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Differential
(Click to cross reference)
abdominal distention
abducens nerve paralysis
acanthocytosis
acetazolamide
acetylcholine
acoustic nerve
acoustic neurinoma, bilateral
Addison's disease
adrenomyeloneuropathy
advances in neurology
adverse drug reaction
aggression
akinetic mute
alcohol intolerance
alcohol, neurologic complications with
alcoholism
Alexanders disease
Alexanders disease, adult onset
algorithm
alkylating agents
alpha-fetoprotein
altered states of consciousness
alternating hemiplegia
alternating hemiplegia of childhood
alternating rapid movement
alternating rapid movement, impaired
Alzheimer's disease
amyloid plaques
amyotrophic lateral sclerosis
Angelman syndrome
aniridia
ankle reflex, absent
antibodies to voltage-gated calcium channels
anticholinesterase
anticonvulsants
anticonvulsants, effectiveness
antimetabolite
antioxidant
apraxia
apraxia of eye movements
areflexia
Arnold Chiari malformation
arrhythmia, cardiac
asparginase
aspiration
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, congenital
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
ataxic-dystonia syndromes
ataxin
ataxin-2
atherosclerosis, premature
atonic bladder
ATP1A3 gene
attention span
atypical
auditory evoked brainstem potentials
autonomic dysfunction
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
axonal spheroid
Babinski sign
baclofen
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
Bassen-Kornzweig syndrome
behavior, combative
behavioral disorder
biologic markers
bladder dysfunction
blindness
blood dyscrasias, neurologic findings with
bone marrow biopsy
brachycephaly
bradykinesia
brain atrophy
brainstem, atrophy
brainstem, lesion of
brainstem, neoplasms of
cachexia
CAG repeats
calcification, intracranial
calcium channel dysfunction
cane
carcinoembryonic antigen
carcinoma
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
cataracts, congenital
celiac disease, adult
central core disease
cerebellar ataxia, autosomal recessive
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar ataxia, hereditary
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hemangioma
cerebellar hypoplasia
cerebellar lesion
cerebellar plaques, amyloid
cerebellar vermis
cerebellum
cerebellum, disease of
cerebellum, neoplasms of
cerebral cortex
cerebral cortical atrophy
cerebral palsy
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, pressure low
cerebrospinal fluid, proteincytologic dissociation
cerebrotendinous xanthomatosis
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
children
chloride channel dysfunction
choking
cholestanol
chorea
chorea, familial
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 12
chromosome 14
chromosome 15
chromosome 18
chromosome 19
chromosome 2
chromosome 6
chromosome 9
chronic progressive external ophthalmoplegia
cirrhosis
cisterna magna, enlarged
Clinical Pathologic Conference(C.P.C.)
clonus
clubfoot as related to neurologic disease
Cockayne's syndrome
cognition
cognition, slowed
cogwheel rigidty
Collier's sign
cone-rod dystrophy
congestive heart failure
conjunctival biopsy
consanguinity
contractures, joint
controversies in neurology
conus medullaris, lesion of
cornea, abnormal
corpus callosum
corpus callosum, atrophy of
corpus callosum, lesion of
corpus callosum, thinning
cortical blindness
cough
cranial neuropathy, multiple
cranio-cervical junction
creatine phosphokinase(CPK)elevated
Creutzfeldt-Jakob disease, genetic
Cuba
cultured skin fibroblasts
cyst
cyst, peritumoral
cyst, neoplastic cerebellum
deafmute
deafness
deep gray nuclei
deep tendon reflexes
degenerative diseases of CNS
delay in diagnosis
delayed dentition
dementia
dementia, familial
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, transmissible
demyelinating disease
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
dermatoglyphics
developmental disability
developmental milestones
developmental milestones, loss of
developmental retardation
dexterity, impaired
diabetes insipidus
diabetes mellitus
diagnostic criteria
diarrhea
differential diagnosis
difficulty climbing stairs
dilantin
diplopia
dizziness
down-beat nystagmus
down-beat nystagmus, primary position of gaze
Dravet syndrome
drooling
dwarfism
dysarthria
dysdiadochokinesia
dysmetria
dysmorphic
dysphagia
dyspraxia
dyssynergia cerebellaris myoclonica
dystonia
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
electroretinograph
encephalopathy
enzyme, defect
epicanthal folds
epidemiology of neurology
episodic neurologic deficits
erectile dysfunction
ethics in neurology
evoked potentials
excitotoxin
exome sequencing
extraocular muscle lesion
eye movement, disorders of
facial appearance, abnormal
facial expression abnormality
facial nerve palsy, bilateral
facial pain
falling
familial
familial hemiplegic migraine
familial periodic ataxia
family planning
