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Differential
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abdominal muscle paralysis
acetylcholine
acetylcholine in CNS
acid maltase deficiency
acid maltase deficiency, adult
acral sensory symptoms
acyl CoA dehydrogenase deficiency
adenosine deaminase deficiency
adrenoleukodystrophy
adrenomyeloneuropathy
advances in neurology
adverse drug reaction
agalsidase alfa
alopecia
alpha galactosidase A deficiency
alpha glucosidase
Alzheimer's disease
aminoacidopathies
aminoacidurias
aminoacylase 1 deficiency
ammonia
amniocentesis
anemia
anemia, hemolytic
aneurysm
angiokeratoma
angiotensin-converting enzyme
anorexia nervosa
anterior horn cell disease
anticonvulsants
anticonvulsants, untoward effects of
apraxia
apraxia of eye movements
aromatic amino acid decarboxylase deficiency
arthropathy
arthropathy, neuropathic
arylsulfatase A
aspartate aminotransferase
aspartocyclase
asymptomatic
ataxia
ataxia, cerebellar
athetosis
autism
autonomic dysfunction
Babinski sign
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
biotin deficiency
biotinidase deficiency
blindness
blood dyscrasias, neurologic findings with
bone marrow transplantation
brain atrophy
brain biopsy
brain purpura
brainstem
brainstem, infarction of
brainstem, lesion of
burning feet
burning feet, differential diagnosis of
burning hands
burning paresthesia
calcification, intracranial
calf hypertrophy
Canavan's disease
carbamyl phosphate synthetase-I deficiency
carbidopa
carbonic anhydrase II deficiency
cardiomegaly
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataracts
caudate nucleus, lesion of
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hemorrhage
cerebellar infarction
cerebellar lesion
cerebellar vermis
cerebral cortical atrophy
cerebral infarction, hemorrhagic
cerebral ischemia
cerebral palsy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, glycine
cerebrospinal fluid, protein of
cerebrospinal fluid, proteincytologic dissociation
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, cryptogenic
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cerebrovascular disease
cherry red spot
cherry red spot-myoclonus syndrome
children
cholesterol
choline acetyltransferase
choline chloride
choreoathetosis
chromosomal abnormality
chromosome 20
chromosome 6
cirrhosis
cirrhosis, infancy
Clinical Pathologic Conference(C.P.C.)
codfish vertebrae
coenzyme Q10 deficiency
coma
compression fracture
confusion
congestive heart failure
conjunctivitis
consanguinity
contractures, joint
coprolalia
cornea, opacification in infancy-causes of
cornea, opacity of
corneal dystrophy
cranial nerve enlargement
cranial nerve palsies
creatine phosphokinase(CPK)elevated
creatinine, elevated
cry, abnormal
crying
cultured skin fibroblasts
cystinuria
cytochrome c oxidase
cytochrome c oxidase, deficiency
deep gray nuclei
deficiency of ADA2
degenerative diseases of CNS
dementia
dementia, presenile
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
developmental milestones, loss of
developmental retardation
diaphragmatic paralysis
diet
distal muscle atrophy
distal muscle weakness
dopa responsive dystonia
dopamine
drooling
dropped head syndrome
dysarthria
dysmorphic
dysostosis multiplex
dysphagia
dyspnea
dyspraxia
dystonia
dystonia, children
dystonic reaction, acute
echolalia
efficacy
electrocardiogram, abnormal
electromyogram
electron microscopy
emergencies, neurologic
encephalopathy
encephalopathy, neonatal
encephalopathy, progressive
enzyme treatment
enzyme, defect
enzyme, muscle disease
epidemiology of neurology
exercise
exercise intolerance
eye movement, disorders of
Fabry's disease
facial anomalies
facial appearance, abnormal
facial hypoplasia
facial weakness
failure to thrive
familial
Farber's disease
fatigue
fatty acid, elevated plasma content
feeding disorder
fever
floppy infant
flow study, carotid artery
fornix, lesion of
fracture, pathologic
frontal bossing
frontal lobe, behavior with disease of
frontal lobe, lesion of
fucosidosis
fundus, abnormality of
gait disorder
galactocerebrosidase
galactorrhea
galactosemia
galactosidase
gangliosidosis GM1
gangliosidosis GM2
gangliosidosis GM2-AB variant
Gaucher's disease
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
Gilles de la Tourette syndrome
globoid cells
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glucocerebrosidase
glutamate dehydrogenase deficiency
glutaric acidemia
glutaric aciduria
glycine
glycogen debranching enzyme deficiency
glycogen storage disease
glycoprotein
growth retardation
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
hallucination
hallucination, auditory
hand pain
hands, fisted
head lag
headache
headache, progressive
headache, thunderclap
headbanging
hearing loss
heart murmur
hematopoietic tissue, extramedullary
hemianopia, homonymous
hepatic failure
hepatomegaly
hepatosplenomegaly
heralding manifestation
herniated disc, thoracic
hexosaminidase-A
hexosaminidase-A and B
histochemistry
histochemistry of muscle
homocystinuria
Hurler's syndrome
hydrocephalus
hydrocephalus, normal pressure
hydroxytryptophan L-5(L-5 HTP)
hyperammonemic encephalopathy
hyperbilirubinemia
hyperglycinemia
hyperhomocysteinemia
hyperreflexia
hypertension
hypertonia
hypogammaglobulinemia
hypoglycemia
hypomyelination
hyponatremia
hyporeflexia
hypothermia
hypotonia
