Neudle.com: muscle atrophy proximal

Differential
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abdominal distention

abdominal muscle paralysis

abdominal protrusion

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

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

ankle reflex, preserved

anterior horn cell disease

anti signal recognition particle antibody

arthrogryposis multiplex

aspartate aminotransferase

atrioventricular block

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

calcification, intracranial

cardiovascular disease

carpal tunnel syndrome

case studies

CAT scan

CAT scan, abnormal

CAT scan, false negative

central core disease

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar edema

cerebellar lesion

cerebral cortical atrophy

cerebral edema

cerebral embolism

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, eosinophilia of

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular accident, young adult

Charcot-Marie-Tooth

chewing, impaired

children

chromosomal abnormality

chromosome 5

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

cold temperature

coma

conduction block

congenital heart disease

congestive heart failure

consanguinity

contractures, joint

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

deafness

delay in diagnosis

dementia

dementia, frontotemporal

dermatomyositis

developmental milestones

developmental retardation

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic amyotrophy

diarrhea

differential diagnosis

difficulty climbing stairs

diplopia

dislocated hip, congenital

distal muscle atrophy

distal muscle weakness

drug induced neurologic disorders

dystrophic calcification

dystrophin

echocardiogram

electrocardiogram, abnormal

electromyogram

electromyogram, decremental response

electron microscopy

Emery-Dreifuss muscular dystrophy

encephalomyelitis

encephalomyelitis, parainfectious

encephalopathy

encephalopathy, progressive

entrapment neuropathy

enzyme treatment

enzyme, defect

enzyme, muscle disease

epidemiology of neurology

exercise

extraocular muscle lesion

facial weakness

facial weakness, bilateral

finger flexor weakness

gammaglobulin therapy, intravenous

gastrocnemius muscle weakness

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic neurologic disorders

genetic screening

genetic testing

glycogen debranching enzyme deficiency

glycogen storage disease

gray matter

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

headache, worst of life

hearing loss

heart block

heart block, complete

heart murmur

hepatomegaly

heralding manifestation

hip flexor weakness

histochemistry of muscle

hoarseness

Hoesch test

human immunodeficiency virus type 1

immunosuppressive agents

inability to stand on tiptoes

inclusion bodies

inclusion bodies, eosinophilic intranuclear

inclusion body myositis

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

klippel feil syndrome

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

leg weakness, bilateral

leg weakness, unilateral

leukodystrophy

level of consciousness, decreased

lid closure, weakness of

life expectancy

lumbosacral plexopathy

lumbosacral plexus

lumbosacral plexus, neuritis

lymphadenopathy

lymphadenopathy, cervical

lysosomal storage disease

lysosomes, abnoral

malignant hyperpyrexia

McArdle's disease

medulla oblongata, lesion of

MELAS syndrome

meningeal enhancement

meningismus

meningoencephalomyelitis

mental retardation

mental status, abnormal

mimics

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve prolapse

MNGIE syndrome

molecular genetics

monoclonal gammopathy

monoclonal gammopathy of uncertain significance

mononeuritis multiplex

motor neuron disease, spontaneous recovery

MRI, spinal cord, increased intramedullary cord signal

multiple myeloma

muscle atrophy, focal

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle pain

muscle phosphorylase deficiency

muscle stiffness

muscle strength, testing

muscle tenderness

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, cardiovascular changes with

muscular dystrophy, classification

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, differential diagnosis

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenic crisis

mycoplasma

mycoplasma pneumoniae

myopathy, carcinomatous

myopathy, drug-induced

myopathy, hereditary

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, mitochondrial

myopathy, necrotizing

myopathy, proximal

myopathy, quadriceps

myopathy, steroid induced

myopathy, thyroid disease causing

nemaline rod myopathy

nemaline rod myopathy, adult onset

nerve conduction studies

neuritis, causes of

neuroendocrinology

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neuropathy, hereditary peripheral

