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Differential
(Click to cross reference)
abscess, intracerebral
acanthosis nigricans
alpha-fetoprotein
anemia
apraxia of eye movements
areflexia
Arnold Chiari malformation
arteriovenous malformation
arteriovenous malformation, pulmonary
aspiration
astrocytoma
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
ataxic gait
athetosis
autoimmune disease
biologic markers
blood dyscrasias, neurologic findings with
brain biopsy
brain biopsy, stereotaxic
cafe au lait spots
carcinoembryonic antigen
carcinoma
carcinoma of breast
CAT scan
CAT scan, abnormal
CAT scan, chest
cerebellar ataxia, autosomal recessive
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar vermis
cerebral palsy
cerebrospinal fluid, xanthochromia of
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
cisterna magna
cisterna magna, enlarged
Clinical Pathologic Conference(C.P.C.)
C-reactive protein, elevated
degenerative diseases of CNS
dental procedure, neurologic complications with
diabetes mellitus
DiGeorge syndrome
drooling
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dystonia
electromyogram
electronystagmography
electrophoretic pattern, serum
epistaxis
Epstein-Barr virus
eye movement, disorders of
familial
fistula, arterio-venous, pulmonary
fourth ventricle, enlargement of
Friedreich's ataxia
gait disorder
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
glioma
gray hair
growth retardation
head injury
hepatolenticular degeneration(Wilson's disease)
hepatosplenomegaly
hereditary hemorrhagic telangiectasia(HHT)
hyperglycemia
hypogonadism
hypotonia
imbalance
immunodeficiency
immunoelectrophoresis, serum
immunologic disease
immunosuppression
incoordination
infection
insulin resistance
Leigh's disease
leukemia
leukemia, neurologic findings assoc.with
leukocytosis
leukoencephalopathy
lipid storage disorder of CNS
liver disease
lymphadenopathy
lymphoma
Marinesco-Sjogren syndrome
masked facies
meningismus
mental retardation
microhemorrhage, intracerebral
misdiagnosis
mitral valve prolapse
molecular genetics
mongolism
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, hypointense signal foci on
MRI, negative
MRI, perfusion
MRS
multiple sclerosis
multiple system atrophy
myelomalacia
neoplasm, primary intracerebral
nerve biopsy
nerve conduction studies
neurocutaneous disease
neuroendocrinology
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic examination, focal
neuropathology
neuropathy
nystagmus
ocular motility, disorders of
ophthalmoplegia
optokinetic nystagmus(O.K.N.)
papilledema
pathology
pneumonia
poliomyelitis
poliomyelitis vaccine
polyneuropathy
progeria
prognosis
progressive neurologic disorder
pulmonary infection
pulmonary infiltrates
radiation hypersensitivity
remote effect of cancer on the nervous system
review article
risk factors
saccadic eye movements
saccadic eye movements, abnormal
scannig speech
skin, darkening of
skin, lesions in neurologic disorders
slurred speech
spinal muscular atrophy
spinocerebellar degeneration
staggering
tandem gait, ataxic
telangiectases
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
vaccination, neurologic complications with
vaccine
vertigo
viral infection
viral infection, CNS
vitamin E deficiency
vitiligo
Von Hippel Lindau
walking, difficulty with
weight loss
wheelchair
white matter disease
workup
Showing articles 150 to 200 of 1234 << Previous Next >>

A 78-year-old Man with a Gait Disorder
Neurol 93:223-227, Saucedo, M.,et al, 2019

Relapsing-Remitting Severe Bickerstaffs Brainstem Encephalitis
BMJ 394:684, Tyrakowska, Z.,et al, 2019

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

Bilateral Claude Syndrome
Neurol 93:599-600, Witsch, J.,et al, 2019

Stridor in Multiple System Atrophy
Neurol 93:630-639, Cortelli, P.,et al, 2019

Neurosyphilis
NEJM 381:1358-1363, Ropper, A.H.,et al, 2019

A 55-Year-Old Woman Presenting with Ataxia and Numbness 1 Year After Ileum Resection
Neurol 93:675-679, Cassano, V.,et al, 2019

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

Clinicopathologic Conference, Powassan Virus Encephalitis
NEJM 380:380-387, Case 3-2019, 2019

Leg Weakness and Stiffness at the Emergency Room
Neurol 92:e622-e625, af Edholm, K.,et al, 2019

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

Toxic Diffuse Isolated Cerebellar Edema from Over-the-Counter Health Supplements
Neurol 92:965-966, Kim, D.D.,et al, 2019

