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Variant late infantile neuronal ceroid lipofuscinosis because of CLN1 mutations. [electronic resource] by
- Simonati, Alessandro
- Tessa, Alessandra
- Bernardina, Bernardo Dalla
- Biancheri, Roberta
- Veneselli, Edvige
- Tozzi, Giulia
- Bonsignore, Maria
- Grosso, Salvatore
- Piemonte, Fiorella
- Santorelli, Filippo M
Producer: 20090522
In:
Pediatric neurology vol. 40
Availability: No items available.
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19.
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Clinical and molecular characterization of a patient with interstitial 6q21q22.1 deletion. [electronic resource] by
- Tassano, Elisa
- Mirabelli-Badenier, Marisol
- Veneselli, Edvige
- Puliti, Aldamaria
- Lerone, Margherita
- Vaccari, Carlotta Maria
- Morana, Giovanni
- Porta, Simona
- Gimelli, Giorgio
- Cuoco, Cristina
Producer: 20150608
In:
Molecular cytogenetics vol. 8
Availability: No items available.
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20.
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Response to rituximab in 3 children with opsoclonus-myoclonus syndrome resistant to conventional treatments. [electronic resource] by
- Battaglia, Teresa
- De Grandis, Elisa
- Mirabelli-Badenier, Marisol
- Boeri, Luca
- Morcaldi, Guido
- Barabino, Paola
- Intra, Chiara
- Naselli, Francesca
- Pistoia, Vito
- Veneselli, Edvige
- Conte, Massimo
Producer: 20120612
In:
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 16
Availability: No items available.
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