Neudle.com: limb girdle weakness

Differential
(Click to cross reference)

abdominal distention

abdominal muscle paralysis

abdominal protrusion

abducens nerve paralysis

abducens nerve paralysis, bilateral

acanthocytosis

acetylcholine receptor antibody

acetylcholinesterase

acetylcholinesterase deficiency

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

acquired immunodeficiency syndrome-related complex

acromegaly

acute disseminated encephalomyelitis

acute intermittant porphyria

acyl CoA dehydrogenase deficiency

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

advances in neurology

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, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis-like syndrome

aneurysm, intracranial

angiotensin-converting enzyme

anorexia

anterior horn cell disease

anterior spinal artery

anterior spinal artery infarction

anterior tibial muscle weakness

anti Jo1 antibody

anti Ku antibody

anti Mi2 antibody

anti signal recognition particle antibody

antibiotics

antibiotics, neurologic complications with

antibodies to voltage-gated calcium channels

anticoagulant, treatment

anticonvulsants, hypersensitivity syndrome

anticonvulsants, untoward effects of

arterial dissection, vertebral

artery of Adamkiewicz

arthralgia

arthritis

arthrogryposis multiplex

atrioventricular block

attention deficit disorder with hyperactivity

automatic implantable cardioverter-defibrillator

autonomic dysfunction

basement membrane thickening

basophilic stippling of red blood cells

Benedict's solution test

beta adrenergic blocker

Borrelia burgdorferi infection

botulinum toxin

botulinum toxin, complications of

botulism

brachial amyotrophic diplegia

brachial neuritis

brachial neuritis, acute

brachial neuritis, bilateral

brachial neuritis, prognosis of

brachial plexus

brachial plexus injury

brachial plexus neuropathy

brachial plexus neuropathy, bilateral

brachial plexus neuropathy, children

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

brachial plexus, lesion of

brachial radiculoplexopathy

bradycardia

brain biopsy

brain biopsy, false negative

brainstem, lesion of

bulbar palsy

bulbar palsy, acute

bulbar palsy, progressive

calcification, intracranial

calf amyotrophy

calf atrophy

calf hypertrophy

calpain III deficiency

campylobacter infection

cancer associated myopathy

canned food

carcinoma

carcinoma of esophagus

carcinoma of lung

cardiac surgery, neurologic complications with

cardiomegaly

cardiomyopathy

cardiotoxicity

cardiovascular disease

carnitine deficiency

carnitine deficiency myopathy

carpal tunnel syndrome

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, myelogram with

cataracts

cauda equina, enhancement

CD4 counts

ceftriaxone

central cord syndrome

central core disease

central nervous system, infection of

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellum

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, artery to artery

cerebral embolism, cardiac origin

cerebral infarction

cerebral palsy

cerebral palsy, associated problems with

cerebral palsy, pure ataxic

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, appearance of

cerebrospinal fluid, cloudy

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, flow cytometry

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, leak

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, etiology

cerebrovascular accident, location of

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, prognosis in

cerebrovascular accident, recurrent

cerebrovascular accident, rehabilitation of

cerebrovascular accident, vascular territory involved

cerebrovascular accident, young adult

cerebrovascular disease

cervical myelopathy

cervical radiculopathy

cervical spondylosis

cervical spondylosis, differential diagnosis of

cervical traction

Charcot-Marie-Tooth

chelation therapy

chemotherapy, CNS treatment and complications with

chromosomal abnormality

chromosome 5

chronic progressive external ophthalmoplegia

chymopapain

cigarette smoking

cleft palate

Clinical Pathologic Conference(C.P.C.)

