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Differential
(Click to cross reference)
altered states of consciousness
angiography, cerebral, beaded vessels
angiography, cerebral
angiokeratoma
anorexia
anticonvulsants
anticonvulsants, selection of
aphasia
arteritides
arthralgia
arthritis
asymptomatic
ataxia
ataxia, cerebellar
ataxic gait
basal ganglia, calcification of
blepharospasm
blind spot, enlarged
blindness
bone marrow biopsy
brain biopsy
brainstem, infarction of
calcification, intracranial
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, false negative
cataracts
cerebral cortical atrophy
cerebral glucose metabolism
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gold sol.curve of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, red cells in
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
cherry red spot
cherry red spot-myoclonus syndrome
chest x-ray, abnormal
children
chronic progressive external ophthalmoplegia
cisternogram, radionuclide
Clinical Pathologic Conference(C.P.C.)
coccidioidomycosis
coenzyme Q10 deficiency
coma
dementia
dentatorubral-pallidoluysian atrophy
diabetes mellitus
diarrhea
diplopia
downward gaze, paralysis of
drowsiness
dystonia
Ekbom's Syndrome
encephalopathy
encephalopathy, progressive
enzyme, defect
eye movement, disorders of
facial pain
falling
familial
fasciculation
fever
frontal lobe, pathologic signs of
F-wave response
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene mutation
gene therapy
genetic counselling
genetic neurologic disorders
genetic testing
granuloma, pulmonary
grasp reflex
headache
headache, severe
hearing loss
heart block
hemiplegia
hepatomegaly
herpes virus
hydrocephalus
hydrocephalus, normal pressure
hypersomnia
hypoglycorrhachia
immunohistochemistry
immunosuppression
impotence
intellectual deterioration
intestinal pseudoobstruction
jaw pain
Kearns-Sayre syndrome
lactic acidemia
Lafora's disease
Leber's hereditary optic neuropathy
Leigh's disease
leukocyte enzyme abnormality
leukocytosis
lipid storage disorder of CNS
lymphadenopathy
MELAS syndrome
memory, defect of recent
memory, impairment of
meningismus
meningitis
meningitis, aseptic
meningitis, fungal
meningitis, syphilitic
meningitis, TB
mental retardation
mental status, abnormal
MERRF syndrome
midbrain, infarction of
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
MRI
MRI, abnormal
muscle biopsy
muscle tenderness
muscle weakness
muscle weakness, proximal
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myelopathy
myoclonic jerks
myoclonus
myoclonus, epilepsy
myopathy
myopathy, mitochondrial
negative
neuraminidase deficiency
neuroendocrinology
neurologic complications of, systemic cancer
neurologic disease, diagnoses of
neurologic symptoms
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathy
neuropathy, ataxia, retinitis pigmentosa
night sweats
normal
nystagmus
nystagmus, vertical
ocular motility, disorders of
ophthalmoplegia
ophthalmoplegia, progressive external
opportunistic infection
optic atrophy
optic neuropathy
pain, leg
pain, thigh
pancytopenia
papilledema
PAS positive
periarteritis nodosa
pericarditis
personality change
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
pleurisy
pneumoencephalogram(PEG)
pneumonia
polymerase chain reaction
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
psychiatric problems in neurologic disorders
ptosis
ragged-red fibers
retinal hemorrhages
retinopathy
review article
sedimentation rate, elevated
seizure
seizure, paradoxical
seizure, treatment of
sensorineural hearing loss
short stature
startle reaction
steroid therapy, CNS treatment and complications with
strokelike episodes
symmetric brain lesions
treatment of neurologic disorder
Unverricht-Lundborg disease
upgaze
upgaze, paralysis of
uveitis
varicella zoster virus
viral infection
viral infection, CNS
vision, blurred
visual acuity, decreased
visual loss
vitreous opacities
weakness
weight loss
Whipple's disease
white matter disease
wide based gait
wrist drop
zoster sine herpete
Showing articles 0 to 50 of 3842 Next >>

Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009

Brain Magnetic Resonance Imaging Findings in Patients with Mitochondrial Cytopathies
Arch Neurol 62:737-742, Barragan-Campos,H.M.,et al, 2005

Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
Lancet Neurol 4:239-248, Shahwan, A., et al, 2005

A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
The Neurologist 8:302-312, Thambisetty,M.,et al, 2002

