Neudle.com: muscle weakness insidious onset of

Differential
(Click to cross reference)

abdominal distention

abdominal muscle paralysis

abdominal protrusion

abscess, brainstem

abscess, intracerebral

abscess, lung

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome-related complex

acute intermittant porphyria

acyl CoA dehydrogenase deficiency

addiction, heroin

addiction, heroin-neurologic complications with

adult polyglucosan body disease

advances in neurology

adverse drug reaction

alcoholism

alternating rapid movement, impaired

amyloid

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

anasarca

anemia

anemia, megaloblastic

aneurysm

aneurysm, abdominal aortic

aneurysm, aortic arch

aneurysm, intracranial

anterior horn cell disease

anterior tibial muscle weakness

anti DNA agent

anti GQ1b IgG antibody

anti signal recognition particle antibody

antibodies to voltage-gated calcium channels

antiganglioside antibodies

aspartate aminotransferase

atrioventricular block

atypical

autoantibodies

autoimmune disease

autonomic dysfunction

basophilic stippling of red blood cells

brachial neuritis, acute

brachial neuritis, bilateral

brachial plexus neuropathy

brachial plexus neuropathy, bilateral

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

brain natriuretic peptide

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

Brown-Vialetto-Van Laere syndrome

brucellosis

brucellosis, nervous system involvement with

campylobacter infection

cardiovascular disease

carnitine deficiency myopathy

cauda equina, enhancement

cauda equina, lesion of

CD4 counts

central nervous system, infection of

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebral cortical atrophy

cerebral embolism

cerebral venous thrombosis

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, location of

cerebrovascular accident, recurrent

cerebrovascular accident, topographic pattern

cerebrovascular disease

Charcot-Marie-Tooth

chelation therapy

chemotherapy, CNS treatment and complications with

chest pain

chest x-ray, abnormal

chronic progressive external ophthalmoplegia

Churg-Strauss syndrome

Clinical Pathologic Conference(C.P.C.)

congenital heart disease

controversies in neurology

conversion reaction

copper

copper deficiency

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

degenerative diseases of CNS

delay in diagnosis

delirium

dementia

dementia, frontotemporal

demyelinating disease

denervation of muscle

denervation potentials

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diabetes mellitus, chemical

diagnostic criteria

diaphragmatic paralysis

diarrhea

diarrhea, bloody

differential diagnosis

difficulty climbing stairs

diplegia, brachial

diplopia

disorientation

distal muscle atrophy

distal muscle weakness

dizziness

down-beat nystagmus

dropped head syndrome

drug abuse

drug abuse, neurologic complications of

drug induced neurologic disorders

dyskinesia, buccal lingual facial

dystrophin associated proteins

efficacy

electrocardiogram, abnormal

electrocorticogram

electroencephalogram, abnormalities of

electromyogram

electromyogram, decremental response

electromyogram, incremental response

electron microscopy

electronystagmography

electrophoretic pattern, serum

Emery-Dreifuss muscular dystrophy

empty sella

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, episodic

encephalitis, Powassan

encephalitis, Rasmussen's

enzyme, muscle disease

enzyme, serum

eosinophilia

eosinophilic granulomatosis with polyangiitis

epidemiology of neurology

epilepsia partialis continua

episodic disorders

episodic neurologic deficits

epistaxis

exercise

exercise intolerance

exercise-related muscle strength increase

extraocular muscle lesion

eye movement, disorders of

facial nerve palsy

facial nerve palsy, recurrent

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failed medical management

fine motor function, impaired

foot drop, differential diagnoses of

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastric partitioning

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

genetic diagnosis, prenatal

genetic neurologic disorders

glucose tolerance test, abnormal

glycogen storage disease

GM1 ganglioside antibodies

Google

Gowers maneuver

granuloma, eosinophilic

granulomatous disease

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, complications

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, prognosis of

Guillain Barre syndrome, variant forms of

gynecomastia

hallucination, auditory

heart block, complete

heart murmur

heliotrope rash

hemiatrophy, cerebral

hemidiaphragm, paralysis of

hemiparesis

hemiplegia

hemiplegia, progressive

hemispherectomy

hemorrhagic diathesis

hepatomegaly

hepatosplenomegaly

heralding manifestation

hereditary myopathy with early respiratory failure

herpes simplex virus

herpes virus

herpes virus infection

herpes, genital

hiccoughs

high arched feet

highly active antiretroviral therapy

hip pain

histochemistry of muscle

HMGcoA reductase inhibitors

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

homocysteine, serum

homosexual

H-reflex testing

human diploid cell rabies vaccine

human immunodeficiency virus type 1

hypertension, intracranial causes of

hypertension, paroxysmal

hyperviscosity

hypoglycorrhachia

hypokalemia

hypokalemic paralysis

hypokinesia

hyponatremia

hyponatremia with cerebral disorders

hypoosmolality of serum

hypotension, systemic

hypotonia

hypotonia, infants

iatrogenic neurologic disorders

immunosuppressive agents

inability to sit up

inappropriate antidiuretic(A.D.H.)hormone

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inborn errors of metabolism

inclusion bodies

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

infant, evaluation of

infection

intellectual deterioration

internet

intestinal pseudoobstruction

intracerebral hemorrhage

intrauterine

intrinsic hand muscles, wasting of

lactic dehydrogenase(LDH)

