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Differential
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acrochordon
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
advances in neurology
adverse drug reaction
affect, inappropriate
alcoholism
anemia
anemia, megaloblastic
ankle, swelling of
anorexia
arrhythmia, cardiac
arthralgia
ascites
aspartate aminotransferase
ataxia
ataxia, cerebellar
ataxic gait
autoantibodies
autonomic dysfunction
B 12 deficiency
bladder dysfunction
blindness
bone marrow transplantation
brain natriuretic peptide
burning hands
burning paresthesia
calf hypertrophy
cardiomyopathy
cardiovascular disease
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellum, disease of
cerebrovascular accident
cervical spondylosis
children
cirrhosis
Clinical Pathologic Conference(C.P.C.)
complications
contractures, joint
cortical blindness
cough
creatine phosphokinase(CPK)elevated
critical care unit
crying, pathologic
cultured skin fibroblasts
dantrolene sodium
deafness
decerebrate posture
delay in diagnosis
dementia, childhood
demyelinating disease
depression
dermal sinus tract
dermoid
developmental retardation
dexterity, impaired
diagnostic criteria
diamond on quadriceps
diastematomyelia
diet
differential diagnosis
difficulty climbing stairs
dimple
down-beat nystagmus
drug induced neurologic disorders
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dyspraxia
dysraphism, spinal
dystrophin
electroencephalogram, abnormalities of
electromyogram
epidemiology of neurology
exercise
facial weakness
falling
familial
fatigue
fatty acid, elevated plasma content
fever
fibrillations
fine motor function, impaired
foot numbness
gait disorder
gait, waddling
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glucose tolerance test, abnormal
Gowers maneuver
hand weakness
hemochromatosis
hemochromatosis, primary
hepatic encephalopathy
hepatolenticular degeneration(Wilson's disease)
HMGcoA reductase inhibitors
hung reflex
hyperpigmentation of skin
hyperreflexia
hypersegmented polys
hypertrichosis
hypogonadism
hypopigmentation of skin
hypothyroidism
iatrogenic neurologic disorders
intellectual deterioration
jaundice
lactic dehydrogenase(LDH)
learning disability
learning disability, in children
leukodystrophy
level of consciousness, decreased
limb-girdle weakness
lipoma of CNS
lipoma of skin
liver function enzymes
Lorenzo's oil
metabolic disorder, primary
methylmalonic acid, serum
misdiagnosis
mood change
mortality
movement disorder
MRI
MRI, abnormal
MRI, spine
multiple system atrophy
muscle biopsy
muscle pain
muscle stiffness
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, Duchenne
muscular dystrophy, limb-girdle
muscular dystrophy, pattern of muscle involvement
myelopathy
myoedema
myoglobinuria
myopathy
myopathy, drug-induced
myopathy, necrotizing, autoimmune
myxedema, neurologic manifestations of
neurocutaneous disease
neurofibromatosis 1
neuroleptic
neuroleptic malignant syndrome
neurologic disease, diagnoses of
neurologic signs
neuronopathy, sensory
neuropathy
neuropathy, sensory
nutritional deficiency
nystagmus
ochronosis
osteoarthrosis
osteoporosis
pain, abdominal
paraparesis
paraparesis, spastic
paresthesias
paresthesias, hands
peripheral blood smear, abnormal
pernicious anemia
peroxisomal disease
personality change
phlebotomy
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proximal muscle atrophy
pruritus
pseudobulbar palsy
ptosis
quadriparesis
renal failure
renal stones
respiratory failure
review article
RFC1 gene
rhabdomyolysis
rigidity
Romberg's sign
sarcoglycan
sarcoglycanopathy
sclerae, hyperpigmented
seizure
sensorineural hearing loss
sensory loss, leg
serum alanine aminotransferase
sex reassignment surgery
skin, biopsy
skin, darkening of
skin, lesions in neurologic disorders
sleep apnea
speech disorder
speech disorder, childhood
speech, delayed development of
speech, slowed
spina bifida
spondylolysis
statin therapy
systemic illness
tandem gait, ataxic
testicular atrophy
tethered spinal cord
toe walking
tongue, smooth
tongue, swelling
transgender
treatment of neurologic disorder
tremor
tremor, intention
trifluoperazine
tripping
urinary incontinence
urine, dark
very long chain fatty acids
vestibular areflexia
walking, difficulty with
walking, difficulty with in dark
weakness
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
white matter disease
wide based gait
winging of scapula
workup
Showing articles 150 to 200 of 1557 << Previous Next >>

Clinicopathologic Conference, AA Amyloidosis, Complicated by Cerebral Mucormycosis
NEJM 382:1457-1466, Case 11-2020, 2020

Progressive Ataxia and Palatal Tremor
Neurol 94:e1445-e1447, Pradeep, S.,et al, 2020

