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Differential
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abdominal distention

abdominal muscle paralysis

abdominal protrusion

abscess, brainstem

abscess, intracerebral

acetylcholine receptor antibody

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

alternating rapid movement, impaired

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

anemia, megaloblastic

aneurysm, abdominal aortic

aneurysm, aortic arch

aneurysm, intracranial

ankle reflex, absent

ankle, swelling of

anoctaminopathy

antecedent illness

anterior horn cell disease

anterior tibial muscle weakness

anti GQ1b IgG antibody

anti signal recognition particle antibody

antibodies to voltage-gated calcium channels

antiganglioside antibodies

antiviral agents

aorta, abdominal

aorta, abnormal

ascending paralysis

aspartate aminotransferase

ataxia, cerebellar

ataxia, progressive

atrioventricular block

autoimmune disease

autonomic dysfunction

axonal degeneration

B 12 deficiency

bacterial infection

basilar artery stenosis

basophilic stippling of red blood cells

Behcet's syndrome

bent spine syndrome

Bing-Neel syndrome

biologic markers

bladder dysfunction

bone marrow biopsy

brachial neuritis

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, nervous system involvement with

burning paresthesia

calf hypertrophy

campylobacter infection

carcinoma of bladder

carcinoma of lung

cardiovascular disease

carnitine deficiency myopathy

CAT scan, abdomen

CAT scan, abnormal

CAT scan, chest

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, muscle

cauda equina, enhancement

cauda equina, lesion of

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

cerebrospinal fluid, proteincytologic dissociation

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 x-ray, abnormal

chewing, impaired

choreoathetosis

chronic progressive external ophthalmoplegia

Churg-Strauss syndrome

cigarette smoking

Clinical Pathologic Conference(C.P.C.)

