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acid maltase deficiency
advances in neurology
alveolar hypoventilation
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
analgesic
anesthesia, general
anterior interosseous neuropathy
anterior tibial muscle weakness
anxiety
apnea
arrhythmia, cardiac
arthrogryposis multiplex
aspiration
asymptomatic
atrioventricular block
axonopathy, distal
baldness
benign congenital hypotonia
benzodiazepine
brachial neuritis
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cachexia
CAG repeats
calf atrophy
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cardiomyopathy
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CAT scan
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cataracts
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cervical spine injury
Charcot-Marie-Tooth
children
chromosome 19
chronic polyneuritis, children
Clinical Pathologic Conference(C.P.C.)
collagen vascular disease
coma
complications
compression neuropathy
concussion
congenital myopathy
congestive heart failure
contractures, joint
controversies in neurology
cost
cost effectiveness
CPAP
creatine phosphokinase(CPK)elevated
degenerative diseases of CNS
dementia
dentatorubral-pallidoluysian atrophy
dermatomyositis
diaphragmatic paralysis
differential diagnosis
distal muscle atrophy
distal muscle weakness
dying
DYSF gene
dysferlin
dysferlinopathy
dysphagia
dyspnea
dystrophic calcification
dystrophin
electrocardiogram, abnormal
electromyogram
electron microscopy
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
entrapment neuropathy
enzyme, defect
enzyme, muscle disease
epidemiology of neurology
ethics in neurology
euthanasia
evidence-based research
exercise
facial appearance, abnormal
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
falling
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fibrillations
floppy infant
foot drop
fragile-X syndrome
gastrocnemius muscle weakness
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gene mutation
genetic counselling
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genetic neurologic disorders
genetic screening
genetic testing
glycogen debranching enzyme deficiency
glycogen storage disease
Guillain Barre syndrome
Guyon's canal
hand weakness
head injury
headache
heart block
heavy metal intoxication
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high arched palate
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Huntington's chorea
hypercapnia
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hypoglycemic coma
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hypotonia, infants
hypoxic encephalopathy
immunohistochemistry
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immunosuppressive agents
inability to stand on tiptoes
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, intracytopasmic
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inclusion body myositis
intermittent positive pressure breathing
intrinsic hand muscles, wasting of
klippel feil syndrome
Kugelberg-Welander syndrome
leg weakness, bilateral
leukoencephalopathy
leukoencephalopathy, differential diagnosis
level of consciousness, decreased
lid closure, weakness of
life sustaining treatment
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median neuropathy
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muscle pain
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muscle strength, testing
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muscle, metabolic disorders of
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muscular dystrophy, congenital
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muscular dystrophy, distal, Miyoshi
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myopathy, thyroid disease causing
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myositis
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myotonia dystrophica
neck weakness
nemaline rod myopathy
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nerve biopsy
neuritis, causes of
neurofibrillary degeneration
neurogenic vs.myopathic atrophy
neurologic complications of, systemic cancer
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neuromuscular junction, abnormality of
neuronal migration disorder
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neuropathy, diabetic
neuropathy, motor, multifocal
neuropathy, peripheral
newborn, evaluation of
next-generation sequencing
oculopharyngeal muscular dystrophy
old age, neurology of
ophthalmoplegia
Oppenheim muscular dystrophy
oxygen therapy
palliative care
Parkinson disease
percussion induced muscle contraction
phosphorylase b kinase deficiency
phrenic nerve pacemaker
physician assisted suicide
poison, mercury
poison, neurologic problems with
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polymerase chain reaction
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polyneuropathy
porphyria
posterior interosseous neuropathy
practice guidelines
pregnancy, neurologic complications in
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progressive muscular dystrophy
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
pseudohypertrophy
ptosis
quadriceps atrophy
quadriceps weakness
quality of life
rash
respirator
respiratory depression
respiratory failure
review article
RFLPs
right to die
sarcoidosis
sedation
seizure
short stature
sleep apnea
slit lamp examination
spinal cord, injury of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinocerebellar ataxia type 1
spinocerebellar degeneration
standing difficulty
steppage gait
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
teleconsulting
telemedicine
teleneurology
telestroke
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
thoracic outlet syndromes
torticollis
treatment of neurologic disorder
tricresylphosphate
trinucleotide repeats
ulnar neuropathy
valium
walking frame
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
Werdnig-Hoffman disease
wheelchair
whistle, inability to
winging of scapula
workup
X-linked bulbospinal neuronopathy
Showing articles 300 to 350 of 1368 << Previous Next >>

Rapid Direct Diagnosis of Deletions Carriers of Duchenne and Becker Muscular Dystrophies
Lancet 344:302-303, Fassati,A.,et al, 1994

Intestinal Pseudo-Obstruction in Adult Spinal Muscular Atrophy
Muscle & Nerve 17:946-948994., Ionasescu,V.,et al, 1994

Location of the Corticospinal Tract in the Internal Capsule at MR Imaging
Radiology 191:455-460, Yagishita,A.,et al, 1994

Motor Neuron Disease
JNNP 57:886-896, Leigh,P.N.&Ray-Chaudhuri,K., 1994

Recent Developments in the Drug Treatment of Motor Neurone Disease
BMJ 309:140-141, , 1994

Sequences Specific for Enterovirus Detected in Spinal Cord from Patients with Motor Neurone Disease
BMJ 308:1541-1543, Woodall,C.J.,et al, 1994

Pseudoneurogenic Thoracic Outlet Syndrome
Muscle & Nerve 17:242-244, Simpson,D.M., 1994

Conjugal Amyotrophic Lateral Sclerosis:Report of a Young Married Couple
Neurol 43:2378-2380, Cornblath,D.R.,et al, 1993

