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abiotrophy
adult polyglucosan body disease
advances in neurology
algorithm
Alzheimer's disease
aminoacidopathies
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, childhood
amyotrophic lateral sclerosis, conjugal
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
amyotrophic lateral sclerosis, juvenile
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis, Parkinson-dementia-complex
amyotrophic lateral sclerosis, post-encephalitic
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
anterior horn cell disease
aphasia
aphasia, progressive, primary
areflexia
arm weakness
arthrogryposis multiplex
ataxia
ataxia, progressive
autonomic dysfunction
axonal degeneration
Babinski sign
behavioral disorder
bladder dysfunction
brain atrophy
bulbar palsy
bulbar palsy, childhood
bulbar palsy, progressive
C0ORF72
CAG repeats
calf hypertrophy
camptocormia
cane
CAT scan, abnormal
CAT scan, emission, abnormal
cataracts
central core disease
cerebellar atrophy, primary
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cell count
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, protein of
cerebrovascular accident
Charcot-Marie-Tooth
children
chorea
chromosomal abnormality
chromosome 5
cognition
congenital heart disease
crying, pathologic
deafness
degenerative diseases of CNS
Dejerine-Sottas syndrome
delusion
dementia
dementia, age at onset
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dermatomyositis
developmental retardation
diagnostic criteria
differential diagnosis
difficulty climbing stairs
distal muscle atrophy
distal muscle weakness
DNA probes
drooling
dying
dysarthria
dysphagia
dyspnea
dystonia
electromyogram
emotional lability
epidemiology of neurology
episodic neurologic deficits
exercise
exercise intolerance
facial weakness
facial weakness, bilateral
falling
familial
fasciculation
Fazio-Londe's disease
fibrillations
floppy infant
fluency
foot drop
free radical
Friedreich's ataxia
frontal lobe, atrophy
frontotemporal dementia, behavioral variant
gait disorder
gait, spastic
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glycogen storage disease
Guillain Barre syndrome
gynecomastia
hallucination
hand weakness
hearing loss
heavy metal intoxication
hemiparesis
heralding manifestation
history of neurology
hoarseness
Huntington's chorea
hyperpigmentation of skin
hyperreflexia
hyporeflexia
hypotension, systemic
hypotonia
hypotonia, infants
imbalance
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
incontinentia pigmenti
infant, evaluation of
inflexibility, mental
intellectual deficit
intellectual deterioration
intrinsic hand muscles, wasting of
Isaacs syndrome
Jakob-Creutzfeldt disease
jaw jerk, abnormal
Jewish
klippel feil syndrome
Kugelberg-Welander syndrome
lactic acidemia
lathyrism
laughing
laughing, pathologic
leg atrophy
leg weakness, bilateral
leg weakness, unilateral
leukodystrophy
leukoencephalopathy
Lewy body
life expectancy
lobar atrophy
lysosomal storage disease
malformation, CNS, congenital
memory, defect of recent
memory, impairment of
mental retardation
metabolic disorder, primary
Mills syndrome
mimics
misdiagnosis
molecular genetics
monomelic amyotrophy
mononeuropathy
mortality
motor neuron disease
MRI, abnormal
multiple sclerosis, differential diagnosis of
muscle atrophy, progressive
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
muscle twitching
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenic crisis
myelomalacia
myeloneuropathy
myokymia
myopathy
myopathy, carcinomatous
myopathy, thyroid disease causing
myositis
myotonia dystrophica
nasal speech
neck weakness
nerve conduction studies
neuritis, causes of
neuroendocrinology
neurofibrillary degeneration
neurofibromatosis 1
neurofibromatosis 2
neurogenic bladder
neurologic disease
neurologic disease, diagnoses of
neurologic testing
neuromyotonia
neuronal degeneration
neuronopathy
neuropathology
neuropathy
neuropathy, diabetic
neuropathy, hereditary peripheral
next-generation sequencing
nusinersen
optic atrophy
pain, increased response
palliative care
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
Parkinson disease
Parkinson disease, dementia with
Parkinson disease, familial
Parkinson disease, rapid progression
Parkinson disease, young onset
Parkinsonism syndrome
Parkinsonism-dementia complex
paroxysmal neurologic deficits
patient information and support
peroneal muscle atrophy, causes of
peroxisomal disease
personality change
pleocytosis of cerebrospinal fluid
poison, mercury
poison, neurologic problems with
poliomyelitis
polyglucosan body
polyglucosan body disease
polymyositis
polyneuropathy
porphyria
post polio syndrome
preclinical
pregnancy, neurologic complications in
primary lateral sclerosis
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
pseudobulbar palsy
pseudohypertrophy
psychiatric problems in neurologic disorders
psychomotor retardation
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
radiculopathy
recombinant DNA
Refsum's disease
release phenomena
respirator
respiratory failure
review article
RFLPs
riluzole
risk factors
Roussy Levy syndrome
sarcoidosis
scoliosis
scoliosis, neurologic association with
screening
seizure
single photon emission computed tomography
skin, lesions in neurologic disorders
SMN1 gene
spastic ataxia
spasticity
speech disorder
speech, loss of
spinal cord
spinal cord degeneration
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinocerebellar ataxia
stereotyped behavior
stiff man syndrome
superoxide dismutase
survival motor neuron gene
temporal lobe, atrophy
term infant
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
tongue, weakness
torticollis
trauma
treatment of neurologic disorder
tremor
tremor, postural
tricresylphosphate
trinucleotide repeats
urea-cycle enzymopathies
urinary incontinence
vestibular function, tests of
walking, difficulty with
weakness
weakness, generalized
weakness, infant
weakness, progressive
weight loss
Werdnig-Hoffman disease
wheelchair
white matter disease
word-finding difficulty
X-linked bulbospinal neuronopathy
Showing articles 500 to 550 of 4485 << Previous Next >>

