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Differential
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abscess, intracerebral
abscess, intracranial
abscess, sphenoid sinus
amyloidosis
anemia
angiography, cerebral
angiography, posterior fossa
anhidrosis
aqueduct of Sylvius, stenosis
aqueductal stenosis
areflexia
arteriopathy
arthrogryposis multiplex
arylsulfatase B
atlanto-axial subluxation
band keratopathy
basal ganglia, calcification of
birth injury
blindness
bone marrow transplantation
calcification, intracranial
carcinoma
carotid artery occlusion, neck
CAT scan
CAT scan, abdomen
CAT scan, abnormal
cataracts
cataracts, congenital
cavernous sinus, syndrome
central nervous system, infection of
cerebellar hypoplasia
cerebral infarction, hemorrhagic
cerebral ischemia
cerebral palsy
cerebral venous thrombosis
cerebro hepato renal syndrome
cerebrovascular accident
cerebrovascular accident, infancy and childhood
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cerebrovascular disease
cervical spine
children
chorioretinitis
chromosomal abnormality
chronic graft versus host disease
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
congenital heart disease
congenital infection, CNS
conjunctival injection
contractures, joint
cornea
cornea, abnormal
cornea, opacification in infancy-causes of
cornea, opacity of
corneal dystrophy
corneal edema
corpus callosum
corpus callosum, hypoplastic
cranial neuropathy, multiple
cultured skin fibroblasts
cytomegalovirus infection
cytomegalovirus infection, congenital
deafness
dementia
dementia, presenile
developmental retardation
diarrhea
diplopia
diplopia, monocular
dissociated sensory loss
donut sign
dural sinus thrombosis
dwarfism
dysmorphic
dysostosis multiplex
dyspraxia
ear, abnormal
echocardiogram
ectatic basilar artery
eculizumab
edema, pedal
electroretinograph
empyema, epidural
empyema, subdural
encephalocele
enzyme treatment
enzyme, defect
epidermal nevus syndrome
eye movement, painful
Fabry's disease
facial appearance, abnormal
facial weakness, bilateral
fatty acid, elevated plasma content
fever
fungal infection, CNS
gangliosidosis GM1
gangliosidosis GM2
gene
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic neurologic disorders
genu valgum
glaucoma
headache
headache, severe
hearing loss
hemianopia
hemiparesis
hemoglobinuria
hemolysis
hemorrhoids
hepatomegaly
hepatosplenomegaly
Hurler's syndrome
hydrocephalus
hydrocephalus, congenital
hydronephrosis
hypertension
hypopyon
hypotonia
hypotonia, infants
inclusion bodies
inclusion bodies, intracytopasmic
intelligence quotient
intracerebral hemorrhage
intraocular pressure, increase
intrauterine
intrauterine infection
intrauterine infection, viral
intrauterine infection, viral of CNS
iritis
jugular foramen syndrome
Krabbe's disease
kyphoscoliosis, neurologic causes of
lactic dehydrogenase(LDH)
life expectancy
lipid storage disorder of CNS
lissencephaly
lymphadenopathy
lymphoma
lymphoma, ocular
lymphoma, systemic
lysosomal storage disease
lysosomes, abnoral
macrocephaly
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
mastoiditis
memory, impairment of
meningitis
mental retardation
metabolic disorder, primary
metachromatic leukodystrophy
microcephaly
micropolygyria
micropthalmia
mitral valve prolapse
monoclonal antibodies
Morquio syndrome
mortality
MRI
MRI, abnormal
mucopolysaccharidoses
multiple sclerosis, differential diagnosis of
myelopathy
myotonia dystrophica
nasal stuffiness
neck pain
neoplasm, metastatic to eye
nerve conduction studies
neurocutaneous disease
neurofibromatosis 2
neurolipidosis IV
neurologic disease, diagnoses of
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, hereditary peripheral
neuropathy, peripheral
neurosis
nevus
Niemann-Pick disease
nystagmus
ophthalmoplegia
optic atrophy
optic nerve
optic nerve, hypoplasia of
optic nerve, neoplasm of
optic neuritis
oral contraceptives
orbit, lesions of
osteomyelitis
osteomyelitis, skull
osteoporosis
otitis, neurologic complications with
pachygyria
pain
pain, abdominal
pain, head
papilledema
paraparesis, spastic
paroxysmal nocturnal hemoglobinuria
patent ductus arteriosus
pectus carinatum
periventricular leukomalacia
photosensitivity, skin
polycystic kidneys
polyneuropathy
pregnancy, neurologic complications in
premature infant
prenatal diagnosis by amniocentesis
prognosis
proteinuria
pseudohypopyon
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychomotor retardation
pupil, abnormality in neurologic disorders
quadriparesis
rash
red eye
renal failure
respiratory failure
retinal degeneration
retinal detachment
retinal dysplasia
retinitis pigmentosa
retinopathy
review article
rubella syndrome
sarcoidosis
seizure
seizure, neonatal
sensorineural hearing loss
short neck
short stature
sinusitis
skin, biopsy
skin, lesions in neurologic disorders
skull x-ray, bony defect on
slit lamp examination
spinal cord, compression of
splenic-vein thrombosis
splenomegaly
stem cell transplantation
stillbirth
sweating, abnormality of
Tangier's disease
third nerve palsy
thrombocytopenia
tinnitus
tongue, enlarged
torticollis
treatment of neurologic disorder
uremia
urinary incontinence
uveitis
varicose veins
vasculopathy
vertebral-basilar insufficiency
vertigo
vertigo, episodic
viral infection, CNS
vision, failure of in childhood
visual acuity
visual acuity, decreased
visual impairment
visual loss
Walker-Warburg syndrome
white matter disease
Showing articles 0 to 50 of 519 Next >>

