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Differential
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acalculia
acquired immunodeficiency syndrome
Africa
agitation
alcohol intolerance
alopecia
alternating rapid movement
alternating rapid movement, impaired
ankle reflex, absent
anorexia
antiviral agents
apraxia, constructional
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
atypical
automobile accidents
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
Babinski sign
Balint's syndrome
basal ganglia, lesion, bilateral
behavioral disorder
bone age
cachexia
CAG repeats
caloric testing
CAT scan, abnormal
CAT scan, chest
CD4 counts
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebellum, disease of
children
choking
chromosomal abnormality
cleft palate
Clinical Pathologic Conference(C.P.C.)
clinodactyly
clonus
cognition, slowed
coinfection
congenital malformation
consanguinity
Cornelia de Lange syndrome
corpus callosum, thinning
Creutzfeldt-Jakob disease, genetic
cry, abnormal
deep gray nuclei
dementia
dementia, familial
dementia, frontotemporal
dementia, rapidly progressive
difficulty climbing stairs
digits, abnormal
diplopia
dizziness
dysarthria
dysdiadochokinesia
dysmetria
dysmorphic
dysphagia
eye movement, disorders of
eyebrows, abnormal
failure to thrive
falling
familial
fatigue
fever
finger nose finger test
foot deformity
frontotemporal dementia, behavioral variant
gait disorder
gene mutation
genetic neurologic disorders
genetic testing
growth retardation
hammertoes
handwriting
headache
headache, progressive
heel-knee-shin test
hirsutism
human immunodeficiency virus type 1
human immunodeficiency virus type 1, false positive
human immunodeficiency virus type 2
hyperreflexia
imbalance
immune reconstitution inflammatory syndrome
immunohistochemistry
immunosuppression
incoordination
insomnia
irritability
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
labyrinth, disorder of
labyrinthitis
labyrinthitis, acute
leg weakness, bilateral
leptospirosis
lethargy
Lewy body disease, diffuse
low birth weight
lymphopenia
memory, defect of recent
memory, impairment of
meningeal enhancement
meningismus
meningitis
meningitis, aseptic
meningitis, leptospira
mental retardation
metamyelocytes
micrognathia
micromelia
middle cerebellar peduncle, lesion
mortality
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, false negative
MRI, punctate pattern
MRI, ring sign
myoclonic jerks
myoclonus
nausea and vomiting
neurologic disease, diagnoses of
neuropathology
neuropathy
nystagmus
nystagmus, direction fixed
nystagmus, rotary
nystagmus, spontaneous
oligodactyly
opportunistic infection
opportunistic infection, CNS
optic atrophy
paranoia
past pointing
phocomelia
polymerase chain reaction
polymerase chain reaction, false negative
pons, lesion of
posterior cortical atrophy
prion disease
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychomotor retardation
pupil, ectopic-congenital
pursuit eye movements, abnormal
rapidly progressing neurologic illness
real-time quaking-induced conversion
Romberg's sign
saccadic eye movements, abnormal
saddle nose
serologic testing
simian crease
simultanagnosia
single photon emission computed tomography
snout reflex
spasticity
spinocerebellar ataxia
spinocerebellar ataxia type 7
spirochete infection
square wave jerks
startle myoclonus
subconjunctival hemorrhage
subcortical U fibers
symmetric brain lesions
syndactyly
synophrys
tandem gait, ataxic
tau protein
thalamus, lesion of-bilateral
thrush
toxoplasmosis, CNS
treatment of neurologic disorder
tremor
tremor, intention
trinucleotide repeats
upgaze, paralysis of
vertigo
vision, blurred
visual acuity, decreased
visuospatial disturbance
walking frame
walking, difficulty with
weight loss
wheelchair
wide based gait
workup
WORLD spelling test
Showing articles 150 to 200 of 209 << Previous Next >>

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

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

"Numb, Clumsy Hands" and Tactile Agnosia Sescondary to High Cervical Spondylotic Myelopathy: A Clinical and Electrophysiological Correlation
Acta Neurol Scand 86:622-625, Chang,M.,et al, 1992

Fucosidosis Revisited:A Review of 77 Patients
Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991

Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
NEJM 325:1487-1498, Dalakas,M.C., 1991

Scleroderma and Central Nervous System Vasculitis
Stroke 22:410-413, Pathak,R.&Gabor,A.J., 1991

Fetal Alcohol Syndrome in Adolescents and Adults
JAMA 265:1961-1967, Streissguth,A.P.,et al, 1991

Congenital Inflammatory Myopathy
Neurol 40:1111-1114, Shevell,M.,et al, 1990

Congenital Brain Anomalies Associated with the Hypoplastic Left Heart Syndrome
Pediatrics 85:984-990, Glauser,T.A.,et al, 1990

Clinicopath Conf
Eosinophilic Fasciitis, Case Study 4-1990, NEJM 322:252-261, 93190., , 1990

Development of Diffuse Fasciitis with Eosinophilia During L-Tryptophan Treatment:Elevated Type I Collagen Gene
Ann Int Med 112:344-351, Varga,J.,et al, 1990

