Neudle.com: hypertrophy muscle

Differential
(Click to cross reference)

abdominal distention

acid maltase deficiency

acid maltase deficiency, adult

acromegaly

acute intermittant porphyria

advances in neurology

adverse drug reaction

alcohol, neurologic complications with

alcoholic polyneuropathy

aneurysm, thoracic aortic

anterior horn cell disease

anticonvulsants

aortic wall, thickened

aortitis

areflexia

arrhythmia, cardiac

arterial dissection, aorta

arterial dissection, wall thickness

brachial neuritis, acute

cardiovascular disease

CAT scan

CAT scan, abnormal

CAT scan, angiography

CAT scan, emission, abnormal

CAT scan, metrizamide

CAT scan, muscle

CAT scan, myelogram with

cataracts

cauda equina

cauda equina, enhancement

cauda equina, lesion of

cavernous sinus

cavernous sinus, lesion of

central nervous system, infection of

cerebellar lesion

cerebral ischemia

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular disease, cardiovascular disease with

cerebrovascular disease, risk factors in

chromosomal abnormality

chromosome 17

claudication, intermittent of cauda equina

Clinical Pathologic Conference(C.P.C.)

CLOVES syndrome

complications

confusion

congenital malformation

congenital myopathy

congestive heart failure

contractures, joint

coronary artery disease

corticotropin level

corticotropin-releasing factor

cortisol, elevated

cranial nerve enlargement

cranial nerves

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cysticercosis, cerebral

cysticercosis, disseminated

cysticercosis, intraventricular

cysticercosis, miliary

deafness

deep gray nuclei

Dejerine-Sottas syndrome

delay in diagnosis

denervation of muscle

dentate nuclei

dentate nuclei, lesion of

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

diamond on quadriceps

diaphragmatic paralysis

differential diagnosis

difficulty climbing stairs

dilantin

diplopia

distal muscle atrophy

distal muscle weakness

dysthyroid ocularmyopathy

dystonia

dystonia, post traumatic

dystrophin

dystrophin associated proteins

echocardiogram

echocardiogram, LVH

edema, periorbital

electrocardiogram, abnormal

electrocardiogram, LVH

electroencephalogram

electroencephalogram, abnormalities of

electromyogram

electron microscopy

encephalopathy

encephalopathy, progressive

entrapment neuropathy

enzyme, defect

eosinophilic fasciitis

epidermal nevus syndrome

exercise

exophthalmus

extraocular muscle enlargement

facial hair, excessive

facial pain

facial pain, atypical

facial weakness

facial weakness, bilateral

failed medical management

fine motor function, impaired

fistula, arterio-venous, carotid-cavernous

fistula, arterio-venous, dural

gammaglobulin therapy, intravenous

genetic diagnosis, prenatal

genetic neurologic disorders

Graves ophthalmopathy

Guillain Barre syndrome

hemiatrophy, congenital

hemidiaphragm, paralysis of

hemihypertrophy, congenital

hemihypertrophy, facial

hemimegalencephaly

hemiparesis

hepatomegaly

hereditary myopathy with early respiratory failure

hypopigmentation of skin

intrinsic hand muscles, wasting of

irritability

Isaacs syndrome

Kobberling-Dunnigan syndrome

Krabbe's disease

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lacrimal gland enlargement

laminectomy, cervical

laminectomy, lumbar

learning disability

learning disability, in children

left ventricular dilatation

leg atrophy

leg numbness

leg swelling

leg weakness, unilateral

leukemia

leukocyte enzyme abnormality

liver function enzymes

lordosis

lumbosacral plexopathy

lymphoma

lymphopenia

macrocephaly

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malignant hyperpyrexia

masseter muscle hypertrophy

mental status, abnormal

monoclonal gammopathy

mononeuritis multiplex

mononeuropathy

mononeuropathy chronic inflammatory demyelinating

MRI, contrast enhanced

MRI, cranial nerves

MRI, hypointense signal foci on

MRI, lumbosacral plexus

MRI, muscle

MRI, optic nerve

MRI, orbit

MRI, peripheral nerve

MRI, spinal cord

MRI, spine

MRI, vessel wall

MRI, vessel wall enhancement

MRS

mucormycosis

multimodal neuroimaging

multiple myeloma

muscle atrophy, focal

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle hypertrophy

muscle hypertrophy, congenital

muscle weakness, proximal

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, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, dystrophin normal

