Neudle.com: amyotrophic lateral sclerosis 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

angiostrongylus cantonensis

anterior horn cell disease

anti citrullinated antibody

anti IgLON5

antiviral agents

aphasia

aphasia, progressive, primary

autonomic dysfunction

Babinski sign

basophilic stippling of red blood cells

brachial amyotrophic diplegia

bulbar palsy

bulbar palsy, acute

bulbar palsy, progressive

CAT scan, emission, abnormal

CD4 counts

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 spine

cervical spondylosis

cervical spondylosis, differential diagnosis of

cervical spondylosis, misdiagnosis

Chinese paralytic syndrome

chondroitin sulfate C

ciguatera poisoning

Clinical Pathologic Conference(C.P.C.)

creatine phosphokinase(CPK)elevated

crying, pathologic

cyclophosphamide

degenerative diseases of CNS

delay in diagnosis

delusion

dementia

dementia, age at onset

dementia, frontotemporal

dementia, presenile

denervation of muscle

denervation potentials

differential diagnosis

distal muscle atrophy

distal muscle weakness

electrophoretic pattern, serum

emotional lability

encephalitis

encephalitis, autoimmune

encephalopathy

endemic area

eosinophilia

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

evoked potentials

exercise

facial weakness

facial weakness, bilateral

fine motor function, impaired

frontotemporal dementia, behavioral variant

F-wave response

gag reflex, depressed

gait disorder

gait, waddling

gammaglobulin therapy, intravenous

gene

gene mutation

genetic counselling

genetic neurologic disorders

genetic screening

genetic testing

GM1 ganglioside antibodies

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, variant forms of

headache, progressive

heavy metal intoxication

helminthic infection of CNS

heralding manifestation

highly active antiretroviral therapy

hoarseness

hospice

human immunodeficiency virus type 1

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

immunosuppressive agents

immunotherapy

inclusion bodies

inclusion bodies, eosinophilic intranuclear

inclusion body myositis

inflexibility, mental

intellectual deficit

internuclear ophthalmoplegia

intrinsic hand muscles, wasting of

laminectomy, cervical

laughing, pathologic

lead and the nervous system

lead poisoning

leg atrophy

leg weakness, bilateral

leg weakness, unilateral

lid closure, weakness of

lymphoma involving CNS

Man-In-The-Barrel syndrome

masseter muscle wasting

meningismus

meningitis, eosinophilic

mimics

misdiagnosis

monoclonal gammopathy

monomelic amyotrophy

mortality

motor neuron disease

motor neuron disease, misdiagnosis

motor neuron disease, spontaneous recovery

MRI

MRI, abnormal

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

muscle atrophy, progressive

muscle biopsy

muscle cramp

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, chronic progressive

myopathy, steroid responsive

nerve conduction studies

nerve conduction studies, motor

neuroendocrinology

neurologic complications of, surgery

neurologic disease, diagnoses of

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuronopathy

neuropathology

neuropathology, peripheral nerves

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

osteomalacia

pain

pain, abdominal

pain, increased response

palliative care

paralysis, acute

paralysis, acute areflexic

paralysis, asymmetric

paranoia

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraproteinemia

parasitic infection

parasitic infection, CNS

Parkinsonism syndrome

pathology

patient information and support

personality change

Pick's disease

pleocytosis of cerebrospinal fluid

poison, mercury

poliomyelitis

poliomyelitis-like illness

polyglucosan body disease

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyradiculoneuropathy

porphyria

positive sharp waves

primary lateral sclerosis

prognosis

progressive neurologic disorder

progressive spinal muscular atrophy

proximal muscle atrophy

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychomotor retardation

pyramidal tract dysfunction

radial nerve, palsy of

raw fish ingestion

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

respiratory tract infection

retrovirus

review article

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

single photon emission computed tomography

sleep

sleep pathology and physiology

snail

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

steroid

steroid therapy, CNS treatment and complications with

tongue, fasciculations of

tongue, impaired movements of

toxins, nervous system

trauma

travel history

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, generalized

weakness, progressive

weight loss

wheelchair

word-finding difficulty

wrist drop

X-linked bulbospinal neuronopathy

Showing articles 100 to 150 of 4087 << Previous Next >>

Venous Thromboembolism in Amyotrophic Lateral Sclerosis
Neurol 82:1674-1677, Gladman, M.,et al, 2014

