Latest Articles

Subject

Article
New family with HSPB8-associated autosomal dominant rimmed vacuolar myopathy
Sejad Al-Tahan, Lan Weiss, Howard Yu, et al.

July 10, 2019
Article
Genetic risk of Parkinson disease and progression:An analysis of 13 longitudinal cohorts
Hirotaka Iwaki, Cornelis Blauwendraat, Hampton L. Leonard, et al.

July 09, 2019
Article
Novel mutation in HTRA1 in a family with diffuse white matter lesions and inflammatory features
Amin Ziaei, Xiaohong Xu, Leila Dehghani, et al.

July 08, 2019
Article
MAPT p.V363I mutationA rare cause of corticobasal degeneration
Sarah Ahmed, Monica Diez Fairen, Marya S. Sabir, et al.

June 25, 2019
Clinical/Scientific Notes
Adult-onset variant ataxia-telangiectasia diagnosed by exome and cDNA sequencing
Martin Krenn, Ivan Milenkovic, Gertrud Eckstein, et al.

June 25, 2019
Article
Genome-wide brain DNA methylation analysis suggests epigenetic reprogramming in Parkinson disease
Juan I. Young, Sathesh K. Sivasankaran, Lily Wang, et al.

June 24, 2019
Article
Systematic review and meta-analysis of cardiac involvement in mitochondrial myopathy
Asfia Quadir, Carly Sabine Pontifex, Helen Lee Robertson, et al.

June 12, 2019
Article
Altered CSF levels of monoamines in hereditary spastic paraparesis 10A case series
Mattias Andréasson, Kristina Lagerstedt-Robinson, Kristin Samuelsson, et al.

June 12, 2019
Article
Human GABRG2 generalized epilepsyIncreased somatosensory and striatothalamic connectivity
Mangor Pedersen, Magdalena Kowalczyk, Amir Omidvarnia, et al.

June 07, 2019
Clinical/Scientific Notes
Missense mutations in DYT-TOR1A dystonia
Zafar Iqbal, Jeanette Koht, Lasse Pihlstrøm, et al.

June 06, 2019

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