lacunar infarction

lacunar infarction, progressive

learning disability, in children

leg numbness

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

leukemia

leukemia, neurologic findings assoc.with

leukocytosis

leukodystrophy

leukoencephalopathy

level of consciousness, decreased

Lhermitte's sign

lid closure, weakness of

life expectancy

limbic encephalitis

liver function enzymes

lymphadenopathy, hilar

lymphadenopathy, paraaortic

lymphoma

lymphoma involving CNS

macroglobulinemia

malabsorption

malaise

malformation, vascular

malignant hyperpyrexia

malignant papulosis

Man-In-The-Barrel syndrome

masseter muscle wasting

mediastinum, mass of

medulla oblongata, lesion of

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningeal enhancement

meningismus

meningitis, basilar

meningoencephalitis

mental status, abnormal

methylmalonic acid, serum

methylmalonic acidemia

mitochondrial disease

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

MNGIE syndrome

molecular genetics

monoclonal gammopathy

mononeuritis multiplex

mononeuritis multiplex, causes of

mononeuropathy

mortality

Morvan's fibrillary chorea

motor neuron disease

motor symptoms

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, brachial plexus

MRI, contrast enhanced

MRI, diffusion weighted

MRI, fetal

MRI, muscle

MRI, peripheral nerve

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRS

multiple sclerosis

muscle atrophy, focal

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle hypertrophy

muscle pain

muscle stiffness

muscle strength, testing

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

muscle weakness, insidious onset of

muscle weakness, intermediate onset of

muscle weakness, proximal

muscle weakness, sudden onset 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, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, dystrophin normal

muscular dystrophy, facioscapulohumeral

muscular dystrophy, female occurrence of

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, treatment of

myasthenic syndrome

mycobacterial infection

mycobacterium bovis

mycotic aneurysm

myelitis, longitudinal

myelopathy, chronic progressive

myopathy, critically ill

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, genetic

myopathy, hereditary

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, inclusion body, hereditary

myopathy, inflammatory

myopathy, metabolic

myopathy, mitochondrial

myopathy, myofibrillar

myopathy, necrotizing

myopathy, necrotizing, autoimmune

myopathy, necrotizing, immune-mediated

myopathy, steroid induced

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, intracranial

neoplasm, intracranial assoc.with systemic hypertension

neoplasm, primary of CNS

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve root biopsy

nerve root enhancement

nerve root hypertrophy

neuroendocrinology

neurogenic bladder

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuromyelitis optica (Devic's disease)

neuromyelitis optica spectrum disorder

neuromyotonia

neuronal intranuclear inclusion disease

neuropathy, asymptomatic

neuropathy, hereditary peripheral

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, peripheral

neuropathy, sensory

neuropathy, toxic

neurotoxic

newborn, evaluation of

next-generation sequencing

nitrous oxide

numbness, ascending

numbness, extremity

numbness, generalized

nusinersen

nutritional deficiency

nystagmus

ocular motility, disorders of

oculopharyngeal muscular dystrophy

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

pacemaker, cardiac-transvenous

paralysis, asymmetric

paraparesis

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

paresthesias

paresthesias, feet

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinsonism syndrome

PAS positive

PAS positive material in the brain

pathology

pedicles of vertebrae, erosion of

periarteritis nodosa

perineurioma

peripheral blood smear

phosphorylase b kinase deficiency

plasmapheresis

PLEDs

PLEDs, bilateral independent

pleocytosis of cerebrospinal fluid

pleural effusion

POLG1 gene

polyglucosan body

polyglucosan body disease

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic inflammatory demyelinating, childhood

polyneuropathy, subacute idiopathic demyelinating

pons, infarction of

porphyria

positive sharp waves

posterior column disease

postural abnormality

precipitating factors

pregnancy, neurologic complications in

prenatal

prenatal diagnosis by amniocentesis

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive spinal muscular atrophy

proprioception, abnormal

proteinuria

protozoan infection

proximal muscle atrophy

pruritus

pseudobulbar palsy

pseudomyotonia

psychiatric problems in neurologic disorders

pulmonary infiltrates

pulmonary nodules

pupil, abnormality in neurologic disorders

pupil, dilated, bilateral

pyramidal tract

pyramidal tract dysfunction

quadriparesis

quadriparesis, acute

quadriparesis, progressive

quadriplegia

quadriplegia, transient

quality of life

rabies, nervous system involvement with

radiation therapy, CNS treatment and complications with

radiculopathy

ragged-red fibers

rapidly progressing neurologic illness

remote effect of cancer on the nervous system

renal failure

renal tubular acidosis

repetitive nerve stimulation

respirator

respiratory failure

respiratory tract infection

reversible neurologic disorder

review article

rhabdomyolysis

riboflavin

riboflavin transporter deficiency

scoliosis, neurologic association with

screening

season

sedimentation rate

sedimentation rate, elevated

seizure, surgical treatment of

seizure, treatment of

sensorineural hearing loss

sensory loss

sensory loss, band distribution

sensory loss, patchy

serum alanine aminotransferase

sex reassignment surgery

skin, lesions in neurologic disorders

sloped shoulders

slow virus infection of CNS

small vessel disease

small vessel vasculitis

small-bowel resection

speech disorder, childhood

speech, delayed development of

spinal cord, cervical

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, extramedullary

spinal cord, neoplasm, intramedullary

spinal cord, vascular malformation of

spinal muscular atrophy

spinal muscular atrophy, classification

steroid therapy, CNS treatment and complications with

stooped posture

stroke, progression of

subarachnoid hemorrhage

sudden death

suspended sensory loss

syringomyelia

systemic illness

systemic lupus erythematosus

temporalis muscle wasting

term infant

thrush

thymoma

thymus and neuromuscular function

tick bite

tick-borne encephalitis

tongue, fasciculations of

tongue, weakness

tonsillar herniation of cerebellum

torticollis

transgender

transient ischemic attack

transverse smile

treatment of neurologic disorder

urine osmolality, elevated

vibratory sensation, abnormal

vincristine neurotoxicity

Waldenstrom's macroglobulinemia

walking frame

walking, difficulty with

Watson-Schwartz reaction

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

x-linked myopathy with excessive autophagy

zinc

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