Neudle.com: "muscle 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

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 3

chromosome 5

chronic graft versus host disease

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clofibrate

clubfoot as related to neurologic disease

Coats syndrome

colchicine

cold temperature

collagen vascular disease

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

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

exercise-related muscle strength increase

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 atrophy

leg numbness

leg swelling

leg weakness, bilateral

leg weakness, unilateral

lethargy

leukocytosis

leukodystrophy

level of consciousness, decreased

lid closure, weakness of

life expectancy

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

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

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

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, brain

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, systemic

neurotoxin

neutropenia

next-generation sequencing

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

paraspinal muscle weakness

Parkinsonism syndrome

parotid gland swelling

periodic paralysis, thyrotoxic

personality change

photophobia

pinched face

plasma cell dyscrasia

plasmapheresis

pleocytosis of cerebrospinal fluid

pleurisy

pneumonia

poison, neurologic problems with

poison, organophosphate

poliomyelitis

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

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

reversible neurologic disorder

review article

rhabdomyolysis

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

salivation, excessive

sarcoglycan

sarcoidosis

schizophrenia

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

thirst

thymectomy

thymoma

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

urine, dark

vasculitides

vecuronium

vibratory sensation, abnormal

vincristine neurotoxicity

walking, difficulty with

Watson-Schwartz reaction

weakness, fluctuating

weakness, generalized

weakness, progressive

weakness, proximal

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 0 to 50 of 2727 Next >>

Progressive Camptocormia with Head Drop and Dysphagia
JAMA Neurol 80:209-210, El-Wahsh,S., 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, Hypocalcemic Myopathy Due to Hypoparathyroidism
NEJM 388:1513-1520, Case 12-2023, 2023

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

Epidemiology, Survival, and Clinical Characteristics of Inclusion Body Myositis
Ann Neurol 92:201-212, Lindgren, U.,et al, 2022

A 63-Year-Old Woman Presenting with Bilateral Leg Pain
Neurol 96:343-348, Budhu, J.,et al, 2021

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

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

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

Acetylcholine Receptor-Antibody-Positive Myasthenia Gravis Presenting with Early Atrophy and Nonfluctuating Weakness of Proximal Limb Muscles
J Clin Neurol 16:714-716, Pancheri, E.,et al, 2020

Progressive Proximal Weakness in a 61-Year-Old Man
Neurol 98:122-127, Yu, M.,et al, 2020

A 59-year-old Woman with Multiple Myeloma and Lower Extremity Weakness and Numbness
Neurol 94:794-800, Gadot, R.,et al, 2020

Neuromuscular Adverse Events Associated with Anti-PD-1 Monoclonal Antibodies
Neurol 92:663-674, Johansen, 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

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

Metabolic Lipid Muscle Disorders: Biomarkers and Treatment
Ther Adv Neurol Disord 12:1-15, Angelini, C.,et al, 2019

Dysphagia and a rash
BMJ 361:k1590, McFarlane, M. & Disney, B., 2018

Clinicopathologic Conference, Cushings syndrome due to a well-differentiated, low-grade thymic neuroendocrine tumor with corticotropin
NEJM 378:2322-2332, Case 18-2018, 2018

A 42-year-old man with unilateral leg weakness
Neurol 90:e1085-e1090, Schneider, R.,et al, 2018

A Child with Arthrogryposis
Neurol 91:e995-e998, Irumudomom, O. & Ghosh, P.S., 2018

Progressive Gait Difficulty and Incontinence in a 40-year-old Man with HIV
Neurol 91:1065-1070, Silverman, A.,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 27-year-old man with unsteady gait
Neurol 89:e120-e123, Fernandez, D.,et al, 2017

A Child with Delayed Motor Milestones and Ptosis
Neurol 88:e158-e163, Ghosh, P.S., 2017

Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017

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

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

A 38-Year-Old Man with Respiratory Failure and Progressive Leg Weakness
Neurol 86:e190-e194, McIntosh, P. & Karam, C., 2016

A 64-year-old Man with Progressive Paraspinal Muscle Weakness
Neurol 86:e4-e9, Schneider, R.,et al, 2016

Clinicopathologic Conference, Botulism
NEJM 372:364-372, Case 3-2015, 2015

Inflammatory Muscle Diseases
NEJM 372:1734-1747, Dalakas, M.C., 2015

Diseases of the Nervous System Caused by Nutritional Deficiency, Vitamin E Deficiency
Adams & Victors Principles of Neurology Chp 41, pg 1176, Ropper, A.H.,et al, 2014

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

Clinicopathologic Conference, Parainfectious Encephalomyelitis Associated with Systemic Mycoplasma Infection
NEJM 370:2427-2438, Case 19-2012, 2014

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

A 49-year-old Man with Fever and Proximal Weakness in his Arms
Neurol 82:e65-e69, Seliger, C.,et al, 2014

Degenerative Diseases of the Nervous System, Kugelberg-Welander Syndrome SMAIII
Adams & Victors Principles of Neurology, Chp 39, pg 1118, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Kennedy Syndrome (X-Linked Bulbospinal Muscular Atrophy)
Adams & Victors Principles of Neurology, Chp 39, pg 1119, Ropper, A.H.,et al, 2014

The Limbic-Girdle Muscular Dystrophies
Neuro Clin 32:729-749, Wicklund, M.P. and Kissel, J.T., 2014

Diagnosis of Lambert-Eaton Myasthenic Syndrome in Children
Neurol 80:e220-e222, Morgan-Followell,B.& de los Reyes,E., 2013

The Spectrum of Statin Myopathy
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Inflammatory Myopathies with Anti-Ku Antibodies
Medicine 91:95-102, Rigolet,A.,et al, 2012

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

Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
Brain 134:3326-3332, Garone, C.,et al, 2011

Redefining Dysferlinopathy Phenotypes Based on Clinical Findings and Muscle Imaging Studies
Neurol 75:316-323,298, Paradas,C., et al, 2010

New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
JNNP 81:946-953, Klinge,L.,et al, 2010

Juvenile Dermatomyositis and Other Idiopathic Inflammatory Myopathies of Childhood
Lancet 371:2201-2212, Feldman,B.M.,et al., 2008

Proximal Paresis of the Upper Extremity in Patients With Stroke
Neurol 69:348-355, Hatakenaka,M.,et al, 2007

Showing articles 0 to 50 of 2727 Next >>