Neudle.com: quadriparesis progressive

Differential
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abdominal distention

abducens nerve paralysis

abducens nerve paralysis, bilateral

abscess, intracerebral

abscess, intracerebral, multiple

abscess, spinal cord

abulia

acetylcholine receptor

acetylcholine receptor antibody

achilles tendon, enlarged

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome myelopathy

acquired immunodeficiency syndrome, heralded by neurologic invol

acral sensory symptoms

acute intermittant porphyria

acyclovir

acyl CoA dehydrogenase deficiency

addiction, heroin

Addison's disease

adverse drug reaction

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis-like syndrome

aneurysm, intracranial

angiography, cerebral

angiography, spinal

angiotensin-converting enzyme

ankylosing spondylitis

anorexia

anorexia nervosa

anterior horn cell disease

anterior spinal artery

anterior spinal artery infarction

anti citrullinated antibody

anti GQ1b IgG antibody

anti MAG antibodies

antiarrhythmic drugs

antibiotics

antibodies to voltage-gated calcium channels

anticholinesterase

anticoagulant, treatment

anticonvulsants

anticonvulsants, untoward effects of

antineutrophil cytoplasmic autoantibodies

arteriovenous malformation

aspartate aminotransferase

atlanto-axial subluxation

atrial fibrillation

atypical

auditory evoked brainstem potentials

autoantibodies

autoimmune disease

autonomic dysfunction

autonomic dysfunction, acute

bacterial endocarditis, neurologic manifestations of

bacterial infection

bacterial infection, CNS

barium poisoning

Barkhof MR criteria for MS

basal cistern

basal ganglia

basal ganglia, lesion of

basilar artery occlusion

basophilic stippling of red blood cells

bat bite

beriberi

Bickerstaff's brainstem encephalitis

Borrelia miyamotoi infection

botulinum toxin

botulinum toxin, complications of

botulism

botulism antitoxin

botulism immune globulin

botulism, infant

bowel urgency

brachial plexus neuropathy

brain biopsy

brain natriuretic peptide

brainstem

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

brainstem, tuberculoma of

Brown Sequard syndrome

Brown-Vialetto-Van Laere syndrome

calcification, intracranial

calcification, membrane

campylobacter infection

carnitine deficiency myopathy

carpal tunnel syndrome

CAT scan, angiography

CAT scan, chest

CAT scan, contrast enhanced

CAT scan, demyelinating disease

CAT scan, dense artery sign

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, myelogram with

CAT scan, spinal cord

cauda equina, enhancement

cauda equina, lesion of

cavernous hemangioma

CD4 counts

cecum perforation

celiac disease, adult

celiac disease, childhood

central nervous system, infection of

central pontine myelinolysis

cerebellar atrophy, secondary

cerebellar degeneration

cerebellum, disease of

cerebral arteries

cerebral edema

cerebral embolism

cerebral embolism, mechanical extraction

cerebral infarction

cerebral infarction, small, deep

cerebral palsy

cerebral palsy, associated problems with

cerebral vasculature

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, culture of, viral

cerebrospinal fluid, cytology

cerebrospinal fluid, cytology, false negative

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, recurrent

cerebrovascular accident, three territory involvement

cerebrovascular accident, young adult

cerebrovascular disease

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

chewing, impaired

children

chills

Chinese paralytic syndrome

chronic fatigue syndrome

Churg-Strauss syndrome

cigarette smoking

ciguatera poisoning

clam poisoning

Clinical Pathologic Conference(C.P.C.)

