Neudle.com: focal myopathy

Differential
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abdominal protrusion

acetylcholine receptor antibody

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

addiction, heroin

Addison's disease

Adies pupil

adverse drug reaction

akinesia of eyelid function

algorithm

amaurosis fugax

amphiphysin antibodies

amyloid

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, misdiagnosis

anemia

anoctaminopathy

anorexia

anterior horn cell disease

anterior interosseous neuropathy

anterior tibial muscle weakness

anticholinergic drugs

anticoagulant, treatment

anticoagulant, treatment in CVD

aphasia

apraxia of eyelid opening

aqueduct of Sylvius, obstruction

arthrogryposis multiplex

ascending paralysis

aspiration

asthma

asthma, poliomyelitis-like syndrome with

autonomic dysfunction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basophilic stippling of red blood cells

benign essential tremor

bent spine syndrome

bitemporal visual field defect

blepharophimosis

blepharospasm

bone biopsy

bone marrow suppression

brain biopsy, negative

brain biopsy, stereotaxic

calcification, intracranial

cardiovascular disease

CAT scan, disappearing lesion on

CAT scan, false negative

cerebellar ataxia, children

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellum

cerebral cortex

cerebral cortical atrophy

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, prognosis in

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

chromosomal abnormality

chromosome 17

chronic progressive external ophthalmoplegia

Chvostek sign

cisterna magna

Clinical Pathologic Conference(C.P.C.)

cogwheel rigidty

collagen vascular disease

collapsin response mediator protein 5 IgG

coma

complications

compression neuropathy

confusion

congenital myopathy

congestive heart failure

conjunctivitis

constipation

contactin associated protein like 2 antibodies

contractures, joint

conversion reaction

corpus callosum, atrophy of

cortical blindness

coumarin

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

cryptococcal meningitis

cultured skin fibroblasts

Cushing's syndrome

cyst, cortical parenchyma

cyst, ventricular

cysticercosis

cysticercosis, cerebral

cysticercosis, intraventricular

cysticercosis, subarachnoid

cystinosis

cytomegalovirus infection

delay in diagnosis

dementia

dementia, frontotemporal

dementia, rapidly progressive

depression

dermatitis

dermatomyositis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic amyotrophy

diaphragmatic paralysis

diarrhea

differential diagnosis

difficulty climbing stairs

diplopia

disability rating scale, neurological

disability, neurological

distal muscle atrophy

distal muscle weakness

doxycycline

dropped head syndrome

dystonia, drug induced

dystonia, face

dystonia, focal

dystonia, post traumatic

dystonia, treatment of

dystrophin

ear, abnormal

edema, pedal

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram

electromyogram, decremental response

electron microscopy

ELISA

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, focal

encephalitis, human immunodeficiency virus type 1

encephalitis, paraneoplastic

encephalomyelitis

encephalopathy

encephalopathy, progressive

endemic area

enterovirus

entrapment neuropathy

enzyme, defect

enzyme, muscle disease

eosinophilia

epidemiology of neurology

epilepsia partialis continua

episodic neurologic deficits

extrapyramidal movement disorder, progressive

eye movement, disorders of

fetal movements, reduced

fetus

fever

fibrillations

fine motor function, impaired

finger flexor weakness

finger weakness

fingernails, abnormal

fourth ventricle, cyst

gadolinium

gait disorder

gait, waddling

gammaglobulin therapy, intravenous

gastroenteritis

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

glabellar sign

glycogen debranching enzyme deficiency

glycogen storage disease

Gowers maneuver

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guyon's canal

gynecomastia

hallucination, auditory

hammertoes

hand deformity

hand weakness

Hand-Schuller-Christian disease

heavy metal intoxication

helminthic infection of CNS

hemianopia

hemianopia, homonymous

heralding manifestation

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

histochemistry of muscle

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

homosexual

hot bath test

human immunodeficiency virus type 1

human immunodeficiency virus type 1, pathogenesis

hydrocephalus

hydrocephalus, non-communicating(obstructive)

