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80044117 - The Spectrum of Developmental Disabilities XL


The Spectrum of Developmental Disabilities XL Banner

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Add to Calendar The Spectrum of Developmental Disabilities XL 3/19/2018 6:00:00 AM 3/21/2018 11:00:00 PM America/New_York For More Details: https://hopkinscme.cloud-cme.com/course/courseoverview?EID=11139 Description: Please click here to view speaker disclosures DESCRIPTION Genetics has rapidly become integral to the evaluation and treatment of a wide variety of neurodevelopmental disabilities. Modern techniques now allow identification of genetic etiologies in as many as 40% of patients with developmental disabilities. The potential benefits in identifying comorbidities, prognostication, and counselin... Johns Hopkins School of Medicine, Turner Auditorium false MM/DD/YYYY


Date & Location
Monday, March 19, 2018, 6:00 AM - Wednesday, March 21, 2018, 11:00 PM, Johns Hopkins School of Medicine, Turner Auditorium

Overview


Please click here to view speaker disclosures

DESCRIPTION
Genetics has rapidly become integral to the evaluation and treatment of a wide variety of neurodevelopmental disabilities. Modern techniques now allow identification of genetic etiologies in as many as 40% of patients with developmental disabilities. The potential benefits in identifying comorbidities, prognostication, and counseling are clear; the American Academy of Pediatrics, American Academy of Neurology, and American College of Medical Genetics all now recommend high-resolution chromosomal microarray testing as first-line evaluation for intellectual disability and autism spectrum disorder. Regardless, there remain significant financial and practical barriers to obtaining this testing. Further, output of these complex tests produce results that can be unexpected and difficult to interpret even for experienced clinicians. Many non-genetics clinicians do not feel equipped to interpret results and articulate a need for further education. The advent and gaining utilization of even higher-resolution techniques such as whole-exome and whole-genome sequencing will further compound this problem over coming years.

Once a genetic variant is identified, incorporating rapidly evolving information from testing into comprehensive care and counseling remains challenging. The number of recognized contributing variants is rapidly growing. In order to make use of the wealth of data now available and to realize the promise of individualized medicine, clinicians must become familiar with the tools and concepts needed to navigate the new genetic information landscape.

WHO SHOULD ATTEND
This activity is intended for pediatricians, genetic counselors, neuro-developmentalists, developmental behavioral pediatricians, child neurologists, child psychiatrists, educators, nurses, nurse practititioners, occupational therapists, psychologists, speech language pathologists, physical therapists, physician assistants and social workers.

FEES
Methods of Payment: We require full payment prior to the start of the activity. On-site payments by credit card only. The registration fee includes instructional materials, continental breakfasts, refreshment breaks and lunches.

Registration Fee ........................................................................$545
Printed Syllabus...........................................................................$35

LATE FEE AND REFUND POLICY
A $50 late fee applies to registrations received after 5:00 p.m. ET on March 13, 2018. A handling fee of $50 will be deducted for cancellation. An additional fee may apply for cancellation of other events, including workshops and social activities. Refund requests must be received by fax or mail by March 13, 2018. No refunds will be made thereafter. Transfer of registration to another Johns Hopkins activity in lieu of cancellation is not possible.


Objectives
After attending this activity, the participant will demonstrate the ability to:

  1. Identify and obtain appropriate genetic testing for children with developmental disabilities.
  2. Interpret genetic testing using current research results.
  3. Counsel patients and families regarding results and implications of genetic testing.
  4. Critically evaluate emerging targeted therapies.

Accreditation


ACCREDITATION STATEMENT
This activity has been planned and implemented in accordance with the accreditation requirements and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint providership of Johns Hopkins University School of Medicine and Kennedy Fellows Association. The Johns Hopkins University School of Medicine is accredited by the ACCME to provide continuing medical education for physicians.

CREDIT DESIGNATION STATEMENT
The Johns Hopkins University School of Medicine designates this live activity for a maximum of 18.25 AMA PRA Category 1 Credits™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.

MAINTENANCE OF CERTIFICATION
The American Board of Psychiatry and Neurology has reviewed The Spectrum of Developmental Disabilities XL: The New Genetics: Implications for Neurodevelopmental Disabilities and has approved this program as part of a comprehensive self-assessment program, which is mandated by the ABMS as a necessary component of Maintenance of Certification.

OTHER CREDIT
This program is offered for up to 1.8 ASHA CEUs (Various level; Professional area)


American Nurses Credentialing Center (ANCC) accepts AMA PRA Category 1 Credits™ from organizations accredited by the ACCME.

