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Author Details
Full Name
Richard P Morse
Affiliation
Geisel School of Medicine at Dartmouth
ORCID
Career Start Year
1987
Papers
30
H Index
17
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
30767900
Functional brain connectivity in electrical status epilepticus in sleep.
Epileptic Disord
2019
23911277
Transitory effect of spike and spike-and-wave discharges on EEG power in children.
Brain Dev
2014
25498516
A comparison of continuous video-EEG monitoring and 30-minute EEG in an ICU.
Epileptic Disord
2014
24794162
Brain connectivity in West syndrome.
Seizure
2014
23848835
Stiripentol in Dravet syndrome: results of a retrospective U.S. study.
Epilepsia
2013
21940124
Maturation of EEG oscillations in children with sodium channel mutations.
Brain Dev
2012
22780836
Outcome of frontal lobe epilepsy surgery.
Epilepsia
2012
22302400
The neurologic findings in Taybi-Linder syndrome (MOPD I/III): case report and review of the literature.
Am J Med Genet A
2012
22341965
SCN1A mutations in Dravet syndrome: impact of interneuron dysfunction on neural networks and cognitive outcome.
Epilepsy Behav
2012
22380859
Epilepsy surgery in tuberous sclerosis: a review.
Neurosurg Focus
2012
21163495
Dravet syndrome: inroads into understanding epileptic encephalopathies.
J Pediatr
2011
22036483
Education of a child neurologist: epilepsy and electroencephalography.
Semin Pediatr Neurol
2011
19953647
Ifosfamide-induced encephalopathy and movement disorder.
Pediatr Blood Cancer
2010
20662891
Intractable occipital lobe epilepsy: clinical characteristics and surgical treatment.
Epilepsia
2010
18378549
Choreoathetosis after herpes simplex encephalitis with basal ganglia involvement on MRI.
Pediatrics
2008
16418593
Deletion of chromosome 21 disturbs human brain morphogenesis.
Genet Med
2006
15901860
Transplantation of umbilical-cord blood in babies with infantile Krabbe's disease.
N Engl J Med
2005
16417876
Novel form of intermediate salla disease: clinical and neuroimaging features.
J Child Neurol
2005
15096412
Rasmussen encephalitis.
Arch Neurol
2004
15172001
Clinical, biochemical, and molecular diagnosis of a free sialic acid storage disease patient of moderate severity.
Mol Genet Metab
2004
11706967
Human herpesvirus 6 limbic encephalitis after stem cell transplantation.
Ann Neurol
2001
11286229
Recombinant human acid alpha-glucosidase enzyme therapy for infantile glycogen storage disease type II: results of a phase I/II clinical trial.
Genet Med
2001
10190829
Neurofibromatosis type 1.
Arch Neurol
1999
9740121
Tuberous sclerosis.
Arch Neurol
1998
7861191
Clonal analysis of human astrocytomas.
J Neurooncol
1994
8429443
Diagnosis of occult muscular dystrophy: importance of the "chance" finding of elevated serum aminotransferase activities.
J Pediatr
1993
1476580
Eastern equine encephalitis presenting with a focal brain lesion.
Pediatr Neurol
1992
2251026
Diagnosis and management of infantile marfan syndrome.
Pediatrics
1990
3317388
Bilateral renal agenesis in three consecutive siblings.
Prenat Diagn
1987
3321025
Prenatal diagnosis of a new syndrome: holoprosencephaly with hypokinesia.
Prenat Diagn
1987
1 - 30 of 30
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