Neudle.com: metabolic myopathy

Differential
(Click to cross reference)

abdominal distention

abdominal muscle paralysis

abducens nerve paralysis

abscess, intracerebral

acetazolamide

acid maltase deficiency

acid maltase deficiency, adult

acoustic nerve

acquired immunodeficiency syndrome

activities of daily living scale

acyl CoA dehydrogenase deficiency

adrenoleukodystrophy

advances in neurology

adverse drug reaction

alcohol

alcohol intolerance

alcohol, heart involvement with

alcohol, neurologic complications with

alcoholism

alkylating agents

alpha glucosidase

altered states of consciousness

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

anemia

aneurysm

aneurysm, intracranial

ankle, swelling of

anterior horn cell disease

anterior tibial muscle weakness

arthrogryposis multiplex

ascending paralysis

asparginase

aspartate aminotransferase

auditory evoked brainstem potentials

autoimmune disease

autonomic dysfunction

azidodeoxythymidine

Babinski sign

BAL

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery stenosis

basophilic stippling of red blood cells

Bassen-Kornzweig syndrome

blood dyscrasias, neurologic findings with

bone marrow suppression

bone marrow transplantation

brainstem, dysfunction

calcification, intracranial

calf hypertrophy

caloric testing

camptocormia

cancer, cerebrovascular accident complicating patients with

canned food

carbon monoxide poisoning

carbon monoxide poisoning, chronic

carnitine deficiency myopathy

CAT scan

CAT scan, abnormal

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, muscle

cataracts

cataracts, congenital

central core disease

central nervous system, infection of

cerebellar atrophy, secondary

cerebellar degeneration

cerebral cortex

cerebral cortical atrophy

cerebral glucose metabolism

cerebral ischemia

cerebro hepato renal syndrome

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure low

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, nonvascular territory

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

Charcot-Marie-Tooth

chemical weapons

chemotherapy, CNS treatment and complications with

cherry red spot-myoclonus syndrome

chromosomal abnormality

chromosome 11

chronic fatigue syndrome

chronic graft versus host disease

chronic progressive external ophthalmoplegia

Chvostek sign

ciguatera poisoning

Clinical Pathologic Conference(C.P.C.)

Cockayne's syndrome

coenzyme Q10

coenzyme Q10 deficiency

congestive heart failure

corticotropin-releasing factor

cortisol, elevated

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cricopharyngeal bar

critical care unit

cultured skin fibroblasts

Cushing's syndrome

cyclic vomiting

cytochrome c oxidase

cytochrome c oxidase, deficiency

cytokines

deafness

DEET

degenerative diseases of CNS

delay in diagnosis

delirium

dementia

dementia, rapidly progressive

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

diaphragmatic paralysis

diarrhea

differential diagnosis

difficulty climbing stairs

diphtheria

diplopia

distal muscle atrophy

distal muscle weakness

dropped head syndrome

drowsiness

drug induced neurologic disorders

electrocardiogram, abnormal

electromyogram

electron microscopy

electronystagmography

electroretinograph

emergencies, medical

emergencies, neurologic

emtricitabine

encephalitis

encephalitis, autoimmune

encephalomalacia

encephalomyopathy

encephalopathy

encephalopathy, anoxic

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, progressive

enzyme treatment

enzyme, defect

enzyme, muscle disease

enzyme, serum

eosinophilia

epidemiology of neurology

epilepsia partialis continua

episodic disorders

episodic neurologic deficits

exercise-induced neurologic dysfunction

exercise-related muscle strength increase

extraocular muscle atrophy

eye movement, disorders of

facial appearance, abnormal

facial hair, excessive

facial nerve palsy

facial nerve palsy, bilateral

facial pain

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

Fazio-Londe's disease

feeding disorder

fever

fibrillations

fingernails, abnormal

fundus, abnormality of

gag reflex, depressed

gait disorder

gammaglobulin therapy, intravenous

gangliosidosis GM2

gastroenteritis

gastrointestinal motility

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

glucocerebrosidase

glycogen debranching enzyme deficiency

glycogen storage disease

gonadal dysgenesis

Gowers maneuver

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Gulf War syndrome

gyrus, abnormal

Hallervorden Spatz disease

hallucination

hand weakness

headache

headache, sudden onset of

hearing loss

heart block

heavy metal intoxication

hemianopia

hemianopia, transient

heralding manifestation

hexosaminidase-A

hip flexor weakness

hirsutism

histochemistry of muscle

human immunodeficiency virus type 1

hypoparathyroidism, idiopathic

hypophonia

hyporeflexia

hypotension, systemic

hypoxic encephalopathy

iatrogenic neurologic disorders

ileus, paralytic

imbalance

immune checkpoint inhibitors

immune-related adverse events

immunologic disease

immunosuppression

immunosuppressive agents

immunotherapy

impotence

impulsivity

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

inborn errors of metabolism

inborn errors of metabolism, screening

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion body myositis

insect repellent

insecticides

intellectual deficit

intellectual deterioration

intelligence quotient

intestinal pseudoobstruction

intracerebral hemorrhage

ipecac

ipilimumab

ischemic exercise test

Kearns-Sayre syndrome

klippel feil syndrome

Korsakoff's psychosis

Kugelberg-Welander syndrome

kyphosis

lactic acidemia

lactic dehydrogenase(LDH)

