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Differential
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abdominal reflex, absent

abducens nerve paralysis

abscess, intracerebral

abscess, spinal cord

achilles tendon, enlarged

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome myelopathy

ACTH, ectopic syndrome of

acyl CoA dehydrogenase deficiency

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

alcohol injection

alcohol, neurologic complications with

Alexanders disease

Alexanders disease, adult onset

Alzheimer's disease

aminoacidopathies

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, juvenile

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

anemia, megaloblastic

anesthesia, general

aneurysm, intracranial

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiography, cerebral

angiography, neurologic complications with

angiography, spinal

angiotensin-converting enzyme

ankle, swelling of

ankylosing spondylitis

anterior spinal artery

anti MAG antibodies

anticonvulsants

anticonvulsants, untoward effects of

antispasticity drugs

arteriovenous malformation

arteritis, temporal

ascending paralysis

asterixis, causes of

asterixis, unilateral

ataxia, cerebellar

ataxia, progressive

ataxia, sensory

atherosclerosis, premature

atlanto-axial subluxation

atrioventricular block

auditory evoked brainstem potentials

autoimmune disease

autonomic dysfunction

azidodeoxythymidine

B 12 deficiency

bacterial infection

bacterial infection, CNS

Barkhof MR criteria for MS

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

behavioral disorder, acute

Behcet's syndrome

bladder dysfunction

blood dyscrasias, neurologic findings with

blood transfusion

bone marrow transplantation

brachial plexus neuropathy

brain biopsy, stereotaxic

brainstem, dysfunction

brainstem, lesion of

Brown Sequard syndrome

brucellosis, nervous system involvement with

bulbar palsy, progressive

calcification, membrane

carcinoma of lung

carotid angiogram

CAT scan, abnormal

CAT scan, demyelinating disease

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, myelogram with

CAT scan, serial

CAT scan, spinal cord

CAT scan, spine

cauda equina, enhancement

cavernous hemangioma

central nervous system, infection of

central nervous system, infection, cancer patient

central pontine myelinolysis

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar plaques, amyloid

cerebral cortical atrophy

cerebral palsy, associated problems with

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, amonia

cerebrospinal fluid, cell count, normal

cerebrospinal fluid, culture of, viral

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, glutamine

cerebrospinal fluid, oligoclonal IgG in

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

cervical myelopathy

cervical osteoarthritis

cervical osteophyte

cervical spine cyst

cervical spine injury, compression

cervical spondylosis

cervical spondylosis, differential diagnosis of

cervical spondylosis, misdiagnosis

chemotherapy, CNS treatment and complications with

chenodeoxycholic acid

choreoathetosis

chorioretinitis

chromosomal abnormality

chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

color vision, impaired

compression fracture

copper deficiency

cornea, opacity of

corpus callosum

corpus callosum, atrophy of

corpus callosum, thinning

cortical blindness

Coxiella burnetti

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

cranio-cervical junction

creatine phosphokinase(CPK)elevated

crossed adductor reflex

crying, pathologic

cryptococcal meningitis

cultured skin fibroblasts

cyclophosphamide

cytomegalovirus infection

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

decerebrate posture

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, childhood

dementia, familial

dementia, presenile

dementia, subcortical

dementia, thalamic

demyelinating disease

dental prostheses

dentate nuclei, lesion of

dermatomyositis

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diagnostic criteria

diarrhea, bloody

differential diagnosis

difficulty climbing stairs

diffuse idiopathic skeletal hyperostosis

digital subtraction angiography

digits, abnormal

disability rating scale, neurological

disability, neurological

distal muscle weakness

drug abuse, inhalation

drug abuse, neurologic complications of

dysarthria-clumsy hand syndrome

dyskinesia, buccal lingual facial

dystonia musculorum deformens

dystonia, cervical

dystrophic calcification

ears of the Lynx MR sign

electrical sensation

electroencephalogram

electroencephalogram, abnormalities of

embolization, therapeutic

emergencies, neurologic

emotional lability

encephalitis, focal

encephalitis, human immunodeficiency virus type 1

encephalitis, recurrent

encephalitis, viral

encephalopathy, metabolic

endovascular therapy

enzyme, muscle disease

epicanthal folds

epidemiology of neurology

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

Epstein-Barr virus

erythema migrans

escherichia coli

evoked potentials

exome sequencing

eye movement, disorders of

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, recurrent

facial weakness

facial weakness, bilateral

failure to thrive

FARS2 deficiency

fatty acid, elevated plasma content

fine motor function, impaired

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

flaccid paralysis

flu-like illness

fluorescent treponema antibody absorption(FTA-ABS)

