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Differential
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abdominal cramps
acral sensory symptoms
activated protein C resistance
alopecia
alpha galactosidase A deficiency
amyloid angiopathy, cerebral
amyloid angiopathy, hereditary cystatin C
amyloidosis
aneurysm
aneurysm, intracranial
aneurysm, intracranial, familial
angina pectoris
angiography, cerebral
anhidrosis
antiphospholipid antibodies
aphasia
arrhythmia, cardiac
arterial dissection
arterial dissection, carotid
arterial dissection, ruptured
arterial dissection, vertebral
arteriopathy
arteriovenous malformation
arteriovenous malformation, cerebral
asymptomatic
atrial fibrillation
atrial myxoma
autonomic dysfunction
basal ganglia, calcification of
basal ganglia, infarction
basal ganglia, lesion of
Binswanger disease
brain biopsy
brainstem, infarction of
brainstem, lesion of
burning paresthesia
calcification, intracranial
cardiomyopathy
carotid angiogram
carotid artery disease
CAT scan
CAT scan, abnormal
cavernous hemangioma
cerebral atherosclerosis
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral embolism
cerebral embolism, cardiac origin
cerebral infarction
cerebral infarction, hemorrhagic
cerebral infarction, small, deep
cerebral infarction, subcortical
cerebral ischemia
cerebral vasculature, calcification
cerebral venous thrombosis
cerebral venous thrombosis, etiology
cerebrospinal fluid, gammaglobulin of
cerebrovascular accident
cerebrovascular accident, cardiac disease causing
cerebrovascular accident, familial occurrence
cerebrovascular accident, genetic
cerebrovascular accident, infancy and childhood
cerebrovascular accident, location of
cerebrovascular accident, multiple
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, prevention of
cerebrovascular accident, recurrent
cerebrovascular accident, women
cerebrovascular accident, work up for
cerebrovascular accident, young adult
cerebrovascular disease
cerebrovascular disease, cardiovascular disease with
cerebrovascular disease, risk factors in
children
chromosomal abnormality
chromosome 12
chromosome 19
chromosome 5
Clinical Pathologic Conference(C.P.C.)
coagulopathy
cognition
collagen vascular disease
congestive heart failure
corpus callosum
corpus callosum, infarction of
corpus callosum, lesion of
cortical blindness
cystic infarction
deep gray nuclei
dementia
dementia, cerebrovascular disease causing
dementia, subcortical
depression
diarrhea
differential diagnosis
diplopia
DNA probes
dural sinus thrombosis
dysarthria
echocardiogram
Ehlers-Danlos syndrome
electroencephalogram, pediatric patients
encephalopathy
enzyme, defect
epidemiology of neurology
Fabry's disease
Factor V Leiden
factor V, deficiency
familial
familial hemiplegic migraine
fever
fibrinogen
fibromuscular dysplasia
fistula, arterio-venous
fistula, arterio-venous, carotid-cavernous
fistula, arterio-venous, pulmonary
gene
gene mutation
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glioblastoma multiforme(astrocytoma Gr.III)
glioma
granular osmiphilic material
headache
headache, thunderclap
hearing loss
hemianopia, homonymous
hemiparesis
hemoglobin abnormality, neurologic complications of
hereditary hemorrhagic telangiectasia(HHT)
herpes simplex encephalitis
herpes simplex encephalitis, differential diagnosis of
homocystinuria
HTRA1 gene
human genome
hypercoagulable state
hyperlipidemia
hypertension
hypertension, cerebrovascular disease with
hypertrophic cardiomyopathy
ileus, paralytic
infantile hemiplegia
intellectual deficit
intellectual deterioration
intracerebral hemorrhage
intracerebral hemorrhage, familial
intracerebral hemorrhage, young adult
intracranial hemorrhage
lactic acidemia
lacunar infarction
leukoencephalopathy
lipid storage disorder of CNS
livedo reticularis
lupus anticoagulant
malformation, vascular
malformation, vascular, cerebral
malformation, vascular, familial
malformation, vascular, screening for
mania
manic-depressive
Marfan syndrome
marihuana
MELAS syndrome
microangiopathy, brain
middle cerebral artery territory infarction
middle cerebral artery, occlusion of
migraine
migraine with aura
migraine, hemiplegic
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitral valve lesion
mitral valve prolapse
molecular genetics
mortality
moyamoya
MRI
MRI, abnormal
MRI, black holes on
MRI, diffusion weighted
MRI, serial
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, familial
multiple sclerosis, misdiagnosis
myocardial infarction
myopathy
myopathy, mitochondrial
neoplasm, primary intracerebral
neoplasm, primary of CNS
neoplasm, primary of CNS-familial occurrence
neurocutaneous disease
neurofibromatosis 1
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurons
neuropathology
Notch3 gene
obesity
occipital lobe
osteogenesis imperfecta
PAS positive
PAS positive material in the brain
patent foramen ovale
polycythemia, primary
polymerase chain reaction
prethrombotic state
prognosis
protein C deficiency
protein S deficiency
pseudobulbar palsy
pseudoxanthoma elasticum
psychosis
psychosis, acute
pulmonary embolism
quadriparesis
ragged-red fibers
Red flags
renal failure
review article
risk factors
screening
seizure
sensorineural hearing loss
short stature
sibling
sick sinus syndrome
sickle cell disease
skin, biopsy
skin, lesions in neurologic disorders
small vessel disease
Sneddon's syndrome
spinal cord, infarction of
spondylosis
straight sinus
subarachnoid hemorrhage
sudden death
superior sagittal sinus thrombosis
syncope
systemic illness
telangiectases
telangiectases, retinal
temporal lobe, lesion
temporal lobe, lesion, bilateral
thrombocytopenia
thrombophlebitis
transient ischemic attack
treatment of neurologic disorder
tuberous sclerosis
twins
vasculopathy
visual loss
visual loss, transient
Von Hippel Lindau
white matter disease
white matter disease, location
workup
Showing articles 150 to 200 of 12689 << Previous Next >>

