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Differential
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advances in neurology
ammonia
anesthesia, general
anterior tibial muscle weakness
antiviral agents
areflexia
arrhythmia, cardiac
ataxia
ataxic gait
atrial fibrillation
atrial paralysis
atrioventricular block
attention deficit disorder with hyperactivity
Babinski sign
biopterin deficiency
bradycardia
bradykinesia
calf hypertrophy
cardiomegaly
cardiomyopathy
cardiovascular disease
cerebral embolism
cerebral embolism, carotid origin
cerebral palsy
cerebrovascular accident
cerebrovascular accident, cardiac disease causing
cerebrovascular accident, young adult
Charcot-Marie-Tooth
children
chromosomal abnormality
chromosome 14
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
consanguinity
contractures, joint
corpus callosum, lesion of
cough
creatine phosphokinase(CPK)elevated
developmental disability
developmental milestones, loss of
diamond on quadriceps
differential diagnosis
difficulty going down stairs
distal muscle weakness
diurnal variation
dopa responsive dystonia
dysarthria
dyspraxia
dystonia
dystonia, treatment of
dystrophin
electrocardiogram, abnormal
electromyogram
Emery-Dreifuss muscular dystrophy
encephalopathy
epileptic encephalopathy
exercise
exome sequencing
failure to thrive
falling
familial
FARS2 deficiency
fasciculation
fever
fibrillations
fine motor function, impaired
foot deformity
foot drop
gait disorder
gait, spastic
gene
gene mutation
gene therapy
genetic neurologic disorders
genetic testing
Gowers maneuver
growth retardation
heart block
heart block, complete
heart murmur
high arched feet
hyperreflexia
hyporeflexia
hypotonia
imbalance
implantable cardioverter defibrillator
influenza A virus
influenza B virus
Krabbe's disease
L-dopa
leukodystrophy
life expectancy
limb-girdle weakness
liver disease
lysosomal storage disease
malignant hyperpyrexia
meningitis, CSF cell count-normal
mental retardation
microcephaly
misdiagnosis
mitochondrial disease
molecular genetics
movement disorder
MRI, abnormal
muscle atrophy, progressive
muscle biopsy
muscle pain
muscle tenderness
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, limb-girdle
muscular dystrophy, pattern of muscle involvement
myoglobinuria
myopathy
myopathy, quadriceps
myositis
myositis, acute of childhood
myositis, post infectious
neurologic disease, diagnoses of
neuropathy
neuropathy, demyelinating
neuropathy, hereditary peripheral
pacemaker, cardiac-transvenous
pain, calf
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, familial spastic, variants
paraparesis, spastic
Parkinson disease, differential diagnosis of
Parkinson disease, juvenile
Parkinsonism syndrome
pes cavus
positive sharp waves
prognosis
progressive neurologic disorder
proximal muscle atrophy
pyramidal tract dysfunction
Red flags
respiratory failure
review article
rhabdomyolysis
rippling muscle disease
sarcoglycan
sarcoglycanopathy
scoliosis
seizure
seizure, children
short stature
sinemet
spastic diplegia
spasticity
steroid therapy, CNS treatment and complications with
sudden death
tandem gait, ataxic
tenderness
toe walking
treatment of neurologic disorder
tremor
tremor, intention
tremor, postural
tripping
urea-cycle enzymopathies
urine, dark
viral infection
viral myopathy
walking
walking frame
walking, delayed
walking, difficulty with
weakness
weakness, progressive
weakness, proximal
web sites
wheelchair
white matter disease
wide based gait
winging of scapula
workup
Showing articles 200 to 250 of 402 << Previous Next >>

Holmes-Adie Syndrome
Lancet 356:1760-1761, Martinelli,P., 2000

Acute Renal Failure with Neurological Involvement in Adults Associated with Measles Virus Isolation
Lancet 354:992-995, Wairagkar,N.S.,et al, 1999

Clinicopath Conf,Guillain-Barre Syndrome, Campylobacter Jejuni Enteritis,Case 39-1999
NEJM 341:1996-2003, , 1999

Hypophosphatemia-Induced Neuropathy: Clinical and Electrophysiologic Findings
Muscle Nerve 21:650-652, Siddiqui,M.F. &Bertorini,T.E., 1998

Secondary Hyperkalaemic Paralysis
JNNP 64:249-252, Evers,S.,et al, 1998

Guillain-Barre Syndrome
Lancet 352:635-641, Hahn,A.F., 1998

Clinicopath Conf
Chronic Inflammatory Demyelinating Polyneuropathy, Case 13-1998, NEJM 338:1212-1219998., , 1998

Genetic Analysis Enables Definite and Rapid Diagnosis of Cerebrotendinous Xanthomatosis
Neurol 51:865-867, Chen,W.,et al, 1998

Alcohol-Related Acute Axonal Polyneuropathy,A Differential Diagnosis of Guillain-Barre Syndrome
Arch Neurol 55:1329-1334, Wohrle,J.C.,et al, 1998

Pregnant,Vomiting,and Going Blind
Lancet 352:1594, Tesfaye,S.,et al, 1998

Clinicopath Conf
Acute Critical-Illness Myopathy, with Loss of Myosin Filaments, ? Induced by Steroid, Case 11-1997,, EJM 379-1088,1997., 1997

Clinicopath Conf
Botulism, Case 22-1997, NEJM 337:184-190997., , 1997

Broadened Friedreich's Ataxia Phenotype after Gene Cloning, Minimal GAA Expan Causes Late Spastic Ataxia
Neurol 49:1617-1620, Ragno,M.,et al, 1997

