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Differential
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advances in neurology
adverse drug reaction
amyloidosis
amyotrophic lateral sclerosis
anesthesia, general
anterior tibial muscle weakness
arrhythmia, cardiac
arthrogryposis multiplex
asymptomatic
automatic implantable cardioverter-defibrillator
bradycardia
bulging of biceps
calf atrophy
calf hypertrophy
calpain III deficiency
cardiomegaly
cardiomyopathy
cardiovascular disease
case studies
central core disease
Charcot-Marie-Tooth
children
complications
conduction block
congenital myopathy
congestive heart failure
contractures, joint
creatine phosphokinase(CPK)elevated
dermatomyositis
diamond on quadriceps
differential diagnosis
distal muscle atrophy
distal muscle weakness
DNA probes
DYSF gene
dysferlin
dysferlinopathy
dystroglycanopathies
dystrophin
dystrophin associated proteins
echocardiogram
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electromyogram
Emery-Dreifuss muscular dystrophy
epidemiology of neurology
erythrocyte
exercise
facial weakness
facioscapulohumeral syndrome
familial
fibrillations
foot drop
gait disorder
gait, waddling
gastrocnemius muscle weakness
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
Gowers maneuver
Guillain Barre syndrome
hand weakness
heart block
histochemistry of muscle
immunohistochemistry
inability to stand on tiptoes
klippel feil syndrome
Kugelberg-Welander syndrome
laminopathies
leg weakness, bilateral
lid closure, weakness of
life expectancy
limb-girdle weakness
LMNA gene
lordosis
lymphocyte capping, diminished
misdiagnosis
molecular genetics
mononeuropathy
motor neuron disease
MRI
MRI, abnormal
MRI, muscle
muscle atrophy, focal
muscle atrophy, progressive
muscle biopsy
muscle diseases, characteristics of
muscle hypertrophy
muscle pain
muscle stiffness
muscle swelling
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
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, congenital
muscular dystrophy, differential diagnosis of
muscular dystrophy, distal, Miyoshi
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, dystrophin normal
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
muscular dystrophy, lymphocyte capping, diminished
muscular dystrophy, pattern of muscle involvement
muscular dystrophy, systemic membrane defect
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myasthenic crisis
myoglobinuria
myopathy
myopathy, carcinomatous
myopathy, centronuclear
myopathy, distal
myopathy, distal, vacuolar
myopathy, mitochondrial
myopathy, quadriceps
myopathy, thyroid disease causing
myopathy, vacuolar
myositis
myotonia dystrophica
neck weakness
nemaline rod myopathy
neuritis, causes of
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination
neuropathy
neuropathy, diabetic
next-generation sequencing
oculopharyngeal muscular dystrophy
old age, neurology of
pacemaker, cardiac-transvenous
poliomyelitis
polymerase chain reaction
polymyositis
polyneuropathy
porphyria
pregnancy, neurologic complications in
progeria
prognosis
progressive neurologic disorder
proximal muscle atrophy
pseudohypertrophy
quadriceps atrophy
quadriceps weakness
quality of life
respirator
respiratory failure
review article
RFLPs
rhabdomyolysis
rippling muscle disease
sarcoglycan
sarcoglycanopathy
sarcoidosis
scoliosis
spinal muscular atrophy
standing difficulty
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
sudden death
syncope
systemic illness
toe walking
torticollis
treatment of neurologic disorder
urine, dark
walking frame
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weakness, proximal
web sites
Werdnig-Hoffman disease
wheelchair
whistle, inability to
winging of scapula
workup
Showing articles 500 to 550 of 1006 << Previous Next >>

A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats
NEJM 330:1401-1406, 14501994., Kremer,B.,et al, 1994

Antibiotic Induced Meningitis
JNNP 57:705-708, River,Y.,et al, 1994

Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
Neurol 44:721-727, Hirano,M.,et al, 1994

Further Reg Var of Acute Polyneuro:Bifacial or 6th Nerve Paresis, Lumbar Polyrad & Ataxia/Phary Cervical-Brachial Wkness
Arch Neurol 51:671-675, Ropper,A.H., 1994

Ekbom's Syndrome:Lypomas, Ataxia, and Neuropathy with MERRF
Muscle & Nerve 17:943-945994., Calabresi,P.,et al, 1994

Congenital Myopathies
Muscle & Nerve 17:131-144994., Bodensteiner,J.B., 1994

Early-Onset Respiratory Failure Caused by Severe Congenital Neuromuscular Disease
J Pediatr 124:636-638, Sandler,D.L.,et al, 1994

Benign Familial Disease with Muscle Mounding and Rippling
JNNP 57:344-347, Burns,R.J.,et al, 1994

The Dropped Head Syndrome with Chronic Inflammatory Demyelinating Polyneuropathy
Muscle & Nerve 17:808-810994., Hoffman,D.&Gutmann,L., 1994

Osteomalacic Myopathy
Muscle & Nerve 17:578-580994., Russell,J.A., 1994

Clinicopath Conf
Small Cell CA (of lung) with Lambert-Eaton Myasthenic Syndr, Case 32-1994, NEJM 331:528-5354., , 1994

Cerebrotendinous Xanthomatosis:Molecular Diagnosis Enables Presymptomatic Detection of a Treatable Disease
Neurol 44:288-290, Meiner,V.,et al, 1994

Cerebral Involvement in McLeod Syndrome
Neurol 44:117-120, Danek,A.,et al, 1994

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

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

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

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

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

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

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

Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes (MELAS) :Clinical, Radiological, Pathol & Genetic Observ
Ann Neurol 34:25-31, Koo,B.,et al, 1993

Ophthalmologic Manifestations in MELAS Syndrome
Arch Neurol 50:977-980, Fang,W.,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

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

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

The Syndrome of MELAS Presenting without Stroke
Arch Neurol 50:275-278, Mosewich,R.K.,et al, 1993

Cerebral Blood Flow in Mitochondrial Myopathy, Encephalopathy, lactic Acidosis, & Strokelike episodes
Stroke 24:304-309, Ooiwa,Y.,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

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



Showing articles 500 to 550 of 1006 << Previous Next >>