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Differential
(Click to cross reference)
aciduria
adverse drug reaction
algorithm
ataxia
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
basal ganglia, lesion of
basal ganglia, lesion, bilateral
caudate nucleus, lesion of, bilateral
central nervous system, infection of
cerebral palsy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, lactic acid concentration
children
chromosomal abnormality
chromosome 1
delay in diagnosis
developmental retardation
diet
differential diagnosis
dopa responsive dystonia
drug induced neurologic disorders
dyskinesia
dystonia
dystonia, children
encephalitis, autoimmune
familial
gene
gene mutation
genetic counselling
genetic neurologic disorders
GLUT1
GLUT1 deficiency syndrome
hypoglycemia
hypoglycorrhachia
hypoglycorrhachia, causes of
hypotonia
inborn errors of metabolism
iron, brain
islet cell tumor
ketogenic diet
lactate
lenticular nucleus, lesion of, bilateral
lumbar puncture
mental retardation
metabolic disorder, primary
microcephaly
mimics
molecular genetics
movement disorder
MRI, abnormal
MRI, paramagnetic effect
neurologic disease, diagnoses of
neurotomy
next-generation sequencing
paroxysmal exertion-induced dyskinesia
review article
seizure
seizure, children
seizure, familial
seizure, neonatal
seizure, petit mal
spasticity
striatal encephalitis
symmetric brain lesions
treatment of neurologic disorder
walking, difficulty with
workup
Showing articles 700 to 750 of 1263 << Previous Next >>

Chronic Encephalitis (Rasmussen's Syndrome) and Ipsilateral Uveitis
Ann Neurol 32:826-829, Harvey,A.S.,et al, 1992

Superior Sagittal Sinus Thrombosis in a Child with Protein S Deficiency
Neurol 42:2303-2305, Prats,J.M.,et al, 1992

Cortical Biopsy in Alzheimer's Disease:Dx Accuracy & Neurochem Neuropath, & Cognit Correl
Ann Neurol 32:625-632, Dekosky,S.T.,et al, 1992

Haemorrhagic Thiamine Deficient Encephalopathy Following Prolonged Parenteral Nutrition
JNNP 55:826-829, Vortmeyer,A.O.,et al, 1992

Three-and Four-Year Cognitive Outcome in Children with Noncortical Brain Tumors & Whole-Brain RT
Ann Neurol 32:551-554, Radcliffe,J.,et al, 1992

Long-Term Neurologic Consequences of Nutritional Vitamin B12 Deficiency in Infants
J Pediatr 121:710-714, Graham,S.M.,et al, 1992

Cognitive Assessment of Human Immunodeficiency Virus-Exposed Children
Am J Dis Child 146:1479-1483, Levenson,R.L.,et al, 1992

Cerebral Artery Aneurysms in Children Infected with Human Immunodeficiency Virus
J Pediatr 121:927-930, Husson,R.N.,et al, 1992

Confusion & Memory Loss from Capsular Genu Infarction:A Thalamocortical Disconnection Syndrome?
Neurol 42:1966-1979, Tatemichi,T.K.,et al, 1992

Twinning and Neurologic Morbisity
Am J Dis Child 146:1110-1113, Scheller,J.M.&Nelson,K.B., 1992

Coma Assoc with Bursts of Abnor Movements & Cognitive Disturb:Acute Encephalopathy of Obscure Origin
J Pediatr 121:845-851, Sebire,G.,et al, 1992

Clinical and NEuroradiol Findings of Congen Hydroceph in Infant Born to Mother with HTLV-I-Assoc Myelopathy
Neurol 42:1406-1408, Tohyama,J.,et al, 1992

Neurologic Syndrome in 25 Workers from an Aluminim Smelting Plant
Arch Int Med 152:1443-1448, White,D.M.,et al, 1992

Gastrointestinal Dysfunction in Parkinson's Disease:Frequency and Pathophysiology
Neurol 42:726-732, Edwards,L.L.,et al, 1992

Long-Term Outcome of Neonatal Meningitis
Am J Dis Child 146:567-571, Franco,S.M.,et al, 1992

Postneonatal Vitamin B6-Dependent Epilepsy
Pediatr 90:221-223, Coker,S.B., 1992

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

Population Screening for Fragile X
Lancet 339:1210-1213, Turner,G.,et al, 1992

Cerebellar Symptoms as Presenting Manifest of Bilirubin Encephal in Children with Crigler-Najjar Type I Disease
Pediatrics 89:768-770, Labrune,P.H.,et al, 1992

