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SPG50
0:02:16
Toronto family of child with rare SPG50 disease raises $3 million for gene therapy
0:09:02
Lincoln’s Light - Rare Disease - SPG50
0:03:59
Family races against time to raise $3m to treat son’s ultra-rare disease
0:03:25
#EsperanzaparaAlberto 🖐️✊, el pequeño con SPG50.
0:03:54
GTACC WIL 2023 SPG50
0:29:21
Season 3 Episode 1: Against All Odds: Finding a Treatment for SPG50
0:05:15
Boy with ultra-rare disease begins groundbreaking gene therapy
0:00:48
Physical Activities Training in SPG50 (For All AP4 Patients)
0:01:04
Alberto, 1 de los 3 casos con SPG50 españoles.
0:00:15
SPG50 challenge
0:02:28
Southport parents fight to save their son and others from rare genetic disorder
0:03:30
Audio-Technica AT-SPG50 Compact Speaker Short Sound Test
0:00:39
JUNTOS aceleramos la esperanza.
0:01:48
Boy with rare disease gets skin transplant
0:03:33
Naomi's Story
0:02:31
Family hopeful about therapy after baby diagnosed with rare disease
0:02:01
ResumenFestival RenHacer 2023
0:02:40
Colorado family pushes for more funding, awareness around rare neurological disorder
0:41:50
Season 2, Episode 8: Jack’s Corner Foundation, SPG 50: Devin and Mike Dwyer
0:02:29
Southport couple searches for cure for son's rare genetic disorder
0:11:46
Entrevista a la neuropediatra Itxaso Martí, responsable del ensayo para SPG50.
0:13:09
EL PARTIDO PARA RENHACER / THE MATCH FOR A NEW LIFE
0:23:57
How Do We Treat the Untreatable? SickKids VS Rare Disease
0:06:36
El sueño de Alejandro SPG50
Вперёд
0:02:16
0:09:02
0:03:59
0:03:25
0:03:54
0:29:21
0:05:15
0:00:48
0:01:04
0:00:15
0:02:28
0:03:30
0:00:39
0:01:48
0:03:33
0:02:31
0:02:01
0:02:40
0:41:50
0:02:29
0:11:46
0:13:09
0:23:57
0:06:36