Association Between Familial Atrial Fibrillation and Risk of New-Onset Atrial Fibrillation
JAMA 304:2263-2269, Lubitz,S.A.,et al, 2010

Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
Brain 133:655-670, Leen,W.G., et al, 2010

Whole-Genome Sequencing in a Patient with Charcot-Marie-Tooth Neuropathy
NEJM 362:1181-1191, Lupski,J.R., et al, 2010

Optimal Screening Strategy for Familial Intracranial Aneurysms: A Cost-Effectiveness Analysis
Neurol 74:1671-1679, Bor,A.S.E., et al, 2010

Familial Mediterranean Fever and Central Nervous System Involvement: A Case Series
Medicine 89:75-84, Kalyoncu,U.,et al, 2010

Pediatric Moyamoya Disease: An Analysis of 410 Consecutive Cases
Ann Neurol 68:92-101, Kim,S.-K., et al, 2010

A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
Neurol 75:259-264, Herv�,D., et al, 2010

Autism
Lancet 374:1627-1638, Levy,S.,et al, 2009

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

Leukodystrophies: Classification, Diagnosis, and Treatment
Neurologist 15:319-328, Costello,D.,et al, 2009

Neurofibromatosis Type 2
Lancet 373:1974-1986, Astagiri,A.R.,et al, 2009

Diagnosis and New Treatments in Muscular Dystrophies
JNNP 80:706-714, Manzur,A.Y. &Muntoni,F., 2009

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

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

Extension of the Clinical Spectrum of Danon Disease
Neurol 70:1358-1359, van der Kooi,A.J.,et al, 2008

Neurologic Manifestations of von Hippel-Lindau Disease
JAMA 300:1334-1342, Butman,J.A.,et al, 2008

Insights into the Dynamics of Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids
Neurol 71:925-929, Van Gerpen,J.A.,et al, 2008

Neurofibromatosis
JAMA 300:352, Torpy,J.M.,et al., 2008

MR Imaging of Familial Creutzfeldt-Jakob Disease: A Blinded and Controlled Study
AJNR 29:1638-1643, Fulbright,R.K.,et al, 2008

