Neudle.com: hereditary spastic paraplegia

Differential
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abdominal reflex, absent

abducens nerve paralysis

abscess, spinal cord

achilles tendon, enlarged

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome myelopathy

acrocyanosis

addiction, heroin-neurologic complications with

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

Africa

agenesis of corpus callosum

Aicardi-Goutieres syndrome

alcohol

alcohol injection

alcohol, neurologic complications with

alcoholism

Alexanders disease

Alexanders disease, adult onset

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, juvenile

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

anemia

anemia, megaloblastic

anesthesia, general

angiitis

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiography, neurologic complications with

ankle reflex, absent

anterior spinal artery

asterixis, unilateral

atherosclerosis, premature

atlanto-axial subluxation

atrioventricular block

atypical

auditory evoked brainstem potentials

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

bacterial infection, CNS

basal ganglia

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

blood dyscrasias, neurologic findings with

blood transfusion

bone marrow transplantation

brain atrophy

brain biopsy

brainstem, atrophy

brainstem, dysfunction

brainstem, lesion of

breast feeding

Brown Sequard syndrome

brucellosis

brucellosis, nervous system involvement with

bulbar palsy

bulbar palsy, progressive

CAG repeats

calcification, intracranial

CAT scan, demyelinating disease

CAT scan, emission, abnormal

CAT scan, myelogram with

CAT scan, serial

CAT scan, spinal cord

CAT scan, spine

cataracts

cavernous hemangioma

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar plaques, amyloid

cerebellar vermis

cerebral cortical atrophy

cerebrospinal fluid, abnormal

cerebrospinal fluid, amonia

cerebrospinal fluid, culture of, viral

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, glutamine

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrotendinous xanthomatosis

cerebrovascular accident

cervical spine

cervical spine injury, compression

cervical spondylosis

Charcot-Marie-Tooth

chenodeoxycholic acid

chilbran skin lesions

chromosomal abnormality

chromosome 2

chromosome 6

chronic progressive external ophthalmoplegia

cirrhosis

cleft lip

cleft palate

Clinical Pathologic Conference(C.P.C.)

cognition

color vision, impaired

complications

compression fracture

confusion

congenital malformation

congenital malformation, non CNS

corpus callosum, atrophy of

corpus callosum, thinning

cranial neuropathy, multiple

crossed adductor reflex

crying, pathologic

cultured skin fibroblasts

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

decerebrate posture

deep gray nuclei

degenerative diseases of CNS

dementia, subcortical

dementia, thalamic

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

depression

developmental milestones

developmental milestones, loss of

developmental retardation

diagnostic criteria

diarrhea

diet

differential diagnosis

digits, abnormal

diplopia

distal muscle atrophy

distal muscle weakness

Dravet syndrome

drought

drug abuse

drug abuse, inhalation

drug abuse, neurologic complications of

ears of the Lynx MR sign

electrical sensation

electroencephalogram

electroencephalogram, abnormalities of

electromyogram

ELISA

emergencies, neurologic

encephalopathy, metabolic

endemic area

enzyme, defect

enzyme, muscle disease

epicanthal folds

epidemiology of neurology

epileptic encephalopathy

erythema migrans

evoked potentials

exome sequencing

eye movement, disorders of

facial anomalies

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

facial weakness

facial weakness, bilateral

fatal familial insomnia

fatigue

fatty acid, elevated plasma content

feeding disorder

fetal alcohol syndrome

fetus

fever

fibrillations

fine motor function, impaired

finger nose finger test

fistula, arterio-venous, dural

gamma amino butyric acid-mimetic drug

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

Gerstmann-Straussler-Scheinker disease

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamine

gram negative rod

granulomatosis with polyangiitis

granulomatous disease

Hallervorden Spatz disease

hearing loss, bilateral

hearing problems in children

heart block

heart block, complete

hemangioma

hemangioma, vertebral

hematopoietic tissue, extramedullary

hematuria, microscopic

hemianopia

hemiparesis

hemoglobin abnormality, neurologic complications of

hepatic encephalopathy

hepatic failure

hepatitis

hepatolenticular degeneration, non-Wilsonian

hepatomegaly

herpes virus

herpes virus infection

human immunodeficiency virus type 1

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

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

hydrocephalus

hydrocephalus, congenital

hydrocephalus, fetal

hydrocephalus, intrauterine

hyperammonemic encephalopathy

hypercalcemia

hyperhidrosis

hyperparathyroidism

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypopigmentation of skin

hypothalamus, disturbance of

hypothermia

hypothermia, causes of

hypothyroidism

hypotonia

iatrogenic neurologic disorders

imbalance

immunosuppression

immunosuppressive agents

impotence

impulsivity

inborn errors of metabolism

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

interferon alpha

internal capsule

intracerebral hemorrhage

intrathecal antispasticity drugs

intrauterine

intrinsic hand muscles, wasting of

iron, brain

irritability

Jamaica ginger paralysis

kyphoscoliosis, neurologic causes of

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

lethargy

leukemia

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukocytosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

