7/18/2023
This sugar kills honeybees – it could also help fight cancer
Sanford Burnham Prebys
5/10/2023
Where science meets patients: Sanford Children’s Research Center hosts inaugural symposium
5/2/2023
The Past, Present and Future of Congenital Disorders of Glycosylation with Prof. Hudson Freeze
GlycanAge
2/23/2022
Against all odds, Rare Disease Day is back in San Diego
10/4/2021
Guest commentary: A memorable visit with La Jolla scientist who helps kids with genetic disorders
La Jolla Light
11/24/2020
Sanford Burnham Prebys scientists elected as AAAS Fellows
6/3/2020
6/3/2020 New test for rare disease identifies children who may benefit from simple supplement Sanford Burnham Prebys
3/5/2020
San Diego Child Only Known Person In World With This Rare Form Of Disease
KPBS
2/29/2020
San Diego family hopes for answers, support at Rare Disease Day
The San Diego Union-Tribune
1/13/2020
Why can’t Bertrand Might cry? Scientists offer an answer: missing water channels
12/11/2018
Parents gain answers about their child’s mysterious condition, thanks to SBP scientists
11/15/2018
Meeting the “man who saved my son’s life”
San Diego Biotech Networks
10/4/2018
Solving a medical mystery: Cause of rare type of dwarfism discovered
WDRB, Newsweek, and Fox News Louisville
9/18/2018
Mannose’s Unexpected Effects on the Microbiome and Weight Gain
Australian Women's Health, Australian Men's Health
9/4/2018
Hudson Freeze: Golden Goose Winner talks Mold, Movies and More
AAAS
4/132018
Freeze Lab CDG Support
Sanford Burnham Prebys (YouTube)
3/2/2018
Forming a Rare Disease Network: Bridging Researchers, Physicians and Families
R&D World
2/27/2018
Professor Hudson Freeze helps dreams come true for rare disease patient
CBS 8
2/6/2018
Diagnosing a rare disease in children
9/26/2017
The Golden Goose Award
The Jim Bohannon Show (AM Radio)
9/25/2017
Uncovering the cause of a 12-year-old girl’s rare neurological disorder
9/1/2017
Faced with life-threatening diseases, patients take over
3/22/2017
Proposed federal budget could lead to major cuts in science and medical research
KUSI TV
2/14/2017
Welcome to Accelerating the Conversation: Rare Disease, The Patient Experience and What's Next
Atlantic LIVE (YouTube)
2/5/2017
An Iranian girl’s journey to the US could save her eyesight
New York Post
1/5/2017
From a Pink Squiggle to the Human Genome Project
Nautilus
11/16/2016
What’s Trump’s Plan for U.S. Biomedical Research?
Technology Review
9/19/2016
Hudson Freeze, Ph.D., on the ABC show Speechless
9/9/2016
“No surrender” to CDG
9/8/2016
Hudson Freeze, Ph.D of Sanford Burnham Prebys talks about his research
9/1/2016
The Challenges of Rare-Disease Research
The Scientist
7/18/2016
Focus: Venter’s deep dive into the human genome
3/10/2016
Study triples the number of known cases of a rare disease
3/9/2016
San Diego Lab Helps Families Dealing With Exceedingly Rare Diseases
2/15/2016
What do you do when you have one of the rarest diseases around?
Washington Post
2/12/2016
Fiona Waddell embraces Rare Disease Day as a patient and advocate
1/12/2016
New marker can help sick kids
7/21/2014
One of a Kind
The New Yorker
3/8/2014
The children without tears
Der Spiegel
11/19/2013
A good ambassador’
ASBMB TODAY
9/19/2013
Golden Goose Awards 2013
Vimeo
5/10/2013
A cautionary tale on genome-sequencing diagnostics for rare diseases