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Barbara R Pober

Showing results (11-20 of 57) with videos related to

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Expert Opinion on Drug Safety|December 28, 2020
Psychopharmacology of Williams syndrome: safety, tolerability, and effectivenessRobyn P Thom, Barbara R Pober, Christopher J McDougle
American Journal of Medical Genetics. Part A|November 12, 2005
Cardiovascular malformations in Fryns syndrome: is there a pathogenic role for neural crest cells?Angela E Lin, Barbara R Pober, Mary P Mullen, et al.
American Journal of Medical Genetics. Part A|February 13, 2013
Hearing from parents: the impact of receiving the diagnosis of Williams syndrome in their childJessica L Waxler, Elizabeth M Cherniske, Kristen Dieter, et al.
Journal of the Academy of Consultation-Liaison Psychiatry|October 7, 2021
Functional Neurological Symptom Disorder in Williams Syndrome: Case Series and Review of Relevant LiteratureRobyn P Thom, Kayla Balaj, Christopher J Keary, et al.
Journal of Autism and Developmental Disorders|August 16, 2023
Diversity of Participants in Williams Syndrome Intervention StudiesEva Shin, Caitlin Ravichandran, Danielle Renzi, et al.
Journal of Autism and Developmental Disorders|November 15, 2019
Buspirone for the Treatment of Generalized Anxiety Disorder in Williams Syndrome: A Case SeriesRobyn P Thom, Christopher J Keary, Jessica L Waxler, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
Pulmonary function and emphysema in Williams-Beuren syndromeEmily S Wan, Barbara R Pober, George R Washko, et al.
American Journal of Medical Genetics. Part A|January 7, 2004
FOXC1 gene deletion is associated with eye anomalies in ring chromosome 6Hui Z Zhang, Peining Li, Dongmei Wang, et al.
European Journal of Medical Genetics|March 4, 2017
Altered body composition, lipedema, and decreased bone density in individuals with Williams syndrome: A preliminary reportJessica L Waxler, Cara Guardino, Richard S Feinn, et al.
European Journal of Medical Genetics|August 17, 2019
Mild macrocytosis in Williams-Beuren syndromeEric Yu, Richard Feinn, Robert Bona, et al.
Pageof 6

Showing results (11-20 of 57) with videos related to

Sort By:
Pageof 6
Expert Opinion on Drug Safety|December 28, 2020
Psychopharmacology of Williams syndrome: safety, tolerability, and effectivenessRobyn P Thom, Barbara R Pober, Christopher J McDougle
American Journal of Medical Genetics. Part A|November 12, 2005
Cardiovascular malformations in Fryns syndrome: is there a pathogenic role for neural crest cells?Angela E Lin, Barbara R Pober, Mary P Mullen, et al.
American Journal of Medical Genetics. Part A|February 13, 2013
Hearing from parents: the impact of receiving the diagnosis of Williams syndrome in their childJessica L Waxler, Elizabeth M Cherniske, Kristen Dieter, et al.
Journal of the Academy of Consultation-Liaison Psychiatry|October 7, 2021
Functional Neurological Symptom Disorder in Williams Syndrome: Case Series and Review of Relevant LiteratureRobyn P Thom, Kayla Balaj, Christopher J Keary, et al.
Journal of Autism and Developmental Disorders|August 16, 2023
Diversity of Participants in Williams Syndrome Intervention StudiesEva Shin, Caitlin Ravichandran, Danielle Renzi, et al.
Journal of Autism and Developmental Disorders|November 15, 2019
Buspirone for the Treatment of Generalized Anxiety Disorder in Williams Syndrome: A Case SeriesRobyn P Thom, Christopher J Keary, Jessica L Waxler, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
Pulmonary function and emphysema in Williams-Beuren syndromeEmily S Wan, Barbara R Pober, George R Washko, et al.
American Journal of Medical Genetics. Part A|January 7, 2004
FOXC1 gene deletion is associated with eye anomalies in ring chromosome 6Hui Z Zhang, Peining Li, Dongmei Wang, et al.
European Journal of Medical Genetics|March 4, 2017
Altered body composition, lipedema, and decreased bone density in individuals with Williams syndrome: A preliminary reportJessica L Waxler, Cara Guardino, Richard S Feinn, et al.
European Journal of Medical Genetics|August 17, 2019
Mild macrocytosis in Williams-Beuren syndromeEric Yu, Richard Feinn, Robert Bona, et al.
Pageof 6