collagen vascular disease

coma

complications

compression neuropathy

conduction block

confusion

congenital heart disease

congenital heart disease, CNS complications with

congenital myasthenic syndromes

congenital myopathy

congestive heart failure

consanguinity

constipation

contractures, joint

conus medullaris, lesion of

corona radiata

corpus callosum, infarction of

corpus callosum, lesion of

cortical blindness

cortical hemorrhage

cortical infarction

cortical infarction, small

corticotropin level

corticotropin-releasing factor

cortisol, elevated

coxsackievirus

cranial nerve enhancement

cranial nerve palsies

cranial nerve palsies, recurrent

cranial neuropathy

cranial neuropathy, multiple

creatine kinase

creatine phosphokinase(CPK)elevated

creatinine, elevated

Creutzfeldt-Jakob disease, genetic

degenerative cervical myelopathy

delay in diagnosis

delusion

dementia

dementia, frontotemporal

dementia, rapidly progressive

denervation potentials

developmental retardation

dexterity, impaired

diabetes mellitus

diabetes mellitus, chemical

diabetes mellitus, neurologic manifestations of

diabetic amyotrophy

diagnostic criteria

diamond on quadriceps

diaphragmatic paralysis

diarrhea

diarrhea, bloody

differential diagnosis

difficulty climbing stairs

dilantin

dilantin, hypersensitivity to

dinitrophenylhydrazine(D.N.P.H.)reaction

diplegia, atonic

diplegia, brachial

diplegia, spastic cerebral

diplopia

disability, neurological

dislocated hip, congenital

disorientation

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

DNA probes

docetaxel

dropped head syndrome

drug abuse

drug abuse, neurologic complications of

drug induced neurologic disorders

dural sinus thrombosis

dystrophic calcification

dystrophin

dystrophin associated proteins

ejection fraction, abnormal

electrical sensation

electrocardiogram, abnormal

electroencephalogram

electromyogram

electromyogram, decremental response

electromyogram, fasciculation potentials

electromyogram, incremental response

electron microscopy

ELISA

embolism

embolism, brachial artery

Emery-Dreifuss muscular dystrophy

emotional lability

encephalitis

encephalomyelitis, postinfectious

encephalopathy

encephalopathy, progressive

endemic area

enterovirus

enterovirus infection of CNS

entrapment neuropathy

enzyme treatment

enzyme, defect

enzyme, muscle disease

enzyme, serum

eosinophilia

epidemiology of neurology

episodic neurologic deficits

exercise-induced neurologic dysfunction

exome sequencing

extraocular muscle lesion

extremity, cold

eye closure

eye movement, disorders of

face, elongated

face, numbness of

facial appearance, abnormal

facial asymmetry

facial hair, excessive

facial nerve palsy

facial nerve palsy, recurrent

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

fine motor function, impaired

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

F-wave response

gag reflex, depressed

gait disorder

gait speed

gait, waddling

gammaglobulin therapy, intravenous

ganglioneuroma

gastrocnemius muscle weakness

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic diagnosis, prenatal

genetic neurologic disorders

glucose tolerance test, abnormal

glycogen debranching enzyme deficiency

glycogen storage disease

gout

Gowers maneuver

granulomatosis with polyangiitis

granulomatosis, allergic

granulomatous disease

Guillain Barre syndrome

Guillain Barre syndrome, ataxic form

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, ophthalmoplegia in

Guillain Barre syndrome, pharyngeal-cervical-brachial variant

Guillain Barre syndrome, variant forms of

gynecomastia

hallucination

hallucination, auditory

hearing problems in children

heart block

heart block, complete

heart murmur

heat intolerance

hemianopia

hemidiaphragm, paralysis of

hemiparesis

hepatomegaly

hepatosplenomegaly

heralding manifestation

herniated disc

herniated disc, cervical

highly active antiretroviral therapy

histochemistry of muscle

hoarseness

hospice

hot bath test

hourglass constrictions of nerves

H-reflex testing

human immunodeficiency virus type 1

hung reflex

hyperadrenalism

hypercalcemia

hypereosinophilic syndrome(HES)