cold temperature

conduction block

congenital heart disease

congenital myopathy

contractures, joint

controversies in neurology

conversion reaction

copper deficiency

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

cricopharyngeal bar

critical care unit

cyclic vomiting

cystoisospora belli

cytosine arabinoside

deep tendon reflexes

degenerative diseases of CNS

delay in diagnosis

dementia, frontotemporal

demyelinating disease

denervation of muscle

denervation potentials

dermatomyositis

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diabetes mellitus, chemical

diagnostic criteria

diaphragmatic paralysis

diarrhea, bloody

differential diagnosis

difficulty climbing stairs

diplegia, brachial

distal muscle atrophy

distal muscle weakness

down-beat nystagmus

dropped head syndrome

drug abuse, neurologic complications of

drug induced neurologic disorders

dysdiadochokinesia

dysferlinopathy

dyskinesia, buccal lingual facial

dystroglycanopathies

dystrophin associated proteins

electrocardiogram, abnormal

electrocorticogram

electroencephalogram, abnormalities of

electromyogram, decremental response

electromyogram, fasciculation potentials

electromyogram, incremental response

electron microscopy

electronystagmography

electrophoretic pattern, serum

Emery-Dreifuss muscular dystrophy

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, episodic

encephalitis, Powassan

encephalitis, Rasmussen's

encephalitis, viral

enzyme, muscle disease

eosinophilic granulomatosis with polyangiitis

epidemiology of neurology

epilepsia partialis continua

episodic disorders

episodic neurologic deficits

exercise intolerance

exercise-related muscle strength increase

exome sequencing

extraocular muscle lesion

eye movement, disorders of

facial nerve palsy

facial nerve palsy, recurrent

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failed medical management

failure to thrive

fatigable chewing

fine motor function, impaired

Fisher's syndrome

flaccid paralysis

flu-like illness

foot drop, bilateral

foot drop, differential diagnoses of

F-wave response

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastric partitioning

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

geographic location

gliomatosis cerebri

glucose tolerance test, abnormal

glycogen storage disease

GM1 ganglioside antibodies

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

hallucination, auditory

headache, positional

heart block, complete

heliotrope rash

hemiatrophy, cerebral

hemidiaphragm, paralysis of

hemiplegia, progressive

hemispherectomy

hemorrhagic diathesis

hepatosplenomegaly

heralding manifestation

hereditary myopathy with early respiratory failure

herpes simplex virus

herpes virus infection

herpes, genital

high arched feet

highly active antiretroviral therapy

histochemistry of muscle

HMGcoA reductase inhibitors

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

homocysteine, serum

H-reflex testing

human diploid cell rabies vaccine

human immunodeficiency virus type 1

hydroxychloroquine

hyperhomocysteinemia

hypertension, intracranial causes of

hypertension, paroxysmal

hypoglycorrhachia

hypokalemic paralysis

hyponatremia with cerebral disorders

hypoosmolality of serum

hypopituitarism

hypotension, systemic

hypotonia, infants

iatrogenic neurologic disorders

ileus, paralytic

immunohistochemistry

immunomodulation

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

intellectual deterioration

intestinal pseudoobstruction

intracerebral hemorrhage

intrinsic hand muscles, wasting of

iododeoxyuridine

jaw jerk, abnormal

lactic dehydrogenase(LDH)

lacunar infarction

lacunar infarction, progressive

laughing, pathologic

learning disability

learning disability, in children

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

leukemia, neurologic findings assoc.with

leukoencephalopathy

level of consciousness, decreased

Lhermitte's sign

lid closure, weakness of

life expectancy

limbic encephalitis

liver function enzymes

lung transplantation

lymph node biopsy

lymphadenopathy

lymphadenopathy, hilar

lymphadenopathy, paraaortic

lymphoma involving CNS

macroglobulinemia

malformation, vascular

malignancy screen

malignant hyperpyrexia

malignant papulosis

Man-In-The-Barrel syndrome

masseter muscle wasting

McLeod syndrome

mediastinum, mass of

medulla oblongata, lesion of

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, basilar

meningoencephalitis

mental status, abnormal

methylmalonic acid, serum

methylmalonic acidemia

mitochondrial disease

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

molecular genetics

monoclonal gammopathy

mononeuritis multiplex

mononeuritis multiplex, causes of

Morvan's fibrillary chorea

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, brachial plexus

MRI, contrast enhanced

MRI, diffusion weighted

MRI, peripheral nerve

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

multiple sclerosis

muscle atrophy, focal

muscle atrophy, progressive

muscle diseases, characteristics of

muscle hypertrophy

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

myelogram, cervical

myeloneuropathy

myelopathy, chronic progressive

myelopathy, tract-specific

myeloradiculopathy

myopathy, amyloid

myopathy, autoimmune

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

myopathy, toxic

myopathy, vacuolar

myositis, ocular

myotonic discharges

nausea and vomiting

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, intracranial

neoplasm, intracranial assoc.with systemic hypertension

neoplasm, primary of CNS

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

neuronal intranuclear inclusion disease

neuropathy, acute

neuropathy, asymptomatic

neuropathy, hereditary peripheral

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, peripheral

neuropathy, sensory

neuropathy, toxic

newborn, evaluation of

next-generation sequencing

numbness, ascending

numbness, extremity

numbness, generalized

nutritional deficiency

ocular motility, disorders of

oculopharyngeal muscular dystrophy

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

oral contraceptives

overlap syndrome

pacemaker, cardiac-transvenous

Paget's disease

pain, abdominal

pain, total body

paralysis, acute

paralysis, asymmetric

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

paresthesias, feet

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinsonism syndrome

PAS positive material in the brain

pedicles of vertebrae, erosion of

periarteritis nodosa

peripheral blood smear

pernicious anemia

personality change

pheochromocytoma

phosphorylase b kinase deficiency

PLEDs, bilateral independent

pleocytosis of cerebrospinal fluid

pleural effusion

polyglucosan body

polyglucosan body disease

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic inflammatory demyelinating, childhood