A Young Health Woman with Difficult-to-Wean Acute Ventilator Dependence
Neurol 94:e1340-e1343, Chandrashekhar, S.,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 16-year-old Girl with Ataxia, Oscillopsia, and Behavioral Changes
Neurol 94:713-717, Silverman, A.,et al, 2020

Wall-Eyed Bilateral Internuclear Ophthalmoplegia by Ischemic Stroke
Neurologist 25:82-84, Uzawa, A.,et al, 2020

Pernicious Anaemia
BMJ 369:m1319, Mohamed, M.,et al, 2020

Coagulopathy and Antiphospholipid Antibodies in Patients with Covid-19
NEJM 382:e38, Zhang, Y.,et al, 2020

Spasms and Myoclonus in a Young Woman with Hashimoto Thyroiditis
JAMA Neurol 77:650-651, Shen, D.,et al, 2020

Functional Gait Disorders
Neurol 94:1093-1099, Nonnekes, J.,et al, 2020

Severe Acute Respiratory Syndrome Coronavirus 2 Infection and Ischemic Stroke
Stroke 51:e124-e127, Valdes Valderrama, E.,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

Burning Pain in the Legs
NEJM 383:e18, Sacks, C.A., 2020

Arthralgia as an Initial Presentation of COVID-19
Rheumatol Int doi:10.1007/s00296-020-04561-0, Joob, B. & Wiwanitkit, V., 2020

Ptosis that Resolves with Application of an Ice Pack
BMJ 369:m1147, Chakraborty, A. & Jacob, J., 2020

Tapia Syndrome at the Time of the COVID-19 Pandemic
Neurol 95:312-313, Decavel, P.,et al, 2020

Clinicopathologic Conference, HIV Type 2 Infection & Cerebral Toxoplasmosis
NEJM 383:859-866, Case 27-2020, 2020

A 14-Year-Old Boy with Acute Weakness, Parethesias, and Headache
Neurol 95:e1285-e1289, Seese, R.R.,et al, 2020

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

An Adolescent Girl Presenting with Worsening Vertigo, Headache, and Ataxia
Neurol 95:e1760-e1763, Brigham, E.,et al, 2020

A 57-Year-Old Woman with Progressive Ataxia and Falls
Neurol 95:650-656, Badahdah, A., 2020

Clinicopathologic Conference, Borrelia Miyamotoi Infection
NEJM 383:1578-1586, Case 32-2020, 2020

A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
Neurol 95:e2707-e2710, Lad, M. & Griffiths, T.D., 2020

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

Bithalamic Lesions
Stroke 51:e355-e358, Chen, P.M.,et al, 2020

Clinical features, prognostic factors, and antibody effects in anti-mGluR1 encephalitis
Neurol 95:e3012-e3025, Spatola, M.,et al, 2020

Covd-19-Associated Myopathy Caused by Type 1 Interferonopathy
NEJM 383:2389-2390, Manzano, A.C.,et al, 2020

Clinicopathologic conference, Vitamin D deficiency
NEJM 383:2462-2470, Case 39-2020, 2020

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

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

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

A 40-Year-Old Woman Presenting with Distal Leg Weakness
Neurol 92:242-247, Fam, D.,et al, 2019

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

Peripheral Neuropathy Associated with Silver Toxicity
Neurol 92:481-483, Naddaf, E.,et al, 2019

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

Neuromuscular Adverse Events Associated with Anti-PD-1 Monoclonal Antibodies
Neurol 92:663-674, Johansen, A.,et al, 2019

Clinicopathologic Conference, Amyotrophic Lateral Sclerosis
NEJM 380:1566-1574, Case 12-2019, 2019

Acute Paraplegia in a Healthy Child
BMJ 367:L6257, Haque, A.K.M.,et al, 2019

A 47-year-old Man with Diffuse White Matter Disease and Rapidly Progressive Dementia
Neurol 92:e2832-e2837, Di Luca, D.G.,et al, 2019

Carbon Monoxide Poisoning
BMJ 365:DOI.10.136/BMJ.L2299, Ashcroft, J.,et al, 2019

Kelch-Like Protein 11 Antibodies in Seminoma-Associated Paraneoplastic Encephalitis
NEJM 381:47-54, Mandel-Brehm, C.,et al, 2019

Vestibular Migraine
BMJ 366:L4213, Li, V.,et al, 2019

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

Muscular Dystrophies
Lancet 394:2025-2038, Mercuri, E.,et al, 2019

Orofacial Dyskinesia in a Young Man
JAMA Neurol 76:1517-1518, Tian, X.,et al, 2019

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

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

Case 27-2019:A 16-Year-Old Girl with Head Trauma During a Sailboat Race
CPC,Concussion,Benign Paroxysmal Positional Vertigo, Case 27-2019, NEJM 381:863-871, Iaccarino,M.A.,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



Showing articles 150 to 200 of 1557 << Previous Next >>