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Differential
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abdominal protrusion

abdominal x-ray

abducens nerve paralysis

achilles tendon, enlarged

adult polyglucosan body disease

advance directives

advances in neurology

adverse drug reaction

agnosia, visual

akinesia of eyelid function

Alzheimer's disease

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

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, juvenile

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis-like syndrome

anti GQ1b IgG antibody

anti Ri antibody

aphasia, progressive, primary

apraxia of eyelid opening

arm swing, reduced

ataxia, cerebellar

ataxia, progressive

ataxia, truncal

autonomic dysfunction

autonomic dysfunction, acute

autonomic neuropathy

axonal degeneration

basal ganglia, lesion of

behavioral disorder

Bickerstaff's brainstem encephalitis

biologic markers

bladder dysfunction

botulinum toxin

botulism antitoxin

botulism immune globulin

botulism, infant

brainstem, dysfunction

brainstem, lesion of

bulbar dysfunction

bulbar palsy, acute

bulbar palsy, childhood

bulbar palsy, juvenile

bulbar palsy, progressive

calcification, intracranial

carcinoma of bladder

carotid angiogram

CAT scan, abnormal

CAT scan, emission, abnormal

central hypoventilation

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral infarction, subcortical

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

chewing, impaired

Clinical Pathologic Conference(C.P.C.)

