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Differential
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abdominal distention

abdominal muscle paralysis

abdominal protrusion

abscess, intracranial

acid maltase deficiency

acid maltase deficiency, adult

acoustic neurinoma

acoustic neurinoma, bilateral

acquired immunodeficiency syndrome

acyl CoA dehydrogenase deficiency

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

agammaglobulinemia

agenesis of corpus callosum

Aicardi-Goutieres syndrome

airway obstruction

alcohol intoxication

alcohol, blood level of

alcohol, neurologic complications with

alcoholic blackout

alcoholic dementia

alcoholic polyneuropathy

alcoholic withdrawal states, DT's, convulsions, etc.

alpha glucosidase

alpha-fetoprotein

alternative medicine

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, diagnosis of

Alzheimer's disease, early onset

Alzheimer's disease, familial

Alzheimer's disease, preclinical

Alzheimer's disease, risk factors in

aminoacidopathies

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

amyotrophic lateral sclerosis, misdiagnosis

anesthesia, general

aneurysm, intracranial

Angelman syndrome

angiofibroma, facial

angiomyolipomas

animal exposure

ankle, swelling of

anoctaminopathy

anterior horn cell disease

anterior tibial muscle weakness

antibodies to voltage-gated calcium channels

anticonvulsants

anticonvulsants, absorption

anticonvulsants, bioavailability

anticonvulsants, blood level determination of

anticonvulsants, compliance

anticonvulsants, hypersensitivity syndrome

anticonvulsants, selection of

anticonvulsants, subtherapeutic

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

antiviral agents

apolipoprotein E

arrhythmia, cardiac

arteriovenous malformation

arteriovenous malformation, pulmonary

arthrogryposis multiplex

aspartate aminotransferase

Asperger's syndrome

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

atrial fibrillation

atrioventricular block

attention deficit disorder with hyperactivity

auditory evoked brainstem potentials

autism, screening for

autoimmune disease

automatic implantable cardioverter-defibrillator

autonomic dysfunction

azidodeoxythymidine

bacterial infection

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery stenosis

Bassen-Kornzweig syndrome

behavior, combative

behavioral disorder

benign essential tremor

bent spine syndrome

bicaudate index

black toenail sign

bleeding disorder

bone marrow transplantation

botulinum toxin

bovine spongiform encephalopathy

brain biopsy, negative

brainstem, lesion of

brainstem, neoplasms of

bulging of biceps

calcification, intracranial

calcium channel dysfunction

calf hypertrophy

carcinoma of pancreas

cardiovascular disease

carnitine deficiency

carnitine deficiency myopathy

CAT scan, abnormal

CAT scan, chest

CAT scan, disappearing lesion on

CAT scan, false negative

CAT scan, muscle

cataracts, congenital

caudate nucleus

caudate nucleus, atrophy

Central America

central core disease

central nervous system, infection of

central nuclei, muscle

central pontine myelinolysis

cerebellar ataxia, children

cerebellar ataxia, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemangioma

cerebellum, neoplasms of

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral ischemia

cerebral palsy, etiology

cerebral palsy, work up

cerebro hepato renal syndrome

cerebrospinal fluid, abnormal

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, protein of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, nonvascular territory

