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anticonvulsants, discontinuation in seizure-free epileptics
apraxia
asymptomatic
ataxia
behavioral disorder
bone pain
calcification, intracranial
CAT scan
CAT scan, abnormal
CAT scan, false negative
cerebral cortical atrophy
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
chromosome 8
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
color vision, impaired
coma
degenerative diseases of CNS
dementia
dementia, presenile
dementia, rapidly progressive
depression
diplopia
electroencephalogram
electroencephalogram, abnormalities of
encephalopathy
encephalopathy, progressive
familial
familial adult myoclonic epilepsy
Gaucher's disease
Gaucher's disease, adult onset
gaze palsy, supranuclear
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
hallucination
hallucination, visual
headache
hearing loss
hepatosplenomegaly
inclusion bodies
inclusion bodies, intracytopasmic
intellectual deficit
intellectual deterioration
juvenile myoclonus epilepsy
lactic acidemia
Lafora body
Lafora's disease
Leigh's disease
Leigh's disease, adult variety
lethargy
MELAS syndrome
mental retardation
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
MRI, abnormal
muscle biopsy
muscle weakness
muscle weakness, proximal
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myoclonic jerks
myoclonus
myoclonus, epilepsy
negative
neuroendocrinology
neurologic disease, diagnoses of
neuroophthalmology
neuropathology
neuropathology, brain
neuropsychiatry
normal
ophthalmoplegia
optic atrophy
optic atrophy, hereditary
paraparesis, spastic
PAS positive
PAS positive material in the brain
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychosis
ptosis
ragged-red fibers
review article
seizure
seizure, children
seizure, diagnosis of
seizure, familial
seizure, intractable
seizure, prognosis in adults
seizure, teenager
seizure, treatment of
short stature
skin, biopsy
sodium valproate
sphingolipodoses
strokelike episodes
treatment of neurologic disorder
upgaze, paralysis of
weakness
Showing articles 250 to 300 of 5884 << Previous Next >>

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

Occult Celiac Disease Presenting as Epilepsy and MRI Changes That Responded to Gluten-Free Diet
Neurol 68:533-534, Harper,E.,et al, 2007

Hemispherectomy for Intractable Epilepsy in Adults: The First Reported Series
Ann Neurol 61:372-376, McClelland,S. III &Maxwell,R.E., 2007

Wilson Disease: Description of 282 Patients Evaluated Over 3 Decades
Medicine 86:112-121, Taly,A.B., et al, 2007

The Clinical and Radiological Spectrum of Reversible Cerebral Vasoconstriction Syndrome. A Prospective Series of 67 Patients
Brain 130:3091-3101, Ducros, A.,et al, 2007

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

Adult Epilepsy
Lancet 367:1087-1100, Duncan,J.S.,et al, 2006

The First Seizure and Its Management in Adults and Children
BMJ 332:339-342, Pohlmann-Eden,B.,et al, 2006

Late-Onset Metachromatic Leukodystrophy: Genotype Strongly Influences Phenotype
Neurol 67:859-863, Rauschka,H.,et al, 2006

GAMT Deficiency: Features, Treatment, and Outcome in an Inborn Error of Creatine Synthesis
Neurol 67:480-484, Mercimek-Mahmutoglu,S.,et al, 2006

First Seizure Presentation:Do Multiple Seizures Within 24 Hours Predict Recurrence?
Neurol 67:1047-1049,927, Kho,L.K.,et al, 2006

The Tuberous Sclerosis Complex
NEJM 355:1345-1356, Crino,P.B.,et al, 2006

Prevalence of Fabry Disease in Patients with Cryptogenic Stroke: A Prospective Study
Lancet 366:1794-1796,1754, Rolfs,A.,et al, 2006

Community-Acquired Bacterial Meningitis in Adults
NEJM 354:44-53, van de Beek,D.,et al, 2006

Glycogen-Storage Disease Type II
eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006

Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
Brain 129:1674-1684, Horvath, R.,et al, 2006

