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abdominal distention
advances in neurology
adverse drug reaction
amyloidosis
amyotrophic lateral sclerosis
anesthesia, general
anterior tibial muscle weakness
areflexia
arrhythmia, cardiac
arthrogryposis multiplex
asymptomatic
ataxia
atrioventricular block
automatic implantable cardioverter-defibrillator
blepharophimosis
blepharospasm
bradycardia
bulging of biceps
cachexia
calcification, intracranial
calf atrophy
calf hypertrophy
calpain III deficiency
carcinoma
cardiomegaly
cardiomyopathy
cardiovascular disease
carnitine deficiency myopathy
case studies
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataracts
central core disease
cerebellar atrophy, secondary
cerebellar degeneration
cerebral cortical atrophy
cerebral embolism
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
Charcot-Marie-Tooth
children
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
Coats syndrome
coma
complications
conduction block
congenital myopathy
congestive heart failure
consanguinity
contractures, joint
creatine kinase
creatine phosphokinase(CPK)elevated
deafness
dementia
dermatomyositis
descending paralysis
developmental retardation
diamond on quadriceps
diarrhea
differential diagnosis
diplopia
distal muscle atrophy
distal muscle weakness
DNA probes
drug induced neurologic disorders
DYSF gene
dysferlin
dysferlinopathy
dysphagia
dyspraxia
dystroglycanopathies
dystrophic calcification
dystrophin
dystrophin associated proteins
ear, abnormal
echocardiogram
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electromyogram
electron microscopy
Emery-Dreifuss muscular dystrophy
encephalopathy
encephalopathy, progressive
enzyme, defect
enzyme, muscle disease
enzyme, serum
epidemiology of neurology
erythrocyte
exercise
exercise intolerance
extraocular muscle lesion
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
falling
familial
fatigue
fibrillations
foot drop
gait disorder
gait, waddling
gastrocnemius muscle weakness
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glycogen debranching enzyme deficiency
glycogen storage disease
Gowers maneuver
Guillain Barre syndrome
hammertoes
headache
hearing loss
heart block
heart block, complete
heart murmur
hepatomegaly
heralding manifestation
high arched feet
hip dysplasia
hip flexor weakness
hip pain
histochemistry of muscle
hyperthyroidism
hypoglycemia
hypokalemia
hyporeflexia
hypotonia
hypotonia, infants
imbalance
immunohistochemistry
immunosuppressive agents
inability to stand on tiptoes
inclusion body myositis
insulin
intestinal pseudoobstruction
klippel feil syndrome
Kugelberg-Welander syndrome
lactic acidemia
lactic dehydrogenase(LDH)
laminopathies
leg weakness, bilateral
leukodystrophy
lid closure, weakness of
life expectancy
limb-girdle weakness
LMNA gene
lordosis
lymphocyte capping, diminished
MELAS syndrome
mental retardation
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
mononeuropathy
motor neuron disease
MRI
MRI, abnormal
MRI, muscle
muscle atrophy, focal
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
muscle pain
muscle stiffness
muscle strength, testing
muscle swelling
muscle tenderness
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, congenital, Fukuyama type
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, female occurrence of
muscular dystrophy, limb-girdle
muscular dystrophy, lymphocyte capping, diminished
muscular dystrophy, pattern of muscle involvement
muscular dystrophy, systemic membrane defect
myasthenia gravis
myasthenia gravis, differential diagnosis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenic crisis
myocarditis
myoclonus
myoglobinuria
myopathy
myopathy, carcinomatous
myopathy, centronuclear
myopathy, distal
myopathy, drug-induced
myopathy, hypokalemic
myopathy, metabolic
myopathy, mitochondrial
myopathy, myofibrillar
myopathy, proximal
myopathy, quadriceps
myopathy, steroid induced
myopathy, thyroid disease causing
myositis
myotonia
myotonia dystrophica
myotonic discharges
neck weakness
negative
nemaline rod myopathy
nerve conduction studies
neuritis, causes of
neuroendocrinology
neurologic complications of, surgery
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination
neuroophthalmology
neuropathy
neuropathy, diabetic
next-generation sequencing
normal
ocular myopathy
oculopharyngeal muscular dystrophy
old age, neurology of
ophthalmoplegia
ophthalmoplegia, plus syndrome
ophthalmoplegia, progressive external
optic atrophy
pacemaker, cardiac-transvenous
pain, abdominal
pain, leg
pinched face
poliomyelitis
polymerase chain reaction
polymyositis
polyneuropathy
porphyria
positive sharp waves
pregnancy, neurologic complications in
progeria
prognosis
progressive neurologic disorder
proteinuria
proximal muscle atrophy
proximal myotonic myopathy
pseudohypertrophy
ptosis
quadriceps atrophy
quadriceps weakness
quality of life
ragged-red fibers
recurrent
respirator
respiratory failure
retina, abnormal
retinal lesion
review article
RFLPs
rhabdomyolysis
rippling muscle disease
sarcoglycan
sarcoglycanopathy
sarcoidosis
Schwartz-Jampel syndrome
scoliosis
seizure
sensorineural hearing loss
short stature
shoulder, pain in
shoulder-girdle wasting
sloped shoulders
spinal muscular atrophy
spinal muscular atrophy, adult onset
standing difficulty
statin therapy
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
strokelike episodes
sudden death
syncope
systemic illness
toe walking
torticollis
transverse smile
treatment of neurologic disorder
trinucleotide repeats
upgaze, paralysis of
urine, dark
walking frame
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weakness, proximal
weaning from respirator, failure to
web sites
Werdnig-Hoffman disease
wheelchair
whistle, inability to
white matter disease
winging of scapula
workup
Showing articles 1550 to 1600 of 2171 << Previous Next >>