fungal infection, CNS

galactocerebrosidase

gamma amino butyric acid-mimetic drug

gastric partitioning

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

geographic location

girdle sensation

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

gram negative rod

granulomatosis with polyangiitis

granulomatous disease

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

hearing loss, bilateral

hearing problems in children

heart block, complete

hemangioma, vertebral

hematoma, epidural-spinal

hematopoietic tissue, extramedullary

hematuria, microscopic

hemoglobin abnormality, neurologic complications of

hemophagocytosis

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration, non-Wilsonian

herniated disc, cervical

herniated disc, thoracic

herpes simplex encephalitis

herpes simplex virus

herpes virus infection

high arched feet

Horner's syndrome

human herpesvirus 6

human immunodeficiency virus type 1

human immunodeficiency virus type 1, pathogenesis

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

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

hydrocephalus, congenital

hydrocephalus, fetal

hydrocephalus, intrauterine

hyperammonemic encephalopathy

hypereosinophilic syndrome(HES)

hyperparathyroidism

hyperpigmentation of skin

hyperthyroidism

hypoglycorrhachia

hypokalemic alkalosis

hypomyelination

hypopigmentation of skin

hypothalamus, disturbance of

hypothermia, causes of

iatrogenic neurologic disorders

immunologic disease

immunology and the nervous system

immunosuppression

immunosuppressive agents

inborn errors of metabolism

inclusion bodies

incontinence, fecal

intellectual deficit

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

internal capsule

intestinal pseudoobstruction

intracerebral hemorrhage

intrathecal antispasticity drugs

intrinsic hand muscles, wasting of

Jamaica ginger paralysis

jaw jerk, abnormal

Kearns-Sayre syndrome

Krabbe's disease

kyphoscoliosis, neurologic causes of

laminectomy, cervical

laughing, pathologic

Leber's hereditary optic neuropathy

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

Lhermitte's sign

ligamentum flavum, ossification of

limbic encephalitis

listeria monocytogenes

lymphadenopathy

lymphocytic pneumonitis

lymphoma involving CNS

lymphomatoid granulomatosis

malabsorption syndrome

malformation, vascular

malformation, vascular, dural

malformation, vascular, treatment of

medulla oblongata, lesion of

Melkersson's syndrome

memory, impairment of

meningeal enhancement

meningeal sarcomatosis

meningitis, aseptic

meningitis, bacterial

meningitis, brucellosis

meningitis, cancer patients with

meningitis, chronic

meningitis, CSF cell count-normal

meningitis, escherichia coli

meningitis, fungal

meningitis, pseudomonas

meningomyelitis

meningovascular syphilis

mental retardation

mental status, abnormal

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

methylmalonic aciduria

middle cerebellar peduncle

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

mononeuritis multiplex

mononeuropathy multiplex

Morquio syndrome

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, angiography

MRI, angiography, contrast enhanced

MRI, brachial plexus

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, demyelinating disease

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, flow void, blood

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

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, late-onset

multiple sclerosis, misdiagnosis

multiple sclerosis, prognosis

multiple sclerosis, spinal form

multiple sclerosis, treatment of

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

myasthenia gravis

myasthenic syndrome

myelinolysis, extrapontine

myelitis, longitudinal

myelitis, transverse

myelogram, cervical

myelogram, thoracic

myeloneuropathy

myelopathy, ischemic

myelopathy, ascending

myelopathy, carcinomatous

myelopathy, chronic progressive

myelopathy, hepatic

myelopathy, necrotizing

myelopathy, radiation induced

myelopathy, tract-specific

myelopathy, transverse

myelopathy, vacuolar

myelopathy, venous hypertensive

myeloradiculopathy

myoclonic jerks

myopathy, metabolic

myopathy, mitochondrial

myopathy, vacuolar

myositis, ocular

Native Americans

nausea and vomiting

neoplasm, hormone producing

neoplasm, hormone producing, ectopic

neoplasm, peripheral nerve

neoplasm, primary intracerebral

neoplasm, primary of CNS

nerve conduction studies

nerve root enhancement

nerve root hypertrophy

neuritis, causes of

neurocutaneous disease

neuroendocrinology

neurofibromatosis 1

neurogenic bladder

neuroichthyosis

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination

neurologic signs

neuromyelitis optica (Devic's disease)