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

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

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

Thrombosis of the Cerebral VEins and Sinuses
NEJM 352:1791-1798, Stam,J., 2005

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

New OnsetGeriatric Epilepsy, A Randomized Study of Gabapentin, Lamotrigine, and Carbamazepine
Neurol 64:1868-1873,1834, Rowan,A.J.,et al, 2005

Four-Year Outcome after Early Withdrawal of Antiepileptic Drugs in Childhood Epilepsy
Neurol 64:2136-2138, Geerts,A.T.,et al, 2005

The Frequency of Intractable Seizures After Stopping AEDs in Seizure-Free Children With Epilepsy
Neurol 64:973-975, Camfield,P & Camfield,C., 2005

Adrenoleukodystrophy
JAMA 294:3131-3134, Moser,H.W.,et al, 2005

Late-Onset Seizures as a Predictor of Subsequent Stroke
Lancet 363:1184-1186,1175, Cleary,P.,et al, 2004

Seizure Outcomes After Stereotactic Radiosurgery for Cerebral Arteriovenous Malformations
Neurol 63:683-687, Schauble,B.,et al, 2004

Early and Late Seizures After Cryptogenic Ischemic Stroke in Young Adults
Neurol 60:400-404,365, Lamy,C.,et al, 2003

Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
Neurol 60:1413-1417, Pearl,P.L.,et al, 2003

Autosomal Dominant Acute Necrotizing Encephalopathy
Neurol 61:226-230, Neilson,D.E.,et al, 2003

Seizure Frequency is Associated with Age at Menopause in Women with Epilepsy
Neurol 61:451-455, Harden,C.L.,et al, 2003

Seizure Remission and Antiepileptic Drug Discontinuation in Children with Tuberous Sclerosis Complex
Arch Neurol 60:1286-1289, Sparagana,S.P.,et al, 2003

Clinical Features and ATTCT Repeat Expansion in Spinocerebellar Ataxia Type 10
Arch Neurol 59:1285-1290, Grewal,R.P.,et al, 2002

Familial Temporal Lobe Epilepsy with Febrile Seizures
Neurol 58:1429-1433, Depondt,C.,et al, 2002

Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
NEJM 347:672-680, Case 27-2002, 2002

Discontinuing Antiepileptic Drugs in Patients who are Seizure Free on Monotherapy
JNNP 72:22-25,5, Specchio,L.M.,et al, 2002

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

Spinocerebellar Ataxia Type 10 is Rare in Populations Other Than Mexicans
Neurol 58:983-984, Matsuura,T.,et al, 2002

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

Glutamic Acid Decarboxylase Autoantibodies and Neurological Disorders
Neurol Sci 23:145-151, Vianello,M.,et al, 2002

Subacute Sclerosing Panencephalitis Clinical and Magnetic Resonance Imaging Evaluation of 36 Patients
J Child Neurol 17:25-29, Ozturk, A.,et al, 2002

Subacute Sclerosing Panencephalitis
Postgrad Med J 78:63-70, Garg, R.K.,et al, 2002

Phenylketonuria Presenting in Adulthood as Progressive Spastic Paraparesis With Dementia
JNNP 71:795-797, Kasim,S.,et al, 2001

Postictal Language Dysfunction in Complex Partial Seizures: Effect of Contralateral Ictal Spread
Neurol 56:1590-1592, Ficker,D.M.,et al, 2001

Fits and Strokes
Lancet 358:120, Sharma,P.,et al, 2001

Cerebral Sinovenous Thrombosis in Children
NEJM 345:417-423, DeVeber,G.,et al, 2001

Epilepsy
NEJM 344:1145-1151, Browne,T.R. & Holmes,G.L., 2001

Gluten Sensitivity in Sporadic and Hereditary Cerebellar Ataxia
Ann Neurol 49:540-543, Bushara,K.O.,et al, 2001

Is Patent Foramen Ovale a Family Trait?
Stroke 32:1563-1566, Arquizan,C.,et al, 2001

Niemann-Pick Disease Type C: Two Cases and an Update
Movement Disorders 15:1199-1203, Uc,E.Y.,et al, 2000



Showing articles 250 to 300 of 5884 << Previous Next >>