Amyotrophic Lateral Sclerosis:T2 Shortening in Motor Cortex at MR Imaging
Radiology 189:843-846, Oba,H.,et al, 1993

Evidence for a Dopaminergic Deficit in Sporadic Amyoptrophic Lateral Sclerosis on Positron Emission Scanning
Lancet 324:1016-1018, Takahashi,H.,et al, 1993

Cardiomyopathy May Be the Only Clinical Manifestation in Female Carriers of Duchenne Muscular Dystrophy
Neurol 43:2342-2345, Mirabella,M.,et al, 1993

Sudden Death of a Carrier of X-Linked Emery-Dreifuss Muscular Dystrophy
Ann Int Med 119:900-905, Fishbein,M.C.,et al, 1993

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

Ophthalmologic Manifestations in MELAS Syndrome
Arch Neurol 50:977-980, Fang,W.,et al, 1993

Competent Pts with Adv States of Perm Paralysis Have the Right to Forgo Life-Sustaining Therapy
Neurol 43:224-225, Bernat,J.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

Signal Loss in the Motor Cortex on Magnetic Resonance Images in Amyotrophic Lateral Sclerosis
Ann Neurol 33:218-222, Ishikawa,K.,et al, 1993

Amyotrophic Lateral Sclerosis:Hyperintensity of the Corticospinal Tracts on MR of Spinal Cord
AJR 160:604-606, Friedman,D.P.&Tartaglino,L.M., 1993

Cell Culture Evidence for Neuronal Degeneration in ALS to Glutamate AMPA/Kainate Receptors
Lancet 341:265-268, Couratier,P.,et al, 1993

Home Ventilation for ALS Patients:Outcomes, Costs, and Patient, Family and Physician Attitudes
Neurol 43:438-443, Moss,A.H.,et al, 1993

Motor Neuron Diseases and Amyotrophic Lateral Sclerosis:GM1 Antibodies and Paraproteinemia
Neurol 43:418-420, Sanders,K.A.,et al, 1993

Lymphocytic Infiltrates in the Spinal Cord in Amyotrophic Lateral Sclerosis
Arch Neurol 50:30-36, Engelhardt,J.I.,et al, 1993

Polyglucosan Body Disease Simulating Amyotrophic Lateral Sclerosis
Neurol 43:785-790, McDonald,T.D.,et al, 1993

Analysis of Dystrophin Expression after Activation of Myogenesis in Amniocytes, Chorionic-Villus Cells, and Fibroblasts
NEJM 329:915-920, Sancho,S.,et al, 1993

Duchenne Muscular Dystrophy:Deficiency of Dystrophin-Associated Proteins in the Sarcolemma
Neurol 43:795-800, Ohlendieck,K.,et al, 1993

Gene Therapy for Duchenne Dystrophy
Ann Neurol 34:3-4, Engel,A.G., 1993

Myoblast Transfer in Duchenne Muscular Dystrophy
Ann Neurol 34:8-18, Karpati,G.,et al, 1993

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

Single-Photon Emission Computed Tomographic Investigation of Patients with Motor Neuron Disease
Neurol 43:1569-1573, Abe,K.,et al, 1993

Spinal Fluid Cells and Protein in Amyotrophic Lateral Sclerosis
Arch Neurol 50:489-491, Norris,F.H.,et al, 1993

The Natural History of Amyotrophic Lateral Sclerosis
Neurol 43:1316-1322, Ringel,S.P.,et al, 1993

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

Diag of Occult Muscular Dystrophy:"Chance"Finding of Elevated Serum Aminotransferase Act
J Pediatr 122:254-256, Morse,R.P.&Rosman,N.P., 1993

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

Duchenne Dystrophy:Randomized, Controlled Trial of Prednisone (18 months) & Azathioprine (12 months)
Neurol 43:520-527, Griggs,R.C.,et al, 1993

Cyclosporine Increases Muscular Force Generation in Duchenne Muscular Dystrophy
Neurol 43:527-532, Sharma,K.R.,et al, 1993

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

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

Upper Gastrointestinal Tract Motility in Children with Progressive Muscular Dystrophy
J Pediatr 121:720-724, Staiano,A.,et al, 1992

Clinicopath Conf
Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992

Decreased Glutamate Transport by the Brain and Spinal Cord in Amyotrophic Lateral Sclerosis
NEJM 326:1464-1468, 14931992., Rothstein,J.D.,et al, 1992

Intrafamilial Heterogeneity in Hereditary Motor Neuron Disease
Neurol 42:1488-1492, Applebaum,J.S.,et al, 1992

Amyotrophic Lateral Sclerosis and Lymphoma:Bone Marroe Examination and Other Diagnostic Tests
Neurol 42:1101-1102, Rowland,L.P.,et al, 1992

Werdnig-Hoffman Disease & Chronic Distal Spinal Muscular Atrophy with Apparent Autosomal Dom Inherit
Ann Neurol 32:404-407, Boylan,K.B.&Cornblath,D.R., 1992

Surgical Treatment of Cervical Spondylotic Myelopathy:Time for a Controlled Trial
Neurol 42:5-13, Rowland,L.P., 1992

Dystrophinopathy in Isolated Cases of Myopathy in Females
Neurol 42:967-975, Hoffman,E.P.,et al, 1992

Detection of Duchenne and Becker MD Carriers by Quant Multiplex Polymerase Chain Reaction
Neurol 42:1783-1790, Ioannou,P.,et al, 1992

Diagnosis of Duchenne & Becker Muscular Dystrophies by Polymerase Chain Reaction
Multicenter Study Group, JAMA 267:2609-26151992., , 1992



Showing articles 300 to 350 of 1368 << Previous Next >>