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Differential
(Click to cross reference)
abdominal muscle paralysis
acid maltase deficiency
acid maltase deficiency, adult
activities of daily living scale
alpha glucosidase
aneurysm
anterior horn cell disease
aspartate aminotransferase
asymptomatic
calf hypertrophy
cardiomegaly
cardiomyopathy
congestive heart failure
consanguinity
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
delay in diagnosis
developmental retardation
diaphragmatic paralysis
difficulty climbing stairs
distal muscle atrophy
distal muscle weakness
dyspnea
efficacy
electrocardiogram, abnormal
electromyogram
electron microscopy
enzyme treatment
enzyme, defect
enzyme, muscle disease
exercise
exercise intolerance
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
hepatomegaly
hip flexor weakness
histochemistry of muscle
hypoglycemia
hypotonia
hypotonia, infants
hypoxia
imbalance
inborn errors of metabolism, screening
ischemic exercise test
leg weakness, bilateral
low back pain
lysosomal storage disease
lysosomes, abnoral
McArdle's disease
misdiagnosis
mortality
MRI, muscle
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
muscle pain
muscle phosphorylase deficiency
muscle stiffness
muscle strength, testing
muscle wasting, diffuse
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
myoglobinuria
myopathy
myopathy, distal, vacuolar
myopathy, genetic
myopathy, metabolic
myopathy, necrotizing
myopathy, vacuolar
myotonic discharges
neck weakness
neurologic disease
neurologic disease, diagnoses of
orthopnea
pain, back
paraspinal muscle
paraspinal muscle weakness
PAS positive
patient in waiting
phosphorylase b kinase deficiency
Pompe's disease of glycogen storage
preclinical
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
pseudomyotonia
pulmonary function tests
pulmonary hypertension
renal failure
respiratory failure
review article
screening
second wind phenomena
short stature
subarachnoid hemorrhage
tongue, enlarged
tongue, weakness
treatment of neurologic disorder
urine, dark
vital capacity
walking, difficulty with
weakness
weakness, progressive
weakness, proximal
winging of scapula
Showing articles 1550 to 1600 of 1619 << Previous Next >>

Genetic Counseling in Retinitis Pigmentosa
MCV Quart 8:283, Noah,V., 1972

Pediatric Neurology
Psych Annals 2:1, , 1972

The Effect of Thyroid Deficiency on Myelination of Brain
Neurol 22:99, Rosman,N.P.,et al, 1972

Burning Feet
BMJ Leading Article 3:193, 1972, July., , 1972

Cerebral Palsy
Med Clin North Am 56:1273, Low,N., 1972

Coarse Facies, Calvarial Thickening & Hyperphosphatasia Associated with Long-Term Anticonvulsant Therapy
NEJM 286:1301, 1972; 287:721972., Lefebvre,E.,et al, 1972

Intracranial Leukemia & the Cerebrospinal Fluid
BMJ 444, 1972 May., Rawabone,R.G.,et al, 1972

Effect of Chronic Anticonvulsant Therapy on Serum 25-Hydroxycalciferol Levels in Adults
NEJM 287:898, Hahn,T.,et al, 1972

Megaloblastic Anemia After Anticonvulsive Therapy
Corres, NEJM 287:9901972., , 1972

Neurological Symptoms in Blood Disease
Book Univ Park Press, Balt 1972., D'Eramo,N.,et al, 1972

Chinese-Restaurant Syndrome, Recurrence, (Letter)
NEJM 286:893, Upton,A.R.M.,et al, 1972

Basilar Impression of the Skull in Patients with Adult Coeliac Disease & After Gastric Surgery
JNNP 35:92-93, Hurwitz,L.J.,et al, 1972

Neurocutaneous Disease
in Dermatology in General Medicine, Fitzpatrick, et al, eds, McGraw Hill, 1971, pp. 1379-1434., Adams,R., 1971

Encephalomyelopathy of Leigh
Editorial BMJ 238, 1971, May., , 1971

Electroencephalogram in Anitconvulsant-Induce Folate Deficiency
BMJ 2:207, Dow,W., 1971

Progressive Paresis of Vertical Gaze in Lipid Storage Disease
Neurol 21:896, Grover,W., 1971

Glutamic Oxalacetic Transaminase, Lactic Dehydrogenase, & Creatine Phosphokinase Content in CSF
Clevel Clinic Quarterly 38:113, Culebras,F.A., 1971

