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Matteo di Capua

Research Profile

Disorders

Concepts & Ideas

Physiology

Chemicals & Drugs

Anatomy

Procedures

DNA Mutational Analysis

Living Beings

Infants

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Publications

TOP 3
Nicola Specchio; Antonio Carotenuto; Marina Trivisano; Simona Cappelletti; Cristina Digilio; Rossella Capolino; Matteo di Capua; Lucia Fusco; Federico Vigevano
Ring 21 chromosome presenting with epilepsy and intellectual disability: clinical report and review of the literature.
Gaëtan Lesca; Eleonore Eymard-Pierre; Filippo M Santorelli; R Cusmai; Matteo di Capua; E M Valente; Jocelyne Attia-Sobol; Henri Plauchu; Vincenzo Leuzzi; A Ponzone; Odile Boespflug-Tanguy; Enrico Bertini
Infantile ascending hereditary spastic paralysis (IAHSP): clinical features in 11 families.
Eleonore Eymard-Pierre; Gaëtan Lesca; Sandra Dollet; Filippo M Santorelli; Matteo di Capua; Enrico Bertini; Odile Boespflug-Tanguy
Infantile-onset ascending hereditary spastic paralysis is associated with mutations in the alsin gene.

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All Publications

2011: Nicola Specchio; Antonio Carotenuto; Marina Trivisano; Simona Cappelletti; Cristina Digilio; Rossella Capolino; Matteo di Capua; Lucia Fusco; Federico Vigevano
Ring 21 chromosome presenting with epilepsy and intellectual disability: clinical report and review of the literature.
American journal of medical genetics. Part A 2011;155A(4):911-4.
2003: Gaëtan Lesca; Eleonore Eymard-Pierre; Filippo M Santorelli; R Cusmai; Matteo di Capua; E M Valente; Jocelyne Attia-Sobol; Henri Plauchu; Vincenzo Leuzzi; A Ponzone; Odile Boespflug-Tanguy; Enrico Bertini
Infantile ascending hereditary spastic paralysis (IAHSP): clinical features in 11 families.
Neurology 2003;60(4):674-82.
2002: Eleonore Eymard-Pierre; Gaëtan Lesca; Sandra Dollet; Filippo M Santorelli; Matteo di Capua; Enrico Bertini; Odile Boespflug-Tanguy
Infantile-onset ascending hereditary spastic paralysis is associated with mutations in the alsin gene.
American journal of human genetics 2002;71(3):518-27.
2001: S Salvi; Filippo M Santorelli; Enrico Bertini; Renata Boldrini; C Meli; A Donati; A B Burlina; C Rizzo; Matteo di Capua; Giuseppe Fariello; Carlo Dionisi Vici
Clinical and molecular findings in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome.
Neurology 2001;57(5):911-4.
2001: Matteo di Capua; M L Lispi; A Giannotti; Daniela Longo; Giuseppe Fariello
Neurofibromatosis type 1 presenting with hand dystonia.
Journal of child neurology 2001;16(8):606-8.
2000: Vincenzo Leuzzi; A Rinna; M Gallucci; Matteo di Capua; Carlo Dionisi Vici; Daniela Longo; Enrico Bertini
Ataxia, deafness, leukodystrophy: inherited disorder of the white matter in three related patients.
Neurology 2000;54(12):2325-8.

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