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Differential
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abdominal muscle paralysis
acid maltase deficiency
acid maltase deficiency, adult
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
acyl CoA dehydrogenase deficiency
adverse drug reaction
algorithm
aneurysm
anterior tibial muscle weakness
arthralgia
arthritis
autoimmune disease
azathioprine
azidodeoxythymidine
brachial plexus neuropathy
brain biopsy
brain biopsy, stereotaxic
calf hypertrophy
carcinoma
cardiomegaly
CAT scan, abnormal
CD4 counts
cerebral venous thrombosis
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cerebrovascular accident, recurrent
cerebrovascular disease
children
chloroquine
chromosomal abnormality
chromosome 9
cranial neuropathy
creatine phosphokinase(CPK)elevated
cryptococcal meningitis
cyclic vomiting
cystinosis
cytomegalovirus infection
delay in diagnosis
dementia
dermatitis
dermatomyositis
diaphragmatic paralysis
diarrhea
diarrhea, bloody
differential diagnosis
difficulty climbing stairs
disability rating scale, neurological
distal muscle atrophy
distal muscle weakness
dropped head syndrome
dysarthria
dysphagia
dyspnea
electrocardiogram, abnormal
electromyogram
electron microscopy
encephalitis
encephalitis, focal
encephalitis, human immunodeficiency virus type 1
enzyme, defect
enzyme, muscle disease
epidemiology of neurology
exercise
exercise intolerance
facial nerve palsy
facial nerve palsy, recurrent
facial weakness
falling
familial
fatigue
fibrillations
foot drop
foot drop, bilateral
fracture, long bone
gait disorder
gene
gene mutation
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glycogen storage disease
Guillain Barre syndrome
hand weakness
headache
hearing loss
heart block
heart block, complete
hepatomegaly
heralding manifestation
histochemistry of muscle
human immunodeficiency virus type 1
human immunodeficiency virus type 1, pathogenesis
hyperreflexia
imbalance
immunosuppressive agents
inability to stand on tiptoes
inclusion bodies
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
inclusion body myositis
intrinsic hand muscles, wasting of
leg weakness, bilateral
limb-girdle weakness
lymphoma
lymphoma involving CNS
lysosomal storage disease
Melkersson's syndrome
memory, impairment of
methotrexate
misdiagnosis
mitochondrial disease
molecular genetics
mononeuritis multiplex
mononeuropathy multiplex
MRI
MRI, abnormal
MRI, brachial plexus
MRI, muscle
multiple sclerosis
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
muscle pain
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, classification
muscular dystrophy, distal, Miyoshi
myasthenia gravis
myelopathy
myelopathy, chronic progressive
myelopathy, vacuolar
myopathy
myopathy, distal
myopathy, distal, vacuolar
myopathy, drug-induced
myopathy, genetic
myopathy, hereditary
myopathy, inclusion body
myopathy, inclusion body, hereditary
myopathy, metabolic
myopathy, necrotizing
myopathy, proximal
myopathy, toxic
myopathy, vacuolar
myositis
myositis, ocular
myotonic discharges
nausea and vomiting
neck weakness
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neuromuscular disease, electrodiagnosis of
neuropathology
neuropathy
neurosyphilis
next-generation sequencing
optic neuritis
orthopnea
pain, abdominal
paraspinal muscle
paraspinal muscle weakness
phosphorylase b kinase deficiency
polymyositis
polyneuropathy, chronic inflammatory demyelinating
Pompe's disease of glycogen storage
prenatal diagnosis by amniocentesis
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
proximal muscle atrophy
pseudomyotonia
quality of life
regional enteritis
research
respiratory failure
review article
riboflavin
screening
sedimentation rate, elevated
seizure
sensorineural hearing loss
short stature
standing difficulty
steppage gait
subarachnoid hemorrhage
syphilis, neurologic complications with
tongue, enlarged
tongue, weakness
toxoplasmosis, CNS
transient ischemic attack
treatment of neurologic disorder
ulcerative colitis
vital capacity
weakness
weakness, progressive
weakness, proximal
weight loss
winging of scapula
X-linked myopathy
x-linked myopathy with excessive autophagy
Showing articles 950 to 1000 of 1026 << Previous Next >>

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

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

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

Cardiac Features of Unusual X-linked Humeroperoneal Neuromuscular Disease
et al NEJM 293:1017, Waters,D.D., 1975

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

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

Neurologic Complications of Rheumatoid Arthritis
Orth Clin North Am 6:861-881, Nakano,K.K., 1975

Neuro Complica of Coeliac Disease & Trop Sprue, Neurology of GI Disease
1974, Major Problems in Neurology V-3, W. B. Saunders Co, Ltd., Pallis,C.A.&Lewis,P.D., 1974

Quadriceps Myopathy-Entity or Syndrome
Arch Neurol 31:60, Boddie,H.,et al, 1974

Neurotoxicity of Commonly Used Antineoplastic Agents
NEJM 291:75, 1271974., Weiss,H.,et al, 1974

Acute Bulbar Dysfunction & Hyperthyroidism
Am J Med 56:464, Kammer,G.M.,et al, 1974

Neuromuscular Disease in Primary Hyperparathyroidism
Ann Int Med 80:182, Patten,B.M.,et al, 1974

Polymyalgia Rheumatica & Giant Cell Arteritis
Disease-A-Month, 1974. , Jan., Anderson,L.,et al, 1974

Coccidioidomycosis in N. Calif
Calif Med 119:16, Werner,S.B.&Pappagianis,D., 1973

Epidemiology of Motor-Neuron Diseases
NEJM 288:1047, Bobwick,A.R.,et al, 1973

Neurologic Complications of Heroin Addiction
Bull NY Acad Sci 49:4, Ritcher,R.W.,et al, 1973

Pathology of Malignant Hyperpyrexia
BMJ Editorial 249, 1973, Feb., , 1973

Neurologic Manifestations of Progressive Systemic Sclerosis, 1972
Nebraska Med J 58:106, Aita,J.A., 1973

Case Records of MGH-NEJM 289:366
1973 Tuberculoma of Cerebral hemisphere & Brain Stem., , 1973

Hereditary Quadriceps Myopathy
JNNP 36:1041, Espir,M.L.E.,et al, 1973

The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica
p498-501, VanWijngaarden,G.K.&Bethlem,J., 1973

Trichinosis with Central Nervous System Involvement
Neurol 22:485-491, Kramer,M.D.,et al, 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

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

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

Neurologic Manifestations of SLE 1972
Nebraska State Journ Med, Oct 1972, pp 395., Aita,J., 1972

Acute & Chronic Alcoholic Myopathy
Neurol, April 1972. Vol. 22., Martinez,A.J.,et al, 1972

SLE in the Elderly
Arch Int Med 130:743, Foad,B.S.,et al, 1972

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

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

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

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

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

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

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

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

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

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



Showing articles 950 to 1000 of 1026 << Previous Next >>