Luca Black

Jan 18, 2024 | academic.oup.com | Noah Lewis |Yan Xin |Luca Black

Heterozygous de novo mutations in the neuronal protein Munc18-1/STXBP1 cause syndromic neurological symptoms, including severe epilepsy, intellectual disability, developmental delay, ataxia, and tremor, summarized as STXBP1 encephalopathies.

Jan 18, 2024 | academic.oup.com | Noah Lewis |Yan Xin |Luca Black |Scheller RH

Mutations in Munc18-1 (encoded by the STXBP1 gene) cause a variety of neurodevelopmental disorders known collectively as STXBP1 encephalopathies.1,2 STXBP1 encephalopathies include severe early-onset epileptic encephalopathies3-5 as well as non-syndromic epilepsies, atypical Rett syndrome and severe intellectual disability without epilepsy.6-9 These devastating and often fatal infantile encephalopathies are all characterized by intellectual disability and cerebral dysfunction, and most...

Oct 2, 2023 | manutd.com | Luca Black

Whether the Reds should play in Rome or Mandalay, we want the chance to be there supporting the players in our beloved shirts. And we want to be represented within and recognised by the football club.  The generations that came before us had the Stretford End, Scoreboard Paddock, United Road - sacred names that echoed with the elation and unity of lifelong friends who travelled the world, bound together by their love for Manchester United.

Jul 12, 2023 | manutd.com | Luca Black

As a Mancunian fan of Manchester United, there are few matches that get me as as fired up and anxious as playing against Leeds does. As I'm sure you'll know, there aren't many historic rivalries in football that run as deep as the two roses of Lancashire and Yorkshire going head to head. At 17, I'm not really old enough to fully gauge the fierce rivalry my dad and his generation encountered and have since told us story after story about.