Research conference summary from the 2014 International Task Force on ATP1A3-Related Disorders
Citation Manager Formats
Make Comment
See Comments

Article Information
- Received August 25, 2016
- Accepted in final form January 18, 2017
- First Published March 2, 2017.
Author Disclosures
- Hendrik Rosewich, MD,
- Matthew T. Sweney, MD,
- Suzanne DeBrosse, MD,
- Kevin Ess, MD, PhD,
- Laurie Ozelius, PhD,
- Eva Andermann, MD, PhD,
- Frederick Andermann, MD,
- Gene Andrasco,
- Alice Belgrade, BCBA,
- Allison Brashear, MD,
- Sharon Ciccodicola, RN,
- Lynn Egan,
- Alfred L. George Jr, MD,
- Aga Lewelt, MD,
- Joshua Magelby, PhD,
- Mario Merida, MD,
- Tara Newcomb, MS,
- Vicky Platt,
- Dominic Poncelin,
- Sandra Reyna, MD,
- Masayuki Sasaki, MD,
- Marcio Sotero de Menezes, MD,
- Kathleen Sweadner, PhD,
- Louis Viollet, MD, PhD,
- Mary Zupanc, MD,
- Kenneth Silver, MD and
- Kathryn Swoboda, MD
- Hendrik Rosewich, MD,
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Matthew T. Sweney, MD,
NONE
NONE
I received one-time honoraria for a speaking engagement on behalf of LivaNova regarding Vagal Nerve Stimulation and neuromodulation.
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Suzanne DeBrosse, MD,
NONE
NONE
Alternating Hemiplegia of Childhood Foundation (non- profit), travel support
NONE
NONE
1) Clinical Decision Support: Pediatrics (chapter on Angelman syndrome); DECISION SUPPORT IN MEDICINE, LLC, online electronic resource, updated 2016 2) Reference Module in Neuroscience and Biobehavioral Psychology (chapter on Alpers syndrome); Elsevier; 2016
NONE
NONE
NONE
NONE
NONE
NONE
(1) NIH, 2U54 NS078059-04, site PI, 2014-2019 (2) NIH, U54 NS078059-04, site PI, 2014-2019
NONE
Philanthropic Account for Pyruvate Dehydrogenase Complex Deficiency Research, University Hospitals Case Medical Center
NONE
NONE
NONE
NONE
NONE
NONE
- Kevin Ess, MD, PhD,
Data Monitoring Committee for Novartis Pharmaceuticals sponsored studies 2013-2015 EXIST-3
NONE
NONE
(1) Journal of Child Neurology 2011-present, member of Editorial Board, no compensation (2) Epilepsy Currents 2014-present, member of Editorial Board, no compensation
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
(1) NINDS, NIH 1R01 NS078289, P.I., 2012-2017 (2) Alternating Hemiplegia Childhood Foundation, P.I., 2012-2017
NONE
NONE
NONE
NONE
NONE
NONE
NONE
Expert witness for defense, unrelated to present study
- Laurie Ozelius, PhD,
NONE
NONE
NONE
NONE
Patents related to DYT1 and DYT6 gene tests
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NIH, DC011805 (Co-I), NS081282 (PI), NS087997 (Co-PD, PIProject 1), NS058949 (Co-I), NS088160 (Co-I)
Icahn School of Medicine at Mount Sinai
NONE
NONE
NONE
Genetic test for DYT1, DYT6, Athena Diagnostics, Inc,
NONE
NONE
NONE
- Eva Andermann, MD, PhD,
NONE
NONE
NONE
Editorial advisory board member: 1) Turkish Journal of Neurology 2) Epilepsy and Behavior 3) Journal of Epileptology
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Frederick Andermann, MD,
NONE
NONE
NONE
Brain and Development Epilepsy and Behavior Journal of Epileptology Turkish Journal of Neurology
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Gene Andrasco,
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Alice Belgrade, BCBA,
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Allison Brashear, MD,
Scientific advisory board for Ipsen and Allergan for protocol development. No DSMB.