neuromyelitis optica spectrum disorder

neuromyelitis optica, IgG

neuronopathy, sensory

neuropathology, brain

neuropathy, demyelinating

neuropathy, peripheral

neuropathy, sensory

neuropathy, vasculitic, systemic

neuroradiology, interventional

next-generation sequencing

numb clumsy hands syndrome

nutritional deficiency

nystagmus, dissociated

nystagmus, vertical

occupational neurologic disorders

oculodentodigital dysplasia

odontoid process

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

opportunistic infection

opportunistic infection, CNS

optic atrophy, hereditary

optic disc edema

optic nerve, lesion of

optic neuritis, bilateral

optic neuropathy

oral contraceptives

oral ulcerations

osmotic demyelination syndrome

pain, abdominal

palatal myoclonus

paralysis, acute

paralysis, acute areflexic

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, painful

paraparesis, spastic

paraparesis, spastic, tropical

parasitic infection, CNS

paraspinal muscle

parathyroid adenoma

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinsonism syndrome

Pelizaeus Merzbacher

perineum, numbness of

peripheral nerve, lesion of

pernicious anemia

peroneal nerve palsy

peroneal nerve, lesion of

peroxisomal disease

personality change

phenylketonuria

phenylketonuria, adult onset

physical activity

pigmentary retinopathy

PLEDs, bilateral independent

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

poison, organophosphate

poliomyelitis-like illness

polycythemia, primary

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

pons, lesion of

portal caval shunt

posterior column disease

posterior leukoencephalopathy syndrome

posterior longitudinal ligament, ossification of

precocious puberty

prenatal diagnosis by amniocentesis

primary lateral sclerosis

prisoners of war, neurologic complications in

progressive multifocal leucoencephalopathy

progressive neurologic disorder

proprioception, abnormal

proteus mirabilis

pseudobulbar palsy

pseudomonas aeruginosa

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

pulmonary infiltrates

pyramidal tract

pyramidal tract dysfunction

quadriparesis, acute

quadriparesis, progressive

quadriplegia, transient

quality of life

rabies, nervous system involvement with

radiation encephalopathy, delayed

radiation therapy, CNS treatment and complications with

ragged-red fibers

rapidly progressing neurologic illness

Raynaud's phenomenon

rectal sphincter tone, decreased

reflex, brainstem

reflex, brainstem, absent

regional enteritis

release phenomena

remote effect of cancer on the nervous system

respiratory failure

reticulum cell sarcoma

retinitis pigmentosa

reversible neurologic disorder

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

rickettsial organism

root lesion, nerve

Rosenthal fibers

sarcoidosis, CNS

Schilder's disease

sclerae, hyperpigmented

scleroderma, neurologic involvement with

sedimentation rate, elevated

seizure, children

sensorineural hearing loss

serologic testing

serologic testing of cerebrospinal fluid

sickle cell disease

Sjogren-Larsson syndrome

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, darkening of

skin, lesions in neurologic disorders

sodium valproate

solitary scerlosis

somatosensory evoked potentials

somatosensory evoked potentials, dermatomal

spastic diplegia

spastic paraplegia, type 11

spastic paraplegia, type 15

spastic paraplegia, type 7

spasticity, treatment of

speech disorder

speech, loss of

spinal cord, biopsy

spinal cord, cervical

spinal cord, compression of

spinal cord, enlargement

spinal cord, extramedullary cyst of

spinal cord, herniation

spinal cord, infarction of

spinal cord, injury of

spinal cord, injury, management of

spinal cord, injury, prognosis in

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, extramedullary

spinal cord, neoplasm, extramedullary intradural

spinal cord, neoplasm, intramedullary

spinal cord, neoplasm, meningioma

spinal cord, neoplasm, neurofibroma

spinal cord, pathologic exam of

spinal cord, vascular disorders Affecting

