Neudle.com: weakness proximal

Differential
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abdominal distention

abdominal muscle paralysis

abdominal protrusion

abducens nerve paralysis

abducens nerve paralysis, bilateral

acetylcholine receptor

acetylcholine receptor antibody

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome-related complex

acromegaly

acute intermittant porphyria

acyl CoA dehydrogenase deficiency

addiction, heroin

Addison's disease

adverse drug reaction

alcohol

alcohol, heart involvement with

alcohol, neurologic complications with

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, prognosis

ANA

anemia

aneurysm

angiotensin-converting enzyme

anisocoria

ankle edema

ankle reflex, preserved

anterior horn cell disease

anterior tibial muscle weakness

anti signal recognition particle antibody

antibodies to voltage-gated calcium channels

anticholinesterase

anticonvulsants, hypersensitivity syndrome

anticonvulsants, untoward effects of

arthrogryposis multiplex

Asians

aspartate aminotransferase

atrioventricular block

atypical

autoantibodies

autoimmune disease

autonomic dysfunction

beta adrenergic blocker

bone marrow transplantation

brachial neuritis, acute

brachial neuritis, bilateral

brachial plexus neuropathy

brachial plexus neuropathy, bilateral

brachial plexus neuropathy, children

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

bradycardia

bradyphrenia

brain natriuretic peptide

bulbar palsy

bulbar palsy, acute

bulbar palsy, progressive

calcification, intracranial

calf atrophy

calf hypertrophy

camptocormia

cancer associated myopathy

canned food

carbenoxolone

carcinoma

carcinoma of esophagus

cardiovascular disease

carnitine deficiency

carnitine deficiency myopathy

carpal tunnel syndrome

CAT scan, emission, abnormal

CAT scan, false negative

cataracts

CD4 counts

central core disease

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar edema

cerebellar lesion

cerebral cortical atrophy

cerebral edema

cerebral embolism

cerebral infarction

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, eosinophilia of

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chromosomal abnormality

chromosome 19

chromosome 3

chromosome 5

chronic graft versus host disease

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

collagen vascular disease

coma

complications

compression neuropathy

conduction block

confidentiality

confusion

congenital heart disease

congenital myasthenic syndromes

congenital myopathy

congestive heart failure

corticotropin-releasing factor

cortisol, elevated

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine kinase

creatine phosphokinase(CPK)elevated

critical care unit

cultured skin fibroblasts

dementia, frontotemporal

dementia, rapidly progressive

dementia, subcortical

dental procedure, neurologic complications with

developmental milestones

developmental retardation

diabetes mellitus

diabetes mellitus, chemical

diabetes mellitus, congenital and infectious disease with

diabetes mellitus, neurologic manifestations of

diabetic amyotrophy

diabetic cranialneuropathies

diabetic mononeuropathy

diabetic radiculopathy

diabetic spinal syndromes

diabetic visceral neuropathy

diamond on quadriceps

diaphragmatic paralysis

diarrhea

diarrhea, bloody

differential diagnosis

difficulty climbing stairs

dilantin

dilantin, hypersensitivity to

diplegia, brachial

diplopia

disability, neurological

dislocated hip, congenital

disorientation

distal muscle atrophy

distal muscle weakness

diuretic

docetaxel

dropped head syndrome

drug abuse

drug abuse, inhalation

drug induced neurologic disorders

dystrophic calcification

electrocardiogram, abnormal

electromyogram

electromyogram, decremental response

electromyogram, incremental response

electron microscopy

Emery-Dreifuss muscular dystrophy

encephalitis, autoimmune

encephalitis, human immunodeficiency virus type 1

encephalomyelitis

encephalomyelitis, parainfectious

encephalopathy

encephalopathy, progressive

entrapment neuropathy

enzyme treatment

enzyme, defect

enzyme, muscle disease

enzyme, serum

eosinophilia

eosinophilia-myalgia syndrome

epidemiology of neurology

epsilon-aminocaproic acid(E.A.C.A.)

evoked potentials

exercise

exercise intolerance

exercise-induced neurologic dysfunction

exome sequencing

extraocular muscle lesion

eye closure

eye movement, disorders of

face, elongated

facial appearance, abnormal

facial hair, excessive

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, recurrent

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

finger flexor weakness

foot ulcer, neuropathic

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

gag reflex, depressed

gait disorder

gait, waddling

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastrocnemius muscle weakness