collagen vascular disease

confusional state, acute

consanguinity

constipation

contractures, joint

contrast agents, neurotoxicity of

conversion reaction

copper deficiency

corneal reflex, abnormal

corpus callosum

corpus callosum, lesion of

corpus callosum, thinning

cough

Coxiella burnetti

cranial nerve enhancement

cranial nerve enlargement

cranial nerve palsies

cranial nerves

cranial neuropathy

cranial neuropathy, multiple

cranio-cervical junction

C-reactive protein

C-reactive protein, elevated

creatine phosphokinase isoenzyme elevation

creatine phosphokinase MB isoenzyme elevation

creatine phosphokinase(CPK)elevated

cytomegalovirus infection

degenerative diseases of CNS

delay in diagnosis

delirium

dementia

demyelinating disease

denervation of muscle

denervation potentials

dense basilar artery sign

dense middle cerebral artery sign

dental prostheses

dentate nuclei

dentate nuclei, lesion of

dermatitis herpetiformis

dermatomyositis

descending paralysis

developmental milestones

developmental milestones, loss of

developmental retardation

diaphragmatic paralysis

diarrhea

diarrhea, bloody

diet

differential diagnosis

difficulty climbing stairs

diffuse idiopathic skeletal hyperostosis

digital subtraction angiography

digitalis

digitalis intoxication

diplegia, brachial

diplopia

diplopia, transient

disability, neurological

disorientation

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

drug abuse, inhalation

drug abuse, neurologic complications of

drug induced neurologic disorders

dysarthria

dysarthria-clumsy hand syndrome

DYSF gene

dysferlinopathy

dyskinesia, buccal lingual facial

dystonia musculorum deformens

dystonia, cervical

dystonia, drug induced

dystonia, face

dystonia, focal

dystonia, treatment of

dystrophic calcification

dystrophin

ears of the Lynx MR sign

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram

electromyogram, decremental response

electromyogram, electrical silence

electromyogram, incremental response

electrophoretic pattern, serum

ELISA

embolism, paradoxical

embolism, vertebral-basilar artery

embolization, therapeutic

emergencies, neurologic

emergency room

emotional lability

encephalitis

encephalitis, acanthamoeba

encephalitis, amebic

encephalitis, brainstem

encephalitis, Japanese

encephalitis, Powassan

encephalitis, recurrent

endocarditis, acute bacterial

endocarditis, infectious

endovascular therapy

enteritis

enterovirus

enterovirus infection of CNS

enzyme, muscle disease

eosinophilia

eosinophilic granulomatosis with polyangiitis

epidemic

epidemiology of neurology

episodic disorders

episodic neurologic deficits

exercise-related muscle strength increase

extraocular muscle lesion

eye movement, disorders of

eye movement, painful

eye, pain in

face, numbness of

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, recurrent

facial pain

facial rigidity

facial weakness

facial weakness, bilateral

fine motor function, impaired

fish poisoning

Fisher's syndrome

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

fluorescent treponema antibody absorption(FTA-ABS)

fundus, abnormality of

F-wave response

gadolinium

gag reflex, depressed

gait disorder

gait, spastic

gait, waddling

gammaglobulin therapy, intravenous

gastric dilatation, acute

gastric partitioning

gastroenteritis

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

gastroparesis

gaze palsy

gaze palsy, horizontal

genetic neurologic disorders

genetic testing

geographic location

girdle sensation

glioblastoma multiforme(astrocytoma Gr.III)

glioma

gluten-free diet

glycogen storage disease

GM1 ganglioside antibodies

granuloma, eosinophilic

granulomatosis with polyangiitis

granulomatous disease

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, infantile and childhood form

Guillain Barre syndrome, variant forms of

gynecomastia

hallucination

hallucination, auditory

hallucination, visual

hand-foot-mouth disease

headache, progressive

headache, recurrent

headache, severe

hearing loss

hearing loss, unilateral

heart murmur

heat intolerance

heavy metal intoxication

heliotrope rash

hematochezia

hematoma, epidural-spinal

hematuria, microscopic

hemianopia, homonymous

hemifacial spasm

hemiparesis

hemophagocytosis

hemorrhagic diathesis

hepatomegaly

hepatosplenomegaly

heralding manifestation

herniated disc

herniated disc, cervical

herniated disc, thoracic

herniation syndromes, intracranial

herpes encephalitis

herpes simplex virus

herpes virus

herpes virus infection

herpes, genital

hiccoughs

highly active antiretroviral therapy

Hispanics

histochemistry

histochemistry of muscle

HLA

HMGcoA reductase inhibitors

hoarseness

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

human diploid cell rabies vaccine

human herpesvirus 6

human immunodeficiency virus type 1

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

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

hypereosinophilic syndrome(HES)

