Neudle.com: muscle atrophy diffuse

Differential
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abdominal distention

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

acrocyanosis

Adies pupil

adult polyglucosan body disease

advances in neurology

adverse drug reaction

agenesis of corpus callosum

Aicardi-Goutieres syndrome

Alexanders disease

alpha glucosidase

alveolar hypoventilation

Alzheimer's disease

amyloid angiopathy, cerebral

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, juvenile

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis-like syndrome

anesthesia, general

angiography, cerebral, false negative

angiography, cerebral, negative

ankylosing spondylitis

anterior horn cell disease

anterior tibial muscle weakness

antibodies to measles

aspartate aminotransferase

ataxia telangiectasia

ataxia, cerebellar

ataxic gait

attention deficit disorder with hyperactivity

atypical

audiogram

auditory evoked brainstem potentials

autoimmune disease

autonomic dysfunction

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basement membrane

basement membrane thickening

brucellosis, nervous system involvement with

bulbar palsy

bulbar palsy, progressive

burning skin

cachexia

CAG repeats

calcification, intracranial

Canavan's disease

cardiac arrest

cardiac arrest and resuscitation

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, spine

cataracts

cataracts, congenital

cauda equina, enhancement

CD4 counts

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebral cortex

cerebral cortical atrophy

cerebral venous thrombosis

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, recurrent

cerebrovascular accident, women

cervical spine

Charcot-Marie-Tooth

chilbran skin lesions

Clinical Pathologic Conference(C.P.C.)