hypotonia, infants
ileus, paralytic
imbalance
immunosuppression
inborn errors of metabolism
inborn errors of metabolism, screening
inclusion bodies, intracytopasmic
infection
infection, recurrent
insulin resistance
intellectual deficit
intellectual deterioration
intelligence quotient
internal capsule
internuclear ophthalmoplegia
internuclear ophthalmoplegia, unilateral
intrauterine
iron, brain
irritability
ischemic exercise test
jaundice
Jewish
Kearns-Sayre syndrome
Korsakoff's psychosis
Krabbe's disease
kyphoscoliosis, neurologic causes of
lactate
lacunar infarction
L-dopa
Leber's hereditary optic neuropathy
leg weakness, bilateral
Leigh's disease
Leigh's disease, adult variety
lens, dislocation of
lens, ectopic
Lesch-Nyhan syndrome
lethargy
leukocyte enzyme abnormality
leukodystrophy
life expectancy
lipid storage disorder of CNS
livedo reticularis
liver disease
lysosomal storage disease
lysosomes, abnoral
macrocephaly
marihuana
McArdle's disease
meconium staining
melanomatosis, primary malignant
MELAS syndrome
memory, defect of recent
mental retardation
mental status, abnormal
MERRF syndrome
mesial temporal lobe
metabolic acidosis
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
microspherophakia
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, demyelinating disease
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, eye of tiger sign
MRI, hypointense signal foci on
MRI, paramagnetic effect
MRI, vessel wall
MRI, vessel wall enhancement
MRS
mucopolysaccharidoses
multiple sclerosis, differential diagnosis of
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
muscle pain
muscle phosphofructokinase deficiency
muscle phosphorylase deficiency
muscle spasm
muscle stiffness
muscle wasting, diffuse
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, neonatal screening
myelopathy
myoclonic jerks
myoclonus
myoglobinuria
myopathy
myopathy, distal, vacuolar
myopathy, metabolic
myopathy, mitochondrial
myopathy, necrotizing
myopathy, vacuolar
myopia
nausea and vomiting
neck weakness
neonatal screening, genetic neurologic disorders
nerve biopsy
nerve conduction studies
neuraminidase deficiency
neurologic disease, diagnoses of
neurologic examination
neurologic signs
neuropathology
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neuropathy, painful
neuropathy, peripheral
neurotransmitter
nystagmus
oculogyric crisis
ophthalmoplegia
ophthalmoplegia, progressive external
opisthotonus
optic atrophy
optic chiasm, enlarged
optic nerve
optic nerve, enlarged
ornithine transcarbamylase deficiency
orthopnea
osteoporosis
pain
palilalia
PANK2 mutation
paraparesis, spastic
paraspinal muscle
paraspinal muscle weakness
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
PAS positive
PAS positive material in the brain
pectus excavatum
pediatric neurology
peroxisomal disease
peroxisomes
phenylketonuria
phosphorylase b kinase deficiency
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
polymerase chain reaction
polyneuropathy
Pompe's disease of glycogen storage
porphyria
postpartum
postpartum coma
postural abnormality
precipitating factors
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prognathism
prognosis
progressive neurologic disorder
prolactin, elevated
proteinuria
pseudomyotonia
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychomotor retardation
psychosis
putamen, lesion of
pyramidal tract
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
pyruvate-kinase deficiency anemia
rash
recurrent
renal failure
renal tubular acidosis
respiratory failure
respiratory tract infection
retinal degeneration
retinopathy
reversible cerebral vasoconstrictive syndromes
reversible neurologic disorder
review article
Reye's syndrome
rigidity
Sandhoff's disease
Sanfilippo syndrome
schizophrenia
scoliosis
scoliosis, neurologic association with
screaming
screening
second wind phenomena
seizure
seizure, children
seizure, neonatal
seizure, psychomotor-temporal lobe
self-mutilation
semialdehyde dehydrogenase deficiency
short stature
skin, biopsy
skin, lesions in neurologic disorders
small vessel disease
sodium valproate
sodium valproate, toxicity
somnolence
spasticity
speech disorder
speech disorder, childhood
sphingolipodoses
spinal cord
spinal cord, compression of
spinal cord, lesion of
spinocerebellar ataxia type 1
spinocerebellar degeneration
splenomegaly
spongy degeneration of brain
startle reaction
stem cell transplantation
strabismus
striatum, lesion of
stuporous
stuttering
subarachnoid hemorrhage
subarachnoid hemorrhage, cerebral convexity
substantia nigra
suck, poor
symmetric brain lesions
systemic illness
Tay-Sachs disease
temporal lobe, lesion
term infant
tetrahydrobiopterin
thalamus, lesion of
thalamus, lesion of-bilateral
thiamine
tinnitus
tone, muscle, increased
tongue, enlarged
tongue, weakness
transketolase
treatment of neurologic disorder
tyrosine
tyrosine hydroxylase deficiency
tyrosinemia
umbilical-cord blood transplantation
urea
urea-cycle enzymopathies
uremia
urinary incontinence
urine test for metabolic disorders
urine, dark
vasculitides
vasculopathy
vertebral-basilar insufficiency
vertigo
vertigo, episodic
visual loss
vital capacity
vitamin deficiency
weakness
weakness, progressive
weakness, proximal
Wernicke's encephalopathy
wheelchair
white matter disease
winging of scapula
Showing articles 250 to 300 of 524 << Previous Next >>