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

glucose tolerance test, abnormal

glycogen debranching enzyme deficiency

glycogen storage disease

gout

Gowers maneuver

granulomatosis with polyangiitis

granulomatosis, allergic

granulomatous disease

gray matter

Guillain Barre syndrome

Guillain Barre syndrome, ataxic form

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, ophthalmoplegia in

Guillain Barre syndrome, variant forms of

gynecomastia

hallucination

hallucination, auditory

headache, worst of life

hearing loss

heart block

heart block, complete

heralding manifestation

high arched feet

high arched palate

highly active antiretroviral therapy

histochemistry of muscle

HLA

HMGcoA reductase inhibitors

human immunodeficiency virus type 1

hung reflex

hyperadrenalism

hypercalcemia

hypereosinophilic syndrome(HES)

hypergammaglobulinemia

hyperparathyroidism

hyperparathyroidism, secondary

hyperphosphatasia

hyperreflexia

hypersensitivity reaction

hypokalemic periodic paralysis

hypomagnesemia

hyponatremia

hypoosmolality of serum

iatrogenic neurologic disorders

idiopathic inflammatory myopathy

ileus, paralytic

imbalance

immediate recall

immune checkpoint inhibitors

immune-related adverse events

immunohistochemistry

immunomodulation

immunosuppressive agents

impotence

impulsivity

inability to stand on tiptoes

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

inclusion bodies

inclusion bodies, eosinophilic intranuclear

inclusion body myositis

insecticides

insulin

intellectual deficit

interstitial pulmonary fibrosis

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

ipecac

ipilimumab

ischemic exercise test

jaw jerk, abnormal

klippel feil syndrome

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

leg weakness, bilateral

leg weakness, unilateral

lethargy

leukocytosis

leukodystrophy

level of consciousness, decreased

lid closure, weakness of

life expectancy

limb-girdle weakness

limbic encephalitis

lipid storage myopathy

lipoma of skin

lipomatosis

lipomatosis, multiple symmetrical

liquorice

livedo reticularis

liver disease

liver function enzymes

lordosis

low back pain

lumbosacral plexopathy

lumbosacral plexus

lumbosacral plexus, neuritis

lumbosacral radiculopathy

lumbosacral radiculoplexopathy

lung transplantation

lymphadenopathy

lymphadenopathy, cervical

lymphadenopathy, hilar

lymphocytic meningoradiculitis

lymphopenia

lysosomal storage disease

lysosomes, abnoral

malabsorption

malabsorption syndrome

malignancy, occult

malignant hyperpyrexia

McArdle's disease

McArdle's disease, adult onset

medulla oblongata, lesion of

MELAS syndrome

Melkersson's syndrome

memory, impairment of

meningeal enhancement

meningismus

meningitis

meningitis, aseptic

meningoencephalomyelitis

mental retardation

mental status, abnormal

middle cerebellar peduncle

migraine

mimics

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve prolapse

MNGIE syndrome

molecular genetics

monoclonal antibodies

monoclonal gammopathy

monoclonal gammopathy of uncertain significance

mononeuritis multiplex

mononeuropathy

mononeuropathy multiplex

monoparesis

mortality

motor neuron disease

motor neuron disease, spontaneous recovery

MRI, disappearing lesion on

MRI, muscle

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

multicore myopathy

multiple myeloma

multiple sclerosis

muscle atrophy, focal

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle hypertrophy

muscle pain

muscle phosphorylase deficiency

muscle spasm

muscle stiffness

muscle strength, testing

muscle swelling

muscle tenderness

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscle weakness, sudden onset of

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, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, dystrophin normal

muscular dystrophy, facioscapulohumeral

muscular dystrophy, female occurrence of

muscular dystrophy, limb-girdle

muscular dystrophy, pattern of muscle involvement

myasthenia gravis

myasthenia gravis, classification

myasthenia gravis, congenital

myasthenia gravis, diagnosis

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, drug induced

myasthenia gravis, etiology of

myasthenia gravis, familial incidence of

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, neuromuscular junction in

myasthenia gravis, presenting manifestations

myasthenia gravis, receptor site in

myasthenia gravis, seronegative

myasthenia gravis, thymectomy in

myasthenia gravis, treatment of

myasthenic crisis

myasthenic syndrome

myasthenic syndrome, treatment of

mycoplasma

mycoplasma pneumoniae

myelitis

myeloneuropathy

myelopathy

myelopathy, chronic progressive

myopathy, carcinomatous

myopathy, critically ill

myopathy, drug-induced

myopathy, hereditary

myopathy, hypocalcemic

myopathy, hypokalemic

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, inflammatory

myopathy, metabolic

myopathy, mitochondrial

myopathy, myofibrillar

myopathy, necrotizing

myopathy, necrotizing, autoimmune

myopathy, necrotizing, immune-mediated

myopathy, painful

myopathy, proximal

myopathy, quadriceps

myopathy, steroid induced

myopathy, steroid responsive

myopathy, thyroid disease causing

myositis, granulomatous

myositis, ocular

myotonia

myotonia dystrophica

myotonia dystrophica, classification

myotonia dystrophica, type 2

myotonic discharges

myxedema, neurologic manifestations of

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, hormone producing, ectopic

