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Differential
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achilles tendon, enlarged
acromicria
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adult polyglucosan body disease
advances in neurology
affect, inappropriate
amniocentesis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
Angelman syndrome
antidepressant
antitoxin
apnea
applause sign
arm weakness
aspiration
asymmetric crying facies
ataxia
autonomic dysfunction
axonal degeneration
Babinski sign
basal ganglia, calcification of
basal ganglia, lesion of
behavior, combative
behavioral disorder
BiPAP
bladder dysfunction
blindness
bone marrow transplantation
botulinum toxin
botulism
botulism antitoxin
botulism immune globulin
botulism, infant
brainstem, infarction of
brainstem, lesion of
bulbar palsy
bulbar palsy, childhood
bulbar palsy, progressive
cachexia
calcification, intracranial
caries
CAT scan, abnormal
CAT scan, emission, abnormal
cataracts
cerebral dominance
cerebrovascular accident
cerebrovascular accident, bilateral
children
chromosomal abnormality
chromosome 15
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
congenital birth defects
congenital heart disease
congenital malformation
constipation
contractures, joint
conversion reaction
cortical blindness
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, weak
crying
crying, pathologic
cryptorchidism
cultured skin fibroblasts
cystatin C mutation
deafness
decerebrate posture
degenerative diseases of CNS
dementia
dementia, frontotemporal
depression
developmental disability
developmental retardation
differential diagnosis
disability rating scale, neurological
disability, neurological
distal muscle weakness
drooling
dying
dysarthria
dysdiadochokinesia
dysmorphic
dysphagia
dysphonia
dystonia
dystonia, cervical
eating disorder
echocardiogram
efficacy
electroencephalogram, abnormalities of
electromyogram
emotional lability
epidemiology of neurology
Erdheim-Chester disease
eye movement, disorders of
eyes, sunken
facial appearance, abnormal
facial asymmetry
facial weakness
facial weakness, bilateral
failure to thrive
falling
familial
fasciculation
fatigue
feeding disorder
fibrillations
flail arm syndrome
floppy infant
fluoxetine
foam cells
food poisoning
food-borne infection
foot drop
gait disorder
gait, spastic
gammaglobulin therapy, intravenous
gaze palsy
gaze palsy, horizontal
gaze palsy, supranuclear
gender
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glycogen storage disease
growth hormone deficiency
growth retardation
hand flapping
head bobbing
hearing loss
heel swelling
hemiparesis
heralding manifestation
histiocytosis
honey
hospice
hyperphagia
hyperpigmentation of skin
hyperreflexia
hypertension
hypogonadism
hypometric saccades
hypopigmentation of skin
hyporeflexia
hypotension, systemic
hypotonia
hypotonia, infants
imbalance
inappropriate antidiuretic(A.D.H.)hormone
inclusion bodies
infant, evaluation of
intellectual deficit
intellectual deterioration
internal capsule
internuclear ophthalmoplegia
intrinsic hand muscles, wasting of
intubation
irritability
irritable baby
jaw jerk, abnormal
Jewish
laughing
laughing, pathologic
leg weakness, unilateral
lethargy
leukodystrophy
leukoencephalopathy
life expectancy
locked-in syndrome
masked facies
memory, defect of recent
memory, impairment of
mental retardation
merosin
middle cerebellar peduncle, lesion
mimics
misdiagnosis
molecular genetics
monoparesis
mortality
motor neuron disease
MRI
MRI, abnormal
MRI, mouse ears
multiple sclerosis, differential diagnosis of
muscle biopsy
muscle cramp
muscle wasting, diffuse
muscular dystrophy
muscular dystrophy, congenital
mutism
myelomalacia
myeloneuropathy
neck weakness
neurogenic bladder
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuroophthalmology
neuropathology
neuropathy
neuroprotective agents
neurotoxin
next-generation sequencing
obesity
ocular bobbing
opened mouth
ophthalmoplegia
optic neuropathy
palliative care
paraparesis, spastic
Parkinsonism syndrome
pathologic reflex
peroxisomal disease
personality change
photosensitivity, skin
pigmentary retinopathy
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polymicrogyria
pons, infarction of
Prader-Labhart-Willi syndrome
prenatal diagnosis by amniocentesis
primary lateral sclerosis
prognosis
progressive neurologic disorder
progressive supranuclear palsy
pseudobulbar palsy
psychomotor retardation
ptosis
ptosis, bilateral
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
radiculopathy
rash
release phenomena
respirator
respiratory arrest
respiratory failure
retinopathy
review article
riluzole
risk factors
saccadic eye movements, abnormal
seizure
sensorineural hearing loss
sertraline
short stature
skew deviation
skin, lesions in neurologic disorders
sleep
sleep pathology and physiology
spasticity
speech disorder
speech, loss of
stooped posture
strabismus
suck, poor
symmetric brain lesions
systemic illness
tachycardia
temper tantrums
term infant
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
tongue, protrusion of
toxins, nervous system
tracheostomy
trauma
treatment of neurologic disorder
tremulousness
tripping
ultrasonography
urinary incontinence
very long chain fatty acids
walking, difficulty with
weakness
weakness, generalized
weakness, infant
weakness, progressive
wheelchair
white matter disease
wide based gait
Showing articles 0 to 50 of 2560 Next >>