muscular dystrophy, facioscapulohumeral

muscular dystrophy, female occurrence of

muscular dystrophy, limb-girdle

muscular dystrophy, pattern of muscle involvement

myelogram

myelopathy

myeloradiculopathy

myocardial infarction

neoplasm, hormone producing, ectopic

neoplasm, metastatic to muscle

neoplasm, metastatic to orbit

neoplasm, peripheral nerve

nerve biopsy

nerve conduction studies

nerve enlargement

nerve hypertrophy

nerve injury

nerve root enhancement

nerve root hypertrophy

neuritis

neuritis, causes of

neuritis, heavy metals causing

neurocutaneous disease

neurologic disease, diagnoses of

neurologic examination

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, medication induced

neuropathy, onion bulb

neuropathy, peripheral

optic chiasm, enlarged

optic nerve

optic nerve sheath enhancement

optic nerve, compression of

optic nerve, enlarged

optic nerve, lesion of

optic neuropathy

optic neuropathy, bilateral

orbit, cellulitis of

orbit, inflammation in

orbit, pseudotumor of

paresthesias, lower extremity

PAS positive material in the brain

pathology

percussion induced muscle contraction

perineuritis

perineuritis, optic

peripheral nerve, lesion of

plasma cell dyscrasia

polyneuropathy

polyneuropathy, chronic idiopathic

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic relapsing

polyneuropathy, familial

post polio syndrome

postural abnormality

prenatal diagnosis by amniocentesis

prognosis

progressive neurologic disorder

proptosis

proximal muscle atrophy

rhabdomyosarcoma of orbit

rigidity

rippling muscle disease

sensorineural hearing loss

skin, lesions in neurologic disorders

somnolence

spasticity

speech disorder, childhood

speech, delayed development of

spinal accessory nerve

spinal cord, compression of

spinal cord, neoplasm

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, intermediate form

spinal stenosis

spinal stenosis, familial

startle reaction

steppage gait

steroid

steroid therapy, CNS treatment and complications with

subarachnoid hemorrhage

subcutaneous nodules

sudden death

superior ophthalmic vein

survival motor neuron gene

symmetric brain lesions

syncope

syringomyelia

systemic illness

telangiectases, retinal

temporal artery

temporalis muscle enhancement

temporalis muscle hypertrophy

temporalis muscle swelling

thalamus, lesion of-bilateral

transient ischemic attack

trauma

treatment of neurologic disorder

trigeminal nerve

trigeminal nerve, abnormality of

trigeminal nerve, hypertrophy

trigeminal nerve, lesion of

trigeminal neuralgia

tripping

ultrasonography, nerve

urinary frequency

urine, dark

vasculitis, large vessel

vertebral artery wall thickness

vision, blurred

visual acuity, decreased

visual fields, constricted

visual loss

vital capacity

weakness

weakness, generalized

weakness, progressive

Showing articles 1250 to 1300 of 2814 << Previous Next >>

CSF Antigliadin Antibodies and the Ramsay Hunt Syndrome
Neurol 49:1131-1133, Chinnery,P.F.,et al, 1997

Prognosis in Familial ALS:Progr & Surv in Pts with glu100gly & ala4val Mutations in Cu, Zn Superoxide Dismutase
Neurol 48:55-57, Juneja,T.,et al, 1997

Mononeuropathy of a Distal Branch of the Femoral Nerve in a Body Building Champion
JNNP 63:669-671, Padua,L.,et al, 1997

AIDS Dementia Complex with Generalized Myoclonus
Mov Disord 12:593-597, Maher,J.,et al, 1997

Clinical Epidemiology of Nocturnal Leg Cramps in Male Veterans
Am J Med Sci 313:210-214, Haskell,S.G.&Fiebach,N.H., 1997

Pediatric Ulnar Mononeuropathy:Report of 21 Electromyography-Documented Cases & Review of Literature
J Child Neurol 11:116-120, Felice,K.J.&Jones,H.R., 1996

Needle Electromyography in the Thoracic Paraspinal Muscles of Motor Neuron Disease
No to Shinkei-Brain & Nerve 48:637-642996., Kyuno,K.,et al, 1996

Motor Neuron Disease with Parkinsonism
Arch Neurol 53:987-991, Qureshi,A.I.,et al, 1996

Age on Onset, Sex, & Cardiomyopathy as Predictors of Disability and Survival in Friedreich's Disease
Neurol 47:1260-1264, DeMichele,G.,et al, 1996

Linomide Reduces the Rate of Active Lesions in Relapsing-Remitting Multiple Sclerosis
Neurol 47:895-900, Anderson,O.,et al, 1996

Angiotropic Large-Cell Lymphoma with Peripheral Nerve & Skeletal Muscle Involvement:Early Diagnosis & Treatment
Neurol 47:1009-1011, Levin,K.H.&Lutz,G., 1996

Progressive Encephalomyelitis with Rigidity Responsive to Plasmapheresis and Immunosuppression
Ann Neurol 40:451-453, Fogan,L., 1996

Axillary Neuropathy in Volleyball Players:Report of Two Cases and Literature Review
JNNP 60:345-347, Paladini,D.,et al, 1996

Critical Illness Myopathy and Neuropathy
Lancet 347:1579-1582, Latronico,N.,et al, 1996

Clinicopath Conf
Tangier Disease, Case 16-1996, NEJM 334:1389-1394996., , 1996

Motor Neuropathy Due to Docetaxel and Paclitaxel
Neurol 47:115-118, Freilich,R.J.,et al, 1996

