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Ultrastructural Localization of Gelsolin in Lattice Corneal Dystrophy Type I.
Published in:
Ophthalmologica, 1998, v. 212, n. 6, p. 415, doi. 10.1159/000027379
By:
- Longanesi, Lora;
- Cavallini, Gian Maria;
- Iammarino, Antonello;
- Vaccina, Fabiana;
- Guerra, Roberto;
- De Pol, Anto
Publication type:
Article
Autoantibody Profile of a Cohort of 78 Italian Patients with Mucous Membrane Pemphigoid: Correlation Between Reactivity Profile and Clinical Involvement.
Published in:
Acta Dermato-Venereologica, 2016, v. 96, n. 6, p. 768, doi. 10.2340/00015555-2311
By:
- COZZANI, Emanuele;
- DI ZENZO, Giovanni;
- CALABRESI, Valentina;
- CARROZZO, Marco;
- BURLANDO, Martina;
- LONGANESI, Lora;
- CERRI, Amilcare;
- CAPRONI, Marzia;
- SERA, Francesco;
- ANTIGA, Emiliano;
- QUAGLINO, Pietro;
- MARZANO, Angelo V.;
- PARODI, Aurora
Publication type:
Article
Deficit of in vivo mitochondrial ATP production in OPA1‐related dominant optic atrophy.
Published in:
Annals of Neurology, 2004, v. 56, n. 5, p. 719
By:
- Raffaele Lodi;
- Caterina Tonon;
- Maria Lucia Valentino;
- Stefano Iotti;
- Valeria Clementi;
- Emil Malucelli;
- Piero Barboni;
- Lora Longanesi;
- Simone Schimpf;
- Bernd Wissinger;
- Agostino Baruzzi;
- Bruno Barbiroli;
- Valerio Carelli
Publication type:
Article
A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 10, p. 1893, doi. 10.1093/hmg/ddr071
By:
- Carelli, Valerio;
- Schimpf, Simone;
- Fuhrmann, Nico;
- Valentino, Maria Lucia;
- Zanna, Claudia;
- Iommarini, Luisa;
- Papke, Monika;
- Schaich, Simone;
- Tippmann, Sabine;
- Baumann, Britta;
- Barboni, Piero;
- Longanesi, Lora;
- Rugolo, Michela;
- Ghelli, Anna;
- Alavi, Marcel V.;
- Youle, Richard J.;
- Bucchi, Laura;
- Carroccia, Rosanna;
- Giannoccaro, Maria Pia;
- Tonon, Caterina
Publication type:
Article

Found: 4

Ultrastructural Localization of Gelsolin in Lattice Corneal Dystrophy Type I.

Autoantibody Profile of a Cohort of 78 Italian Patients with Mucous Membrane Pemphigoid: Correlation Between Reactivity Profile and Clinical Involvement.

Deficit of in vivo mitochondrial ATP production in OPA1‐related dominant optic atrophy.

A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16.