검색결과 : 6건
| No. | Article |
|---|---|
| 1 |
Involvement of the mitochondrial compartment in human NCL fibroblasts Pezzini F, Gismondi F, Tessa A, Tonin P, Carrozzo R, Mole SE, Santorelli FM, Simonati A Biochemical and Biophysical Research Communications, 416(1-2), 159, 2011 |
| 2 |
Variant late infantile ceroid lipofuscinoses associated with novel mutations in CLN6 Cannelli N, Garavaglia B, Simonati A, Aiello C, Barzaghi C, Pezzini F, Cilio MR, Biancheri R, Morbin M, Bernardina BD, Granata T, Tessa A, Invernizzi F, Pessagno A, Boldrini R, Zibordi F, Grazian L, Claps D, Carrozzo R, Mole SE, Nardocci N, Santorelli FM Biochemical and Biophysical Research Communications, 379(4), 892, 2009 |
| 3 |
Identification of a new mtDNA mutation (14724G > A) associated with mitochondrial leukoencephalopathy Pereira C, Nogueira C, Barbot C, Tessa A, Soares C, Fattori F, Guimaraes A, Santorelli FM, Vilarinho L Biochemical and Biophysical Research Communications, 354(4), 937, 2007 |
| 4 |
The NDUFB11 gene is not a modifier in Leber hereditary optic neuropathy Petruzzella V, Tessa A, Torraco A, Fattori F, Dotti MT, Bruno C, Cardaioli E, Papa S, Federico A, Santorelli FM Biochemical and Biophysical Research Communications, 355(1), 181, 2007 |
| 5 |
POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changes Biancheri R, Falace A, Tessa A, Pedernonte M, Scapolan S, Cassandrini D, Aiello C, Rossi A, Broda P, Zara F, Santorelli FM, Minetti C, Bruno C Biochemical and Biophysical Research Communications, 363(4), 1033, 2007 |
| 6 |
A new method for analysis of mitochondrial DNA point mutations and assess levels of heteroplasmy Cassandrini D, Calevo MG, Tessa A, Manfredi G, Fattori F, Meschini MC, Carrozzo R, Tonoli E, Pedemonte M, Minetti C, Zara F, Santorelli FM, Bruno C Biochemical and Biophysical Research Communications, 342(2), 387, 2006 |