neuropathy, motor, multifocal

neuropathy, painful

neuropathy, peripheral

neuropathy, short-fiber

neurotoxin

next-generation sequencing

occupational neurologic disorders

occupational neuropathies

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy

osteomalacia

pacemaker, cardiac-transvenous

paralysis, use-related

paraspinal muscle weakness

plasma cell dyscrasia

plasmapheresis

pleocytosis of cerebrospinal fluid

poliomyelitis

poliomyelitis, provocation

polymyositis

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

Pompe's disease of glycogen storage

porphyria

positive sharp waves

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prognosis

progressive neurologic disorder

progressive spinal muscular atrophy

proximal muscle atrophy

rabies, nervous system involvement with

radionuclide imaging, heart

ragged-red fibers

rapidly progressing neurologic illness

rash

recurrent

renal stones

repetitive nerve stimulation

respiratory failure

respiratory tract infection

retina, abnormal

retinal lesion

retrograde axonal flow

scoliosis, neurologic association with

screening

seizure

sensorineural hearing loss

sensory symptoms

serologic testing

short stature

shoulder, subluxation

SMN1 gene

spinal cord

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

standing difficulty

steroid

steroid therapy, CNS treatment and complications with

stiff man syndrome

strokelike episodes

sudden death

survival motor neuron gene

systemic illness

tandem gait, ataxic

temporalis muscle wasting

tetanus

toe walking

tongue, enlarged

tongue, fasciculations of

tongue, weakness

torticollis

toxins, nervous system

transverse smile

treatment of neurologic disorder

trinucleotide repeats

upgaze, paralysis of

upward deviation of eyes

walking, difficulty with

weakness

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

weight loss

Werdnig-Hoffman disease

wheelchair

white matter disease

winging of scapula

X-linked bulbospinal neuronopathy

X-linked myopathy

x-linked myopathy with excessive autophagy

Showing articles 800 to 850 of 4643 << Previous Next >>

Inclusion Body Myositis
Arch Neurol 39:760-764, Danon,M.J.,et al, 1982

Distal Myopathy, Histochemical & Ultrastructural Studies
Arch Neurol 39:367-371, Kumamoto,T.,et al, 1982

Cardiomyopathy Associated with the Syndrome of Amyotrophic Chorea & Acanthocytosis
Ann Int Med 96:616-617, Faillace,R.T.,et al, 1982

Enigmatic Dyspnoea:An Unusual Presentation of Motor-Neuron Disease
Lancet 1:933-935, Nightingale,S.,et al, 1982

Long-Term Management of Respiratory Failure in Amyotrophic Lateral Sclerosis
Ann Neurol 12:18-23, Sivak,E.,et al, 1982

Benign Familial Spinal Muscular Atrophy With Hypertrophy of the Calves
Arch Neurol 39:657-660, D'Alessandro,R.,et al, 1982

Exacerbation of Charcot-Marie-Tooth Disease in Pregnancy
Neurol 32:1311-1314, Pollock,M.,et al, 1982

Clinical & Electrophysiological Studies in Primary Lateral Sclerosis
Jr. , Arch Neurol 39:662-664982., Russo,L.S., 1982

Amyotrophic Lateral Sclerosis & Paraproteinemia
Neurol 32:896-898, Krieger,C.,et al, 1982

A Prospective Study of Lacunar Infarction Using Computerized Tomography
Neurol 32:49-56, Donnan,G.A.,et al, 1982

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

Preservation of the Phrenic Motorneurons in Werdnig-Hoffman Disease
Ann Neurol 9:506-510, Kuzuhara,S.,et al, 1981

Circulating Immune Complexes in Neurologic Disease
Neurol 31:1402-1407, Noronha,A.B.C.,et al, 1981

Lipid Storage Myopathy:Successful Treatment with Propranolol
BMJ 282:1997-1999, Martyn,C.,et al, 1981

Myopathy Induced by Rifampicin
BMJ 283:105-106, Jenkins,P.,et al, 1981

Motor Neuron Disease:Decremental Responses to Repetitive Nerve Stimulation
Neurol 31:202-204, Bernstein,L.P.,et al, 1981

Arthrogryposis Multiplex Congenita
Editorial, BMJ 283:2-31981., , 1981

Progressive Pontobulbar Palsy With Deafness
Arch Neurol 38:186-190, Brucher,J.M.,et al, 1981

Vitamin E Deficiency in Werdnig-Hoffmann Disease
Ann Neurol 10:266-268, Shapira,Y.,et al, 1981

Primary Lateral Sclerosis
Arch Neurol 38:630-633, Beal,M.F.,et al, 1981

Pattern Reversal Visual Evoked Potentials
Arch Neurol 38:739-741, Bird,T.D.,et al, 1981