lymphocytic pneumonitis

lymphoma

lymphoma involving CNS

lymphomatoid granulomatosis

Maghreb

magnetic stimulation

magnetic stimulation, brain

malformation, CNS, congenital

malformation, vascular

malformation, vascular, treatment of

medulla oblongata, lesion of

meningeal enhancement

meninges

meningitis

meningitis, brucellosis

meningitis, CSF cell count-normal

meningomyelitis

meningovascular syphilis

mental retardation

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

methyl benzene

methylmalonic aciduria

microcephaly

microdontia

micrognathia

middle cerebellar peduncle

middle cerebellar peduncle, lesion, bilateral

Mills syndrome

mimics

misdiagnosis

mitochondrial disease

molecular genetics

mononeuropathy multiplex

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, demyelinating disease

MRI, emergent

MRI, false negative

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, T1 weighted high signal foci

MRI, target sign

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, chronic progressive

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, prognosis

multiple sclerosis, spinal form

multiple sclerosis, treatment of

multiple system atrophy

muscle wasting, diffuse

muscle weakness

mutism

myelitis

myelitis, longitudinal

myelopathy, chronic progressive

nerve conduction studies

nerve culture

nerve root enhancement

neurocutaneous disease

neuroendocrinology

neurogenic bladder

neuroichthyosis

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination

neurologic signs

neurologic symptoms

neuronal ceroid-lipofuscinosis

neuropathology

neuropathology, brain

neuropathy

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, sensory

neuropathy, vasculitic, systemic

neurosyphilis

neurotoxic

neurotoxin

next-generation sequencing

night blindness

nitrous oxide

nystagmus

nystagmus, dissociated

nystagmus, rotary

nystagmus, vertical

occupational neurologic disorders

ochronosis

ocular motility, disorders of

oculodentodigital dysplasia

ophthalmoplegia

ophthalmoplegia, progressive external

opportunistic infection

optic ataxia

optic atrophy

optic atrophy, hereditary

optic nerve, lesion of

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, painful

paraparesis, spastic

paraparesis, spastic, tropical

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

peroneal nerve, lesion of

phenylketonuria, adult onset

phlebotomy

pleocytosis of cerebrospinal fluid

poison, organophosphate

polycythemia, primary

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy, familial

pons, lesion of

portal caval shunt

posterior longitudinal ligament, ossification of

precocious puberty

prenatal

prenatal diagnosis by amniocentesis

primary lateral sclerosis

prion disease

prisoners of war, neurologic complications in

progeria

prognosis

progressive neurologic disorder

proteinuria

pseudobulbar palsy

pseudomonas aeruginosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

psychosis

ptosis

pulmonary infiltrates

pursuit eye movements, abnormal

pyramidal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

quadriplegia

radiation encephalopathy, delayed

radiation therapy, CNS treatment and complications with

reticulum cell sarcoma

retinitis pigmentosa

retrovirus

reversible neurologic disorder

review article

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

sclerae, hyperpigmented

scleroderma

scleroderma, neurologic involvement with

SCN1A gene

screening

sea-blue histiocytes

sedimentation rate, elevated

seizure, tonic-clonic

sensorineural hearing loss

sensory level

sensory loss

serologic testing

serologic testing of cerebrospinal fluid

Sjogren-Larsson syndrome

Sjogren's syndrome

skin, darkening of

skin, lesions in neurologic disorders

sleep pathology and physiology

sodium channel dysfunction

solvent

somatosensory evoked potentials

spartin

spastic ataxia

spastic diplegia

spastic paraplegia, type 11

spastic paraplegia, type 15

spastic paraplegia, type 7

spasticity

spasticity, treatment of

