Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
acid maltase deficiency
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, heralded by neurologic invol
advances in neurology
adverse drug reaction
alpha-fetoprotein
Alzheimer's disease
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis-like syndrome
anterior horn cell disease
anterior tibial muscle weakness
antiviral agents
apraxia of eye movements
areflexia
arm atrophy
arm weakness
arthrogryposis multiplex
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
Brugada syndrome
bulbar palsy
bulbar palsy, progressive
CAG repeats
calf hypertrophy
carcinoembryonic antigen
carcinoma
CD4 counts
central core disease
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
Charcot-Marie-Tooth
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 5
Clinical Pathologic Conference(C.P.C.)
coma
complications
congenital heart disease
congenital myopathy
constipation
creatine phosphokinase(CPK)elevated
degenerative diseases of CNS
dementia
denervation of muscle
denervation potentials
dentatorubral-pallidoluysian atrophy
developmental milestones
developmental retardation
diabetes mellitus
diaphragmatic paralysis
differential diagnosis
distal muscle atrophy
distal muscle weakness
DNA probes
drooling
dysarthria
dysphagia
dystonia
dystrophin
efficacy
electrocardiogram, abnormal
electromyogram
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
enzyme, muscle disease
epidemiology of neurology
eye movement, disorders of
facial weakness, bilateral
facioscapulohumeral syndrome
familial
fasciculation
Fazio-Londe's disease
fibrillations
floppy infant
foot drop
fragile-X syndrome
Friedreich's ataxia
gait disorder
gait, waddling
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
growth retardation
gynecomastia
heavy metal intoxication
highly active antiretroviral therapy
history of neurology
human immunodeficiency virus type 1
huntingtin
Huntington's chorea
hypercapnia
hypertension
hypoglycemia
hypoglycemic coma
hyporeflexia
hypotonia
hypotonia, infants
hypoxic encephalopathy
immunodeficiency
immunosuppression
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
infant, evaluation of
intestinal pseudoobstruction
intrinsic hand muscles, wasting of
Isaacs syndrome
jaw closure weakness
Kugelberg-Welander syndrome
leg weakness, bilateral
leg weakness, unilateral
leukemia
lid closure, weakness of
life expectancy
liver disease
lordosis
lymphoma
masseter muscle weakness
mental retardation
misdiagnosis
molecular genetics
monomelic amyotrophy
mortality
motor neuron disease
motor system
movement disorder
movement disorder, extrapyramidal
multiple system atrophy
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle hypertrophy
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, differential diagnosis of
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myocardial injury
myocytolysis
myokymia
myopathy
myopathy, centronuclear
myopathy, mitochondrial
myopathy, quadriceps
myotonia congenita
myotonia dystrophica
nemaline rod myopathy
neoplasm, primary intracranial
neoplasm, primary of CNS
nerve conduction studies
neurocutaneous disease
neuroendocrinology
neurofibrillary degeneration
neurogenic vs.myopathic atrophy
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neuromyotonia
neuronal degeneration
neuronal migration disorder
neuronopathy
neuropathology
neuropathy
neuropathy, hereditary peripheral
neuropathy, motor, multifocal
newborn, evaluation of
nusinersen
ocular motility, disorders of
Parkinson disease
pathology
patient information and support
placebo
poison, mercury
poison, neurologic problems with
polymerase chain reaction
polymyositis
polyneuropathy
post polio syndrome
preclinical
pregnancy, neurologic complications in
primary lateral sclerosis
progeria
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
pseudohypertrophy
quadriceps atrophy
quadriceps weakness
radiation hypersensitivity
radiculopathy
respiratory failure
retrovirus
review article
RFLPs
risk-benefit assessment
safety
scoliosis
scoliosis, neurologic association with
screening
skin, lesions in neurologic disorders
SMN1 gene
spinal cord
spinal cord degeneration
spinal cord, pathologic exam of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar degeneration
sudden death
survival motor neuron gene
telangiectases
term infant
testicular atrophy
tongue, fasciculations of
treatment of neurologic disorder
tremor
tremor, postural
tricresylphosphate
trinucleotide repeats
viral infection
walking, difficulty with
weakness
weakness, generalized
weakness, infant
weakness, progressive
weaning from respirator, failure to
weight loss
Werdnig-Hoffman disease
wheelchair
whistle, inability to
winging of scapula
workup
X-linked bulbospinal neuronopathy
Showing articles 50 to 100 of 7091 << Previous Next >>