hyperintense vessel sign

hyperkalemia

hypermagnesemia

hyperparathyroidism, secondary

hyperphosphatasia

hyperpigmentation of skin

hypogammaglobulinemia

hypoglycorrhachia

hypogonadism

hypokalemia

hypokalemic paralysis

hypokalemic periodic paralysis

hyponatremia

hypophonia

hypophosphatemia

hypopigmentation of skin

hypoprothrombinemia

hyporeflexia

hypotension, systemic

hypothalamus, lesion of

hypothyroidism

hypotonia

hypotonia, infants

iatrogenic neurologic disorders

immunology and the nervous system

immunosuppression

immunosuppressive agents

immunotherapy

impotence

inappropriate antidiuretic(A.D.H.)hormone

inattention

inborn errors of metabolism

inclusion bodies

inclusion body myositis

incontinence, fecal

India

industrial neurologic disorders

infant, evaluation of

infection

intellectual deficit

intellectual deterioration

interstitial pulmonary fibrosis

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial hypertension, benign

intracranial pressure, increased

intrathecal chemotherapy

intrinsic hand muscles, wasting of

irritability

irritable baby

Jamaica ginger paralysis

lead and the nervous system

lead poisoning

leg numbness

leg weakness, bilateral

leg weakness, unilateral

Legionnaires'disease

lesions too numerous to count

lethargy

leukemia

leukemia, neurologic findings assoc.with

leukocytosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy, toxic

leukopenia

level of consciousness, decreased

lid closure, weakness of

ligamentum flavum, ossification of

limbic encephalitis

lipid storage myopathy

lipoprotein receptor-related protein 4

liver function enzymes

lymphadenopathy, hilar

lymphocytic pneumonitis

lymphoma

lymphoma involving CNS

malabsorption syndrome

malformation, vascular

malformation, vascular, dural

malformation, vascular, treatment of

malignant papulosis

masked facies

masseter muscle wasting

mastoiditis

McArdle's disease

mediastinum, mass of

medulla oblongata, lesion of

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningeal enhancement

meningeal sarcomatosis

meninges

meningismus

meningitis

meningitis, acinetobacter calcoaceticus var.antitratus

meningitis, aseptic

meningitis, bacterial

meningitis, basilar

meningitis, chronic

meningitis, fungal

meningitis, fungal-negative CSF culture

meningitis, leukemic

meningitis, monocytic

meningitis, neutrophilic

meningitis, recurrent

meningitis, TB

meningitis, treatment of

meningoencephalitis

meningoencephalitis, amoebic

meningomyelitis

mental retardation

mental status, abnormal

MERCI trial

merosin

mestinon

metabolic disorder, primary

methotrexate

methyl benzene

microcephaly

microscopic polyangiitis

midbrain, lesion of

middle cerebellar peduncle, lesion

mimics

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

MNGIE syndrome

molecular genetics

monoclonal antibodies

monoclonal gammopathy

monocytosis

mononeuritis multiplex

mononeuritis multiplex, causes of

mononeuropathy

mononeuropathy multiplex

MRI, angiography, contrast enhanced

MRI, brachial plexus

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, cranial nerves

MRI, demyelinating disease

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, emergent

MRI, false negative

MRI, fast

MRI, FLAIR, hyperintense vessels

MRI, high signal foci on

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, sulcal hyperintensity

MRI, target sign

multinucleated giant cell

multiple myeloma

multiple sclerosis

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple sclerosis, late-onset

multiple sclerosis, misdiagnosis

multiple sclerosis, prognosis

multiple sclerosis, spinal form

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle pain

muscle phosphorylase deficiency

muscle relaxant

muscle stiffness

muscle strength, testing

muscle tenderness

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, limb-girdle