American Academy of Nurse Practitioners National Certification Program accepts AMA PRA Category 1 Credits™ from organizations accredited by the ACCME.

American Academy of Physician Assistants (AAPA) accepts certificates of participation for educational activities certified for AMA PRA Category 1 Credits™ from organizations accredited by ACCME. Physician assistants may receive a maximum of 18.25 AAPA Category 1 CME credits for completing this program.

The Johns Hopkins University School of Medicine is authorized by the Maryland State Board of Examiners of Psychologists as a provider of continuing education. The Johns Hopkins University School of Medicine maintains responsibility for this program. A certificate for 18.25 CEUs will be awarded upon completion of this activity.

The Maryland Board of Social Work Examiners
certifies that this program meets the criteria for 18.25 credit hours of Category 1 or 1.8 CEUs of continuing education for social workers and associates licensed in Maryland. The Johns Hopkins University School of Medicine is an approved sponsor of the Maryland Board of Social Work Examiners for continuing education credits for licensed social workers in Maryland.

The National Society of Genetic Counselors (NSGC) has authorized the Johns Hopkins University School of Medicine to offer up to 1.79 CEUs or 17.91 Category 1 contact hours for the activity The Spectrum of Developmental Disabilities XL: The New Genetics: Implications for Neurodevelopmental Disabilities. The American Board of Genetic Counseling (ABGC) will accept CEUs earned at this program for the purposes of genetic counselor certification and recertification.

The Johns Hopkins University has approved this activity for 18.25 contact hours for non-physicians.




Keywords: LIVE

HOTEL RESERVATION CUT-OFF DATE: FEBRUARY 19, 2018

Homewood Suites by Hilton
625 South President Street
Baltimore, Maryland 21202
Phone: 410-234-0999
FAX: (443) 392-9020
Make your reservation online at http://group.homewood-suites.com/JohnsHopkinsDevelopmentDisabilies2018

Pasquale Accardo, MD
James H. Franklin Professor of Developmental Research in Pediatrics
Virginia Commonwealth University
Kristin Baranano, MD, PhD
Assistant Professor of Neurology
Johns Hopkins University School of Medicine
Hans Bjornsson, MD
Assistant Professor of Pediatrics and Genetics
Johns Hopkins University School of Medicine
Mary E Blue, PhD
Kennedy Krieger Institute
Joann Bodurtha, MD, MPH
Professor of Pediatrics
Johns Hopkins University School of Medicine
George T Capone, MD
Director, Down Syndrome Clinic; Associate Professor of Pediatrics
Kennedy Krieger Institute
Tina L Cheng, MD, MPH
Director, Department of Pediatrics
Johns Hopkins University School of Medicine
Julie S Cohen, ScM, CGC
Senior Genetic Counselor
Kennedy Krieger Institute
Anne M Comi, MD
Associate Professor
Kennedy Krieger Insitute
Kevin Ess, MD, PhD
Associate Professor of Pediatrics and Neurology; Director, Pediatric Neurology
Vanderbilt University Medical Center
Seyed Ali Fatemi, MD
Chief Medical Officer
Kennedy Krieger Institute
Brenda Finucane, MS
Associate Director
Geisinger Autism & Developmental Medicine Institute
Gary Goldstein, MD
President and Chief Executive Officer, Professor of Neurology and Pediatrics
Kennedy Krieger Institute Johns Hopkins University School of Medicine
Andrea L Gropman, MD
Professor
Children's National Health System
David Gutmann, MD,PhD
Donald O Schnuck Family Professor Vice Chairman for Research Affairs
Washington University School of Medicine
James C Harris, MD
Director Developmental Neuropsychiatry
Johns Hopkins University
Ingo Helbig, MD
Assistant Professor of Neurology and Pediatrics
Perelman School of Medicine
Michael V Johnston, MD
Blum Moser Chair for Pediatric Neurology; Executive Vice President and Chief Medical Officer
Kennedy Krieger Institute
Nicholas Katsanis, PhD
Professor, Department of Cell Biology
Duke University School of Medicine
Walter E Kaufmann, MD
Director, Center for Translational Research; Professor of Neurology; Research Professor of Pediatrics; Adjunct Professor of Human Genetics
Greenwood Genetic Center University of South Carolina School of Medicine Emory University School of Medicine
Michael Kruer, MD
Director, Pediatric Movement Disorders Program Barrow
Neurological Institute Phoenix Childrens Hospital
Mary Leppert, MD
Associate Professor of Pediatrics
Kennedy Krieger Institute/Johns Hopkins School of Medicine
Paul H Lipkin, MD
Associate Professor of Pediatrics
Johns Hopkins School of Medicine and Kennedy Krieger Institute
Thomas M Lock, MD
Professor of Clinical Pediatrics
Indiana University School of Medicine
Sonal Mahida, MGC
MGC, CGC
Kennedy Krieger Institute
Eric M. Morrow, MD, PhD
Associate Professor
Brown University
Scott M Myers, MD
Associate Professor of Pediatrics
Geisinger Commonwealth School of Medicine
Jonathan Pevsner, PhD
Professor of Psychiatry and Behavioral Sciences
Johns Hopkins University School of Medicine
Brian T Rogers, MD
Professor of Pediatrics
Oregon Health and Science University
Bruce Shapiro, MD
Vice President of Training; Professor of Pediatrics
Kennedy Krieger Institute and Johns Hopkins University School of Medicine