congestive heart failure

corpus callosum, infarction of

corpus callosum, lesion of

cortical blindness

cortical blindness, transient

cortical infarction

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

critical care unit

crying, pathologic

cultured skin fibroblasts

degenerative diseases of CNS

Dejerine-Sottas syndrome

delayed dentition

dementia

dementia, childhood

dementia, frontal lobe type

dementia, frontotemporal

denervation of muscle

denervation potentials

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

diarrhea

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

diffuse idiopathic skeletal hyperostosis

diplopia

diplopia, transient

disability, neurological

distal muscle weakness

disulfiram

drooling

dural sinus thrombosis

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

encephalopathy, acute

encephalopathy, anoxic

encephalopathy, metabolic

encephalopathy, post anoxic

enzyme treatment

enzyme, defect

enzyme, muscle disease

episodic neurologic deficits

evoked potentials

exercise intolerance

exome sequencing

extraocular muscle lesion

eye movement, disorders of

facial appearance, abnormal

facial nerve palsy

facial weakness

facial weakness, bilateral

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, lesion of

frontal lobe, pathologic signs of

fundus, abnormality of

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

genu of corpus callosum

globus pallidus, hemorrhage

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glycogen storage disease

GM1 ganglioside antibodies

gray matter

Guillain Barre syndrome, differential diagnosis of

hearing loss, bilateral

hearing loss, sudden, bilateral

heart block

hemiparesis

hemiparesis, transient

hepatomegaly

heralding manifestation

high arched feet

high arched palate

highly active antiretroviral therapy

hoarseness

hospice

human immunodeficiency virus type 1

hyperpyrexia, CNS disorder causing

hypotension, systemic

hypotonia

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

imbalance

immunosuppressive agents

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

incoordination

infection

intellectual deficit

intellectual deterioration

interferon alpha

intestinal pseudoobstruction

intrauterine

intrinsic hand muscles, wasting of

irritability

Jakob-Creutzfeldt disease

laminar necrosis, cortical

laughing

laughing, pathologic

leg weakness, bilateral

leg weakness, unilateral

lenticular nucleus, lesion of, bilateral

leukodystrophy

leukoencephalopathy

Lewy body disease, diffuse

life expectancy

life support, withdrawal of

lobar atrophy

lymphoma

lymphoma involving CNS

lysosomal storage disease

lysosomes, abnoral

macrocephaly

Marinesco-Sjogren syndrome

masseter muscle wasting

MELAS syndrome

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal enhancement

meningismus

meningitis, melanomatous

mental retardation

merosin

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

methylene tetrahydrofolate reductase

methylenetetrahydrofolate reductase deficiency

microangiopathy, brain

microangiopathy, retina

microcephaly

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

Middle east

mimics

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

MNGIE syndrome

molecular genetics

monoclonal gammopathy

MRI, contrast enhanced

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, FLAIR

MRI, functional

MRI, high signal foci on

MRI, negative

MRI, serial

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, susceptibility weighted

multiple organ failure

multiple sclerosis

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, progressive

muscle biopsy

muscle pain

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, congenital

muscular dystrophy, limb-girdle

myelomalacia

myeloneuropathy

myelopathy

myelopathy, chronic progressive

myopathy, critically ill

myopathy, drug-induced

myopathy, steroid induced

nerve conduction studies

nerve root enhancement

neurogenic bladder

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic evaluation

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuronal degeneration

neuronopathy

neuropathology

neuropathology, brain

neuropathy

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, sensory

neuroprotective agents

neurotoxic

neurotoxicity, acute

next-generation sequencing

nutritional deficiency

nystagmus

obesity

occipital lobe, lesion of

old age, neurology of

ophthalmoplegia

optic atrophy

optic nerve, hypoplasia of

optic neuropathy

optic neuropathy, nutritional

patient information and support

pediatric neurology

percussion induced muscle contraction

persistent vegetative state

personality change

pes cavus

pleocytosis of cerebrospinal fluid

POLR3B

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, critically ill

polyneuropathy, critically ill, children

polyradiculoneuropathy

Pompe's disease of glycogen storage

pons, atrophy

pons, lesion of

posterior column disease

posterior longitudinal ligament, ossification of

pregnancy, neurologic complications in

prenatal

prenatal diagnosis by amniocentesis

primary lateral sclerosis

prognosis

progressive myoclonic epilepsy

progressive neurologic disorder

proximal muscle atrophy

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

ptosis

pupil, abnormality in neurologic disorders

pupil, tonic

pyramidal tract

pyramidal tract dysfunction

quadriparesis

quadriplegia

quadriplegia, transient

radiculopathy

ragged-red fibers

rapidly progressing neurologic illness

reading disorder, acquired

retinal artery occlusion

retinal branch artery occlusion

reversible neurologic disorder

saccadic eye movements, abnormal

Schilder's disease

sedimentation rate, elevated

seizure

seizure, children

sensorineural hearing loss

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

sleep

sleep pathology and physiology

slit lamp examination

slow virus infection of CNS

small vessel disease

SMN1 gene

spasticity

speech disorder, childhood

spinal cord

spinal cord degeneration

spinal cord, cervical

spinal cord, compression of

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinal stenosis

spinal stenosis, cervical canal

splenium of corpus callosum

spondylosis

spongy degeneration of brain

spontaneous remission

steroid therapy, CNS treatment and complications with

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subdural hematoma

superior sagittal sinus thrombosis

sural nerve

survival motor neuron gene

Susac's syndrome

symmetric brain lesions

systemic illness

tandem gait, ataxic

teeth, abnormal

teeth, number of in infants

temporal lobe, atrophy

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

thalamus, lesion of

thalamus, lesion of-bilateral

tongue, fasciculations of

tongue, weakness

toxic encephalopathy

transient neurologic deficit

trauma

treatment of neurologic disorder

trinucleotide repeats

tripping

urinary incontinence

urine test for metabolic disorders

visual acuity, decreased

visual loss

visual tracking

visuospatial disturbance

vitamin deficiency

vitamin E deficiency

Waldenstrom's macroglobulinemia

walking, delayed

walking, difficulty with

weakness

weakness, acute

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

weight loss

wheelchair

white matter disease

white matter disease, periventricular

white matter disease, subcortical

wide based gait

winging of scapula

word-finding difficulty

Showing articles 850 to 900 of 5194 << Previous Next >>

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

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

Chronic Focal Polymyositis in the Adult
JNNP 44:419-425, Bharucha,N.E.,et al, 1981

Subcortical Arteriosclerotic Encephalopathy:A Clinical & Radiological Investigation
JNNP 44:294-304, Loizou,L.A.,et al, 1981

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

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

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

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

Meningeal Gliomatosis:A Review of 12 Cases
Ann Neurol 8:605-608, Young,W-k.A.,et al, 1980

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

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

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

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

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

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

Hereditary Myoclonus & Progressive Distal Muscular Atrophy
Ann Neurol 6:227-231, Jankovic,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

Spirometry in Amyotrophic Lateral Sclerosis
Arch Neurol 36:74-80, Fallat,R.J.,et al, 1979

Age & Cerebrospinal-Fluid Protein in Motor-Neuron Disease
NEJM 300:437-438, Guiloff,R.J.,et al, 1979

Double-Blind Study of Modified Neurotoxin in Motor Neuron Disease
Neurol 29:77-81, Tyler,H.R., 1979

Central Vestibular Involvement in Peroneal Muscle Atrophy:A Preliminary Report
Ann Neurol 5:118-120, Melgaard,B.,et al, 1979

Neurologic Disturbances in Pagets Disease of Bone:Response to Calcitonin
Neurol 29:448-457, Chen,J.R.,et al, 1979

Use of the ECG in the Diagnosis of Childhood Spinal Muscular Atrophy
Arch Neurol 36:317-318, Russman,B.S.,et al, 1979

Subacute Motor Neuronopathy:A Remote Effect of Lymphoma
Ann Neurol 5:271-287, Schold,S.C.,et al, 1979

Presenile Dementia With Motor Neuron Disease in Japan, A New Entity
Arch Neurol 36:592-593, Mitsuyama,Y.,et al, 1979

Haemophilic Neuromyopathy
JNNP 42:600-605, Defaria,C.R.,et al, 1979

Amyotrophic Lateral Sclerosis With Ophthalmoplegia; A Cliniocopathologic Study
Arch Neurol 36:615-617, Harvey,D.G.,et al, 1979

Remission of a Syndrome Indistinguishable from Motor Neuron Disease after Resection of Bronchial Carcinoma
BMJ 2:176-177, , 1979

Clinical Pathological Conference
Amyotrophic Lateral Sclerosis, Case Record 46-1979, NEJM 301:1104-1111979., , 1979

Familial Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome)
Ann Neurol 6:200-206, Kalimo,H.,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

Quadriceps Myopathy in Two Brothers
Rhode Island Med J 62:125, Finelli,P.F., 1979

Clinical Pathological Conference, Peripheral Neuropathy in Leprosy
NEJM 300:546-553, Dawson,D., 1979

Acute Anterior Myelitis Complicating West Nile Fever
Arch Neurol 36:172-173, Gadoth,N.,et al, 1979

Showing articles 850 to 900 of 5194 << Previous Next >>