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Differential
(Click to cross reference)
abdominal distention
abducens nerve paralysis
adverse drug reaction
alopecia
amenorrhea
anasarca
anemia
anorexia
arteriopathy
arteritides
arteritis, temporal
arthralgia
arthritis
ascites
aspirin
ataxia
ataxia telangiectasia
ataxic gait
autonomic dysfunction
B 12 deficiency
bacterial infection
basal ganglia, lesion of
Beau's lines
biologic markers
biotin deficiency
biotinidase deficiency
brain atrophy
brain scan, abnormal
brainstem, lesion of
breast feeding
cafe au lait spots
carcinoma
cardiomyopathy
Castleman's disease
CAT scan, emission, abnormal
cataracts
cerebral arteries
cerebral atherosclerosis
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortical atrophy
cerebral infarction
cerebral infarction, subcortical
cerebral ischemia
cerebral peduncle
cerebral vasculature
cerebral venous infarction
cerebral venous thrombosis
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, pressure increased
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, young adult
children
chorea
chromosome 8
Clinical Pathologic Conference(C.P.C.)
clubbing of fingers
coma
comorbidities
confusion
confusional state, acute
congestive heart failure
conjunctival injection
conjunctivitis
Coombs test, positive
cortical vein thrombosis
corticotropin level
corticotropin-releasing factor
cortisol, elevated
cranial nerve palsies
cranial neuropathy, multiple
Cushing's syndrome
cytoid bodies
degenerative diseases of CNS
delirium
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
diet
diplopia
dural sinus thrombosis
dyspnea
echocardiogram
echocardiogram, LVH
edema, pedal
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
emergencies, neurologic
encephalopathy
enzyme, defect
erythema nodosum
evoked potentials
eye movement, disorders of
facial hair, excessive
facial pain
facial weakness
failure to thrive
false positive VDRL
familial
fatigue
fever
fingernails, abnormal
fingernails, white
foot drop
fornix, lesion of
gait disorder
gammaglobulin therapy, intravenous
gene
gene mutation
genetic linkage
genetic neurologic disorders
genetic testing
glaucoma
glycosuria
gray hair
Griscelli syndrome
growth retardation
gynecomastia
hair analysis
hair, loss
hallucination
hand pain
headache
hearing loss
hemifacial atrophy
hepatomegaly
hepatosplenomegaly
herniated disc, thoracic
hirsutism
Horner's syndrome
HTRA1 gene
hypercoagulable state
hyperhidrosis
hyperhomocysteinemia
hyperpigmentation of skin
hypertension
hypertrichosis
hypocomplementemia
hypogonadism
hypokalemia
hyponatremia
hypothermia
hypotonia
immunodeficiency
immunoelectrophoresis, serum
immunosuppression
impotence
infant, evaluation of
infantile tremor syndrome
infection
internal capsule
intracranial pressure, increased
jaw pain
Kawasaki disease
leg swelling
leukemia
leuko-araiosis
leukocytosis
leukoencephalopathy
leukopenia
life expectancy
liver disease
liver function enzymes
low back pain
lymphadenopathy
lymphadenopathy, hilar
lymphohistiocytosis
lymphoma involving CNS
lymphopenia
meningitis
meningitis, aseptic
meningoencephalitis
mental status, abnormal
mesial temporal lobe
metabolic acidosis
metabolic alkalosis
microhemorrhage, intracerebral
midbrain, lesion of
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
mimics
misdiagnosis
mitoxantrone
monoclonal gammopathy
mononeuritis multiplex
mononeuropathy
mortality
MRI
MRI, abnormal
MRI, diffusion weighted
multiple myeloma
multiple sclerosis
multiple sclerosis, treatment of
muscle pain
muscle weakness, proximal
myelination of nervous system
myelitis
myeloma, osteosclerotic
myelopathy
myocardial injury
myocarditis
myoclonus
myocytolysis
myositis
nausea and vomiting
neck trauma
neonatal screening, genetic neurologic disorders
neoplasm, hormone producing, ectopic
nephritis
nerve biopsy
neuroendocrinology
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neuropathy
neuropathy, motor, multifocal
neuropathy, peripheral
neutropenia
night sweats
nystagmus
nystagmus, rotary
nystagmus, spontaneous
oculocutaneous albinism
ophthalmoplegia
optic atrophy
optic neuritis
P300
pain, back
palpitations
papilledema
paranoia
pericarditis
photophobia
pink eye
plasmacytoma
pleocytosis of cerebrospinal fluid
pleural effusion
pleurisy
POEMS syndrome
poliosis
polymyalgia rheumatica
polyneuropathy
pons, lesion of
postpartum
pregnancy, neurologic complications in
progeria
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychosis
ptosis
pulmonary embolism
purpura
quadriparesis
radiation therapy, CNS treatment and complications with
rash
Raynaud's phenomenon
retinal detachment
reversible neurologic disorder
review article
risk factors
scalp necrosis
schizophrenia
scleroderma
scleroderma, neurologic involvement with
scotoma
screening
sedimentation rate, elevated
seizure
seizure, children
seizure, drug resistance
seizure, neonatal
short stature
skin cancer
skin, lesions in neurologic disorders
skin, pale
skin, thickened
slurred speech
small vessel disease
somatosensory evoked potentials
spinal cord, lesion of
splenomegaly
spondylolysis
spondylosis
steroid psychosis
steroid therapy, CNS treatment and complications with
subcortical U fibers
subcutaneous nodules
substantia nigra
symmetric brain lesions
systemic illness
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
systemic lupus erythematosus, skin changes in
temporal lobe, lesion
term infant
thirst
thrombocytopenia
thrombocytosis
thrombotic thrombocytopenia purpura
tinnitus
treatment of neurologic disorder
tremor
tremor, intention
trichopoliodystrophy
tuberculosis
tuberculosis, miliary
urinary frequency
urinary tract infection
urticaria
uveitis
vasculitides
vegetarianism
Venereal Disease Research Laboratory test
vertigo
vision, blurred
visual acuity, decreased
visual loss
vitamin deficiency
vitiligo
Vogt-Koyanagi-Harada syndrome
weakness, generalized
weight loss
Werner's syndrome
white hair
white matter disease
whites
Showing articles 0 to 50 of 1368 Next >>

