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acanthocytosis
acetylcholine
advances in neurology
algorithm
Alzheimer's disease
amantadine
amyotrophic lateral sclerosis
anticholinesterase
antioxidant
areflexia
Arnold Chiari malformation
arrhythmia, cardiac
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
ataxia, truncal
ataxic gait
atypical
Babinski sign
Bassen-Kornzweig syndrome
biologic markers
blindness
blood dyscrasias, neurologic findings with
brainstem, atrophy
CAG repeats
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
cerebellar ataxia, autosomal recessive
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar vermis
cerebral glucose metabolism
cerebrovascular accident
chromosomal abnormality
chromosome 9
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Cockayne's syndrome
congestive heart failure
consanguinity
controversies in neurology
cornea, abnormal
deafmute
deafness
deep tendon reflexes
degenerative diseases of CNS
delay in diagnosis
dentatorubral-pallidoluysian atrophy
dexterity, impaired
diabetes mellitus
disability, neurological
dwarfism
dysarthria
dysdiadochokinesia
dysmetria
dysmorphic
echocardiogram
echocardiogram, LVH
electrocardiogram, abnormal
electrocardiogram, LVH
electroencephalogram, abnormalities of
electromyogram
electronystagmography
electronystagmography, abnormal
endocardial fibrosis
ethics in neurology
eye movement, disorders of
falling
familial
frataxin
Friedreich's ataxia
Friedreich's ataxia, late onset
gait disorder
gargoylism
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glaucoma
Guillain Barre syndrome
Hallgren's syndrome
hammertoes
head injury
hearing loss
heart block
hepatolenticular degeneration(Wilson's disease)
Huntington's chorea
Hurler's syndrome
hydroxytryptophan L-5(L-5 HTP)
hyperreflexia
hypertonia
hypotonia
imbalance
incoordination
jaw jerk, abnormal
Kearns-Sayre syndrome
keratoconus
kyphoscoliosis, neurologic causes of
kyphosis
Laurence-Moon-Bardet-Biedl syndrome
lecithin
leg weakness, bilateral
Leigh's disease
leukoencephalopathy
life expectancy
lipid storage disorder of CNS
malformation, CNS, congenital
malondialdehyde
Marinesco-Sjogren syndrome
mental retardation
metabolic disorder, primary
misdiagnosis
mitochondrial disease
molecular genetics
MRI
MRI, abnormal
MRI, negative
MRI, spinal cord
mucopolysaccharidoses
multiple sclerosis
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, Duchenne
myelomalacia
myopathy
myopia
myotonia dystrophica
nerve conduction studies
neuritis
neurologic disease, diagnoses of
neurologic signs
neuropathy
neuropathy, amyloid
nystagmus
obesity
ocular motility, disorders of
ocular myopathy
optic atrophy
paraparesis, familial spastic
Parkinson disease
pathologic reflex
pes cavus
physostigmine
polydactyly
polyneuropathy
prognosis
progressive neurologic disorder
proprioception, abnormal
pseudoretinitis pigmentosa
psychiatric disorder
remote effect of cancer on the nervous system
retinitis pigmentosa
retinopathy
review article
Romberg's sign
saccadic eye movements, abnormal
schizophrenia
scoliosis
seizure
sensory loss
spastic ataxia
spasticity
Spielmeyer Vogt syndrome
spinal cord, cervical
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 2
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 6
spinocerebellar ataxia type 7
spinocerebellar degeneration
staggering
tandem gait, ataxic
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trinucleotide repeats
Usher's syndrome
vibratory sensation
vibratory sensation, abnormal
visual evoked response
visual field defect
visual fields, constricted
vitamin deficiency
vitamin E
vitamin E deficiency
Von Hippel Lindau
walking, difficulty with
wheelchair
white matter disease
wide based gait
workup
Showing articles 350 to 400 of 1233 << Previous Next >>

Risk Factors for Spinal Cord Lesions in Dystonic Cerebral Palsy and Generalised Dystonia
JNNP 83:159-163, Guettard,E.,et al, 2012

Clincopathologic Conference,Graves Disease with Thyrotoxic Periodic Paralysis
NEJM 366:553-560, Case 4-2012, 2012

A Case of Delayed Encephalopathy after Carbon Monoxide Poisoning Longitudinally Monitored by Diffusion Tensor Imaging
AJNR 33:e52-e54, Kuroda,H.,et al, 2012

Clinical Reasoning: A Middle-Aged Woman with Progressive Symmetric Weakness and a CSF Pleocytosis
Neurol 78:e88-e92, Marks,D.,et al, 2012

Clinicalpathologic Conference, Vitamin B12 Deficiency due to Pernicious Anemia
NEJM 366:1626-1633, Case 13-2012, 2012

Central Nervous System Neuronal Surface Antibody Associated Syndromes: Review and Guidelines for Recognition
JNNP 83:638-645, Zuliani,L.,et al, 2012

Cortical Restricted Diffusion as the Predominant MRI Finding in Sporadic Creutzfeldt-Jakob Disease
Acta Radiologica 52:336-339, Talbott,S.D.,et al, 2011

Clinicopathologic Conference, Thymoma with Paraneoplastic Myasthenia Gravis, Polymyositis and Myocarditis, and Brain Stem Encephalitis
NEJM 365:2413-2422, Case 39-2011, 2011

Epstein-Barr Virus Infections of the Nervous System
www.medlink.com, Nov, Amlie-Lefond,C., 2011

Skin biopsy is useful for the antemortem diagnosis of neuronal intranuclear inclusion disease
Neurol 76:1372-1376, Sone, J.,et al, 2011