fasciculation
fatigue
feeding disorder
fever
finger nose finger test
fingerprint bodies
fish
fluorescene in situ hybridization
fluorouracil
flush syndrome
foam cells
foot deformity
foot drop
foot numbness
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
frataxin
Friedreich's ataxia
Friedreich's ataxia, late onset
frontotemporal dementia, behavioral variant
fundus, abnormality of
gadolinium
gait disorder
gait, spastic
galactosemia
gargoylism
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gaze palsy
gaze palsy, supranuclear
gender
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
Gerstmann-Straussler-Scheinker disease
Gillespie syndrome
glaucoma
gliosis
globus pallidus, lesion of
glucose tolerance test, abnormal
glutamate dehydrogenase deficiency
glutamic acid
granular osmiphilic material
growth retardation
Hallervorden Spatz disease
Hallgren's syndrome
hallucination
hammertoes
handwriting
head injury
head nodding
headache
hearing loss
heart block
heel-knee-shin test
hemangioblastoma
hematuria, gross
hemiplegia
hemochromatosis
hemochromatosis, primary
hepatic encephalopathy
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
heralding manifestation
HLA
hot cross bun sign
human T-lymphotropic virus type II(HTLV-II)
huntingtin
Huntington's chorea
Hurler's syndrome
hydrocephalus
hydroxytryptophan L-5(L-5 HTP)
hyperactivity
hyperreflexia
hypertonia
hypodontia
hypogonadism
hypogonadism, hypogonadotropic
hypokalemic periodic paralysis
hypomyelination
hyponatremia
hypopigmentation of skin
hyposmia
hypotonia
hypoxia
imbalance
imbalance, postural
immunodeficiency
immunosuppression
impotence
impulsivity
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intranuclear
inclusion bodies, ubiquitin
incoordination
infection
intellectual deficit
intellectual deterioration
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
intestinal pseudoobstruction
intracranial pressure, increased
iris, abnormal
irritability
isoniazid
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
jaw pain
karyotyping
Kearns-Sayre syndrome
keratoconus
Korsakoff's psychosis
kyphosis
lactic acidemia
laughing, pathologic
Laurence-Moon-Bardet-Biedl syndrome
L-dopa
leg weakness, bilateral
Leigh's disease
leukemia
leukemia, neurologic findings assoc.with
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
leukoencephalopathy, hereditary diffuse
life expectancy
lipid storage disorder of CNS
lymphoma
macrognathia
macular degeneration
malformation, CNS, congenital
malignant hyperpyrexia
marche a petits pas
Marinesco-Sjogren syndrome
masked facies
memory, impairment of
meningismus
meningitis, carcinomatous
meningoencephalopathy
mental retardation
metabolic acidosis
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
methotrexate
methylhydrazine derivatives
Mexican
microcephaly
microdontia
microhemorrhage, intracerebral
midbrain, atrophy
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
migraine, hemiplegic
Minamata disease
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
monoamine oxidase inhibitors
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
movement disorder, hyperkinetic
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, FLAIR
MRI, negative
MRI, punctate pattern
MRI, serial
MRI, spinal cord
MRS
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle biopsy
muscle cramp
muscle pain
muscle weakness
muscle weakness, proximal
muscular dystrophy
myasthenic syndrome
myelomalacia
myelopathy
myoclonic jerks
myoclonus
myoclonus, epilepsy
myopathy
myopia
myotonia congenita
myotonia dystrophica
Native Americans
nausea and vomiting
negative
neoplasm, metastatic to CNS
neoplasm, primary of CNS
neoplasm, primary of CNS-surgical treatment of
nerve conduction studies
neuritis
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neuroaxonal dystrophy, juvenile
neuroaxonal leukodystrophy
neurocutaneous disease
neuroendocrinology
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neuronal ceroid-lipofuscinosis
neuronal intranuclear inclusion disease
neuronopathy
neuronopathy, sensory
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, demyelinating
neuropathy, hereditary peripheral
neuropathy, peripheral
neuropathy, sensory
neurotoxin
neurotransmitter
next-generation sequencing
Niemann-Pick disease
nitrogen mustard
nutritional deficiency
nystagmus
nystagmus, gaze-evoked
nystagmus, gaze-paretic
nystagmus, hereditary
nystagmus, monocular
nystagmus, periodic
nystagmus, primary position of gaze
nystagmus, rotary
nystagmus, upbeating-in primary position of gaze
nystagmus, vertical
obesity
ocular motility, disorders of
ocular myopathy
oculodentodigital dysplasia
old age, neurology of
ophthalmoplegia
ophthalmoplegia, progressive external
optic ataxia
optic atrophy
optical coherence tomography
orbit, tomograms of
orthostatic hypotension
oscillopsia
ovarian dysgenesis
pain
pain, abdominal