Ten Steps in Characterizing and Diagnosing Patients with Peripheral Neuropathy
Neurol 47:10-17, Dyck,P.J.,et al, 1996

Multifocal Motor Neuropathy
JNNP 60:599-603, Nobile-Orazio,E., 1996

Hereditary Spastic Paraplegia:Advances in Genetic Research
Neurol 46:1507-1514, Fink,J.K.,et al, 1996

Classification of Daily and Near-Daily Headaches:Field Trial of Revised IHS Criteria
Neurol 47:871-875, Silberstein,S.D.,et al, 1996

Diagnostic Guidelines in Central Nervous System Whipple's Disease
Ann Neurol 40:561-568, Louis,E.D.,et al, 1996

Human T-Cell Lymphotrophic Virus Type II-Associated Myelopathy:Clinical and Immunologic Profiles
Ann Neurol 40:714-723, Lenky,T.J.,et al, 1996

Distal WEakness in Dystrophin-Deficient Muscular Dystrophy
Muscle & Nerve 19:1608-1610996., Felice,K.J., 1996

Total Alopecia, Diabetes Mellitus, and Falls
Lancet 348:1420, Mueller-Schoop,J.W., 1996

Cognitive Dysfunction as the Major Presenting Feature of Becker's Muscular Dystrophy
Neurol 46:461-465, North,K.N.,et al, 1996

Unusual Clinical Presentations of Cortical-Basal Ganglionic Degeneration
Ann Neurol 40:893-900, Bergeron,C.,et al, 1996

Clozapine-Induced Myotoxicity in Patients with Chronic Psychotic Disorders
Neurol 47:1518-1523, Scelsa,S.N.,et al, 1996

Acute Myopathy of Intensive Care:Clinical, Electromyographic, and Pathological Aspects
Ann Neurol 40:645-654, Lacomis,D.,et al, 1996

Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy
Ann Neurol 40:782-791, Pegoraro,E.,et al, 1996

Inclusion Body Myositis:Clinical and Pathological Boundaries
Ann Neurol 40:581-586, Amato,A.A.,et al, 1996

Investigation of Muscle Disease
JNNP 60:256-274, Mastaglia,F.L.&Laing,N.G., 1996

Brain and Spinal Cord MRI in Motor Neuron Disease
JNNP 61:314-317, Thorpe,J.W.,et al, 1996

Amyotrophic Lateral Sclerosis and Occupational History
Arch Neurol 53:730-733, Strickland,D.,et al, 1996

Avoiding False Positive Diagnoses of Motor Neuron Disease:Lessons from the Scottish Motor Neuron Disease Register
JNNP 60:147-151, Davenport,R.J.,et al, 1996

Diagnosing Motor Neurone Disease
BMJ 312:650-651, Chancellor,A.M., 1996

Motor Neuron Disease
BMJ 313:244, Shneerson,J.M., 1996

Motor Neuron Disease Presenting as Acute Respiratory Failure:A Clinical and Pathological Study
JNNP 60:455-458, Chen,R.,et al, 1996

Dose-Ranging Study of Riluzole in Amyotrophic Lateral Sclerosis
Lancet 347:1425-1431, Lacomblez,L.,et al, 1996

Skin Involvement in Amyotrophic Lateral Sclerosis
lancet 347:1226-1227, Kolde,G.,et al, 1996

Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
Ann Neurol 39:352-360, Scolding,N.J.,et al, 1996

AAEM Case Report#13:Diabetic Amyotrophy
Muscle & Nerve 19:939-945996., Chokroverty,S.&Sander,H.W., 1996

Ethylene Oxide Neurotoxicity:A Cluster of 12 Nurses with Peripheral and Central Nervous System Toxicity
Neurol 46:992-998, Brashear,A.,et al, 1996

Clinicopath Conf
Hypertension, MI, and Cerebral Infarctions with Pheochromocytoma, Am J Med 100:357-36496., , 1996

Opsoclonus
Semin Neurol 16:21-26, Averbuch-Heller,L.&Remler,B., 1996

Diffuse Lewy Body Disease:Clinical Features in Nine Cases without Coexistent Alzheimer's Disease
JNNP 60:531-538, Hely,M.A.,et al, 1996

Development of General Weakness in a Patient with Amyotrophic Lateral Sclerosis after Focal Botulinum Toxin Injection
Neurol 46:845-846, Mezaki,T.,et al, 1996

Chronic Inflammatory Demyelinating Polyradiculoneuropathy:Unusual Clinical Features and Therapeutic Responses
Neurol 46:1206-1212, Midroni,G.&Dyck,P.J., 1996

Yelling Attacks and Wasted Hands
Lancet 348:238, Bosboom,W.M.J.,et al, 1996

Diagnosis of McArdle's Disease by Molecular Genetic Analysis of Blood
Neurol 47:579-580, El-Schahawi,M.,et al, 1996

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996

Showing articles 1250 to 1300 of 2814 << Previous Next >>