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Differential
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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

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

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

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

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

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

hyponatremia

hyponatremia with cerebral disorders

hypoosmolality of serum

iatrogenic neurologic disorders

immunosuppressive agents

inability to sit up

inappropriate antidiuretic(A.D.H.)hormone

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

inclusion bodies

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

infection

intellectual deterioration

internet

intestinal pseudoobstruction

intracerebral hemorrhage

intrinsic hand muscles, wasting of

lactic dehydrogenase(LDH)

lacunar infarction

lacunar infarction, progressive

lead poisoning

learning disability

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, muscle

MRI, peripheral nerve

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRS

multiple sclerosis

muscle atrophy, focal

muscle atrophy, progressive

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

myelogram, cervical

myeloneuropathy

myelopathy

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

neuroendocrinology

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

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

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

pedicles of vertebrae, erosion of

periarteritis nodosa

perineurioma

peripheral blood smear

phosphorylase b kinase deficiency

plasmapheresis

PLEDs

PLEDs, bilateral independent

pleocytosis of cerebrospinal fluid

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 diagnosis by amniocentesis

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive spinal muscular atrophy

proprioception, abnormal

proteinuria

protozoan infection

proximal muscle atrophy

pruritus

pseudomyotonia

psychiatric problems in neurologic disorders

pulmonary infiltrates

pulmonary nodules

pupil, abnormality in neurologic disorders

pupil, dilated, bilateral

pyramidal tract dysfunction

quadriparesis

quadriparesis, acute

quadriparesis, progressive

quadriplegia

quality of life

rabies, nervous system involvement with

radiation therapy, CNS treatment and complications with

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

SMN1 gene

solitary scerlosis

somnolence

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

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

weakness, acute

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

x-linked myopathy with excessive autophagy

zinc

Showing articles 0 to 50 of 3825 Next >>

A 60-Year Old Man with Asymmetric Weakness and Persistent Fever
Neurol 100:530-536, Zheng,Y.,et al, 2023

A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
Neurol 100:631-637, Zeng,T.f.,et al, 2023

Clinicopathologic Conference, Functional Vitamin B12 Deficiency from Use of Nitrous Oxide
NEJM 388:1893-1900, Case 15-2023, 2023

A Young Woman with Rapidly Progressive Weakness and Paresthesia
Neurol 101:676-681, Alwakeel,S.S.,et al, 2023

Miller Fisher Syndrome and Acute Motor and Sensory Axonal Neuropathy (AMSAN) Variant Guillain-Barre Overlap Syndrome (MFS/AMSAN-GBS) After Upper Respiratory Tract Infection (URTI)
Acta Sci Clin Case Reports 3:19-24, Chau,T.C. & Muhamad,N.A.N., 2022

A 36-Year-Old Man With Asymmetric Muscle Weakness
Neurol 99"1057-1061, Harada,Y.,et al, 2022

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

A 59-Year-Old Man with Progressive Proximal Weakness Since Childhood
Neurol 97:958-963, Davalos, L.,et al, 2021

Clinicopathologic Conference, Disseminated Mycobacterium Bovis Infection
NEJM 384:651-662, Case 5-2021, 2021

A 68-Year-Old Man with Proximal Weakness and Seizures
Neurol 97:e423-e428, Chen, T., 2021

Bilateral Ptosis, Dysphagia, and Progresive Weakness in a Patient of French-Canadian Background
Neurol 95:933-938, Paul,P.,et al, 2020

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

Muscular Dystrophies
Lancet 394:2025-2038, Mercuri, E.,et al, 2019

A 54-year-old man with Dyspnea and Muscle Weakness
Neurol 92:e1136-e1140, Chertcoff, A.,et al, 2019

Clinicopathologic Conference, Amyotrophic Lateral Sclerosis
NEJM 380:1566-1574, Case 12-2019, 2019

Clinicopathologic Conference, Statin-Associated Autoimmune Myopathy
NEJM 381:275-283, Case 22-2019, 2019

A 65-year-old man with Asymmetric Weakness and Parethesias
Neurol 93:856-861, Harada, Y.,et al, 2019

Progressive Proximal Weakness in a 56-year-old Man with Bone Pain
Neurol 93:939-944, Torabi,T.,et al, 2019