Spinal Muscular Atrophy
Lancet 371:2120-2133, Lunn,M.R. &Wang,C.H., 2008

Tuberous Sclerosis
Lancet 372:657-658, Curatolo,P.,et al., 2008

Decoding Cryptogenic Cardioembolism
Ann Neurol 64:364-365, Meschia,J.F., 2008

Parkinson Disease, 10 Years After Its Genetic Revolution: Multiple Clues to a Complex Disorder
Neurol 69:2093-2104, Klein,C. &Schlossmacher,M.G., 2007

Seizures on Hearing the Alarm Clock
Lancet 370:2172, Vollmar,C.,et al, 2007

Pulmonary Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia: A Series of 126 Patients
Medicine 86:1-7, Cottin,V.,et al, 2007

Neuroimaging Findings in Human Prion Disease
JNNP 78:664-670, Macfarlane,R.G.,et al, 2007

Amyotrophic Lateral Sclerosis
Lancet 369:2031-2041, Mitchell,J.D. & Borasio,G.D., 2007

Paroxysmal Extreme Pain Disorder (Previously Familial Rectal Pain Syndrome)
Neurol 69:586-595, Fertleman,C.R.,et al, 2007

A Genetic Risk Factor for Periodic Limb Movements in Sleep
NEJM 357:639-647, Stefansson,H.,et al, 2007

Differential Diagnosis of Bilateral Thalamic Lesions
Clin Neuroradiol 17:3-22, Linn,J.,et al, 2007

Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
Brain 130:2484-2493, Jen, J.C.,et al, 2007

Glycogen-Storage Disease Type II
eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006

Prevalence of Fabry Disease in Patients with Cryptogenic Stroke: A Prospective Study
Lancet 366:1794-1796,1754, Rolfs,A.,et al, 2006

Metabolic Disease and Stroke: MELAS
emedicine.com, Mandava,P.,et al, 2006

Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene
NEJM 354:2584-2592, Case 18-2006, 2006

Common Misdiagnosis of a Common Neurological Disorder: How Are We Misdiagnosing Essential Tremor?
Arch Neurol 63:1100-1104, Jain,S.,et al, 2006

The Tuberous Sclerosis Complex
NEJM 355:1345-1356, Crino,P.B.,et al, 2006

Familial Cervical Artery Dissections: Clinical, Morphologic, and Genetic Studies
Stroke 37:2924-2929, Martin,J.J.,et al, 2006

Restless Legs Syndrome: Is Treatable But Under-Recognised
BMJ 333:457-458, Medcalf,P. &Bhatia,K.P., 2006

Mitochondrial DNA Polymerase-y and Human Disease
Hum Mol Genet 15:R244-R252, Hudson, G.,et al, 2006

Adrenoleukodystrophy
JAMA 294:3131-3134, Moser,H.W.,et al, 2005

Value of Gradient-Echo Magnetic REsonance Imaging in the Diagnosis of Familial Cerebral Cavernous Malformation
Arch Neurol 62:653-658, Lehnhardt,F-G.,et al, 2005

Phaeochromocytoma
Lancet 366:665-675, Lenders,J.W.M.,et al, 2005

Malignant Hyperthermia, Update on Susceptibility Testing
JAMA 293:2918-2924,2958, Litman,R.S.&Rosenberg,H., 2005

Heritability of Carotid Artery Atherosclerotic Lesions
Stroke 36:5-8, Moskau,S.,et al, 2005

Migraine and Cerebral White Matter Lesions
The Neurologist 11:19-29, Gladstone,J.P. &Dodick,D.W., 2005

Psychosocial Impact of Screening for Intracranial Aneurysms in Relatives with Familial Subarachnoid Hemorrhage
Stroke 36:836-840, Wermer,M.J.H.,et al, 2005

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

Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
Neurol 64:1196-1203, Bosley, T.M.,et al, 2005

Neurobrucellosis:Clinical and Neuroimaging Correlation
AJNR 25:395-401, Al-Sous,M.W.,et al, 2004



Showing articles 150 to 200 of 12689 << Previous Next >>