Infantile Spinal Muscular Atrophy
Arch Neurol 25:276, Wilkins,R.,et al, 1971

Neurogenic Muscular Atrophy of Infancy with Prolonged Survival
Brain 92:9, Munsat,T.,et al, 1969

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

Chronic Spinal Muscular Atrophy in Adults
J Neurol Sci 9:551, Meadows,J.C.,et al, 1969

Neurogenic Muscular Atrophy Simulating Facioscapulohumeral Muscular Dystrophy
J Neurol Sci 9:389, Furukawa,T.,et al, 1969

Amyotrophic Lateral Sclerosis
Lancet 400:1363-1380, Feldman, E.L.,et al, 2022

Complete Evaluation of Dementia: PET and MRI Correlation and Diagnosis for the Neuroradiologist
AJNR 42:998-1007, Oldan, J.D.,et al, 2021

Amyotrophic Lateral Sclerosis
NEJM 377:162-172, Brown, R.H.,et al, 2017

Spectrum of Imaging Appearances of Intracranial Cryptococcal Infection in HIV/AIDS Patients in the Anti-Retroviral Therapy Era
Clin Radiol 71:9-17, Offiah, C.E. & Naseer, A., 2016

The Spectrum of Mutations in Progranulin: A Collaborative Study Screening 545 Cases of Neurodegeneration
Arch Neurol 67:161-170,145, Yu,C.-E.,et al, 2010

Frontotemporal Lobar Degeneration with Motor Neuron Disease
Arch Neurol 63:489-490, Clark,C.M. &Forman,M.S., 2006

Linkage of Familial Amyotrophic Lateral Sclerosis with Frontotemporal Dementia to Chromosome 9q21-q22
JAMA 284:1664-1669, Hosler,B.A.,et al, 2000

The Central Nervous system and Infection by Candida Species
Diagn Microbial Infect Dis 37:169-179, Sanchez-Portocarrero, J.,et al, 2000

Hypertrophy of Multiple Cranial Nerves and Spinal Roots in Chronic Inflammatory Demyelinating Neuropathy
JNNP 67:685-687, Duarte,J.,et al, 1999

MR Findings in AIDS-Associated Myelopathy
AJNR 20:1412-1416,1387, Chong,J.,et al, 1999

Olfactory Dysfunction in Guamanian ALS,Parkinsonism,and Dementia
Neurol 51:1672-1677, Ahlskog,J.E.,et al, 1998

MR Findings of Werdnig-Hoffmann Disease in Two Infants
AJNR 19:550-552, Hsu,C.,et al, 1998

Familial Nature and Continuing Morbidity of the Amyotrophic Lateral Sclerosis-Parkinsonism Dementia Complex of Guam
Neurol 49:400-409, McGeer,P.L.,et al, 1997

Candidal Meningitis in HIV-Infected Patients: Analysis of 14 Cases
Clin Inf Dis 25:473-476, Casado, J.L.,et al, 1997

Cytomegalovirus Encephalitis
Ann Int Med 125:577-578, Arribas,J.R.,et al, 1996

Tuberculous Meningitis Among Adults with and without HIV Infection
Arch Int med 156:1710-1716, Yechoor,V.K.,et al, 1996

Neuroimaging Findings in Patients with AIDS
Clin Inf Dis 22:906-919, Walot,I.,et al, 1996