Dr. Brashear has salary support from NINDS (5R01NS058949-04 (AB), performs research for Allergan, Merz USA, Revance, and Ipsen, and consults for Ispsen, Allegan, Revance, Worldmeds. All research grants are paid directly to Wake Forest School of Medicine. Her conflict of interest is being managed by Wake Forest School of Medicine. Dr. Brashear is also on the Board of Directors of the American Board of Psychiatry and Neurology and the Association of University Professors of Neurology. She also reviews for NINDS. Dr. Brashear has received book royalties from Demos.
Dr. Brashear has consulting agreements with Ispsen, Allegan, Revance, Worldmeds for research program development. Dr. Brashear does not participate in any speakers bureaus. All research grants are paid directly to Wake Forest School of Medicine. Her conflict of interest is being managed by Wake Forest School of Medicine. Dr. Brashear is also on the Board of Directors of the American Board of Psychiatry and Neurology and the Association of University Professors of Neurology. She also reviews for NINDS.
NONE
Application for care management- patent pending.
Spasticity- Demos publishing book. Royalities in 2011, 2012
NONE
Dr. Brashear has consulting agreements with Ispsen, Allegan, Revance, Worldmeds for research program development. Dr. Brashear does not participate in any speakers bureaus. All research grants are paid directly to Wake Forest School of Medicine. Her conflict of interest is being managed by Wake Forest School of Medicine. Dr. Brashear is also on the Board of Directors of the American Board of Psychiatry and Neurology and the Association of University Professors of Neurology. She also reviews for NINDS.
NONE
NONE
NINDS grant is about ATP1A3 diseases. I am PI and I have 20% salary effort.
Dr. Brashear has salary support from NIH (R01-NS058949). This grant is focused on ATP1A3 diseases. Dr. Brashear has consulting agreements with Ispsen, Allegan, Revance, Worldmeds for research program development. These are all on clinical trials with botulinum toxin. Dr. Brashear does not participate in any speakers bureaus. All research grants are paid directly to Wake Forest School of Medicine. Her conflict of interest is being managed by Wake Forest School of Medicine.
NIH (R01-NS058949- PI 4/2008-2/2013. I also have 1% effort on clinical trails funded as noted above.
NONE
NONE
NONE
NONE
NONE
NONE
NONE
Dr. Brashear has been an expert reviewer for one of her patients in the last year.
- Sharon Ciccodicola, RN,
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Lynn Egan,
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Alfred L. George Jr, MD,
Amgen, SAB for cardio-metabolic disorders
NONE
EpiPM Therapeutics (now called Praxis Therapeutics),travel to San Francisco to discuss licensing of leadcompound with another company
Journal of Clinical Investigation, Editorial Consultant,2001 - presentHeart Rhythm Journal, Editorial Board, 2010-presentJournal of General Physiology, Editorial Board, 2004-present
NONE
NONE
NONE
NONE
NONE
NONE
NONE
MerckXenon Pharmaceuticals
NIH, NS0323287, PINIH, HL122010, PINIH, HL083374, PINIH, HL131914, PI
NONE
Alternating Hemiplegia of Childhood FoundationDravet Syndrome Foundation
NONE
NONE
NONE
NONE
NONE
NONE
- Aga Lewelt, MD,
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Joshua Magelby, PhD,
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Mario Merida, MD,
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Tara Newcomb, MS,
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
(1) NICHD, R01-HD69045, genetic counselor,2011-2016 (2) CDC, U01DD001108, coordinator, 2015-2020
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Vicky Platt,
NONE
NONE
NONE
NONE
NONE
NONE
(1) Willamette Management Associates, Director of Research, 19 years
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Dominic Poncelin,
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Sandra Reyna, MD,
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Masayuki Sasaki, MD,
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Marcio Sotero de Menezes, MD,
NONE
NONE
NONE
NONE
NONE
NONE
Employed by a non-profit organization
NONE
Cyberonics advisory board talk
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Kathleen Sweadner, PhD,
