Friday 27th Programme
Session 1: Clinical manifestations and care
30 years after the detection of the LAMA2 gene - Haluk Topaloğlu
10:30 - 10:40 . ——
10:40 - 10:55 —
Exercise therapy for LAMA2 patients - Eric Voorn
Physiotherapy for congenital LAMA2-RD patients - Numan Bulut, Göknur Haliloğlu
10:55 - 11:15 ————
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
Lunch
12:15 - 13:15
Session 2: Natural history and trial readiness
Türkiye - Didem Ardıçlı, Hacer Durmuş
13:15 - 13:35
Spain - Gabriela Urcuyo
13:35 - 13:55 —
France - Susana Quijano Roy
13:55 - 14:15
UK - Anna Sarkozy, Alberto Zambon
14:15 - 14:35 ———
Italy - Alberto Zambon, Stefano Previtali
14:35 - 14:55 ———
Russia - Polina Chausova
14:55 - 15:15
Wrap-up
15:15 - 15:45
Coffee-break
15:45 - 16:15
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
Triple AAV gene therapy to express full-length LAMA2 - Marc Güell
17:35 - 17:55
19:30
Dinner