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

Charcot-Marie-Tooth

cherry red spot-myoclonus syndrome

chewing, impaired

chloride channel dysfunction

chorea, familial

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

clubfoot as related to neurologic disease

Cockayne's syndrome

coenzyme Q10 deficiency

collagen vascular disease

compression neuropathy

conduction block

confidentiality

congenital birth defects

congenital heart disease

congenital heart disease, CNS complications with

congenital malformation

congenital myasthenic syndromes

congenital myopathy

congenital myopathy, inflammatory

congestive heart failure

contractures, joint

conversion reaction

cornea, abnormal

corneal dystrophy

corpus callosum

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

cricopharyngeal bar

cultured skin fibroblasts

cyclic vomiting

cyst, peritumoral

cyst, neoplastic cerebellum

cyst, parenchymal

cytochrome c oxidase

cytochrome c oxidase, deficiency

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

delay in diagnosis

dementia, childhood

dementia, familial

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, transmissible

demyelinating disease

dentatorubral-pallidoluysian atrophy

developmental abnormality of brain

developmental disability

developmental evaluation

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

diamond on quadriceps

diaphragmatic paralysis

differential diagnosis

difficulty climbing stairs

digits, abnormal

dilantin, hypersensitivity to

dislocated hip, congenital

distal muscle atrophy

distal muscle weakness

diurnal variation

dopa responsive dystonia

dropped head syndrome

drug induced neurologic disorders

dysarthria-clumsy hand syndrome

dyschromatopsia

dysferlinopathy

dystonia musculorum deformens

dystonia musculorum deformens, carrier

dystonia, cervical

dystonia, etiology of

dystonia, painful

dystonia, post traumatic

dystonia, treatment of

dystroglycanopathies

dystrophin associated proteins

eating disorder

edema, periorbital

Ehlers-Danlos syndrome

Ehlers-Danlos syndrome, classification

ejection fraction

ejection fraction, abnormal

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electron microscopy

electronystagmography

electroretinograph

embolism, paradoxical

embolism, septic

Emery-Dreifuss muscular dystrophy

encephalomalacia

encephalopathy, anoxic

encephalopathy, neonatal

encephalopathy, progressive

enzyme treatment

enzyme, induction

enzyme, muscle disease

epidemiology of neurology

episodic disorders

episodic neurologic deficits

epistaxis, recurrent

erectile dysfunction

esophageal varices

ethics in neurology

evoked potentials

executive dysfunction

exercise intolerance

exercise-induced neurologic dysfunction

exome sequencing

extraocular muscle lesion

eye movement, disorders of

Fabry's disease

facial anomalies

facial appearance, abnormal

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failure to thrive

familial hemiplegic migraine

family planning

fatty acid, elevated plasma content

Fazio-Londe's disease

feeding disorder

fetal alcohol syndrome

fibroma, ungual

fine motor function, impaired

fistula, arterio-venous, pulmonary

foot drop, bilateral

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal balding

fundus, abnormality of

gangliosidosis GM1

gangliosidosis GM2

gastrocnemius muscle weakness

gastrointestinal bleeding

gastrointestinal disease, neurologic complications

gastrointestinal motility

Gaucher's disease

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann-Straussler-Scheinker disease

glucocerebrosidase

GLUT1 deficiency syndrome

glycogen storage disease

glycosyltransferase

gonadal dysgenesis

Gowers maneuver

growth hormone deficiency

Guillain Barre syndrome

gyrus, abnormal

Hallervorden Spatz disease

Hallgren's syndrome

head circumference

headache, positional

heart block, complete

heavy metal intoxication

hemangioblastoma

hematuria, gross

hemianopia, homonymous

hemidiaphragm, paralysis of

hemorrhagic diathesis

hepatic encephalopathy

hepatic failure

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

hereditary myopathy with early respiratory failure

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

hexosaminidase-A

high arched feet

high arched palate

histochemistry of muscle

hormone replacement

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's chorea, presymptomatic detection of