Palliative Care and Neurology
Neurol 83:561-567, Boersma, I.,et al, 2014

Neuropsychiatric Changes Precede Classic Motor Symptoms in ALS and Do Not Affect Survival
Neurol 82:149-155, Mioshi, E.,et al, 2014

Macroglossia in Amyotrophic Lateral Sclerosis
JAMA Neurol 70:1432-1435, McKee, H.R.,et al, 2013

Bright Tongue Sign in ALS
Neurol 79:1520, Fox, M.D. & Cohen, A.B., 2012

Neurodegenerative causes of death among retired National Football League Players
Neurol 79:1970-1974, Lehman, E.,et al, 2012

Spectrum of Paraneoplastic Disease Associated With Lymphoma
Neurol 76:705-710, Briani,C.,et al, 2011

Spinal Muscular Atrophy A Timely Review
Arch Neurol 68:979-984, Kolb, S.J.,et al, 2011

The Spectrum of Mutations in Progranulin: A Collaborative Study Screening 545 Cases of Neurodegeneration
Arch Neurol 67:161-170,145, Yu,C.-E.,et al, 2010

A Large-Scale International Meta-Analysis of Paraoxonase Gene Polymorphisms in Sporadic ALS
Neurol 73:16-24,11, Wills,A.-M.,et al, 2009

Practice Parameter Update: The Care of the Patient with Amyotrophic Lateral Sclerosis: Drug, Nutritional, and Respiratory Therapies (An Evidence-Based Review)
Neurol 73:1218-1226, Miller,R.G.,et al, 2009

Spinal Muscular Atrophy
Lancet 371:2120-2133, Lunn,M.R. &Wang,C.H., 2008

Primary Lateral Sclerosis With HIV-1 Infection
Neurol 70:575-577, Verma,A. &Berger,J.R., 2008

What Are the Prospects of Stem Cell Therapy for Neurology?
BMJ 337:1325-1327, Chandran,S., 2008

Genetics of Familial Amyotrophic Lateral Sclerosis
Neurol 70:144-152, Valdmanis,P.N. &Rouleau,G.A., 2008

Palliative Care for Patients With Amyotrophic Lateral Sclerosis
JAMA 298:207-216,248, Mitsumoto,H. &Rabkin,J.G., 2007

Cerebral Cortical and White Matter Lesions in Amyotrophic Lateral Sclerosis With Dementia; Correlation With MR and Pathologic Examinations
AJNR 28:1505-1510, Matsusue,E.,et al, 2007

Frontotemporal Lobar Degeneration with Motor Neuron Disease
Arch Neurol 63:489-490, Clark,C.M. &Forman,M.S., 2006

The Natural History of Primary Lateral Sclerosis
Neurol 66:647-653, Gordon,P.H.,et al, 2006

Clinicopath Conf,Encephalomyelitis Due to West Nile Virus and CLL, Case 22-2005
NEJM 353:287-295, Hollande,H.,et al, 2005

West Nile Virus: A Case Report with Flaccid Paralysis and Cervical Spinal Cord MR Imaging Findings
AJNR 26:26-29, Kraushaar, G., et al, 2005

Hemiplegic ALS:Mills Syndrome
Neurol 64:1984-1985, Rajabally,Y.A.,et al, 2005

ALS Corticospinal Degeration on DWI
Neurol 62:1834, Cabello,J.P.,et al, 2004

ALS Patients on TPPV
Neurol 61:135-137, Hayashi,H. &Oppenheimer,E.A., 2003

Occurrence of Amyotrophic Lateral Sclerosis Among Gulf War Veterans
Neurol 61:742-749, Horner,R.D.,et al, 2003

