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Differential
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abducens nerve paralysis
abducens nerve paralysis, bilateral
Addison's disease
adducted thumb
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
advances in neurology
adverse drug reaction
algorithm
allergic angiitis
alopecia
amaurosis fugax
amniocentesis
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, misdiagnosis
ANA
anemia
anergy
anesthesia, general
aneurysm
angiotensin-converting enzyme
anorexia
antibiotics
anticonvulsants, hypersensitivity syndrome
anticonvulsants, untoward effects of
anti-myeloperoxidase
antineutrophil cytoplasmic autoantibodies
aortic valve, insufficiency
aphasia
arachnoiditis
arcuate scotoma, differential diagnosis of
areflexia
arrhythmia, cardiac
arsenic
arteritides
arthralgia
arthritis
ascending paralysis
aspirin
asthma
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
atrial fibrillation
atrioventricular block
attention deficit disorder with hyperactivity
autism
autoimmune disease
autonomic dysfunction
Babinski sign
bacterial infection
BAL
Balint's syndrome
basal ganglia
basophilic stippling of red blood cells
Bassen-Kornzweig syndrome
Beau's lines
bitemporal visual field defect
blindness
blood cultures
bone marrow suppression
bone marrow transplantation
brain atrophy
brain biopsy
brainstem, infarction of
brainstem, lesion of
brainstem, neoplasms of
brainstem, tuberculoma of
bulbar palsy
burning feet
burning paresthesia
CAG repeats
calcification, intracranial
calcification, muscle
calf hypertrophy
carcinoma
carcinoma of lung
carcinoma of pancreas
cardiomegaly
cardiomyopathy
cardiovascular disease
carpo-pedal spasm
CAT scan
CAT scan, abnormal
CAT scan, chest
CAT scan, muscle
cataracts
cauda equina
cauda equina, lesion of
central nervous system, infection of
central nuclei, muscle
cerebellum, disease of
cerebellum, neoplasms of
cerebral edema
cerebral infarction
cerebro hepato renal syndrome
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cervical spine
cervical spine abnormality
chest pain
chest x-ray, abnormal
children
chills
cholelithiasis
chorea
chromosomal abnormality
chromosome 14
Churg-Strauss syndrome
Chvostek sign
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
Cogan's syndrome
cognition
collagen vascular disease
coma
complications
confusion
congenital myopathy
congestive heart failure
conjunctival injection
conjunctivitis
contractures, joint
coronavirus
corpus callosum, lesion of
corpus callosum, thinning
COVID-19
cranial nerve palsies
cranial neuropathy, multiple
craniopharyngioma
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
Cushing's syndrome
cyclophosphamide
Danon disease
deafness
deafness, bilateral
deafness, unilateral
degenerative diseases of CNS
delirium
dementia
dementia, childhood
demyelinating disease
depression
dermatitis
dermatomyositis
dermatomyositis, childhood
diabetes insipidus
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diagnostic criteria
diarrhea
diet
differential diagnosis
difficulty climbing stairs
digits, abnormal
dilantin
dilantin, hypersensitivity to
diplopia
disseminated intravascular coagulation(DIC)
distal muscle atrophy
distal muscle weakness
diurnal variation
DNA probes
dopa responsive dystonia
drug induced neurologic disorders
dysarthria
dysarthria-clumsy hand syndrome
dysmetria
dysmorphic
dysphagia
dyspnea
dystonia
dystonia, etiology of
dystonia, painful
dystrophic calcification
dystrophin
ear, abnormal
echocardiogram
echocardiogram, transesophageal
edema, pedal
edema, periorbital
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electromyogram
electronystagmography
electroretinograph
Emery-Dreifuss muscular dystrophy
encephalitis
encephalomyelitis
encephalopathy
endocarditis
endocarditis, acute bacterial
endophthlamitis
eosinophilia
eosinophilia-myalgia syndrome
eosinophilic fasciitis
epidemiology of neurology
epistaxis
equinovarus
erectile dysfunction
erythema multiforme
erythrocyte
exophthalmus
eye movement, disorders of
eye, pain in
face, numbness of
facial nerve palsy
facial nerve palsy, bilateral
facial weakness
falling
false positive VDRL
familial
fasciculation
fatigue
fatty acid, elevated plasma content
fetus
fever
fingernails, abnormal
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
Friedreich's ataxia
