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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 0 to 50 of 1392 Next >>

Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019

Review of the Neurological Implications of von Hippel-Lindau Disease
JAMA Neurol 75:620-627, Dornbos, D.,et al, 2018

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

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

Clinicopath Conf, Von Hippel Lindau Disease, Adrenal Pheochromocytoma, Brain-Stem and Spinal Cord Hemangioblastoma
NEJM 355:394-402, Case 23-2006, 2006

A Variant in the HS1-BP3 Gene is Associated with Familial Essential Tremor
Neurol 64:417-421, Higgins, J.J., et al, 2005

Variable Presentation of Brugada Syndrome: Lessons from Three Generations with Syncope
BMJ 326:1078-1079, Plunkett,A.,et al, 2003

von Hippel-Lindau Disease
Lancet 361:2059-2067, Lonser,R.R.,et al, 2003

New Nomenclature and DNA Testing Guidelines for Myotonic Dystrophy Type 1 (DM1)
Neurol 54:1218-1221, The International Myotonic Dystrophy Consortium (I, 2000

Getting a Grip on the Myotonic Dystrophies
Neurol 52:12-13, Thornton,C.A.&Ashizawa,T., 1999

Linkage of Proximal Myotonic Myopathy to Chromosome 3q
Neurol 52:170-171,12, Ricker,K.,et al, 1999

Chromosome 20 Ring:A Chromosomal Disorder Associated with a Particular Electroclinical Pattern
Epilepsia 39:942-951, Canevini,M.P.,et al, 1998

Angelman Syndrome: Clinical Profile
J Child Neurol 7:270-280, Zori,R.T.,et al, 1992

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

A 32 Year-Old Woman with Recurrent Intracerebral Hemorrhages
Neurol 104:e213422, Hindsholm,M.F.,et al, 2025

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

Severe Myotonic Crisis Resembling Malignant Hyperthermia
Neurol 104:e213497, Wadhwani,A.R.,et al, 2025

Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
Ann Neurol 97:611-628, Coppens,S.,et al, 2025

A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
Neurol 104:e213593, Pence, K.L. &Clark, R.A., 2025

A 26-Year-OldWoman with Headache and Eosinophilia
Neurol 104:e213434, Goh,W.G.W.,et al, 2025

A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,et al, 2025

Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency
Neurol 104:e213636, Chanda,G.,et al, 2025

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,et al, 2025

RNF213 Polymorphisms in Intracranial Artery Dissection
Genes doi.org/10.3390/genesis 15060725, Zedde,M.,et al, 2024

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

Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
JAMA Neurol 81:1-82, Chu,X.C.,et al, 2024

A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,et al, 2024

A 65-Year-Old Woman with Isolated Macroglossia as the Initial Presentation of a Rare Disease
Neurol 103:e210070, Lara,C.,et al, 2024

Genome Sequencing in the NICU and PICU is Here to Stay
Neurol 104:e210267, Hoffman,E.P. and Kesari,A., 2024

A 35-Year-Old Woman with Personality Change and Gait Impairment
Neurol 104:e210252, Bernardes,C.,et al, 2024

Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
Neurol 104:e210253, Chadha,D.,et al, 2024

Clinicopathologic Conference, Myeloperoxidase antineutrophil cytoplasmic antibody-associated vasculitis
NEJM 390:843-851, Case 7-2024, 2024

Diagnosis and Management of ANCA-Associated Vasculitis
Lancet 403:683-698, Kronbichler, A., et al, 2024

Cavernous Maliformations of the Central Nervous System
NEJM 390:1022-1028, Smith,E.R., 2024

Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
Neurol 102:e209385, Nishida,K.,, 2024

A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
Neurol 102:e209358, Barbosa,A.R.,et al, 2024

A 24-Year-Old Man with Spastic Ataxia and Hypodontia
JAMA Neurol 81:658-659, Marien,L.,et al, 2024

A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis
Neurol 103:e209708, Wannarong,T.,et al, 2024

A 26-Year-Old Woman with Chronic Progressive Gait Dysfunction
Neurol 103:e2098-e2030, Jones,F.J.S. & Orthmann-Murphy,J., 2024

Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
Neurol 103:e209844, Dhawan,A.,et al, 2024

Pomalidomide for Epistaxis in Hereditary Hemorrhagic Telangiectasia
NEJM 391:1015-1027, Al-Samkari,H.,et al, 2024

A 50-YEar-Old Man with Intracerebral Hemorrhage and Tortuous Retinal Arterioles
Neurol 103:e209796, Bouchart,J.,et al, 2024

Focusing on the Eye Signs of Alport Syndrome in a 40-Year-Old Man Who Previously Had a Kidney Transplant and Hearing Loss
Lancet 401:e2, Kovalchuk,B. & Khoramnia,R., 2023

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
Neurol 100:206-212, Stamm,B.,et al, 2023

Neuroimaging Features of Biotinidase Deficiency
AJNR 44:328-333, Biswas,A.,et al, 2023

A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
Neurol 100:631-637, Zeng,T.f.,et al, 2023

Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023

Neonatal Seizures
NEJM 388:1692-1700, Ropper.A.H., 2023



Showing articles 0 to 50 of 1392 Next >>