Gadolinium-Enhanced MRI in a Case of Cytomegalovirus Polyradiculopathy
Neurol 41:1522-1523, Bazan,C.,et al, 1991

Primary Leptomeningeal Lymphoma:Report of 9 Cases, Dx with Immunocytochemical Analysis & Review
Neurol 41:95-100, Lachance,D.H.,et al, 1991

Lymphoma, Motor Neuron Diseases, and Amyotrophic Lateral Sclerosis
Ann Neurol 29:78-86, Younger,D.S.,et al, 1991

Symptoms and Disease Associations in Idiopathic Intracranial Hypertension (Pseudotumor Cerebri) :A Case-Control Study
Neurol 41:239-244, Siuseffi,V.,et al, 1991

Anterior Femoral Cutaneous Nerve Injury Following Femoral Artery Reconstructive Surgery
Arch Neurol 48:230-232, Belsh,J.M., 1991

Transient Entrapment Neuropathy of the Posterior Interosseous Nerve in Violin Players
J Comput Assist Tomogr 15:39-44, Maffulli,N.&Maffulli,F., 1991

Eosinophilia-Myalgia Syndrome, A Clinical Case Series of 21 Patients
Arch Int Med 151:533-537, Philen,R.M.,et al, 1991

Congenital Monomelic Hypertrophy with Progressive Myopathy
Arch Neurol 48:107-110, Shukla,A.,et al, 1991

Clinical and Electrophysiological Aspects of Acute Paralytic Disease of Children and Young Adults in Northern China
Lancet 338:593-597, McKhann,G.M.,et al, 1991

Spinal Cord Schistosomiasis:A Pediatric Case Mimicking Intrinsic Cord Neoplasm
Neurol 41:755-757, Selwa,L.M.,et al, 1991

Diagnosis of Hematogenous Pyogenic Vertebral Osteomyelitis by Magnetic Resonance Imaging
Arch Int Med 151:683-687, Meyers,S.P.&Wiener,S.N., 1991

HTLV-I-Associated Myelopathy/Tropical Spastic Paraparesis in the United States
Neurol 41:1355-1357, Janssen,R.S.,et al, 1991

HTLV-I-Associated Myelopathy Endemic in Texas-Born Residents and Isolation of Virus from CSF Cells
Neurol 41:831-836, McKendall,R.R.,et al, 1991

Clinicopath Conf
Spinal Cord Infarction, Acute, Secondary to Fibrocartilaginous Emboli, Case 5-1991, NEJM 324:322-332, 1991, 1991

Progressive Neuropathy & Recurrent Myoglobinuria in a Child with Long-chain 3-Hydroxyacylcoenzyme A Dehydrogenase Defic
J Pediatr 118:744-746, Dionisi,C.,et al, 1991

Complete Ophthalmoplegia as a Complication of Acute Corticosteroid-and Pancuronium-Associated Myopathy
Neurol 41:921-922, Sitwell,L.D.,et al, 1991

Bilateral Diaphragmatic Paralysis Presenting with Orthopnoea & Apparent Radiological Evidence of Pulmonary Embolism
BMJ 302:954-955, Nisbet,A.,et al, 1991

Sciatic Endometriosis:MR Appearance
J Comput Assist Tomogr 15:508-510, Binkovitz,L.A.,et al, 1991

Immunosuppressive Treatment in Multifocal Motor Neuropathy
Ann Neurol 30:397-401, Feldman,E.L.,et al, 1991

Isolated Muscle Hypertrophy as a Sign of Radicular or Peripheral Nerve Injury
JNNP 54:325-329, Mattle,H.P.,et al, 1991

