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abdominal distention

acetylcholine receptor antibody

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

acute intermittant porphyria

adrenoleukodystrophy

adverse drug reaction

agenesis of corpus callosum

Aicardi-Goutieres syndrome

airway obstruction

alpha glucosidase

alpha-fetoprotein

alternating hemiplegia

alternating hemiplegia of childhood

alveolar hypoventilation

amaurosis fugax, unilateral vs.bilateral

aminoacidopathies

aminoacylase 1 deficiency

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

aneurysm, aortic arch

Angelman syndrome

ankle, swelling of

anterior horn cell disease

antiviral agents

aortic arch stenosis

aortic arch study

apraxia of eye movements

aromatic amino acid decarboxylase deficiency

arrhythmia, cardiac

arterial dissection, aorta

arteritis, temporal

arthrogryposis multiplex

aspartate aminotransferase

ataxia telangiectasia

ataxia, cerebellar

ataxia, progressive

ataxia, truncal

athetosis, infant

auditory and vestibular pathways

autoimmune disease

autonomic dysfunction

axonal degeneration

B 12 deficiency

B 12 deficiency, infants

Babinski sign in new born

bacterial infection

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavior, combative

behavioral disorder

biologic markers

biopterin deficiency

biotin deficiency

biotin deficiency, acquired

biotin deficiency, juvenile form

biotinidase deficiency

blindness, sudden

bone density, increased

bone marrow biopsy

bone marrow transplantation

botulinum toxin

botulism antitoxin

botulism immune globulin

botulism, infant

brainstem, atrophy

brainstem, lesion of

breech delivery

Brown-Vialetto-Van Laere syndrome

brucellosis, nervous system involvement with

bulbar palsy, childhood

calcification, intracranial

Canavan's disease

carcinoembryonic antigen

carcinoma of breast

cardiac surgery, hypothermia and circulatory arrest for

cardiac surgery, neurologic complications with

carnitine deficiency

carnitine deficiency myopathy

CAT scan, abnormal

CAT scan, angiography

CAT scan, chest

CAT scan, emission, abnormal

cataracts, congenital

cauda equina, enhancement

caudate nucleus, atrophy

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

celiac disease, childhood

central core disease

central hypoventilation, congenital

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hypoplasia

cerebellar vermis

cerebral cortical atrophy

cerebral embolism

cerebral infarction

cerebral palsy, associated problems with

cerebral vasculature

cerebral venous thrombosis

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, glycine

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, infancy and childhood

cerebrovascular accident, intrauterine

cerebrovascular accident, neonatal

cerebrovascular accident, postpartum

ceruloplasmin, serum

cervical spine injury

chelation therapy

cherry red spot

chest x-ray, abnormal

chilbran skin lesions

chorea, Sydenham's

chorea, Sydenham's, recurrent

chorea, treatment of

choreoathetosis

chorioamnionitis

chorioretinitis

chromosomal abnormality

chronic progressive external ophthalmoplegia

cirrhosis, infancy

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cobalamin C deficiency

Coffin-Siris syndrome

cognitive delay

cogwheel rigidty

cold hands sign

cold intolerance

collagen vascular disease

conduction block

congenital heart disease

congenital heart disease, CNS complications with

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital myopathy

congenital myopathy, inflammatory

congestive heart failure

contactin associated protein like 2 antibodies

contractures, joint

conversion reaction

cornea, abnormal

cornea, opacification in infancy-causes of

cornea, opacity of

corpus callosum

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cranial nerve enhancement

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

crying, pathologic

cultured skin fibroblasts

cyst, parenchymal

cytochrome c oxidase

cytochrome c oxidase, deficiency

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

Dandy Walker malformation

dantrolene sodium

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

delayed dentition

delayed muscle relaxation

delivery, complicated

dementia, childhood

dementia, rapidly progressive

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

descending paralysis

developmental abnormality of brain

developmental disability

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

differential diagnosis

digits, abnormal

diphtheria-tetanus-pertussis immunization

disability, neurological

dislocated hip, congenital

distal muscle atrophy

distal muscle weakness

dropped head syndrome

dural sinus thrombosis

dysdiadochokinesia

dysferlinopathy

dysostosis multiplex

dystonia, children

eating disorder

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electron microscopy

embolism, paradoxical

emergencies, neurologic

emotional lability

