• 7151 Citations
  • 14 h-Index
1990 …2019
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Fingerprint Dive into the research topics where Michele Carmine Sacco is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 2 Similar Profiles
Prader-Willi Syndrome Medicine & Life Sciences
Uniparental Disomy Medicine & Life Sciences
Italy Medicine & Life Sciences
Therapeutics Medicine & Life Sciences
Insulin-Like Growth Factor I Medicine & Life Sciences
Mycoplasma Pneumonia Medicine & Life Sciences
Bartter Syndrome Medicine & Life Sciences
Mutation Medicine & Life Sciences

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

Research Output 1990 2019

  • 7151 Citations
  • 14 h-Index
  • 45 Article
  • 1 Editorial
  • 1 Review article
2 Citations (Scopus)

A novel dominant-negative FGFR1 variant causes Hartsfield syndrome by deregulating RAS/ERK1/2 pathway

Palumbo, P., Petracca, A., Maggi, R., Biagini, T., Nardella, G., Sacco, M. C., Di Schiavi, E., Carella, M., Micale, L. & Castori, M., Jan 1 2019, In : European Journal of Human Genetics.

Research output: Contribution to journalArticle

MAP Kinase Signaling System
Fibroblast Growth Factor 2
Holoprosencephaly
Exome
Autophagy

Anthropometric characteristics of newborns with Prader-Willi syndrome

Salvatoni, A., Moretti, A., Grugni, G., Agosti, M., Azzolini, S., Bonaita, V., Cianci, P., Corica, D., Crinò, A., Delvecchio, M., Ferraris, S., Greggio, N. A., Iughetti, L., Licenziati, M. R., Madeo, S. F., Nosetti, L., Pajno, R., Rutigliano, I., Sacco, M., Salvatore, S. & 3 others, Scarano, E., Trifirò, G. & Wasniewska, M., Oct 1 2019, In : American journal of medical genetics. Part A. 179, 10, p. 2067-2074 8 p.

Research output: Contribution to journalArticle

Prader-Willi Syndrome
Newborn Infant
Birth Weight
Gestational Age
Mothers

Complications and risk factors for severe outcome in children with measles

Group, SITIP. M. S., Lo Vecchio, A., Krzysztofiak, A., Montagnani, C., Valentini, P., Rossi, N., Garazzino, S., Raffaldi, I., Di Gangi, M., Esposito, S., Vecchi, B., Melzi, M. L., Lanari, M., Zavarise, G., Bosis, S., Valenzise, M., Cazzato, S., Sacco, M., Govoni, M. R., Mozzo, E. & 10 others, Cambriglia, M. D., Bruzzese, E., Di Camillo, C., Pata, D., Graziosi, A., Sala, D., Magurano, F., Villani, A., Guarino, A. & Galli, L., Jan 12 2019, In : Archives of Disease in Childhood.

Research output: Contribution to journalArticle

Measles
C-Reactive Protein
Genotype
Hospitalized Child
Encephalitis

Long QT syndrome in chromosome 7q35q36.3 deletion involving KCNH2 gene: Warning for chlorpheniramine prescription

Di Stolfo, G., Accadia, M., Mastroianno, S., Leone, M. P., Palumbo, O., Palumbo, P., Potenza, D., Maccarone, P., Sacco, M., Russo, A. & Carella, M., Sep 1 2019, In : Molecular Genetics and Genomic Medicine. 7, 9, e855.

Research output: Contribution to journalArticle

Open Access
Chlorpheniramine
Genetic Databases
Long QT Syndrome
Chromosome Deletion
Prescriptions