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Differential
(Click to cross reference)
adrenal mass
aggression
Aicardi-Goutieres syndrome
akinetic mute
Angelman syndrome
arrhythmia, cardiac
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
attention span
basal ganglia, calcification of
behavior, combative
behavioral disorder
benign essential tremor
brachycephaly
brainstem, lesion of
Brugada syndrome
calcification, intracranial
carcinoma
cardiac arrest
carotid artery occlusion, neck
CAT scan, abdomen
CAT scan, abnormal
catecholamine
cerebellar atrophy, primary
cerebellar hemangioma
cerebellar lesion
cerebral cortex
cerebral cortical atrophy
children
chromosomal abnormality
chromosome 15
chromosome 19
chromosome 20
chromosome 20 ring
chromosome 3
Clinical Pathologic Conference(C.P.C.)
confidentiality
cyst
cyst, peritumoral
cyst, neoplastic cerebellum
cyst, parenchymal
deep gray nuclei
dementia
dementia, rapidly progressive
developmental milestones, loss of
developmental retardation
dexterity, impaired
drooling
dysarthria
dysmorphic
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
encephalopathy
endolymphatic sac tumors
eye movement, disorders of
facial appearance, abnormal
facial expression abnormality
familial
feeding disorder
fever
fish
fluorescene in situ hybridization
fundus, abnormality of
gait disorder
gene
gene mutation
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
Gerstmann-Straussler-Scheinker disease
headache
hearing loss
hearing loss, sudden, unilateral
hemangioblastoma
heralding manifestation
hydrocephalus
hyperactivity
hypertension
hypopigmentation of skin
hypotonia
interferon alpha
laughing, pathologic
leukoencephalopathy
macrognathia
medulla oblongata, lesion of
medulla oblongata, neoplasm of
mental retardation
microcephaly
molecular genetics
mortality
MRI
MRI, abdomen
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
muscular dystrophy
muscular dystrophy, classification
myopathy
myopathy, proximal
myotonia
myotonia dystrophica
myotonia dystrophica, classification
myotonia dystrophica, type 2
neurocardiology
neurologic disease, diagnoses of
pancreatic cyst
pheochromocytoma
pleocytosis of cerebrospinal fluid
postural abnormality
prion disease
prion protein gene
prognathism
prognosis
progressive neurologic disorder
protein 14-3-3, cerebrospinal fluid
proximal myotonic myopathy
radiation therapy, stereotactic
renal cell carcinoma
renal cyst
retinal hemangioma
retinal lesion
review article
seizure
skin, lesions in neurologic disorders
smiling
speech disorder
speech disorder, childhood
speech, delayed development of
spinal cord, lesion of
spinal cord, neoplasm
sudden death
syncope
syncope, recurrent
tandem gait, ataxic
teeth, wide-spaced
tinnitus
tongue, protrusion of
treatment of neurologic disorder
tremor
trinucleotide repeats
tumor suppressor gene
ventricular tachycardia
vertigo
Von Hippel Lindau
Von Hippel Lindau, screening protocol for
von Hippel-Lindau, screening
white matter disease
Showing articles 100 to 150 of 1417 << Previous Next >>

A 47-Year-Old With Headache, Vertigo, and Double Vision
Neurol 97:e535-e539, Frey, J.,et al, 2021

Clinical and Genetic Features in Patients with Reflex Bathing Epilepsy
Neurol 97:e577-e586, Accogli, A.,et al, 2021

Genetics of Cluster Headache Takes a Leap
Ann Neurol 90:191-192, Palotie, A., 2021

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

CLOVES Syndrome
Neurol 96:e1487-e1488, Collins, M.,et al, 2021

Bilateral Temporal Pole Involvement in Adult-Onset X-Linked Adrenoleukodystrophy
JAMA Neurol 78:367-368, Liu, M.,et al, 2021

Brain and Skin Involvement in Erdheim-Chester Disease
Neurol 96:e1590-e1592, Budhram, A.,et al, 2021

Alzheimers Disease
Lancet 397:1577-1590, Scheltens, P.,et al, 2021

Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
NEJM 385:1317-1325, Case 30-2021, 2021

Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
Neurol 97:813-816,801, Appleby, B.S.,et al, 2021

Hypotonia and Delayed Teeth Eruption in a 2-Year-Old Girl
Neurol 97:875-878, Dinov, D.,et al, 2021

