Sam Amin (S Amin)

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 13

Top Topics

Duchenne Muscular Dystrophy

Tyrosine Kinase

Autism Spectrum Disorder

Top Venues

Developmental medicine and child neurology

Orphanet journal of rare diseases

British journal of clinical pharmacology

This page only lists publications with an associated author ORCID identifier.

Publications

Sam Amin, B Ruban-Fell, I Newell, J Evans, K Vyas, C Nortvedt, R F Chin
Treatment guidelines for rare, early-onset conditions associated with epileptic seizures: a literature review on Rett syndrome and tuberous sclerosis complex. Orphanet journal of rare diseases 19 (1) (2024)
Sam Amin, Rikke Steensjerre Moller, Angel Aledo-Serrano, Alexis A Arzimanoglou, Patrick Bager, Sergiusz Jóźwiak, Gerhard Josef Kluger, Sandra López-Cabeza, Rima Nabbout, Carol-Anne Partridge, Susanne Schubert-Bast, Nicola Specchio, Reetta Kälviäinen
Providing quality care for people with CDKL5 deficiency disorder: A European expert panel opinion on the patient journey. Epilepsia open 9 (3) (2024)
Sam Amin, Rikke Steensjerre Moller, Angel Aledo-Serrano, Alexis A Arzimanoglou, Patrick Bager, Sergiusz Jóźwiak, Gerhard Josef Kluger, Sandra López-Cabeza, Rima Nabbout, Carol-Anne Partridge, Susanne Schubert-Bast, Nicola Specchio, Reetta Kälviäinen
Providing quality care for people with CDKL5 deficiency disorder: A European expert panel opinion on the patient journey. Epilepsia open (2024)
Jill Cadwgan, Jane Goodwin, Barbara Babcock, Molly Brick, Richard F M Chin, Ava Easton, Ben Green, Siobhan Hannan, Rhys P D Inward, Suzannah Kinsella, Callum King, Manju A Kurian, Phillip Levine, Andrew A Mallick, Jeremy R Parr, Carol Anne Partridge, Sam Amin, Daniel E Lumsden, Judith Helen Cross, Ming J Lim, null null
UK research priority setting for childhood neurological conditions. Developmental medicine and child neurology (2024)
Sam Amin, B Ruban-Fell, I Newell, J Evans, K Vyas, C Nortvedt, R F Chin
Treatment guidelines for rare, early-onset conditions associated with epileptic seizures: a literature review on Rett syndrome and tuberous sclerosis complex. Orphanet journal of rare diseases 19 (1) (2024)
Sam Amin, Rikke Steensjerre Moller, Angel Aledo-Serrano, Alexis A Arzimanoglou, Patrick Bager, Sergiusz Jóźwiak, Gerhard Josef Kluger, Sandra López-Cabeza, Rima Nabbout, Carol-Anne Partridge, Susanne Schubert-Bast, Nicola Specchio, Reetta Kälviäinen
Providing quality care for people with CDKL5 deficiency disorder: A European expert panel opinion on the patient journey. Epilepsia open 9 (3) (2024)
Sam Amin, B Ruban-Fell, I Newell, J Evans, K Vyas, C Nortvedt, R F Chin
Treatment guidelines for rare, early-onset conditions associated with epileptic seizures: a literature review on Rett syndrome and tuberous sclerosis complex. Orphanet journal of rare diseases 19 (1) (2024)
Sam Amin, Rikke Steensjerre Moller, Angel Aledo-Serrano, Alexis A Arzimanoglou, Patrick Bager, Sergiusz Jóźwiak, Gerhard Josef Kluger, Sandra López-Cabeza, Rima Nabbout, Carol-Anne Partridge, Susanne Schubert-Bast, Nicola Specchio, Reetta Kälviäinen
Providing quality care for people with CDKL5 deficiency disorder: A European expert panel opinion on the patient journey. Epilepsia open 9 (3) (2024)
Sam Amin
Rare epilepsy treatment: What is on the gene-code lottery list? Developmental medicine and child neurology (2023)
Kingsley Wong, George Davies, Helen Margaret Leonard, Jennepher Anne Downs, Mohammed Junaid, Sam Amin
Growth patterns in individuals with CDKL5 deficiency disorder. Developmental medicine and child neurology (2023)
Sam Amin, Andrew Lux, Finbar O'Callaghan
The journey of metformin from glycaemic control to mTOR inhibition and the suppression of tumour growth. British journal of clinical pharmacology 85 (1) (2018)
Sam Amin, A Lux, Muhammad Amjad Khan, F O'Callaghan
Sirolimus Ointment for Facial Angiofibromas in Individuals with Tuberous Sclerosis Complex. International scholarly research notices 2017 (2017)
Sam Amin, N Forrester, A Norman, A Lux, K Vijayakumar
Novel 9 amino acid in-frame deletion in the NTRK1 tyrosine kinase domain in a patient with congenital insensitivity to pain with anhydrosis. Clinical genetics 92 (5) (2017)