spinal cord, vascular malformation of

spinal epidural arteriovenous malformation

spinal stenosis

spinal stenosis, cervical canal

spinal xanthomatosis

spine, infection of

spirochete infection

sternocleidomastoid muscle

steroid therapy, CNS treatment and complications with

strokelike episodes

subarachnoid hemorrhage

subcortical U fibers

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

systemic illness

teeth, abnormal

tendon, enlarged

testicular atrophy

thalamus, lesion of

thrombocytopenia

tinnitus, pulsatile

tongue, atrophy

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

toxins, nervous system

toxoplasma gondii

toxoplasmosis, acquired

toxoplasmosis, CNS

transient ischemic attack

transposition of the great vessels

treatment of neurologic disorder

treatment, empirical

tuberculoma of CNS

tuberculosis, spinal

ulcerative colitis

ulcers, fingertip

ultrasonography, spinal

unconsciousness

urinary frequency

urinary incontinence

urinary retention

urinary urgency

venous engorgement

vibratory sensation, abnormal

viral infection

viral infection, CNS

viral isolation

vision loss, sequential

visual acuity, decreased

visual evoked response

visual loss, progressive

visual loss, sudden

walking, difficulty with

water channel antibodies

watershed infarcts

weakness, episodic

weakness, generalized

weakness, progressive

weakness, proximal

Werner's syndrome

Western immunoblot test

white matter disease

wide based gait

xanthoma, tendon

x-linked hydrocephalus

Showing articles 950 to 1000 of 5267 << Previous Next >>

An Ultramicroscopic Study of Skin & Conjunctival Biopsies in Chronic Neuro. Disorders of Childhood
Ann Neurol 9:163-173, Arsenio-Nunes,M.L.,et al, 1981

Motor Neuron Disease:Decremental Responses to Repetitive Nerve Stimulation
Neurol 31:202-204, Bernstein,L.P.,et al, 1981

Circulating Immune Complexes in Neurologic Disease
Neurol 31:1402-1407, Noronha,A.B.C.,et al, 1981

Abrupt Neurological Deterioration in Children With Kearns-Sayre Syndrome
Arch Neurol 38:247-250, Coulter,D.L.,et al, 1981

Ophthalmoplegia-Plus
Arch Neurol 38:423-426, Okamoto,T.,et al, 1981

Demyelinating Radiculopathy in the Kearns-Sayre Syndrome:A Clinicopathological Study
Ann Neurol 8:373-380, Groothuis,D.R.,et al, 1980

Mitral Valve Prolapse & Ophthalmoplegia:A Progressive, Cardioneurologic Syndrome
Ann Int Med 92:735-741, Darsee,J.R.,et al, 1980

Extramedullary Hematopoiesis & Spinal Cord Compression Complicating Polycythemia Rubra Vera
Ann Neurol 7:81-84, Rice,G.P.A.,et al, 1980

Neuropathy & Mitochondrial Myopathy
Ann Neurol 7:262-268, Peyronnard,M.J.,et al, 1980

Management of Hypoventilation in Motor Neuron Disease Presenting with Respiratory Insufficiency
Ann Neurol 7:188-191, Sivak,E.D.,et al, 1980

Epidural Spinal Cord Compression in Acute Myelogenous Leukemia
Arch Neurol 37:319, Hildebrand,J.,et al, 1980

Clinical Criteria for Diagnosis of Machado-Joseph Disease:Report of a Non-Azorean Portuguese Family
Neurol 30:319-322, Lima,L.,et al, 1980

Leukaemia:Neurological Involvement
in Handbk of Clinical Neurology, Vinkin PJ & Bruyn GW, Ed, North-Holland Publ Co, Amsterdam 39:1, Yuill,G.M., 1980

Neurologic Manifestations in Macroglobulinemia
In Vinken PJ, Bruyn GW, Eds, Handbook of Clin Neurol, Vol 39, North-Holland Publ Co, p. 189, Abramsky,O., 1980

Skeletel Fluorosis
In Vinken PJ, Bruyn GE, Ed, Handbook of Clin Neurol, Vol 36, North-Holland Publ Co, 465, Reddy,D.R., 1979

Familial Kearns-Sayre syndrome
Neurol 29:1172-1174, Schnitzler,E.R.,et al, 1979

Basal Ganglia Calcification in Kearns-Sayre Syndrome
Arch Neurol 36:711-713, Robertson,W.C.Jr., 1979

Amyotrophic Lateral Sclerosis With Ophthalmoplegia; A Cliniocopathologic Study
Arch Neurol 36:615-617, Harvey,D.G.,et al, 1979

Remission of a Syndrome Indistinguishable from Motor Neuron Disease after Resection of Bronchial Carcinoma
BMJ 2:176-177, , 1979

Clinical Pathological Conference
Amyotrophic Lateral Sclerosis, Case Record 46-1979, NEJM 301:1104-1111979., , 1979

Necrotizing Myelopathy Complicating Hodgkin's Disease
Arch Neurol 36:583-585, Lester,E.P.,et al, 1979

