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Differential
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abdominal muscle paralysis
acid maltase deficiency
acid maltase deficiency, adult
activities of daily living scale
adverse drug reaction
alpha glucosidase
aminoacidopathies
aneurysm
anterior horn cell disease
aspartate aminotransferase
asymptomatic
bright tongue sign
bulbar palsy
calf hypertrophy
cardiomegaly
cardiomyopathy
CAT scan, abnormal
children
chromosomal abnormality
chromosome 11
Clinical Pathologic Conference(C.P.C.)
compartment syndrome
complications
congenital myopathy
congestive heart failure
consanguinity
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
delay in diagnosis
developmental retardation
diaphragmatic paralysis
differential diagnosis
difficulty climbing stairs
distal muscle atrophy
distal muscle weakness
dysarthria
dysphagia
dyspnea
efficacy
electrocardiogram, abnormal
electromyogram
electron microscopy
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
enzyme treatment
enzyme, defect
enzyme, muscle disease
exercise
exercise intolerance
exercise-related muscle strength increase
facial weakness
falling
familial
fatigue
fibrillations
floppy infant
gene
gene mutation
gene therapy
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glycogen debranching enzyme deficiency
glycogen storage disease
Gowers maneuver
hepatomegaly
heralding manifestation
hip flexor weakness
histochemistry of muscle
hypoglycemia
hypotonia
hypotonia, infants
hypoxia
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
immunohistochemistry
immunomodulation
immunosuppressive agents
inborn errors of metabolism, screening
ischemic exercise test
leg weakness, bilateral
leukocytes
limb-girdle weakness
lipid storage myopathy
low back pain
lysosomal storage disease
lysosomes, abnoral
McArdle's disease
McArdle's disease, adult onset
misdiagnosis
molecular genetics
monoclonal gammopathy
monoclonal gammopathy of uncertain significance
mortality
MRI
MRI, abnormal
MRI, muscle
mucopolysaccharidoses
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle hypertrophy
muscle pain
muscle phosphofructokinase deficiency
muscle phosphorylase deficiency
muscle stiffness
muscle strength, testing
muscle wasting, diffuse
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
muscular dystrophy
myoglobinuria
myopathy
myopathy, acquired
myopathy, amyloid
myopathy, distal, vacuolar
myopathy, genetic
myopathy, glycogen storage
myopathy, metabolic
myopathy, necrotizing
myopathy, scleromyxedema
myopathy, vacuolar
myositis
myotonia congenita
myotonic discharges
neck weakness
nemaline rod myopathy
nemaline rod myopathy, adult onset
nerve biopsy
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neuropathy
newborn, evaluation of
next-generation sequencing
old age, neurology of
orthopnea
pain
pain, arm
pain, back
paraspinal muscle
paraspinal muscle weakness
PAS positive
patient in waiting
phosphorylase b kinase deficiency
polymerase chain reaction
Pompe's disease of glycogen storage
Pompe's disease, infantile
preclinical
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
proximal muscle atrophy
pseudomyotonia
pulmonary function tests
pulmonary hypertension
renal failure
respiratory failure
respiratory tract infection
review article
RFLPs
screening
second wind phenomena
seizure
short stature
sphingolipodoses
spinal muscular atrophy
spinocerebellar degeneration
stem cell transplantation
storage disease of CNS
subarachnoid hemorrhage
systemic illness
tongue, enlarged
tongue, weakness
treatment of neurologic disorder
urine, dark
vital capacity
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
winging of scapula
workup
Showing articles 900 to 950 of 1146 << Previous Next >>

Tubular Aggregates, Their Association with Neuromuscular Diseases, Including the Syndrome of Myalgias/Cramps
Arch Neurol 42:973-976, Rosenberg,N.L.,et al, 1985

The Cherry-Red Spot in Tay-Sachs & Other Storage Diseases
Ann Neurol 17:356-360, Kivlin,J.D.,et al, 1985

The Frequency of Malignant Neoplasms in Patients with Polymyositis-Dermatomyositis, A Controlled Study
Arch Int Med 145:1835-1839, Manchul,L.A.,et al, 1985

GM1 Gangliosidosis:Clinical and Laboratory Findings in Eight Families
Hum Genet 70:347-354, Giugliani,R.,et al, 1985

Abnormalities of Eyelid Closure
In Walsh & Hoyt's Clinical Neuro-ophthalmology, Williams & Wilkins, Baltimore, 2:967, Miller,M.R., 1985

Takayasu Arteritis, A Study of 32 North American Patients
Medicine 64:89-99, Hall,S.,et al, 1985

Cysticercosis-Review of 230 Patients
Bull Clin Neurosci 50:76-101, McCormick.G.F., 1985

Nemaline Myopathy Appearing in Adults as Cardio-myopathy
Arch Neurol 41:443-445, Meier,C.,et al, 1984

Familial Occurrences of Adult-Type Neuronal Ceroid Lipofuscinosis
Arch Neurol 41:1091-1094, Tobo,M.,et al, 1984

Polymyositis Associated with Monoclonal Gammopathy
Lancet 2:1183-1186, Kiprov,D.D.,et al, 1984

Penicillamine-Induced Myositis
Am J Med 77:719-722, Halla,J.T.,et al, 1984

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome
Ann Neurol 16:481-488, Pavlakis,S.G.,et al, 1984

Mitochondrial Encephalomyopathy:Fluctuating Symptoms & CT
Neurol 34:1456-1460, Yamamoto,T.,et al, 1984