Clinicopath Conf
Arteritis, Unclassified, with Giant-Cell Reaction & Multiple Infarcts of the Brain & Neuropathy, Cas, 5-199532:452-459,1995., 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Ekbom's Syndrome:Lypomas, Ataxia, and Neuropathy with MERRF
Muscle & Nerve 17:943-945994., Calabresi,P.,et al, 1994

Mitochondril Encephalopathies:Molecular Genetic Diagnosis from Blood Samples
Lancet 337:1311-1313, Hammans,S.R.,et al, 1991

Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
J Comput Assist Tomogr 12:854-857, DeVolder,A.,et al, 1988

Progressive Myoclonus Epilepsies:Specific Causes & Diagnosis
NEJM 315:296-305, Berkovic,S.F.,et al, 1986

Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
Ann Neurol 6:232-244, Miyatake,T.,et al, 1979

The Cherry-red Spot-Myoclonus Syndrome
Ann Neurol 3:234, Rapin,I.,et al, 1978

Neurologic Complications After Treatment for Whipple's Disease:A Report of Four Patients
Medicine 55:467, Knox,D.L.,et al, 1976

Case Records of MGH-NEJM 285:621
1971., , 1971

Whipple's Disease & Papilledema
Arch Int Med 123:74, Switz,D.M.,et al, 1969

Behcets Syndrome
NEJM 390:640-651, Saadoun,D.,et al, 2024

Posttransplant Anti-GABAA Receptor Antibody-Associated Autoimmune Encephalitis
Neurol 102:e209245, Togni,C.L.,et al, 2024

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD): Clinical Features and Diagnosis
UptoDate.com, March, Flanagan,E.P. & Tillema,J-M, 2023

Clinicopathologic Conference, Factitious Disorder
NEJM 388:1609-1615, Case 13-2023, 2023

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

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD):Clinical Features and Diagnosis
www.UptoDate.com, Sept, Flanagan,E.P. & Tillema,J-M, 2023

Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
Neurol 101:e1884-e1892, van der Veen,S.,et al, 2023

Diagnosis of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease:International MOGAD Panel Proposed Criteria
Lancet Neurol doi.org110.1016/51474-4422(22)00431-8, Banwell,B.,et al, 2023

Autoimmune Encephalitis Misdiagnosis in Adults
JAMA Neurol 80:30-39, Flanagan,E.P.,et al, 2023

A 48-Year-Old Woman Presenting with Vertigo, Ptosis, and Red Eyes
Neurol 98:678-683, Kim, K.T.,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

Clinicopathologic Conference, Anti-IgLON5 IgG-Associated Neurologic Disorder
NEJM 386:173-180, Case 1-2022, 2022

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

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

FDA Approves Fenfluramine for Treatment of Seizures Associated with Dravet Syndrome
FDA June2020, , 2020

An Adolescent Girl Presenting with Worsening Vertigo, Headache, and Ataxia
Neurol 95:e1760-e1763, Brigham, E.,et al, 2020

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

Neurological Impairments in a Patient Returning from Cuba
JAMA Neurol 77:1570-1571, Serlin, Y.,et al, 2020

Rapid Progression of Prion Disease Associated with Transverse Myelitis
Neurol 94:e1670-e1672, Hussein, O.,et al, 2020

A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,et al, 2019

A Middle-Aged Man with New Onset Seizures and Myoclonic Jerks
Neurol 92:e274-e281, Chen, Z. & Neo, S., 2019

Recurrent Involuntary Contractions of the Face, Arm, and Leg in an Elderly Man
JAMA Neurol 76:728-729, Kim, D.D.,et al, 2019

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

Behcet Disease
emedicine.medscape.com Dec, Davey-Ranasinghe, N. & Diamond, H.S., 2018

A 22-year-old Man Presenting with Headache and Right Leg Jerks
Neurol 91:891-895, Schupper, A.J.,et al, 2018

Antibody-Mediated Encephalitis
NEJM 378:840-851, Dalmau, J.,et al, 2018

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

Human Parechovirus: An Increasingly Recognized Cause of Sepsis-Like Illness in Young Infants
Clin Microbiol Reviews 31:1-17, Olijve, L.,et al, 2018

Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet Syndrome
NEJM 376:2011-2020, Devinsky, O.,et al, 2017

Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
JAMA Neurol 74:737-740, Cohen, A.L.,et al, 2017

A 54-year-old woman with Dementia, Myoclonus, and Ataxia
Neurol 89:e7-e12, Ali, F.,et al, 2017

A Case of Altered Mental Status, Not Otherwise Specified
Neurol 89:e154-e158, Swor, D.E.,et al, 2017

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

A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017



Showing articles 0 to 50 of 3842 Next >>