palatal myoclonus
paramyotonia congenita
paranoia
paraparesis
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
paresthesias
Parkinson disease
Parkinson disease, dystonia with
Parkinson disease, familial
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
past pointing
pathology
Pelizaeus Merzbacher
periodic paralysis
Perrault syndrome
personality change
pes cavus
pheochromocytoma
phlebotomy
physostigmine
pleocytosis of cerebrospinal fluid
pneumonia
poison, mercury
poison, neurologic problems with
POLG1 gene
POLR3B
polydactyly
polymerase chain reaction
polyneuropathy
pons, atrophy
pons, lesion of
pontocerebellar atrophy
positional head-hanging test
postural abnormality
potassium channel antibodies
potassium channel dysfunction
precipitating factors
pregnancy, neurologic complications in
prevention of neurologic disorders
prion disease
prion protein gene
procarbazine
progeria
prognathism
prognosis
progressive infantile poliodystrophy
progressive neurologic disorder
progressive pallidum atrophy
proprioception, abnormal
protein 14-3-3, cerebrospinal fluid
pseudobulbar palsy
pseudoretinitis pigmentosa
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
psychomotor retardation
psychosis
ptosis
ptosis, bilateral
pulmonary infection
Purkinje cell
pursuit eye movements, abnormal
putamen, lesion of
putamen, lesion of, bilateral
pyramidal
pyramidal tract
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
radiation hypersensitivity
radiation therapy, CNS treatment and complications with
radiation therapy, stereotactic
ragged-red fibers
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
reading disorder, acquired
real-time quaking-induced conversion
recurrent
release phenomena
remote effect of cancer on the nervous system
respiratory failure
respiratory tract infection
retina, abnormal
retinal degeneration
retinal hemangioma
retinal lesion
retinitis pigmentosa
retinopathy
review article
RFC1 gene
rigidity
Romberg's sign
Rosenthal fibers
saccadic eye movements, abnormal
schizophrenia
SCN1A gene
scoliosis
screening
seizure
seizure, children
seizure, familial
seizure, febrile
seizure, intractable
seizure, neonatal
seizure, paradoxical
seizure, photosensitive
seizure, psychomotor-temporal lobe
seizure, tonic-clonic
seizure, treatment of
sensorineural hearing loss
sensory loss
sensory loss, leg
Shy-Drager syndrome
sinemet
skin, biopsy
skin, darkening of
skin, lesions in neurologic disorders
sleep apnea
sleep pathology and physiology
smiling
sodium channel dysfunction
somatosensory evoked potentials
spastic ataxia
spastic paraplegia, type 7
spasticity
speech disorder
speech disorder, childhood
speech disorder, non aphasic
speech, delayed development of
speech, loss of
Spielmeyer Vogt syndrome
spinal cord, lesion of
spinal cord, neoplasm
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 10
spinocerebellar ataxia type 12
spinocerebellar ataxia type 14
spinocerebellar ataxia type 17
spinocerebellar ataxia type 2
spinocerebellar ataxia type 28
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 5
spinocerebellar ataxia type 6
spinocerebellar ataxia type 7
spinocerebellar ataxia type 8
spinocerebellar degeneration
spinopontine atrophy, dominant
splenomegaly
spongy degeneration of brain
staggering
startle myoclonus
status epilepticus
stereotaxic surgery
storage disease of CNS
striatonigral degeneration
striatonigral degeneration, infantile
striopallidodentate calcifications, familial idiopathic
stuttering
subcortical U fibers
superior cerebellar peduncle
symmetric brain lesions
syndactyly
syphilis, neurologic complications with
systemic illness
tandem gait, ataxic
tauopathy
teeth, abnormal
teeth, number of in infants
teeth, wide-spaced
telangiectases
thalamus, lesion of
thalamus, lesion of-bilateral
tinnitus
titubation
tongue, protrusion of
topiramate
toxins, nervous system
transient neurologic deficit
trazodone
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trinucleotide repeats
trisomes
trisomy 9p
upgaze, paralysis of
urinary incontinence
urinary urgency
Usher's syndrome
vertigo, episodic
vestibular areflexia
vestibulopathy
vibratory sensation, abnormal
vinblastine
vincristine neurotoxicity
vision, failure of in childhood
visual acuity, decreased
visual field defect
visual fields, constricted
visual loss
visual loss, progressive
visual loss, slow
vitamin deficiency
vitamin E
vitamin E deficiency
vitamin supplementation
vocal cord paralysis
voice, abnormality of
Von Hippel Lindau
walking frame
walking, difficulty with
walking, difficulty with in dark
weakness
weakness, generalized
weakness, progressive
weaning from respirator, failure to
weight loss
Western immunoblot test
wheelchair
white matter disease
wide based gait
Wolfram syndrome
workup
wrist drop
writing
X-linked bulbospinal neuronopathy
Showing articles 350 to 400 of 3297 << Previous Next >>