A 28-Year-Old Woman with Vision Loss and an Unusual Gait
Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021

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

"Disappearing Infarct" Is Late-Onset MELAS
Ann Neurol 90:1001-1002, Landis,T.M.,et al, 2021

Molecular Diagnostic Yield of Exome Sequencing in Patients with Cerebral Palsy
JAMA 325:467-475, Moreno-De-Luca, A.,et al, 2021

A 6-Year-Old Boy with Muscle Twitching
Neurol 96:e301-e304, Lewis, H.S.,et al, 2021

Clinicopathologic Conference,Aceruloplasminemia, Hereditary
NEJM 383:1974-1983, Case 35-2020, 2020

Bilateral Ptosis, Dysphagia, and Progresive Weakness in a Patient of French-Canadian Background
Neurol 95:933-938, Paul,P.,et al, 2020

Hypointensity of the Basal Ganglia in Adults with Glucose Transporter Protein Type 1 Deficiency Syndrome: A Novel Magnetic Resonance Imaging Finding
Ann Neurol 87:10-11, Van Samkar, A.,et al, 2020

"Boule Du Biceps" in Dysferlinopathy
Neurol 94:83-84, El Sherif, R.,et al, 2020

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

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

A 22-Year-Old Man with Progressive Bilateral Visual Loss
Neurol 94:625-630, Yang, S.L.,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

A 42-year-old Woman with Progressive Cognitive Difficulties and Gait Imbalance
Neurol 94:e1219-e1226, Slama, M.C.C.,et al, 2020

A 25-year-old Woman with Recurrent Episodes of Collapse and Loss of Consciousness
Neurol 94:994-999, Wildman, J.,et al, 2020

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

Ears of the Lynx Magnetic Resonance Imaging Sign
Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

A 10-Year-Old Girl with Muscle Stiffness
Neurol 95:e773-e778, Prior, D.E. & Ghosh, P.S., 2020

Pediatric Leigh Syndrome
Ann Neurol 88:218-232, Alves, C.A.P.F.,et al, 2020

Spinal Xanthomatosis
Neurol 95:e1615-e1616, Valencia-Sanchez, C.,et al, 2020

Muscle Stiffness, Gait Instability, and Liver Cirrhosis in Wilsons Disease
Lancet 396:990, Kronlage, C.,et al, 2020

Recurrent Cerebral Ischemia During Pregnancies
Neurol 95:e2453-e2457, Bulwa, Z.,et al, 2020

Dressing Apraxia as Initial Manifestation of Creutzfeldt-Jakob Disease
Tremor and Other Hyperkinetic Movements 10:1-3, Heckmann, J.G.,et al, 2020

Acute Cortical Lesions in MELAS Syndrome: Anatomic Distribution, Symmetry, and Evolution
AJNR 41:167-173, Bhatia,K.D.,et al, 2020

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
Neurol Sci 40:2251-2263, Donzuso,G.,et al, 2019

Neurodegeneration with Brain Iron Accumulation
AIAN 22:267-276, Batla, A. & Gaddipati, C., 2019

GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
Ann Neurol 86:962-968,809, Okubo, M.,et al, 2019

Metabolic Lipid Muscle Disorders: Biomarkers and Treatment
Ther Adv Neurol Disord 12:1-15, Angelini, C.,et al, 2019

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

"Ears of the Lynx" MRI Sign is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia
AJNR 40:199-203, Pascual, B.,et al, 2019

CRAO and Silent Brain Infarcts caused by Cardiac Myxomas in Carney Complex
Neurol 92:e286-e287, Huang, L-T.,et al, 2019

Fibromuscular Dysplasia and Its Neurologic Manifestations
JAMA Neurol 76:217-226, Touze, E.,et al, 2019

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

A 15-year-old Boy with Bilateral Wrist Pain in the Setting of Weight Loss
Neurol 92:486-492, Lau, K.H.V.,et al, 2019

A Teenager with Persistent Headache
Neurol 92:e1526-e1531, Hu, Y.,et al, 2019

Limbic-Predominant Age-Related TDP-43 Encephalopathy (LATE): Consensus Working Group Report
Brain DOI: 10.1093/brain/awz099, Nelson, P.T.,et al, 2019

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019



Showing articles 100 to 150 of 1417 << Previous Next >>