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Author/Creator Mole, Sara E

1. Clinical challenges and future therapeutic approaches for neuronal ceroid lipofuscinosis. Issue 1 (January 2019)

Authors:
Mole, Sara E; Anderson, Glenn; Band, Heather A; Berkovic, Samuel F; Cooper, Jonathan D; Kleine Holthaus, Sophia-Martha; McKay, Tristan R; Medina, Diego L; Rahim, Ahad A; Schulz, Angela; Smith, Alexander J
Journal:
Lancet neurology
Issue:
Volume 18:Issue 1(2019)
Page Start:
107
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Neonatal brain-directed gene therapy rescues a mouse model of neurodegenerative CLN6 Batten disease. (6th September 2019)

Authors:
kleine Holthaus, Sophia-Martha; Herranz-Martin, Saul; Massaro, Giulia; Aristorena, Mikel; Hoke, Justin; Hughes, Michael P; Maswood, Ryea; Semenyuk, Olha; Basche, Mark; Shah, Amna Z; Klaska, Izabela P; Smith, Alexander J; Mole, Sara E; Rahim, Ahad A; Ali, Robin R
Journal:
Human molecular genetics
Issue:
Volume 28:Number 23(2019)
Page Start:
3867
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Revealing the clinical phenotype of atypical neuronal ceroid lipofuscinosis type 2 disease: Insights from the largest cohort in the world. (30th December 2020)

Authors:
Lourenço, Charles M; Pessoa, Andre; Mendes, Carmen C; Rivera‐Nieto, Carolina; Vergara, Diane; Troncoso, Mónica; Gardner, Emily; Mallorens, Francisca; Tavera, Lina; Lizcano, Luis A; Atanacio, Nora; Guelbert, Norberto; Specola, Norma; Mancilla, Nury; de Souza, Carolina F M; Mole, Sara E
Journal:
Journal of paediatrics and child health
Issue:
Volume 57:Number 4(2021)
Page Start:
519
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