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3 results for author:"Adobbati L." in Literature citations

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NOTCH3 gene mutations in subjects clinically suspected of CADASIL.

Mosca L., Marazzi R., Ciccone A., Santilli I., Bersano A., Sansone V., Grosso E., Mandrile G., Giachino D.F., Adobbati L. et al.

J. Neurol. Sci. 307:144-148(2011) · Mapped (3)

Free insulin-like growth factor (IGF)-1 and IGF-binding proteins-2 and -3 in serum and cerebrospinal fluid of amyotrophic lateral sclerosis patients.

Corbo M., Lunetta C., Magni P., Dozio E., Ruscica M., Adobbati L., Silani V.

Eur. J. Neurol. 17:398-404(2010) · Mapped (26)

Novel Twinkle (PEO1) gene mutations in Mendelian progressive external ophthalmoplegia.

Virgilio R., Ronchi D., Hadjigeorgiou G.M., Bordoni A., Saladino F., Moggio M., Adobbati L., Kafetsouli D., Tsironi E., Previtali S. et al.

J. Neurol. 255:1384-1391(2008) · UniProtKB (3) · Mapped (14)

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