• 276 Citations
  • 8 h-Index
20132019
If you made any changes in Pure these will be visible here soon.

Fingerprint Dive into the research topics where Maurizio Rondinelli is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 6 Similar Profiles
Glucagon-Like Peptide 1 Medicine & Life Sciences
Type 2 Diabetes Mellitus Medicine & Life Sciences
Liddle Syndrome Medicine & Life Sciences
Mutation Medicine & Life Sciences
Induced Pluripotent Stem Cells Medicine & Life Sciences
RNA Splice Sites Medicine & Life Sciences
pioglitazone Medicine & Life Sciences
Hypoglycemia Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 2013 2019

  • 276 Citations
  • 8 h-Index
  • 18 Article

Generation of Human-Induced Pluripotent Stem Cells from Wolfram Syndrome Type 2 Patients Bearing the c.103 + 1G>A CISD2 Mutation for Disease Modeling

La Spada, A., Ntai, A., Genovese, S., Rondinelli, M., De Blasio, P. & Biunno, I., Feb 15 2018, In : Stem Cells and Development. 27, 4, p. 287-295 9 p.

Research output: Contribution to journalArticle

Induced Pluripotent Stem Cells
Wolfram Syndrome
Mutation
Premature Aging
Optic Atrophy
3 Citations (Scopus)

Generation of Human-Induced Pluripotent Stem Cells from Wolfram Syndrome Type 2 Patients Bearing the c.103 + 1G>A CISD2 Mutation for Disease Modeling

La Spada, A., Ntai, A., Genovese, S., Rondinelli, M., De Blasio, P. & Biunno, I., Feb 15 2018, In : Stem Cells and Development. 27, 4, p. 287-295 9 p.

Research output: Contribution to journalArticle

Induced Pluripotent Stem Cells
Wolfram Syndrome
Mutation
Premature Aging
Optic Atrophy
2 Citations (Scopus)

Three reportedly unrelated families with liddle syndrome inherited from a common ancestor

Pagani, L., Diekmann, Y., Sazzini, M., De Fanti, S., Rondinelli, M., Farnetti, E., Casali, B., Caretto, A., Novara, F., Zuffardi, O., Garagnani, P., Mantero, F., Thomas, M. G., Luiselli, D. & Rossi, E., Feb 1 2018, In : Hypertension. 71, 2, p. 273-279 7 p.

Research output: Contribution to journalArticle

Liddle Syndrome
Y Chromosome
Mitochondrial DNA
Alleles
Epithelial Sodium Channels

Three Reportedly Unrelated Families With Liddle Syndrome Inherited From a Common Ancestor

Pagani, L., Diekmann, Y., Sazzini, M., De Fanti, S., Rondinelli, M., Farnetti, E., Casali, B., Caretto, A., Novara, F., Zuffardi, O., Garagnani, P., Mantero, F., Thomas, M. G., Luiselli, D. & Rossi, E., Feb 2018, In : Hypertension. 71, 2, p. 273-279 7 p.

Research output: Contribution to journalArticle

Liddle Syndrome
Y Chromosome
Mitochondrial DNA
Alleles
Epithelial Sodium Channels