophy with Multiple Bilateral Cranial Nerve Enhancement
Neurol 93:e1742-e1743, Sonowal, P.,et al, 2019

Pantothenate Kinase - Associated Neurodegeneration (PKAN)
Emedicine.Medscape Sept, Hanna, P.A. & Benbadis, S.R., 2018

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

Neuroimaging Changes in Menkes Disease, Part 1
AJNR 38:1850-1857, Manara, R.,et al, 2017

Hydrocephalus in Children
Lancet 387:788-799, Kahle, K.T.,et al, 2016

Clinicopathologic Conference, Aqueductal Stenosis with Hydrocephalus
NEJM 375:2583-2593, Case 40-2016, 2016

Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis)
NEJM 370:1830-1841, Case 14-2014, 2014

Inherited Metabolic Diseases of the Nervous System, Tay Sachs Disease
Adams & Victors Principles of Neurology, Chp 37, pg 957, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Infantile Gaucher Disease
Adams & Victors Principles of Neurology, Chp 37, pg 958, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Neuroaxonal Dystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 972, Ropper, A.H.,et al, 2014

Juvenile Myasthenia Gravis: Recommendations for Diagnostic Approaches and Treatment
Neuropediatrics 45:75-83, Marina, A.D.,et al, 2014

Rapidly Progressive Leukoencephalopathy in Mitochondrial Complex I Deficiency
Neurol 81:e10-e11, Baertling, F.,et al, 2013

Intracranial Optic Nerve Enlargement in Infantile Krabbe Disease
Neurol 78: e126, Shah, S.,et al, 2012

Encephalitis Associated with Glutamic Acid Decarboxylase Autoantibodies in a Child A Treatable Condition?
Arch Neurol 68:1065-1068, Korff, C.M.,et al, 2011

Clinicopath Conf, Infantile Krabbe Disease
NEJM 362:346-356, Case 3-2010, 2010

Aicardi-Gouti�res Syndrome: Neuroradiologic Findings and Follow-up
AJNR 30:1971-1976, Uggetti,C.,et al, 2009

Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
NEJM 347:672-680, Case 27-2002, 2002

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

Niemann-Pick Disease Type C:Diagnosis and Outcome in Children, with Particular Reference to Liver disease
J Pediatr 123:242-247, Kelly,D.A.,et al, 1993

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Long-Term Neurologic Consequences of Nutritional Vitamin B12 Deficiency in Infants
J Pediatr 121:710-714, Graham,S.M.,et al, 1992

Cerebral Artery Aneurysms in Children Infected with Human Immunodeficiency Virus
J Pediatr 121:927-930, Husson,R.N.,et al, 1992

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

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

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

Elevated Serum Levels of Tumor Necrosis Factor are Associated with Prog Encephalopathy in Children with AIDS
Am J Dis Child 143:771-774, Mintz,M.,et al, 1989

Neurological Manifestations in Three German Children with AIDS
Neuropediatrics 18:99-106, Biggemann,B.,et al, 1987

Alexander's Disease, A Disease of Astrocytes
Brain 108:367-385, Borrett,D.&Becker,L.E., 1985

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

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

A 67-Year-Old Woman with Progressive Tingling Sensations and Imlalance
Neurol 100:151-157, Horta,L.F.B.,et al, 2023

Clinicopathologic Conference, Hypocalcemic Myopathy Due to Hypoparathyroidism
NEJM 388:1513-1520, Case 12-2023, 2023

Clinicopathologic Conference, Functional Vitamin B12 Deficiency from Use of Nitrous Oxide
NEJM 388:1893-1900, Case 15-2023, 2023

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

Updates on Sturge-Weber Syndrome
Stroke 53:3769-3779, Yeom,S.E.&Comi,A.M., 2022

A 49-Year-OLD Woman with Progressive Numbness and Gait Instability
Neurol 97:342-347, Zahid, A.,et al, 2021

Leg Weakness and Paraesthesia Provide a Clue to Sudden Death due to Aortic Dissection
Lancet 397:128, Agarwal, M.,et al, 2021

Paraneoplastic Myeloneuropathies
Neurol 96:e632-e639, Shah, S.,et al, 2021

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

A 53-year-old Woman with Lower Extremity Paresthesias
Neurol 94:1105-1108, Dehbashi, S.,et al, 2020

Distal Symmetric Polyneuropathy in 2020
JAMA 324:90-92, Callaghan, B.C.,et al, 2020

COVID-19 Presenting with Ophthalmoparesis from Cranial Nerve Palsy
Neurol 95:221-223, Dinkin, M.,et al, 2020



Showing articles 0 to 50 of 230 Next >>