Neuromyelitis Optica Spectrum Disorder (NMOSD) in a Male with Hiccups and Quadriparesis
IJCMR 5:K28-K30, Tuteja,H.S.,et al, 2018

Clinical Reasoning: A 49-year-old man with Progressive Numbness, Weakness, and Evidence of Leptomeningeal Enhancement
Neurol 90:e90-e93, Lovett, A.,et al, 2018

Subacute Paresis in a 28-year-old man with HIV
Neurol 90:432-435, Harada, Y.,et al, 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

Progressive Weakness and Memory Impairment in a Middle-aged Man
JAMA 320:197-198, DeFilippis, E.M.,et al, 2018

A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
Neurol 91:187-190, Silva,A.M.S.,et al, 2018

A Man with Rapidly Progressive Weakness and Respiratory Failure
Neurol 91:e686-e691, Xu,D.,et al, 2018

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
Neurol 88:e185-e189, Vazquez do Campo, R.,et al, 2017

A Case of Statin-Associated Autoimmune Myopathy
Clin Med Insights: Case Reports 10:1-4, Sweidan, A.J.,et al, 2017

A 30-year-old Man with Progressive Weakness and Atrophy
Neurol 87:e227-e230, Quinn, C.,et al, 2016

Rapidly Progressive Quadriplegia and Encephalopathy
JAMA Neurol 73:1363-1366, Wynn, D.,et al, 2016

Statin-Associated Autoimmune Myopathy
NEJM 374:664-669, Mammen, A.L., 2016

A 44-year-old Woman with Rapidly Progressive Weakness and Ophthalmoplegia
Neurol 85:e22-e27, Schreck, K.C.,et al, 2015

Motor Neurone Disease
BMJ 349:g4052, Nageshwaran, S.,et al, 2014

A 52-year-old Woman with Progressive Proximal Weakness
Neurol 83:e106-e109, Enduri, S.,et al, 2014

Clinicopathologic Conference, Chronic Meningoencephalitis Consistent with Rasmussens Encephalitis
NEJM 371:1737-1746, Case 34-2014, 2014

Mystery Case: A 63-year-old Man with Progressive Proximal Pain and Weakness
Neurol 82:e26-e29, Scripko, P.D.,et al, 2014

Clinical Case Conference: A 41-Year-Old Woman with Progressive Weakness and Sensory Loss
Ann Neurol 75:9-19, Stephen, C.D.,et al, 2014

Chronic and Slowly Progressive Weakness of the Legs and Hands
BMJ 348:g459, Nightingale, H.,et al, 2014

A 20-year-old Woman with Rapidly Progressive Weakness
Neurol 82:e200-e204, Paganoni, S.,et al, 2014

Clinicopathologic Conference, Dermatomyositis. Malignant Atrophic Papulosis (Degoss Disease), Involving the Skin and Gastrointestinal Tract
NEJM 370:2327-2337, Case 18-2014, 2014

Degenerative Diseases of the Nervous System, Amyotrophic Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1109, Ropper, A.H.,et al, 2014

The Limbic-Girdle Muscular Dystrophies
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Peripheral Neuropathy - Lead Astray?
LANCET 381:1156, Pickrell, W.,et al, 2013

A Case of Necrotizing Myopathy with Proximal Weakness and Cardiomayopathy
Neurol 78:1527-1532, Matthews,E.,et al, 2012

Guillain-Barre Syndrome
NEJM 366:2294-2304, Yuki, N. & Hartung, H.P., 2012

Topographic Location of Acute Pontine Infarction is Associated with the Development of Progressive Motor Deficits
Stroke 43:708-713, Oh,S.,et al, 2012

Solitary Sclerosis
Neurol 78:540-544, Schmalstieg,W.F.,et al, 2012

Clinicopathologic Conference,Necrotizing Noninflammatory Myopathy Consistent with Exposure to Statins
NEJM 36:944-954, Case 7-2012, 2012

Progressive Weakness with Respiratory Failure in a Patient with Sarcoidosis
Arch Neurol 69:534-537, Chaudhry,P.,et al, 2012

Showing articles 0 to 50 of 3825 Next >>