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

A 59-Year-Old Man with Progressive Dysarthria and Gait Instability
Neurol 104:e213729, Shen,D.,et al, 2025

Clinicopathologic Conference, Infant Botulism, Case 3-2024
NEJM 390:358-366, Case 3-2024, 2024

Pharmaceutical Interventions for Emotionalism After Stroke
Stroke 54:e213-e214, Hackett,M.L.,et al, 2023

Congenital Asymmetric Crying Facies Syndrome, A Case Report
Medicine 97:31(e11403), Liang,X. & He,B., 2018

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

My Weeping Patient
Neurol 89:e202, Peters, J.,et al, 2017

Inherited Metabolic Diseases of the Nervous System, Adrenoleukodystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 988, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Progressive Supranuclear Palsy
Adams & Victors Principles of Neurology, Chp 39, pg 1096, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Progressive Bulbar Palsy
Adams & Victors Principles of Neurology, Chp 39, pg 1111, Ropper, A.H.,et al, 2014

Diagnosis and Management of Motor Neurone Disease
BMJ 336:658-662, McDermott,C.J. &Shaw,P.J., 2008

Amyotrophic Lateral Sclerosis
Lancet 369:2031-2041, Mitchell,J.D. & Borasio,G.D., 2007

Case 35-2006: A Newborn Boy with Hypotonia
NEJM 355:2132-2142, Brown,R.H.,et al, 2006

Human Botulism Immune Globulin for the Treatment of Infant Botulism
NEJM 354:462-471, Arnon,S.S.,et al, 2006

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

Paramedian Pontine Infarction
Stroke 28:809-815, Kataoka,S.,et al, 1997

Primary Lateral Sclerosis, Clin Features, Neuropath & Dx Criteria
Brain 115:495-520, Pringle,C.E.,et al, 1992

Cockayne Syndrome: Review of 140 Cases
Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992

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

Emotionalism after Stroke
BMJ 298:991-994, House,A.,et al, 1989

Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
Arch Neurol 45:509-513, Gastaut,J.L.,et al, 1988

Pathological Laughter & Crying
In Frederiks, J. A. M. (Ed) Handbook of Clinical Neurology, Elsevier Science Publ, 45:219, Poeck,K., 1985

Control of Emotional Expression in Pseudobulbar Palsy
Arch Neurol 34:717, Lieberman,A.,et al, 1977

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,et al, 2025

A 56-Year-Old Woman with New-Onset Hoarsement and Dysphagia
Neurol 104:e213363, McAree,M. & Frontera, J.A., 2025

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

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

Postprocedural Brachial Neuritis:Clinical, Electrodiagnostic, and Neuroimaging Features
AJNR 46:1050-1055, Ambati,V.S.,et al, 2025

A 72-Year-Old Man With Meningoencephalitis
Neurol 104:e213658, Isaza-Pierotti,D.F.,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

A 19-Year-Old Woman with Progressive Weakness and Numbness in Her Arms and Legs
Neurol 104:e213495, Alsabah,A-A.,et al, 2025

Sarcoidosis of the Pituitary Gland and Stalk in a Man Presenting Asthenia, Impotence, Loss of Libido, Polyuria, and Polydipsia
Lancet 404:2460-2461, Clement,J., et al, 2024

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

Clinicopatholigic Conference, Rheumatoid Arthritis with Vasculitis Causing A Confluent Mononeuritis Multiplex
NEJM 390:1312-1322, Case 11-2024, 2024

Clinicopathologic Conference, Thyrotoxic Periodic Paralysis Associated with Graves Disease
NEJM 390:1514-1522, Case 13-2024, 2024

A 65-Year-Old Woman with Isolated Macroglossia as the Initial Presentation of a Rare Disease
Neurol 103:e210070, Lara,C.,et al, 2024

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

Clinical and Imaging Features of Cobb Syndrome
Neurol 102:e208118, Yang,X.,et al, 2024

A 26-Year-Old Woman with Chronic Progressive Gait Dysfunction
Neurol 103:e2098-e2030, Jones,F.J.S. & Orthmann-Murphy,J., 2024

A 61-Year-Old Man With Progressive Right Leg Numbness and Weakness
Neurol 103:e209900, Jones,F.J.S.,et al, 2024

A 32-Year-Old Man with Painless Bilateral Shoulder Girdle Weakness and Atrophy
Neurol 103:e209915, Gutti,N.B.,et al, 2024

A 22-Year-Old Woman with Episodic Weakness and Jaundice
Neurol 103:e210018, Rathinasbapathi,M.,et al, 2024

Clinicopathologic Conference, Myasthenia Gravis
NEJM 391:1441-1450, Case 32-2024, 2024

Intracranial Hypertension Associated with Poly-Cranio-Radicular-Neuropathies A Case Report and Review of the Literature
Neurologist 29:166-169, Eaton,J.E.,et al, 2024

A 55-Year -Old Woman with Painless Hand Weakness and Atrophy
Neurol 103:e209561, Ticku,H. & Katirji,B.,, 2024

The "Chameleon Eyes Sign" in Myasthenia Gravis
Neurol 103:e209756, Zara,P.,et al, 2024

A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis
Neurol 103:e209708, Wannarong,T.,et al, 2024

Behcets Syndrome
NEJM 390:640-651, Saadoun,D.,et al, 2024

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



Showing articles 0 to 50 of 2560 Next >>