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

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019

Paraoxysmal Tonic Upgaze in Children, Three Case Reports and a Review of the Literature
Pediatr Emer Care 35:e67-e69, Kartal,A., 2019

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

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

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

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

Subacute Progressive Ptosis, Ophthalmoplegia, Gait Instability, and Cognitive Changes
JAMA Neurol 75:1284-1285, Lin, J.,et al, 2018

Clinical Presentation and Cranial MRI Findings of Listeria Monocytogenes Encephalitis
Neurologist 23:198-203, Arslan, F.,et al, 2018

Neuronal Intranuclear Inclusion Disease Showing Intranuclear Inclusions in Renal Biopsy 12 Years Earlier
Neurol 91:884-886, Motoki, M.,et al, 2018

A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
Neurol 91:e1942-e1946, Bauer, Z.,et al, 2018

Progressive Gait Difficulty and Incontinence in a 40-year-old Man with HIV
Neurol 91:1065-1070, Silverman, A.,et al, 2018

Neuro-Sweet Disease Presenting as Ischemic Stroke and Aseptic Meningitis
Neurol 91:e2197-e2199, Das, A.S.,et al, 2018

An Unusual Fundus Finding in a Teenage Girl
JAMA Neurol 75:1566-1567, Filho, F.M.R.,et al, 2018

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

A 52-year-old woman with a 3 weeks of progressive gait ataxia and dysarthria
Neurol 90:e985-e989, Ly, C.,et al, 2018

A 60-year-old woman with ataxia
Neurol 90:e1627-e1630, Dandapat, S.,et al, 2018

Disability in adults with arthrogryposis is severe, partly invisible, and varies by genotype
Neurol 90:e1596-e1604, Dai, S.,et al, 2018

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

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

IgLON5-mediated neurodegeneration is a differential diagnosis of CNS Whipple disease
Neurol 90:1113-1115, Morales-Briceno, H.,et al, 2018

Risk of Ischemic and Hemorrhagic Strokes in Occult and Manifest Cancers
Stroke 49:1585-1592, Andersen, K.K. & Olsen, T.S., 2018

Progressive Weakness and Memory Impairment in a Middle-aged Man
JAMA 320:197-198, DeFilippis, E.M.,et al, 2018

A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
Neurol 91:187-190, Silva,A.M.S.,et al, 2018

Isolated Gait Dysfunction Due to Intracranial Hypotension
Neurol 91:271-272, Sasikumar,S.,et al, 2018

Coxa Saltans Misdiagnosed as Functional Gait Disorder
Neurol 91:276-277, Gilbert,D.L.,et al, 2018

Glutamate Receptor D2 Serum Antibodies in Pediatric Opsoclonus Myoclonus Ataxia Syndrome
Neurol 91:e714-e723, Berridge, G.,et al, 2018

Clnicopathologic Conference Anti-N-Methyl-D-Aspartate (NMDA) Receptor Encephalitis
NEJM 379:870-878, CASE 27-2018, 2018

The Laser Shoes
Neurol 90:e164-e171, Barthel, C.,et al, 2018

Recurrent Dysarthria and Ataxia in a Young Girl
JAMA Neurol 75:125-126, Romba, M.,et al, 2018

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

Persistent Postural-Perceptual Dizziness (PPPD): A Common, Characteristic and Treatable Cause of Chronic Dizziness
Pract Neurol 18:5-13, Popkirov, S.,et al, 2018

Clinical Reasoning: A 49-year-old man with Progressive Numbness, Weakness, and Evidence of Leptomeningeal Enhancement
Neurol 90:e90-e93, Lovett, A.,et al, 2018

A 58-year-old Woman with Systemic Scleroderma and Progressive Cervical Cord Compression
Neurol 91:e1262-e1264, Karschnia, P.,et al, 2018

Progressive Multifocal Leukoencephalopathy: Epidemiology, Clinical Manifestations, and Diagnosis
www.UptoDate.com, May, Koralnik, I.J., 2018

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
Front Neurol doi:10.3389/fneur.2017.00472, Velazquez-Perez, L.C.,et al, 2017

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

Glial Fibrillary Acidic Protein Immunoglobulin G as Biomarker of Autoimmune Astrocytopathy: Analysis of 102 Patients
Ann Neurol 81:298-309, Flanagan, E.P.,et al, 2017



Showing articles 150 to 200 of 1234 << Previous Next >>