Encephalitis in Cat Scratch Disease with Persistent Dementia
JNNP 55:133-135, Revol,A.,et al, 1992

Cardioskeletal Mitochondrial Myopathy Associated with Chronic Magnesium Deficiency
Neurol 42:128-130, Riggs,J.E.,et al, 1992

The Neuropsychological Features of Mitochondrial Myopathies and Encephalomyopathies
Arch Neurol 49:158-160, Kartsounis,L.D.,et al, 1992

Cognitive Functioning in Cancer Patients:Effect of Previous Treatment
Neurol 42:434-436, Meyers,C.A.&Abbruzzese,J.L., 1992

Girls with Fragile X Syndrome:Physical and Neurocognitive Status and Outcome
Pediatrics 89:395-400, Hagerman,R.J.,et al, 1992

Cerebromeningeal Haemophagocytic Lymphohistiocytosis
Lancet 239:104-107, Henter,J.&Elinder,G., 1992

Psychiatric Disturbances in Metachromatic Leukodystrophy
Arch Neurol 49:401-406, Hyde,T.M.,et al, 1992

Protein S Deficiency in Middle-Aged Women with Stroke
Neurol 42:1029-1033, Green,D.,et al, 1992

Familial Intracranial Haemorrhage Due to Factor V Deficiency
JNNP 55:227-228, Wadia,R.S.,et al, 1992

New Research in Tuberous Sclerosis, Probably More Common with More Adult Complications
BMJ 304:1647-1648, Mitchell,S.&Bradbeer,C., 1992

Wilson Disease
Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992

Vitamin B12 Metabolism in Multiple Sclerosis
Arch Neurol 49:649-652, Reynolds,E.H.,et al, 1992

Wernicke's Encephalopathy and Central Pontine Myelinolysis Associated with Hyperemesis Gravidarum
BMJ 305:517-518, Bergin,P.S.&Harvey,P., 1992

Plasma Vitamin B12 Level as a Potential Cofactor in Studies of HIV Type 1-Related Cognitive Changes
Arch Neurol 49:501-506, Beach,R.S.,et al, 1992

Detection of Full Fragile X Mutation
Lancet 339:271-272, Pergolizzi,R.G.,et al, 1992

Is Aluminium a Dementing Ion?
Editorial, Lancet 339:713-7141992., , 1992

Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
Ann Int Med 116:896-900, Coleman,R.A.,et al, 1992

Genetic Diagnosis of Gaucher's Disease
Lancet 339:889-892, Mistry,P.K.,et al, 1992

Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
Neurol 42:1220-1224, 1992,, Rando,T.A.,et al, 1992

McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature
JNNP 55:407-408, Felice,K.J.,et al, 1992

A Synd of Autosomal Dominant Alternating Hemiplegia:Mimicking Intractable Epilepsy; Chromosomal Studies; Physiol Investig
Neurol 42:2251-2257, Mikati,M.A.,et al, 1992

Prevention of First Occur of Neural-Tube Defects by Periconceptional Vitamin Suppl
NEJM 327:1832-1835, 18751992., Czeizel,A.E.&Dudas,I., 1992

Cognitive Development of Yu-Cheng ('Oil Disease') Children Prenatally Exposed to Heat-Degraded PCBs
JAMA 268:3213-3218, Chen,Y.J.,et al, 1992

Chemotherapy for Acute Lymphocytic Leukemia:Cognitive and Academic Sequelae
J Pediatr 121:885-889, Brown,R.T.,et al, 1992

Factors Impairing Daytime Performance in Patients with Sleep Apnea/Hypopnea Syndrome
Arch Int Med 152:538-541, Cheshire,K.,et al, 1992

Hypomelanosis of Ito
Editorial, Lancet 339:651-6521992., , 1992

Cognitive and Motor Development in Infants at Risk for Human Immunodeficiency Virus
Am J Dis Child 146:218-222, Aylward,E.H.,et al, 1992

Clinical Outcome in Aggressively Treated Meningeal Gliomatosis
Neurol 42:252-254, Grant,R.,et al, 1992

Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
Neurol 42:85-91, Aubourg,P.,et al, 1992

Cerebral Infarction Associated with Protein C Deficiency
Stroke 23:108-111, Matsushita,K.,et al, 1992

Hypoglycemia Presenting as Basilar Artery Thrombosis
Stroke 23:112-113, Rother,J.,et al, 1992



Showing articles 700 to 750 of 1263 << Previous Next >>