Emanuele Bellacchio
Bambino Gesù Children's Hospital(IT)Istituti di Ricovero e Cura a Carattere Scientifico(IT)
Publications by Year
Research Areas
Mitochondrial Function and Pathology, Genetic Neurodegenerative Diseases, Metabolism and Genetic Disorders, Porphyrin and Phthalocyanine Chemistry, Connective tissue disorders research
Most-Cited Works
- → Mitochondrial import and enzymatic activity of PINK1 mutants associated to recessive parkinsonism(2005)443 cited
- → Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome(2006)401 cited
- → Absence of Mn-Centered Oxidation in the S2→ S3Transition: Implications for the Mechanism of Photosynthetic Water Oxidation(2001)303 cited
- → Template-Imprinted Chiral Porphyrin Aggregates(1998)152 cited
- → NF1 Gene Mutations Represent the Major Molecular Event Underlying Neurofibromatosis-Noonan Syndrome(2005)151 cited
- → AHI1 gene mutations cause specific forms of Joubert syndrome–related disorders(2006)138 cited