hydrocephalus, transient

hypokalemic periodic paralysis

hypoparathyroidism

hyporeflexia

hypothalamus

hypothalamus, disturbance of

immunology and the nervous system

inability to stand on tiptoes

inattention

inclusion bodies

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

inclusion body myositis

incoordination

INR values

intellectual deficit

interstitial pulmonary fibrosis

intracranial hypertension, benign

intracranial pressure, increased

intranasal medication

intrinsic hand muscles, wasting of

islet cell tumor

Jakob-Creutzfeldt disease

jaundice

jaw jerk, abnormal

Kearns-Sayre syndrome

klippel feil syndrome

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

kyphosis

lactate

lactic acidemia

laminar necrosis, cortical

leg weakness, bilateral

leg weakness, unilateral

leptospirosis

lethargy

leucine rich glioma inactivated 1 antibodies

leukocytosis

leukodystrophy

leukopenia

level of consciousness, decreased

lid closure, weakness of

life expectancy

limbic encephalitis

linear lesion

lipid storage disorder of CNS

liver disease

liver function enzymes

low back pain

lymphoma

lymphoma involving CNS

malignancy screen

malignancy, occult

Marinesco-Sjogren syndrome

memory, impairment of

meningeal enhancement

meningitis, cysticercosis

meningitis, eosinophilic

meningitis, leptospira

meningitis, neutrophilic

meningoencephalitis

mental retardation

mental status, abnormal

mitochondrial disease

mitochondrial encephalomyopathy

mixed connective tissue disease

MNGIE syndrome

molecular genetics

monoclonal gammopathy

monomelic myositis

mononeuropathy

mononeuropathy multiplex

movement disorder, drug induced

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, muscle

MRI, perfusion

MRI, sulcal hyperintensity

MRI, susceptibility weighted

MRS

multiple myeloma

muscle atrophy, focal

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle hypertrophy

muscle hypertrophy, congenital

muscle pain

muscle stiffness

muscle swelling

muscle swelling, focal

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, diagnosis

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, paraneoplastic

myoclonus, stimulus sensitive

myopathy, carcinomatous

myopathy, distal

myopathy, distal, vacuolar

myopathy, distal, Welander's

myopathy, focal

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, inclusion body, hereditary