Acute Corticosteroid Myopathy in Intensive Care Patients
Muscle & Nerve 20:1371-1380997., Hanson,P.,et al, 1997

Erroneous Diagnosis Corrected After 28 Years
Arch Neurol 53:1194-1196, Gordon,P.H.,et al, 1996

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996

Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
Neurol 46:810-814, Connolly,A.M.,et al, 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Acute Lumbosacral Polyradiculopathy Due to Cytomegalovirus in Advanced HIV Disease:CSF Findings in 17 Patients
JNNP 61:456-460, Miller,R.F.,et al, 1996

Multifocal Demyelinating Motor Neuropathy:Pathologic Evidence of Inflammatory Demyelinasting Polyradiculoneuropathy
Neurol 45:1828-1832, Oh,S.J.,et al, 1995

Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
Neurol 45:2266-2271, Schwankhaus,J.D.,et al, 1995

Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,et al, 1995

Critical Illness Neuromuscular Disease in Children Manifested as Ventilatory Dependence
J Pediatr 126:259-261, Sheth,R.D.,et al, 1995

The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
Neurol 45:311-317, Barth,P.G.,et al, 1995

Serotonin Syndrome
Neurol 45:219-223, Bodner,R.A.,et al, 1995

Kayser-Fleischer Ring:Hepatolenticular Degeneration (Wilson's Disease)
Neurol 45:1261-1262, Finelli,P.F., 1995

Reflex Sympathetic Dystrophy
BMJ 310:1645-1648, Paice,E., 1995

Reflex Sympathetic Dystrophy in Children
BMJ 310:1648-1649, Lloyd-Thomas,A.R.&Lauder,G., 1995

Combined System Disease after Nitrous Oxide Anesthesia:A Case Report
Neurol 45:1224-1225, McMorrow,A.M.,et al, 1995

X-Linked Pure Familial Spastic Paraparesis
Arch Neurol 52:665-669, Cambi,F.,et al, 1995

Site of Autonomic Dysfunction in a Patient with Ross'Syndrome and Postganglionic Horner's Syndrome
Neurol 45:2094-2096, Wolfe,G.I.,et al, 1995

Systemic Sclerosis Sine Scleroderma:An Unusual Presentation in Scleroderma Renal Crisis
J Rheumatol 22:557-560, Molina,J.F.,et al, 1995

Adult-Onset Spinocerebellar Dysfunction Caused by a Mutation in the Gene for the a-Tocopherol-Transfer Protein
NEJM 333:1313-1318, 13511995., Gotoda,T.,et al, 1995

Clinicopath Conf
Progressive Muscular Atrophy, Case 36-1995, NEJM 333:1406-1412995., , 1995

Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
Muscle & Nerve 18:267-275995., Ionasecu,V.V., 1995

Polyarteritis Nodosa-Induced Quadriplegia
Ann Int MEd 122:731-732, Smith,D.L.,et al, 1995

A Comparison of Two Techniques for Ankle Jerk Assessment in Elderly Subjects
Lancet 344:1619-1620, O'Keefe,S.T.,et al, 1994

Clinicopath Conf
Chronic Idiopathic Anhidrosis, Case 29-1994, NEJM 331:259-265994., , 1994

Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
Ann Neurol 36:368-378, Lampe,T.H.,et al, 1994

Peripheral Nerve Injury and Causalgia Secondary to Routine Venipuncture
Neurol 44:962-964, Horowitz,S.H., 1994

Further Reg Var of Acute Polyneuro:Bifacial or 6th Nerve Paresis, Lumbar Polyrad & Ataxia/Phary Cervical-Brachial Wkness
Arch Neurol 51:671-675, Ropper,A.H., 1994

Clinicopath Conf
Small Cell CA (of lung) with Lambert-Eaton Myasthenic Syndr, Case 32-1994, NEJM 331:528-5354., , 1994

Acute Sensory Neuronopathy:Report of a Child with Remarkable Clinical Recovery
Neurol 44:762-764, Fernandez,J.M.,et al, 1994

Cerebrotendinous Xanthomatosis:Molecular Diagnosis Enables Presymptomatic Detection of a Treatable Disease
Neurol 44:288-290, Meiner,V.,et al, 1994

Cerebral Involvement in McLeod Syndrome
Neurol 44:117-120, Danek,A.,et al, 1994

Acute Lumbosacral Polyradiculopathy in Acquired Immunodeficiency Syndrome:Experience in 23 Patients
Ann Neurol 35:53-58, So,Y.T.&Olney,R.K., 1994

Rapidly Evolving Myopathy with Myosin-Deficient Muscle Fibers
Ann Neurol 35:273-279, 2571994., Al-Lozi,M.T.,et al, 1994

Clinicopath Conf
Acquired Demyelinating Neuropathy, ? CIDP, ? Motor Neuropathy with Multifocal Conduction Blocks, Cas, 41-1EJM 329:1182-1190,1993., 1993

Acute Myopathy and Neuropathy in Status Asthmaticus:Case Report and Literature Review
Muscle & Nerve 16:84-90993., Lacomis,D.,et al, 1993

The Neurologic Syndrome of Vitamin E Deficiency:A Significant Cause of Ataxia
Neurol 43:2167-2169, Kayden,H.J., 1993



Showing articles 200 to 250 of 402 << Previous Next >>