spastin

speech disorder

speech disorder, childhood

speech, loss of

spinal cord

spinal cord, biopsy

spinal cord, cervical

spinal cord, compression of

spinal cord, enlargement

spinal cord, herniation

spinal cord, infarction of

spinal cord, injury of

spinal cord, injury, management of

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, extramedullary

spinal cord, neoplasm, meningioma

spinal cord, pathologic exam of

spinal cord, vascular disorders Affecting

spinal cord, vascular malformation of

spinal xanthomatosis

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

spirochete infection

splenomegaly

spondylolysis

spongy degeneration of brain

startle reaction

status epilepticus

steroid

steroid therapy, CNS treatment and complications with

stiff legs

striatonigral degeneration

striatonigral degeneration, infantile

striopallidodentate calcifications, familial idiopathic

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subarachnoid hemorrhage

subcortical U fibers

substantia nigra

symmetric brain lesions

syndactyly

syphilis, meningomyelitis

syphilis, neurologic complications with

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

toxins, nervous system

transposition of the great vessels

trauma

treatment of neurologic disorder

tremor

tremor, intention

trinucleotide repeats

vibratory sensation, abnormal

viral infection

viral infection, CNS

viral isolation

visual acuity, decreased

visual evoked response

visual loss

walking frame

walking, difficulty with

war

weakness

weakness, progressive

weight loss

Werdnig-Hoffman disease

Werner's syndrome

West disease

Western immunoblot test

x-linked hydrocephalus

x-ray, spine

Showing articles 1600 to 1650 of 2292 << Previous Next >>

Adrenomyeloneuropathy Presenting as Addison's Disease in Childhood
NEJM 322:13-16, 54-551990., Sadeghi-Nejad,A.&Senior,B., 1990

The Dystonias
BMJ 300:139-144, Marsden,C.D.&Quinn,N.P., 1990

Dystonia Gene in Ashkenazi Jewish Population is Located on Chromosome 9q32-34
Ann Neurol 27:114-120, Kramer,P.L.,et al, 1990

Transmission and Age-At-Onset Patterns in Familial Alzheimer's Disease:Evidence for Heterogeneity
Neurol 40:395-403, Farrer,L.A.,et al, 1990

Intracranial Hemorrhage in Patients with Polycystic Kidney Disease
Stroke 21:291-294, Ryu,S.J., 1990

Cerebrotendinous Xanthomatosis:Clinical and MRI Study (A Case Report)
JNNP 53:76-78, Fiorelli,M.,et al, 1990

Premature Stroke in a Family with Lupus Anticoagulant and Antiphospholipid Antibodies
Stroke 21:66-71, Ford,P.M.,et al, 1990

Neurologic Crises in Hereditary Tyrosinemia
NEJM 322:432-437, Mitchell,G.,et al, 1990

Familial Meningioma
Neurol 40:312-314, McDowell,J.R., 1990

Dopa-Responsive Dystonia:The Spectrum of Clinical Manifestations in a Large North American Family
Neurol 40:66-69, Nygaard,T.G.,et al, 1990

A Large Kindred with Autosomal Dominant Parkinson's Disease
Ann Neurol 27:276-282, Golbe,L.I.,et al, 1990

Treatment of Late Infantile Metachromatic Leukodystrophy by Bone Marrow Transplantation
NEJM 322:28-32, 541990., Krivit,W.,et al, 1990

Hyperostosis Cranialis Interna
NEJM 322:450-463, Manni,J.J.,et al, 1990

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

Retroviruses and Multiple Sclerosis. I. Analysis of Seroreactivity by Western Blot and Radioimmune Assay
Neurol 40:1251-1253, Weinshenker,B.G.,et al, 1990

Retroviruses & Multiple Sclerosis. II. Failure of Gene Amplification Techniques to Detect Viral Sequences
Neurol 40:1254-1258, Dekaban,G.A.&Rice,G.P.A., 1990

Combined Resting-Postural Tremor of Lower Limbs:Another Essential Trem, or Variant
Neurol 40:1006, Rapoport,A.,et al, 1990

Botulinum Toxin Treatment of Cranial-Cervical Dystonia, Spasmodic Dystonia, Focal Dystonias & Hemifacial Spasm
JNNP 53:633-639, Jankovic,J.,et al, 1990

Prion Dementia Without Characteristic Pathology
Lancet 336:7-9, 21-221990., Collinge,J.,et al, 1990

Assessment:The Clinical Usefulness of Botulinum Toxin-A in Treating Neurologic Disorders
Subcommittee Report, Neurol 40:1332-13361990., , 1990