A Progressive Neurologic Disorder with Supranuclear Vertical Gaze Paresis & Distinctive Bone Marrow Cells
Mayo Clin Proc 59:404-410, Yan-go,F.L.,et al, 1984

Myasthenia Gravis & Myasthenic Syndromes
Ann Neurol 16:519-534, Engel,A.G., 1984

Clin. Path. Conference
Coproporphyria with Polyneuropathy, Case Record 39-1984, NEJM 311:839-847984., , 1984

Graves'Disease Presenting with Bilateral Acute Painful Proptosis, Ptosis, Ophthalmoplegia, & Visual Loss
Lancet 2:431-433, Leonard,T.J.K.,et al, 1984

Clinicopathological Conference
Case 2-1984, Fabry's Disease, NEJM 310:106-114984., , 1984

Unilateral Myopathy:An Unusual Presentation of Thyrotoxicosis
BMJ 288:1124, Gimlette,T.,et al, 1984

Pentazocine Abuse Masquerading as Familial Myopathy
Neurol 34:524-527, Choucair,A.K.,et al, 1984

Prenatal Diagnosis of Neuronal Ceroid Lipofuscinosis
NEJM 310:595, MacLeod,P.M.,et al, 1984

Presentation, Treatment, & Prognosis of Idiopathic Inflammatory Muscle Disease in a Rural Hospital
Am J Med 75:433-438, Hoffman,G.S.,et al, 1983

Implications of Diagnostic Delay in Duchenne Muscular Dystrophy
BMJ 287:1106-1107, Zellweger,H., 1983

Recognising & Preventing Duchenne Muscular Dystrophy
BMJ 287:1083-1084, Firth,M.A.,et al, 1983

Chronic Progressive External Ophthalmoplegia (CPEO) :Clinical, Morphologic, & Biochemical Studies
Neurol 33:452-461, Mitsumoto,H.,et al, 1983

Infantile Osteopetrosis & Neuronal Storage Disease
Neurol 33:437-441, Ambler,M.W.,et al, 1983

Neurodegenerative Disease of Infancy & Childhood
Ann Neurol 13:351-364, Dyken,P.,et al, 1983

Myopathy & Hypersensitivity to Phenytoin
Neurol 33:790-791, Harney,J.,et al, 1983

Fibrous Myopathy in Association with Pentazocine
Arch Int Med 143:2203-2204, Adams,F.M.,et al, 1983

Clinical Epidemology of Toxic-Oil Syndrome
NEJM 309:1408-1414, Kilbourne,E.M.,et al, 1983

Idiopathic Recurrent Myoglobinuria & Persistent Weakness
Neurol 33:1613-1615, Bermils,C.,et al, 1983

Endocrine Myopathies
BMJ 287:705-708, Kendall-Taylor,P.,et al, 1983

Childhood-Type Myositis & Linear Scleroderma
Neurol 33:928-930, Miike,T.,et al, 1983

Isolated Ocular Myopathy & Celiac Disease in Childhood
Neurol 33:792, Sandyk,R.,et al, 1983

Carpal Tunnel Syndrome, Complication of Toxic Shock Syndrome
Arch Neurol 40:414-415, Sahs,A.L.,et al, 1983

Quadriceps Myopathy:A Varient of the Limb-Girdle Dystrophy Syndrome
JNNP 46:355-357, Swash,M.,et al, 1983

Nemaline Myopathy in the Neonate
Neurol 33:351-356, Norton,P.,et al, 1983

Nemaline Myopathy Presenting as Cardiomyopathy
NEJM 308:1536-1537, Meier,C.,et al, 1983

Proximal Myopathy Due to Discrete Carcinomatous Metastases in Muscle
JNNP 46:358-360, Doshi,R.,et al, 1983

Investigative Strategies for Muscle Pain
J Neurol Sci 58:73-88, Mills,K.R.,et al, 1983

An Unusual Cause of Hypokalemic Muscle Weakness
Neurol 33:1242-1243, Valeriano,J.,et al, 1983

Myositis of Chronic Graft Versus Host Disease
Neurol 33:1222-1224, Reyes,M.G.,et al, 1983

Acute Myopathy Associated with Gasoline Sniffing
Neurol 33:629-631, Kovanen,J.,et al, 1983

Childhood Dermatomyositis:Factors Predicting Functional Outcome and Development of Dystrophic Calcification
Pediatrics 103:882-888, Bowyer,L.S.,et al, 1983

Fibrodysplasia Ossificans Progressiva, The Clinical Features & Natural Hx of 34 Pts
J Bone Joint Surg 64B:76-83, Connor,J.M.&Evans,D.A.P., 1982

Necrotizing Myopathy Associated with Steroid Therapy, Report of Two Cases
Pathology 14:435-438, Ojeda,V.J., 1982

Transient Myopathy Apparently Due to Tetracycline
NEJM 307:821-822, Sinclair,D.,et al, 1982

Myopathy Due to Mercaptopropionyl Glycine
BMJ 285:939, Hales,D.S.M.,et al, 1982

Inflammatory Facioscapulohumeral Muscular Dystrophy & Coats Syndrome
Ann Neurol 12:398-401, Wulff,J.D.,et al, 1982

Adult Dystonic Lipidosis, Clin Histo & Biochem Findings of a Neurovisceral Storage Dis
Neurol 32:1295-1299, Longstreth,W.T.Jr.,et al, 1982



Showing articles 900 to 950 of 1146 << Previous Next >>