Hurler's syndrome

hydrocephalus, congenital

hydrocephalus, fetal

hydrocephalus, intrauterine

hyperkalemic periodic paralysis

hypersensitivity reaction

hyperthyroidism

hypertrophic cardiomyopathy

hypoglycemic coma

hypoglycorrhachia

hypokalemic periodic paralysis

hypopigmentation of skin

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

ileus, paralytic

imbalance, postural

immunodeficiency

immunohistochemistry

immunology and the nervous system

immunosuppressive agents

inability to sit up

inability to stand on tiptoes

inborn errors of metabolism

inborn errors of metabolism, screening

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

infantile spasm

informed consent

intellectual deficit

intellectual deterioration

interferonopathy

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial pressure, increased

intranasal medication

intrauterine infection

intrauterine infection, viral

intrinsic hand muscles, wasting of

ischemic exercise test

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, variant

joint hypermobility

Kearns-Sayre syndrome

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

Lafora's disease

laminar necrosis, cortical

Laurence-Moon-Bardet-Biedl syndrome

Leber's hereditary optic neuropathy

leg spasms, painful

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

lens, dislocation of

leukocyte enzyme abnormality

leukoencephalopathy

lid closure, weakness of

life expectancy

limb-girdle weakness

lipid storage disorder of CNS

lipid storage myopathy

liver function enzymes

lymphadenopathy

lymphangiomyomatosis

lymphocyte capping, diminished

lysosomal storage disease

lysosomes, abnoral

macular degeneration

magnetoencephalography

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malignant hyperpyrexia

McArdle's disease

McLeod syndrome

medical-legal aspects of neurology

memory, impairment of

meningeal enhancement

meningitis, basilar

meningitis, leptospira

meningoencephalitis

mental retardation

mental retardation, familial

mesial temporal lobe

metabolic acidosis

metabolic disorder, primary

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

Miller-Dieker syndrome

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

mitral valve prolapse

molecular genetics

molybdenum cofactor deficiency

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI lesion location

MRI, contrast enhanced

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, functional

MRI, gyral enhancement

MRI, gyral swelling

MRI, intrauterine

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

mucopolysaccharidoses

multicore myopathy

multiminicore disease

multiple sclerosis, misdiagnosis

muscle atrophy, focal

muscle atrophy, progressive

muscle atrophy, static

muscle hypertrophy

muscle phosphorylase deficiency

muscle stiffness

muscle swelling

muscle tenderness

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, Duchenne, neonatal screening

muscular dystrophy, Duchenne, presymptomatic detection

muscular dystrophy, dystrophin normal

muscular dystrophy, facioscapulohumeral

muscular dystrophy, female occurrence of

muscular dystrophy, limb-girdle

muscular dystrophy, lymphocyte capping, diminished

muscular dystrophy, neurogenic hypothesis of

muscular dystrophy, pattern of muscle involvement

muscular dystrophy, systemic membrane defect

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, familial incidence of

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, neuromuscular junction in

myasthenia gravis, receptor site in

myasthenia gravis, seronegative

myasthenic syndrome

myoclonic jerks

myoclonus, cortical

myoclonus, epilepsy

myoclonus, stimulus sensitive

myopathy, alcoholic

myopathy, centronuclear

myopathy, desmin

myopathy, distal

myopathy, distal Laing

myopathy, distal, vacuolar

myopathy, distal, Welander's

myopathy, drug-induced

myopathy, genetic

myopathy, hereditary

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, inclusion body, hereditary

myopathy, metabolic

myopathy, mitochondrial

myopathy, myofibrillar

myopathy, necrotizing

myopathy, proximal

myopathy, quadriceps

myopathy, vacuolar

myotonia congenita

myotonia dystrophica

myotonia dystrophica, classification

myotonia dystrophica, type 2

myotonic discharges

nasal bridge, wide

nausea and vomiting

nemaline rod myopathy

nemaline rod myopathy, adult onset

neonatal screening, genetic neurologic disorders

neoplasm, metastatic to CNS

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplasm, primary of CNS-surgical treatment of

