Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Andrea Gropman"'
Autor:
Dragana Protic, Elizabeth Breeze, Guadalupe Mendoza, Marwa Zafarullah, Leonard Abbeduto, Randi Hagerman, Christopher Coffey, Merit Cudkowicz, Blythe Durbin-Johnson, Paul Ashwood, Elizabeth Berry-Kravis, Craig A Erickson, Robin Filipink, Andrea Gropman, Lenora Lehwald, Angela Maxwell-Horn, Stephanie Morris, Amanda Palladino Bennett, Lisa Prock, Amy Talboy, Nicole Tartaglia, Jeremy Veenstra-VanderWeele, Flora Tassone
Publikováno v:
SAGE Open Medicine, Vol 12 (2024)
Background: Fragile X syndrome, with an approximate incidence rate of 1 in 4000 males to 1 in 8000 females, is the most prevalent genetic cause of heritable intellectual disability and the most common monogenic cause of autism spectrum disorder. The
Externí odkaz:
https://doaj.org/article/4350d693f92447c5b032e073bc4ebe02
Publikováno v:
Neurotherapeutics, Vol 21, Iss 4, Pp e00397- (2024)
Externí odkaz:
https://doaj.org/article/b6350046adc446099d384929db196a36
Autor:
Kara Simpson, Nicholas Ah Mew, Ljubica Caldovic, Annette Feigenbaum, Raquel Fernandez, Emily Groopman, Andrea Gropman, Emily Kudalkar, Uta Lichter-Konecki, McKenna Kyriss, Elaine Spector, Meredith Weaver, Manya Warrier, Diane Zastrow, Amanda Thomas-Wilson
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 100884- (2024)
Externí odkaz:
https://doaj.org/article/cd6c80da050b43fc9abb2af511554055
Autor:
Elizabeth Pickup, Kuntal Sen, Steven Moore, Pim Suwannarat, Christina Grant, Nicholas Ah Mew, Andrea Gropman
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 100901- (2024)
Externí odkaz:
https://doaj.org/article/0ca6d180434d4315b0e83ae956ece33d
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 100933- (2024)
Externí odkaz:
https://doaj.org/article/5955ea22b60a4b538325e8110919e624
Autor:
Cristal Hernandez Hernandez, Nhat Duong, Andrea Cohen, Elmer Rajah, Eric Vilain, Daniel Felten, Andrea Gropman, Seth Berger
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101101- (2024)
Externí odkaz:
https://doaj.org/article/a47875e0271546358eddc6375a171096
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101308- (2024)
Externí odkaz:
https://doaj.org/article/6c7cba3ecbe448788517962195b27895
Autor:
Kuntal Sen, Amitha Ananth, Rachel Gottlieb-Smith, Daniel Calalme, Jeffrey Strelzik, Kristin Baranano, Lisa Emrick, Julie Ziobro, Christa Habela, Margie Ream, Divakar Mithal, Andrea Gropman, Louis Dang
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101466- (2024)
Externí odkaz:
https://doaj.org/article/25ed3c23cc0542b49dcdeda4a0460486
Publikováno v:
Transportation Research Interdisciplinary Perspectives, Vol 22, Iss , Pp 100983- (2023)
Previous studies have shown that lack of attention and delayed reactions cause most car crashes. Populations with known deficits in executive function domains such as inattention and lack of mobility would potentially be vulnerable. Understanding the
Externí odkaz:
https://doaj.org/article/fc55c3cb341a465381afba4c5b514d7a
P224: An exploration of the neurodevelopmental phenotype of two patients with 48,XXYY during infancy
Autor:
Lindsey Lang, Andrea Gropman, Debra Counts, Antonie Kline, Francie Mitchell, Elizabeth Buscema, Teresa Sadeghin, Carole Samango-Sprouse
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100252- (2023)
Externí odkaz:
https://doaj.org/article/91edbfaef11046a9826f46be426be53f