Lafora's disease

laminar necrosis, cortical

Laurence-Moon-Bardet-Biedl syndrome

Leber's hereditary optic neuropathy

leg swelling

leg weakness, bilateral

Leigh's disease

lens, dislocation of

leukemia

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

level of consciousness, decreased

lid closure, weakness of

life expectancy

limb-girdle weakness

lipid storage disorder of CNS

lipid storage myopathy

liver disease

liver function enzymes

lordosis

low back pain

lymphopenia

lysosomal storage disease

McArdle's disease, adult onset

memory, impairment of

meningeal enhancement

meningismus

meningitis

meningitis, leukemic

meningoencephalopathy

mental retardation

mental status, abnormal

metabolic disorder, primary

metallic taste

methotrexate

methylhydrazine derivatives

microcephaly

migraine

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

MNGIE syndrome

molecular genetics

molybdenum cofactor deficiency

monoamine oxidase inhibitors

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, gyral enhancement

MRI, gyral swelling

MRI, hypointense signal foci on

MRI, muscle

MRI, serial

MRI, T1 weighted high signal foci

MRS

mucopolysaccharidoses

multiple organ failure

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle hypertrophy

muscle pain

muscle phosphofructokinase deficiency

muscle phosphorylase deficiency

muscle spasm

muscle stiffness

muscle strength, testing

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, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, neonatal screening

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, ocular

myopathy, carcinomatous

myopathy, centronuclear

myopathy, critically ill

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, genetic

myopathy, inflammatory

myopathy, metabolic

myopathy, mitochondrial

myopathy, necrotizing

myopathy, necrotizing, immune-mediated

myopathy, proximal

myopathy, steroid induced

myopathy, thyroid disease causing

myotonia, treatment of

nemaline rod myopathy

neonatal screening, genetic neurologic disorders

neoplasm, hormone producing, ectopic

neoplasm, metastatic

neoplasm, metastatic to CNS

nephrotic syndrome

nerve agents

nerve biopsy

nerve conduction studies

nerve conduction studies, sensory

neuritis, causes of

neuritis, heavy metals causing

neuroendocrinology

neurofibrillary degeneration

neurogenic vs.myopathic atrophy

neurologic complications

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuronal ceroid-lipofuscinosis

