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You are here: Home / Archives for ECTS Rare Webinar

Mar 06 2023

Webinar Series Rare Bone Diseases: The pathogenesis and consequences of having too much bone

Organisers: European Calcified Tissue Society and ERN BOND
Topic: The pathogenesis and consequences of having too much bone
Chairs: Natasha Appelman-Dijkstra, additional chair TBC
Speaker: Prof Wim van Hul
Date & Time: 31 May 2023, from 16:00 to 17:00 CET

Learning Objectives

After participating in this webinar, participants will:

  • Have better knowledge about the classification of sclerosing bone dysplasias
  • Have gained insight into the pathogenic mechanisms underlying sclerosing bone dysplasias
  • Understand the clinical consequences of having too much bone
  • Be able to review their daily practice thanks to case discussions.

Registration

This webinar is free and open to everyone with an interest in the field.

REGISTER HERE

 

Accreditation

This live Webinar has been submitted to EACCME for CME Accreditation.

 

Supported by

This programme is supported by Kyowa Kirin in the form of an educational grant. The scientific programme has not been influenced in any way by its sponsor.

Dec 13 2022

Webinar Series Rare Bone Diseases: Melorheostosis

Organisers: European Calcified Tissue Society and ERN BOND
Topic: Melorheostosis
Chairs: Dr Natasha Appelman-Dijkstra & Dr Natalie Butterfield
Speaker: Prof Geert Mortier
Date & Time: 14 March 2023, from 16:00 to 17:00 CET

Learning Objectives

After watching this webinar, participants will be able to discuss:

  • What are clinical and radiographic features of melorheostosis?
  • How can dysregulation of the TFGbeta pathway cause melorheostosis?
  • How can we identify the genetic cause in rare sporadic bone disorders?

 

Registration

This webinar is free and open to everyone with an interest in the field.

REGISTER HERE

 

Accreditation

The ECTS webinar “Melorheostosis,” streamed live and on-demand, 14 March 2023 has been accredited by the European Accreditation Council for Continuing Medical Education (EACCME®) with 1 European CME credit (ECMEC®s).

Each medical specialist should claim only those hours of credit that he/she actually spent in the educational activity, live or on-demand.

Through an agreement between the Union Européenne des Médecins Spécialistes and the American Medical Association, physicians may convert EACCME® credits to an equivalent number of AMA PRA Category 1 CreditsTM.

Information on the process to convert EACCME® credit to AMA credit can be found at www.ama-assn.org/education/earn-credit-participation-international-activities.

Live educational activities, occurring outside of Canada, recognised by the UEMS-EACCME® for ECMEC®s are deemed to be Accredited Group Learning Activities (Section 1) as defined by the Maintenance of Certification Program of the Royal College of Physicians and Surgeons of Canada.

 

Sponsored by

This programme is supported by Kyowa Kirin in the form of an educational grant. The scientific programme has not been influenced in any way by its sponsor.

 

About the Speaker

Geert Mortier is currently Director of the Department Medical Genetics and Head of the Center for Rare Diseases in the Antwerp University Hospital. He is also Chairman of GENOMED, a research center of excellence at the University of Antwerp where he is funded by the prestigious Methusalem grant. He is full professor at the University of Antwerp and affiliated professor at the Manipal University in India. He is a Belgian-certified pediatrician and clinical geneticist. He has a strong research interest in growth diseases and genetic disorders of the skeleton. He participates in several expert networks for skeletal dysplasias and is member of the scientific medical committee and medical advisory board for several companies and agencies. He is currently coordinator of the Flemish Network for Rare Bone Disorders and International Coordinating Investigator for the Dreambird study (natural history study for achondroplasia sponsored by Therachon). His research bibliography is available at Researcher ID:D-2542-2012 and ORCID ID: 0000-0001-9871-4578 

Sep 21 2021

Webinar Series Rare Bone Diseases: Sorting out Sclerosing Bone Dysplasias

Date & Time: 2 March 2022, 4-5pm CET

Organised by ECTS

Sponsored by Industry

Featuring: Stuart Ralston Chaired by Gavin Clunie & Ciro Menale

Learning Objectives:

  • To be aware of the various conditions that can present with osteosclerosis
  • To be aware of the clinical features and investigations that can help differentiate between different osteosclerotic disorders
  • To be aware of the treatment options for individual osteosclerotic disorders

Format:

  • 5 min introduction
  • 25 min meet-the-expert presentation
  • 30 min Q&A and Case Discussion

Costs: Live & On-demand webinar is free for ECTS members and non-members, but a registration is required.

READ MORE

REGISTER

 

The ECTS Rare Bone Diseases Webinar – Sorting out Sclerosing Bone Dysplasias, 2 March, has been submitted for accreditation by the European Accreditation Council for Continuing Medical Education (EACCME®) for European CME credits (ECMEC®s).