fundus, abnormality of
gait disorder
gallium scan
gammaglobulin therapy, intravenous
gastroenteritis
gastrointestinal bleeding
gaze palsy
gaze palsy, horizontal
gaze palsy, supranuclear
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
Gowers maneuver
granuloma, eosinophilic
granulomatosis, allergic
granulomatous disease
granulomatous hypophysitis
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
gynecomastia
Hallervorden Spatz disease
hallucination
hallucination, auditory
hallucination, visual
hand weakness
Hand-Schuller-Christian disease
headache
headache, bifrontal
headache, positional
hearing loss
heart block
heart murmur
heavy metal intoxication
heliotrope rash
hemangioblastoma
hematuria, microscopic
hemianopia, homonymous
hemiparesis
hemoglobinuria
hepatitis
hepatomegaly
hepatosplenomegaly
histochemistry of muscle
hormone replacement
Huntington's chorea
hydrocephalus
hydrocephalus, congenital
hydrocephalus, fetal
hydrocephalus, intrauterine
hyperadrenalism
hyperamylasemia
hypercalcemia
hypereosinophilic syndrome(HES)
hyperesthesia
hypergammaglobulinemia
hyperinsulinism
hyperkalemia
hyperkeratosis
hyperparathyroidism
hypersensitivity reaction
hypersomnia
hypertension
hyperthyroidism
hypertrophic intracranial pachymeningitis
hypoglycorrhachia
hypogonadism
hypokalemic periodic paralysis
hypokinetic left ventricle
hyponatremia
hypoparathyroidism
hypopyon
hyporeflexia
hypothalamus
hypothalamus, disturbance of
iatrogenic neurologic disorders
imbalance
immunohistochemistry
immunosuppressive agents
impulsivity
inclusion body myositis
Indonesia
infection
intellectual deficit
interferonopathy
intestinal biopsy
intracerebral hemorrhage
intracranial pressure, increased
intrinsic hand muscles, wasting of
intubation
iritis
islet cell tumor
karyotyping
Kawasaki disease
Kearns-Sayre syndrome
keratitis
lacrimation
lactic dehydrogenase(LDH)
Laurence-Moon-Bardet-Biedl syndrome
L-dopa
leg spasms
leg spasms, painful
leg weakness, bilateral
leptospirosis
leukocytosis
leukodystrophy
leukopenia
level of consciousness, decreased
life expectancy
livedo reticularis
liver disease
liver function enzymes
Lorenzo's oil
L-tryptophan
lymphadenitis
lymphadenopathy
lymphadenopathy, hilar
lymphocyte capping, diminished
lymphoid adenohypophysitis
lymphoma
macular degeneration
malabsorption
malignant hyperpyrexia
mastoiditis
mediastinum, mass of
medulla oblongata, lesion of
Mees lines
memory, impairment of
meningitis
meningitis, aseptic
meningitis, basilar
meningitis, chronic
meningitis, recurrent
meningoencephalitis
meningomyelitis
mental retardation
mental retardation, familial
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
misdiagnosis
molecular genetics
mononeuritis multiplex
mononeuropathy
mononeuropathy multiplex
mortality
mosquito
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, muscle
mucopolysaccharidoses
multiple sclerosis, misdiagnosis
muscle biopsy
muscle cramp
muscle pain
muscle stiffness
muscle tenderness
muscle weakness
muscle weakness, causes of
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
muscular dystrophy, lymphocyte capping, diminished
muscular dystrophy, systemic membrane defect
myasthenia gravis
myasthenia gravis, receptor site in
myelitis, longitudinal
myelopathy
myocarditis
myoclonus
myoedema
myoglobinuria
myopathy
myopathy, centronuclear
myopathy, distal
myopathy, drug-induced
myopathy, hereditary
myopathy, inflammatory
myopathy, mitochondrial
myopathy, quadriceps
myopathy, vacuolar
myopia
myositis
myotonia dystrophica
myotonic discharges
myotubularin
myxedema coma
myxedema, neurologic manifestations of
nasal polyp
nasal septum, perforation of
nausea and vomiting
neck extension
neoplasm, pituitary
neoplasm, primary intracranial
neoplasm, primary of CNS
neoplastic angioendotheliosis
nerve biopsy
nerve conduction studies
neuritis, heavy metals causing
neuroendocrinology
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neuromuscular disease, electrodiagnosis of
neuronal ceroid-lipofuscinosis
neuronal migration disorder
neuronopathy
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, hereditary peripheral
neuropathy, painful
neuropathy, peripheral
neuropathy, toxic
neuropathy, vasculitic, systemic
neurotoxic
night blindness
night sweats
nystagmus
obsessive-compulsive disorder
ocular myopathy
odynophagia
ophthalmoplegia
ophthalmoplegia, plus syndrome