polyneuropathy, subacute idiopathic demyelinating

pons, infarction of

positive sharp waves

posterior column disease

postural abnormality

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive spinal muscular atrophy

proprioception, abnormal

protozoan infection

proximal muscle atrophy

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychosis, acute

psychotic behavior

ptosis, bilateral

pulmonary embolism

pulmonary infiltrates

pulmonary nodules

pupil, abnormality in neurologic disorders

pupil, dilated, bilateral

purkinje cell cytoplastic autoantibody

pyramidal tract

pyramidal tract dysfunction

quadriparesis, acute

quadriparesis, progressive

quadriplegia, transient

quality of life

rabies, nervous system involvement with

radiation therapy, CNS treatment and complications with

ragged-red fibers

rapidly progressing neurologic illness

regional enteritis

release phenomena

remote effect of cancer on the nervous system

renal tubular acidosis

repetitive nerve stimulation

respiratory failure

respiratory tract infection

retina, abnormal

retinal hemorrhages

retroperitoneal mass

reversible neurologic disorder

riboflavin transporter deficiency

sarcoidosis, CNS

sclerosis, bone

scoliosis, neurologic association with

sedimentation rate

sedimentation rate, elevated

seizure, intractable

seizure, repetitive

seizure, surgical treatment of

seizure, treatment of

sensorineural hearing loss

sensory loss, band distribution

sensory loss, patchy

serum alanine aminotransferase

sex reassignment surgery

Sheehan's syndrome

shoulder, pain in

skin, lesions in neurologic disorders

sloped shoulders

slow virus infection of CNS

small vessel disease

small vessel vasculitis

small-bowel resection

solitary scerlosis

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

standing difficulty

steroid therapy, CNS treatment and complications with

stooped posture

stroke, progression of

subarachnoid hemorrhage

suspended sensory loss

systemic illness

systemic lupus erythematosus

temporalis muscle wasting

thrombophlebitis

thymus and neuromuscular function

tick-borne encephalitis

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, weakness

tonsillar herniation of cerebellum

transient ischemic attack

transverse smile

treatment of neurologic disorder

treatment, empirical

tremor, postural

ulcerative colitis

unconsciousness

upgaze, paralysis of

urinary incontinence

urine osmolality, elevated

vascular endothelial growth factor

vectors of infection

vestibular migraine

vibratory sensation, abnormal

vincristine neurotoxicity

viral infection

viral infection, CNS

vision, blurred

vitamin deficiency

Waldenstrom's macroglobulinemia

walking, difficulty with

Watson-Schwartz reaction

weakness, acute

weakness, congenital

weakness, episodic

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

white matter disease

wide based gait

winging of scapula

X-linked myopathy

x-linked myopathy with excessive autophagy

Showing articles 100 to 150 of 4298 << Previous Next >>

Clinicopath Conf
Hodgkin's Disease and Guillain Barre Syndrome, Case Record 39-1990, NEJM 323:895-908990., , 1990

Adult Phosphorylase b Kinase Deficiency
Ann Neurol 28:529-538, Clemens,P.R.,et al, 1990

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

Inclusion Body Myositis, Observations in 40 Patients
Brain 112:727-747, Lotz,B.P.,et al, 1989

Hyponatremia and Inappropriate Secretion of Vasopressin (Antidiuretic Hormone) in Patients with Hypopituitarism
NEJM 321:492-496, 5381989., Oelkers,W., 1989

Duchenne Muscular Dystrophy Manifesting Carriers
Arch Neurol 46:673-675, Barkhaus,P.E.&Gilchrist,J.M., 1989

Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989

Human Immunodeficiency Virus-Associated Myopathy:Analysis of 11 Pts
Ann Neurol 24:79-84, Simpson,D.M.&Bender,A.N., 1988

Clinincopath Conf
Progressive Muscular Atrophy & Diabetic Neuromuscular Disease, Case 21-1987, NEJM 316:1326-13357., , 1987

Clinicopath Conf
Myopathy Due to Adult Acid Maltase Deficiency, 36-1986, NEJM 315:694-701986., , 1986

Facioscapulohumeral Dystrophy, in Myology, Basic & Clinical
McGraw-Hill Book Co, NY, p1251986., Munsat,T.L., 1986

Acid Maltase Deficiency
Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986

Ipecac-induced Myopathy Simulating Dermatomyositis
Neurol 32:91-94, Bennett,H.S.,et al, 1982

Neurologic Manifestations in Macroglobulinemia
In Vinken PJ, Bruyn GW, Eds, Handbook of Clin Neurol, Vol 39, North-Holland Publ Co, p. 189, Abramsky,O., 1980

