Friday 27th Programme
Session 1: Clinical manifestations and care
12:15 - 13:15
Lunch
10:30 - 10:40 . ——
30 years after the detection of the LAMA2 gene - Haluk Topaloğlu
10:40 - 10:55 —
Exercise therapy for LAMA2 patients - Eric Voorn
10:55 - 11:15 ————
Physiotherapy for congenital LAMA2-RD patients - Numan Bulut, Göknur Haliloğlu
11:15 - 11:35
Dysphagia in patients with LAMA2-RD - Clara Gontijo Camelo
11:35 - 11:55—
Pulmonary care - John Pascoe
11:55 - 12:15
Session 2: Natural history and trial readiness
13:15 - 13:35
13:35 - 13:55 —
13:55 - 14:15
14:15 - 14:35 ———
14:35 - 14:55 ———
14:55 - 15:15
Türkiye - Didem Ardıçlı, Hacer Durmuş
Spain - Gabriela Urcuyo
France - Susana Quijano Roy
UK - Anna Sarkozy, Alberto Zambon
Italy - Alberto Zambon, Stefano Previtali
Russia - Polina Chausova
15:45 - 16:15
Coffee-break
Wrap-up
15:15 - 15:45
Session 3: The road to therapy
LAMA2-RD modifier genes - Veronica Pini
16:15 - 16:35——
Targeting the Dutch LAMA2 Founder mutation - Zheping Cai
16:35 - 16:55————
Cellular sources of laminin-α2 in skeletal muscle - Judith Reinhard
16:55 - 17:15————
Laminin chains in the cardiorespiratory and muscular systems - Kinga Gawlik
17:15 - 17:35
Single and dual AAV treatment of LAMA2 deficiency: Mechanisms, advances and challenges - Peter Yurchenco
17:55 - 18:15
Novel cellular models for LAMA2-RD -Leslie Caron
17:35 - 17:55
19:30
Dinner