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Author/Creator Berry, Gerard

1. A 7-year old female with arthrogryposis multiplex congenita, Duane retraction syndrome, and Marcus Gunn phenomenon due to a ZC4H2 gene mutation: a clinical presentation of the Wieacker-Wolff syndrome. (3rd September 2021)

Authors:
Godfrey, Deena; Torres, Alcy; Heidary, Gena; Zahoor, Hovra; Lee, Arthur; Berry, Gerard; Engle, Elizabeth
Journal:
Ophthalmic genetics
Issue:
Volume 42:Number 5(2021)
Page Start:
612
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Effects of triheptanoin (UX007) in patients with long‐chain fatty acid oxidation disorders: Results from an open‐label, long‐term extension study. Issue 1 (14th September 2020)

Authors:
Vockley, Jerry; Burton, Barbara; Berry, Gerard; Longo, Nicola; Phillips, John; Sanchez‐Valle, Amarilis; Chapman, Kimberly; Tanpaiboon, Pranoot; Grunewald, Stephanie; Murphy, Elaine; Lu, Xiaoxiao; Cataldo, Jason
Journal:
Journal of inherited metabolic disease
Issue:
Volume 44:Issue 1(2021)
Page Start:
253
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. Uridine‐responsive epileptic encephalopathy due to inherited variants in CAD: A Tale of Two Siblings. Issue 3 (26th January 2021)

Authors:
McGraw, Christopher M.; Mahida, Sonal; Jayakar, Parul; Koh, Hyun Yong; Taylor, Alan; Resnick, Trevor; Rodan, Lance; Schwartz, Marc A.; Ejaz, Ayesha; Sankaran, Vijay G.; Berry, Gerard; Poduri, Annapurna
Journal:
Annals of clinical and translational neurology
Issue:
Volume 8:Issue 3(2021)
Page Start:
716
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