The Adult Form of Acid Maltase (a-1, 4-Glucosidase) Deficiency
Ann Neurol 1:276, Karpati,G.,et al, 1977

Case Records of the MassGeneral Hospital, Case 41-1975, Acute Intermittent Porphyria
NEJM 293:817, Woods,B., 1975

Astrocytoma Mimicking the Features of Pheochromocytoms
NEJM 286:1397, Evans,C.,et al, 1972

Case Records of MGH-NEJM 286:1047
1972 Progressive Multifocal Leukoencephalopathy., , 1972

Complains of Muscle Weakness
Patient Care Clinical Concepts, 21, 1970 Jan., , 1970

Neuro CPC of MGH
Congenital Vascular Malfor. of Spinal Cord, NEJM 258:949-954958., , 1958

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,et al, 2025

A 59-Year-Old Man with Acute-Onset Encephalopathy and Aphasia
Neurol 105:e214299, Gutierrez-Abizuri,C.,et al, 2025

Clinicopathologic Features, Pathogenesis, and Treatment of Monoclonal Gammopathy-Associated Myopathies
Neurol 105:213101, Soontrapa,P.,et al, 2025

Clinicopathologic Conference, Myasthenia Gravis
NEJM 391:1441-1450, Case 32-2024, 2024

Unpacking the CNS Manifestations of Epstein-Barr Virus:An Imaging Perspective
AJNR 44:1002-1008, Soni,N.,et al, 2023

A 48-Year-Old Man With Spasticity and Progressive Ataxia
Neurol 101:e1747-e1752, Vizcarra,J.A.,et al, 2023

Progressive Camptocormia with Head Drop and Dysphagia
JAMA Neurol 80:209-210, El-Wahsh,S., et al, 2023

Re-Emergency of Poliovirus in the United States:Considerations and Implications
Ann Neurol 92:725-728, Russo,G.B.,et al, 2022

Spontaneous Subarachnoid Haemorrhage
Lancet 400:846-862, Claassen, J. & Park, S., 2022

Thyrotoxic Periodic Paralysis
UptoDate Jan, Gutmann, L. & Conwit, R., 2022

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

An 8-Year-Old with Acute Onset Ataxia
Neurol 99:305-310, McLaren, J.R.,et al, 2022

What All Physicians Need to Know About the Polio Resurgence in New York State
JAMA online e1-e3, Larkin, H., 2022

The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022

Lumbar Sediment Sign Seen in an Unusual Presentation of Meningitis
Lancet 398:1436, Hegde, A.,et al, 2021

Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
Neurol 97:813-816,801, Appleby, B.S.,et al, 2021

Congenital Cytomegalovirus Infection
BMJ 373:m1212, Pesch, M.H.,et al, 2021

A Teenager with Shortness of Breath and Difficulty Walking
Neurol 96:e2346-e2350, Liu, S.C.,et al, 2021

A 71-Year-Old Man Presenting with Acute Onset Dysarthria and Dysphagia
Neurol 96:180-184, Spagni, G.,et al, 2021

Acute Flaccid Myelitis: Cause, Diagnosis, and Management
Lancet 394:334-397, Murphy, O.C.,et al, 2021

A Case of Monocytic Pleocytosis in West Nile Virus Encephalitis and Review of the Literature
Case Reports 23:687-688, Villafuerte, B.J.,et al, 2020

Clinicopathologic conference, Vitamin D deficiency
NEJM 383:2462-2470, Case 39-2020, 2020

A 14-Year-Old Boy with Acute Weakness, Parethesias, and Headache
Neurol 95:e1285-e1289, Seese, R.R.,et al, 2020

When the Temporal Artery Biopsy is Negative
Neurologist 25:70-72, Ford, E. & Smith, J.H., 2020

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

A Headache of a Diagnosis
NEJM 379:475-479, Stern,R.M.,et al, 2018

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

A 22-year-old Man Presenting with Headache and Right Leg Jerks
Neurol 91:891-895, Schupper, A.J.,et al, 2018

Mystery Myelitis in Children
JAMA 320:2069, Kuehn, B., 2018

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

Showing articles 100 to 150 of 4298 << Previous Next >>