hypergammaglobulinemia

hyperparathyroidism

hyperparathyroidism, secondary

hyperphosphatasia

hyperreflexia

hypersensitivity reaction

hypokalemic periodic paralysis

hypokinetic left ventricle

hyponatremia

hypoosmolality of serum

hypotension, systemic

iatrogenic neurologic disorders

idiopathic inflammatory myopathy

ileus, paralytic

imbalance

immune checkpoint inhibitors

immune-related adverse events

immunohistochemistry

immunomodulation

immunosuppression

immunosuppressive agents

impotence

impulsivity

inability to sit up

inability to stand on tiptoes

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

incidence

inclusion bodies

inclusion body myositis

intellectual deficit, treatable causes of

intelligence quotient

interstitial pulmonary fibrosis

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial hypotension

intravenous drug abuse

intrinsic hand muscles, wasting of

ischemic exercise test

Jakob-Creutzfeldt disease

jugular foramen syndrome

juvenile distal and segmental muscular atrophy

juxtacortical hemorrhage

karyotyping

klippel feil syndrome

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

lacunar infarction

laminectomy

laminectomy, cervical

laminopathies

language disorders in children

laughing, pathologic

lead poisoning

Leber's hereditary optic neuropathy

left handedness

leg atrophy

leg swelling

leg weakness, bilateral

leg weakness, unilateral

lethargy

leukemia

leukemia, neurologic findings assoc.with

leukocytosis

leukodystrophy

Lhermitte's sign

lid closure, weakness of

life expectancy

life support, withdrawal of

limb-girdle weakness

linear lesion

lipid storage myopathy

lumbosacral plexopathy

lumbosacral plexus

lumbosacral plexus, neuritis

lumbosacral radiculopathy

lumbosacral radiculoplexopathy

Lyme disease

lymphadenopathy

lymphocyte capping, diminished

lymphocytic meningoradiculitis

lymphoma

lymphoma involving CNS

lymphopenia

lysosomal storage disease

malabsorption

malabsorption syndrome

malignancy screen

malignant hyperpyrexia

Man-In-The-Barrel syndrome

maple syrup urine disease

McArdle's disease

McArdle's disease, adult onset

McLeod syndrome

medulla oblongata, lesion of

MELAS syndrome

Melkersson's syndrome

memory, impairment of

meningeal enhancement

meningismus

meningitis

meningitis, aseptic

meningitis, late neurologic sequelae in

meningitis, leukemic

meningitis, neurologic aspects and complications of

meningomyelitis

mental retardation

mental status, abnormal

mestinon

metabolic acidosis

metabolic alkalosis

microangiopathy, brain

middle cerebellar peduncle

midline defect in children

migraine

mimics

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve prolapse

MNGIE syndrome

molecular genetics

monoclonal antibodies

monoclonal gammopathy

monoclonal gammopathy of uncertain significance

monomelic amyotrophy

mononeuritis multiplex

mononeuropathy

mononeuropathy multiplex

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, susceptibility weighted

MRI, vertebral bone marrow

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, Becker, carrier

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, lymphocyte capping, diminished

muscular dystrophy, pattern of muscle involvement

muscular dystrophy, systemic membrane defect

myasthenia gravis

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, infantile and juvenile

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, neonatal

myasthenia gravis, neuromuscular junction in

myasthenia gravis, presenting manifestations

myasthenia gravis, treatment of

myasthenic crisis

myasthenic syndrome

myasthenic syndrome, treatment of

myelitis

myelitis, longitudinal

myelitis, post infectious

myelopathy, chronic progressive

myelopathy, tract-specific

myoclonus, stimulus sensitive

myopathy, carcinomatous

myopathy, centronuclear

myopathy, distal

myopathy, drug-induced

myopathy, glycogen storage

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, immune-mediated

myopathy, proximal

myopathy, quadriceps

myopathy, scleromyxedema

myopathy, steroid induced

myopathy, thyroid disease causing

myopathy, toxic

myopathy, vacuolar

myositis

myositis, granulomatous

myxedema, neurologic manifestations of

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, hormone producing, ectopic

