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acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

acute intermittant porphyria

advances in neurology

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis, work up

amyotrophic lateral sclerosis-like syndrome

angiostrongylus cantonensis

anterior horn cell disease

anti citrullinated antibody

antiviral agents

aphasia, progressive, primary

ascending paralysis

ataxia, progressive

autonomic dysfunction

basophilic stippling of red blood cells

behavioral disorder

bone marrow biopsy

brachial amyotrophic diplegia

bulbar palsy, acute

bulbar palsy, progressive

burning paresthesia

CAT scan, emission, abnormal

central nervous system, infection of

cerebellar atrophy, primary

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, eosinophilia of

cerebrospinal fluid, proteincytologic dissociation

cervical osteophyte

cervical spondylosis

cervical spondylosis, differential diagnosis of

cervical spondylosis, misdiagnosis

Chinese paralytic syndrome

chondroitin sulfate C

ciguatera poisoning

Clinical Pathologic Conference(C.P.C.)

conduction block

conversion reaction

cranial neuropathy

creatine phosphokinase(CPK)elevated

crying, pathologic

cyclophosphamide

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delay in diagnosis

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denervation of muscle

denervation potentials

dexterity, impaired

diabetes mellitus

diagnostic criteria

differential diagnosis

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distal muscle atrophy

distal muscle weakness

electrophoretic pattern, serum

emotional lability

encephalitis, autoimmune

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evoked potentials

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fine motor function, impaired

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frontotemporal dementia, behavioral variant

F-wave response

gag reflex, depressed

gammaglobulin therapy, intravenous

genetic counselling

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GM1 ganglioside antibodies

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, variant forms of

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heavy metal intoxication

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inflexibility, mental

intellectual deficit

internuclear ophthalmoplegia

intrinsic hand muscles, wasting of

laminectomy, cervical

laughing, pathologic

lead and the nervous system

leg weakness, bilateral

leg weakness, unilateral

lid closure, weakness of

life expectancy

locked-in syndrome

lymphoma involving CNS

Man-In-The-Barrel syndrome

masseter muscle wasting

meningitis, eosinophilic

monoclonal gammopathy

monomelic amyotrophy

motor neuron disease

motor neuron disease, misdiagnosis

motor neuron disease, spontaneous recovery

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

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muscle stiffness

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

myasthenia gravis

myasthenia gravis, diagnosis

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelopathy, ischemic

myelopathy, chronic progressive

myeloradiculopathy

myopathy, autoimmune

myopathy, quadriceps

myopathy, steroid responsive

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nerve conduction studies, motor

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neuropathy, peripheral, treatment

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neuroprotective agents

next-generation sequencing

pain, abdominal

pain, increased response

palliative care

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paraparesis, familial spastic

paraparesis, familial spastic, classification

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paraspinal muscle

parathyroid adenoma

Parkinsonism syndrome

patient information and support

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poison, mercury

poliomyelitis-like illness

polyglucosan body disease

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

polyradiculoneuropathy

positive sharp waves

primary lateral sclerosis

progressive neurologic disorder

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proximal muscle atrophy

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psychiatric problems in neurologic disorders

psychomotor retardation

pyramidal tract dysfunction

quadriceps atrophy

quadriceps weakness

radial nerve, palsy of

raw fish ingestion

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal cell carcinoma

respiratory failure

respiratory tract infection

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

sensory symptoms

shell fish poisoning

single photon emission computed tomography

sleep pathology and physiology

somatosensory evoked potentials

somatosensory evoked potentials, dermatomal

speech disorder

speech, loss of

spinal cord, cervical

spinal cord, compression of

spinal cord, lesion of

spinal muscular atrophy

stereotyped behavior

sternocleidomastoid muscle

steroid therapy, CNS treatment and complications with

tandem gait, ataxic

tongue, atrophy

tongue, fasciculations of

tongue, impaired movements of

toxins, nervous system

travel, foreign

treatment of neurologic disorder

tremor, postural

trinucleotide repeats

unconsciousness

unconsciousness, episodic

unconsciousness, transient

urinary incontinence

viral infection

viral infection, CNS

viral isolation

Waldenstrom's macroglobulinemia

walking, difficulty with

weakness, generalized

weakness, progressive

word-finding difficulty

X-linked bulbospinal neuronopathy

Showing articles 0 to 50 of 4087 Next >>

Clinicopathological Conference, Eosinophilic meningitis due to Angiostrongylus cantonensis infection
NEJM 392:699-709, Case 5-2025, 2025

Clinicopathologic Conference, Anti-IgLON5 IgG-Associated Neurologic Disorder
NEJM 386:173-180, Case 1-2022, 2022

Amyotrophic Lateral Sclerosis
Lancet 400:1363-1380, Feldman, E.L.,et al, 2022

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

Non-Alzheimers Dementia 1 Frontotemporal Dementia
Lancet 386:1672-1682, Bang, Jee.,et al, 2015

Motor Neurone Disease
BMJ 349:g4052, Nageshwaran, S.,et al, 2014

Diagnosis and Management of Motor Neurone Disease
BMJ 336:658-662, McDermott,C.J. &Shaw,P.J., 2008

Clinicopath Conf., Multifocal Motor Neuropathy With Conduction Block
NEJM 357: 2707-2715, Case 40-2007, 2007

Lead Poisoning From the Beauty Case: Neurologic Manifestations in an Elderly Woman
Neurol 69:929-930, Fluri,F.,et al, 2007

Amyotrophic Lateral Sclerosis
Lancet 369:2031-2041, Mitchell,J.D. & Borasio,G.D., 2007

Brachial Amyotrophic Diplegia in a Patient with Human Immunodeficiency Virus Infection
Arch Neurol 62:817-823, Berger,J.R.,et al, 2005

