Articles

Adult-Onset Niemann–Pick Disease Type C: Rapid Treatment Initiation Advised but Early Diagnosis Remains Difficult

in Movement Disorders

• Tobias Piroth
• Kai Boelmans
• Florian Amtage
• Michel Rijntjes
• Anna Wierciochin
• Thomas Musacchio
• Cornelius Weiller
• Jens Volkmann
• Stephan Klebe

Clinical, genotypic, and neuropsychological profile in a series of patients with Niemann-Pick type C disease

in Pediatric Neurology

• Rita dos Santos Mendes
• Daniel Almeida do Valle
• Tiago dos Santos Bara
• Vanessa Furlin
• Michelle da Silva Zeny
• Mara Lúcia Schmitz Ferreira Santos
• Mara L. Cordeiro

New Approaches to Tay-Sachs Disease Therapy

in Lipid and Fatty Acid Research

• Valeriya V. Solovyeva
• Alisa A. Shaimardanova
• Daria S. Chulpanova
• Kristina V. Kitaeva
• Lisa Chakrabarti
• Albert A. Rizvanov

Differently increased volumes of multiple brain areas in Npc1 mutant mice following various drug treatments

• Veronica Antipova
• Diana Heimes
• Katharina Seidel
• Jennifer Schulz
• Oliver Schmitt
• Carsten Holzmann
• Arndt Rolfs
• Hans-Jürgen Bidmon
• Estibaliz González de San Román Martín
• Pitter F. Huesgen

Cipaglucosidase alfa plus miglustat: linking mechanism of action to clinical outcomes in late-onset Pompe disease

in Neuromuscular Disorders and Peripheral Neuropathies

• Barry J. Byrne
• Giancarlo Parenti
• Benedikt Schoser
• Ans T. van der Ploeg
• Hung Do
• Brian Fox
• Mitchell Goldman
• Franklin K. Johnson
• Jia Kang
• Nickita Mehta