Clinical Outcomes and Selection Criteria for Prodromal Huntington's Disease Trials

por Langbehn, Douglas R., Hersch, Steven
Publicado 2020

Utility of the Huntington's Disease Prognostic Index Score for a Perimanifest Clinical Trial

por Langbehn, Douglas R., Fine, Elisabeth M., Meier, Andreas, Hersch, Steven
Publicado 2022

A Phenotypic Atlas for Huntington Disease Based on Data From the Enroll-HD Cohort Study

por Langbehn, Douglas R., Sathe, Swati S., Loy, Clement, Sampaio, Cristina, Mccusker, Elizabeth A.
Publicado 2023

Developmental Trajectory of Height, Weight, and BMI in Children and Adolescents at Risk for Huntington’s Disease: Effect of mHTT on Growth

por Tereshchenko, Alexander, van der Plas, Ellen, Mathews, Katherine D., Epping, Eric, Conrad, Amy L., Langbehn, Douglas R., Nopoulos, Peg
Publicado 2020

Behavioral features in child and adolescent huntingtin gene‐mutation carriers

por Reasoner, Erin E., van der Plas, Ellen, Al‐Kaylani, Hend M., Langbehn, Douglas R., Conrad, Amy L., Schultz, Jordan L., Epping, Eric A., Magnotta, Vincent A., Nopoulos, Peggy C.
Publicado 2022

Early atrophy of pallidum and accumbens nucleus in Huntington’s disease

por van den Bogaard, Simon J. A., Dumas, Eve M., Acharya, Tanka P., Johnson, Hans, Langbehn, Douglas R., Scahill, Rachael I., Tabrizi, Sarah J., van Buchem, Mark A., van der Grond, Jeroen, Roos, Raymund A. C.
Publicado 2010

Progressive alterations in white matter microstructure across the timecourse of Huntington's disease

por Estevez‐Fraga, Carlos, Elmalem, Michael S., Papoutsi, Marina, Durr, Alexandra, Rees, Elin M., Hobbs, Nicola Z., Roos, Raymund A. C., Landwehrmeyer, Bernhard, Leavitt, Blair R., Langbehn, Douglas R., Scahill, Rachael I., Rees, Geraint, Tabrizi, Sarah J., Gregory, Sarah
Publicado 2023

Neuropsychiatry and White Matter Microstructure in Huntington’s Disease

por Gregory, Sarah, Scahill, Rachael I., Seunarine, Kiran K., Stopford, Cheryl, Zhang, Hui, Zhang, Jiaying, Orth, Michael, Durr, Alexandra, Roos, Raymund A.C., Langbehn, Douglas R., Long, Jeffrey D., Johnson, Hans, Rees, Geraint, Tabrizi, Sarah J., Craufurd, David
Publicado 2015

Operationalizing compensation over time in neurodegenerative disease

por Gregory, Sarah, Long, Jeffrey D., Klöppel, Stefan, Razi, Adeel, Scheller, Elisa, Minkova, Lora, Papoutsi, Marina, Mills, James A., Durr, Alexandra, Leavitt, Blair R., Roos, Raymund A. C., Stout, Julie C., Scahill, Rachael I., Langbehn, Douglas R., Tabrizi, Sarah J., Rees, Geraint
Publicado 2017

A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes

por Ciosi, Marc, Maxwell, Alastair, Cumming, Sarah A., Hensman Moss, Davina J., Alshammari, Asma M., Flower, Michael D., Durr, Alexandra, Leavitt, Blair R., Roos, Raymund A.C., Holmans, Peter, Jones, Lesley, Langbehn, Douglas R., Kwak, Seung, Tabrizi, Sarah J., Monckton, Darren G.
Publicado 2019

Neurological disease in xeroderma pigmentosum: prospective cohort study of its features and progression

por Garcia-Moreno, Hector, Langbehn, Douglas R, Abiona, Adesoji, Garrood, Isabel, Fleszar, Zofia, Manes, Marta Antonia, Morley, Ana M Susana, Craythorne, Emma, Mohammed, Shehla, Henshaw, Tanya, Turner, Sally, Naik, Harsha, Bodi, Istvan, Sarkany, Robert P E, Fassihi, Hiva, Lehmann, Alan R, Giunti, Paola
Publicado 2023

Huntington’s disease blood and brain show a common gene expression pattern and share an immune signature with Alzheimer’s disease

por Hensman Moss, Davina J., Flower, Michael D., Lo, Kitty K., Miller, James R. C., van Ommen, Gert-Jan B., ’t Hoen, Peter A. C., Stone, Timothy C., Guinee, Amelia, Langbehn, Douglas R., Jones, Lesley, Plagnol, Vincent, van Roon-Mom, Willeke M. C., Holmans, Peter, Tabrizi, Sarah J.
Publicado 2017