Neurology of the Leukemias & Lymphomas-Editorial
BMJ 442, 1971 Nov., , 1971

The Mucopolysaccharidoses
(Ed) , 4th Edition, the C. V. Mosby Co, 1971, Chp. 11, p. p. 521-686., McKusick,V.A., 1971

Hunter's Syndrome, In Recognizable Patterns Of Human Malformation, Genetic, Embryologic, & Clinical Aspects, by Smith
W. B. , Saunders Co. , 1970, 248-249., David,W., 1970

Microcephaly & Mental Retardation
Am J Dis Child 119:128, Martin,H.P., 1970

Complains of Muscle Weakness
Patient Care Clinical Concepts, 21, 1970 Jan., , 1970

Restless Legs
Lead Article BMJ 758, Dec1970., , 1970

Fetal & Newborn Virus Infections
J Pediatr 77:315, Overall,J.,et al, 1970

Monoamine Oxidase Inhibitor & L-Dopa
BMJ 3:388, Hunter,H.R.,et al, 1970

Neurological Disorders & Adult Coeliac Disease
Gut 11:549, Morris,J.S.,et al, 1970

Rubella, Clinical Manifestations & Management
Am J Dis Child 118:18-29, Cooper,L.Z.,et al, 1969

Mental Retradation Due to Germinal Matrix Infarction
Science 164:156, Towbin,A., 1969

Head Circumference & Cellular Growth of the Brain in Normal & Marasmic Children
J Pediatr 74:774, Winick,M.,et al, 1969

Creatine Phosphokinase Content in Cerebrospinal Fluid (Findings in M. S. )
Cleveland Clin Quart 36:47, Culebras,A., 1969

Chronic Spinal Muscular Atrophy in Adults
J Neurol Sci 9:527, Meadows,J.C.,et al, 1969

Malnutrition & Brain Development
J Pediatr 74:667, Winick,M., 1969

The Use of Serum Lactate Dehydrogenase Isoenzymens in the Diagnosis of Muscle Disease
Neurol 19:26, Hooshmard,H.,et al, 1969

Case Records of MGH
NEJM 280:1009, 1969 Systemic Lupus Erythematosus with Necrotizing Angiitis., , 1969

Neurologic Syndromes Associated with Primary Thrombocythemia
J Mount Sinai Hosp NY 36:317, Korenman,G., 1969

Nonatherosclerotic Causes of Stroke
Ann Int Med 70:807, Levine,J.,et al, 1969

Benign Intracranial Cyst, In Neurosurgery of Infancy & Childhood
(Ed) , 1969, Charles C. Thomas p. 179., Matson,D.D., 1969

Intracranial Ventricular Haemorrhage as a First Presentation of Haemophilia
JNNP 32:470-473, Adeloye,A.,et al, 1969

Folic Acid & the Nervous System
BMJ 722, 1968 Dec., , 1968

Idiopathic Thrombocytosis
Neurol 18:711-713, Levine,J.,et al, 1968

Corticodentatonigral Degeneration with Neuronal Achromasia
Arch Neurol 18:20-33, Rebeiz,J.J.,et al, 1968

Benign Intracranial Hypertension
Pediatr Clin North Am 14:819-830, Greer,M., 1967

The Brain in Multiple Neurofibromatosis:A Suggested Neuropathological Basis for the Assoc. Mental Defect
Brain 90:829, Rosman,N.P.,et al, 1967

A Spectrum of Myopathy Associated with Alcoholism (I. Clinical & Laboratory Features)
Ann Int Med 67:481, Perkoff,G.T.,et al, 1967

Contributions of Serum Enzymes to the Diagnosis of Myocardial Injury
Med Concepts of CVD 36:49, , 1967

Dementia & Folate Deficiency
Quart J Med 36:, 1967 Apr., Strachan,R.,et al, 1967

Contributions of Serum Enzymes & Isozymes to the Diagnosis of Myocardial Injury
Med Concept of CVD 36:43, Cohen,L., 1967

Infantile Spasms Favorable Response to Steroid Therapy
JAMA 201:116, Snyder,C.H., 1967

Mental Deficiency Associated with Muscular Dystrophy
Brain 89:769, Rosman,N.P.,et al, 1966

Central Potine Myelinolysis in a Child with Leukemia
Arch Neurol 14:273, Rosman,N.P.,et al, 1966



Showing articles 1550 to 1600 of 1619 << Previous Next >>