Magnetic Resonance Imaging in Clinically Isolated Lesions of the Brain Stem
JNNP 49:737-743, Ormerod,I.E.C.,et al, 1986

Clinicopath Conf
Tuberous Sclerosis, Case 41-1986, NEJM 315:1013-1022986., , 1986

A Population-Based Study of Multiple Sclerosis in Twins
NEJM 315:1638-1642, Ebers,G.C.,et al, 1986

Cerebrospinal Fluid Findings in Healthy Siblings of Multiple Sclerosis Patients
Neurol 36:727-729, Duquette,P.&Charest,L., 1986

Bilateral Pontine Gaze Palsy
Arch Neurol 42:93-94, Joseph,R.,et al, 1985

Conjugal Multiple Sclerosis
In Handbook of Clinical Neurol, Elsivier Publ, Amsterdam 47:291985., Myrianthopoulos,N.C., 1985

Hereditary Adult-Onset Leukodystrophy Simulating Chronic Progressive Multiple Sclerosis
NEJM 311:948-953, Eldridge,R.,et al, 1984

Clinicopathological Conference
Case 2-1984, Fabry's Disease, NEJM 310:106-114984., , 1984

Taste & Smell in Disease (First of Two Parts)
NEJM 308:1275-1279, Schiffman,S.S., 1983

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

Family Studies in Tuberous Sclerosis
JAMA 249:1302-1304, Cassidy,S.B.,et al, 1983

The Genetics of Susceptibility to Multiple Sclerosis
Epidemiol Rev 4:45-65, Spielman,R.S.&Nathanson,N., 1982

Epidermoid Tumors Involving the Fourth Ventricle
Neurosurgery 9:9-13, Rosario,M.,et al, 1981

The Familial Nature of MS:Empiric Recurrence Risks for First, Second-, & Third-degree Relatives of Pts
Neurol 31:1039-1041, Sadovnick,A.D.,et al, 1981

Optic Neuritis in Familial MS
Neurol 31:1138-1142, Ebers,G.C.,et al, 1981

Demyelinating Disease Presenting As Wallenberg's Syndrome
Stroke 12:877-878, Smith,D.B.,et al, 1981