neoplasm, metastatic to muscle

nerve biopsy

nerve conduction studies

neuritis, causes of

neuroblastoma

neuroendocrinology

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuroophthalmology

neuropathology

neuropathology, brain

neuropathology, peripheral nerves

neuropathy

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, recurrent

neuropathy, sensory

neuropathy, short-fiber

neuropathy, toxic

neuropathy, vasculitic, nonsystemic

neuropathy, vasculitic, systemic

neurotoxin

neutropenia

next-generation sequencing

occupational neurologic disorders

occupational neuropathies

ocular myopathy

oculopharyngeal muscular dystrophy

old age, neurology of

opened mouth

ophthalmoplegia

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

ophthalmoplegia, total

owl's eye sign of spinal cord

pacemaker, cardiac-transvenous

paralysis, acute areflexic

paralysis, use-related

paraspinal muscle weakness

Parkinsonism syndrome

parotid gland swelling

periodic paralysis, thyrotoxic

plasma cell dyscrasia

plasmapheresis

pleocytosis of cerebrospinal fluid

pleurisy

pneumonia

poison, neurologic problems with

poison, organophosphate

poliomyelitis

poliomyelitis, provocation

polymerase chain reaction

polymyositis

polymyositis, eosinophilic

polyneuritis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic inflammatory demyelinating, variant form

polyneuropathy, chronic inflammatory demyelinating-pure motor syn

polyneuropathy, chronic inflammatory demyelinating-sens atax var

polyneuropathy, chronic inflammatory demyelinating-variant forms

polyradiculoneuropathy

polyuria

Pompe's disease of glycogen storage

porphyria

position sensation, abnormal

positive sharp waves

posterior column disease

postpartum

potassium

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prognosis

progressive neurologic disorder

progressive spinal muscular atrophy

propranolol

proteinuria

proximal muscle atrophy

proximal myotonic myopathy

pseudohypertrophy

pseudomyotonia

psychiatric problems in neurologic disorders

psychological testing

pulmonary function tests

pulmonary hypertension

pulmonary infiltrates

pupil, abnormality in neurologic disorders

rabies, nervous system involvement with

radiculitis

radiculopathy

radionuclide imaging, heart

ragged-red fibers

rapidly progressing neurologic illness

remote effect of cancer on the nervous system

renal failure

renal stones

repetitive nerve stimulation

respirator

respiratory failure

respiratory tract infection

retina, abnormal

retinal lesion

retrograde axonal flow

reversible neurologic disorder

review article

rhabdomyolysis

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

salivation, excessive

Schwartz-Jampel syndrome

scleroderma

sclerosis, bone

scoliosis

scoliosis, neurologic association with

screening

sedimentation rate, elevated

seizure

seizure, focal

sensorineural hearing loss

serum alanine aminotransferase

sex reassignment surgery

short stature

shoulder, pain in

shoulder, subluxation

single-fiber electromyography

sinusitis

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, lesions in neurologic disorders

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinocerebellar degeneration

starvation, therapeutic

statin therapy

statin therapy, discontinuation

status asthmaticus

status epilepticus

stem cell transplantation

steroid

steroid therapy, CNS treatment and complications with

subarachnoid hemorrhage

subcutaneous edema

sudden death

suicide

survival motor neuron gene

systemic illness

systemic lupus erythematosus

telangiectases, periungual

temporal lobe, lesion

temporalis muscle wasting

tensilon test, false positive

thymus and neuromuscular function

thyroid function tests

thyroiditis

thyrotoxicosis

tick bite

tick-borne encephalitis

toe walking

tongue, enlarged

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

torticollis

toxins, nervous system

transgender

transient ischemic attack

transverse smile

treatment of neurologic disorder

tremor

tremor, intention

trinucleotide repeats

upward deviation of eyes

uremia

urinary frequency

urinary incontinence

urine osmolality, elevated

vibratory sensation, abnormal

vincristine neurotoxicity

walking, difficulty with

Watson-Schwartz reaction

weakness, fluctuating

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

weight loss

Werdnig-Hoffman disease

X-linked bulbospinal neuronopathy

X-linked myopathy

x-linked myopathy with excessive autophagy

Showing articles 50 to 100 of 191 << Previous Next >>

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Juvenile Dermatomyositis and Other Idiopathic Inflammatory Myopathies of Childhood
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Amyloid Myopathy Presenting with Distal Atrophic Weakness
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Clinicopath Conf., Colchicine Myoneuropathy
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Oculopharyngeal Muscular Dystrophy in Hispanic New Mexicans
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New Nomenclature and DNA Testing Guidelines for Myotonic Dystrophy Type 1 (DM1)
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Distinctive Pathologic Findings in Proximal Diabetic Neuropathy (Diabetic Amyotrophy)
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Linkage of Proximal Myotonic Myopathy to Chromosome 3q
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Atypical Form of Amyotrophic Lateral Sclerosis
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Microvasculitis and Ischemia in Diabetic Lumbosacral Radiculoplexus Neuropathy
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Chloroquine Myopathy and Neuropathy with Elevated CSF Protein
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Clinical Heterogeneity of Adhalin Deficiency
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Showing articles 50 to 100 of 191 << Previous Next >>