Neudle.com: myotonia

Neurology Specific Literature Search

Differential
(Click to cross reference)

abortion, spontaneous

acid maltase deficiency

advances in neurology

adverse drug reaction

adynamia episodica hereditaria

airway obstruction

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, familial

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

anesthesia, general

anterior interosseous neuropathy

antiarrhythmic drugs

antibodies to voltage-gated calcium channels

anticoagulant, treatment

anticoagulant, treatment in CVD

anticonvulsants

anticonvulsants, untoward effects of

arrhythmia, cardiac

arthrogryposis multiplex

ataxia, hereditary

ataxia, paroxysmal

atrial fibrillation

atrioventricular block

auditory and vestibular pathways

auditory evoked brainstem potentials

autoimmune disease

autoimmune encephalopathy

automatic implantable cardioverter-defibrillator

autonomic dysfunction

axonal degeneration

axonopathy, distal

basal ganglia, calcification of

behavioral disorder

beta adrenergic agonist

blepharophimosis

brachial neuritis

brainstem, lesion of

calcification, intracranial

calcium antagonist

calcium channel dysfunction

calf hypertrophy

cancer of colon

carbamazepine, toxicity

carcinoma of ovary

carcinoma of pancreas

carcinoma of uterus

cardiac arrest and resuscitation

cardiac surgery, neurologic complications with

cardiac transplantation

carotid angiogram

CAT scan, abnormal

CAT scan, muscle

central core disease

central nervous system, infection of

cerebral blood flow

cerebral embolism

cerebral embolism, cardiac origin

cerebral ischemia

cerebrospinal fluid, elevated protein of

cerebrovascular accident

cerebrovascular accident, prevention of

cerebrovascular accident, young adult

Charcot-Marie-Tooth

chewing, impaired

chloride channel dysfunction

chromosomal abnormality

chronic progressive external ophthalmoplegia

ciguatera poisoning

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cold hands sign

cold intolerance

cold temperature

compression neuropathy

conduction block

confidentiality

congenital birth defects

congenital heart disease

congenital myopathy

congestive heart failure

contactin associated protein like 2 antibodies

contractures, joint

controversies in neurology

corneal dystrophy

corpus callosum

corpus callosum, thinning

cranial nerve palsies

cranial neuropathy

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

cylindrical spiral

dantrolene sodium

defibrillator, implanted

degenerative diseases of CNS

delay in diagnosis

delayed muscle relaxation

dementia, thalamic

dentatorubral-pallidoluysian atrophy

dermatomyositis

diabetes mellitus

diaphragmatic paralysis

differential diagnosis

difficulty climbing stairs

dilantin, toxicity

disability, neurological

distal muscle weakness

down-beat nystagmus

dropped head syndrome

drug induced neurologic disorders

electrocardiogram, abnormal

electron microscopy

electronystagmography

electronystagmography, abnormal

electrophoretic pattern, serum

electroretinograph

emergencies, neurologic

encephalopathy, anoxic

encephalopathy, neonatal

entrapment neuropathy

enzyme treatment

eosinophilic fasciitis

epidemiology of neurology

episodic disorders

episodic neurologic deficits

evoked potentials

exercise electrocardiography

