M. Zortea

发表

Ataxia and Congenital Muscular Dystrophy: the follow-up of a new specific phenotype

A. Tormene, M. Armani, C. Trevisan, 2001, Brain and Development.

A novel 9-bp insertion in the GJB1 gene causing a mild form of X-linked CMT with late onset

G. Vazza, M. Mostacciuolo, L. Merlini, 2006, Neuromuscular Disorders.

Charcot‐Marie‐Tooth disease type I and related demyelinating neuropathies: Mutation analysis in a large cohort of Italian families

G. Siciliano, M. Mostacciuolo, F. Taroni, 2001, Human mutation.

A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28.

F. Boaretto, G. Vazza, M. Mostacciuolo, 2000, American journal of human genetics.

Prevalence of Inherited Ataxias in the Province of Padua, Italy

S. di Donato, C. Gellera, M. Armani, 2004, Neuroepidemiology.

Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1

M. Armani, A. Vettori, G. Vazza, 2002, Journal of medical genetics.

Friedreich’s ataxia: clinical heterogeneity in two sisters

M. Armani, L. Zuliani, C. Trevisan, 2006, Neurological Sciences.

A genetic polymorphism in the human HOXB1 homeobox gene implying a 9bp tandem repeat in the amino-terminal coding region. Mutations in brief no. 200. Online.

E. Boncinelli, A. Faiella, V. Capra, 1998, Human Mutation.

Glass tanks as models for convection in the upper mantle

M. Zortea, I. Peychès, 1971 .