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Differential
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abstinence syndrome

acrocyanosis

acromicria

addiction, heroin

aggression

Aicardi-Goutieres syndrome

algorithm

altered states of consciousness

antimicrosomal antibodies

antithyroid antibodies

autoimmune cerebellar ataxia

autoimmune disease

automobile accidents

autonomic dysfunction

Babinski sign

basal ganglia, calcification of

basal ganglia, lesion, bilateral

botulism immune globulin

bronchopulmonary dysplasia

bulbar palsy

burn injury

cachexia

calcification, intracranial

cerebellar atrophy, primary

cerebellar degeneration

cerebellar lesion

cerebral cortical atrophy

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident, mimics

chilbran skin lesions

children

chorioretinitis

chromosomal abnormality

chromosome 15

chromosome 3

Clinical Pathologic Conference(C.P.C.)

congenital heart disease

congenital heart disease, CNS complications with

congenital infection, CNS

congenital infection, viral

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

cyst

cyst, parenchymal

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

deep gray nuclei

degenerative diseases of CNS

delivery, complicated

dementia

dementia, differential diagnosis of

dementia, rapidly progressive

dementia, reversible

dementia, treatment of

dentate nuclei

dentate nuclei, lesion of

developmental abnormality of brain

developmental disability

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

diagnostic criteria

diet

differential diagnosis

disability, neurological

drug abuse, toxic screen In

drug withdrawal

dyskinesia, buccal lingual facial

electroencephalogram, abnormalities of

electroencephalogram, focal delta activity

electroencephalogram, triphasic delta waves

electromyogram

emotional lability

encephalitis, autoimmune

encephalopathy

encephalopathy, Hashimoto's

encephalopathy, neonatal

encephalopathy, progressive

enzyme, defect

epidemiology of neurology

evoked potentials

eye movement, disorders of

eyes, sunken

facial anomalies

facial appearance, abnormal

facial expression abnormality

fluorescene in situ hybridization

gamma amino butyric acid receptor antibody

gene

gene mutation

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

globoid cells

growth hormone deficiency

head circumference and brain development

hemorrhage, intracranial, newborn

hemorrhagic diathesis

hyperammonemic encephalopathy

hyperbilirubinemia

hyperphagia

hyperpyrexia, CNS disorder causing

hypertrophic cardiomyopathy

hypogonadism

hypopigmentation of skin

immunosuppressive agents

inappropriate antidiuretic(A.D.H.)hormone

inattention

inborn errors of metabolism

incoordination

infant, evaluation of

infection

intellectual deficit

intellectual deterioration

interferon alpha

intrauterine

intrauterine infection

intrauterine infection, viral

intraventricular hemorrhage

intubation

irritability

irritable baby

Jakob-Creutzfeldt disease

leukocyte enzyme abnormality

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

level of consciousness, fluctuating

limbic encephalitis

lissencephaly

liver function enzymes

low birth weight

lymphadenopathy, hilar

macrocephaly

macrognathia

malformation, CNS, congenital

maple syrup urine disease

meconium staining

memory, impairment of

meningeal enhancement

mental retardation

mental status, abnormal

merosin

mesial temporal lobe

metabolic disorder, primary

metabolic disorder, primary-screening tests

methadone

microcephaly

micrognathia

migraine, seizures in

mimics

misdiagnosis

molecular genetics

molybdenum cofactor deficiency

mortality

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, disappearing lesion on

MRI, functional

MRI, hypointense signal foci on

muscular dystrophy, congenital

nemaline rod myopathy

neonatal abstinence syndrome

neonatal infection, viral

nerve conduction studies

neuroendocrinology

neurologic complications of, chronic pulmonary disease

neurologic disease, diagnoses of

neurologic examination

neurologic examination, focal

neurologic signs

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuronal migration disorder

optic chiasm, enlarged

optic nerve, enlarged

optic neuropathy

ornithine transcarbamylase deficiency

oxycodone

panic attacks

parietal lobe, lesion of

PAS positive material in the brain

pectus excavatum

personality change

petechiae

photosensitivity, skin

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

polyhydramnios

polymerase chain reaction

polymicrogyria

postural abnormality

Prader-Labhart-Willi syndrome

precipitating factors

pregnancy, neurologic complications in

premature infant

premature infant, problems in

prenatal

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

prognathism

prognosis

progressive neurologic disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pyramidal tract dysfunction

quadriplegia

rash

remote effect of cancer on the nervous system

respirator

respiratory arrest

respiratory distress syndrome, neurologic status with

seizure, complications following

seizure, injury following

seizure, intractable

seizure, neonatal

seizure, petit mal

seizure, stimulus sensitive

seizure, violence associated with

seizure, withdrawal

sensorineural hearing loss

serum alanine aminotransferase

short stature

skin, lesions in neurologic disorders

small for dates infant, problems in

speech disorder, childhood

speech, delayed development of

spongy degeneration of brain

startle reaction

status epilepticus

status epilepticus, recurrent

steroid

steroid responsive encephalopathy

steroid therapy, CNS treatment and complications with

symmetric brain lesions

tachycardia

teeth, wide-spaced

temper tantrums

temporal lobe, lesion

temporal lobe, lesion, bilateral

term infant

thalamus, lesion of-bilateral

thrombocytopenia

thyroglobulin antibodies

thyroid peroxidase antibodies

thyroiditis

thyrotropin

tongue, protrusion of

toxins, nervous system

tracheostomy

transient neurologic deficit

trauma

treatment of neurologic disorder

tremor

tremulousness

ultrasonography, head

urea-cycle enzymopathies

uric acid, low

urine test for metabolic disorders

valvulopathy

visual evoked response

weakness, generalized

Showing articles 0 to 40 of 40

Clinicopathologic Conference, Infant Botulism, Case 3-2024
NEJM 390:358-366, Case 3-2024, 2024