encephalomyelitis

encephalopathy, acute

encephalopathy, anoxic

encephalopathy, neonatal

enzyme treatment

epidemiology of neurology

epileptic encephalopathy

evoked potentials

executive dysfunction

exome sequencing

eye movement, disorders of

facial anomalies

facial appearance, abnormal

facial expression abnormality

facial nerve palsy, bilateral

facial weakness

facial weakness, bilateral

failure to thrive

FARS2 deficiency

fatty acid, elevated plasma content

feeding disorder

fetal alcohol syndrome

fetal movements, reduced

fine motor function, impaired

fingernails, abnormal

fingernails, hypoplastic

food-borne infection

Friedreich's ataxia

fundus, abnormality of

gag reflex, depressed

gammaglobulin therapy, intravenous

gangliosidosis GM1

gangliosidosis GM2

gastrocnemius muscle weakness

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genital hypoplasia

globus pallidus, hemorrhage

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

GLUT1 deficiency syndrome

glutamic acid decarboxylase, antibody

gluten-free diet

glycogen storage disease

Gowers maneuver

growth hormone deficiency

growth retardation

Guillain Barre syndrome

head circumference

headache, bifrontal

headache, positional

health insurance

hemorrhagic diathesis

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

hexosaminidase-A

high arched feet

Hirschprung's disease

histochemistry of muscle

Horner's syndrome

Horner's syndrome, bilateral

Horner's syndrome, congenital

Hunter's syndrome

Huntington's chorea

Huntington's disease, children

hydrocephalus, communicating

hydrocephalus, congenital

hydrocephalus, exvacuo

hydroxyglutaric aciduria

hyperbilirubinemia

hyperglycinemia

hyperhomocysteinemia

hyperpyrexia, CNS disorder causing

hypertrophic cardiomyopathy

hypogammaglobulinemia

hypoglycorrhachia

hypomelanosis of Ito

hypomyelination

hypopigmentation of skin

hypotonia, causes of

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

immunization, neurologic complications with

immunodeficiency

immunomodulation

immunosuppression

immunosuppressive agents

inability to stand on tiptoes

inappropriate antidiuretic(A.D.H.)hormone

inborn errors of metabolism

inclusion bodies

inclusion bodies, intracytopasmic

infant, evaluation of

infantile hemiplegia

infantile neuronal degeneration

infection, recurrent

intellectual deficit

intellectual deterioration

interferon alpha

intestinal biopsy

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

Isaacs syndrome

islet cell tumor

Jakob-Creutzfeldt disease

joint hypermobility

keratoconjunctivitis

kyphoscoliosis, neurologic causes of

lactic acidemia

leg spasms, painful

leg weakness, bilateral

Leigh's disease

lens, dislocation of

leukoencephalopathy

leukoencephalopathy, differential diagnosis

lid closure, weakness of

lipid storage disorder of CNS

listeria monocytogenes

liver function enzymes

Lowe's syndrome

lumbar puncture

lymphadenopathy

lysosomal storage disease

lysosomes, abnoral

malformation, CNS, congenital

malignant hyperpyrexia

mediastinum, mass of

memory, impairment of

meningitis, carcinomatous

meningitis, CSF cell count-normal

mental retardation

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

methylene tetrahydrofolate reductase

methylenetetrahydrofolate reductase deficiency

methylmalonic acidemia

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine, seizures in

mitochondrial disease

mitral valve prolapse

molecular genetics

Morvan's fibrillary chorea

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI, angiography

MRI, contrast enhanced

MRI, diffusion weighted

MRI, high signal foci on

MRI, hypointense signal foci on

MRI, spinal cord

MRI, susceptibility weighted

mucopolysaccharidoses

mucopolysacchariduria

multicore myopathy

multiminicore disease

multiple sclerosis

multiple sclerosis, diet in

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, progressive

muscle atrophy, static

muscle diseases, characteristics of

muscle stiffness

muscle tenderness

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscle-eye-brain disease

muscular dystrophy

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, LAMA2

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, neonatal

myasthenic syndrome

myasthenic syndrome, treatment of

myoclonic jerks

myopathy, centronuclear

myopathy, mitochondrial

myopathy, necrotizing

myotonia congenita

myotonia dystrophica

nasal bridge, wide

nausea and vomiting

neonatal infection, viral

neonatal intensive care unit

neonatal screening, genetic neurologic disorders

nerve conduction studies

nerve conduction studies, motor

nerve root enhancement

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neurocutaneous disease

neuroendocrinology

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic evaluation

neurologic examination

neurologic signs

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuromyotonia and axonal neuropathy