Monday, March 19, 2018
Welcome and Conference Goals
8:45AM - 9:00AM
Bruce Shapiro, MD
Welcome and Conference Goals
8:45AM - 9:00AM
Tina L Cheng, MD, MPH
Welcome and Conference Goals
8:45AM - 9:00AM
Gary Goldstein, MD
Genetics of NDD: It's Not as Simple as it Used to Be
9:00AM - 9:40AM
Seyed Ali Fatemi, MD
Genomics Gateway to Individualized Medicine
9:40AM - 10:20AM
Jonathan Pevsner, PhD
Genetics of Motor Disability: From DCD to CP
10:40AM - 11:25AM
Michael Kruer, MD
Newborn Screening in the Era of Medical Genomics
11:25AM - 12:10PM
Nicholas Katsanis, PhD
Questions and Answers
12:10PM - 12:30PM
Brian T Rogers, MD
Autism Behavioral and Endophenotypes: Relevance for Specific Behavioral Treatment Strategies
1:30PM - 2:15PM
James C Harris, MD
A Staged Evaluation to the Child With Developmental Delay
2:15PM - 3:00PM
Kristin Baranano, MD, PhD
Unexpected Findings, Unknown Significance and Informed Consent
3:20PM - 4:05PM
Julie S Cohen, ScM, CGC
Genetic Counseling for NDD in an Evolving Theoretical Landscape
4:05PM - 4:50PM
Brenda Finucane, MS
Questions and Answers
4:50PM - 5:10PM
Thomas M Lock, MD
Tuesday, March 20, 2018
Epigenetics, Complex Traits, and Environment
8:30AM - 9:20AM
Hans Bjornsson, MD
The Genetics of Epilepsy
9:20AM - 10:10AM
Ingo Helbig, MD
What Have We Learned From Syndromic Autism
10:30AM - 11:15AM
Eric M. Morrow, MD, PhD
NDD Genetics: Molecular Pathways and Therapeutic Potential
11:15AM - 12:00PM
Mary E Blue, PhD
Questions and Answers
12:00PM - 12:30PM
Mary Leppert, MD
Fragile X: Linking the Clinical Manifestations
1:30PM - 2:15PM
Walter E Kaufmann, MD
Down Syndrome: A Lifespan Approach
2:15PM - 3:05PM
George T Capone, MD
Neurofibromatosis Type 1: Precision Medicine Meets Its Match
3:25PM - 4:10PM
David Gutmann, MD,PhD
Sturge Weber: From the Clinic to the Gene
4:10PM - 4:55PM
Anne M Comi, MD
Questions and Answers
4:55PM - 5:25PM
Scott M Myers, MD
Wednesday, March 21, 2018
Hooking Up Parent Support for Genetic and Rare Disorders
8:30AM - 9:15AM
Sonal Mahida, MGC
What's a Primary Care Provider to Do?
9:15AM - 10:00AM
Joann Bodurtha, MD, MPH
Tuberculosis Sclerosis Complex and Epilepsy: What's Next
10:00AM - 10:40AM
Kevin Ess, MD, PhD
Therapeutic Approaches to Genetic Disorders: Symptomatic, Ameliorative, Curative
11:00AM - 11:45AM
Andrea L Gropman, MD
The Kallikaks and the Jukes
11:45AM - 12:30PM
Pasquale Accardo, MD
Questions and Answers
12:30PM - 1:00PM
Paul H Lipkin, MD

Contact Us:
410-955-2959
Or by email: [email protected]

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