K. Haas

发表

People with mesial temporal lobe epilepsy have altered thalamo-occipital brain networks

Graham W. Johnson, V. Morgan, D. Englot, 2020, Epilepsy & Behavior.

Inter-rater agreement on identification of electrographic seizures and periodic discharges in ICU EEG recordings

J. C. Sackellares, B. C. Dean, S. Sinha, 2015, Clinical Neurophysiology.

De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies.

Michael R. Johnson, I. Scheffer, H. Mefford, 2014, American journal of human genetics.

The Epilepsy Phenome/Genome Project

I. Scheffer, N. Risch, R. Kuzniecky, 2013, Clinical trials.

Phenotypic analysis of 303 multiplex families with common epilepsies

I. Scheffer, H. Mefford, D. Goldstein, 2017, Brain : a journal of neurology.

New-onset refractory status epilepticus

J. Szaflarski, L. Hirsch, P. Kaplan, 2015, Neurology.

Non-convulsive Status Epilepticus and Non-convulsive Seizures in Neurological ICU Patients

John Barwise, Bassel Abou-Khalil, Hasan H. Sonmezturk, 2015, Neurocritical Care.

Erratum: De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies (American Journal of Human Genetics (2014) 95(4) (360–370)(S0002929714003838)(10.1016/j.ajhg.2014.08.013))

Michael R. Johnson, I. Scheffer, H. Mefford, 2017 .

Brainstem Functional Connectivity Disturbances in Epilepsy may Recover After Successful Surgery.

Sarah E. Goodale, B. Landman, V. Morgan, 2019, Neurosurgery.

Dosing feasibility and tolerability of intranasal diazepam in adults with epilepsy

M. Sperling, G. Krauss, A. Rabinowicz, 2014, Epilepsia.

Seizure‐onset regions demonstrate high inward directed connectivity during resting‐state: An SEEG study in focal epilepsy

Benoit M Dawant, Saramati Narasimhan, Victoria L Morgan, 2020, Epilepsia.

Video-EEG results and clinical characteristics in patients with psychogenic nonepileptic spells: The effect of a coexistent epilepsy

Hasan H. Sonmezturk, N. Azar, B. Abou-Khalil, 2016, Epilepsy & Behavior.

Ultra-rare genetic variation in common epilepsies: a case-control sequencing study

Michael R. Johnson, I. Scheffer, H. Mefford, 2017, The Lancet Neurology.

Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies

Christian Gieger, Norman Delanty, Ellen Campbell, 2018, Nature Communications.

Does adherence to epilepsy quality measures correlate with reduced epilepsy‐related adverse hospitalizations? A retrospective experience

N. Azar, B. Abou-Khalil, T. Ladner, 2015, Epilepsia.

Diverse genetic causes of polymicrogyria with epilepsy

I. Scheffer, H. Mefford, E. Eichler, 2021, Epilepsia.

Tissue-specific variation of Ube3a protein expression in rodents and in a mouse model of Angelman syndrome

A. Deutch, I. Filonova, E. Weeber, 2010, Neurobiology of Disease.

Cough syncope in a 43-year-old woman with glomus jugulare tumor☆

Hasan H. Sonmezturk, Susanta Bandyopadhyay, B. Abou-Khalil, 2014, Epilepsy & Behavior Case Reports.

Analysis of EEG patterns and genotypes in patients with Angelman syndrome

T. Loddenkemper, M. Gregas, S. Kothare, 2012, Epilepsy & Behavior.

Using common genetic variants to find drugs for common epilepsies

David F. Smith, C. Gieger, I. Scheffer, 2021, Brain Communications.

Epidemiology of Functional Seizures Among Adults Treated at a University Hospital.

L. Davis, E. Torstenson, K. Haas, 2020, JAMA network open.

Development and Feasibility Testing of a Critical Care EEG Monitoring Database for Standardized Clinical Reporting and Multicenter Collaborative Research

J. Szaflarski, J. Hopp, Pearce J. Korb, 2016, Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society.

A randomized controlled trial of levodopa in patients with Angelman syndrome

E. Weeber, A. Rotenberg, S. Skinner, 2018, American journal of medical genetics. Part A.

Role of the Nucleus Basalis as a Key Network Node in Temporal Lobe Epilepsy

Graham W. Johnson, P. Konrad, M. Rubinov, 2021, Neurology.

Functional seizures are associated with cerebrovascular disease and functional stroke is more common in patients with functional seizures than epileptic seizures

L. Davis, S. Goleva, K. Haas, 2022, Epilepsy & Behavior.

Visual Field Defects After Selective Amygdalohippocampectomy and Standard Temporal Lobectomy

P. Konrad, Y. Song, K. Haas, 2009, Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society.

Experience From 211 Transcortical Selective Amygdalohippocampectomy Procedures: Relevant Surgical Anatomy and Review of the Literature.

P. Konrad, D. Englot, Rushna Ali, 2021, Operative neurosurgery.

Quantitative analysis of phenotypic elements augments traditional electroclinical classification of common familial epilepsies

I. Scheffer, H. Mefford, D. Goldstein, 2019, Epilepsia.

De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies.

H. Mefford, P. May, R. Krause, 2017, American journal of human genetics.

GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture

Ethan M. Goldberg, Andreas M. Koupparis, W. C. Stewart, 2023, Nature Genetics.

Analysis of EEG patterns and genotypes in patients with Angelman syndrome

T. Loddenkemper, M. Gregas, S. Kothare, 2012, Epilepsy & Behavior.