Neurology Specific Literature Search   
 
[home][thesaurus]
    

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 0 to 8 of 8

Hypointensity of the Basal Ganglia in Adults with Glucose Transporter Protein Type 1 Deficiency Syndrome: A Novel Magnetic Resonance Imaging Finding
Ann Neurol 87:10-11, Van Samkar, A.,et al, 2020

Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm
JNNP 86:774-781, Van Egmond, M.E.,et al, 2015

Cerebrospinal Fluid Analysis in the Workup of GLUT1 Deficiency Syndrome
JAMA Neurol 70:1440-1444, Leen, W.G.,et al, 2013

Differential Diagnosis of a Low CSF Glucose in Children and Young Adults
Neurol 81:e178-e181, Leen, W.G.,et al, 2013

Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
Brain 133:655-670, Leen,W.G., et al, 2010

Absence Epilepsies With Widely Variable Onset are a Key Feature of Familial GLUT1 Deficiency
Neurol 75:432-440, Mullen,S.A., et al, 2010

The Expanding Phenotype of GLUT1-Deficiency Syndrome
Brain & Dev 31:545-552, Brockmann,K., 2009

Defective Glucose Transport Across the Blood-Brain Barrier as Cause of Hypoglycorrhachia, Seizures, and Devel Delay
NEJM 325:703-709, 7311991., DeVivo,D.C.,et al, 1991



Showing articles 0 to 8 of 8