neurons

neuroophthalmology

neuropathology

neuropathology, peripheral nerves

neuropathy

neuropathy, acute

neuropathy, ataxia, retinitis pigmentosa

neuropathy, diabetic

neuropathy, diphtheritic

neuropathy, hereditary peripheral

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, peripheral

newborn, evaluation of

next-generation sequencing

occipital lobe, lesion of

occupational neurologic disorders

ocular motility, disorders of

ocular myopathy

old age, neurology of

ophthalmoplegia

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

ophthalmoplegia, total

organ transplantation

orthopnea

orthostatic hypotension

paramyotonia congenita

paraparesis

paraspinal muscle

paraspinal muscle weakness

patient information and support

peripheral blood smear

peripheral blood smear, abnormal

peripheral nerve, lesion of

peroxisomal disease

personality change

phosphorylase b kinase deficiency

pigmentary retinopathy

plasmapheresis

pleocytosis of cerebrospinal fluid

pleural effusion

poison, mercury

poison, neurologic problems with

poison, organophosphate

POLG1 gene

poliomyelitis

polymerase chain reaction

polymyalgia rheumatica

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, critically ill

Pompe's disease of glycogen storage

Pompe's disease, infantile

porphyria

position sensation, abnormal

postpartum

postural abnormality

precipitating factors

preclinical

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

procarbazine

prognosis

progressive neurologic disorder

proprioception, abnormal

proteinuria

proximal muscle atrophy

pruritus

pseudomyotonia

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pulmonary function tests

pulmonary hypertension

pulmonary infiltrates

quadriparesis

quadriparesis, acute

quadriparesis, progressive

quadriplegia

quadriplegia, transient

radionuclide imaging, heart

ragged-red fibers

rapidly progressing neurologic illness

rash

recurrent

recurrent laryngeal nerve paralysis

respiratory tract infection

reversible neurologic disorder

second wind phenomena

sensorineural hearing loss

sensory symptoms

sensory testing

sensory testing, quantitative

short stature

skin, lesions in neurologic disorders

sleep pathology and physiology

sodium channel dysfunction

sodium valproate

sodium valproate, toxicity

somatosensory evoked potentials

Southern immunoblot test

spasticity

spinal cord, compression of

spinal cord, metastasis to

spinal muscular atrophy

spinocerebellar degeneration

spongy degeneration of brain

spontaneous remission

steroid therapy, CNS treatment and complications with

stiff man syndrome

stooped posture

storage disease of CNS

strokelike episodes

subarachnoid hemorrhage

suicide

sweating, abnormality of

symmetric brain lesions

systemic illness

tachycardia

tapetoretinal degeneration

taxol

Tay-Sachs disease

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thirst

thrombocytopenia

tinnitus

tone, muscle, increased

toxins, nervous system

transient neurologic deficit

transverse smile

treatment of neurologic disorder

Unverricht-Lundborg disease

urine test in toxic screen

urine, dark

Usher's syndrome

vaccination, neurologic complications with

vecuronium

vinblastine

vincristine neurotoxicity

walking, difficulty with

weakness, fluctuating

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weight loss

Werdnig-Hoffman disease

wheelchair

whistle, inability to

white matter disease

whole genome sequencing

winging of scapula

workup

wrist drop

Showing articles 400 to 450 of 1936 << Previous Next >>

Clinicopathologic Conference, Inflammatory Myopathy and Myasthenia Gravis Assoc. with Thymoma
NEJM 369:764-773, Case 26-2013, 2013

Head Drop in Huntington Disease: Insights into the Pathophysiology
Neurol 81:769-770, Morgante, F.,et al, 2013

Clinicopathologic Conference, Rabies Encephalitis
NEJM 368:172-180, Case 1-2013, 2013

A 62-Yeal-Old Man with Fluctuating Neurological Deficits and Skin Lesions
JAMA Neurol 70:120-124, Konikkara, J.,et al, 2013

Everolimus Long-Term Safety and Efficacy in Subependymal Giant Cell Astrocytoma
Neurol 80:574-580, Krueger, D.,et al, 2013

Clinicopatholic Conference, Acute Infection with Hepatitis B Virus
NEJM 368:1239-1245, Case 10-2013, 2013

Retrospective Review of Cerebral Mycotic Aneurysms in 26 Patients: Focus on Treatment in Strongly Immunocompromised Patients with a Brief Literature Review
AJNR 34:823-827, Allen, L.M.,et al, 2013

Correlation of Clinicoserologic and Pathologic Classifications of Inflammatory Myopathies
Medicine 92:15-24, Fernandez, C.,et al, 2013

Polymyalgia Rheumatica
Lancet 381:63-72, Kermani, T. & Washington, K., 2013

Primary CNS Posttransplant Lymphoproliferative Disease (PTLD): An International Report of 84 Cases in the Modern Era
Am J Transplant 13:1512-1522, Evens, A.M.,et al, 2013

Diffusion-Weighted Imaging in Acute Hyperammonemic Encephalopathy
Neurohosp 3:125-130, Rosario, M.,et al, 2013

The Spectrum of Statin Myopathy
Curr Opin Rheumatol 25:747-752, Mohassel, P. & Mammen, A.L., 2013

Neurological Immune-Related Adverse Events of Ipilimumab
Pract Neurol 13:278-280, Bot, I.,et al, 2013

Clinical Findings and Diagnosis in Human Granulocytic Anaplasmosis: A Case Series from Massachusetts
Mayo Clin Proc 87:233-239, Weil, A.A.,et al, 2012

Primary Sjogren Syndrome
BMJ 344:e3821, Ramos-Casals, M.,et al, 2012

The Ever-Expanding Spectrum of Congenital Muscular Dystrophies
Ann Neurol 72:9-17, Mercuri, E. & Muntoni, F., 2012

A Young Man with Progressive Subcortical Lesions and Optic Nerve Atrophy
Neurol 79:e63, Komatsuzaki, S.,et al, 2012

Clincopathologic Conference,Graves Disease with Thyrotoxic Periodic Paralysis
NEJM 366:553-560, Case 4-2012, 2012

Characteristics of Intravascular Large B-Cell Lymphoma on Cerebral MR Imaging
AJNR 33:292-296, Yamamoto,A.,et al, 2012

Reversible Paraneoplastic Tonic Pupil
Neurol 78:1820-1822, Horta, E.,et al, 2012

Intracranial Optic Nerve Enlargement in Infantile Krabbe Disease
Neurol 78: e126, Shah, S.,et al, 2012