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuroophthalmology

neuropathology, brain

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, peripheral

neurophysiology

neurotoxicity, acute

neurotransmitter

newborn, evaluation of

next-generation sequencing

Niemann-Pick disease

Noonan Syndrome

nystagmus, monocular

nystagmus, periodic

obstetric neurologic injuries

ocular motility, disorders of

ocular myopathy

oculogyric crisis

old age, neurology of

ophthalmoplegia

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

optic atrophy, infants

optic nerve, hypoplasia of

optic neuropathy

optic neuropathy, ischemic

optic neuropathy, ischemic, anterior

palmomental response

paraparesis, familial spastic

paraparesis, spastic

paraspinal muscle weakness

parenteral alimentation

Parkinson disease

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

patient information and support

pectus excavatum

pediatric neurology

periventricular leukomalacia

peroxisomal disease

personality change

pertussis immunization

phenylketonuria, variant form of

physical therapy

placenta, infection of

placenta, thrombosis of

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, neurologic problems with

poliomyelitis vaccine

polycystic kidneys

polymerase chain reaction

polymyalgia rheumatica

polymyositis, infantile

polyneuropathy, chronic inflammatory demyelinating

Pompe's disease of glycogen storage

pons, lesion of

pontocerebellar atrophy

postoperative neurologic complications

postural abnormality

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

progressive neurologic disorder

psychiatric problems in neurologic disorders

psychomotor retardation

ptosis, bilateral

pulmonary stenosis

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriparesis, acute

radiation hypersensitivity

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

Refsum's disease

remote effect of cancer on the nervous system

renal tubular acidosis

repetitive nerve stimulation

respirations in CNS disease

respiratory arrest

respiratory failure

respiratory tract infection

retinal degeneration

retinal dysplasia

Rett's syndrome

rheumatic fever

riboflavin transporter deficiency

rigid spine syndrome

rippling muscle disease

risus sardonicus

rubella vaccine

saccadic eye movements, abnormal

Schmidt syndrome

scoliosis, neurologic association with

sedimentation rate

sedimentation rate, elevated

segmental demyelination

seizure, children

seizure, injury following

seizure, neonatal

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

serum alanine aminotransferase

shoulder, pain in

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep pathology and physiology

small for dates infant, problems in

sodium valproate

sodium valproate, toxicity

spastic diplegia

speech disorder

speech disorder, childhood

speech, delayed development of

spinal cord, enlargement

spinal cord, injury of

spinal cord, injury, New Born

spinal cord, intramedullary cyst of

spinal cord, transection

spinal muscular atrophy

spinal muscular atrophy, classification

spinocerebellar ataxia

spongy degeneration of brain

standing difficulty

startle reaction

status epilepticus

stereotyped behavior

steroid therapy, CNS treatment and complications with

stiff limb syndrome

stiff man syndrome

streptococcal infection

subdural effusion

sulfite oxidase deficiency

superior sagittal sinus thrombosis

sweating, abnormality of

symmetric brain lesions

syphilis, neurologic complications with

tandem gait, ataxic

Tay-Sachs disease

teeth, abnormal

teeth, number of in infants

temper tantrums

temporal artery, biopsy

temporal artery, tender

temporalis muscle wasting

tetrahydrobiopterin

thalamus, lesion of

thalamus, lesion of-bilateral

thiamine deficiency

thrombocytopenia

tone, muscle, increased

tongue, enlarged

tongue, fasciculations of

tongue, protrusion of

tongue, weakness

toxic encephalopathy

toxins, nervous system

toxoplasmosis, CNS

transient loss of muscle tone

transient neurologic deficit

transilumination of skull

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

trichopoliodystrophy

trinucleotide repeats

ultrasonography

ultrasonography, head

ultrasonography, head, fetus-neonate

urinalysis, abnormal

urinary incontinence

urine test for metabolic disorders

vaccination, neurologic complications with

vertigo, cervical

vertigo, treatment of

viral infection, CNS

vision, failure of in childhood

visual evoked response

visual impairment

visual tracking

vitamin deficiency

vitamin E deficiency

vomiting, recurrent

Walker-Warburg syndrome

walking, difficulty with

weakness, acute

weakness, congenital

weakness, generalized

weakness, infant

weakness, progressive

weakness, proximal

Werdnig-Hoffman disease

white matter disease

wide based gait

x-linked mental retardation

Showing articles 350 to 400 of 6177 << Previous Next >>

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

Cogan Syndrome
www.medlink.com, Feb, Ramachandran, T.S., 2010

Subacute sclerosing panencephalitis: An Update
Dev Med Child Neurol 52:901-907, Guitierrez, J.,et al, 2010

Case 38-2009: A 16-Year-Old Boy with Paroxysmal Headaches and Visual Changes
NEJM 361:2367-2378, Brass,S.,et al, 2009

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

Carbon Monoxide Poisoning
NEJM 360:1217-1225, Weaver,L.K., 2009

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

A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia
Neurol 72:1262-1276, DiMauro,S.,et al, 2009

