Neudle.com: mitochondrial myopathy

Differential
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abdominal distention

acanthocytosis

acquired immunodeficiency syndrome

adrenoleukodystrophy

advances in neurology

adverse drug reaction

agammaglobulinemia

alcoholism

aminoacidopathies

anterior tibial muscle weakness

anticonvulsants

anticonvulsants, selection of

basal ganglia, calcification of

basal ganglia, infarction

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

calcification, intracranial

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, muscle

CAT scan, xenon-enhanced

cataracts

cataracts, congenital

cause of death

central core disease

central nervous system, infection of

cerebellar ataxia, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebral blood flow

cerebral cortical atrophy

cerebral edema, cytotoxic

cerebral embolism

cerebral embolism, cardiac origin

cerebral glucose metabolism

cerebral infarction

cerebro hepato renal syndrome

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

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

cherry red spot-myoclonus syndrome

children

chromosomal abnormality

chronic progressive external ophthalmoplegia

Chvostek sign

Clinical Pathologic Conference(C.P.C.)

Cockayne's syndrome

coenzyme Q10

coenzyme Q10 deficiency

coma

congenital birth defects

congenital myopathy

consanguinity

cornea, abnormal

corpus callosum, lesion of

cortical blindness

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cricopharyngeal bar

cultured skin fibroblasts

cyst, parenchymal

cytochrome c oxidase

cytochrome c oxidase, deficiency

deafmute

deafness

deep gray nuclei

degenerative diseases of CNS

dementia

dementia, rapidly progressive

dentatorubral-pallidoluysian atrophy

depression

developmental retardation

diabetes mellitus

diarrhea

differential diagnosis

diplopia

distal muscle weakness

dizziness

DNA probes

drug induced neurologic disorders

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram

electron microscopy

electronystagmography

electroretinograph

encephalomyopathy

encephalopathy

encephalopathy, progressive

enzyme, defect

epilepsia partialis continua

evoked potentials

exercise

exercise intolerance

extraocular muscle atrophy

extraocular muscle lesion

eye closure

eye movement, disorders of

facial nerve palsy

facial nerve palsy, bilateral

facial nerve, lesion of

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

foot ulcer, neuropathic

Friedreich's ataxia

fundus, abnormality of

gadolinium

gait disorder

gargoylism

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic neurologic disorders

Hallervorden Spatz disease

Hallgren's syndrome

headache

headache, sudden onset of

hearing loss

heart block

hemianopia

hemianopia, homonymous

hemianopia, transient

hemiparesis

hepatic failure

hepatomegaly

heralding manifestation

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

hirsutism

histochemistry of muscle

human immunodeficiency virus type 1

hypoparathyroidism, idiopathic

inclusion bodies, intranuclear

inclusion body myositis

intellectual deficit

intellectual deterioration

intelligence quotient

intestinal pseudoobstruction

ischemic exercise test

Kearns-Sayre syndrome

laminar necrosis, cortical

Laurence-Moon-Bardet-Biedl syndrome

Leber's hereditary optic neuropathy

leg numbness

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leukocyte enzyme abnormality

