Neudle.com: multiple sclerosis familial

Differential
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abdominal cramps

abdominal reflex, absent

acute disseminated encephalomyelitis

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

Alexanders disease, adult onset

aminoacidopathies

aminoacidurias

amnestic syndrome

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, prognosis

anatomy of

angiitis

angiitis, granulomatous of CNS

angiitis, isolated of CNS

attention deficit disorder with hyperactivity

autonomic dysfunction

Babinski sign

baclofen

basal ganglia, infarction

basal ganglia, lesion of

behavioral disorder

benign essential tremor

beta adrenergic blocker

bladder dysfunction

blink reflex

bone marrow transplantation

brain biopsy

brainstem

brainstem, infarction of

brainstem, lesion of

burning paresthesia

calcification, intracranial

Canavan's disease

CAT scan

CAT scan, abnormal

CAT scan, demyelinating disease

CAT scan, serial

catecholamine

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortical atrophy

cerebral infarction

cerebral infarction, small, deep

cerebral infarction, subcortical

cerebral ischemia

cerebral palsy

cerebral venous infarction

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cell count

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, immunoglobulins of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, multiple

cerebrovascular accident, nonvascular territory

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease, cardiovascular disease with

Charcot-Marie-Tooth

children

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

cognition

congenital malformation

congestive heart failure

corneal dystrophy

cortical blindness

cortical blindness, transient

degenerative diseases of CNS

dementia

dementia, cerebrovascular disease causing

dementia, presenile

dementia, subcortical

dementia, thalamic

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

differential diagnosis

dilantin

diplopia

disability, neurological

dopamine

drug induced neurologic disorders

dysarthria

dysarthria-clumsy hand syndrome

dysdiadochokinesia

dysphagia

dystonia

dystonia musculorum deformens

echocardiogram

echolalia

electrical sensation

electrocardiogram, abnormal

electroencephalogram, abnormalities of

encephalopathy, metabolic

facial weakness, bilateral

gamma amino butyric acid

gamma amino butyric acid-mimetic drug

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gilles de la Tourette syndrome

glioma

glutaric acidemia

granular osmiphilic material

hearing loss, bilateral

heavy metal intoxication

hemianopia

hemianopia, transient

hemiparesis

hemiparesis, transient

hemiplegia

hepatic encephalopathy

hepatic encephalopathy, treatment of

hepatolenticular degeneration(Wilson's disease)

human immunodeficiency virus type 1

human T-lymphotropic virus type I(HTLV-I)

hypoxic encephalopathy

iatrogenic neurologic disorders

imbalance

incoordination

intellectual deficit

intellectual deterioration

interferon

interferon beta 1-a

interferon beta 1-b

intrathecal antispasticity drugs

Leber's hereditary optic neuropathy

Leigh's disease

Leigh's disease, adult variety

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

Lhermitte's sign

lipid storage disorder of CNS

liver disease

Lorenzo's oil

low birth weight

magnetic susceptibility

malformation, CNS, congenital

maple syrup urine disease

MELAS syndrome

mental retardation

metabolic disorder, primary

metachromatic leukodystrophy

metronidazole

microhemorrhage, intracerebral

migraine

misdiagnosis

mitochondrial disease

MRI, CAT scan compared to

MRI, complications with

MRI, contrast enhanced

MRI, demyelinating disease

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, negative

MRI, paramagnetic effect

MRI, serial

MRI, spinal cord

MRI, T1 weighted high signal foci

MRI, volumetry

multiple sclerosis

multiple sclerosis, asymptomatic

multiple sclerosis, chronic progressive

multiple sclerosis, clinical patterns

multiple sclerosis, conjugal

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple sclerosis, etiology of

multiple sclerosis, familial

multiple sclerosis, linoleic acid in

multiple sclerosis, misdiagnosis

multiple sclerosis, parental transmission

multiple sclerosis, pathogenesis

multiple sclerosis, prognosis

multiple sclerosis, risk factors for

multiple sclerosis, spinal form

multiple sclerosis, treatment of

muscle biopsy

myelin basic protein gene

myelinolysis, extrapontine

myelitis

myelitis, longitudinal

myelitis, transverse

myelomalacia

myelopathy

myelopathy, chronic progressive

myocardial infarction

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neuromyelitis optica (Devic's disease)