Cholesterol-Lowering Agent Myopathy (CLAM)
Neurol 41:1159-1160, London,S.F.,et al, 1991

Staphylococcal Pyomyositis in Patients Infected by the Human Immunodeficiency Virus
Am J Med 90:595-600, Schwartzman,W.A.,et al, 1991

Pyomyositis Presenting as Rapidly Progressive Generalized Weakness
Neurol 41:944-945, Felice,K.,et al, 1991

Parental Sex Effect in Familial Amyotrophic Lateral Sclerosis
Neurol 41:1292-1294, Leone,M., 1991

Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
NEJM 324:1381-1384, 1430-14321991., Siddique,T.,et al, 1991

Late Effects of Paralytic Poliomyelitis in Olmsted County, Minnesota
Neurol 41:501-507, Windebank,A.J.,et al, 1991

Epidermal Nevus Synd:A Neurologic Variant with Hemimegalencephaly, Gyral Malf, Mental Retard, Seizures & Facial Hemihyper
Neurol 41:266-271, Pavone,L.,et al, 1991

HTLV-I-Associated Myelopathy Associated with Blood Transfusion in the US:Epidemiologic & Molecular Evidence
Neurol 41:192-197, Kaplan,J.E.,et al, 1991

Syphilitic Meningomyelitis
Neurol 41:325-326, Strom,T.&Schneck,S.A., 1991

Myelopathic Neurosarcoidosis:Diagnostic Value of Enhanced MRI
Neurol 41:150-151, Sauter,M.K.,et al, 1991

Idiopathic Myelopathies with White Matter Vacuolation in Non-AIDS Patients
Human Pathol 22:816-824, Kamin,S.S.&Petito,C.K., 1991

Venous Infarction of the Spinal Cord Resulting from Dural Arteriovenous Fistula:MR Imaging Findings
Larsson, E-M, AJNR 12:739-743991., , 1991

Infant Botulism:A Review of 12 Years'Experience at the Children; s Hosp of Phila
Pediatrics 87:159-165, Schreiner,M.S.,et al, 1991

Joubert Syndrome:A Clinico-Radiological Study
Neuroradiology 31:502-506, Kendall,B.,et al, 1990

Clinicopath Conf
Hodgkin's Disease and Guillain Barre Syndrome, Case Record 39-1990, NEJM 323:895-908990., , 1990

Acute Sensorineural Deafness in Lassa Fever
JAMA 264:2093-2096, 21191990., Cummins,D.,et al, 1990

Causalgia and Other Reflex Sympathetic Dystrophies
In the Management of Pain, Lea & Febiger, Phila, p. 220, Bonica,J.J., 1990

OKT3 Encephalopathy
Ann Neurol 28:837-838, Coleman,A.E.&Norman,D.J., 1990

Sexual Expression in Paraplegia
BMJ 301:1007-1008, , 1990

Polyclonal IgM Anti-GM1 Ganglioside Antibody in Patients with Motor Neuron Disease and Variants
Ann Neurol 27:558-563, Salazar-Grueso,E.F.,et al, 1990

Immunologic Reactivity Against Borrelia Burgdorfi in Patients with Motor Neuron Disease
Arch Neurol 47:586-594, Halperin,J.J.,et al, 1990

2-Amino-3- (methylamino) -Propanoic Acid (BMAA) in Cycad Flour:An Unlikely Cause of ALS & Parkinsonism-Dementia of Guam
Neurol 40:767-772, Duncan,M.W.,et al, 1990

Clinicopath Conf
Acute Multiple Sclerosis, Case Record 42-1990, NEJM 323:1123-1135990., , 1990

Fulminant Monophasic Multiple Sclerosis, Marburg's Type
JNNP 53:918-921, Johnson,M.D.,et al, 1990

Cavernous Hemangioma of the Spinal Cord:Report of 2 Unusual Cases
Neurol 40:1791-1793, Lopate,G.,et al, 1990

L-Tryptophan-Associated Eosinophilic Perimyositis, Neuritis, and Fasciitis
Medicine 69:187-199, Kaufman,L.D.,et al, 1990

Congenital Inflammatory Myopathy
Neurol 40:1111-1114, Shevell,M.,et al, 1990

Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
Lancet 336:271-273, Melki,J.,et al, 1990

Spinal Muscular Atrophies
Editorial, Lancet 336:280-2811990., , 1990

Vaccine-Associated Paralytic Poliomyelitis, Regional Case Series and Review
Arch Neurol 47:541-544, Querfurth,H.&Swanson,P.D., 1990



Showing articles 1550 to 1600 of 2171 << Previous Next >>