Neudle.com: motor neuron disease misdiagnosis

Differential
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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, ischemic

myelopathy, chronic progressive

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 50 to 100 of 4138 << Previous Next >>

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

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

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

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

HIV-Related Neuromuscular Syndrome Simulating Motor Neuron Disease
Neurol 40:544-546, Verma,R.K.,et al, 1990

Paraneoplastic Motor Neuron Disease and Renal Cell Carcinoma:Improvement after Nephrectomy
Neurol 40:960-962, Evans,B.K.,et al, 1990

Misdiagnosis in Patients with Amyotrophic Lateral Sclerosis
Arch Int Med 150:2301-2305, Belsh,J.M.&Schiffman,P.L., 1990

HTLV-1 Associated Myelopathy and Polymyositis in a US Native
Neurol 39:1572-1575, Evans,B.K.,et al, 1989

Amyotrophic Lateral Sclerosis, Recent Advances in Pathogenesis & Therapeutic Trials
Arch Neurol 45:189-202, Mitsumoto,H.,et al, 1988

Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
Arch Neurol 45:509-513, Gastaut,J.L.,et al, 1988

Misdiagnosis of Myasthenia Gravis
J Nat'l Medical Assoc, 79:425-4291987., Wheeler,S.D., 1987

Amyotrophic Lateral Sclerosis:Part 1. Clinical Features, Pathology, & Ethical Issues in Management
Ann Neurol 18:271-280, Tandan,R.,et al, 1985

Neuromuscular Disease in Primary Hyperparathyroidism
Ann Int Med 80:182, Patten,B.M.,et al, 1974

Amyotrophic Lateral Sclerosis:Clinical Syndrome Differential Diagnosis
Med Clin North Am 44:1013, Mulder,D.W., 1960

Reversible Leukoencephalopathy and Parkinsonism Due to CNS Involvement in Cryoglobulinemia
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Deep Venous Dural Arteriovenous Fistula Mimicking Progressive Dementia
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Cerebral Amyloid Angiopathy
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Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
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Clinodactyly as a Key Finding in Distal Spinal Muscular Atrophy
Neurol 104: e213682, Hayakawa,I.,et al, 2025

Risdiplam in Presymptomatic Spinal Muscular Atrophy
NEJM 393:671-682, Finkel,R.S.,et al, 2025

Pan-Neurofascin Nodo-Paranodopathy Presenting as Fulminant Guillain-Barre Syndrome
Neurol 105:e213848, Cabral,A.,et al, 2025

A 59-Year-Old Female Patient with Urinary Dysfunction and Lightheadedness
Neurol 105:e214233, Bu,S.,et al, 2025

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

Powassan Virus Encephalitis: A Tertiary Center Experience
Clin Inf Dis 78:80-89, Mendoza,M.A.,et al, 2024

Primary Central Nervous System Vasculitis
NEJM 391:1028-1037, Salvarani,C.,et al, 2024

Ocular Myasthenia Gravis, Central Ocular Motor Signs and Unilateral Visual Loss Caused by the Great Neuro-Ophthalmologic Impersonator
Neurol 102:e209260, Young,A. & Johnston,J.L., 2024

Cognitive and Clinical Characteristics of Patients with Limbic-Predominant Age-Related TDP-43 Encephalopathy
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Multidisciplinary End-of-Life Care for a Patient with Amyotrophic Lateral Sclerosis Requesting Euthanasia
Lancet 402:484, Kruithof,W.J.,et al, 2023

A 17-Year-Old Girl with Progressive Cognitive Impairment
Neurol 101:e1466-e1472, Zhao,B.,et al, 2023

Rapidly Progressive Dementia in a Man With HIV Infection and Undetectable Plasma Viral Load
Neurol 100:344-348, Chishimba,L.C.,et al, 2023

Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022

Re-Emergency of Poliovirus in the United States:Considerations and Implications
Ann Neurol 92:725-728, Russo,G.B.,et al, 2022

What All Physicians Need to Know About the Polio Resurgence in New York State
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Disabling Jaw Clonus in a Patient with Bulbar-Onset Amyotrophic Lateral Sclerosis Successfully Treated with Botulinum Toxin
Neurol 99:671, Santos, M.O.,et al, 2022

Clinicopathologic Conference, Diffuse Large B-Cell Lymphoma
NEJM 386:977-986, Case 7-2022, 2022

Rapidly Progressive Thalamic Dementia
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Clinicopathologic Conference, Normal Pressure Hydrocephalus
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Natural History of "Pure" Primary Lateral Sclerosis
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Teaching Video NeuroImages: Jaw Clonus in Amyotrophic Lateral Sclerosis
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Complete Evaluation of Dementia: PET and MRI Correlation and Diagnosis for the Neuroradiologist
AJNR 42:998-1007, Oldan, J.D.,et al, 2021

A 71-Year-Old Man Presenting with Acute Onset Dysarthria and Dysphagia
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Clinicopathologic conference, Frontotemporal Lobar Degeneration with tau-positive inclusions consistent with Picks disease
NEJM 383:2666-2675, Case 41-2020, 2020

Ears of the Lynx Magnetic Resonance Imaging Sign
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Isolated Oculomotor Nerve Palsy due to Pituitary Apoplexy Missed on CT scan
Neurol 94:e1774-e1777, Marzoughi, S.,et al, 2020

Contrast-Induced Encephalopathy Following Coronary Angiography
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Clinical Characteristics, Risk Factors, and Outcomes of POEMS Syndrome
Neurol 95:e268-e279, Keddie, S.,et al, 2020

Nusinersen in Adult Patients with Spinal Muscular Atrophy
Neurol 95:e413-e416, Moshe-Lilie, O.,et al, 2020

Telemedicine in Neurology
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Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

Hopkins Syndrome
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Showing articles 50 to 100 of 4138 << Previous Next >>