Aarhus University Scientific Advisory Board DANDRITE
NONE
(1) Weizmann Institute, Israel, speaker travel expenses, 2016. (2) Gordon Research Conferences, Italy, speaker travel expenses and registration, 2016. (3) University of Lausanne, Switzerland, speaker travel expenses, 2016. (4) Harvard Club of Australia; Royal North Shore Hospital, University of New South Wales, Australia, travel expenses for 1 mo
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
(1) Funded by a subcontract from Wake Forest University from NIH grant NS058949, (2015-2020). (2) Funded as principal investigator on NIH grant NS081558 (2013-2015). (3) Funded as principal investigator on P30 DK057521-16 (BADERC) (2015-2017) (4) Funded as principal investigator on P30 DK040561-19 (NORC-H) (2015-2016)
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Louis Viollet, MD, PhD,
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Mary Zupanc, MD,
1. Mallinkrodt Pharma--Advisory Board 2. Insys Pharma--Advisory Board
NONE
1. Insys Pharmaceutical, funding for travel and advisory board meeting. 2. Mallinkrodt Pharma, funding for travel and advisory board meeting. 3. Penry Epilepsy Minifellowship Program--Speaker for educational purposes, non-CME.
1. Pediatric Neurology
NONE
NONE
NONE
NONE
NONE
NONE
NONE
1. Lundbeck 2. Insys Pharma
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Kenneth Silver, MD and
1. Non-profit: Alternating Hemiplegia of Childhood Foundation Medical Advisory Board 2.Commercial: Marathon Pharmaceuticals, PTC Therapeutics, and Retrophin Inc National Advisory Board Meeting
NONE
Non-Profit: Munster Hospital Grand Rounds Honorarium
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Kathryn Swoboda, MD
AveXis
NONE
NONE
1. Journal of Neuromuscular Disorders, Editorial Board, 2015-present
NONE
NONE
NONE
Biogen Nurture Advisory Board
NONE
NONE
NONE
1. Ionis pharmaceuticals: PI for phase I/II trials of Ionis 396443 in SMA patients, University of Utah, 2010- Dec, 2014 2. Biogen: PI for phase II trial of nusinursen in pre-symptomatic infants with SMA; April 2016-present
NIH RO1-HD69045 grant to fund a newborn screening pilot study for SMA, PI, 2011-16, NICHD.
Adjunct Professor, University of Utah Department of Neurology
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- From the Department of Pediatrics and Pediatric Neurology (H.R.), Georg August University, Göttingen, Germany; Division of Clinical Genetics (L.V.), Department of Pediatrics (T.N., M.T.S.) and Department of Neurology (M.T.S.), University of Utah, Salt Lake City; Center for Human Genetics (S.D.), University Hospitals and Case Western Reserve University, Cleveland, OH; Division of Pediatric Neurology (K.E.), Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN; Center for Human Genetics Research (L.O., M.M., K. Swoboda), Department of Neurology, Massachusetts General Hospital, Boston; Neurogenetics Unit (E.A.) and Epilepsy Research Group (E.A., F.A.), Montreal Neurological Hospital and Institute; Department of Neurology and Neurosurgery (E.A., F.A.), Department of Human Genetics (E.A.), and Department of Pediatrics (F.A.), McGill University, Quebec, Canada; Alternating Hemiplegia of Childhood Foundation (G.A., S.C., L.E., V.P.), Southfield, MI; BCBA (A. Belgrade), Belgrade Behavior Consulting, Chicago, IL; Department of Neurology (A. Brashear), Wake Forest School of Medicine, Winston-Salem, NC; Department of Pharmacology (A.L.G.), Northwestern University Feinberg School of Medicine, Chicago, IL; Department of Pediatrics (A.L.), University of Florida College of Medicine, Jacksonville; Integrative Neuropsychology (J.M.), Fairlawn, OH; Association Française de l'Hémiplégie Alternante (D.P.), Paris, France; Rare Disease Innovation Unit (S.R.), Clinical Development Program, Biogen, Cambridge, MA; Department of Child Neurology (M.S.), National Center of Neurology and Psychiatry, Kodaira, Japan; Swedish Neuroscience Institute (M.S.d.M.), Swedish Medical Center, Seattle, WA; Department of Neurosurgery (K. Sweadner), Massachusetts General Hospital and Harvard Medical School, Boston; Neuroscience Institute (M.Z.), Children's Hospital of Orange County, CA; and Departments of Pediatrics and Neurology (K. Silver), University of Chicago and Comer Children's Hospital, Chicago, IL.