Clinicopathologic Conference, Glioblastonoma, WHO grade IV of IV, with Methylation of the MGMT Promoter
NEJM 366:2112-2120, Case 17-2012, 2012

Evidence-based Guideline: Intravenous Immunoglobulin in the Treatment of Neuromascular Disorders
Neurol 78:1009-1015, Patwa,H.S.,et al, 2012

Peripheral Neuropathy after Hip Replacement Failure: Is Vanadium the Culprit?
Lancet 379:1676, Moretti,B.,et al, 2012

Acute Symptomatic Seizures
The Neurologist 18:109-119, Beleza,P., 2012

A Case of Necrotizing Myopathy with Proximal Weakness and Cardiomayopathy
Neurol 78:1527-1532, Matthews,E.,et al, 2012

Central Nervous System Involvement in Dengue
Neurol 78:736-742, Araujo,F.M.C.,et al, 2012

A 21-year old Woman with Multiple Cancers and a New Brain Lesion
Neurol 78:743-749, Schiff,D.,et al, 2012

Inflammatory Myopathies with Anti-Ku Antibodies
Medicine 91:95-102, Rigolet,A.,et al, 2012

Cogan Syndrome An Analysis of Reported Neurological Manifestations
The Neurologist 18:55-63, Antonios,N. and Silliman,S., 2012

Clinicopathologic Conference,Necrotizing Noninflammatory Myopathy Consistent with Exposure to Statins
NEJM 36:944-954, Case 7-2012, 2012

Clinicopathologic Conference, Rocky Mountain Spotted Fever
NEJM 366:1434-1443, Case 11-2011, 2012

Persistent Diffusion-Restricted Lesions in Bevacizumab-Treated Malignant Gliomas are Associated with Improved Survival Compared with Matched Controls
AJNR 33:1763-1770, Mong, S.,et al, 2012

Neurologic Manifestations of E Coli infection - induced Hemolytic-Uremic Syndrome in Adults
Neurol 79:1466-1473, Weissenborn, K.,et al, 2012

Diabetic Ketoacidosis Accompanied by Hypothermia:A Case Report
Diabetes Reser Clin Pract 96:326-330, Nambu,T.,et al, 2012

Primary Central Nervous System T-Cell Lymphoma of the Brain
Open Neurosurg J 4:62-65, Behbahami, M. & Lyons, M., 2011

Infectious Mononucleosis in Adults and Adolescents
UpToDate, May, Aronson,M.D. & Auwaerter,P.G., 2011

Longitudinal Assessment of Oxaliplatin-Induced Neuropathy
Neurol 77:980-986, Burakgazi, A.Z.,et al, 2011

Treatment of Severe Neurological Deficits with IgG Depletion through Immunoadsorption in Patients with Escherichia coli O104:H4-Associated Haemolytic Uraemic Syndrome: A Prospective Trial
Lancet 378:1166-1173,1120, Greinacher, A.,et al, 2011

Clinicopathologic Conference, Cystoisospora Belli Enteritis and HIV Infection
NEJM 365:2306-2316, Case 38-2011, 2011

Clinicopathologic Conference, Thymoma with Paraneoplastic Myasthenia Gravis, Polymyositis and Myocarditis, and Brain Stem Encephalitis
NEJM 365:2413-2422, Case 39-2011, 2011

LMNA Cardiomyopathy:Cell Biology and Genetics Meet Clinical Medicine
Disease Models & Mechanisms 4:562-568, Lu,J.T., et al, 2011

In the Eye of the Cuban Epidemic Neuropathy Storm: Rosaralis Santiesteban MD PhD
MEDICC Review 13:10-15, Mills, C.,et al, 2011

Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
Brain 134:3326-3332, Garone, C.,et al, 2011

Myoglobinuria and Muscle Pain are Common in Patients With Limb-Girdle Muscular Dystrophy 21
Neurol 76:194-195, Mathews,K.D.,et al, 2011

Guidelines for the Prevention of Stroke in Patients With Stroke or Transient Ischemic Attack: A Guideline for Healthcare Professionals From the American Heart Association/American Stroke Association
Stroke 42:227-276, Furie,K.L.,et al, 2011

Current Concepts and Management of Glioblastoma
Ann Neurol 70:9-21, Preusser, M.,et al, 2011

Weighing the Benefits of High-Dose Simvastatin against the Risk of Myopathy
NEJM 365:285-287, Egan, A.,et al, 2011

Clinicopathologic Conference, Susacs Syndrome (retinocochleocerebral vasculopathy)
NEJM 365:549-559, Case 24-2011, 2011

Rituximab Monotherapy for Patients With Recurrent Primary CNS Lymphoma
Neurol 76:929-930, Batchelor,T.T.,et al, 2011

Showing articles 400 to 450 of 1936 << Previous Next >>