Neudle.com: proximal muscle atrophy

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 950 to 1000 of 4643 << Previous Next >>

Surgical Anatomy of the Hand
Clinical Symposia,Ciba 21:66-109, Lampe,E.W., 1969

Corticodentatonigral Degeneration with Neuronal Achromasia
Arch Neurol 18:20-33, Rebeiz,J.J.,et al, 1968

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy (II)
Arch Neurol 18:619, Dyck,P.,et al, 1968

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy
Arch Neurol 18:603, Dyck,P.,et al, 1968

Myopathy of the Quadriceps Muscles
J Neurol Sci 7:201, VanWijngaarden,G.K.,et al, 1968

The Oculopharyngeal Syndrome
JAMA 203:1003, Murphy,S.F.,et al, 1968

The Remote Effects of Cancer on the Nervous System
Proc Roy Soc Med 60:683, Wilkinson,M., 1967

Clinical Cases-Dx:Functional Approach to Neuroanatomy pp 477-490 Earl Lawrence House
McGraw Hill 1967., , 1967

Amyotrphic Lateral Sclerosis
Arch Neurol 16:357, Hirano,A.,et al, 1967

"Myopathic"Changes in Chronically Denervated Muscle
Arch Neurol 16:14-24, Drachman,D.B.,et al, 1967

Pure Motor Hemiplegia of Vascular Origin
Arch Neurol 13:30, Fisher,C.M.,et al, 1965

Motor Neurone Disease as a Manifestation of Neoplasm
Brain 88:479, Brain,L.,et al, 1965

The Neurological Sequelae of Electrical Injury
Can Med Assn J 91:195, Silversides,J., 1964

Cervical Myelopathy with Fasciculations in the Lower Extremities
J Neurosurg 20:948, King,R.B.,et al, 1963

Course & Prognosis in Amyotrophic Lateral Sclerosis
Arch Neurol 8:17, Mackay,R., 1963

Recognition, Prognosis, & Treatment of the Guillain-Barre Syndrome (Acute Idiopathic Polyneuritis)
Med Clin North Am 47:1371, Eiben,R.,et al, 1963

Neuro CPC of MGH
Congenital Toxoplasmosis Involving CNS, NEJM 269:369-3741963., , 1963

Clinical Syndromes in Cerebral Arterial Occlusion
(Ed) , Fields, Wm. Pathogenesis & Treatment of CVD, Charles C. Thomas, Publisher, Fisher,C.M., 1961

Neuro CPC of MGH
Glioblastoma Multiforme, NEJM 262:413-4161960., , 1960

Amyotrophic Lateral Sclerosis:Clinical Syndrome Differential Diagnosis
Med Clin North Am 44:1013, Mulder,D.W., 1960

Myasthenic Syndrome in Patients with ALS
et al Neurol 9:627, Mulder,D.W., 1959

Neuro CPC of MGH
Cervical Spondylosis with Protruded Disk, NEJM 261:715-7201959., , 1959

Neuro CPC of MGH
Myopathy, Severe, Generalized, Chronic, NEJM 258:388-3938., , 1958

Neurologic Signs & Symptoms as Early Manifestations of SLE
Neurol 5:84, Siekert,R.,et al, 1955

Localization of Lesions Causing Horner's Syndrome
Arch Ophthamol 44:710, Jaffe,N., 1950

Degenerative Diseases of the Nervous System, Primary Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1112, Ropper, A.H.,et al,

Electric Shocks and Weakness of the Right Hand in a Young Man:Hirayama Disease
, Witiw,C.D.&OToole,J.E.,

Clinical Study of Nine Patients with ReNU Syndrome
, Okamoto,N.,et al,

Bilateral Posterior Limb Internal Capsule T2 Hyperintensity and Severe Cerebellar Atrophy in 2 Lifelong Friends
Neurol 106:e218014, Inoue,H.,et al, 2026

A 35-Year-Old Patient with Rapidly Progressive Ascending Weakness Leading to Loss of Brainstem Reflexes
Neurol 106:e218059, Lyons,H.J.,et al, 2026

A Woman with Parkinson Disease, Dyskinesia, Rhadomyolysis, Subcutaneous Emphysema, and Pneumomediastinum
Neurol 106:e218064, Iqbal,M.M.,et al, 2026

A 32-Year-Old Woman with Progressive Vision Loss and Confusion
Neurol 106:e214988, Kumar,A.B.,et al, 2026

A 55-Year-Old Man with Rapidly Progressive Weakness and Numbness
Neurol 106:e218063, Li,X.,et al, 2026

An 81-Year-Old Woman with Chronic Isolated Neck Extensor Weakness
Neurol 106:e218060, Chen,J.,et al, 2026

Inflammatory Myopathies
NEJM 394:1925-1938, AllenBach,Y. & Benveniste,O., 2026

Reversible Leukoencephalopathy and Parkinsonism Due to CNS Involvement in Cryoglobulinemia
Neurol 106:e214622, German,A.,et al, 2026

Progressive Quadriparesis and Falls in a 66-Year-Old Man With Longstanding Human Immunodeficiency Virus
Neurol 106:e214621, Ong,B.A. & Carlson,A.K., 2026

Congenital Zika Syndrome
NEJM 394:e2, Bacin,F. & Montenegro,M.A., 2026

Polymyalgia Rheumatica
NEJM 394:1097-1109, Dejaco,C.,et al, 2026

A 67-Year-Old Man with Exercise Intolerance nd Progressive Weakness
Neurol 106:e214830, Gosset,A.,et al, 2026

A 35-Year-Old Man with Recurrent Asymmetric Lumbosacral and Cervical Plexopathy
Neurol 106:e214910, Tayade,K.S., et al, 2026

Niemann-Pick Type C Disease
www.UpToDate.com, Nov, Schiffmann, R., 2026

Association of Changes in Activity Patterns with Brain Atrophy and Disability Progression in People with Multiple Sclerosis
Neurol 106:e214678, e214742, Fitzgerald,K.C.,et al, 2026

Melas Syndrome
Stat PearlsPubl Jan 25, Pia,S. & Lui,F., 2025

Complex Regional Pain Syndrome
NEJM 393:2338-2348, Goebel,A., 2025

A 16-Year-Old Adolescent Boy with Ophthalmoplegia and Unilateral Ptosis
Neurol 105:e214430, Lu,Y.,, 2025

Clinicopathologic Conference, Diffuse Meningeal Melanomatosis
NEJM 393:2152-2162, Case 34-2025, 2025

A Randomized Trial of Shunting for Idiopathic Normal-Pressure Hydrocephalus
NEJM 393:2198-2209, 2264, Luciano,M.G.,et al, 2025

A 5-Year-Old Boy with Subacute and Refractory Myoclonus
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Tiger Man Sign in Sarcoid Myopathy
Neurol 105:e214323, Sun,Q.,et al, 2025

Showing articles 950 to 1000 of 4643 << Previous Next >>