Wiznitzer, Max

Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthase

Simpson, M. A., Cross, H., Proukakis, C., Priestman, D. A., Neville, D. C. A., Reinkensmeier, G., Wang, H., Wiznitzer, M., Gurtz, K., Verganelaki, A., et al. (2004) · Nature Genetics

Lysosomal Storage Disorders ResearchMetabolism and Genetic Disorders

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Evidence-based support for autistic people across the lifespan: maximising potential, minimising barriers, and optimising the person–environment fit

Lai, M.-C., Anagnostou, E., Wiznitzer, M., Allison, C., & Baron-Cohen, S. (2020) · The Lancet Neurology

Autism Spectrum Disorder ResearchFamily and Disability Support Research

Cited by 250

Practice guideline: Treatment for insomnia and disrupted sleep behavior in children and adolescents with autism spectrum disorder: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology

Williams Buckley, A., Hirtz, D., Oskoui, M., Armstrong, M. J., Batra, A., Bridgemohan, C., Coury, D., Dawson, G., Donley, D., Findling, R. L., et al. (2020) · Neurology

Sleep and related disordersAutism Spectrum Disorder Research

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Autism and tuberous sclerosis

Wiznitzer, M. (2004) · Journal of Child Neurology

Tuberous Sclerosis Complex ResearchAutism Spectrum Disorder Research

Cited by 214