Brainstem Gliomas in Adults: Prognostic Factors and Classification
Brain 124:2528-2539, Guillamo,J.-S.,et al, 2001

Ataxia Associated with Hashimotos Disease: Progressive Non-Familial Adult Onset Cerebellar Degeneration with Autoimmune Thyroiditis
JNNP 71:81-87, Selim, M. and Drachman, D.A., 2001

Cardiac Dysfunction in Neuromuscular Diseases
The Neurologist 6:67-82, Pourmand,R., 2000

Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. et al, 2000

Paraneoplastic Cerebellar Ataxia Due to Autoantibodies Against a Glutamate Receptor
NEJM 342:21-27, Smitt,P.S.,et al, 2000

Niemann-Pick Disease Type C: Two Cases and an Update
Movement Disorders 15:1199-1203, Uc,E.Y.,et al, 2000

Vertigo and Gait Ataxia Without Usual Signs of Lateral Medullary Infarction: A Clinical Variant Related to Rostral-dorsolateral Lesions
Cerebrovasc Dis 10:471-474, Kim,J.S., 2000

Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
NEJM 341:901-908, , 1999

Superficial Siderosis of the Central Nervous System,A Late Complication of Cerebellar Tumors
Neurol 52:163-169, Anderson,N.E.,et al, 1999

N-Acetylcysteine Therapy for Unverricht-Lundborg Disease
Neurol 52:426-427, Selwa,L.M., 1999

Paraneoplastic Syndromes
Arch Neurol 56:405-408, Dalmau,J.O.&Posner,J.B., 1999

Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
Neurol 52:1472-1478, Nardocci,N.,et al, 1999

Cerebellar Ataxia Associated with Subclinical Celiac Disease Responding to Gluten-Free Diet
Neurol 53:1606-1608, Pellecchia,M.T.,et al, 1999

Distal Myopathies:Clinical and Molecular Diagnosis and Classification
JNNP 67:703-709, Mastaglia,F.J.&Laing,N.G., 1999

Leukoencephalopathy and Raised Brain Lactate from Heroin Vapor Inhalation ("Chasing the Dragon")
Neurol 53:589-1048, Kriegstein,A.R., et al, 1999

Lateral Medullary Infarction
Stroke, Pathophysiology, Diagnosis and management, Churchhill Livingstone, NY 3rd Ed, Ch 22, p. 534, Amarenco,P.,et al, 1998

Clinical,Radiological,Neurophysiological,and Neuropathological Characteristics of Gluten Ataxia
Lancet 352:1582-1585, Hadjivassiliou,M.,et al, 1998

The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998

Cerebral Manifestation of Wilson's Disease Successfully Treated with Liver Transplantation
Neurol 51:863-865, Bax,R.T.,et al, 1998

