Neudle.com: "motor neuron disease misdiagnosis"

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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

anemia

anterior horn cell disease

anti citrullinated antibody

aphasia, progressive, primary

apraxia of eye movements

ataxia telangiectasia

autonomic dysfunction

Babinski sign

basophilic stippling of red blood cells

brachial amyotrophic diplegia

bulbar palsy, progressive

cachexia

CAG repeats

cane

carcinoembryonic antigen

carcinoma

CAT scan, emission, abnormal

catalepsy

CD4 counts

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar degeneration

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, proteincytologic dissociation

cervical osteophyte

cervical spine

cervical spondylosis

cervical spondylosis, differential diagnosis of

cervical spondylosis, misdiagnosis

chills

Chinese paralytic syndrome

chondroitin sulfate C

chorea

choreoathetosis

chromosomal abnormality

chromosome 11

ciguatera poisoning

Clinical Pathologic Conference(C.P.C.)

cortical-basal ganglionic degeneration

cranial neuropathy

crying, pathologic

cyclophosphamide

degenerative diseases of CNS

delay in diagnosis

delusion

dementia

dementia, age at onset

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

denervation of muscle

denervation potentials

differential diagnosis

distal muscle atrophy

distal muscle weakness

electroencephalogram, abnormalities of

electromyogram

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, Japanese

encephalitis, viral

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

evoked potentials

executive dysfunction

exercise

eye movement, disorders of

facial weakness

facial weakness, bilateral

fine motor function, impaired

frontal behavioral spatial syndrome

frontotemporal dementia, behavioral variant

F-wave response

gag reflex, depressed

gait disorder

gait, apraxic

gamma amino butyric acid

gammaglobulin therapy, intravenous

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic screening

genetic testing

GM1 ganglioside antibodies

grasp reflex

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, variant forms of

heavy metal intoxication

heralding manifestation

highly active antiretroviral therapy

human immunodeficiency virus type 1

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

immunosuppressive agents

immunotherapy

impulsivity

inclusion bodies

inclusion bodies, eosinophilic intranuclear

inclusion body myositis

India

inflexibility, mental

intellectual deficit

intrinsic hand muscles, wasting of

laminectomy, cervical

laughing, pathologic

L-dopa

lead and the nervous system

lead poisoning

leg atrophy

leg weakness, bilateral

leg weakness, unilateral

lymphoma involving CNS

Man-In-The-Barrel syndrome

masked facies

masseter muscle wasting

meningitis

mental retardation

mental status, abnormal

monoclonal gammopathy

motor neuron disease, misdiagnosis

motor neuron disease, spontaneous recovery

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sleep latency test

multiple system atrophy

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle pain

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

myasthenia gravis

myasthenia gravis, diagnosis

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelomalacia

myelopathy

myelopathy, chronic progressive

myelopathy, ischemic-due to trauma or spondylosis

myopathy, steroid responsive

nerve conduction studies

nerve conduction studies, motor

neurocutaneous disease

neuroendocrinology

neurologic complications of, surgery

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuropathology, brain

neuropathy

neuropathy, acute

neuropathy, amyloid

neuropathy, diphtheritic

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, painful

neuropathy, peripheral, treatment

neuropathy, toxic

neuroprotective agents

neurotoxin

next-generation sequencing

night sweats

obsessive-compulsive disorder

ocular motility, disorders of

osteomalacia

pain

pain, abdominal

pain, increased response

pain, leg

palliative care

paralysis, acute

paralysis, acute areflexic

paralysis, asymmetric

paranoia

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraspinal muscle

parathyroid adenoma

Parkinson disease, axial symptoms

Parkinson disease, L-dopa nonresponsive

Parkinson disease, tremor, absence of

Parkinsonism syndrome

pathology

patient information and support

penguin silhouette sign

personality change

Pick bodies

Pick's disease

pleocytosis of cerebrospinal fluid

poliomyelitis

poliomyelitis-like illness

polyglucosan body disease

polymerase chain reaction

polymerase chain reaction, false negative

polymyositis

polyneuropathy, chronic inflammatory demyelinating

polysomnogram

porphyria

positive sharp waves

primary lateral sclerosis

progeria

prognosis

progressive neurologic disorder

progressive spinal muscular atrophy

progressive supranuclear palsy

proximal muscle atrophy

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychomotor retardation

pyramidal tract dysfunction

rabies, nervous system involvement with

radial nerve, palsy of

radiation hypersensitivity

release phenomena

REM sleep

REM sleep behavior disorder

remote effect of cancer on the nervous system

respiratory tract infection

rheumatoid arthritis, neurologic complications of

saccadic eye movements, abnormal

screening

sensory symptoms

sequencing difficulty

shell fish poisoning

sinemet

single photon emission computed tomography

skin, biopsy

skin, lesions in neurologic disorders

sleep

sleep offset paralysis

sleep onset paralysis

sleep paralysis

sleep pathology and physiology

somatosensory evoked potentials

somatosensory evoked potentials, dermatomal

spinal cord, cervical

spinal cord, compression of

spinal cord, lesion of

spinal muscular atrophy

spondylosis

stereotyped behavior

sternocleidomastoid muscle

temporal lobe, atrophy

tick paralysis

tongue, atrophy

tongue, fasciculations of

tongue, impaired movements of

toxins, nervous system

trauma

travel, foreign

treatment of neurologic disorder

tremor

tremor, postural

trinucleotide repeats

tripping

unconsciousness

unconsciousness, episodic

unconsciousness, transient

Waldenstrom's macroglobulinemia

walking, difficulty with

weakness

weakness, acute

weakness, generalized

weakness, progressive

word-finding difficulty

wrist drop

X-linked bulbospinal neuronopathy

Showing articles 0 to 50 of 4003 Next >>

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

Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism
NEJM 372:1151-1162, Miller, B.L.,et al, 2015

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

Criteria for the Diagnosis of Corticobasal Degeneration
Neurol 80:496-503, Armstrong, M.J.,et al, 2013

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

Progressive Supranuclear Palsy: A Current Review
The Neurologist 14:79-88, Lubarsky,M. &Juncos,J.L., 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

Narcolepsy With Cataplexy
Lancet 369:499-511, Dauvilliers,Y.,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

Paralytic Rabies After a Two Week Holiday in India
BMJ 331:501-503, Solomon,T.,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

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

A Poliomyelitis-like Syndrome from West Nile Virus Infection
NEJM 347:1279-1280, Leis,A.A., et al, 2002

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

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

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

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

Poliomyelitis-Like Illness Due to Japanese Encephalitis Virus
lancet 351:1094-1097, Solomon,T.,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

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

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

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

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

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

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

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

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

Showing articles 0 to 50 of 4003 Next >>