ophthalmoplegia, total
optic atrophy
optic nerve
optic neuropathy
orange peel appearance of skin
otitis, neurologic complications with
pain
pain, abdominal
pain, flank
pain, foot
pain, leg
pain, testicular
pancreatitis
pancytopenia
papilledema
paranoia
paraparesis
paraparesis, spastic
parathyroid adenoma
paresthesias
paresthesias, feet
paresthesias, hands
Parkinsonism syndrome
parotitis
PAS positive
periarteritis nodosa
pericardial effusion
pericarditis
periodic paralysis
peripheral blood smear
peripheral blood smear, abnormal
peripheral nerve, lesion of
peroxisomal disease
pheochromocytoma
photophobia
pigmentary retinopathy
pituitary, enlargement
pituitary, lesion of
pleocytosis of cerebrospinal fluid
pleural effusion
pleurisy
pneumonia
polycystic kidneys
polymerase chain reaction
polymerase chain reaction, false negative
polymyositis
polymyositis, eosinophilic
polyneuropathy
pons, lesion of
position sensation, abnormal
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
primary aldosteronism
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
proprioception, abnormal
proteinuria
prothrombin time, prolonged
proximal muscle atrophy
psychiatric problems in neurologic disorders
psychosis
ptosis
ptosis, bilateral
pulmonary edema
pulmonary infiltrates
pyloric stenosis
quadriceps atrophy
quadriparesis
quadriplegia
radiculopathy
rash
rash, hand
Raynaud's phenomenon
recombinant DNA
refractive errors
Refsum's disease
renal cell carcinoma
renal cyst
renal stones
respiratory distress syndrome, neurologic status with
respiratory failure
respiratory tract infection
reticulum cell sarcoma
retinal artery occlusion
retinal degeneration
retinal hemangioma
retinal lesion
retinal tumor
retinitis pigmentosa
retinopathy
reversible neurologic disorder
review article
RFLPs
rhabdomyolysis
rheumatoid arthritis
rheumatoid arthritis factor(R.A.factor)
rhinorrhea
rickettsial organism
rigid spine syndrome
rippling muscle disease
risk factors
Rocky Mountain spotted fever
sarcoidosis
sarcoidosis, CNS
scleroderma
scleroderma, neurologic involvement with
scoliosis
scotoma
sedimentation rate
sedimentation rate, elevated
seizure
seizure, familial
sella turcica, enlargement of
sensorineural hearing loss
serologic testing
serum alanine aminotransferase
serum sickness
severe acute respiratory syndrome
sinemet
sinusitis
skin, biopsy
skin, darkening of
skin, lesions in neurologic disorders
skin, tight
skull x-ray
skull x-ray, abnormal
southeast asia
Southern immunoblot test
spinal cord, lesion of
spinal cord, neoplasm
spinal muscular atrophy
spinocerebellar degeneration
spirochete infection
splenomegaly
splinter hemorrhages
standing difficulty
steroid
steroid therapy, CNS treatment and complications with
Stevens-Johnson syndrome
streptococcus pneumoniae
subarachnoid hemorrhage
subcutaneous edema
suprasellar lesion
sweating
sweating, abnormality of
swimming
systemic illness
systemic lupus erythematosus, drug induced
tachycardia
tandem gait, ataxic
tapetoretinal degeneration
telangiectases
telangiectases, periungual
testicular atrophy
testicular biopsy
testicular enlargement
tetany
third nerve palsy
thrombocytopenia
thrombocytosis
thyrotoxicosis
tick bite
tinnitus
toe walking
tongue, fasciculations of
tonsillar herniation of cerebellum
toxic encephalopathy
toxic oil syndrome
transient ischemic attack
travel, foreign
treatment of neurologic disorder
tremor
tremor, intention
tremor, postural
trigeminal neuropathy
trigeminal neuropathy, sensory
trinucleotide repeats
troponin T
Trousseau's sign
tuberculoma of CNS
tuberculosis
tuberculosis, miliary
tumor necrosis factor inhibitor
uncal herniation
uremia
urine test in toxic screen
Usher's syndrome
uveitis
vasculitides
Venereal Disease Research Laboratory test
vertigo
very long chain fatty acids
viral myopathy
vision, blurred
visual acuity, decreased, monocular
visual field defect
visual loss
visual loss, sudden-unilateral
vital capacity
Von Hippel Lindau
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weakness, proximal
web sites
weight loss
Western immunoblot test
wheelchair
Whipple's disease
white matter disease
xerostomia
X-linked bulbospinal neuronopathy
x-linked hydrocephalus
x-linked mental retardation
X-linked myopathy
x-linked myopathy with excessive autophagy
x-ray, cervical spine
Showing articles 0 to 50 of 1505 Next >>

Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
Lancet 400:1144, Sabino de Oliveira, D.,et al, 2022

A 59-Year-Old Man with Progressive Proximal Weakness Since Childhood
Neurol 97:958-963, Davalos, L.,et al, 2021

Covd-19-Associated Myopathy Caused by Type 1 Interferonopathy
NEJM 383:2389-2390, Manzano, A.C.,et al, 2020

Clinicopathologic Conference, Probable Acute Leptospirosis
NEJM 377:268-278, Case 22-2017, 2017

Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Sarcoidosis
Adams & Victors Principles of Neurology, Chp 32, pg 721, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Kennedy Syndrome (X-Linked Bulbospinal Muscular Atrophy)
Adams & Victors Principles of Neurology, Chp 39, pg 1119, Ropper, A.H.,et al, 2014

Clinicopathologic Conference, Rocky Mountain Spotted Fever
NEJM 366:1434-1443, Case 11-2011, 2012

Diagnosis and New Treatments in Muscular Dystrophies
JNNP 80:706-714, Manzur,A.Y. &Muntoni,F., 2009

Extension of the Clinical Spectrum of Danon Disease
Neurol 70:1358-1359, van der Kooi,A.J.,et al, 2008

Cardiac Involvement in Patients With Limb-Girdle Muscular Dystrophy Type 2 and Becker Muscular Dystrophy
Arch Neurol 65:1196-1201, Sveen,M.-L.,et al., 2008

Whipples Disease
NEJM 356:55-66, Fenollar,F.,et al, 2007

Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
NEJM 355:831-839, Case 26-2006, 2006

Adrenoleukodystrophy
JAMA 294:3131-3134, Moser,H.W.,et al, 2005

Penetrance of the Fragile X-Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population
JAMA 291:460-469, Jacquemont,S.,et al, 2004

Clinicopath Conf., Penumococcal penumonia with Endocarditis and Endophtlhalmitis
NEJM 348:834-842, Case 7-2003, 2003

Diagnosis of X-Linked Myotubular Myopathy by Detection of Myotubularin
Ann Neurol 50:42-46, Laporte,J.,et al, 2001

Cardiac Dysfunction in Neuromuscular Diseases
The Neurologist 6:67-82, Pourmand,R., 2000