Cytomegalovirus Ventriculoencephalitis in AIDS, A Syndrome with Distinct Clin & Path FEatures
Medicine 72:67-77, Kalayjian,R.C.,et al, 1993

Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
Ann Int Med 116:896-900, Coleman,R.A.,et al, 1992

Brain Imaging in Human Immunodeficiency Virus Infection
Semin Neurol 12:57-69, Ketonen,L.&Tuite,M.J., 1992

Recurrent Encephalopathy and Seizures in a US Native with HTLV-I-Associated Myelopathy/Tropical Spastic Paraparesis
Neurol 42:658-661, Smith,C.R.,et al, 1992

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

Multiple Sclerosis-Like Illness Occurring with Human Immunodeficiency Virus Infection
Neurol 39:324-329, Berger,J.R.,et al, 1989

CT, MR, and Pathlogy in HIV Encephalitis and Meningitis
AJR 151:373-380, Post,M.J.D.,et al, 1988

Neurological Clues from Environmental Neurotoxins
BMJ 295:346-347, Martyn,C.N., 1987

Neurological Complications of Acquired Immune Deficiency Syndrome:Analysis of 50 Patients
Ann Neurol 14:403-418, Snider,W.D.,et al, 1983

Neurodegenerative Disease of Infancy & Childhood
Ann Neurol 13:351-364, Dyken,P.,et al, 1983

Preservation of the Phrenic Motorneurons in Werdnig-Hoffman Disease
Ann Neurol 9:506-510, Kuzuhara,S.,et al, 1981

Vitamin E Deficiency in Werdnig-Hoffmann Disease
Ann Neurol 10:266-268, Shapira,Y.,et al, 1981

Cellular Immunity In Guamanians with Amyotrophic Lateral Sclerosis & Parkinsonism-Dementia
NEJM 299:680-685, Hoffman,P.M.,et al, 1978

Sparing of the Onufrowicz Nucleus in Sacral Anterior Horn Lesions
Ann Neurol 4:245-249, Iwata,M.,et al, 1978

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy (II)
Arch Neurol 18:619, Dyck,P.,et al, 1968

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

Amyotrphic Lateral Sclerosis
Arch Neurol 16:357, Hirano,A.,et al, 1967

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

Multidisciplinary End-of-Life Care for a Patient with Amyotrophic Lateral Sclerosis Requesting Euthanasia
Lancet 402:484, Kruithof,W.J.,et al, 2023

Disabling Jaw Clonus in a Patient with Bulbar-Onset Amyotrophic Lateral Sclerosis Successfully Treated with Botulinum Toxin
Neurol 99:671, Santos, M.O.,et al, 2022

Toward Simpler, Safer Treatment of Cryptococcal Meningitis
NEJM 386:1179-1181, Moosa, M.Y.S. & Lessells, R.J., 2022

Natural History of "Pure" Primary Lateral Sclerosis
Neurol 96:e2231-e2238, Hassan, A.,et al, 2021

Teaching Video NeuroImages: Jaw Clonus in Amyotrophic Lateral Sclerosis
Neurol 96:e2563, Goel, A.,et al, 2021

Clinicopathologic Conference, Mycobacterium Tuberculosis Meningitis
NEJM 384:166-176, Case 1-2021, 2021

Clinicopathologic Conference, Acute human immunodeficiency virus type 1
NEJM 385:641-648, Case 24-2021, 2021

Clinicopathologic conference, Cryptococcal meningoencephalitis and advanced HIV infection
NEJM 383:2572-2580, Case 40-2020, 2020

Diagnostic and Prognostic Value of Conventional Brain MRI in the Clinical Work-Up of Patients with Amyotrophic Lateral Sclerosis
J Clin Med 9:1-12, Rizzo, G.,et al, 2020

Telemedicine in Neurology
Neurol 94:30-38,16, Hatcher-Martin, J.M.,et al, 2020



Showing articles 50 to 100 of 7091 << Previous Next >>