exercise intolerance

eye movement, disorders of

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

facial nerve, lesion of

facial weakness

facial weakness, bilateral

familial hemiplegic migraine

Fazio-Londe's disease

fine motor function, impaired

fluorescein angiography

fragile-X syndrome

Friedreich's ataxia

frontal balding

F-wave response

gammaglobulin therapy, intravenous

gastric partitioning

genetic counselling

genetic diagnosis

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

glucose tolerance test, abnormal

Gowers maneuver

Guillain Barre syndrome

heart block, complete

heavy metal intoxication

heralding manifestation

high arched feet

high arched palate

hip flexor weakness

histochemistry of muscle

H-reflex testing

human diploid cell rabies vaccine

Huntington's chorea

hydrops fetalis

hyperinsulinism

hyperkalemic periodic paralysis

hyperparathyroidism

hypokalemic periodic paralysis

hypoparathyroidism

hypoparathyroidism, idiopathic

hypotonia, causes of

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

immunodeficiency

immunologic disease

immunomodulation

immunosuppressive agents

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion body myositis

intellectual deficit

intelligence quotient

Isaacs syndrome

Kearns-Sayre syndrome

klippel feil syndrome

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

laryngeal spasm

leg weakness, bilateral

leucine rich glioma inactivated 1 antibodies

lid abnormalities

lid closure, weakness of

lid retraction, lower

life expectancy

limbic encephalitis

lymphoma, primary of CNS

malignancy screen

malignant hyperpyrexia

manic-depressive

median neuropathy

Melkersson's syndrome

mental retardation

mental status, abnormal

metabolic acidosis

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve prolapse

molecular genetics

Morvan's fibrillary chorea

motor neuron disease

MRI, functional

multiple sclerosis

multiple sclerosis, diet in

multiple sclerosis, treatment of

muscle atrophy, progressive

muscle atrophy, static

muscle diseases, characteristics of

muscle hypertrophy

muscle stiffness

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, cardiovascular changes with

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, non motor symptoms

myasthenic crisis

myasthenic syndrome

myasthenic syndrome, treatment of

myokymia, facial

myopathy, acute

myopathy, carcinomatous

myopathy, distal

myopathy, drug-induced

myopathy, genetic

myopathy, hereditary

myopathy, metabolic

myopathy, mitochondrial

myopathy, myofibrillar

myopathy, necrotizing

myopathy, proximal

myopathy, thyroid disease causing

myopathy, toxic

myopathy, vacuolar

myotonia congenita

myotonia dystrophica

myotonia dystrophica, classification

myotonia dystrophica, type 2

myotonia, causes of

myotonia, treatment of

myotonic crisis

myotonic discharges

neoplasm, metastatic to CNS

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

nerve conduction studies

nerve conduction studies, motor

neuritis, causes of

neurocutaneous disease

neurofibrillary degeneration

neurofibromatosis 1

neurofibromatosis 2

neurogenic vs.myopathic atrophy

neurologic complications of, surgery

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neuromuscular disease, electrodiagnosis of