Creatine Phosphokinase MB Band In Oculopharyngeal Muscular Dystrophy
(Letter) NEJM 301:270979., Diskin,C.J., 1979

Extraocular Muscle Biopsy in Chronic Progressive External Ophthalmoplegia
Ann Neurol 6:326-339, Ringel,S.P.,et al, 1979

Haemophilic Neuromyopathy
JNNP 42:600-605, Defaria,C.R.,et al, 1979

Presenile Dementia With Motor Neuron Disease in Japan, A New Entity
Arch Neurol 36:592-593, Mitsuyama,Y.,et al, 1979

Lactic Acidemia, Mitochondrial Myopathy, & Basal Ganglia Calcification
Neurol 29:1057-1061, Markesbery,Wm.R., 1979

A Familial Mitochondrial Myopathy With Central Defect in Neural Transmission
Arch Neurol 36:553-556, Barron,S.A.,et al, 1979

Reversibility of Human Myopathy Caused by Vitamin E Deficiency
Neurol 29:1182-1186, Tomasi,L.G., 1979

Use of the ECG in the Diagnosis of Childhood Spinal Muscular Atrophy
Arch Neurol 36:317-318, Russman,B.S.,et al, 1979

Spirometry in Amyotrophic Lateral Sclerosis
Arch Neurol 36:74-80, Fallat,R.J.,et al, 1979

Age & Cerebrospinal-Fluid Protein in Motor-Neuron Disease
NEJM 300:437-438, Guiloff,R.J.,et al, 1979

Double-Blind Study of Modified Neurotoxin in Motor Neuron Disease
Neurol 29:77-81, Tyler,H.R., 1979

Combined Myelopathy & Radiculoneuropathy with Malignant Lymphoproliferative Disease
Arch Neurol 36:311-313, Peress,N.S.,et al, 1979

Subacute Motor Neuronopathy:A Remote Effect of Lymphoma
Ann Neurol 5:271-287, Schold,S.C.,et al, 1979

Spinal Cord Compression by Extramedullary Hemopoietic Tissue in Pyruvate-Kinase-Deficiency-Caused Hemolytic Anemia
Neurol 29:510-513, Rutgers,M.J.,et al, 1979

Neurologic Abnormalities of Lyme Disease
Medicine 58:281-294, Reik,L.,et al, 1979

Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
Neurol 28:703, Coutinho,P.,et al, 1978

Diaphragmatic Paralysis in Motor Neuron Disease
Neurol 28:18, Parhad,I.M.,et al, 1978

Free Amino Acid Levels in Amyotrophic Lateral Sclerosis
Ann Neurol 3:305, Patten,B.M.,et al, 1978

Kearns-Sayre Syndrome with Hypoparathyroidism
Ann Neurol 3:513, Horwitz,S.J.,et al, 1978

Kearns-Sayre Syndrome & Hypoparathyroidism
Ann Neurol 3:455, Pellock,J.M.,et al, 1978

Distal Chronic Spinal Muscular Atrophy Involving the Hands
JNNP 41:653-658, O'Sullivan,D.J.,et al, 1978

Amyotrophic Lateral Sclerosis
Arch Neurol 35:638-642, Rosen,A.D., 1978

Cellular Immunity In Guamanians with Amyotrophic Lateral Sclerosis & Parkinsonism-Dementia
NEJM 299:680-685, Hoffman,P.M.,et al, 1978

Leukoencephalopathy in Oculocraniosomatic Neuromuscular Disease With Ragged-Red Fibers
Arch Neurol 35:643-647, Bertorini,T.,et al, 1978

Sparing of the Onufrowicz Nucleus in Sacral Anterior Horn Lesions
Ann Neurol 4:245-249, Iwata,M.,et al, 1978

Intrathecal Methotrexate Causing Paraplegia in a Middle-Aged Woman
Acta Haemat 60:59-60, Weiss,S.,et al, 1978

Chronic Neurogenic Quadriceps Amyotrophy
Ann Neurol 2:528, Furukawa,T.,et al, 1977

Control of Emotional Expression in Pseudobulbar Palsy
Arch Neurol 34:717, Lieberman,A.,et al, 1977

Viruslike Particles in Amytrophic Lateral Sclerosis:Electron Microscopical Study of a Case
Ann Neurol 1:290, Pena,C.E., 1977

Showing articles 950 to 1000 of 5267 << Previous Next >>