neuromyelitis optica spectrum disorder

neuromyelitis optica, IgG

neuropathology

neuropathy

neuropathy, peripheral

obsessive-compulsive disorder

occipital lobe, infarction

occipital lobe, lesion of

old age, neurology of

optic atrophy

optic atrophy, bilateral

optic atrophy, hereditary

optic nerve, hypoplasia of

optic neuritis

optic neuritis, bilateral

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, hereditary

paraparesis, spastic, tropical

paraplegia

paratrigeminal syndrome

paresthesias

Parkinson disease

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

PAS positive

PAS positive material in the brain

Pelizaeus Merzbacher

periventricular leukomalacia

phenylketonuria

phenylketonuria, adult onset

pimozide

pleocytosis of cerebrospinal fluid

poison, neurologic problems with

polymerase chain reaction

pons, lesion of

posterior cerebral artery territory infarction

posterior leukoencephalopathy syndrome

premature infant

prevention of neurologic disorders

primary lateral sclerosis

psychiatric problems in neurologic disorders

pyramidal tract dysfunction

quadriparesis

quadriplegia

quality of life

radiation therapy, stereotactic

reversible neurologic disorder

sensorineural hearing loss

sick sinus syndrome

skin, biopsy

skin, lesions in neurologic disorders

smell

spasticity

spasticity, treatment of

speech disorder

speech, loss of

spinal cord

spinal cord, injury of

spinal cord, injury, management of

spinal cord, lesion of

spontaneous remission

steroid therapy, CNS treatment and complications with

stimulation, deep brain

symmetric brain lesions

systemic lupus erythematosus

tardive dyskinesia

taste

Tay-Sachs disease

temporal lobe, lesion, bilateral

thalamic tumors

thalamic tumors, bilateral

thalamotomy

thalamus

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

tongue, impaired movements of

top of the basilar syndrome

torticollis

transient ischemic attack

transient ischemic attack, recurrent

transient neurologic deficit

trauma

treatment of neurologic disorder

tremor

tremor, cerebellar

tremor, classification

tremor, differential diagnosis of

tremor, surgical treatment of

tremor, thalamic stimulation for suppression of

very long chain fatty acids

viral infection

viral infection, CNS

vision loss, sequential

visual acuity, decreased

visual evoked response

visual loss

visual loss, progressive

visual loss, sudden

visual loss, transient

walking, difficulty with

water channel antibodies

weakness

Wernicke's encephalopathy

white matter disease

workup

Showing articles 3400 to 3450 of 5493 << Previous Next >>

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

Botulinum Toxin is a Useful Treatment in Excessive Drooling of Saliva
JNNP 67:697, Bhatia,K.P.,et al, 1999

Neural-Tube Defects
NEJM 341:1509-1519,1485, Botto,L.D.,et al, 1999

Multiple Cerebral Infarctions Associated with Ovarian Hyperstimulation Syndrome
Neurol 53:225-227, Yoshii,F.,et al, 1999

MR Angiography and Surgery for Unruptured Familial Intracranial Aneurysms in Persons with a Family History of Cerebral Aneurysms
AJR 173:133-138, Brown,B.M.&Soldevilla,F., 1999

Seizure Control and Mortality in Epilepsy
Ann Neurol 46:45-50, Sperling,M.R.,et al, 1999

A Prospecitve Study of Preferences and Actual Treatment Choices in ALS
Neurol 53:278-283,248, Albert,S.M.,et al, 1999

Stereotactic Radiosurgical Pallidotomy and Thalamotomy with the Gamma Knife:MR Imaging Findings with Clinical Correlation-Preliminary Experience
Radiology 212:143-150, Friedman,D.P.,et al, 1999

Serial Magnetic Resonance Imaging of Cerebral Atrophy in Preclinical Alzheimer's Disease
Lancet 353:2125, Fox,N.C.,et al, 1999

Patients with Refractory Seizures
NEJM 340:1565-1570, Devinsky,O, 1999

Practice Advisory:The Use of Felbamate in the Treatment of Patients with Intractable Epilepsy, Report of the quality Standards Subcommittee of the AAN and the American Epilepsy Society
Neurol 52:1540-1545, French,J.,et al, 1999

Vagus Nerve Stimulation for Medication-Resistant Generalized Epilepsy
Neurol 52:1510-1512, Labar,D.,et al, 1999

Left Vagal nerve Stimulation in Children with Medically Refractory epilepsy
J Pediatr 134:563-566, 532, Murphy,J.V.&Pediatric VNS Study Group, 1999

Evaluation of Refractory epilepsy Treated with Vagus Nerve Stimulation for Up to 5 Years
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Vagal Nerve Stimulation in epileptic Encephalopathies
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Supratentorial Cavernous Haemangiomas and Epilepsy:A Review of the Literature and Case Series
JNNP 66:561-568, Moran,N.F.,et al, 1999

Intractable Epilepsy
Lancet 353:1238, Shuper,A.,et al, 1999

Disorientation and Vertebral Fractures
Lancet 353:1848, McConnaughey,D.,et al, 1999

Clinicopath Conf:Lymphoplasmocytic Lymphoma with Motor Neuronopathy,Waldenstrom's Macroglobulinemia
NEJM 340:1661-1669, , 1999