Amyotrophic Lateral Sclerosis & its Association with Dementia, Parkinsonism & Other Neurological Disorders:A Review
Brain 104:217-247, Hudson,A.J., 1981

Correlation of CT Scanning and Pathologic Features of Ophthalmic Graves'Disease
Ophthalmol 88:553-564, Trokel,S.L.&Jakobiec,F.A., 1981

Myotonic Dystrophy
In Harrison's Principles of Internal Medicine, 9th Ed, McGraw-Hill Book Co, NY 206180., Adams,R.D.,et al, 1980

Infantile Neuronal Degeneration Masquerading as Werdnig-Hoffmann Disease
Ann Neurol 8:317-324, Steiman,G.S.,et al, 1980

Unusual Effects of Metrizamide Lumbar Myelography
Arch Neurol 37:588-589, Kelley,R.E.,et al, 1980

Peripheral Neuropathy in the Cherry-Red Spot-Myoclonus Syndrome (Sialidosis Type I)
Ann Neurol 7:450-456, Steinman,L.,et al, 1980

Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
Arch Neurol 37:300-305, Sarnatt,H.B.,et al, 1980

Juvenile Metachromatic Leukodystrophy
Arch Neurol 37:42-46, Haltia,T.,et al, 1980

Poliomyelitis-like Syndrome Associated with Asthma
Arch Neurol 37:52-53, Wheeler,S.D.,et al, 1980

Management of Hypoventilation in Motor Neuron Disease Presenting with Respiratory Insufficiency
Ann Neurol 7:188-191, Sivak,E.D.,et al, 1980

Juvenile Muscular Atrophy Localized to Arms
Arch Neurol 37:297-299, Singh,N.,et al, 1980

Progressive Bulbar Paralysis Associated With Neurgl Deafness, A Nosological Entity
Arch Neurol 37:214-216, Alberica,R.,et al, 1980

Focal Neurologic symptoms in hypercalcemia
Neurol 30:200-201, Longo,D.L.,et al, 1980

Motor Neuropathy Associated with Cimetidine
BMJ 281:974-975, Walls,T.J.,et al, 1980

Masticatory Spasm in Facial Hemiatrophy
Ann Neurol 7:585-587, Kaufman,M.D., 1980

A pedigree of Amyotrophic Chorea With Acantho-cytosis
Arch Neurol 37:514-517, Kito,S.,et al, 1980

Lobar Cerebral Hemorrhages:Acute Clinical Syndromes in 26 Cases
Ann Neurol 8:141-147, Ropper,A.H.,et al, 1980

Proximal Myopathy after Prolonged Total Therapeutic Starvation
BMJ 280:1212-1213, Scobie,I.N.,et al, 1980

Proximal Muscle Weakness in Uremia
Arch Neurol 37:555-558, Lazaro,R.P.,et al, 1980

Acridine Orange-Nucleic Acid Fluorescence
Arch Neurol 37:641-644, Perl,D.P.,et al, 1980

Acne Fulminans with Inflammatory Myopathy
Neurol 8:67-69, Noseworthy,J.H.,et al, 1980

Gross Demonstration of Atrophic Cauda Equina Roots in Motor Neuron Disease, An Improved Method
Arch Neurol 37:394, Meneses,A., 1980

Proximal Myopathy During Beta-blockade
BMJ 2:1331-1332, Forfar,J.C.,et al, 1979

Multiple Endocrine Neoplasia, Type 2b:Phenotype Recognition; Neurological Features & Their Pathological Basis
Ann Neurol 6:302-314, Dyck,P.J.,et al, 1979

Gyrate Atrophy of the Choroid & Retina with Hyperornithinemia:Tubular Aggreg. & Type 2 Fiber Atrophy
Neurol 29:966, Sipila,I.,et al, 1979

Clinical Pathological Conference
Foramen Magnum Meningioma, Case Record 29-1979, NEJM 301:147-154979., , 1979

Hereditary Myoclonus & Progressive Distal Muscular Atrophy
Ann Neurol 6:227-231, Jankovic,J.,et al, 1979

Eosinophilic Polymyositis
Arch Neurol 36:721-722, 1979, Stark,R.J., 1979

Reversibility of Human Myopathy Caused by Vitamin E Deficiency
Neurol 29:1182-1186, Tomasi,L.G., 1979

Showing articles 800 to 850 of 4643 << Previous Next >>