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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 500 to 550 of 1579 << Previous Next >>

In-flight Seizures and Fatal Air Embolism
Arch Neurol 68:661-664, Arnaiz, J.,et al, 2011

Myoglobinuria and Muscle Pain are Common in Patients With Limb-Girdle Muscular Dystrophy 21
Neurol 76:194-195, Mathews,K.D.,et al, 2011

Prediction of Respiratory Insufficiency in Guillain-Barr� Syndrome
Arch Neurol 67:781-787, Walgaard,C.,et al, 2010

Clincopath Conference, Endogenous Endophthalmitis Due to Aspergillus Niger
NEJM 363:1749-1758, Case 33-2010, 2010

Comparative Analysis of Therapeutic Options Used for Myasthenia Gravis
Ann Neurol 68:797-805, Mandawat,A.,et al, 2010

Delirious Deficiency
Lancet 376:1362, Olsen,R.Q &Regis,J.T., 2010

A Meta-Regression of the Long-Term Effects of Deep Brain Stimulation on Balance and Gait in PD
Neurol 75:1292-1299, St. George,R.J.,et al, 2010

New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
JNNP 81:946-953, Klinge,L.,et al, 2010

Sensory Ganglionopathy Due to Gluten Sensitivity
Neurol 75:1003-1008, Hadjivassiliou,M.,et al, 2010

Copper Deficiency as a Treatable Cause of Poor Balance
BMJ 340:864-866, Khaleeli,Z., et al, 2010

Clinicopath Conf., Progressive Multifocal Leukoencephalopathy
NEJM 362:1431-1437, Case 11-2010, 2010

Clinicopath Conf., Brain Abscess, Pulmonary Arteriovenous Malformation Due to Hereditary Hemorrhagic Telangiectasia
NEJM 362:1326-1333, Case 10-2010, 2010

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

Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
NEJM 362:2213-2219, Case 17-2010, 2010

Huntingtons Disease
BMJ 341:34-40, Novak,M.J. &Tabrizi,S.J., 2010

Polyneuritis Cranialis Caused by Varicella Zoster Virus in the Absence of Rash
Neurol 74:85-86, Murata,K.,et al, 2010

Subclinical Hypothyroidism Presenting with Gait Abnormality
The Neurologist 16:115-116, Edvardsson,B. &Persson,S., 2010

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

Clinicopath Conf, Intravascular Large-B-Cell Lympoma
NEJM 362:1129-1138, Case 9-2010, 2010

Sjogren Syndrome: Neurologic Complications
www.Medlink.com,Jan, Roman,G.C., 2010

Epithelial-Myoepithelial Carcinoma of the Tongue Base: A Case for the Case-Report and Review of the Literature
Head & Neck Oncol 2, Peters, P.,et al, 2010

Cauda Equina Syndrome
BMJ 338:881-884, Lavy,C.,et al, 2009

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

A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
Neurol 72:1607-1613, Lossos,A.,et al, 2009

Antivenom for Critically Ill Children with Neurotoxicity from Scorpion Stings
NEJM 360:2090-2098, Boyer,L.V.,et al, 2009

Clinicopath Conf, Neuro-Behcets Disease
NEJM 360:2341-2351, Case 17-2009, 2009

Toxic and Drug-Induced Myopathies
JNNP 80:832-838, Dalakas,M.C., 2009

Neurological Consequences of Atrioesophageal Fistula After Radiofrequency Ablation in Atrial Fibrillation
Arch Neurol 66:884-887, St�llberger,C.,et al, 2009

Positron Emission Tomography in Diagnosis of Visual Variant Alzheimer Disease
J Neuro-Ophthalmol 29:149-150, Finelli,P.F., 2009

A 54-Year-Old Woman with Progressive Gait Disturbance and MRI Abnormalities
Neurol 73:466-474, Hochberg,F.H.,et al, 2009

A 75-Year-Old Woman with Progressive Right-Hand Tremor and Inability to Use Her Right Side
Neurol 73:1399-1405, Kertesz,A.,et al, 2009

Practice Parameter Update: The Care of the Patient with Amyotrophic Lateral Sclerosis: Drug, Nutritional, and Respiratory Therapies (An Evidence-Based Review)
Neurol 73:1218-1226, Miller,R.G.,et al, 2009

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

Syndrome of the Trephined
J Neurosurg 111:650-652, Joseph, V. & Reilly, P., 2009

Long-Term Outcomes Among Adult Survivors of Childhood Central Nervous System Malignancies in the Childhood Cancer Survivor Study
J Natl Cancer Inst 101:946-958, Armstrong,G.T.,et al, 2009

Neuro-Ophthalmologic Manifestations of Paraneoplastic Syndromes
J Neuro-Ophthalmol 28:58-68, Ko,M.W.,et al, 2008

Bilateral Basal Ganglia Lesions in Patients with End-Stage Diabetic Nephropathy
Nephrology 13:68-72, Li, J.,et al, 2008

Practice Parameter: Assessing Patients in a Neurology Practice for Risk of Falls (An Evidence-Based Review)
Neurol 70:473-479, Thurman,D.J.,et al, 2008

Clinicopath Conference, Postpartum Renal Failure Due to Thrombotic Microangiopathy Associated With Antiphospholipid Antibodies
NEJM 358:275-289, Case 2-2008, 2008

A 23-Year-Old Man With Seizures and Visual Deficit
Neurol 70:73-78, Boustany,R.-M.,et al, 2008

Diagnosis and Management of Motor Neurone Disease
BMJ 336:658-662, McDermott,C.J. &Shaw,P.J., 2008

Progressive Supranuclear Palsy: A Current Review
The Neurologist 14:79-88, Lubarsky,M. &Juncos,J.L., 2008

Association of Gait and Balance Disorders With Age-Related White Matter Changes: The LADIS Study
Neurol 70:935-942, Baezner,H.,et al, 2008

A Parkinsonian Syndrome in Methcathinone Users and the Role of Manganese
NEJM 358:1009-1017, Stepens,A.,et al, 2008

Lumbar Spinal Stenosis
NEJM 358:818-825, Katz,J.N. &Harris,M.B., 2008

Guillain-Barr\� Syndrome: Incidence and Mortality Rates in US Hospitals
Neurol 70:16081-1613, Alshekhlee,A.,et al, 2008

Anteroir Cerebral Artery Infarction: Stroke Mechanism and Clinical-Imaging Study in 100 Patients
Neurol 70:2386-2393, Kang,S.Y. &Kim,J.S., 2008

Clinicopath Conf., Endheim-Chester Disease
NEJM 359:736-747, Case 25-2008, 2008

Guillain-Barre Syndrome
BMJ 337:227-231, Winer,J.B., 2008

Juvenile Dermatomyositis and Other Idiopathic Inflammatory Myopathies of Childhood
Lancet 371:2201-2212, Feldman,B.M.,et al., 2008



Showing articles 500 to 550 of 1579 << Previous Next >>