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Differential
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acrocyanosis
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
Africa
Aicardi-Goutieres syndrome
algorithm
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
ataxia
ataxia, progressive
atypical
Babinski sign
basal ganglia, calcification of
bladder dysfunction
bone marrow transplantation
brain atrophy
bulbar palsy
calcification, intracranial
camptocormia
cane
CAT scan, abnormal
cerebellar atrophy, primary
cerebrospinal fluid, abnormal
chilbran skin lesions
children
constipation
corpus callosum
corpus callosum, atrophy of
corpus callosum, thinning
cultured skin fibroblasts
degenerative diseases of CNS
dementia, childhood
demyelinating disease
dentate nuclei, lesion of
diagnostic criteria
diet
differential diagnosis
distal muscle weakness
dysarthria
dysphagia
dystonia
dystonia, children
ears of the Lynx MR sign
ELISA
emergency room
encephalopathy
endemic area
epidemiology of neurology
familial
fasciculation
fatty acid, elevated plasma content
feeding disorder
fever
foot drop
gait disorder
gait, spastic
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
geographic location
hand weakness
head lag
hemiparesis
high arched feet
human T-lymphotropic virus type I(HTLV-I)
hyperpyrexia, CNS disorder causing
hyperreflexia
hypogonadism
hypotonia
intellectual deficit
interferon alpha
intrauterine
intrinsic hand muscles, wasting of
irritability
jaw jerk, abnormal
leg weakness, bilateral
leukodystrophy
leukoencephalopathy
Lorenzo's oil
Maghreb
microcephaly
Mills syndrome
misdiagnosis
motor neuron disease
movement disorder
MRI, abnormal
MRI, emergent
multiple sclerosis, misdiagnosis
muscle cramp
myelopathy
myelopathy, chronic progressive
neck weakness
neurologic disease, diagnoses of
neurologic signs
neuropathology
next-generation sequencing
pain, leg
paraparesis
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, familial spastic, variants
paraparesis, spastic
paraparesis, spastic, tropical
paraplegia
peroxisomal disease
pleocytosis of cerebrospinal fluid
polymerase chain reaction
prenatal
prenatal diagnosis by amniocentesis
primary lateral sclerosis
prognosis
progressive neurologic disorder
psychomotor retardation
pyramidal tract dysfunction
review article
screening
seizure
skin, darkening of
skin, lesions in neurologic disorders
spastic ataxia
spastic paraplegia, type 11
spastic paraplegia, type 15
spasticity
spastin
speech disorder, childhood
startle reaction
stiff legs
testicular atrophy
toe walking
treatment of neurologic disorder
urinary urgency
walking frame
walking, difficulty with
weakness
weakness, progressive
wheelchair
white matter disease
Showing articles 250 to 300 of 3817 << Previous Next >>

Neuronal Intranuclear Inclusion Disease Cases with Leukoencephalopathy Diagnosed via Skin Biopsy
JNNP 85:354-356, Sone, J.,et al, 2014

Chediak-Higashi Syndrome: Pathognomonic Feature
Lancet 382:1514, Antunes, H.,et al, 2013

Polymyalgia Rheumatica
Lancet 381:63-72, Kermani, T. & Washington, K., 2013

The Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale
Stroke 43:2871-2876, Pescini, F.,et al, 2012

Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
NEJM 367:1921-1929, Ligt, J.,et al, 2012

Brain Arteriovenous Malformation Multiplicity Predicts the Diagnosis of Hereditary Hemorrhagic Telangiectasia Quantitive Assessment
Stroke 43:72-78, Bharatha, A.,et al, 2012

Cerebral Amyloid Angiopathy
eMedicine, Jan, Menon, R.S., 2012

Idiopathic Thoracic Spinal Cord Herniation: Retrospective Analysis Supporting a Mechanism of Diskogenic Dural Injury and Subsequent Tamponade
AJNR 33:52-56, Brus-Ramer,M. and Dillon,W.P., 2012

Risk Factors for Spinal Cord Lesions in Dystonic Cerebral Palsy and Generalised Dystonia
JNNP 83:159-163, Guettard,E.,et al, 2012

Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
Neurol 78:e72-e76, Blackburn,J.S. and Cirillo,M.L., 2012

Solitary Sclerosis
Neurol 78:540-544, Schmalstieg,W.F.,et al, 2012

Guillain-Barre Syndrome
NEJM 366:2294-2304, Yuki, N. & Hartung, H.P., 2012

Clinicopathologic Conference, Adult T-cell Leukemia-lymphoma Associated with HTLV-1
NEJM 367:552-563, Case 24-2012, 2012

Clinical Reasoning: A Young Man with Reversible Paralysis, Cerebral White Matter Lesions, and Peripheral Neuropathy
Neurol 79: e70-e72, Zhong, L.,et al, 2012

Range of Genetic Mutations Associated with Severe Non-Syndromic Sporadic Intellectual Disability: An Exome Sequencing Study
Lancet 380:1674-1682, Rauch, A.,et al, 2012

Diagnostic Exome, Sequencing in Persons with Severe Intellectual Disability
NEJM 367:1921-1929, Ligt, J.,et al, 2012

Cerebral White Matter Disruption in Creutzfeldt-Jakob Disease
AJNR 33:1945-1950, Lee,H.,et al, 2012

Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
Brain 134:3326-3332, Garone, C.,et al, 2011

Metastatic spinal cord compression
BMJ 342:d2402, Quraishi, N. & Esler, C., 2011

Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
UpToDate, Feb, Shovlin, C., 2011

Family Paralysis
Lancet 377:352, Sung,C.-C.,et al, 2011

An unusual cause of stroke and hypoxia
BMJ 342:c7200, Bell, S.L. & Eveson, D.J., 2011

Neurological disturbances caused by intravascular lymphomatosis
Brain Nerve 63:443-449, Mizutani, T., 2011

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

Transverse Myelitis
NEJM 363:564-572, Frohman,E.M. &Wingerchuk,D.M., 2010

Comparison of Clinical, Familial, and MRI Features of CADASIL and NOTCH3-Negative Patients
Neurol 74:57-63, Pantoni,L.,et al, 2010

Clinicopath Conf, Infantile Krabbe Disease
NEJM 362:346-356, Case 3-2010, 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

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

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

Spinal Dural Arteriovenous Fistulas
AJNR 30:639-648, Krings,T. &Geibprasert,S., 2009

The Expanding Phenotype of GLUT1-Deficiency Syndrome
Brain & Dev 31:545-552, Brockmann,K., 2009

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

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

Diagnostic Approaches to Imported Schistosomal Myeloradiculopathy in Travelers
Neurol 71:66-67, Makinson,A.,et al, 2008

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

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

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

Curable Cause of Paraplegia: Spinal Dural Arteriovenous Fistulae
Stroke 39:2756-2759, Aghakhani,N.,et al, 2008

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

Pyramidal Tract Degeneration in Sporadic Creutzfeldt-Jakob Disease
Neuropathology 27:434-441, Iwasaki,Y.,et al, 2007

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

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

Spinal Epidural Abscess
NEJM 355:2012-2020, Darouiche,R.O., 2006



Showing articles 250 to 300 of 3817 << Previous Next >>