myopathy, inflammatory

myopathy, metabolic

myopathy, mitochondrial

myopathy, monomelic

myopathy, necrotizing

myopathy, quadriceps

myopathy, radiation-induced

myopathy, thyroid disease causing

myopathy, vacuolar

myositis

myositis, bacterial

myositis, eosinophilic

myositis, focal

myositis, fungal

myositis, granulomatous

myxedema, neurologic manifestations of

nerve conduction studies

nerve hypertrophy

neuritis, causes of

neuritis, heavy metals causing

neuroendocrinology

neurofibrillary degeneration

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuronal cell surface antigen

neuronopathy, sensory

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, motor, multifocal

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, short-fiber

ocular myopathy, differential diagnosis

old age, neurology of

onconeural antibodies

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

opsoclonus-myoclonus syndrome

paralysis, acute areflexic

paralysis, asymmetric

paraneoplastic cerebellar degeneration

paranoia

paraplegia

paraproteinemia

parasitic infection, CNS

paraspinal muscle

paraspinal muscle weakness

peripheral blood smear

peripheral blood smear, abnormal

peripheral nerve, lesion of

PLEDs, bilateral independent

PLEDs, etiology of

pleocytosis of cerebrospinal fluid

pleural effusion

POEMS syndrome

poliomyelitis

poliomyelitis vaccine

poliomyelitis-like illness

polymerase chain reaction

polymerase chain reaction, false negative

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, familial

polyradiculoneuropathy

polyuria

pons, lesion of

porphyria

position sensation, abnormal

positive sharp waves

posterior interosseous neuropathy

postural abnormality

prevention of neurologic disorders

primary aldosteronism

prion disease

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive supranuclear palsy

proprioception, abnormal

proteinuria

proximal muscle atrophy

pseudobulbar palsy

pseudohypertrophy

psychiatric problems in neurologic disorders

psychological testing

pupil, abnormality in neurologic disorders

radiation therapy, CNS treatment and complications with

radiculopathy

ragged-red fibers

rapidly progressing neurologic illness

real-time quaking-induced conversion

Red flags

remote effect of cancer on the nervous system

renal failure

repetitive nerve stimulation

respiratory failure

respiratory tract infection

Schwartz-Jampel syndrome

sedimentation rate, elevated

seizure

seizure, focal

sensorineural hearing loss

serologic testing

short stature

shunt procedure, ventricular

sicca syndrome

single-fiber electromyography

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

spinal cord, lesion of

steroid therapy, CNS treatment and complications with

sweating, abnormality of

symmetric brain lesions

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tandem gait, ataxic

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

tensilon test, false positive

tetany

thalamus, infarction, bilateral

thalamus, lesion of

thirst

thoracic outlet syndromes

thrombocytopenia

thymoma

thyrotoxicosis

tongue, fasciculations of

tongue, weakness

torticollis

torticollis, post traumatic

toxoplasmosis, CNS

transient ischemic attack

trauma

travel, foreign

treatment of neurologic disorder

urine test in toxic screen

visual evoked response

visual field defect

visual loss

walking, difficulty with

weakness, generalized

weakness, progressive

weakness, proximal

weight loss

Werdnig-Hoffman disease

Showing articles 50 to 100 of 2801 << Previous Next >>

Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
Ann Int Med 116:896-900, Coleman,R.A.,et al, 1992

The Dropped Head Syndrome
Neurol 42:1625-1627, Suarez,G.A.&Kelly,J.J., 1992

Chronic Limb-Girdle Myasthenia Gravis
Neurol 42:1153-1156, Oh,S.J.&Kuruoglu,R., 1992

Poliomyelitis-Like paralysis During Recovery from Acute Bronchial Asthma:Possible Etiology and Risk Fators
Pediatrics 88:276-279, Shahar,E.M.,et al, 1991

Staphylococcal Pyomyositis in Patients Infected by the Human Immunodeficiency Virus
Am J Med 90:595-600, Schwartzman,W.A.,et al, 1991

Pyomyositis in Patients with the Human Immunodeficiency Virus:An Unusual Form of Disseminated Bacterial Infection
Am J Med 91:129-136, Widrow,C.A.,et al, 1991

Autosomal Recessive Distal Dystrophy
Neurol 41:1365-1370, Barohn,R.J.,et al, 1991

Congenital Monomelic Hypertrophy with Progressive Myopathy
Arch Neurol 48:107-110, Shukla,A.,et al, 1991

Cervical Dystonia:Clinical Findings and Associated Movement Disorders
Neurol 41:1088-1091, Jankovic,J.,et al, 1991

Cerebral Cortex and Brainstem Involvement in Marinesco-Sjogren Syndrome
Ann Neurol 27:448-449, Katafuchi,Y.,et al, 1990

Quadriceps Myopathy:Forme Fruste of Becker Muscular Dystrophy
Ann Neurol 28:634-639, Sunohara,N.,et al, 1990

A Disorder of Azonal Development, Necrotizing Myopathy, Cardiomyopathy, and Cataracts:A New Familial Disease
Ann Neurol 27:193-199, Lyon,G.,et al, 1990

Life-Threatening Cranial Dystonia Following Trihexyphenidyl Withdrawal
Movement Disorders 4:349-353, Gimenez-Roldan,S.,et al, 1989

Antecollis in Parkinsonism
Lancet 1:1320-1321, Jorens,P.G.,et al, 1989

The Lambert-Eaton Myasthenic Syndrome, A Review of 50 Cases
Brain 111, 577-5961988., O'Neill,J.H.,et al, 1988