cogwheel rigidty

corpus callosum, lesion of

corpus callosum, thinning

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

crying, pathologic

cystatin C mutation

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

degenerative diseases of CNS

delay in diagnosis

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

diabetes mellitus

diaphragmatic paralysis

differential diagnosis

difficulty climbing stairs

disability, neurological

distal muscle weakness

dysdiadochokinesia

dystonia, cervical

ears of the Lynx MR sign

electromyogram, decremental response

emergencies, neurologic

emotional lability

encephalitis, autoimmune

encephalitis, brainstem

encephalomyelitis

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

Erdheim-Chester disease

executive dysfunction

extrapyramidal movement disorder, progressive

eye movement, disorders of

Fabry's disease

facial nerve palsy

facial nerve palsy, bilateral

facial weakness

facial weakness, bilateral

fatigable chewing

feeding disorder

fine motor function, impaired

Fisher's syndrome

flaccid paralysis

flail arm syndrome

food-borne infection

frontal lobe, atrophy

frontotemporal dementia, behavioral variant

gag reflex, depressed

gastrostomy, percutaneous endoscopic

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

gaze palsy, vertical

genetic neurologic disorders

genetic testing

glycogen storage disease

granulomatosis with polyangiitis

granulomatous disease

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, variant forms of

hemifacial spasm

heralding manifestation

histochemistry of muscle

hypometric saccades

hypotension, systemic

hypotonia, infants

ideomotor apraxia

inclusion bodies

inclusion bodies, intracytopasmic

infant, evaluation of

intellectual deficit

intellectual deterioration

internal capsule

intracerebral hemorrhage

intrinsic hand muscles, wasting of

jaw jerk, abnormal

Kugelberg-Welander syndrome

lacunar infarction

language disorder in adults

laughing, pathologic

leg weakness, bilateral

leg weakness, unilateral

leukoencephalopathy

lid closure, weakness of

life expectancy

locked-in syndrome

loss of sympathy

lymphoma involving CNS

lymphomatoid granulomatosis

malignancy screen

memory, defect of recent

memory, impairment of

meningitis, aseptic

mental status, abnormal

microhemorrhage, intracerebral

midbrain, atrophy

middle cerebellar peduncle, lesion

mitochondrial disease

monoclonal gammopathy

motor neuron disease

motor neuron disease, misdiagnosis

MRI, mouse ears

multiple sclerosis, differential diagnosis of

muscle atrophy, progressive

muscle spasm, face

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

myasthenia gravis

myasthenia gravis, presenting manifestations

myasthenic syndrome

myeloneuropathy

myoclonic jerks

myokymia, facial

myopathy, mitochondrial

nausea and vomiting

nemaline rod myopathy

nemaline rod myopathy, adult onset

nerve conduction studies

neurogenic bladder

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic symptoms

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuroophthalmology

neuropathology, brain

neuropathy, peripheral

neuroprotective agents

next-generation sequencing

nystagmus, dissociated

nystagmus, vertical

obsessive-compulsive disorder

ocular myopathy

ocular myopathy, differential diagnosis

oculocephalic reflex

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, progressive external

ophthalmoplegia, total

pain, abdominal

pain, management of chronic

palate, paralysis

palliative care

paralysis, acute

paralysis, acute areflexic

paraneoplastic brainstem encephalitis

paraparesis, familial spastic

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

Parkinson disease

Parkinson disease, axial symptoms

Parkinson disease, tremor, absence of

Parkinsonism syndrome

pathologic reflex

penguin silhouette sign

pleocytosis of cerebrospinal fluid

poliomyelitis vaccine

polyglucosan body

polyglucosan body disease

polymerase chain reaction

post infectious polyneuropathy

post polio syndrome

postural abnormality

practice guidelines

prevention of neurologic disorders

primary lateral sclerosis

progressive neurologic disorder

progressive spinal muscular atrophy

progressive supranuclear palsy

proximal muscle atrophy

pseudobulbar palsy

pseudoxanthoma elasticum

psychiatric problems in neurologic disorders

psychomotor retardation

ptosis, bilateral

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pyramidal tract

pyramidal tract dysfunction

quality of life

radiation therapy, CNS treatment and complications with

ragged-red fibers

rapidly progressing neurologic illness

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

repetitive nerve stimulation

respirations in CNS disease

respiratory failure

respiratory tract infection

retinitis pigmentosa

rigidity, axial

saccadic eye movements, abnormal

salivation, excessive

semantic dementia

sensorineural hearing loss

sequencing difficulty

shell fish poisoning

skin, lesions in neurologic disorders

sleep apnea, obstructive

sleep pathology and physiology

small vessel disease

small vessel disease, cerebral

spastic paraplegia, type 11

speech disorder

speech, loss of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal muscular atrophy

standing difficulty

startle reaction

stem cell transplantation

steroid therapy, CNS treatment and complications with

stooped posture

subarachnoid hemorrhage

systemic illness

tandem gait, ataxic

temporal lobe, atrophy

temporalis muscle wasting

thrombocytopenia

tongue, atrophy

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

toxins, nervous system

transverse smile

treatment of neurologic disorder

tremor, postural

trinucleotide repeats

unconsciousness

unconsciousness, episodic

unconsciousness, transient

urinary incontinence

urinary retention

vestibular function, tests of

viral infection

viral infection, CNS

vision, blurred

visual symptoms

vocal cord paralysis

walking, difficulty with

weakness, acute

weakness, fatiguable

weakness, focal

weakness, generalized

weakness, infant

weakness, progressive

weakness, proximal

weakness, rapidly progressive

West Nile fever

white matter disease

white matter disease, subcortical

word-finding difficulty

X-linked bulbospinal neuronopathy

Showing articles 250 to 300 of 4068 << Previous Next >>

Low Body Weight in Alzheimer's Disease is Associated with Mesial Temporal Cortex Atrophy
Neurol 46:1585-1591, Grundman,M.,et al, 1996

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

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340995., Forestier,N.L.,et al, 1995

Neurologic Aspects of Inflammatory Bowel Disease
Neurol 45:416-421, Lossos,A.,et al, 1995

Some Specific Clinical Features Differentiate Multiple System Atrophy (Striatonigral Variety) from Parkinson's Disease
Arch Neurol 52:294-298, Colosimo,C.,et al, 1995

Parkinsonism-Recognition and Differential Diagnosis
BMJ 310:447-452, Quinn,N., 1995

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

Acute Bilateral Ophthalmoplegia Secondary to Metastatic Prostatic Carcinoma:Demonstr of Magnetic Resonance Imaging
J Neuro-Ophthalmol 15:45-47, Agarwal,P.,et al, 1995

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

Autosomal Dominant Migraine with MRI White-Matter Abnormalities Mapping to the CADASIL Locus
Neurol 45:1086-1091, Chabriat,H.,et al, 1995

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995

Brainstem Ocular Motility Defects and AIDS
Am J Ophthalmol 106:437-442, Hamed,L.M.,et al, 1995

Familial Hemiplegic Migraine and Autosomal Dominant Arteriopathy with Leukoencephalopathy (CADASIL)
Ann Neurol 38:817-824, Hutchinson,M.,et al, 1995

Clinical Spectrum of CADASIL:A Study of 7 Families
Lancet 346:934-939, Chabriat,H.,et al, 1995

Neuromuscular Effects of Papuan Taipan Snake Venom
Ann Neurol 38:916-920, Connolly,S.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340, LeForestier,N.,et al, 1995

Prolonged Paralysis Due to Nondepolarizing Neuromuscular Blocking Agents and Corticosteroids
Muscle & Nerve 17:647-654994., Barohn,R.J.,et al, 1994

Preliminary NINDS Neuropathologic Criteria for Steele-Richardson-Olszewski Syndrome (Progressive Supranuclear Palsy)
Neurol 44:2015-2019, Hauw,J.-J., 1994

Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994

Progress in the Genetics of Cerebrovascular Disease Inherited Subcortical Arteriopathies
Stroke 25:1696-1698, Bowler,J.V.&Hachinski,V., 1994

Diffuse Leukodystrophy with a Large-Scale Mitochondrial DNA Deletion
Lancet 343:1397-1398, Nakai,A.,et al, 1994

Eye Movements in Parkinsonian Syndromes:Vidailhet
M. , et al, Neurol 35:420-42694., , 1994

Diff Diag of parkinson's Disease, Multiple Sys Atrophy, & Steele-Richardson-Olszewski Syndrome:Striatal F-Dopa PET Data
JNNP 57:278-284, Burn,D.J.,et al, 1994

Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
Neurol 44:721-727, Hirano,M.,et al, 1994

Myotonic Dystrophy
In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994

The Syndrome of'Pure Akinesia'and Its Relationship to Progressive Supranuclear Palsy
Neurol 44:1025-1029, Riley,D.E.,et al, 1994

Rapidly Progressing Atrophy of Medial Temporal Lobe in Alzheimer's Disease
Lancet 343:829-830, Jobst,K.A.,et al, 1994

Acute Pseudobulbar Mutism with Good Functional Recovery
Neurol 44:176-177, Chesser,M.Z.,et al, 1994

Botulinum Toxin-A Improves the Rigidity of Progressive Supranuclear Palsy
Ann Neurol 35:237-239, Polo,K.B.&Jabbari,B., 1994

Clinicopath Conf
progressive Supranuclear Palsy, Case 46-1993, NEJM 329:1560-1567993., , 1993

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

Neuropathic Findings in Oculopharyngeal Muscular Dystrophy, Seven Cases & Review of Literature
Arch Neurol 50:481-488, Hardiman,O.,et al, 1993

Magnetic Resonance Imaging of Brain and the Neuromotor Disorder in Endemic Cretinism
Ann Neurol 34:91-94, Ma,T.,et al, 1993

Olfactory Testing Differentiates Between Progressive Supranuclear Palsy & Idiopathic Parkinson's Dis
Neurol 43:962-965, Doty,R.L.,et al, 1993

Multiple System Atrophy & Prog Supranuc Palsy, Dimin Striatal D2 Dopamine Receptor Act by SPECT
Arch Neurol 50:513-516, vanRoyen,E.,et al, 1993

Ophthalmologic Manifestations in MELAS Syndrome
Arch Neurol 50:977-980, Fang,W.,et al, 1993

Pontine and Extrapontine Myelinolysis:A Neurologic Disorder Following Rapid Correction of Hyponatremia
Medicine 72:359-373, Karp,B.I.&Laureno,R., 1993

Congenital Bilateral Perisylvian Syndrome:Study of 31 Patients
Lancet 341:608-612, Kuzniecky,R.,et al, 1993

Clinicopath Conf
B-Cell Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma with Infilt of Orbital Muscle, Case 4, 193,NEJM 328:266-275,1993., 1993

Neurological Involvement in Wegener's Granulomatosis:An Analysis of 324 Consecutive Pts at the Mayo Clin
Neurol 33:4-9, Nishino,H.,et al, 1993

Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy
Bertoni. J. M. , et al, JAMA 268:2413-2415., , 1992

Neurologic Manifestations of Progressive Systemic Sclerosis
Arch Neurol 49:1292-1295, Averbuch-Heller,L.,et al, 1992

Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
Churchhill Livingstone, NY, p285, 30392., Mastaglia,F.L.&Walton,J., 1992

A Familial Disorder with Subcortical Ischemic Strokes, Dementia, and Leukoencephalopathy
Neurol 42:1015-1019, Mas,J.L.,et al, 1992

Striatal D2 Receptor Status in Patients with Parkinson's Disease, Striatonigral Degeneration, and PSP, (PET)
Ann Neurol 31:184-192, Brooks,D.J.,et al, 1992

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

McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature
JNNP 55:407-408, Felice,K.J.,et al, 1992

Detection in Life of Confirmed Alzheimer's Disease, Medial Temporal Lobe Atrophy by Computed Tomography
Lancet 340:1179-1183, Jobst,K.A.,et al, 1992

The Apomorphine Test in Parkinsonian Syndromes
JNNP 54:870-872, D'Costa,D.F.,et al, 1991

Clinicopath Conf
Cerebral Amyloid Angiopathy, Case 27-1991, NEJM 325:42-54991., , 1991

Showing articles 250 to 300 of 4068 << Previous Next >>