Bilateral Pseudohypopyon Causing White Eyes in a Patient with Lymphoma
Lancet 395:e74, Radhakrishnan Iyer, S.S.,et al, 2020

Clinicopathologic Conference, Paroxysmal Nocturnal Hemoglobinuria
NEJM 377:2581-2590, Case 40-2017, 2017

Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases
Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003

Follow-up of Nine Patients with Hurler Syndrome After Bone Marrow Transplantation
J Pediatr 133:119-125, 71998., Guffon,N.,et al, 1998

Mucolipidosis Type IV; Characteristic MRI Findings
Neurol 51:565-569, Frei,K.P.,et al, 1998

Cerebrovascular Complications of Fabry's Disease
Ann Neurol 40:8-17, Mitsias,P.&Levine,S.R., 1996

Visual Impairment in Patients with Neurofibromatosis 2
Neurol 43:622-623, Bouzas,E.A.,et al, 1993

Lethal Cytomegalovirus Infection in Preterm Infants:Clinical, Radiological, and Neuropathological Findings
Ann Neurol 31:64-68, Perlman,J.M.&Argyle,C., 1992

Anderson-Fabry Disease
Editorial, Lancet 336:24-251990., , 1990

Anderson-Fabray Disease, A Commonly Missed Diagnosis
BMJ 297:872-873, Morgan,S.H.&Crawfurd,M., 1988

Ocular Complications of Tangier Disease
Am J Med 83:991-994, Pressley,T.A.,et al, 1987

Familial Amyloidosis with Cranial Neuropathy & Corneal Lattice Dystrophy
Neurol 36:432-435, Darras,B.T.,et al, 1986

Tangier Disease (Hypo-a-Lipoproteinemia)
Textbook of Child Neurology, 3rd Ed. , Phila, Lea & Febiger, Ch 1, p 86, Menkes,J.H., 1985

Congenital Hydrocephalus & Eye Abnormalities with Severe Developmental Brain Defects:Warburg's Syndrome
Ann Neurol 16:60-65, Bordarier,C.,et al, 1984

Cerebro-ocular Dysgenesis (Walker-Warberg Syndrome) :Neuropathologic & Etiologic Analysis
Neurol 34:1531-1541, Williams,R.S.,et al, 1984

The Cerebrohepatorenal (Zellweger) Syndrome
NEJM 310:1141-1146, Moser,A.E.,et al, 1984

Clinicopathological Conference
Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983