nerve conduction studies

nerve growth factor

nerve hypertrophy

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurofibromatosis 2

neurofibromatosis 2, presymptomatic

neurogenic vs.myopathic atrophy

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic examination, focal

neurologic practice

neurologic signs

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuroophthalmology

neuropathy, amyloid

neuropathy, ataxia, retinitis pigmentosa

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, peripheral

newborn, evaluation of

next-generation sequencing

Niemann-Pick disease

night blindness

Noonan Syndrome

obsessive-compulsive disorder

obstetric neurologic injuries

occipital lobe, lesion of

ocular motility, disorders of

ocular myopathy

oculopharyngeal muscular dystrophy

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy, hereditary

optic disc edema

optic nerve, compression of

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, hereditary

oral contraceptives

pacemaker, cardiac-transvenous

Paget's disease

pain, abdominal

paralysis, acute areflexic

paralysis, asymmetric

paramyotonia congenita

paraparesis, familial spastic

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

Parkinson disease

Parkinsonism syndrome

paroxysmal exertion-induced dyskinesia

paroxysmal neurologic deficits

patient in waiting

patient information and support

pectus excavatum

percussion induced muscle contraction

periodic paralysis

periodic paralysis, thyrotoxic

peripheral blood smear

peroxisomal disease

personality change

pheochromocytoma

phosphorylase b kinase deficiency

pigmentary retinopathy

pituitary, hormones of

pleocytosis of cerebrospinal fluid

pleural effusion

poison, mercury

poison, neurologic problems with

polycystic kidneys

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, familial

Pompe's disease of glycogen storage

Pompe's disease, infantile

portal caval shunt

positive sharp waves

postural abnormality

potassium channel antibodies

potassium channel dysfunction

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

pregnancy, anticonvulsants during

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

presenilin-1 gene

presenilin-2 gene

prevention of neurologic disorders

progressive infantile poliodystrophy

progressive myoclonic epilepsy

progressive neurologic disorder

protein 14-3-3, cerebrospinal fluid

proximal muscle atrophy

proximal myotonic myopathy

pseudohypertrophy

pseudomyasthenia

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

psychosis, acute

psychosocial aspects

psychotic behavior

ptosis, bilateral

ptosis, familial

pulmonary hypertension

pulmonary infection

pulmonary stenosis

pyloric stenosis

quadriceps atrophy

quadriceps weakness

quadriparesis, progressive

quadriplegia, transient

quality of life

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

ragged-red fibers

rapidly progressing neurologic illness

real-time quaking-induced conversion

recombinant DNA

refractive errors

Refsum's disease

renal cell carcinoma

repetitive nerve stimulation

respiratory depression

respiratory failure

respiratory tract infection

retina, abnormal

retinal degeneration

retinal hamartoma

retinal hemangioma

retinitis pigmentosa

reversible neurologic disorder

rhabdomyosarcoma of heart

rigid spine syndrome

rippling muscle disease

saccadic eye movements, abnormal

sarcoglycanopathy

sclerosis, bone

scoliosis, neurologic association with

second wind phenomena

seizure, children

seizure, familial

seizure, injury following

seizure, intractable

seizure, laughing as manifestation

seizure, neonatal

seizure, paradoxical

seizure, petit mal

seizure, pregnancy

seizure, treatment of

seizure, treatment of, monotherapy

self-mutilation

sensorineural hearing loss

serum alanine aminotransferase

shoulder, pain in

sick sinus syndrome

single photon emission computed tomography

skin, darkening of

skin, hyperextensible

skin, lesions in neurologic disorders

skin, translucent

skull x-ray, abnormal

slit lamp examination

sloped shoulders

sodium channel dysfunction

Southern immunoblot test

speech disorder

speech, delayed development of

sphingolipodoses

Spielmeyer Vogt syndrome

spinal cord, neoplasm

spinal cord, vascular malformation of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinocerebellar ataxia

