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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 900 to 950 of 1006 << Previous Next >>

Haemophilic Neuromyopathy
JNNP 42:600-605, Defaria,C.R.,et al, 1979

Headache
In Clinical Neurology, Baker & Baker Editor. In Vol. II, Harper & Row, Publishers 1979, Chap. 13, p., 38-43. n,A.P., 1979

Drug-Induced Myopathies In Man
Lancet 2:562-566, Lane,R.J.M.,et al, 1978

Adult Onset Nemaline Myopathy
Neurol 28:1306-1309, Brownell,A.K.W.,et al, 1978

Carnitine Deficiency Acute Postpartum Crisis
Ann Neurol 4:558-561, Angelini,C.,et al, 1978

Muscle Fiber-Type Disproportion
Arch Neurol 35:823-826, Eisler,T.,et al, 1978

Isolated Trigeminal Sensory Neuropathy:Early Manifestation of Mixed Connective Tissue Disease
Neurol 28:1286-1289, Searles,R.P.,et al, 1978

Leukoencephalopathy in Oculocraniosomatic Neuromuscular Disease With Ragged-Red Fibers
Arch Neurol 35:643-647, Bertorini,T.,et al, 1978

Fatal Infantile Form of Muscle Phosphorylase Deficiency
Neurol 28:1124-1129, DiMauro,S.,et al, 1978

HLA-B8 in Polymyositis
NEJM 298:1260, Behan,W.M.H.,et al, 1978

Effects of Acetazolamide on Myotonia
Ann Neurol 3:531, Griggs,R.C.,et al, 1978

Nemaline (Rod) Myopathy:The Need for Histochemical Evaluation of Affected Families
Ann Neurol 4:37, Bender,A.N.,et al, 1978

Inclusion Body Myositis:A Distinct Variety of Idiopathic Inflammatory Myopathy
Neurol 28:8, Carpenter,S.,et al, 1978

A Case of Schwartz-Jampel Syndrome with Unusual Muscle Biopsy Findings
Ann Neurol 3:93, Fariello,R.,et al, 1978

Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
Neurol 28:1135-1140, Dobkin,B.H.,et al, 1978

The Muscular Pain-fasciculation Syndrome
Neurol 28:1105-1109, Hudson,A.J.,et al, 1978

Quinine Sulfate for Pain in the Guillain-Barre Syndrome
Ann Neurol 4:386-387, Nixon,R.A., 1978

Malignant Hyperthermia & Central Core Disease in a Child with Congenital Dislocating Hips
Arch Neurol 35:189, Eng,G.D.,et al, 1978

Alternating Proptosis
Arch Neurol 34:642, Keane,J.R., 1977

Neonatal Ophthalmoplegia with Microfibers:A Reversible Myopathy
Neurol 27:974, Hanson,P.A.,et al, 1977

Clinical Pathological Conference
Dermatomyositis, Case Record, 33-1977, NEJM 297:37877., , 1977

Pellagra
In Brain's Diseases of the Nervous System, 8th Ed. 1977, p 849-851, Oxford University Press., , 1977

Clofibrate-Induced Muscle Damage with Myoglobinuria & Cardiomyopathy
NEJM 296:942, Smals,A.G.H., 1977

Rigid Spine Syndrome:A Type I Fiber Myopathy
Arch Neurol 34:119, Seay,A.R.,et al, 1977

Eosinophilic Polymyositis
Ann Neurol 1:65, Layzer,R.B.,et al, 1977

The Adult Form of Acid Maltase (a-1, 4-Glucosidase) Deficiency
Ann Neurol 1:276, Karpati,G.,et al, 1977

Acute Hypokalemic Myopathy in Alcoholism
Arch Neurol 34:553, Rubenstein,A.E.,et al, 1977

Lower Motor Neuron Disease with Spinocerebellar Degeneration
Ann Neurol 2:524, Page,R.W.,et al, 1977

Neurologic Manifestations in Sarcoidosis
Ann Int Med 87:336, Delaney,P., 1977

Chronic Neurogenic Quadriceps Amyotrophy
Ann Neurol 2:528, Furukawa,T.,et al, 1977

Proximal Diabetic Neuropathy
Ann Neurol 2:179, 1977, (Editorial) ., Asbury,A.K., 1977

Neuropsychiatric Manifest. of SLE:Diagnosis, Clinical Spectrum, & Relationship to Other Features of the Disease
Medicine 55:323, Feinglass,E.J.,et al, 1976

Cardiac Myxoma:A Diagnostic Challenge for the Neurologist
Neurol 26:1060, Yufe,R.,et al, 1976

The Extra-Intestinal Complications of Crohn's Disease & Ulcerative Colitis:A Study of 700 Patients
Medicine 55:401, Greenstein,A.J.,et al, 1976

Granulomatous Myositis & Myopathy Assoc. with Crohn's Colitis
NEJM 295:818, Menard,D.B.,et al, 1976

Antibody Titers to Coxsackieviruses in Amyotrophic Lateral Sclerosis
NEJM 295:107, Cremer,N.E.,et al, 1976

Long-term Administration of Corticosteroids in Myasthenia Gravis
Neurol 26:729, Mann,J.D.,et al, 1976

Cause of Weakness in Myasthenia Gravis
NEJM 294:722, Grob,D., 1976

The Thyroid Gland:Its Relationship to Neurology
In Handbook of Clin Neurol, Vinken & Bruyn (Ed) , North Holland Publ Co, Amsterdam 27:255, Greene,R., 1976

Pseudomalignant Myositis Ossificans, A Pathological Study of Eight Cases
Human path 6:653-665, Lagier,R.&Cox,J.N., 1975

Important Advances in Clinical Medicine
West J Med 123:128, Mosier,J.M.,et al, 1975

Reye's Syndrome-Virus or Artifact in Muscle
NEJM 293:505, Hanson,P.A.,et al, 1975

Chronic Myopathy Associated with Coxsackievirus Type A9-A Combined Electron Microscopical & Viral Isolation Study
NEJM 292:608, 6411975., Tang,T.,et al, 1975

Progressive Supranuclear Palsy-Case Study
NEJM 293:346, Richardson,E.P., 1975

Adult Toxoplasmosis Presenting as Polymyositis & Cerebellar Ataxia
Ann Int Med 82:367, Greenlee,J.,et al, 1975

Serum Creatine Phosphokinase in Leptospirosis
JAMA 233:981, Johnson,W.D.,et al, 1975

Posttraumatic Dysautonomic Cephalgia
Arch Neurol 32:649, Vijayan,N.,et al, 1975

Recurrent Aseptic Meningitis in an Elderly Male, Unusual Prodromal Manifestation of SLE
JAMA 235:1142, Finelli,P.F.,et al, 1975

Case Records of the MassGeneral Hospital, Case 41-1975, Acute Intermittent Porphyria
NEJM 293:817, Woods,B., 1975

Polymyositis & Dermatomyositis
NEJM 292:344, 1975, 292:403975., Bohan,A.,et al, 1975



Showing articles 900 to 950 of 1006 << Previous Next >>