muscular dystrophy, neurogenic hypothesis of

MuSK antibodies

mutism

myasthenia gravis

myasthenia gravis, classification

myasthenia gravis, cold test for

myasthenia gravis, diagnosis

myasthenia gravis, differential diagnosis

myasthenia gravis, etiology of

myasthenia gravis, infantile and juvenile

myasthenia gravis, late-onset

myasthenia gravis, neuromuscular junction in

myasthenia gravis, ocular

myasthenia gravis, presenting manifestations

myasthenia gravis, receptor site in

myasthenia gravis, seronegative

myasthenia gravis, thymectomy in

myasthenia gravis, treatment of

myasthenia gravis, variants

myelinolysis, extrapontine

myelitis

myelitis, longitudinal

myelitis, transverse

myelogram

myeloma, osteosclerotic

myelopathy, ascending

myelopathy, chronic progressive

myelopathy, necrotizing

myelopathy, radiation induced

myelopathy, transverse

myelopathy, venous hypertensive

myopathy, critically ill

myopathy, drug-induced

myopathy, inflammatory

myopathy, metabolic

myopathy, mitochondrial

myopathy, necrotizing

myopathy, necrotizing, autoimmune

myopathy, steroid induced

nasal septum, perforation of

necrotizing granuloma

negative

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, peripheral nerve

neoplasm, primary of CNS

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve hypertrophy

nerve root enhancement

nerve root hypertrophy

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination

neurologic history

neurologic signs

neurologic symptoms

neurological intensive care

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuromyelitis optica (Devic's disease)

neuromyelitis optica spectrum disorder

neuronal degeneration

neuronopathy

neuropathology

neuropathology, brain

neuropathology, peripheral nerves

neuropathy

neuropathy, acute

neuropathy, asymptomatic

neuropathy, chronic

neuropathy, demyelinating

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, recurrent

neuropathy, sensory

neuropathy, toxic

neuropathy, vasculitic, systemic

neuroradiology, interventional

next-generation sequencing

numb clumsy hands syndrome

numbness, generalized

nutritional deficiency

nystagmus

nystagmus, primary position of gaze

ocular bobbing

ocular myopathy

oculopharyngeal muscular dystrophy

odontoid process

old age, neurology of

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, plus syndrome

ophthalmoplegia, recurrent

ophthalmoplegia, total

opportunistic infection

opportunistic infection, CNS

organ transplantation

organomegaly

oropharyngeal weakness

osmotic demyelination syndrome

osteomalacia

osteoporosis

otitis, neurologic complications with

owl's eye sign of spinal cord

paralysis, acute areflexic

paralysis, asymmetric

paranoia

paraparesis

paraparesis, acute

paraparesis, familial spastic

paraparesis, flaccid

paraparesis, spastic

paraparesis, spastic, tropical

paraparesis, transient

paraplegia

paraplegia, acute

paraplegia, recurrent

paraproteinemia

parasitic infection

parasitic infection, CNS

parenteral alimentation

paresthesias

paresthesias, feet

paresthesias, generalized

paresthesias, hands

patent foramen ovale

patient information and support

periodic paralysis, thyrotoxic

perioral numbness

peripheral blood smear, abnormal

peripheral nerve, lesion of

phenothiazine, dyskinesia associated with

plasma cell dyscrasia

plasmacytoma

plasmapheresis

PLEDs

PLEDs, bilateral independent

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pleural effusion

pneumonia

POEMS syndrome

poison, organophosphate

poliomyelitis

poliomyelitis vaccine

poliomyelitis-like illness

polyclonal gammopathy

polymerase chain reaction

polymerase chain reaction, false negative

polymyalgia rheumatica

polymyositis

polymyositis, infantile

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic inflammatory demyelinating, childhood

