Walter E Kaufmann

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 10

Top Topics

Cross Sectional

Subarachnoid Hemorrhage

Top Venues

Developmental medicine and child neurology

Orphanet journal of rare diseases

American journal of medical genetics. Part A

Journal of autism and developmental disorders

This page only lists publications with an associated author ORCID identifier.

Publications

Walter E Kaufmann, Alan K Percy, Jeffrey L Neul, Jenny Downs, Helen Leonard, Paige Nues, Girish D Sharma, Theresa E Bartolotta, Gillian S Townend, Leopold M G Curfs, Orietta Mariotti, Claude Buda, Heather M O'Leary, Lindsay M Oberman, Vanessa Vogel-Farley, Katherine V Barnes, Christopher U Missling
Burden of illness in Rett syndrome: initial evaluation of a disorder-specific caregiver survey. Orphanet journal of rare diseases 19 (1) (2024)
Walter E Kaufmann, Alan K Percy, Jeffrey L Neul, Jenny Downs, Helen Leonard, Paige Nues, Girish D Sharma, Theresa E Bartolotta, Gillian S Townend, Leopold M G Curfs, Orietta Mariotti, Claude Buda, Heather M O'Leary, Lindsay M Oberman, Vanessa Vogel-Farley, Katherine V Barnes, Christopher U Missling
Burden of illness in Rett syndrome: initial evaluation of a disorder-specific caregiver survey. Orphanet journal of rare diseases 19 (1) (2024)
Walter E Kaufmann, Alan K Percy, Jeffrey L Neul, Jenny Downs, Helen Leonard, Paige Nues, Girish D Sharma, Theresa E Bartolotta, Gillian S Townend, Leopold M G Curfs, Orietta Mariotti, Claude Buda, Heather M O'Leary, Lindsay M Oberman, Vanessa Vogel-Farley, Katherine V Barnes, Christopher U Missling
Burden of illness in Rett syndrome: initial evaluation of a disorder-specific caregiver survey. Orphanet journal of rare diseases 19 (1) (2024)
Ave M Lachiewicz, Tracy M Stackhouse, Kristin Burgess, Debra Burgess, Howard F Andrews, Tse-Hwei Choo, Walter E Kaufmann, Sharon A Kidd
Sensory Symptoms and Signs of Hyperarousal in Individuals with Fragile X Syndrome: Findings from the FORWARD Registry and Database Multisite Study. Journal of autism and developmental disorders (2023)
Walter E Kaufmann
CDKL5 deficiency disorder: At the intersection between Rett syndrome and developmental epileptic encephalopathies. Developmental medicine and child neurology (2023)
Walter E Kaufmann, Melissa Raspa, Carla M Bann, Julia M Gable, Holly K Harris, Dejan B Budimirovic, Reymundo Lozano, null null
Latent Class Analysis Identifies Distinctive Behavioral Subtypes in Children with Fragile X Syndrome. Journal of autism and developmental disorders (2022)
Patricia Cogram, Robert M J Deacon, Daniel Klamer, Nell Rebowe, Jeffrey Sprouse, Samantha T Reyes, Christopher U Missling, Walter E Kaufmann
Brain cell signaling abnormalities are detected in blood in a murine model of Fragile X syndrome and corrected by Sigma-1 receptor agonist Blarcamesine. American journal of medical genetics. Part A 188 (8) (2022)
Dejan B Budimirovic, Dragana D Protic, Carol M Delahunty, Howard F Andrews, Tse-Hwei Choo, Qing Xu, Elizabeth M Berry-Kravis, Walter E Kaufmann, null null
Sleep problems in fragile X syndrome: Cross-sectional analysis of a large clinic-based cohort. American journal of medical genetics. Part A (2021)
Heather E Olson, Julia G Costantini, Lindsay C Swanson, Walter E Kaufmann, Timothy A Benke, Anne B Fulton, Ronald Hansen, Annapurna Poduri, Gena Heidary
Cerebral visual impairment in CDKL5 deficiency disorder: vision as an outcome measure. Developmental medicine and child neurology 63 (11) (2021)
Walter E Kaufmann
Long QT interval in Rett syndrome: expanding the knowledge of a poorly understood phenomenon. Developmental medicine and child neurology 62 (7) (2020)