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Cry your eyes out: detecting huntingtin in tears

Cry your eyes out: detecting huntingtin in tears

Is someone cutting onions? Expanded huntingtin can now be detected in tears to help scientists track disease progression.

Dr Sarah HernandezApril 10, 2024

How many is too many? Exploring the toxic CAG threshold in the Huntington’s disease brain

How many is too many? Exploring the toxic CAG threshold in the Huntington’s disease brain

New work from researchers in London uses mice to narrow in on the number of CAG repeats needed to cause symptoms of Huntington’s disease. Their work points to fewer than 185 CAGs as a threshold.

Dr Chris KayApril 21, 2024

A new era for HDBuzz

A new era for HDBuzz

For over a decade HDBuzz has reported unbiased news about Huntington’s disease research and trials. As our beloved Ed and Jeff step back, Rachel, Sarah, and Leora look forward to upholding the HDBuzz mission.

Dr Sarah Hernandez, Dr Leora Fox, and Dr Rachel HardingMay 01, 2024

The VIP section: velvet ropes for the brain and how to get in

The VIP section: velvet ropes for the brain and how to get in

New work from two groups advances tools to model the blood-brain barrier and could improve the way drugs are delivered for brain diseases. This builds on our ability to study, and eventually treat, Huntington’s disease.

Dr Sarah HernandezJune 10, 2024

Hereditary Disease Foundation (HDF) conference 2024 – Day 2

Hereditary Disease Foundation (HDF) conference 2024 – Day 2

Read updates from clinical trials and scientific research on Huntington’s disease from Day 2 of the 2024 HDF Milton Wexler Biennial Symposium #HDF2024

Dr Tamara Maiuri, Dr Sarah Hernandez, and Dr Rachel HardingAugust 10, 2024

Hereditary Disease Foundation (HDF) conference 2024 – Day 3

Hereditary Disease Foundation (HDF) conference 2024 – Day 3

Read our live tweet compilation from clinical trials and scientific research on Huntington’s disease from Day 3 of the 2024 HDF Milton Wexler Biennial Symposium #HDF2024

Dr Rachel Harding and Dr Sarah HernandezAugust 12, 2024

Hereditary Disease Foundation (HDF) conference 2024 – Day 4

Hereditary Disease Foundation (HDF) conference 2024 – Day 4

Read our live tweet compilation from clinical trials and scientific research on Huntington’s disease from Day 4 of the 2024 HDF Milton Wexler Biennial Symposium #HD2024

Dr Sarah Hernandez and Dr Rachel HardingAugust 13, 2024

Hope vs. hype: seeking truth in recent Prilenia headlines

Hope vs. hype: seeking truth in recent Prilenia headlines

Although pridopidine has suffered four negative trials for HD, the message from Prilenia continues to be positive. What is hope and what is hype in this sixteen-year quest for regulatory approval?

Dr Sarah HernandezSeptember 10, 2024

14 changes for a healthier brain

14 changes for a healthier brain

In 2019, there were ~57 million people living with dementia. By 2050, that number is expected to climb to 153 million. Changes in the 14 factors highlighted here can improve brain health and be applied to Huntington’s disease.

Dr Sarah HernandezSeptember 30, 2024

Bringing HD Treatments to Market: The Role of Regulatory Oversight

Bringing HD Treatments to Market: The Role of Regulatory Oversight

Moving drugs from the lab bench to pharmacy shelves is no small task. In this article we delve into the role regulatory oversight plays in clinical trials and the approval of medicines for Huntington’s disease.

Dr Rachel HardingOctober 21, 2024

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