Eosinophilia-Myalgia Syndrome-New Mexico
JAMA 262:3116, Belvins,W.L.,et al, 1989

Peripheral Nerve Disorders in Instrumentalists
Ann Neurol 26:640-646, Lederman,R.J., 1989

Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989

Congenital Muscular Dystrophy
J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989

Dopa Responsive Dystonia:A Treatable Condition Misdiagnosed as Cerebral Palsy
BMJ 298:1019-1020, Boyd,K.&Patterson,V., 1989

Rigid Spine Syndrome and Rigid Spine Sign in Myopathies
J Child Neurol 4:273-282, Merlini,L.,et al, 1989

Lesions of the Head & Neck in Patients with AIDS:CT and MR Findings
AJNR 9:693-698, Olsen,W.L.,et al, 1988

Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
Neuropediatrics 19:62-71, Voit,T.,et al, 1988

Autoantibodies to Glutamic Acid Decarboxylase in Pt with Stiff-Man Syndr, Epilepsy & Type I Diabetes Mellitus
NEJM 318:1012-1020, Solimena,M.,et al, 1988

Early-Onset Benign Autosomal Dominant Limb-Girdle with Contractures (Bethlem Myopathy)
Neurol 38:573-580, Mohire,M.D.,et al, 1988

Rett Syndrome:Natural History and Management
Pediatrics 82:1-10, Moeschler,J.B.,et al, 1988

Hand Contractures in Parkinson's Disease
JNNP 51:1221-1223, Kyriakides,T.&Hewer,R.L., 1988

Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia (Osler-Wever-Rendu Disease)
Am J Med 82:989-997, Perry,W.H., 1987

Progressive Multifocal Leukoencephalopathy Associated with Human Immunodeficiency Virus Infection
Ann Int Med 107:78-87, Berger,J.R., 1987

Central Core Disease, Clinical Features in 13 Patients
Medicine 66:389-396, Shuaid,A.,et al, 1987

Myelopathy Hand
Editorial, Lancet 2:721-7221987., , 1987

Acute Arsenic Intoxication Presenting as Guillain-Barre-Like Syndrome:Donofrio
P. D. , et al, Muscle & Nerve 10:114-120, , 1987

Clinicopath. Conference
Acquired Immunodeficiency Syndrome, Rhabdomyosarcoma, with Extensive Metastases, Case 9-1986, NEJM 3, 4:620,1986., 1986

Natural History of the Fetal Alcohol Syndrome:A 10-Year Follow-Up of Eleven Patients
Lancet 2:85-91, Streissguth,A.P.,et al, 1985

Central Nervous System Infections Associated with Hereditary Hemorrhagic Telangiectasia
Am J Med 77:86-92, Press,O.L.W.,et al, 1984

Sclerosteosis:Neurogenetic & Pathophysiologic Analysis of an American Kinship
Neurol 33:267-277, Stein,S.A.,et al, 1983

Clinical Epidemology of Toxic-Oil Syndrome
NEJM 309:1408-1414, Kilbourne,E.M.,et al, 1983

Fibrodysplasia Ossificans Progressiva, The Clinical Features & Natural Hx of 34 Pts
J Bone Joint Surg 64B:76-83, Connor,J.M.&Evans,D.A.P., 1982

Confrontation Visual Field Techniques in the Detection of Anterior Visual Pathway Lesions
Ann Neurol 10:28-34, Trobe,J.D.,et al, 1981

Finger Wrinkling after Immersion in Water
BMJ 281:586-587, Alvarez,G.,et al, 1980

Congenital Myotonic Dystrophy
Arch Neurol 37:693-696, Argov,Z.,et al, 1980

Midline Granuloma
Topel J. L. in Vinken P. J. & Bruyn, G. N. (Eds) Handbook of Clin Neurol, Vol 39, North-Holland Publ, Co, Amsterda, 1980

Skin Wrinkling on Immersion of Hands
Arch Neurol 36:113-114, Braham,J.,et al, 1979

Emery-Dreifuss Muscular Dystrophy
Ann Neurol 5:111-117, Rowland,L.P.,et al, 1979

Sarcoid Encephalopathy with Diffuse Inflammation & Focal Hydrocephalus Shown by Sequential CT
Neurol 29:1161-1165, Ho,S.U.,et al, 1979

Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
Neurol 28:1135-1140, Dobkin,B.H.,et al, 1978

Chiasmal Syndrome in Sphenoid Sinus Mucocele
Ann Neurol 4:440-444, Goodwin,J.A.,et al, 1978

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

Spontaneous Dissecting Aneurysm of the Internal Carotid Artery
Arch Neurol 34:251, Roome,N.S.,et al, 1977

Carotidynia
Neurol 27:43, Raskin,N.H.,et al, 1977

Neurologic Aspects of Hereditary Hemorrhagic Telangiectasia
Arch Neurol 34:101, Adams,H.P.,et al, 1977

The Spectrum of Mild X-Linked Recessive Muscular Dystrophy
Arch Neurol 34:408, Ringer,S.P.,et al, 1977

Rigid Spine Syndrome:A Type I Fiber Myopathy
Arch Neurol 34:119, Seay,A.R.,et al, 1977

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



Showing articles 150 to 200 of 209 << Previous Next >>