neuromyotonia and axonal neuropathy

neuromyotonia, ocular

neuronal migration disorder

neuroophthalmology

neuropathy, amyloid

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, medication induced

neuropathy, motor, multifocal

neuropathy, peripheral

newborn, evaluation of

next-generation sequencing

nystagmus, vertical

ocular myopathy

oculovestibular reflex

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegic migraine

orbicularis oculi muscle

orbit, lesions of

pacemaker, cardiac-transvenous

paramyotonia congenita

paraspinal muscle

Parkinson disease

paroxysmal neurologic deficits

percussion induced muscle contraction

pericardial effusion

periodic paralysis

peripheral nerve, lesion of

physical activity

platelet inhibiting drugs

pleural effusion

poison, mercury

poison, neurologic problems with

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

Pompe's disease of glycogen storage

positive sharp waves

post polio syndrome

posterior fossa

posterior interosseous neuropathy

postoperative neurologic complications

potassium channel antibodies

potassium channel dysfunction

precipitating factors

pregnancy, neurologic complications in

premature infant

prevention of neurologic disorders

primary episodic ataxia

progressive neurologic disorder

proximal muscle atrophy

proximal myotonic myopathy

psychiatric problems in neurologic disorders

psychological testing

ptosis, bilateral

pulmonary function tests

pulmonary hypertension

radiation neuropathy

radiation therapy, CNS treatment and complications with

radionuclide angiocardiography

ragged-red fibers

recombinant DNA

red cell aplasia

remote effect of cancer on the nervous system

respiratory failure

respiratory tract infection

rippling muscle disease

risk-benefit assessment

saccadic eye movements

saccadic eye movements, abnormal

salivation, excessive

Schwartz-Jampel syndrome

second wind phenomena

sedimentation rate, elevated

sensorineural hearing loss

shoulder, pain in

single photon emission computed tomography

skin, lesions in neurologic disorders

skin, thickened

sleep pathology and physiology

slit lamp examination

sodium channel dysfunction

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 6

spinocerebellar degeneration

standing difficulty

steroid therapy, CNS treatment and complications with

stiff man syndrome

sweating, abnormality of

syphilis, neurologic complications with

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

testicular atrophy

thiamine deficiency

thoracic outlet syndromes

tone, muscle, increased

transient ischemic attack

treatment of neurologic disorder

tricresylphosphate

trigeminal nerve

trigeminal nerve, lesion of

trigeminal neuropathy

trinucleotide repeats

tubular aggregates, muscle

ulnar neuropathy

ultrasonography

ventricular tachycardia

vertigo, cervical

vertigo, treatment of

viral infection, CNS

visual evoked response

vitamin deficiency

vocal cord paralysis

walking, difficulty with

weakness, acute

weakness, episodic

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

Werdnig-Hoffman disease

Wernicke's encephalopathy

white matter disease

white matter disease, periventricular

winging of scapula

X-linked bulbospinal neuronopathy

X-linked myopathy

x-linked myopathy with excessive autophagy

Showing articles 50 to 100 of 138 << Previous Next >>

Anesthetic and Surgical Complictions in 219 Cases of Myotonic Dystrophy
Neurol 49:1646-1650, Mathieu,J.,et al, 1997

Proximal Myotonic Myopathy with MRI White Matter Abnormalities of the Brain
Neurol 48:33-37, Hund,E.,et al, 1997

Myotonic Dystrophy, The Role of Large Triplet Repeat Length in the Develop of Mental Retardation
Arch Neurol 54:251-254, Spranger,M.,et al, 1997

Pure Motor Hand Weakness
Semin Neurol 16:75-81, Lewis,R.A., 1996

Neurogenic Muscle Hypertrophy
Muscle & Nerve 19:811-818996., Gutmann,L., 1996

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

Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
Arch Neurol 52:25-31, Ricker,K.,et al, 1995

Cardiac Involvement in a Large Kindred with Myotonic Dystrophy:Quant Assess & Relation to Size of CTG Repeat Expansion
JAMA 274:813-819, Tokgozoglu,L.S.,et al, 1995

Proximal Myotonic Myopathy Syndrome in the Absence of Trinucleotide Repeat Expansions
Muscle & Nerve 18:782-783995., Stoll,G.,et al, 1995

Acquired Neuromyotonia:Evidence for Autoantibodies Directed Against K+Channels of Peripheral Nerves
Ann Neurol 38:714-722, 7011995., Shillito,P.,et al, 1995

Myotonic Dystrophy
In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994

The Nondystrophic Myotonias
In Myology, McGraw-Hill, 2nd Ed, Ch49, p1291-13024., Rudel,R.,et al, 1994

Myotonic Dystrophy with No Trinucleotide Repeat Expansion
Neurol 35:269-272, 2551994., Thornton,C.A.,et al, 1994

Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994

Direct Diagnosis of Myotonic Dystrophy with a Disease-Specific DNA Marker
NEJM 328:471-475, Shelbourne,P.,et al, 1993

Brief Report:Reverse Mutation in Myotonic Dystrophy
NEJM 328:476-480, Brunner,H.G.,et al, 1993

Genetics and Physiology of the Myotonic Muscle Disorders
NEJM 328:482-489, Ptacek,L.J.,et al, 1993

Cerebral Abnormalities in Myotonic Dystrophy
Arch Neurol 50:917-923, Chang,L.,et al, 1993

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

The Polymerase Chain Reaction:Application to Nervous System Disease
Ann Neurol 34:513-523, Darnell,R.B., 1993

The Heart in Myotonic Dystrophy
Editorial, Lancet 339:528-5291992., , 1992

Post-Irradation Neuromyotona Affecting Trigeminal Nerve Distribution:An Unusual Presentation
Neurol 42:1102-1104, Diaz,J.M.,et al, 1992

Oculomotor, Auditory, and Vestib ular Responses in Myotonic Dystrophy
Arch Neurol 49:954-960, Verhagen,W.I.M.,et al, 1992

Unstable DNA Sequence in Myotonic Dystrophy
Lancet 339:1125-1128, Harley,H.G.,et al, 1992