Parkinsons Disease
Lancet 373:2055-2066, Lees,A.J.,et al, 2009

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

Woke Up Paralysed--Without Injury or Stroke
Lancet 371:870, Bawaskar,H.S. &Bawaskar,P.H., 2008

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

Voltage-Gated Potassium Channel Autoimmunity Mimicking Creutzfeldt-Jakob Disease
Arch Neurol 65:1341-1346, Geschwind,M.D.,et al, 2008

A Young Man with Rapidly Progressive Multifocal Disease Affecting the White matter
Pract Neurol 7:172-181, Hilton-Jones,D.,et al, 2007

Clinicopath Conf., Multifocal Motor Neuropathy With Conduction Block
NEJM 357: 2707-2715, Case 40-2007, 2007

A 46-Year-Old Woman With Severe Weakness Following Acute Respiratory Distress Syndrome
Neurol 68:1529-1535, Waclawik,A.J.,et al, 2007

Clinicopath Conf., Severe Microangiopathy of Diabetic Vasculopathy with Multiple Cerebral Infarcts
NEJM 357:164-173, Case Study 21-2007, 2007

Neurologic Complications of Gastric Bypass Surgery for Morbid Obesity
Neurol 68:1843-1850, Juhasz-Pocsine,K.,et al, 2007

Orthostatic Myoclonus: A Contributor to Gait Decline in Selected Elderly
Neurol 68:1826-1830, Glass,G.A.,et al, 2007

Clinicopath Conf., Left Atrial Myxoma with Systemic Embolization
NEJM 357:1137-1145, Case 28-2007, 2007

Whipples Disease
NEJM 356:55-66, Fenollar,F.,et al, 2007

Tiagabine-Induced Myoclonic Status Epilepticus in a Nonepileptic Patient
Neurol 68:310, Vollmar,C. &Noachtar,S., 2007

Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
Brain 130:2484-2493, Jen, J.C.,et al, 2007

Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
NEJM 355:831-839, Case 26-2006, 2006

West Nile Virus Neuroinvasive Disease
Ann Neurol 60:286-300, Davis,L.E.,et al, 2006

Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene
NEJM 354:2584-2592, Case 18-2006, 2006

Hanging Leg Syndrome: Combined Bilateral Femoral and Sciatic Neuropathies
Neurol 66:1124-1125, Scherer,K.,et al, 2006

Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006

Concomitant Chronic Inflammatory Demyelinating Polyneuropathy and Myasthenia Gravis Following Cytomegalovirus Infection
J Neurol Sci 240:103-106, Mori, M.,et al, 2006

The Clinical Spectrum of Neuralgic Amyotrophy in 246 cases
Brain 129:438-450, Alfen, N.V. & Baziel, G.M., 2006

Mitochondrial DNA Polymerase-y and Human Disease
Hum Mol Genet 15:R244-R252, Hudson, G.,et al, 2006

Initial DWI and ADC Imaging May Predict Outcome in Acute Disseminated Encephalomyelitis: Report of Two Cases of Brain Stem Encephalitis
JNNP 76:996-998, Axer,H.,et al, 2005

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

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

Cervical Radiculopathy
NEJM 353:392-399, Carette,S. &Fehlings,M.G., 2005

Acute Painful Neuropathy in Thallium Poisoning
Neurol 65:302-304, Kuo,H.-C.,et al, 2005

Dysphagia as the Sole Manisfestation of Myasthenia Gravis
JNNP 76:1297-1300, Llabrs,M.,et al, 2005

Clinicopath Conf, Prion Disease (Sporadic Creutzfeldt-Jakob Disease)
NEJM 353:1042-1050, Case 27-2005, 2005

The Serotonin Syndrome
NEMJ 352:1112-20, Boyer, E.W. & Shannon, M., 2005

Neurologic Manifestations in Welders with Pallidal MRI T1 Hyperintensity
Neurol 64:2033-2039,2001, Josephs,K.A.,et al, 2005

Clinicopath Conf,Encephalomyelitis Due to West Nile Virus and CLL, Case 22-2005
NEJM 353:287-295, Hollande,H.,et al, 2005

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

Mitoxantrone Treatment of Multiple Sclerosis
Neurol 63(Suppl 6):S28-S32, Cohen,B.A. &Mikol,D.D., 2004

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

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

Recent Developments in Thyroid Eye Disease
BMJ 329:385-390, Cawood,T.,et al, 2004

Clinicopath Conf, Multiple-System Atrophy
NEJM 351:912-921, Case 27-2004, 2004

Stiff-Person Syndrome
The Neurologist 10:131-137, Murinson,B.B., 2004

Penetrance of the Fragile X-Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population
JAMA 291:460-469, Jacquemont,S.,et al, 2004

Showing articles 350 to 400 of 6177 << Previous Next >>