Multiple large and Small Cerebellar Infarcts
JNNP 66:739-745, Sanaple,S.&Bogousslavsky,J., 1999

Familial Paroxysmal Dystonic Choreoathetosis,Clinical Findings in a Large Japanese Family and Genetic Linkage to 2q
Arch Neurol 56:721-726, Matsuo,H.,et al, 1999

MR Imaging of Dejerine-Sottas Disease
AJNR 20:378-380, Make,D.D.,et al, 1999

Sjogren-Larsson Syndrome, Clinical and MRI/MRS Findings in FALDH-Deficient Patients
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Neurology and the Skin
JNNP 66:417-430, Hurko,O.&Provost,T.T., 1999

MR of CNS Sarcoidosis:Correlation of Imaging Features to Clinical Symptoms and Response to Treatment
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Atypical Form of Amyotrophic Lateral Sclerosis
JNNP 66:581-585, Sasaki,S.&Iwata,M., 1999

Practice Parameter:The Care of the Patient with Amyotrophic Lateral Sclerosis (An Evidence-Based Review), Report of the Quality Standards Subcommittee of the AAN
Neurol 52:1311-1323, Miller,R.G.,et al, 1999

Bilateral Thalamic Stimulation for the Treatment of Essential Tremor
Neurol 53:1447-1450, Pahwa,R.,et al, 1999

Neuropsychological and Quality of Life Outcome after Thalamic Stimulation for Essential Tremor
Neurol 53:1774-1780, Troster,A.I.,et al, 1999

Altered Brain Activation in Cognitively Intact Individuals at High Risk for Alzheimer's Disease
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Aneurysms in Relatives of Patients with Subarachnoid Hemorrhage,Frequency and Risk Factors
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MRI Detection of New Hemorrhages:Potential Marker of Progression in Cerebral Amyloid Angiopathy
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Antiplatelet Treatment Does Not Reduce the Severity of Subsequent Stroke
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Safety and Factors Related to Survival After Percutaneous Endoscopic Gastrostomy in ALS
Neurol 53:1123-1125, Chio,A.,et al, 1999

Neurologic Complications in Children with Enterovirus 71 Infection
NEJM 341:936-942, Huang,C-C.,et al, 1999

Brachial Amyotrophic Diplegia, A Slowly Progressive Motor Neuron Disorder
Neurol 53:1071-1076, Katz,J.S.,et al, 1999

Clinical and MRI Findings in Spinocerebellar Ataxia Type 5
Neurol 53:1355-1357, Stevanin,G.,et al, 1999

Risks and Benefits of Screening for Intracranial Aneurysms in First-Degree Relatives of Patients with Sporadic Subarachnoid Hemorrhage
NEJM 341:1344-1350, The Magnetic Resonance Angiography in Relatives of, 1999

Patient-Oriented Outcome Assessment After Temporal Lobectomy for Refractory Epilepsy
Neurol 53:687-694, 662, Gilliam,F.,et al, 1999

Reassessment:Vagus Nerve Stimulation for Epilepsy
Neurol 53:666-669, Fisher,R.S.&Handforth,A., 1999

Prethrombotic Disorders in Children with Arterial Ischemic Stroke and Sinovenous Thrombosis
Arch Neurol 56:967-971, Bonduel,M.,et al, 1999

Cerebroretinal Vasculopathy Mimicking a Brain Tumor:A Case of a Rare Hereditary Syndrome
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Pediatric Third, Fourth, and Sixth Nerve Palsies:A Population-Based Study
Am J Ophthalmol 127:388-392, Holmes,J.M.,et al, 1999

Rapid-Onset Dystonia-Parkinsonism:Linkage to Chromosome 19q13
Ann Neurol 46:176-182, Kramer,P.L.,et al, 1999

Folic Acid for the Prevention of Neural Tube Defects
Pediartrics 104:325-327, Committee on Genetics, 1999

Adult-Onset Nemaline Myopathy:Another Cause of Dropped Head
Muscle & Nerve 22:1146-1150, Lomen-Hoerth,C.,et al, 1999

Intracerebral Hemorrhage in Young People,Analysis of Risk Factors,Location,Causes,and Prognosis
Stroke 30:537-541, Rutz-Sandoval,J.L.,et al, 1999

Facial Diplegia Complicating a Bilateral Internal Carotid Artery Dissection
Stroke 30:681-686, Gout,O.,et al, 1999

Epidemiology of Recurrent Cerebral Infarction,A Medicare Claims-Based Comparison of First and Recurrent Strokes on 2-Year Survival and Cost
Stroke 30:338-349, Samsa,G.P.,et al, 1999

Multicentre European Study of Thalamic Stimulation in Paarkinsonisn and Essential Tremor
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Showing articles 3400 to 3450 of 5493 << Previous Next >>