Pyomyositis in a Patient with the Acquired Immunodeficiency Syndrome
Arch Int Med 148:1608-1610, Gaut,P.,et al, 1988

MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission
Neurol 38:751-754, Montagne,P.,et al, 1988

Spectrum of Inclusion Body Myositis
Arch Neurol 44:1154-1157, Ringel,S.P.,et al, 1987

Acute Arsenic Intoxication Presenting as Guillain-Barre-Like Syndrome:Donofrio
P. D. , et al, Muscle & Nerve 10:114-120, , 1987

Cysticercosis-Review of 230 Patients
Bull Clin Neurosci 50:76-101, McCormick.G.F., 1985

Autosomal Recessive Distal Muscular Dystrophy:A Comparative Study with Distal Myopathy with Rimmed Vacuole Formation
Ann Neurol 17:51-59, Nonaka,I.,et al, 1985

Inflammatory Myopathies
Ann Neurol 17:215-227, 317-3231985., Mastaglia,F.L.,et al, 1985

Unilateral Myopathy:An Unusual Presentation of Thyrotoxicosis
BMJ 288:1124, Gimlette,T.,et al, 1984

Distal Myopathy, Histochemical & Ultrastructural Studies
Arch Neurol 39:367-371, Kumamoto,T.,et al, 1982

Polymyositis Beginning as a Focal Process
Arch Neurol 38:439-442, Heffner,R.R.Jr.,et al, 1981

Eosinophilic Myositis, An Unusual Cause of Pseudotumor & Eosinophilia
JAMA 246:70-71, Agrawal,B.L.,et al, 1981

Chronic Focal Polymyositis in the Adult
JNNP 44:419-425, Bharucha,N.E.,et al, 1981

Focal Neurologic symptoms in hypercalcemia
Neurol 30:200-201, Longo,D.L.,et al, 1980

Quadriceps Myopathy in Two Brothers
Rhode Island Med J 62:125, Finelli,P.F., 1979

A Case of Schwartz-Jampel Syndrome with Unusual Muscle Biopsy Findings
Ann Neurol 3:93, Fariello,R.,et al, 1978

Chronic Neurogenic Quadriceps Amyotrophy
Ann Neurol 2:528, Furukawa,T.,et al, 1977

Progressive Supranuclear Palsy-Case Study
NEJM 293:346, Richardson,E.P., 1975

Quadriceps Myopathy-Entity or Syndrome
Arch Neurol 31:60, Boddie,H.,et al, 1974

Neurological Problems in Endocrine Diseases
Med Clin North Am 56:1029, Dale,A., 1972

Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
The New Physic 263, 1967, Oct., Boshes,L., 1967

CT Perfusion Abnormality in Hypoglycemic Focal Neurological Deficits
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Niemann-Pick Type C Disease
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A 49-Year-Old Man with Meningoencephalitis and Persistent Altered Mental Status
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A 67-Year-Old Man with Exercise Intolerance nd Progressive Weakness
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Status Epilepticus After Carotid Endarterectomy:An Illustrative Case of Cerebral Hyperfusion Syndrome
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An 81-Year-Old Woman with Chronic Isolated Neck Extensor Weakness
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Inflammatory Myopathies
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Melas Syndrome
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High-Grade Gliomas with Autoimmune Encephalitis-Like Presentation: Case Report and Systematic Review of the Literature
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Niemann-Pick Disease Type C
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From Stroke Workup to Mitochondrial Disease: A Case Report of MELAS
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MELAS Presenting as Bilateral Symmetric Occipital and Temporal Cortices Lesions, A Case Report and Literature Review
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Clinicopathologic Features, Pathogenesis, and Treatment of Monoclonal Gammopathy-Associated Myopathies
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A 40-Year-Old Man With Refractory Status Epilepticus After Small Bowel Resection for Volvulus
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Tiger Man Sign in Sarcoid Myopathy
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