Familial Spastic Paraplg, Peroneal Neuropathy, & Crural Hypopig, A New Neurocut Synd
Neurol 31:754-757, Stewart,R.M.,et al, 1981

A pedigree of Amyotrophic Chorea With Acantho-cytosis
Arch Neurol 37:514-517, Kito,S.,et al, 1980

Chronic Progressive Myelopathy:Investigation with CSF Electrophoresis, Evoked Potentials, & CT Scan
Ann Neurol 6:419-424, Patty,D.W.,et al, 1979

Congenital Ocular Motor Apraxia
Arch Neurol 36:29-31, Orrison,W.W.,et al, 1979

Neurological Manifestations of Fabry Disease in Female Carriers
Ann Neurol 4:537-540, Bird,T.D.,et al, 1978

Familial Degeneration of the Basal Ganglia with Acanthocytosis:a Clinical Neuropathological, & Neurochemical Study
Ann Neurol 3:253, Bird,T.D.,et al, 1978

Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
Neurol 28:703, Coutinho,P.,et al, 1978

Familial Occurrence of Meralgia Paresthetica
Arch Neurol 35:182, Massey,E.W., 1978

CNS Lesions in Cystinuria
Arch Neurol 34:638, Blackburn,C.R.B.,et al, 1977

Reversible Corticospinal Tract Disease Due to Hyperthyrodisim
Arch Neurol 34:647, Garcia,C.A.,et al, 1977

Clinical Correlations of Periodic Lateralized Epileptiform Discharges
Clin Electroenceph 8:191-202, Porecha,H.P.&Reilly,E.L., 1977

Bilateral Sixth Nerve Palsy
Arch Neurol 33:681, Keane,J.R., 1976

Catecholamines & Neurologic Diseases
NEJM 293:274, Moskowitz,M.A.,et al, 1975

Specific Laboratory Test for Diagnosis of MS
BMJ 1:412, Field,E.J.,et al, 1974

Isolated Facial Numbness
Ann Int Med 80:49, Horowitz,S., 1974

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

M. S. :A Review
BMJ 2:292, McAlpine,D., 1973

Leigh's Syndrome:The Adult Form of Subacute Necrotizing Encephalomyelopathy with Predilection for the Brainstem
Neurol 23:1030, Sipe,J.C., 1973

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

Differential Diagnosis of Tremors
Med Clin North Am 56:1363, Fahn,S., 1972

Lymphomatoid Granulomatosis
Human Pathology 3:457, Liebow,A.,et al, 1972

Familial and Conjugal Multiple Sclerosis
Brain 86:315-332, Schapira,K.,et al, 1963

Compression of the Thoracic Spinal Cord in a Patient with Scleroderma
Bull Hosp Joint Dis 18:98, 1957, Kaplan,A.,et al, 1957

Failure of Vision in Childhood
Proc Royal Soc Medicine, pp 494-500., , 1850

Spectrum of Intracranial Hemorrhages in Cerebral Venous Thrombosis, A Pictorial Case Series and Review of Pathophysiology and Management
Neurologist 30:45-51, Jha,S.,et al, 2025

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

Progress Toward Mitigating Disability Progression in Multiple Sclerosis
NEJM 392:1966-1968, Calabresi,P.A., 2025

A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,et al, 2025

Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency
Neurol 104:e213636, Chanda,G.,et al, 2025

Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
Ann Neurol 97:611-628, Coppens,S.,et al, 2025

Vertebrobasilart Dolichoectasia Presenting with Multiple Cranial Nerve Involvement
Neurol 104:213541, Freiherr von Seckendorff,A.,et al, 2025

A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
Neurol 104:e213593, Pence, K.L. &Clark, R.A., 2025

Diagnostic MRI Score to Differentiate Susac Syndrome from Primary Angiitis of the Central Nervous System and Multiple Sclerosis
Ann Neurol 96:846-854, Marrodan,M.,et al, 2024

RNF213 Polymorphisms in Intracranial Artery Dissection
Genes doi.org/10.3390/genesis 15060725, Zedde,M.,et al, 2024



Showing articles 500 to 550 of 4485 << Previous Next >>