Kennedy Disease
Arch Neurol 60:893-894, Paparounas,K.,et al, 2003

Polymyositis Masquerading as Motor Neuron Disease
Arch Neurol 60:1001-1003, Ryan,A.,et al, 2003

Multiple Sclerosis Presenting as Lower Motor Neuron Wasting and Weakness of the Distal Upper Extremity
Neurol 61:1303-1304, Chong,P.S.T.,et al, 2003

Inclusiong Body Myositis Mimicking Motor Neuron Disease
Arch Neurol 58:1253-1256, Dabby,R.,et al, 2001

Nonpoliovirus Poliomyelitis Simulating Guillain-Barre Syndrome
Arch Neurol 58:1460-1464, Gorson,K.C.&Ropper,A.H., 2001

An ALS-Like Syndrome with New HIV Infection and Complete Response to Antiretroviral Therapy
Neurol 57:1094-1097,945, MacGowan,D.J.L.,et al, 2001

Reversible ALS-Like Disorder in HIV Infection
Neurol 57:995-1001,945, Moulignier,A.,et al, 2001

Amyotrophic lateral Sclerosis Mimic Syndromes, A Population-Based Study
Arch Neurol 57:109-113, Traynor,B.J.,et al, 2000

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

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

An Algorithm for ALS Diagnosis and Management
Neurol 53:S58-S62, Swash,M., 1999

Amyloid Neuropathy Simulating Lower Motor Neuron Disease
Neurol 51:600-602, Quattrini,A.,et al, 1998

Steroid-Responsive Myopathy with Deficient Chondroitin Sulfate C in Skeletal Muscle Conn Tissue
Neurol 50:526-529, Al-Lozi,M.T.,et al, 1998

Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
Neurol 49:568-572, Parboosingh,J.S.,et al, 1997

Generalised Motor Neuron Disease as an Unusual Manifestation of Borrelia Burgdorferi Infection
JNNP 63:257-258, Hemmer,B.,et al, 1997

ALS & Severe Cervical Spondylotic Myelopathy in Pt with a Posterior Fossa Archnoid Cyst:Diag Dilemma
South Medical J 80:1580-1583, Lee,S.K.&Kelly,D.L., 1997

Needle Electromyography in the Thoracic Paraspinal Muscles of Motor Neuron Disease
No to Shinkei-Brain & Nerve 48:637-642996., Kyuno,K.,et al, 1996

Inclusion Body Myositis
JNNP 60:251-255, Garlepp,M.J.&Mastaglia,F.L., 1996

Avoiding False Positive Diagnoses of Motor Neuron Disease:Lessons from the Scottish Motor Neuron Disease Register
JNNP 60:147-151, Davenport,R.J.,et al, 1996

Diagnosing Motor Neurone Disease
BMJ 312:650-651, Chancellor,A.M., 1996

Multifocal Motor Neuropathy with Conduction Block:A Study of 24 Patients
JNNP 59:38-44, Bouche,P.,et al, 1995

Clinicopath Conf
Progressive Muscular Atrophy, Case 36-1995, NEJM 333:1406-1412995., , 1995

Multifocal Demyelinating Motor Neuropathy:Pathologic Evidence of Inflammatory Demyelinasting Polyradiculoneuropathy
Neurol 45:1828-1832, Oh,S.J.,et al, 1995

The Electrophysiological Study of Diff Dx Between ALS & Cervical Spondylotic Myelopathy
EMG & Clin Neurophysiology 35:231-238995., Kang,D.X.&Fan,D.S., 1995

Motor Neuron Disease
JNNP 57:886-896, Leigh,P.N.&Ray-Chaudhuri,K., 1994

Monomelic Amyotrophy
Muscle & Nerve 17:1129-1134994., Donofrio,P.D., 1994

Clinicopath Conf
Acquired Demyelinating Neuropathy, ? CIDP, ? Motor Neuropathy with Multifocal Conduction Blocks, Cas, 41-1EJM 329:1182-1190,1993., 1993

Polyglucosan Body Disease Simulating Amyotrophic Lateral Sclerosis
Neurol 43:785-790, McDonald,T.D.,et al, 1993

Differential Diagnosis of Guillain-Barre Synd, In Guillain-Barre Synd
Thieme Med Publ, Ch 3, p 42993., Parry,G.J., 1993

Clinicopath Conf
Motor Neuron Disease, Progressive-Muscular-Atrophy Type, Case 43-1992, NEJM 327:1298-130592., , 1992

Multifocal Demyelinating Motor Neuropathy:Cranial Nerve Involvement and Immunoglobulin Therapy
Neurol 42:506-509, Kaji,R.,et al, 1992

Multifocal Motor Neuropathy with Conduction Block:Is It a Distinct Clinical Entity?
Neurol 42:497-505, Lange,D.J.,et al, 1992

Surgical Treatment of Cervical Spondylotic Myelopathy:Time for a Controlled Trial
Neurol 42:5-13, Rowland,L.P., 1992

Clinicopath Conf
Case 40-1991, Inclusion-Body Myositis, NEJM 325:1026-1035991., , 1991

Subacute, Reversible Motor Neuron Disease
Neurol 41:1541-1544, Tucker,T.,et al, 1991

Pick's Disease:A Case Clinically Resembling Amyotrophic Lateral Sclerosis
Neurol 41:1831-1833, Sam,M.,et al, 1991

Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
Neurol 41:823-828, Olney,R.K.,et al, 1991

Acute Paralytic Poliomyelitis Presenting as Guillain-Barre Syndrome
J Infection 22:129-133, Yohannan,M.D.,et al, 1991

Showing articles 0 to 50 of 4087 Next >>