leukodystrophy

leukoencephalopathy

lid closure, weakness of

life expectancy

lipoma of skin

lipomatosis

lipomatosis, multiple symmetrical

lordosis

macular degeneration

malaise

malformation, CNS, congenital

MELAS syndrome

Melkersson's syndrome

memory, impairment of

mental retardation

MERRF syndrome

microangiopathy, brain

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine

mimics

misdiagnosis

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, muscle

MRI, serial

MRS

mucopolysaccharidoses

muscle atrophy, progressive

muscle biopsy

muscle biopsy, extraocular

muscle cramp

muscle pain

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, congenital

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

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

myasthenia gravis, seronegative

myopathy, centronuclear

myopathy, drug-induced

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, mitochondrial

nemaline rod myopathy

neoplasm, primary of CNS

nephrotic syndrome

neuritis

neuroendocrinology

neurogenic vs.myopathic atrophy

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neurologic symptoms

neuromuscular blockade

neuromuscular junction, abnormality of

neuronal ceroid-lipofuscinosis

neuropathy, ataxia, retinitis pigmentosa

neuropathy, hereditary peripheral

neuropathy, peripheral

next-generation sequencing

occipital lobe, infarction

occipital lobe, lesion of

ocular motility, disorders of

ocular myopathy

ocular myopathy, differential diagnosis

oculopharyngeal muscular dystrophy

old age, neurology of

ophthalmoplegia

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

optic atrophy

optic atrophy, hereditary

optic disc edema

optic nerve

optic nerve, compression of

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, hereditary

orbicularis oculi muscle

Parkinsonism syndrome

pigmentary retinopathy

PLEDs

PLEDs, bilateral independent

PLEDs, etiology of

POLG1 gene

polydactyly

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

polymyalgia rheumatica

polymyositis

polyneuropathy

prognosis

progressive infantile poliodystrophy

progressive myoclonic epilepsy

progressive neurologic disorder

prostigmine

proteinuria

proximal muscle atrophy

pseudomyasthenia

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

rapidly progressing neurologic illness

respiratory tract infection

Reye's syndrome, adult

seizure, treatment of

sensorineural hearing loss

sensory loss

seronegative

short stature

single photon emission computed tomography

sore throat

Southern immunoblot test

spasticity

Spielmeyer Vogt syndrome

spinal muscular atrophy

spinocerebellar degeneration

spongy degeneration of brain

standing difficulty

Stephens syndrome

strokelike episodes

succinate dehydrogenase deficiency

symmetric brain lesions

systemic illness

tapetoretinal degeneration

temporal lobe, lesion

thalamus, lesion of-bilateral

transverse smile

treatment of neurologic disorder

trinucleotide repeats

undiagnosed

Unverricht-Lundborg disease

vision, failure of in childhood

visual acuity, decreased

visual field defect

visual fields, constricted

visual loss

visual loss, progressive

walking, difficulty with

weakness

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

web sites

weight loss

wheelchair

whistle, inability to

white matter disease

white matter disease, pattern

wide based gait

winging of scapula

workup

Showing articles 600 to 650 of 1110 << Previous Next >>

Clinical Genetics in Neurological Disease
JNNP 57:7-15, MacMillan,J.C.&Harper,P.S., 1994

Hypokalemic Myopathy Induced by Giardia Lamblia
NEJM 330:66-67, Addiss,D.G.&Lengerich,e.J., 1994

Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
Neurol 44:461-466, Wilkinson,D.A.,et al, 1994

Rapidly Evolving Myopathy with Myosin-Deficient Muscle Fibers
Ann Neurol 35:273-279, 2571994., Al-Lozi,M.T.,et al, 1994

The Mutations at nt 8993 of Mitochondrial DNA is a Common Cause of Leigh's Syndrome
Ann Neurol 34:827-834, Santorelli,F.M.,et al, 1993

Mitochondrial Involvement in Parkinson's Disease:The Controversy Continues
Neurol 43:2170-2172, DiMauro,S., 1993

Lissencephaly:A Human Brain Malformation Associated with Deletion of the LIS1 Gene Located at Chromosome 17p13
JAMA 270:2838-2842, Dobyns,W.B.,et al, 1993

Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test
JAMA 270:1569-1575, Brown,W.,et al, 1993

Tay-Sachs Disease-Carrier Screening, Prenatal Diagnosis, and the Molecular Era
JAMA 270:2307-2315, Kaback,M.,et al, 1993

Myositis-Specific Autoantibodies, Touchstones for Understanding the Inflammatory Myopathies
JAMA 270:1846-1849, Miller,F.W., 1993

MELAS Syndrome Masquerading as Herpes Simplex Encephalitis
Neurol 43:2471-2473, Johns,D.R.,et al, 1993

Tibial Muscular Dystrophy
Arch Neurol 50:604-608, Udd,B.,et al, 1993

Acute Myopathy and Neuropathy in Status Asthmaticus:Case Report and Literature Review
Muscle & Nerve 16:84-90993., Lacomis,D.,et al, 1993

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

Molecular Genetic Heterogeneity of Myophosphorylase Deficiency (McArdle's Disease)
NEJM 329:241-245, Tsujino,S.,et al, 1993

Myopathy in the Elderly:Evaluation of the Histopathologic Spectrum and the Accuracy of Clinical Diagnosis
Neurol 43:825-828, Lacomis,D.,et al, 1993

Molecular Genetic Characterization of an X-Linked Form of Leigh's Syndrome
Ann Neurol 33:652-655, Matthews,P.M.,et al, 1993

Leber's Hereditary Optic Neuropathy as a Cause of Severe Visual Loss in Childhood
Pediatrics 91:988-989, Moorman,C.M.&Elston,J.S., 1993

Atypical Leber's Hereditary Optic Neuropathy with Molecular Confiramtion
Arch Neurol 50:470-473, Weiner,N.C.,et al, 1993

Leber's Hereditary Optic Neuropathy, New Genetic Considerations
Arch Neurol 50:540-548, Newman,N.J., 1993

Neuropathic Findings in Oculopharyngeal Muscular Dystrophy, Seven Cases & Review of Literature
Arch Neurol 50:481-488, Hardiman,O.,et al, 1993

