Concepedia

S. Cacurri

SC

Statistics

Publications

6

Citations

637

H-Index

6

Active since

1994

Affiliations

Institute of Cell Biology and Neurobiology(Current)

Università Cattolica del Sacro Cuore

Sapienza University of Rome

Istituti di Ricovero e Cura a Carattere Scientifico

Casa Sollievo della Sofferenza

S. Cacurri is an author at Institute of Cell Biology and Neurobiology specializing in medicine, genetics, and molecular genetics.

Top concepts

Publications per year

1994–1999

6

Publications

6

Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number ofKpnI repeats at the 4q35 locus and clinical phenotype

Enzo Ricci, Giuliana Galluzzi, Giancarlo Deidda et al. · Annals of Neurology · 1999 · 296 citations

, , +15

Direct detection of 4q35 rearrangements implicated in facioscapulohumeral muscular dystrophy (FSHD).

Giancarlo Deidda, S. Cacurri, N. Piazzo et al. · Journal of Medical Genetics · 1996 · 142 citations · Full text

, , +15

Physical Mapping Evidence for a Duplicated Region on Chromosome 10qter Showing High Homology with the Facioscapulohumeral Muscular Dystrophy Locus on Chromosome 4qter

Giancarlo Deidda, S. Cacurri, Paola Grisanti et al. · European Journal of Human Genetics · 1995 · 102 citations

, , +8

Sequence Homology between 4qter and 10qter Loci Facilitates the Instability of Subtelomeric KpnI Repeat Units Implicated in Facioscapulohumeral Muscular Dystrophy

S. Cacurri, N. Piazzo, Giancarlo Deidda et al. · The American Journal of Human Genetics · 1998 · 58 citations · Full text

, , +8

Molecular analysis of 4q35 rearrangements in facioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagnosis of the disease

Giuliana Galluzzi, Giancarlo Deidda, S. Cacurri et al. · Neuromuscular Disorders · 1999 · 27 citations

, , +10

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