Excess Incidence of ALS in Young Gulf War Veterans
Neurol 61:750-756, Haleyl,R.W., 2003

Neuropathological Findings in West Nile Virus Encephalitis: A Case Report
Ann Neurol 54:547-551, Agamanolis,D.P.,et al, 2003

Asymmetric Flaccid Paralysis: A Neuromuscular Presentation of West Nile Virus Infection
Ann Neurol 53:703-710,691, Li,J.,et al, 2003

Early or Late Appearance of "Dropped Head Syndrome" in Amyotropic Lateral Sclerosis
JNNP 74:683-686, Gourie-Devi,M.,et al, 2003

Prognosis in Amyotrophic Lateral Sclerosis
Neurol 60:813-819, del Aguila,M.A.,et al, 2003

Early Symptom Progression Rate is Related to ALS Outcome
Neurol 59:99-103, Chio,A.,et al, 2002

Familial Amyotrophic Lateral Sclerosis
Muscle Nerve 25:135-159, Hand,C.K. &Rouleau,G.A., 2002

Euthanasia and Physician-Assisted Suicide Among Patients with Amyotrophic Lateral Sclerosis in the Netherlands
NEJM 346:1638-1644, Veldink,J.H.,et al, 2002

The Final Month of Life in Patients with ALS
Neurol 59:428-431, Ganzini,L.,et al, 2002

Results of Radiotherapy for Drooling in Amyotrophic Lateral Sclerosis
Neurol 58:1308, Stalpers,L.J.A. &Moser,E.C., 2002

Poliomyelitis Due to West Nile Virus
NEJM 347:1280-1281, Glass,J.D.,et al, 2002

Amyotrophic Lateral Sclerosis
NEJM 344:1688-1700, Rowland,L.P. & Shneider,N.A., 2001

Hospitalization in Amyotrophic Lateral Sclerosis, Causes, Costs, and Outcomes
Neurol 56:753-757, Lechtzin,N.,et al, 2001

Poliomyelitic-Like Illness in Central European Encephalitis
Neurol 55:299-302, Schellinger,P.D. et al, 2000

Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. et al, 2000

Injections of Botulinum Toxin A Into the Salivary Glands Improve Sialorrhoea in Amyotrophic Lateral Sclerosis
JNNP 69:121-123, Giess,R. et al, 2000

Linkage of Familial Amyotrophic Lateral Sclerosis with Frontotemporal Dementia to Chromosome 9q21-q22
JAMA 284:1664-1669, Hosler,B.A.,et al, 2000

A 44-Year-Old Woman with Difficulty Walking
JAMA 284:2632-2639, Iezzoni,L.I., 2000

The Split Hand in ALS has a Cortical Basis
J Neurol Sci 180:66-70, Weber,M.,et al, 2000

Disorders of Upper & Lower Motor Neurons
Neurol in Clin Practice, 3rd Ed., Butterworth, Boston: Ch. 78 p. 2007, Mitasumoto,H., 2000

Botulinum Toxin is a Useful Treatment in Excessive Drooling of Saliva
JNNP 67:697, Bhatia,K.P.,et al, 1999

Safety and Factors Related to Survival After Percutaneous Endoscopic Gastrostomy in ALS
Neurol 53:1123-1125, Chio,A.,et al, 1999

Molecular Basis of the Neurodegenerative Disorders
NEJM 340:1970-1980, Martin,J.B., 1999

A Prospecitve Study of Preferences and Actual Treatment Choices in ALS
Neurol 53:278-283,248, Albert,S.M.,et al, 1999

Adult-Onset Nemaline Myopathy:Another Cause of Dropped Head
Muscle & Nerve 22:1146-1150, Lomen-Hoerth,C.,et al, 1999

Showing articles 100 to 150 of 4087 << Previous Next >>