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Differential
(Click to cross reference)
abscess, intracerebral
acanthosis nigricans
alpha-fetoprotein
anemia
apraxia of eye movements
areflexia
Arnold Chiari malformation
arteriovenous malformation
arteriovenous malformation, pulmonary
aspiration
astrocytoma
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
ataxic gait
athetosis
autoimmune disease
biologic markers
blood dyscrasias, neurologic findings with
brain biopsy
brain biopsy, stereotaxic
cafe au lait spots
carcinoembryonic antigen
carcinoma
carcinoma of breast
CAT scan
CAT scan, abnormal
CAT scan, chest
cerebellar ataxia, autosomal recessive
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar vermis
cerebral palsy
cerebrospinal fluid, xanthochromia of
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
cisterna magna
cisterna magna, enlarged
Clinical Pathologic Conference(C.P.C.)
C-reactive protein, elevated
degenerative diseases of CNS
dental procedure, neurologic complications with
diabetes mellitus
DiGeorge syndrome
drooling
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dystonia
electromyogram
electronystagmography
electrophoretic pattern, serum
epistaxis
Epstein-Barr virus
eye movement, disorders of
familial
fistula, arterio-venous, pulmonary
fourth ventricle, enlargement of
Friedreich's ataxia
gait disorder
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
glioma
gray hair
growth retardation
head injury
hepatolenticular degeneration(Wilson's disease)
hepatosplenomegaly
hereditary hemorrhagic telangiectasia(HHT)
hyperglycemia
hypogonadism
hypotonia
imbalance
immunodeficiency
immunoelectrophoresis, serum
immunologic disease
immunosuppression
incoordination
infection
insulin resistance
Leigh's disease
leukemia
leukemia, neurologic findings assoc.with
leukocytosis
leukoencephalopathy
lipid storage disorder of CNS
liver disease
lymphadenopathy
lymphoma
Marinesco-Sjogren syndrome
masked facies
meningismus
mental retardation
microhemorrhage, intracerebral
misdiagnosis
mitral valve prolapse
molecular genetics
mongolism
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, hypointense signal foci on
MRI, negative
MRI, perfusion
MRS
multiple sclerosis
multiple system atrophy
myelomalacia
neoplasm, primary intracerebral
nerve biopsy
nerve conduction studies
neurocutaneous disease
neuroendocrinology
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic examination, focal
neuropathology
neuropathy
nystagmus
ocular motility, disorders of
ophthalmoplegia
optokinetic nystagmus(O.K.N.)
papilledema
pathology
pneumonia
poliomyelitis
poliomyelitis vaccine
polyneuropathy
progeria
prognosis
progressive neurologic disorder
pulmonary infection
pulmonary infiltrates
radiation hypersensitivity
remote effect of cancer on the nervous system
review article
risk factors
saccadic eye movements
saccadic eye movements, abnormal
scannig speech
skin, darkening of
skin, lesions in neurologic disorders
slurred speech
spinal muscular atrophy
spinocerebellar degeneration
staggering
tandem gait, ataxic
telangiectases
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
vaccination, neurologic complications with
vaccine
vertigo
viral infection
viral infection, CNS
vitamin E deficiency
vitiligo
Von Hippel Lindau
walking, difficulty with
weight loss
wheelchair
white matter disease
workup
Showing articles 350 to 400 of 1255 << Previous Next >>

An Unexpected Trismus
Lancet 380:536, Alves, M.,et al, 2012

Clinical Reasoning: A Case of Treatable Spastic Paraparesis
Neurol 79: e50-e53, McKinnon, J.H. & Bosch E.P., 2012

Multimodal Imaging of Reversible Cerebral Vasoconstriction Syndrome: A Series of 6 Cases
AJNR 33:1403-1410, Marder, C.P.,et al, 2012

Heterogeneity of Coenzyme Q10 Deficiency
Arch Neurol 69:978-983, Emmanuele, V.,et al, 2012

Anti-Glutamic Acid Decarboxylase Limbic Encephalitis Without Epilepsy Evolving Into Dementia with Cerebellar Ataxia
Arch Neurol 69:1064-1066, Mirabelli-Badenier, M.,et al, 2012

Clinicopathologic Conference, Paraneoplastic Stiff Person Syndrome with Limbic Encephalitis with Anti-Amphiphysin Antibodies with Metastatic Carcinoma of Breast
NEJM 367:851-861, Case 27-2012, 2012

Clinicopathologic Conference, Acute Ischemic Stroke due to Basilar Artery Embolism. Patent Foramen Ovale
NEJM 367:1450-1460, Case 31-2012, 2012

Granulomatous Meningitis due to Rheumatoid Arthritis
Acta Neurol Belg 112:193-197, Duray, M.C.,et al, 2012

Solitary Sclerosis
Neurol 78:540-544, Schmalstieg,W.F.,et al, 2012

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

Brain Arteriovenous Malformation Multiplicity Predicts the Diagnosis of Hereditary Hemorrhagic Telangiectasia Quantitive Assessment
Stroke 43:72-78, Bharatha, A.,et al, 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

Susceptibility-Weighted MR Imaging for Diagnosis of Capillary Telangiectasia of the Brain
AJNR 33:715-720, El-Koussy,M.,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

An unusual cause of stroke and hypoxia
BMJ 342:c7200, Bell, S.L. & Eveson, D.J., 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

Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
UpToDate, Feb, Shovlin, C., 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

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

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

Pulmonary AVMs, including hereditary hemorrhagic telangiectasia: Diagnosis and Treatment
UpTo Date, August, Gossage, J.R., 2010

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

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



Showing articles 350 to 400 of 1255 << Previous Next >>