Congenital Cytomegalovirus Infection
BMJ 373:m1212, Pesch, M.H.,et al, 2021

An Older Man with Memory Impairment and Convulsions
BMJ 358:J2824, Zhao, X.,et al, 2017

Neonatal Abstinence Syndrome
NEJM 375:2468-2479, McQueen, K. & Murphy-Oikonen, J., 2016

Clinical and Immunological Features of Hashimotos Encephalopathy Presenting with Limbic Symptoms
Neurol 82:suppl P5.160, Matsunaga, A.,et al, 2015

Clinical and Immunological Features of Limbic Form of Hashimotos Encephalopathy
Neurol 84:Suppl P4.045, Kishitani, T.,et al, 2015

Seizures from Solving Sudoku Puzzles
JAMA Neurol 72:1524-1526, Feddersen, B.,et al, 2015

Molybdenum Cofactor Deficiency
Neurol 85:e175-e178, Nagappa, M.,et al, 2015

The Acquired Metabolic Disorders of the Nervous System, Hashimoto Encephalopathy (Steroid Responsive Encephalopathy Syndrome)
Adams & Victors Principles of Neurology Chp 40, pg 1155, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Inherited Hypeammonemia
Adams & Victors Principles of Neurology, Chp 37, pg 952, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Maple Syrup Urine Disease
Adams & Victors Principles of Neurology, Chp 37, pg 953, Ropper, A.H.,et al, 2014

Hashimoto Encephalopathy
Neurol 78:e134, Afshari, M.,et al, 2012

Motor Vehicle Accidents, Suicides, and Assaults in Epilepsy: A Population-Based Study
Neurol 76:801-806, 770, Kwon,C.,et al, 2011

A Case of Hashimoto Encephalopathy Clinical Manifestation, Imaging, Pathology, Treatment, and Prognosis
The Neurologist 17:141-143, Zhao, W.,et al, 2011

Hashimotos Encephalopathy
Radiol Case Reports 6:445-449, Ramalho, J. & Castillo, M., 2011

Clinical Reasoning: A 9-year-old Girl With Seizures and Encephalopathy
Neurol 74:e97-e100, Nguyen,T.P. &El-Hakam,L.M., 2010

Clinicopath Conf, Infantile Krabbe Disease
NEJM 362:346-356, Case 3-2010, 2010

Aicardi-Gouti�res Syndrome: Neuroradiologic Findings and Follow-up
AJNR 30:1971-1976, Uggetti,C.,et al, 2009

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

Non-Herpetic Acute Limbic Encephalitis-like Manifestation in a Case of Hashimotos Encephalopathy with Positive Autoantibodies against Ionotropic Glutamate Receptor Epsilon
Rinsho Shinkeigaku 47:629-634, Shindo, A.,et al, 2007

Case 35-2006: A Newborn Boy with Hypotonia
NEJM 355:2132-2142, Brown,R.H.,et al, 2006

Injuries Due to Seizures in Persons with Epilepsy
Neurol 63:1565-1570, Lawn,N.D.,et al, 2004

An Organic Cause of Neuropsychiatric Illness in Adolescence
Lancet 361:572, Taylor,S.E.,et al, 2003

Hashimoto Encephalopathy
Arch Neurol 60:164-171, Chong,J.Y.,et al, 2003

Mutations in the Molybdenum Cofactor Biosynthetic Genes MOCS1, MOCS2, and GEPH
Hum Mutat 21:569-576, Reiss,J. &Johnson,J.L., 2003

Nemaline Myopathy:A Clinical Study of 143 Cases
Ann Neurol 50:312-320, Ryan,M.M.,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

Hashimoto's Encephalitis as a Differential Diagnosis of Creutzfeldt-Jakob Disease
JNNP 66:172-176, Seipelt,M.,et al, 1999

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

A Woman with a Relapsing Psychosis Who Got Better with Prednisone
Lancet 347:1288, Cohen,L.,et al, 1996

Accidental Injury is a Serious Risk in Children with Typical Absence Epilepsy
Arch Neurol 53:929-932, Wirrell,E.C.,et al, 1996

Electroencephalographic Findings in Hashimoto's Encephalopathy
Neurol 45:977-981, Henchey,R.,et al, 1995

Causal Heterogeneity in Isolated Lissencephaly
Neurol 42:1375-1388, Dobyns,W.B.,et al, 1992

Neurodevelopmental Outcome of Term Infants with Intraventricular Hemorrhage
Am J Dis Child 146:194-197, Jocelyn,L.J.&Casiro,O.G., 1992

Angelman Syndrome: Clinical Profile
J Child Neurol 7:270-280, Zori,R.T.,et al, 1992

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

A Clinical Study of Noonan Syndrome
Arch Dis Child 67:178-183, Sharland, M.,et al, 1992

Infant Botulism:A Review of 12 Years'Experience at the Children; s Hosp of Phila
Pediatrics 87:159-165, Schreiner,M.S.,et al, 1991

Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
Neurol 40:1876-1882, Gascon,G.G.,et al, 1990

Movement Disorder of Premature Infants with Severe Bronchopulmonary Dysplasia:A New Syndrome
Pediatrics 84:215-218, Perlman,J.M.&Volpe,J.J., 1989

Showing articles 0 to 40 of 40