Polymyositis and Dermatomyositis
Lancet 362:971-982, Dalakas,M.C.&Hohlfeld,R., 2003

Should I Start All My Ischaemic Stroke and TIA Patients on a Statin, an ACE Inhibitor, a Diuretic, and Aspirin Today?
JNNP 74:1461-1464, Sandercock,P.A.G., 2003

Stroke Prevention with the Oral Direct Thrombin Inhibitor Ximelagatran Compared with Warfarin in Patients with Non-Valvular Atrial Fibrillation (SPORTIF III): Randomised Controlled Trial
Lancet 362:1691-1698,1686, Executive Steering Committee on Behalf of the SPOR, 2003

Treatment of Wilson Disease With Ammonium Tetrathiomolybdate, III. Initial Therapy in a Total of 55 Neurologically Affected Patients and Follow-up With Zinc Therapy
Arch Neurol 60:379-385, Brewer,G.J.,et al, 2003

Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases
Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003

Blood Pressure-Lowering for Secondary Prevention of Stroke: ACE Inhibition Is Not the Key
Stroke 34:1334-1335,1335, Bath,P., 2003

Blood Pressure--Lowering for Secondary Prevention of Stroke: ACE Inhibition Is the Key
Stroke 34:1333-1334,1334, Anderson,C., 2003

Hemi-orolingual Angioedema and ACE Inhibition After Alteplase Treatment of Stroke
Neurol 60:1525-1527,1403, Hill,M.D.,et al, 2003

Acute Mycoplasma Pneumoniae Infection Presenting as Cholestatic Hepatitis
J Clin Microbiol 41:514-515, Grullich, C.,et al, 2003

Disease-Modifying Therapy in Multiple Sclerosis: Strategies for Optimizing Management
The Neurologist 8:227-236, Frohman,E.,et al, 2002

The PROGRESS Trial: Preventing Strokes by Lowering Blood Pressure in Patients With Cerebral Ischemia
Stroke 33:319-320, van Gijn,J., 2002

Stroke Prevention Therapy Beyond Antithrombotics: Unifying Mechanisms in Ischemic Stroke Pathogenesis and Implications for Therapy
Stroke 33:862-875, Gorelick,P.B., 2002

The Neurological Masquerade of Intravascular Lymphomatosis
Arch Neurol 59:439-443, Beristain,X.&Azzarelli,B., 2002

Patients with Multiple Sclerosis and Risk of Type 1 Diabetes Mellitus in Sardinia,Italy: A Cohort Study
Lancet 359:1461-1465,1450, Marrosu,M.G.,et al, 2002

Cholinergic Vesicular Transporters in Progressive Supranuclesar Palsy
Neurol 58:1013-1018,997, Suzuki,M.,et al, 2002

Use of Ramipril in Preventing Stroke: Double Blind Randomised Trial
BMJ 324:699-702,687, Bosch,J.,et al, 2002

Giant-cell Arteritis
NEJM 347:272-278, Case 23-2002, 2002

Blood Pressure Control in Stroke Patients
Neurol 59:23-25, Messerli,F.H.,et al, 2002