Clinicopath Conf, Granulomatous and Lymphocytic Hypophysitis
NEJM 343:1399-1406, Case 34-2000, 2000

Dermatomyositis
Lancet 355:53-57, Callen,J.P., 2000

Churg-Strauss Syndrome, Clinical Study and Long-Term Follow-Up of 96 Patients
Medicine 78:26-37, Guillevin,L.,et al, 1999

Medical Complications in Long-Term Survivors with X-Linked Myotubular Myopathy
J Pediatr 134:206-214, Herman,G.E.,et al,, 1999

Clinicopath Conf
Rocky Mountain Spotted Fever with Meningoencephalomyelitis, Vasculitis and Focal Myocarditis, Case 3, -17,NEJM 337:1149-1156,1997., 1997

X-Linked Vacuolated Myopathy:Membrane Attack Complex Depos on Muscle Fiber Membr with Calcium Accumul on Sarcolemma
Ann Neurol 41:117-120, Louboutin,J.P.,et al, 1997

X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
JNNP 63:4-14, vanGeel,B.M.,et al, 1997

Distal WEakness in Dystrophin-Deficient Muscular Dystrophy
Muscle & Nerve 19:1608-1610996., Felice,K.J., 1996

Investigation of Muscle Disease
JNNP 60:256-274, Mastaglia,F.L.&Laing,N.G., 1996

Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
Lancet 345:161-162, Jouet,M.&Kenwrick,S., 1995

Becker Muscular Dystrophy with Onset after 60 Years
Neurol 44:2388-2390, Heald,A.,et al, 1994

Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test
JAMA 270:1569-1575, Brown,W.,et al, 1993

Clinicopath Conf
Tuberculosis of Mediastinal Lymph Nodes, Case 3-1993, NEJM 328:195-202993., , 1993

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

Population Screening for Fragile X
Lancet 339:1210-1213, Turner,G.,et al, 1992

Clinicopath Conf
Churg-Strauss Syndrome, Case 18-1992, NEJM 326:1204-1212992., , 1992

Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
Neurol 41:823-828, Olney,R.K.,et al, 1991

Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental Retardation
NEJM 325:1673-1681, Rousseau,F.,et al, 1991

The Frequency of Patients with Dystrophic Abnormalities in a Limb-Girdle Patient Population
Neurol 41:1491-1496, Arikawa,E.,et al, 1991

Molecular Genetics of Duchenne and Becker Muscular Dystrophy
J Pediatr 117:1-15, Darras,B.T., 1990

The Clinical Spectrum of the Eosinophilia-Myalgia Syndrome Associated with L-Tryptophan Ingestion
Ann Int Med 113:124-134, Martin,R.W.,et al, 1990

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

Quadriceps Myopathy:Forme Fruste of Becker Muscular Dystrophy
Ann Neurol 28:634-639, Sunohara,N.,et al, 1990

Familial X-linked Myalgia and Cramps:A Nonprogressive Myopathy Associated with a Deletion in the Dystrophin Gene
Neurol 39:1277-1280, Gospe,S.M.,et al, 1989

Distinction of Becker from Limb-Girdle Muscular Dystrophy by Means of Dystrophin cDNA Probes
Lancet 1:466-468, Norman,A.,et al, 1989

Molecular Biology of Duchenne and Becker's Muscular Dystrophy:Clinical Applications
Ann Neurol 26:189-194, Gutmann,D.H.&Fischbeck,K.H., 1989

Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989

Aseptic Meningitis Complicating Adult Kawasaki Disease:Case Report and Review of the Literature
Am J Med 87:106-110, McIlroy,M.A.,et al, 1989

Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
Medicine 68:1-29, Lamiell,J.M.,et al, 1989

DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
Hum Genet 82:55-58, Defesche,J.C.,et al, 1989

Rigid Spine Syndrome and Rigid Spine Sign in Myopathies
J Child Neurol 4:273-282, Merlini,L.,et al, 1989

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988



Showing articles 0 to 50 of 1505 Next >>