spinocerebellar ataxia type 2

spinocerebellar ataxia type 6

spinocerebellar degeneration

spirochete infection

spongy degeneration of brain

spontaneous remission

standing difficulty

status epilepticus

stereotaxic surgery

stereotyped behavior, drug induced

steroid therapy, CNS treatment and complications with

stooped posture

storage disease of CNS

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

subarachnoid hemorrhage

subependymal nodules

succinate dehydrogenase deficiency

survival motor neuron gene

symmetric brain lesions

systemic illness

systemic lupus erythematosus

tandem gait, ataxic

tapetoretinal degeneration

Tay-Sachs disease

telangiectases, retinal

temper tantrums

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

testicular atrophy

testicular enlargement

thalamus, lesion of-bilateral

thrombocytopenia

thyroid function tests

tissue plasminogen activator, intravenous

tongue, enlarged

tongue, fasciculations of

tongue, protrusion of

tongue, weakness

torticollis, post traumatic

transient neurologic deficit

transverse smile

travel, foreign

treatment of neurologic disorder

tremor, intention

tremor, postural

tricresylphosphate

trinucleotide repeats

tuberous sclerosis

tuberous sclerosis, screening for

type 1 muscle fiber

ultrasonography

ultrasonography, head

ultrasonography, head, fetus-neonate

Unverricht-Lundborg disease

upgaze, paralysis of

Usher's syndrome

very long chain fatty acids

vestibular migraine

viral infection

viral infection, CNS

visceral neuropathy

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss, progressive

vitamin supplementation

vomiting, recurrent

Von Hippel Lindau

walking, difficulty with

weakness, acute

weakness, chronic

weakness, episodic

weakness, fatiguable

weakness, fluctuating

weakness, focal

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

Werdnig-Hoffman disease

Wernicke's encephalopathy

Western immunoblot test

Whipple's disease

white matter disease

white matter disease, pattern

whole genome sequencing

wide based gait

winging of scapula

wound healing, poor

X-linked bulbospinal neuronopathy

x-linked hydrocephalus

x-linked mental retardation

X-linked myopathy

x-linked myopathy with excessive autophagy

Zika virus infection

Showing articles 850 to 900 of 2510 << Previous Next >>

Isolated Dropped Head Due to Adult-Onset Nemaline Myopathy Treated by Posterior Fusion
Neurol 65:1504-1505, Katirji,B.,et al, 2005

Hereditary Motor and Sensory Neuropathies
Peripheral Neuropathy, Dyck,P.J. & Thomas,P.K. (Ed). Elsevier Publ, Vol 2, Ch 69: 1623-1635, Shy,M.E., et al, 2005

Rhabdomyolysis: An Evaluation of 475 Hospitalized Patients
Medicine 84:377-385, Melli,G.,et al, 2005

Late-Onset Friedreich Ataxia
Arch Neurol 62:1865-1869, Bhidayasiri,R.,et al, 2005

Clinicopath Conf., MELAS Syndrome
NEJM 353:2271-2280, Case 36-2005, 2005

Neuroblastoma -- from Genetic Profiles to Clinical Challenge
NEJM 353:2215-2217, Kushner,B.H. &Cheung,N.-K.V., 2005

Heritability of Carotid Artery Atherosclerotic Lesions
Stroke 36:5-8, Moskau,S.,et al, 2005

Migraine and Cerebral White Matter Lesions
The Neurologist 11:19-29, Gladstone,J.P. &Dodick,D.W., 2005

A Variant in the HS1-BP3 Gene is Associated with Familial Essential Tremor
Neurol 64:417-421, Higgins, J.J., et al, 2005

Genetic Screening for a Single Common LRRK2 Mutation in Familial Parkinson's Disease
Lancet 365:410-412, Nichols, W.C., et al, 2005

Genetic Factors in Alzheimer's Disease
NEJM 352: 862-863, 884, Bird, T., 2005

Fatal Avian Influenza A (H5N1) in a Child Presenting with Diarrhea Followed by Coma
NEJM 352:686-691, de Jong,M.D., et al, 2005

Unusual Variants of Alexander's Disease
Ann Neurol 57:327-338, van der Knaap,M.S., et al, 2005

Brain Magnetic Resonance Imaging in Patients with Cowden Syndrome
Medicine 84:129-136, Lok,C.,et al, 2005

Clinicopath Conf, Human Granulocytic Ehrlichiosis
NEJM 352:1358-1364, Case 10-2005, 2005

Psychosocial Impact of Screening for Intracranial Aneurysms in Relatives with Familial Subarachnoid Hemorrhage
Stroke 36:836-840, Wermer,M.J.H.,et al, 2005

The Clinical and Genetic Spectrum of Spinocerebellar Ataxia 14
Neurol 64:1258-1260, Chen,D-H.,et al, 2005

Value of Gradient-Echo Magnetic REsonance Imaging in the Diagnosis of Familial Cerebral Cavernous Malformation
Arch Neurol 62:653-658, Lehnhardt,F-G.,et al, 2005

Autonomic Peripheral Neuropathy
Lancet 365:1259-1270, Freeman,R., 2005

Clinicopath Conf, Neurofibromatosis Type 1, with Multiple Spinal Neurofibromas
NEJM 352:1800-1808, Case 13-2005, 2005

The Genetic Causes of Basal Ganglia Calcification, Dementia, and Bone Cysts
Neurol 64:1502-1507, Klunemann,H.H.,et al, 2005

Pallidal Stimulation Improves Pantothenate Kinase-Associated Neurodegeneration
Ann Neurol 57:738-741,613, Castelnau,P.,et al, 2005