Treatment of Women with Epilepsy
Seminars in Neurology 22:289-297, Pack.A.M.&Morrell,M.J., 2002

Neurological Complications of Coeliac Disease
Postgrad Med J 78:393-398, Tengah, D.S.N.A.,et al, 2002

Acute Disseminated Encephalomyelitis (ADEM) Due to Mycoplasma Pneumoniae Infection in an Adolescent
Infection 29:240-242, Riedel, K.,et al, 2001

Acute Hepatic Encephalopathy with Diffuse Cortical Lesions
Neuroradiology 43:551-554, Arnold, S.M.,et al, 2001

Neuro-Ophthalmic Manifestations of Sarcoidosis. Clincal Spectrum, Evaluation and Management
J Neuroophthalmol 21:132-137, Frohman,L.P,et al, 2001

Pituitary Lymphoma Presenting as Fever of Unknown Origin
J Clin Endocrinol Metab 86:1470-1476, Landman, R.E.,et al, 2001

Postpartum Blindness
Lancet 358:1338, Jurgensen,J.S.,et al, 2001

Long-term Treatment of Acromegaly With Pegvisomant, a Growth Hormone Receptor Antagonist
Lancet 358:1754-1759,1743, van der Lely,A.J.,et al, 2001

Clinicopath Conf,Systemic Sclerosis with Scleroderma Renal Crisis
NEJM 345:596-605, Case 26-2001, 2001

Quantitation of 14-3-3 and Neurol-Specific Enolase Proteins in CSF in Creutzfeldt-Jakob Disease
Neurol 57:728-730, Aksamit,A.L.,et al, 2001

Comtan (Entacapone) The Treatment of Parkinson's Disease, Questions & Answers
APDA Ed Suppl #15, Watts,R.L., 2001

Fomepizole for the Treatment of Methanol Poinsoning
NEJM 344:424-429, Brent,J.,et al, 2001

Enzyme Replacement Therapy in Fabry Disease
JAMA 285:2743-2749, Schiffmann,R.,et al, 2001

Fulminant Liver Failure During Interferon Beta Treatment of Multiple Sclerosis
Neurol 56:1416, Yoshida,E.M.,et al, 2001

Solving the Mysteries of Narcolepsy
Neurol 56:1616-1618, Silber,M.H. &Rye,D.B., 2001

Neurogene Therapy for the 21st Century
Arch Neurol 57:54, Brady,R.O., 2000

Tolcapone and Hepatotoxic Effects
Arch Neurol 57:263-267, Olanow,C.W.&Tasmar Advisory Panel, 2000

Interaction Between HLA-DR2 and Abnormal Brain MRI in Optic neuritis and Early MS
Neurol 54:1859-1861, Hauser,S.L.,et al, 2000

Adverse Effect of Anticonvulsants on Efficacy of Chemotherapy for Acute Lymphoblastic Leukaemia
Lancet 356:285-290, Relling,M.V. et al, 2000

Multiple Sclerosis
NEJM 343:938-952, Noseworthy,J.H. et al, 2000

Prevention of Ischaemic Stroke
BMJ 321:1455-1459, Gubitz,G. & Sandercock,P., 2000

Agranulocytosis Associated with Lamotrigine
BMJ 318:1179, DeCamargo,O.A.K., 1999

Muscle Pain after Exercise
Lancet 353:1062, Nielen,C.&Mazzone,P., 1999

Drug Interactions with Methadone
Presse Med 27:1381-1384, Schlatter,J.,et al, 1999

Multiple Sclerosis, Side Effects of Interferon Beta Therapy and Their Management
Neurol 53:1622-1627, Walther,E.U.&Hohlfeld,R., 1999

Behcet's Disease
NEJM 341:1284-1291, Sakane,T.,et al, 1999

Medical Complications in Long-Term Survivors with X-Linked Myotubular Myopathy
J Pediatr 134:206-214, Herman,G.E.,et al,, 1999

Lamotrigine-Associated Anticonvulsant Hypersentivitiy Syndrome
Neurol 51:1171-1175, Schlienger,R.G.,et al, 1998

Cerebral Sparganosis with Intracerebral Hemorrhage:A Case Report
Neurol 50:503-506, Jeong,S.-C.,et al, 1998

Postpartum Coma
Lancet 351:1700, McCormack,G.,et al, 1998

Loss of Vision in Gaucher's Disease and Its Reversal by Enzyme-Replacement Therapy
NEJM 338:1471-1472, vom Dahl,S.,et al, 1998

Tolcapone for Parkinson's Disease
The Medical Letter 40:60-61, , 1998



Showing articles 250 to 300 of 524 << Previous Next >>