neoplasm, metastatic to CNS

neoplasm, metastatic to muscle

nerve biopsy

nerve conduction studies

nerve root enhancement

neuralgia

neuralgia, intercostal

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neurolymphomatosis

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, acute

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, recurrent

neuropathy, sensory

neuropathy, short-fiber

neuropathy, toxic

neuropathy, vasculitic, systemic

neuroprotective agents

neurotoxin

neutropenia

next-generation sequencing

obstetric neurologic injuries

ocular motility, disorders of

ocular myopathy

oculopharyngeal muscular dystrophy

old age, neurology of

opened mouth

ophthalmoplegia

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

ophthalmoplegia, total

opportunistic infection, CNS

optic atrophy

optic neuritis

optic neuropathy

optic neuropathy, hereditary

oral contraceptives

oropharyngeal weakness

orthopnea

osteomalacia

overlap syndrome

owl's eye sign of spinal cord

pacemaker, cardiac-transvenous

pain, pseudoradicular

pain, scapula

pain, severe

pain, thigh

palate, paralysis-unilateral

palatopharyngeal incompetence

paralysis, acute areflexic

paralysis, asymmetric

paranoia

paraparesis

paraparesis, flaccid

paraparesis, progressive

paraplegia

paraplegia, acute

paraspinal muscle

paraspinal muscle weakness

Parkinsonism syndrome

parotid gland swelling

periodic paralysis, thyrotoxic

peripheral blood smear

peripheral nerve, lesion of

peripheral pulse, absent

phrenic nerve paralysis

pinched face

pitfalls

plasma cell dyscrasia

plasmapheresis

pleocytosis of cerebrospinal fluid

pleurisy

pneumonia

poison, neurologic problems with

poison, organophosphate

poliomyelitis

poliomyelitis-like illness

polymerase chain reaction

polymerase chain reaction, false negative

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

polyneuropathy, lymphomatous

polyradiculoneuropathy

polyuria

Pompe's disease of glycogen storage

porphyria

positive sharp waves

post infectious plexopathy

posterior column disease

posterior fossa

posterior fossa, lesion of

posterior spinal artery infarction

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

primary intracranial hypotension

prion disease

progeria

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

propranolol

proteinuria

proximal muscle atrophy

proximal myotonic myopathy

pseudohypertrophy

pseudomyotonia

psychiatric problems in neurologic disorders

psychological testing, neurologic problems

pulmonary function tests

pulmonary hypertension

pulmonary infiltrates

purkinje cell cytoplastic autoantibody

pyramidal tract

pyramidal tract dysfunction

radial pulse, unilateral decrease of

radiation induced neoplasm

radicular pain

radiculitis

radiculopathy

radionuclide imaging, heart

ragged-red fibers

rapidly progressing neurologic illness

rash

Raynaud's phenomenon

real-time quaking-induced conversion

rehabilitation for neurologic disorders

remote effect of cancer on the nervous system

renal biopsy

renal failure

renal stones

repetitive nerve stimulation

respirator

respiratory failure

respiratory tract infection

retina, abnormal

retinal lesion

retrovirus

reversible neurologic disorder

rheumatoid arthritis factor(R.A.factor)

rheumatoid arthritis, neurologic complications of

rigid spine syndrome

riluzole

rippling muscle disease

scalenus anticus syndrome

schizophrenia

schwannoma

Schwartz-Jampel syndrome

scleroderma

sclerosis, bone

scoliosis

scoliosis, neurologic association with

scotoma

screening

season

sedimentation rate, elevated

seizure

seizure, advice to parents and teachers regarding

seizure, focal

seizure, psychosocial aspects of

seizure, treatment of

sensorineural hearing loss

sensory ganglia

sensory level

sensory loss

sensory loss, pseudoradicular

serologic testing

serologic testing of cerebrospinal fluid

short stature

shoulder, pain in

shoulder, weakness

shoulder-girdle wasting

single-fiber electromyography

sinusitis

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, lesions in neurologic disorders

sleep

sleep apnea

sleep pathology and physiology

speech disorder, childhood

speech, slowed

spina bifida

spinal accessory nerve palsy

spinal cord

spinal cord vasculature

spinal cord, cervical

spinal cord, compression of

spinal cord, enlargement

spinal cord, infarction of

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal cord, vascular disorders Affecting

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spine, metastasis to

spinocerebellar degeneration

spirochete infection

splenium of corpus callosum

splenomegaly

splinter hemorrhages

sports medicine, neurology of

standing difficulty

statin therapy

status epilepticus

stem cell transplantation

steroid

steroid therapy, CNS treatment and complications with

subarachnoid hemorrhage

subcutaneous edema

sudden death

suicide

superior sagittal sinus thrombosis

suprascapular nerve

suprascapular neuropathy

supraspinatus muscle

survival motor neuron gene

suspended sensory loss

swimming

syncope

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

telangiectases, periungual

temporal lobe, lesion

temporalis muscle wasting

tensilon test, false positive

tethered spinal cord

thirst

thoracic outlet syndromes

thrombocytopenia

thyroid function tests

thyroiditis

thyrotoxicosis

tick bite

tissue plasminogen activator, intravenous

toe walking

tomaculous neuropathy

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, weakness

torticollis

toxins, nervous system

transient ischemic attack

transverse smile

trapezius weakness

trauma

treatment of neurologic disorder

tremor

tremor, intention

trinucleotide repeats

urine osmolality, elevated

urine test for metabolic disorders

urine, dark

vasculitides

vasculopathy

ventricular tachycardia

vestibular migraine

vibratory sensation, abnormal

walking, difficulty with

watershed infarcts

Watson-Schwartz reaction

weakness, fluctuating

weakness, focal

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

web sites

weight loss

Werdnig-Hoffman disease

West Nile fever

Western immunoblot test

wheelchair

whistle, inability to

white matter disease

wide based gait

winging of scapula

word-finding difficulty

X-linked bulbospinal neuronopathy

zinc

Showing articles 200 to 250 of 1540 << Previous Next >>

Proximal Myopathy Due to Discrete Carcinomatous Metastases in Muscle
JNNP 46:358-360, Doshi,R.,et al, 1983

Myopathy & Hypersensitivity to Phenytoin
Neurol 33:790-791, Harney,J.,et al, 1983

Endocrine Myopathies
BMJ 287:705-708, Kendall-Taylor,P.,et al, 1983

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

Necrotizing Myopathy Associated with Steroid Therapy, Report of Two Cases
Pathology 14:435-438, Ojeda,V.J., 1982

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

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

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

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

Insulin-Induced Weakness in Hypokalemic Myopathy
Ann Neurol 6:139-140, Ruff,R.L., 1979