Narcolspey
NEJM 323:389-394, Aldrich,M.S., 1990

Screening for Carriers of Tay-Sachs Disease Among Ashkenazi Jews
NEJM 323:6-12, Triggs-Raine,B.L.,et al, 1990

Cerebrovascular Disease in Ehlers-Danlos Syndrome Type IV
Stroke 21:626-632, Schievink,W.I.,et al, 1990

Idiopathic Cerebellar Ataxia of Late Onset:Natural History and MRI Morphology
JNNP 53:297-305, Klockgether,T.,et al, 1990

Neurofibromatosis Type I in Children
J Pediatr 116:845-853, Listernick,R.&Charrow,J., 1990

Neurofibromatosis 2 (Bilateral Acoustic Neurofibromatosis) An Update
Ann Int Med 113:39-52, Mulvihill,J.J.,et al, 1990

Central Nervous System Haemangioblastoma:A Clinical & Genetic Study of 52 Cases
JNNP 53:644-648, Boughey,A.M.,et al, 1990

Electroencephalography Laboratory Diagnosis of Prolonged QT Interval
Ann Neurol 28:387-390, Gospe,S.M.&Gabor,A.J., 1990

Superior Sagittal Sinus Thrombosis in a Patient with Protein S Deficiency
Stroke 21:633-636, Cros,D.,et al, 1990

Progress in Tuberous Sclerosis
Editorial, Lancet 336:598-5991990., , 1990

Cranial MRI in Wilson's Disease
Neuroradiology 32:211-214, Prayer,L.,et al, 1990

Wilson's Disease, Development of Neurological Disease after Beginning Penicillamine Therapy
Arch Neurol 47:595-596, Glass,J.D.,et al, 1990

Neuropsychological Changes in Olivopontocerebellar Atrophy
Arch Neurol 47:997-1001, Berent,S.,et al, 1990

MRI in Familial Multiple Sclerosis
Neurol 40:900-903, Lynch,S.G.,et al, 1990

A Comparison of Sporadic and Familial Multiple Sclerosis
Neurol 40:1354-1358, Weinshenker,B.G.,et al, 1990

Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA
Ann Neurol 26:699-708, Hold,I.J.,et al, 1989

Familial X-linked Myalgia and Cramps:A Nonprogressive Myopathy Associated with a Deletion in the Dystrophin Gene
Neurol 39:1277-1280, Gospe,S.M.,et al, 1989

HTLV-1 and Polymyositis in Jamaica
Lancet 2:1184-1187, Morgan,O.S.,et al, 1989

Cerebral Palsy Diplegia:Improvements for Walking
BMJ 299:1115-1116, Patrick,J., 1989

Dyslexia
Editorial, Lancet 2:719-7201989., , 1989

MRI in Cockayne Syndrome Type 1
Neuroradiology 31:276-277, Boltshauser,E.,et al, 1989

Lumbosacral Plexopathy Secondary to Perirectal Abscess in a Patient with HIV Infection
Neurol 39:1400-1401, Holtzman,D.M.,et al, 1989

Cardioembolic Stroke in Primary Oxalosis with Cardiac Involvement
DiPasquale. G. , et al, Stroke 20:1403-14069., , 1989

Acute and Chronic Effects of Propranolol and Primidone in Essential Tremor
Neurol 39:1587-1588, Koller,W.C.&Vetere-Overfield,B., 1989

Tourette's Syndrome:Current Concepts
Neurol 39:1625-1630, Kurland,R., 1989

Spinal Epidural Lipomatosis:A Serious Complication of Iatrogenic Cushing's Syndrome
Neurol 39:1031-1034, Kaplan,J.G.,et al, 1989

Aicardi Syndrome in Two Sisters
J Pediatr 115:282-283, Molina,J.A.,et al, 1989

Juvenile Myoclonic Epilepsy:An Autosomal Recessive Disease
Ann Neurol 25:440-443, Panayiotopoulos,C.P.&Obeid,T., 1989

Radiologic Screening for von Hippel-Lindau Disease:Role of Gd-DTPA Enhanced MR Imaging of the CNS
J Comput Assist Tomogr 13:743-755, Filling-Katz,M.R.,et al, 1989

Adult-Onset Adrenoleukodystrophy Manifesting as Dementia
Am J Med 87:481-483, Panegyres,P.K.,et al, 1989

Showing articles 1600 to 1650 of 2292 << Previous Next >>