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Differential
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acetazolamide
acid maltase deficiency
advances in neurology
adverse drug reaction
airway obstruction
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
anesthesia, general
antiarrhythmic drugs
antibodies to voltage-gated calcium channels
anticonvulsants
antihistamines
arrhythmia, cardiac
arthrogryposis multiplex
ataxia
ataxia, paroxysmal
autoimmune disease
baldness
botulism
brainstem, lesion of
calcium antagonist
calcium channel dysfunction
carbamazepine
carcinoma
cardiac surgery, neurologic complications with
cardiac transplantation
cardiomyopathy
CAT scan
CAT scan, muscle
cataracts
central core disease
central nervous system, infection of
Charcot-Marie-Tooth
chewing, impaired
children
chloride channel dysfunction
chronic progressive external ophthalmoplegia
clubfoot as related to neurologic disease
complications
congenital birth defects
congenital heart disease
congenital myopathy
controversies in neurology
corpus callosum
corpus callosum, thinning
creatine phosphokinase(CPK)elevated
degenerative diseases of CNS
differential diagnosis
dilantin
dropped head syndrome
drug induced neurologic disorders
electrocardiogram, abnormal
electromyogram
electron microscopy
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
epidemiology of neurology
eye closure
facial appearance, abnormal
facial nerve palsy
facial nerve palsy, bilateral
facial nerve, lesion of
facial weakness
facial weakness, bilateral
falling
familial
familial hemiplegic migraine
Fazio-Londe's disease
floppy infant
frontal balding
gene mutation
genetic neurologic disorders
genetic testing
heavy metal intoxication
high arched feet
high arched palate
Huntington's chorea
hydrocephalus
hyperkalemic periodic paralysis
hypokalemia
hypokalemic periodic paralysis
hypotonia
hypotonia, causes of
hypotonia, infants
hypoxic encephalopathy
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion body myositis
kaliuresis
Kearns-Sayre syndrome
Kugelberg-Welander syndrome
lid closure, weakness of
lordosis
malignant hyperpyrexia
Melkersson's syndrome
metabolic acidosis
mexiletine
micrognathia
migraine
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
motor neuron disease
MRI
MRI, abnormal
MRI, muscle
muscle biopsy
muscle cramp
muscle hypertrophy
muscle pain
muscle stiffness
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, congenital
muscular dystrophy, Duchenne
myasthenia gravis
myoglobinuria
myopathy
myopathy, drug-induced
myopathy, mitochondrial
myotonia
myotonia congenita
myotonia dystrophica
myotonia dystrophica, classification
myotonia, treatment of
neck weakness
neoplasm, metastatic to CNS
neoplasm, primary of CNS
neurofibrillary degeneration
neurologic disease, diagnoses of
neurologic evaluation
newborn, evaluation of
nifedipine
ocular myopathy
orbicularis oculi muscle
paramyotonia congenita
paresthesias
paroxysmal neurologic deficits
percussion induced muscle contraction
periodic paralysis
poison, mercury
poison, neurologic problems with
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
polymyositis
postoperative neurologic complications
potassium channel antibodies
potassium channel dysfunction
procainamide
prognosis
respiratory failure
review article
rhabdomyolysis
seizure
sodium channel dysfunction
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 6
temporalis muscle wasting
term infant
tocainide
treatment of neurologic disorder
tricresylphosphate
trinucleotide repeats
tubular aggregates, muscle
viral infection, CNS
weakness
weaning from respirator, failure to
Werdnig-Hoffman disease
workup
Showing articles 50 to 100 of 1186 << Previous Next >>

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

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

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

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

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

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

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

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

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

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

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

Cardiac Involvement in Myotonic Muscular Dystrophy
Medicine 64:371-387, Moorman,J.R.,et al, 1985

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

Radionuclide Angiocardiographic Analysis of Myocardial Function in Myotonic Muscular Dystrophy
Neurol 33:657-660, Hartwign,G.B.,et al, 1983

The Treatment of Myotonia:Evaluation of Chronic Oral Taurine Therapy
Neurol 33:599-603, Durelli,L.,et al, 1983

Abnormal Visual Evoked Potentials in Myotonic Dystrophy
Neurol 33:1622-1625, Cott,P.S.,et al, 1983

Families with Myotonic Dystrophy with & without Cardiac Involvement
Arch Int Med 143:2134-2136, Hawley,R.J.,et al, 1983

Myotonic Dystrophy, Mitral Valve Prolapse, and Cerebral Embolism
Stroke 13:93-94, Morris,L.K.,et al, 1982

Respiratory Muscle Function and Ventilatory Control in Patients with Myotonic Dystrophy
Q J Med 202:205-226, Serisier,D.E.,et al, 1982

Hypersomnia Associated with Alveolar Hypoventilation in Myotonic Dystrophy
Neurol 31:1336-1337, Hansotia,P.,et al, 1981

Congenital Myotonic Dystrophy
Arch Neurol 37:693-696, Argov,Z.,et al, 1980

Echocardiographic Evaluation of Cardiac Abnormalities in Duchenne's Dystrophy & Myotonic Muscular Dystrophy
Arch Neurol 37:273-277, Reeves,W.C.,et al, 1980

Myotonic Dystrophy
In Harrison's Principles of Internal Medicine, 9th Ed, McGraw-Hill Book Co, NY 206180., Adams,R.D.,et al, 1980

Retraction of the Lower Eyelid
Neurol 29:386-389, Cohen,M.M.,et al, 1979

Cholestasis & Myotonic Dystrophy
(letter) NEJM 301:329-330979., Theodore,Ch.,et al, 1979

Peripheral Neuropathy in Myotonic Dystrophy
Arch Neurol 35:741-745, Olson,N.D.,et al, 1978

Erythrocyte Metabolism in Muscular Dystrophy
Arch Neurol 35:592-595, Danon,M.J.,et al, 1978

Abnormal Iris Vasculature in Myotonic Dystrophy
Arch Neurol 35:224, Stern,L.Z.,et al, 1978

Myasthenia Gravis & Myotonic Dystrophy in a 13-year-old Girl
Neurol 27:546, Schoen,R.T., 1977

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

Preclinical Detection of Dystrophia Myotonica
BMJ 124, 1972 April., , 1972

Thalmic Neuronal Inclusion Disease
Neurol 22, 3961972., Segarra,J., 1972

Electrodiagnosis of Neuromuscular Disease
Bull Univ Maryland School Med 56:33, Kemble,F., 1971

Ophthalmoplegia In Myotonic Dystrophy
Am J Ophthalmol 71:1231-1235, Lessell,S.,et al, 1971

Early Recognition of Heterozygotes for the Gene for Dystrophia Myotonica
JNNP 33:279, Bundey,S.,et al, 1970

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

The Cerebral Defect & Myopathy in Myotonic Dystrophy
Neurol 17:1106, Rosman,N.,et al, 1967

Functional Outcome in Patients with Carotid Artery Dissection Undergoing Thrombectomy or Standard Medical Treatment
Neurol 104:e213465, Sykora,M.,et al, 2025

Severe Myotonic Crisis Resembling Malignant Hyperthermia
Neurol 104:e213497, Wadhwani,A.R.,et al, 2025

Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
Ann Neurol 97:611-628, Coppens,S.,et al, 2025



Showing articles 50 to 100 of 1186 << Previous Next >>