polyneuropathy, chronic relapsing

polyneuropathy, critically ill

polyneuropathy, subacute idiopathic demyelinating

polyneuropathy, uremic

post infectious polyneuropathy

posterior column disease

posterior leukoencephalopathy syndrome

posterior longitudinal ligament, ossification of

postoperative neurologic complications

postpartum

potassium

practice guidelines

precipitating factors

pregnancy, neurologic complications in

prevention of neurologic disorders

primary lateral sclerosis

procainamide

prognosis

progressive infantile poliodystrophy

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive spinal muscular atrophy

proprioception, abnormal

proptosis

protozoan infection

proximal muscle atrophy

pruritus

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary infiltrates

pulmonary nodules

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

pupil, light reflex, abnormal

pupil, oval

pyomyositis

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

Q fever

quadriparesis

quadriparesis, acute

quadriparesis, progressive

quadriplegia

quadriplegia, transient

quality of life

rabies, nervous system involvement with

race

radial nerve, palsy of

radiation therapy, CNS treatment and complications with

radiculopathy

ragged-red fibers

Rankin score

rapidly fatal neurologic illness

rapidly progressing neurologic illness

rash

rash, hand

Raynaud's phenomenon

rectal sphincter tone, decreased

remote effect of cancer on the nervous system

renal failure

renal failure, acute

renal transplantation

renal tubular acidosis

repetitive nerve stimulation

respirator

respiratory arrest

respiratory failure

respiratory paralysis, pharmacologic

respiratory tract infection

reticulum cell sarcoma

retina, abnormal

retinal artery occlusion

reversible neurologic disorder

review article

rhabdomyolysis

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

rheumatoid arthritis, neurologic complications of

rheumatoid vasculitis

rhinorrhea

riboflavin

riboflavin transporter deficiency

salivation, excessive

scleroderma, neurologic involvement with

sedimentation rate, elevated

seizure

sensorineural hearing loss

sensory level

sensory loss

sensory loss, band distribution

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

seronegative

serum alanine aminotransferase

serum lipase, elevated

sex reassignment surgery

single-fiber electromyography

sinuses, diseases of

sinusitis

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, lesions in neurologic disorders

small vessel vasculitis

small-bowel resection

somatosensory evoked potentials

spastic paraplegia, type 11

spinal cord degeneration

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, 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, neurofibroma