Reversible Cerebral Atrophy and Substantia Nigra Changes after Vitamin B12 Treatment in Infantile Tremor Syndrome
Neurol 103:e210076, Singh,R.,et al, 2024

Neuroimaging Features of Biotinidase Deficiency
AJNR 44:328-333, Biswas,A.,et al, 2023

Clinicopathologic Conference, Cushings syndrome due to a well-differentiated, low-grade thymic neuroendocrine tumor with corticotropin
NEJM 378:2322-2332, Case 18-2018, 2018

Neuroimaging Changes in Menkes Disease, Part 1
AJNR 38:1850-1857, Manara, R.,et al, 2017

Poor Vision in a Patient with White Hair and Pale Skin
BMJ 352:i24, Tripathy, K. & Sharma, Y.R., 2016

Characyeristic features and progression of abnormalities on MRI for CARASIL
Neurol 85:459-463, Sekine, Y., etal, 2015

Griscelli Syndrome and CNS Lymphohistiocytosis
Neurol 82:e122-e123, Saini, A.G.,et al, 2014

Unilateral Leukonychia and Hair Depigmentation in Multifocal Motor Neuropathy
Neurol 81: 1800-1801, Turner, M.R., 2013

A Prematurely Aging Patient Presenting with Severe Leukoaraiosis and Stroke
Neurol 78:e113-e114, Seixas,J.C.,et al, 2012

Cerebral Vein Thrombosis Misdiagnosed and Mismanaged
Thrombosis 2012:210676, Sasidharan, P.K., 2012

Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
NEJM 360:1729-1739, Hara,K.,et al, 2009

Mitoxantrone Treatment of Multiple Sclerosis
Neurol 63(Suppl 6):S28-S32, Cohen,B.A. &Mikol,D.D., 2004

POEMS Syndrome:A Study of 25 Cases and a Review of the Literature
Am J Med 97:543-553, Soubrier,M.J.,et al, 1994

Accelerated Aging of the Brain in Werner's Syndrome
Neurol 42:922-924, Kakigi,R.,et al, 1992

Serial MR Studies in Menkes Disease
J Comput Assist Tomogr 13:113-115, Blaser,S.I.,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

Biotinidase Deficiency:Initial Clinical Features & Rapid Diagnosis
Ann Neurol 18:614-617, Wolf,B.,et al, 1985

Ataxia-Telangiectasia:A Multisystem Hereditary Disease with Immunodeficiency
Ann Int Med 99:367-379, Waldmann,T.A.,et al, 1983