Monocular Polyopia
Arch Neurol 40:756-757, Hirst,L.W.,et al, 1983

Mucopolysaccaridosis IV (Morquio Syndrome) , in The Metabolic Basis of Inherited Disease
(Ed) 5th Ed. , McGraw-Hill, New York, p. 766, Stanbury,J.B., 1983

Cockayne Syndrome:Unusual Neuropathological Findings & Review of the Literature
Ann Neurol 6:340-348, 1979, Soffer,D.,et al, 1979

Neurological Involvement in the Epidermal Naevus Syndrome
JNNP 41:466, McAuley,D.L.,et al, 1978

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

Sarcoidosis & Its Ophthalmic Manifestations
Am J Ophthmol 86:648-655, Obenauf,C.D.,et al, 1978

Globoid cells, Glial nodules, & Peculiar Fibrillary Changes in the cerebro-hepato-renal Syndrome of Zellweger
Ann Neurol 2:473, deLeon,G.A.,et al, 1977

Neurological Complications of Infections of the Head & Neck
Otolaryng Clin North Am 9:729, Kaplan,R.J., 1976

Corneal Opacification in Infancy
MCV Quart 8:230, Ching,F., 1972

Mucopolysaccaridosis IV (Morquio Syndrome) , in Heritable Disorders of Connective Tissue
(Ed) 4th Ed, The C. V. Mosby Co, St. Louis, p. 583, McKusick,V.A., 1972

Ophthalmoplegia In Myotonic Dystrophy
Am J Ophthalmol 71:1231-1235, Lessell,S.,et al, 1971

Rubella, Clinical Manifestations & Management
Am J Dis Child 118:18-29, Cooper,L.Z.,et al, 1969

Angiokeratoma Corporis Diffusum
Quart J Med 31:177, 1962 April., Wise,D.,et al, 1962

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

Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
NEJM 388:2379-2387, Case 19-2023, 2023

A Woman with Progressive Painless Sequential Monocular Vision Loss
Neurol 101:e2197-e2201, Ditrapani,J.,et al, 2023

Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
UptoDate 2022 Jan, Darras, B.T., 2022

Bilateral Hearing Loss and Constricted Visual Fields
BMJ 378:e070672, Sachdeva, G. & Shafquat, S., 2022

Facial Numbness, Dysarthria, Muscle Atrophy, and Weakness in a Young Patient
JAMA Neurol 78:1273-1274, Liu, Y.,et al, 2021

A 28-Year-Old Woman with Vision Loss and an Unusual Gait
Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021

Imaging Patterns Characterizing Mitochondrial Leukodystrophies
AJNR 42:1334-1340, Roosendaal, S.D.,et al, 2021

A 42-year-old Woman with Progressive Cognitive Difficulties and Gait Imbalance
Neurol 94:e1219-e1226, Slama, M.C.C.,et al, 2020

Spinal Cord Involvement in Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia
JAMA Neurol 77:1169-1170, Li, S.,et al, 2020

Bilateral Ptosis, Dysphagia, and Progresive Weakness in a Patient of French-Canadian Background
Neurol 95:933-938, Paul,P.,et al, 2020

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

"Boule Du Biceps" in Dysferlinopathy
Neurol 94:83-84, El Sherif, R.,et al, 2020

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

Accuracy of a Machine Learning Muscle MRI - Based Tool for the Diagnosis of Muscular Dystrophies
Neurol 94:e1094-e1102, Verdu-Diaz, J.,et al, 2020

Muscular Dystrophies
Lancet 394:2025-2038, Mercuri, E.,et al, 2019

Heart Transplantation in a Patient with Myotonic Dystrophy Type 1 and End-Stage Dilated Cardiomyopathy: A Short Term Follow-up
Acta Myologica 37:267-271, Papa, A.A.,et al, 2018

Clinical Reasoning: Cardioembolic Stroke in a 23-year-old Man with Elbow Contracture
Neurol 90:e172-e176, Roy, B. & Raynor, E., 2018

Long-term Effects of Glucocorticoids on Function, Quality of Life, and Survival in Patients with Duchenne Muscular Dystrophy: A Prospective Cohort Study
Lancet 391:451-461, McDonald, C.M.,et al, 2018



Showing articles 0 to 50 of 519 Next >>