Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
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 1100 to 1146 of 1146 << Previous

Neurological Problems in Endocrine Diseases
Med Clin North Am 56:1029, Dale,A., 1972

Muscular Syndrome after Clofibrate
NEJM 286:1110, Katsilambros,N., 1972

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

Diphenylhydantoin for Myotonia Congenita-Correspondence
NEJM 286:893, , 1972

Case Record of MGH
NEJM Amyloidosis & Multiple Myeloma, 86:53472., , 1972

Lead Encephalopathy in Adults
Am J Med 52:289, Whitfield,C.L.,et al, 1972

Congenital Dystrophia Myotonica
Neurol 22:443, Dyken,P.D., 1972

Comprehensive Mangagement of Duchenne Muscular Distrophy
Arch Phys Med & Rehab Mar 1971, pp110., Johnson,E.,et al, 1971

Trigeminal Neuropathy in Connective Tissue Disease
Neurol 21:609, Ashworth,B.,et al, 1971

"Sick"Motoneurones A Unifying Concept of Muscle Disease
Lancet 321, 1971 Feb., McComas,A.J.,et al, 1971

Electrodiagnosis Studies in Neuromuscular Disease
NEJM 285:1244, Samaha,F., 1971

Electrodiagnosis of Neuromuscular Disease
Bull Univ Maryland School Med 56:33, Kemble,F., 1971

Diphosphonate Therapy in a Patient with Myosotis Ossificans Progressiva
Ann Int Med 74:933-936, Weiss,I.W.,et al, 1971

Neurologic Manifestation in Progressive Systemic Sclerosis
Arch Neurol 22:l26, Gordon,R.M.,et al, 1970

The Incidence of the Non-Metastatic Neurological Syndromes of Obscure Origin in the Reticuloses
Brain 93:629, Currie,S.,et al, 1970

Prenatal Genetic Diagnosis
NEJM 283:1370, Milunsky,A.,et al, 1970

Abnormal Head Size, In Neurology In Pediatrics
(Ed) , 1970 Year Book Med. Publishers, p. 61., Bray,P.F., 1970

The Neuromyopathy of Vincristine in Man, Clinical, Electrophysiol & Pathological Studies
J Neurol Sci 10:107-131, Bradley,W.G.,et al, 1970

Polymyositis Presenting as Distal Muscle Weakness
J Neurol Sci 8:479-484, Hollinrake,K., 1969

Rocky Mountain Spotted Fever in the Eastern US
NEJM 280:57, Hazard,G.,et al, 1969

Ocular Myopathy
Arch Neurol 20:1, Magora,A.,et al, 1969

Chronic Progressive External Ophthalmoplegia
Arch Ophthalmol 82:845, Daroff,R., 1969

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

Progressive Ophthalmoplegia
Arch Neurol 19:362, Rosenberg,R.,et al, 1968

The Oculopharyngeal Syndrome
JAMA 203:1003, Murphy,S.F.,et al, 1968

Myopathy of the Quadriceps Muscles
J Neurol Sci 7:201, VanWijngaarden,G.K.,et al, 1968

Neuromuscular Disease in Patients with Steatorrhoea
Gut 8:605-611, Binder,H.J.,et al, 1967

A Critical Survey of Stiff-Man Syndrome
Am J Med 42:582-599, Gordon,E.E.,et al, 1967

The Cerebral Defect & Myopathy in Myotonic Dystrophy
Neurol 17:1106, Rosman,N.,et al, 1967

Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
The New Physic 263, 1967, Oct., Boshes,L., 1967

Some Neuro-ophthalmological Observations
JNNP 30:383, Fisher,C.M., 1967

The Remote Effects of Cancer on the Nervous System
Proc Roy Soc Med 60:683, Wilkinson,M., 1967

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

"Myopathic"Changes in Chronically Denervated Muscle
Arch Neurol 16:14-24, Drachman,D.B.,et al, 1967

Involvement of CNS in Collagen Disease
Jap Cir Jour 30:1292, Mozai,T., 1966

Neurological Aspect of SLE
Keio J Med l5:l39, Honda,M., 1966

Neurological Manifestations of Sarcoidosis
Neurol 15:1147, Wiederholt,W.,et al, 1965

Bacterial Meningitis-A Review of Selected Aspects
NEJM 272:725, Swartz,M.&Dodge,P., 1965

Central Nervous System Manifestations of Periarteritis Nodosa
Neurol 15:114, Ford,R.G.,et al, 1965

The Muscular Dystrophies
NEJM 273:537, 5961965., Zundel,W.,et al, 1965

Muscular Dystrophy
Am J Med 35:632, Pearson,C.M., 1963

Recognition, Prognosis, & Treatment of the Guillain-Barre Syndrome (Acute Idiopathic Polyneuritis)
Med Clin North Am 47:1371, Eiben,R.,et al, 1963

Diabetic Amyotrophy
Am J Med 34:775, Locke,S.,et al, 1963

Hysterical Hemiplegia and Hemianesthesia
Postgrad Med 31:339-345, Magee,K.R., 1962

Neuro CPC of MGH
Myopathy, Severe, Generalized, Chronic, NEJM 258:388-3938., , 1958

Five Types of Dystrophy
Together with Other Conditions Producing Insidious Muscle Weakness-Table 1-Hospital Med p. 60., , 1850

Cerebellar Ataxia in Children
Handout & References., Gilbert,J.J., 1850



Showing articles 1100 to 1146 of 1146 << Previous