- Correspondence to Dr. Sweney: matthew.sweney{at}hsc.utah.edu
Article usage
Letters: Rapid online correspondence
REQUIREMENTS
You must ensure that your Disclosures have been updated within the previous six months. Please go to our Submission Site to add or update your Disclosure information.
Your co-authors must send a completed Publishing Agreement Form to Neurology Staff (not necessary for the lead/corresponding author as the form below will suffice) before you upload your comment.
If you are responding to a comment that was written about an article you originally authored:
You (and co-authors) do not need to fill out forms or check disclosures as author forms are still valid
and apply to letter.
Submission specifications:
- Submissions must be < 200 words with < 5 references. Reference 1 must be the article on which you are commenting.
- Submissions should not have more than 5 authors. (Exception: original author replies can include all original authors of the article)
- Submit only on articles published within 6 months of issue date.
- Do not be redundant. Read any comments already posted on the article prior to submission.
- Submitted comments are subject to editing and editor review prior to posting.
You May Also be Interested in
- Article
- Abstract
- GLOSSARY
- CONSENSUS TOWARD AN EXPANDED NON–SYNDROME-BASED DIAGNOSTIC ALGORITHM FOR ATP1A3-RELATED NEUROLOGIC DISORDERS
- STANDARDIZED DEFINITIONS FOR PAROXYSMAL EVENTS IN AHC
- CATASTROPHIC EVENTS IN ATP1A3-RELATED DISORDERS
- CRITICAL GAPS IN OUR CURRENT KNOWLEDGE OF ATP1A3-RELATED DISORDERS
- SUGGESTED ACUTE MANAGEMENT RECOMMENDATIONS FOR COMMONLY ENCOUNTERED ADVERSE EVENTS IN PATIENTS WITH ATP1A3-RELATED DISORDERS
- RECOMMENDATIONS FOR MOLECULAR DIAGNOSTIC TESTING
- ATP1A3-RELATED DISORDERS AND EPILEPSY
- DISCUSSION AND FUTURE DIRECTIONS
- AUTHOR CONTRIBUTIONS
- STUDY FUNDING
- DISCLOSURE
- Footnotes
- REFERENCES
- Figures & Data
- Info & Disclosures
Hastening the Diagnosis of Amyotrophic Lateral Sclerosis
Dr. Brian Callaghan and Dr. Kellen Quigg
► Watch
Topics Discussed
Alert Me
Recommended articles
-
Article
Cardiac phenotype in ATP1A3-related syndromesA multicenter cohort studySimona Balestrini, Mohamad A. Mikati, Reyes Álvarez-García-Rovés et al.Neurology, September 10, 2020 -
Article
The expanding clinical and genetic spectrum of ATP1A3-related disordersHendrik Rosewich, Andreas Ohlenbusch, Peter Huppke et al.Neurology, February 12, 2014 -
Article
Genotype–phenotype correlations in alternating hemiplegia of childhoodMasayuki Sasaki, Atsushi Ishii, Yoshiaki Saito et al.Neurology, January 15, 2014 -
Editorial
ATP1A3 mutationsWhat is the phenotype?Allison Brashear, Laurie J. Ozelius, Kathleen J. Sweadner et al.Neurology, January 15, 2014