Phenotypic Expression of the Myotonic Dystrophy Gene in Monozygotic Twins
Neurol 42:1815-1817, Dubel,J.R.,et al, 1992

Continuous Muscle Fiber Activity, Peripheral Neuropathy, and Thymoma
Ann Neurol 29:215-218, Garcia-Merino,A.,et al, 1991

Myotonic Heart Disease:A Clinical Follow-Up
Neurol 41:259-262, Hawley,R.J.,et al, 1991

Response to Treatment with Antihistamines in a Family with Myotonia Congenita
Lancet 337:28-30, Hughes,E.F.&Wilson,J., 1991

Autoimmune Aetiology for Acquired Neuromyotonia (Isaacs'Syndrome)
Lancet 338:75-77, Sinha,S.,et al, 1991

Ventricular Late Potentials in Myotonic Dystrophy
Ann Int Med 115:607-613, Milner,M.R.,et al, 1991

Presymptomatic and Prenatal Diagnosis in Myotonic Dystrophy by Genetic Linkage Studies
Neurol 40:671-676, Speer,M.C.,et al, 1990

Criteria for Establishing the Validity of Genetic Recombination in Myotonic Dystrophy
Neurol 39:420-421, Griggs,R.C.,et al, 1989

Magnetic Resonance Imaging and Clinical Correlates of Intellectual Impairment in Myotonic Dystrophy
Arch Neurol 46:536-540, Huber,S.J.,et al, 1989

The Molecular Genetic Revolution, Its Impact on Clinical Neurology
Arch Neurol 45:1366-1376, Payne,C.S.&Roses,A.D., 1988

Hearing Loss in Myotonic Dystrophy
Ann Neurol 23:202-203, Wright,R.B.,et al, 1988

Central Nervous System Magnetic Resonance Imaging Findings in Myotonic Dystrophy
Arch Neurol 45:36-37, Glantz,R.H.,et al, 1988

Peripheral Neuropathy in Myotonic Dystrophy:A Nerve Biopsy Study
Ann Neurol 23:470-476, Cros,D.,et al, 1988

Hydrops and Pleural Effusions in Congenital Myotonic Dystrophy
J Pediatr 113:555-557, Curry,C.J.R.,et al, 1988

Cerebral Ischemia with Mitral Valve Prolapse
Am Heart J 113:1308-1315, Wolf,P.A.,et al, 1987

Genetic Linkage in Neurologic Diseases
Editorial, NEJM 316:1018-10201987., Martin,J.B., 1987

Association of Primary Hyperparathyroidism with Myotonic Dystrophy in Two Patients
Arch Int Med 147:777-778, Harada,S.,et al, 1987

Acetazolamide-Responsive Myotonia Congenita
Neurol 37:488-491, Trudell,R.G.,et al, 1987

Computed Tomographic Findings of Brain & Skull in Myotonic Dystrophy
JNNP 50:435-438, Avrahami,E.,et al, 1987

Cerebral Ventricular Dilation in Congenital Myotonic Dystrophy
J Pediatr 111:372-376, Regev,R.,et al, 1987

Treatment of Myotonia
Editorial, Lancet 1:1242-12441987., , 1987

Frequency of Cerebral Infarction in Patients with Inherited Neuromuscular Disease
Stroke 18:805-807, Biller,J.,et al, 1987

Clinicopath Conf
Kearns-Sayre Syndrome (Oculocraniosomatic Neuromuscular Disease with Mitochondrial Myopathy) , Case, 4-1,NEJM 317:493-501,1987., 1987

Adynamia Episodica & Paralysis Periodica Paramyotonica
Neurol 36:682-686, Ricker,K.,et al, 1986

Successful Treatment with Tocainide of Recessive Generalized Congenital Myotonia
Ann Neurol 19:501-504, Streib,E.W., 1986

Cardiac Side Effects of Phenytoin & Carbamazepine, A Dose-Related Phenomenon
Arch Neurol 42:1067-1068, Durelli,L.,et al, 1985

Showing articles 50 to 100 of 138 << Previous Next >>