Brain Magnetic Resonance Imaging Findings in Patients with Mitochondrial Cytopathies
Arch Neurol 62:737-742, Barragan-Campos,H.M.,et al, 2005

Malignant Hyperthermia, Update on Susceptibility Testing
JAMA 293:2918-2924,2958, Litman,R.S.&Rosenberg,H., 2005

Phaeochromocytoma
Lancet 366:665-675, Lenders,J.W.M.,et al, 2005

Underappreciated Statin-Induced Myopathic Weakness Causes Disability
Neurorehabil Neural Repair 19:259-263, Dobkin,B.H., 2005

Spectrum of Mutations in Biopsy-Proven CADASIL: Implications for Diagnostic Strategies
Arch Neurol 62:1091-1094, Peters,N.,et al, 2005

Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
Neurol 64:1196-1203, Bosley, T.M.,et al, 2005

Amyloid Myopathy Presenting with Distal Atrophic Weakness
Muscle Nerve 29:605-609, Smestad, C.,et al, 2004

Hyperhomocysteinemia, Low Folate and Vitamin B12 Concentrations, and Methylene Tetrahydrofolate Reductase Mutation in Cerebral Venous Thrombosis
Stroke 35:1790-1794, Cantu,C.,et al, 2004

The Parkinsonian Phenotype of Spinocerebellar Ataxia Type 2
Arch Neurol 61:35-38, Lu,C.,et al, 2004

Gene Transfer for Neurologic Disease
Neurol 63:2225-2232, Mendell,J.R. &Miller,A., 2004

Neurologic Manifestations in Primary Sjogren Syndrome: A Study of 82 Patients
Medicine 83:280-291, Delalande,S.,et al, 2004

Clinical and Molecular Findings in Patients with Giant Axonal Neuropathy (GAN)
Neurol 62:13-16, Bruno,C.,et al, 2004

Infantile Bilateral Striatal Necrosis Maps to Chromosome 19q
Neurol 62:87-90, Basel-Vanagaite,L.,et al, 2004

The Neurological Complications of Bariatric Surgery
Arch Neurol 61:1185-1189, Berger,J.R., 2004

Neurological Sequelae in Twins Born After Assisted Conception: Controlled National Cohort Study
BMJ 329:311-314, Pinborg,A.,et al, 2004

Pathogenetic Mechanisms of Parkin in Parkinson's Disease
Lancet 364:722-724, Hattori,N. &Mizuno,Y., 2004

Bilateral Extraocular Muscle Atrophy in Myotonic Dystrophy Type 1
Neurol 63:759-760, Yamashita,T.,et al, 2004

Neuromuscular Disorders in Severe Acute Respiratory Syndrome
Arch Neurol 61:1669-1673,1647, Tsai,L.-K.,et al, 2004

The Occurence of Guillain-Barre Syndrome Within Families
Neurol 63:1747-1750, Geleijns,K.,et al, 2004

Natural History of Nonketotic Hyperglycinemia in 65 Patients
Neurol 63:1847-1853, Hoover-Fong,J.E.,et al, 2004

Incidence of Hospitalized Rhabdomyloysis in Patients Treated With Lipid-Lowering Drugs
JAMA 292:2585-2590, Graham,D.J.,et al, 2004

Primary Respiratory Failure in Inclusion Body Myositis
Neurol 63:2191-2192, Voermans,N.C.,et al, 2004

Charcot-Marie-Tooth Disease:Extensive Cranial Nerve Involvement on CT and MR Imaging
AJNR 25:494-497, Aho,T.R.,et al, 2004

Practice Parameter:Diagnostic Assessment of the Child with Cerebral Palsy
Neurol 62:851-863, Ashwal,S.,et al, 2004

Developmental Dyslexia
Lancet 363:1451-60, Demonet,J-F.,et al, 2004

Aromatic L-Amino Acid Decarboxylase Deficiency
Neurol 62:1058-1065, Pons,R.,et al, 2004

Intravenous Immunoglobulin in Autoimmune Neuromuscular Diseases
JAMA 291:2367-2375, Dalakas,M.C., 2004

Recurrent Meningitis of Unknown Aetiology
Lancet 363:1772, Ellerin,T.B.,et al, 2004

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