Rhombencephalitis A Series of 97 Patients
Medicine 90:256-261, Moragas, M.,et al, 2011

N-methyl-D-aspartate Receptor Autoimmune Encephalitis Presenting With Opsoclonus-Myoclonus
Arch Neurol 68:1069-1072, Smith, J.H.,et al, 2011

Opsoclonus and Multiple Cranial Neuropathy as a Manifestation of Neuroborreliosis
Neurol 77:1013-1014, Sabien Van Erp, W.,et al, 2011

A Rare Cause of Gait Ataxia
Lancet 378:1274, Rous, C.,et al, 2011

GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
Neurol 77:1287-1294, Prust, M.,et al, 2011

Basal Ganglia Involvement in Wernicke Encephalopathy: Report of 2 Cases
AJNR 32:E129-E131, Zuccoli, G.,et al, 2011

A Strange Case of Waitress Headache
Lancet 378:1824, Libera, D.D.,et al, 2011

Exercise-Associated Numbness and Tingling in the Legs
Arch Neurol 68:1599-1602, Sharp, L.,et al, 2011

Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 2011

Diagnosis and Management of Cerebral Venous Thrombosis: A Statement for Healthcare Professionals From the American Heart Association/American Stroke Association
Stroke 42:1158-1192, Saposnik,G.,et al, 2011

Clinicopathologic Conference, Sjogrens syndrome with dorsal-root ganglionitis
NEJM 364:1856-1865, Case 14-2011, 2011

Rapidly Progressive Corticobasal Degeneration Syndrome
Case Rep Neurol 3:185-190, Herrero Valverde, A.,et al, 2011

Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
Brain 134:3326-3332, Garone, C.,et al, 2011

Primary Central Nervous System Post-Transplantation Lymphoproliferative Disorder
CANCER 16:863-870, Cavaliere, R.,et al, 2010

Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
NEJM 362:2213-2219, Case 17-2010, 2010

A Meta-Regression of the Long-Term Effects of Deep Brain Stimulation on Balance and Gait in PD
Neurol 75:1292-1299, St. George,R.J.,et al, 2010

3-Methylglutaconic Aciduria Type I Redefined: A Syndrome With Late-Onset Leukoencephalopathy
Neurol 75:1079-1083, Wortmann,S.B.,et al, 2010

Sensory Ganglionopathy Due to Gluten Sensitivity
Neurol 75:1003-1008, Hadjivassiliou,M.,et al, 2010

Opsoclonus-Myoclonus Syndrome in Anti-N-Methyl-D-Aspartate Receptor Encephalitis
Arch Neurol 67:118-121, Kurian,M.,et al, 2010

Subclinical Hypothyroidism Presenting with Gait Abnormality
The Neurologist 16:115-116, Edvardsson,B. &Persson,S., 2010

Assessment: Symptomatic Treatment for Muscle Cramps (an Evidence-Based Review): Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology
Neurol 74:691-696, Katzberg,H.D.,et al, 2010

Copper Deficiency as a Treatable Cause of Poor Balance
BMJ 340:864-866, Khaleeli,Z., et al, 2010

Clinicopath Conf., Progressive Multifocal Leukoencephalopathy
NEJM 362:1431-1437, Case 11-2010, 2010

Clinicopath Conf., Brain Abscess, Pulmonary Arteriovenous Malformation Due to Hereditary Hemorrhagic Telangiectasia
NEJM 362:1326-1333, Case 10-2010, 2010

Clinicopath Conf, Intravascular Large-B-Cell Lympoma
NEJM 362:1129-1138, Case 9-2010, 2010

Cogan Syndrome
www.medlink.com, Feb, Ramachandran, T.S., 2010

MR Imaging Findings in 56 Patients with Wernicke Encephalopathy: Nonalcoholics May Differ from Alcoholics
AJNR 30:171-176, Zuccoli,Z.,et al, 2009

Neurosarcoidosis: A Study of 30 New Cases
JNNP 80:297-304, Joseph,F.G. &Scolding,N.J., 2009

Slurred Speech and Spirochaetes
Lancet 373:978, Thukral,A.,et al, 2009

High Doses of Deferiprone May Be Associated with Cerebellar Syndrome
BMJ 338:653, Beau-Salinas,F.,et al, 2009

A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia
Neurol 72:1262-1276, DiMauro,S.,et al, 2009

A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
Neurol 72:1607-1613, Lossos,A.,et al, 2009

Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, and KCNJ10 Mutations
NEJM 360:1960-1970, Bockenhauer,D.,et al, 2009

Frequency, Characteristics, and Risk Factors for Amiodarone Neurotoxicity
Arch Neurol 66:865-869, Orr,C.F. &Ahlskog,E., 2009

Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
Neurol 73:430-437, Verhagen,M.M.M.,et al, 2009

A 54-Year-Old Woman with Progressive Gait Disturbance and MRI Abnormalities
Neurol 73:466-474, Hochberg,F.H.,et al, 2009

A 75-Year-Old Woman with Progressive Right-Hand Tremor and Inability to Use Her Right Side
Neurol 73:1399-1405, Kertesz,A.,et al, 2009

Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009

Paraneoplastic Syndromes Affecting Brain and Cranial Nerves
UpToDate May 2009, Dalmau,J. &Rosenfeld,M., 2009

The Hot Cross Bun Sign in the Patients with Spinocerebellar Ataxia
Eur J Neurol 16:513-516, Lee, Y.-C.,et al, 2009



Showing articles 350 to 400 of 1233 << Previous Next >>