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List of works by Anna Szuto

A 23 years follow-up study identifies GLUT1 deficiency syndrome initially diagnosed as complicated hereditary spastic paraplegia

scientific article published on 8 October 2016

C9orf72 hexanucleotide repeat expansions as the causative mutation for chromosome 9p21-linked amyotrophic lateral sclerosis and frontotemporal dementia

scientific article published on 01 September 2012

CYP7B1 Mutations in French-Canadian Hereditary Spastic Paraplegia Subjects ⬇️

scientific article published on 01 January 2012

Clinical and genetic study of hereditary spastic paraplegia in Canada

scientific article published on 5 December 2016

Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis

scientific article

Exome sequencing identifies FUS mutations as a cause of essential tremor

scientific article

Exome sequencing identifies recessive CDK5RAP2 variants in patients with isolated agenesis of corpus callosum

scientific article published on 22 July 2015

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

scientific article published on May 2016

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

scientific article published on June 2016

Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis

scientific article published on 28 September 2015

SYNE1 mutations in autosomal recessive cerebellar ataxia

scientific article

UBQLN2 mutations are rare in French and French-Canadian amyotrophic lateral sclerosis

scientific article published on 03 May 2012

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