Polyneuropathy, Skin Hyperpigmentation, Edema, & Hypertrichosis in Localized Osteosclerotic Myeloma
Neurol 27:675, Iwashita,H.,et al, 1977

Bilateral Scalp Necrosis in Temporal Arteritis
Am J Med 61:541, Soderstrom,C.W.,et al, 1976

Neuropsychiatric Manifest. of SLE:Diagnosis, Clinical Spectrum, & Relationship to Other Features of the Disease
Medicine 55:323, Feinglass,E.J.,et al, 1976

Hemifacial Atrophy
Brit J Oral Surg 9:102, Vickery,I.M., 1971

The Natural History of SLE by Prospective Analysis
Medicine 50:85, Estes,D.,et al, 1971

The Uveomeningoencephalitic Syndrome
Neurol 16, 6031966., Riehl,J.L.,et al, 1966

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

Partially Reversible FLAIR Hyperintensity Along the Brainstem Surface in Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
Neurol 102:e208064, Wu, J.,et al, 2024

Supratentorial Lymphocytic Inflammation with Parenchymal Perivascular Enhancement Responsive to Steroids:A Potentially Overlooked Diagnosis
Ann Neurol 95:407-409, Tsibonakis,A.,et al, 2024

A 54-Year-Old Woman with Progressive Headache and Neurologic Decline
Neurol 102:e209190, Cheng,Y. & Zachariah,J., 2024

A 51-Year-Old Woman with Abnormal Corups Callosum Signal
JAMA Neurol 81:192-193, Xie,N. & Sun, Q, 2024

A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
Neurol 102:e209258, Lail,G.,et al, 2024

A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
Neurol 102:e209358, Barbosa,A.R.,et al, 2024

Uncommon Causes of Nontraumatic Intracerebral Hemorrhage
Stroke 55:1416-1427, Tartarin,H.,et al, 2024

Clinicopathological Conference, Glutamic Acid Decarborylase 65 Autoantibody-Associated Stiff-Person Syndrome
NEJM 390:1712-1719, Case 14-2024, 2024

Brainstem Chipmunk Sign: A Diagnostic Imaging Clue Across All Subtypes of Alexander Disease
AJNR 45:769-776, Armangue,T.,et al, 2024

Clinicopathologic Conference, Legionella Infection Complicated by Rhabdomyolysis
NEJM 391:1039-1048, Case 29-2024, 2024

Neuroleptic Malignant Syndrome
NEJM 391:1130-1138, Wijdicks,E.F.M. & Ropper,A.H., 2024

Lentiviral Gene Therapy for Cerebral adrenoleukodystrophy
NEJM 391:1302-1312,1358, Eichler,F.,et al, 2024

Clinicopathologic Conference, Infective Endocarditis Due to Haemophilus Parainfluenza
NEJM 391:2148-2157, Case 38-2024, 2024

A 35-Year-Old Woman with Personality Change and Gait Impairment
Neurol 104:e210252, Bernardes,C.,et al, 2024

Amyloid-Related Imaging Abnormalities:An Update
AJR 220:562-575, Roytman,M.,et al, 2023

Diagnosis of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease:International MOGAD Panel Proposed Criteria
Lancet Neurol doi.org110.1016/51474-4422(22)00431-8, Banwell,B.,et al, 2023

Shrimp Sign in Ataxic Cerebellar Progressive Multifocal Leukoencephalopathy
Neurol 101:918-919, Varela,F.J.,et al, 2023

Severe Amyloid-Related Imaging Abnormalities After Anti-B-Amyloid Monoclonal Antibody Treatment
Neurol 101:1079-1080, Bonami,S.,et al, 2023

Tuberous Sclerosis Complex:Clinical Features
www.UptoDate.com, Dec, Randle,S., et al, 2023

A 60-Year Old Man with Asymmetric Weakness and Persistent Fever
Neurol 100:530-536, Zheng,Y.,et al, 2023

Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023

Monkeypox-Associated Central Nervous System Disease:A Case Series and Review
Ann Neurol 93:893-905, Money,K.M.,et al, 2023

Posterior Reversible Encephalopathy Syndrome
NEJM 388:2171-2178, Geocadin,R.G., 2023

Progressive Hemiparesis and White Matter Abnormalities in an HIV-Negative Patient
Neurol 100:1156-1163, Jabbari,E.,et al, 2023



Showing articles 0 to 50 of 1368 Next >>