Evidence for Mitochondrial Dysfunction in Patients with Alternating Hemiplegia of Childhood
Ann Neurol 33:604-607, Arnold,D.L.,et al, 1993

Abnormal Expression of Dystrophin-Associated Proteins in Fukuyama-Type Congenital Muscular Dystrophy
Lancet 341:521-522, Matsumura,K.,et al, 1993

Neuromuscular Manifestations of Wegener's Granulomatosis:A Case Report
Neurol 43:617-618, Finkelman,R.,et al, 1993

The Neurological Complciations of Sepsis
Ann Neurol 33:94-100, Bolton,C.F.,et al, 1993

Clinicopath Conf
Tuberculosis of Mediastinal Lymph Nodes, Case 3-1993, NEJM 328:195-202993., , 1993

Experience with Screening Newborns for Duchenne Muscular Dystrophy in Wales
BMJ 306:357-360, 3491993., Bradley,D.M.,et al, 1993

Treatment of Inclusion-Body Myositis with High-Dose Intravenous Immunoglobulin
Neurol 43:876-879, Soueidan,S.A.&Dalakas,M.C., 1993

Inclusion Body Myositis Presenting Solely as Dysphagia
Neurol 43:1241-1243, Riminton,D.S.,et al, 1993

Acute Myopathy Associated with Large Parenteral Dose of Corticosteroid in Myasthenia Gravis
JNNP 56:702-704, Panegyres,P.K.,et al, 1993

Sudden Onset of Profound Weakness in a Toddler
J Pediatr 122:663-667, Carraccio,C.,et al, 1993

Clinicopath Conf
Axonal Polyneuritis Assoc with IgA Lambda Multiple Myeloma, Case 21-1993, NEJM 328:1550-1558993., , 1993

Acute Neuromuscular Respiratory Paralysis
JNNP 56:334-343, Hughes,R.A.C.&Bihari,D., 1993

The DNA Laboratory and Neurolgoical Practice
JNNP 56:229-233, Harding,A., 1993

Human Immunodeficiency Virus Type 1 Infection and Myopathy:Clinical Relevance of Zidovudine Therapy
Ann Neurol 34:206-211, Grau,J.M.,et al, 1993

Myopathies Assoc with HIV and Zidovudine:Can Their Effects be Distinguished?
Neurol 43:971-976, Simpson,D.M.,et al, 1993

MRI Changes in Intracranial Hypotension
Neurol 43:919-926, Pannullo,S.C.,et al, 1993

Fulminant Rhabdomyolysis in a Patient with Dermatomyositis
Neurol 43:844-845, Caccamo,D.V.,et al, 1993

Drug Therapy of Idiopathic Inflammatory Myopathies:Response to Prednisone Azathioprine, & Methotrexate
Am J Med 94:379-387, Joffe,M.M.,et al, 1993

The Treatment of Inclusion Body Myositis:A Retrospective Review & Random, Prospective Trial of Immunosupp Therapy
Medicine 72:225-235, Leff,R.L.,et al, 1993

Ipecac Myopathy and Cardiomyopathy
JNNP 56:560-562, Dresser,L.P.,et al, 1992

Travel and Ciguatera Fish Poisoning
Arch Int Med 152:2049-2053, Lange,W.R.,et al, 1992

Severe Phenytoin Hypersensitivity with Myopathy:A Case Report
Neurol 42:2303, Barclay,C.L.,et al, 1992

Mosaic Express of Dystrophin in Carriers of Becker's Muscular Dyst & X-Linked Synd of Myalgia & Cramps
NEJM 327:1100, Minetti,C.&Bonilla,E., 1992

Skeletal Muscle Toxoplasmosis in Patients with Acquired Immunodeficiency Syndrome:A Clinicopath Study
Ann Neurol 32:535-542, Gherardi,R.,et al, 1992

The Psychological Consequences of Predictive Testing for Huntington's Disease
NEJM 327:1401-1405, 14491992., Wiggins,S.,et al, 1992

Neurologic Manifestations of Progressive Systemic Sclerosis
Arch Neurol 49:1292-1295, Averbuch-Heller,L.,et al, 1992

Immunologic Aspects of Neurological and Neuromuscular Diseases
JAMA 268:2918-2922, Zweiman,B.&Levinson,A.I., 1992

Acute Quadriplegic Myopathy:A Complic of Treat with Steroids, Nondepolarizing Blocking Agents, or Both
Neurol 42:2082-2087, Hirano,M.,et al, 1992

Myopathy in Severe Asthma
Am Rev Respir Dis 146:517-519, Douglass,J.A.,et al, 1992

Showing articles 600 to 650 of 1110 << Previous Next >>