nikola's story: parents of child with rare disease push va. to update newborn screening
Published 5 years ago • 90 plays • Length 0:54Download video MP4
Download video MP3
Similar videos
-
3:14
parents of child with rare disease push va. to update newborn screening
-
4:13
nikola's law: committee declines to add rare disease to newborn screening, parents and legislators t
-
1:48
alabama families advocate for bill adding more rare diseases to newborn screening
-
4:00
delegate takes on virginia department of health and the governor to get funds for krabbe disease ear
-
2:21
children's hospital colorado provides children with critical screenings
-
10:14
nikola's krabbe disease story: extended interview
-
6:41
vote yes on aidan's law (ald) | bk stories
-
6:17
pediatric life limiting illness/courageous stories: soul mates, a love story
-
5:08
newborn screening programs feel pinch of funding struggles
-
1:10:58
newborn screening bootcamp clip session
-
0:29
nc newborns now screened for two additional disorders
-
2:26
children & anxiety: lowering screening age
-
1:01:03
rare webinar series newborn screening
-
48:57
2023 ulf family conference: newborn screening update
-
0:13
am i the problem?: stories from czi's rare as one project | the story collider
-
2:35
during newborn screening month, children's hospital colorado offers important services
-
0:16
pediatrics | peyton manning children's hospital | dr. monica wehby | 15 | ascension st. vincent
-
1:01:51
from lab to clinical trial: rare disease and newborn screening
-
0:54
special report: continued fight to provide funding for early screening of krabbe disease
-
1:53
savannah doctor says screening for newborns can be lifesaving
-
2:16
talking to parents about newborn screening
-
2:03
a better approach to newborn screening