Neurological Channelopathies, Dysfunctional Ion Channels May Cause Many Neurological Diseases
BMJ 316:1104-1105, Rose,M.R., 1998

Dopa-Responsive Dystonia, Some Pieces of the Puzzle are Still Missing
Neurol 50:853-855, Nygaard,T.G.&Wooten,G.F., 1998

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

Wobbly Handwriting
Lancet 351:336, Rosario,M.A.F.,et al, 1998

Cerebellar Degeneration Associated With Human Immunodeficiency Virus Infection
Neurol 50:244-251, Tagliati,M.,et al, 1998

Multiple-System Atrophy is Genet Distinct from Ident Inherited Causes of Spinocerebellar Degen
Neurol 49:1598-1604, Brandmann,O.,et al, 1997

Atrophy of Cerebellum & Brainstem in Dentatorubral Pallidoluysian Atrophy, CAG Repeat Size on MRI Findings
Neurol 49:1605-1612, Koide,R.,et al, 1997

Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
Neurol 49:1702-1705, Bohlega,S.,et al, 1997

Rapid Spongiform Degeneration of the Cerebrum and Cerebellum in Creutzfeldt-Jakob Encephalitis:Serial MR Findings
AJNR 18:583-586, Tzeng,B-C.,et al, 1997

Ataxia and Slurred Speech after Artesunate Treatment for Falciparum Malaria
NEJM 336:1328, Miller,L.G.&Panosian,C.B., 1997

Clinicopath Conf
Hodgkin's Disease, Paraneoplastic Cerebellar Degeneration, Case 21-1997, NEJM 337:115-12297., , 1997

Paraneoplastic Cerebellar Degeneration
Arch Int Med 157:1258-1262, Bolla,L.&Palmer,R.M., 1997

Frataxin Gene of Friedreich's Ataxia is Targeted to Mitochondria
Ann Neurol 42:265-269, Priller,J.,et al, 1997

Familial episodic Ataxia:Clinical Heterogeneity in Four Families Linked to Chromosome 19p
Ann Neurol 41:8-16, 41997., Baloh,R.W.,et al, 1997

Autoantibodies to Glutamic Acid Decarboxylase in Three Patients With Cerebellar Ataxia, Late-Onset Insulin-Dependent Diabetes Mellitus, and Polyendocrine Autoimmunity
Neurol 49:1026-1030, Saiz,A.,et al, 1997

Hereditary Spastic Paraplegia:Advances in Genetic Research
Neurol 46:1507-1514, Fink,J.K.,et al, 1996

Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
Ann Neurol 39:352-360, Scolding,N.J.,et al, 1996

Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

Clinicopath Conf
Q Fever, Acute (with Cerebellar and Meningeal Involvement) , Case 38-1996, NEJM 335:1829-1834., , 1996

MR Findings in Listerial Rhombencephalitis
AJNR 17:593-596, Alper,G.,et al, 1996

Chronic Lymphocytic Leukemia and the Central Nervous System:A clinical and Pathological Study
Neurol 46:19-25, Cramer,S.C.,et al, 1996

Delayed-Onset Cerebellar Syndrome
Arch Neurol 53:450-454, Louis,E.D.,et al, 1996

Mycoplasma Pneumoniae Infection Associated with an Acute Brainstem Syndrome
Acta Neurol Scand 93:203-206, OBrien, P.M.,et al, 1996

Management of Acoustic Neuroma
BMJ 311:1141-1144, Wright,A.&Bradford,R., 1995

Erdheim-Chester Disease and Slowly Progressive Cerebellar Dysfunction
JNNP 58:238-240, Fukazawa,T.,et al, 1995

A Novel Mutation in Exon 3 of the Proteolipid Protein Gene in Pelizaeus-Merzabacher Disease
Neurol 45:394-395, Pratt,V.M.,et al, 1995

A Positron Emission Tomography Study of Cerebral Activation Associated with Essential and Writing Tremor
Arch Neurol 52:299-305, Wills,A.J.,et al, 1995

Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
Lancet 346:741-742, Brahe,C.,et al, 1995

Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
Neurol 45:1739-1743, Shulman,L.M.,et al, 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995



Showing articles 350 to 400 of 3297 << Previous Next >>