spinal cord, pathologic exam of

spinal cord, vascular disorders Affecting

spinal cord, vascular malformation of

spinal epidural arteriovenous malformation

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinal stenosis

spinal stenosis, cervical canal

spinal xanthomatosis

spirochete infection

spironolactone

splenium of corpus callosum

splenomegaly

spondylosis

spontaneous remission

standing difficulty

staphylococcus aureus

stem cell transplantation

steppage gait

steroid

steroid therapy, CNS treatment and complications with

stiff legs

stool culture

strokelike episodes

subarachnoid hemorrhage

substantia nigra

suck, poor

suprasellar lesion

survival motor neuron gene

suspended sensory loss

sweating

sweating, abnormality of

synovitis

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

systemic illness

tachycardia

tachypnea

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

tendon, enlarged

tensilon test

tensilon test, false positive

testicular biopsy

tetany

thalamus, infarction, bilateral

thymus and neuromuscular function

thyroid function tests

tick-borne encephalitis

tinnitus

tinnitus, pulsatile

tongue, atrophy

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

tonic spasms

toxic encephalopathy

toxins, nervous system

transgender

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

treatment, empirical

tremor

trigeminal neuropathy

trigeminal neuropathy, sensory

tuberculoma of CNS

tuberculosis

tuberculosis, miliary

tuberculosis, spinal

ulcerative colitis

ulcers, fingertip

ultrasonography, spinal

vaccination, neurologic complications with

vaccine

vascular endothelial growth factor

vibratory sensation, abnormal

vincristine neurotoxicity

vision, blurred, monocular

visual acuity, decreased

visual evoked response

voice, abnormality of

Waldenstrom's macroglobulinemia

walking frame

walking, difficulty with

weakness, generalized

weakness, infant

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

weight gain

weight loss

Wernicke's encephalopathy

West Nile fever

Western immunoblot test

word-finding difficulty

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Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
Lancet 345:161-162, Jouet,M.&Kenwrick,S., 1995

Late-Onset Mitochondrial Myopathy
Ann Neurol 37:16-23, 31995., Johnston,W.,et al, 1995

Evaluation of the Cardiomyopathy in Becker Muscular Dystrophy
Muscle & Nerve 18:283-291995., Nigro,G.,et al, 1995

Amyotrophic Lateral Sclerosis:Correlation of Clinical & MR Imaging Findings
Radiology 194:263-270, Cheung,G.,et al, 1995

Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,et al, 1995

Critical Illness Neuromuscular Disease in Children Manifested as Ventilatory Dependence
J Pediatr 126:259-261, Sheth,R.D.,et al, 1995

Progressive Multifocal Leukoencephalopathy:Unusual MR Findings
J Comput Assist Tomogr 19:302-305, Ng,S.,et al, 1995

Clinicopath Conf
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Neurofibromatosis Type 1:Pathologic Substrate of High-Signal-Intensity Foci in the Brain
Radiology 195:721-724, DiPaolo,D.P.,et al, 1995

Medial Medullary Syndrome:Report of 18 New Patients and a Review of the Literature
Stroke 26:1548-1552, Kim,J.S.,et al, 1995

MRI of the Brain in Wilson Disease:T2 Signal Loss Under Therapy
J Comput Assist Tomogr 19:635-638, Engelbrecht,V.,et al, 1995

Apolipoprotein E Genotype in Diverse Neurodegenerative Disorders
Ann Neurol 38:131-135, Schneider,J.A.,et al, 1995

Prolonged Paralysis After Neuromuscular Blockage
Muscle & Nerve, 18:937-94295., Gooch,J., 1995

Reflex Sympathetic Dystrophy in Children
BMJ 310:1648-1649, Lloyd-Thomas,A.R.&Lauder,G., 1995

The Prevention of Neurogenetic Disease
Arch Neurol 52:356-362, 3451995., Rosenberg,R.N.&Iannaccone,S.T., 1995

AIDS-Associated Progressive Multifocal Leukoencephalopathy Revealed by New-Onset Seizures
Am J Med 99:64-68, Moulignier,A.,et al, 1995

Myositis:Immunologic Contributions to Understanding Cause, Pathogenesis, and Therapy
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Deficiency of Brain Synaptic Dystrophin in Human Duchenne Muscular Dystrophy
Ann Neurol 38:446-449, Kim,T.W.,et al, 1995

Brain Abnormalities in Duchenne Muscular Dystrophy:Phosphorus-31 Magnetic Resonance Spectroscopy & Neuropsych Study
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Cardiac Involvement in a Large Kindred with Myotonic Dystrophy:Quant Assess & Relation to Size of CTG Repeat Expansion
JAMA 274:813-819, Tokgozoglu,L.S.,et al, 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Primary Adhalin Deficiency as a Cause of Muscular Dystrophy in Patients with Normal Dystrophin
Ann Neurol 38:367-372, 3531995., Ljunggren,A.,et al, 1995

Amyloidosis Causing A Progressive Myopathy
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Hypoglycaemia in Spinal Muscular Atrophy
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Natural History in Proximal Spinal Muscular Atrophy
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Persistence of MRI Hyperintensity of the Globus Pallidus in Cirrhotic Patients:A 2-year Follow-up Study
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