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

A Case of Schwartz-Jampel Syndrome with Unusual Muscle Biopsy Findings
Ann Neurol 3:93, Fariello,R.,et al, 1978

Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
Neurol 28:1135-1140, Dobkin,B.H.,et al, 1978

Systemic Membrane Defect in the Proximal Muscular Dystrophies
NEJM 299:841-846, Pickard,N.A.,et al, 1978

Clinical Syndromes of Myasthenia in Infancy & Childhood
Arch Neurol 35:97, Fenichel,G.M., 1978

Adult Onset Nemaline Myopathy
Neurol 28:1306-1309, Brownell,A.K.W.,et al, 1978

Carnitine Deficiency Acute Postpartum Crisis
Ann Neurol 4:558-561, Angelini,C.,et al, 1978

Muscle Fiber-Type Disproportion
Arch Neurol 35:823-826, Eisler,T.,et al, 1978

Acute Hypokalemic Myopathy in Alcoholism
Arch Neurol 34:553, Rubenstein,A.E.,et al, 1977

Rigid Spine Syndrome:A Type I Fiber Myopathy
Arch Neurol 34:119, Seay,A.R.,et al, 1977

Eosinophilic Polymyositis
Ann Neurol 1:65, Layzer,R.B.,et al, 1977

The Adult Form of Acid Maltase (a-1, 4-Glucosidase) Deficiency
Ann Neurol 1:276, Karpati,G.,et al, 1977

Clinical Pathological Conference
Dermatomyositis, Case Record, 33-1977, NEJM 297:37877., , 1977

Proximal Diabetic Neuropathy
Ann Neurol 2:179, 1977, (Editorial) ., Asbury,A.K., 1977

Granulomatous Myositis & Myopathy Assoc. with Crohn's Colitis
NEJM 295:818, Menard,D.B.,et al, 1976

Cardiac Features of Unusual X-linked Humeroperoneal Neuromuscular Disease
et al NEJM 293:1017, Waters,D.D., 1975

Case Records of the MassGeneral Hospital, Case 41-1975, Acute Intermittent Porphyria
NEJM 293:817, Woods,B., 1975

Brachial Plexus Neuropathies
In Peripheral Neuropathy, Ed by PJ Dyck, PK Thomas, EH Lambert, WB Saunders Co. , Phila, Vol 1, p 65, Tsairis,P., 1975

Quadriceps Myopathy-Entity or Syndrome
Arch Neurol 31:60, Boddie,H.,et al, 1974

Neuromuscular Disease in Primary Hyperparathyroidism
Ann Int Med 80:182, Patten,B.M.,et al, 1974

The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica
p498-501, VanWijngaarden,G.K.&Bethlem,J., 1973

Nontraumatic Plexitis and Heroin Addiction
JAMA 225:958-961, Challenor,Y.B.,et al, 1973

Case Records of MGH-NEJM 286:934
1972 Osteochondrosarcoma & Residual Ganglioneuroma., , 1972

Pediatric Neurology
Psych Annals 2:1, , 1972

Comprehensive Mangagement of Duchenne Muscular Distrophy
Arch Phys Med & Rehab Mar 1971, pp110., Johnson,E.,et al, 1971

Chronic Spinal Muscular Atrophy in Adults
J Neurol Sci 9:527, Meadows,J.C.,et al, 1969

Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
The New Physic 263, 1967, Oct., Boshes,L., 1967

The Muscular Dystrophies
NEJM 273:537, 5961965., Zundel,W.,et al, 1965

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

Muscular Dystrophy
Am J Med 35:632, Pearson,C.M., 1963

Five Types of Dystrophy
Together with Other Conditions Producing Insidious Muscle Weakness-Table 1-Hospital Med p. 60., , 1850

Brachial artery embolus mimicking acute stroke
, Holmstedt, C. & Chimowitz, M.,

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

Clinicopathologic Conference, Lyme Neuroborreliosis and Coinfection with Babesia Microti
NEJM 394:383-391, Case 3-2026, 2026

A Woman with Subacute Progression of Distal Upper Extremity Weakness
Neurol 105:e214212, Zhao,A.J.,et al, 2025

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,et al, 2025

A 69-Year-Old Woman with Ophthalmoplegia
Neurol 104:e213763, Yu, H & Frey, J, 2025

Clinical, Prognostic, and Longitudinal Functional and Neuropsychological Features of West Nile Virus Neuroinvasive Disease in the United States: A Systematic Review and Meta-Analysis
Ann Neurol 98:93-106, Roberts,J.A.,et al, 2025

Showing articles 200 to 250 of 1540 << Previous Next >>