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 3200 to 3250 of 5493 << Previous Next >>

Brain Calcifications in Systemic Sclerosis
Arch Neurol 59:1642-1643, Gusbi,O. &Bernardini,G.L., 2002

Familial Dementia With Lewy Bodies
Arch Neurol 59:1622-1630, Tsuang,D.W.,et al, 2002

Indications and Usefulness of Nerve Biopsy
Arch Neurol 59:1532-1535, Said,G., 2002

Clinicopath Conf., Adenocarcinoma with Metastasis to Liver, with Hypercoagulable State Resulting in Thrombophlebitis & Nonbacterial Thrombotic Endocarditis, with Multiple Embolic Infarcts (Trousseau's
NEJM 347:1187-1194, Case 31-2002, 2002

Subarachnoid Hemorrhage
Stroke 33:1321-1326, Kissela,B.M.,et al, 2002

Familial Infantile Bilateral Striatal Necrosis
Neurol 59:983-989, Straussberg,R.,et al, 2002

Rectal Diazepam Gel for Treatment of Acute Repetitive Seizures in Adults
Arch Neurol 59:1915-1920, Cereghino,J.J.,et al, 2002

Outcomes of 32 Hemispherectomies for Sturge-Weber Worldwide
Neurol 59:1735-1738, Kossoff,E.H.,et al, 2002

New Players in the Genetics of Stroke
NEJM 347:1711-1712, Tournier-Lasserve,E., 2002

Prospective Assessment of Risk Factors for Recurrent Stroke During Childhood--A 5-year Follow-up Study
Lancet 360:1540-1545,1526, Strater,R.,et al, 2002

Tourette's Syndrome
Lancet 360:1577-1586, Leckman,J.F., 2002

Posterior Circulation Stroke in Childhood
Neurol 59:1552-1556, Ganesan,V.,et al, 2002

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

Unilateral Cranial and Phrenic Nerve Involvement in Axonal Guillain-BarrT Syndrome
Muscle Nerve 25:297-299, Sakakibara,Y.,et al, 2002

Hearing Loss is a Common Feature of Symptomatic Children with Profound Biotinidase Deficiency
J Pediatr 140:242-246, Wolf,B.,et al, 2002

Recurrent Stroke as a Manifestation of Primary Angiitis of the Central Nervous System in a Patient Infected With Human Immunodeficiency Virus
Arch Neurol 59:468-473, Nogueras,C.,et al, 2002

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

Emergent Use of Anticoagulation for Treatment of Patients with Ischemic Stroke
Stroke 33:856-861, Adams,H.P., 2002

Gluten Sensitivity as a Neurological Illness
JNNP 72:560-563, Hadjivassiliou,M.,et al, 2002

Therapies for Movement Disorders
Arch Neurol 59:699-702, Goetz,C.G &Hinson,V.K., 2002

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

Hyperammonemic Encephalopathy in Multiple Myeloma
NEJM 346:1674-1675, Kwan,L.,et al, 2002

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

Mimic Syndromes in Sporadic Cases of Progressive Spinal Muscular Atrophy
Neurol 58:1593-1596, Visser,J.,et al, 2002

Sudden Coma From Acute Bilateral Internal Carotid Artery Territory Infarction
Neurol 58:1846-1849, Kwon,S.U.,et al, 2002

The Final Month of Life in Patients with ALS
Neurol 59:428-431, Ganzini,L.,et al, 2002

The Behavioral Spectrum of Tic Disorders
Neurol 59:414-420, Kurlan,R.,et al, 2002

Warfarin-Aspirin Recurrent Stroke Study (WARSS) Trial
Stroke 33:1723-1726, Hankey,G.J., 2002

Evolving Treatment Strategies for Epilepsy
JAMA 287:2917-2920, Diaz-Arrastia,R.,et al, 2002

Responding to Medical Events During Commercial Airline Flights
NEJM 346:1067-1073, Gendreau,M.A. &DeJohn,C., 2002

Mitochondrial Optic Neuropathies
JNNP 72:423-425, Sadun,A.A., 2002

Results of Radiotherapy for Drooling in Amyotrophic Lateral Sclerosis
Neurol 58:1308, Stalpers,L.J.A. &Moser,E.C., 2002

Mutations in Each of the Five Subunits of Translation Initiation Factor eIF2B Can Cause Leukoencephalopathy with Vanishing White Matter
Ann Neurol 51:264-270, van der Knaap,M.S.,et al, 2002

Middle Cerebral Artery Stenosis Is a Major Clinical Determinant in Striatocapsular Small, Deep Infarction
Arch Neurol 59:259-263, Bang,O.Y.,et al, 2002

Diffusion-weighted MRI Differentiates the Parkinson Variant of Multiple System Atrophy from PD
Neurol 58:575-580, Schocke,M.F.H.,et al, 2002

Serial MRI Findings in a Case of Primary Lateral Sclerosis
Neurol 58:647-649, Smith,C.D., 2002

Clinicopath Conf, Hyperviscosity Syndrome Due to IgG Multiple Myeloma
NEJM 346:603-610, Case 6-2002, 2002

Angiotropic Large Cell Lymphoma with Imaging Characteristics of CNS Vasculitis
AJNR 23:239-242, Song,D.K.,et al, 2002

Bilateral Carotid Dissection. A Not to Underestmiate Cause of Neurological Loss After Road Accident
Unfallchirurg 105:919-922, Stock,K.,et al, 2002

Hypertrophic Cardiomyopathy A Systematic Review
JAMA 287:1308-1320, Maron, B.J., 2002

Clinical Profile of Stroke in 900 Patients with Hypertrophic Cardiomyopathy
J Am Coll Cardiol 39:301-307, Maron,B.J.,et al, 2002

Cardiac Papillary Fibroelastoma as a Cause of Recurrent Ischemic Strokes: The Diagnostic Value of Serial Transesophageal Echocardiography
Cerebrovasc Dis 14:256-259, Baba, Y.,et al, 2002

Antiphospholipid Syndrome and Multiple Ischemic Strokes in a Patient with Myasthenia Gravis
Kurume Med J 49:211-216, Kaji, M.,et al, 2002

Isolated Third Nerve Palsy Due to Sarcoidosis
Can J Ophthalmol 36:416-419, Ueyama,H.,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

Balos Concentric Sclerosis Demonstrated by Contrast MRI
Neurol 57:1610, Kastrup, O.,et al, 2001

Repeated Thalamic Haemorrhage: Case Report and Review of the Literature
Acta Neurol Scand 104:48-53, Tatara, N.,et al, 2001

Traumatic Bilateral Carotid Dissection with Concomitant Cerebral Infarction
J Emerg Med 20:33-38, Pittock,S.J.,et al, 2001

MRI Hyperintensities of the Temporal Lobe and External Capsule in Patients with CADASIL
Neurol 56:628-634, O'Sullivan,M.,et al, 2001

Showing articles 3200 to 3250 of 5493 << Previous Next >>