Sep 21 2021

Webinar Series Rare Bone Diseases: Managing adults with low alkaline phosphatase

Date & Time: 9 February 2022, 4-5pm CET

Organised by ECTS

Sponsored by Industry

Featuring: Prof. Dr. José A. Riancho Chaired by Nuria Guanabens & Cristiana Cipriani

Learning Objectives:

  • To raise awareness of the presentation of hereditary skeletal disorders in adults
  • To understand the diagnostic work up of patients with low alkaline phosphatase
  • To know the skeletal consequences of mild hypophosphatasia in adults
  • To understand the benefits and drawbacks of therapy in adult patients with hypophosphatasia

Format:

  • 5 min introduction
  • 25 min meet-the-expert presentation
  • 30 min Q&A and case Discussion

Costs: Live & on-demand webinar is free for ECTS members and non-members, but a registration is required.

READ MORE

REGISTER

 

“The ECTS Rare Bone Diseases Webinar – Managing adults with low alkaline phosphatase, Brussels, Belgium, 09/02/2022-09/02/2022 has been accredited by the European Accreditation Council for Continuing Medical Education (EACCME®) with 1 European CME credits (ECMEC®s). Each medical specialist should claim only those hours of credit that he/she actually spent in the educational activity.”

“Through an agreement between the Union Européenne des Médecins Spécialistes and the American Medical Association, physicians may convert EACCME® credits to an equivalent number of AMA PRA Category 1 CreditsTM. Information on the process to convert EACCME® credit to AMA credit can be found at www.ama-assn.org/education/earn-credit-participation-international-activities.

“Live educational activities, occurring outside of Canada, recognised by the UEMS-EACCME® for ECMEC®s are deemed to be Accredited Group Learning Activities (Section 1) as defined by the Maintenance of Certification Program of the Royal College of Physicians and Surgeons of Canada.”

 

Sep 21 2021

Webinar Series Rare Bone Diseases: Fibrodysplasia Ossificans Progressiva

from 4:00pm to 5:00pm

Speaker: Prof Marelise Eekhoff

Chaired by Dr Geneviève Baujat & Dr Carolina Maria Medina Gomez

Learning Objectives:

  • to understand the background of the disease
  • being able to diagnose FOP
  • to know which treatments are available  (or not available yet)

Format:

  • 5 min introduction
  • 25 min meet-the-expert presentation
  • 30 min Q&A and Case Discussion

Registration for On-Demand Access

The Live & On-demand webinar is free for ECTS members and non-members, but a registration is required.                                            REGISTER HERE

 

Accreditation:

The ECTS Rare Bone Diseases Webinar – Fibrodysplasia ossificans progressiva, Brussels, (Online), Belgium, 27/01/2022-27/01/2022 has been accredited by the European Accreditation Council for Continuing Medical Education (EACCME®) with 1 European CME credits (ECMEC®s).

Each medical specialist should claim only those credits that he/she actually spent in the educational activity, live or on-demand.  To obtain your Certificate, you will be required to fill in a short feedback evaluation form.

Faculty:

Featuring Prof. Marelise Eekhoff

Marelise Eekhoff is an internist-endocrinologist, associate professor, working as a staff member at the Department of Internal Medicine, Department of Endocrinology of the University Medical Centers Amsterdam, location VU (VUmc), Amsterdam, the Netherlands since 2002.

She completed her internal medical education at the Leiden University Medical Center (LUMC), Leiden, the Netherlands. She then worked for more than a year in the Intensive Care Unit, followed by her endocrinology studies at the Endocrinology Department of the LUMC in Leiden. In the same period, she conducted her thesis “Paget’s bone disease in the Netherlands: epidemiology, genetics and treatment” (PhD 2004).

Read full biography

Moderated by

Dr Geneviève Baujat

Genevieve Baujat (MD, MSc), pediatrician by training, is clinical geneticist, consultant in the Centre of Reference for Skeletal Dysplasia, at the Imagine institute of Necker-Enfants malades Hospital, Paris, France. She is also member of the ERN BOND (Rare Bone Disease) and ICC (International Clinical Council on FOP). She has an active interest for skeletal dysplasia diagnosis (from antenatal period to adulthood) and pediatric management. She participates to several research projects through the Centre of Reference, including the development of databases and registries for better known epidemiology and natural history of skeletal conditions, and clinical trials for emergent therapies, including Fibrodysplasia Ossificans Progressiva. 

Dr Carolina Maria Medina Gomez

Dr Carolina Medina Gomez is a postdoctoral researcher at the Erasmus MC University Medical Center Rotterdam, the Netherlands and current member of the ECTS academy. She obtained her PhD in 2016 and was awarded multiple recognitions including the New Investigator award by ECTS, ASBMR and ICBBH. Her work in genetic epidemiology in admixed populations gave her the opportunity to visit the Children Hospital of Philadelphia financed by the European Union. She is the main genetic analysts of the ErasmusMC cohorts and has led many projects within the GEFOS/GENOMOS consortium. Her findings have contributed to underscore the importance of molecules such as WNT16 in bone biology. Her work is at the forefront of cutting-edge methods in genomics (including not only genetic data but also transcriptomics). She has now extended her research to include the microbiome and has a lead role in the MiBioGen consortium trying to bring together genetic, genomic and gut microbiome data.

 

Sponsorship:

This webinar is supported by an educational grant from industry.  The content of the session has not been influenced by the sponsors.

 

 

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