Simona Di Modica @simonadimodica

Regulation of Iron Metabolism Unit, Ospedale San Raffaele Joined November 2012

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touchHAEMATOLOGY @touchHAEMA

a month ago

🩸We’re delighted to spotlight Dr Simona Maria Di Modica as a touchHAEMATOLOGY Future Leader 2025 @simonadimodica In this feature, Dr Di Modica shares her inspirations, and the lessons learned from both successful and unexpected experimental outcomes. touchhaematology.com/insight/4-ques…

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BioIronSocial @BioIronSocial

a year ago

Commentary on the combo therapies studies for b-thalassemia from Rivella’s and Nai’s labs! Have a look! onlinelibrary.wiley.com/doi/epdf/10.10…

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BioIronSocial @BioIronSocial

a year ago

Tribute to Clara Camaschella by all her colleagues in the iron field: such dedication and commitment, as well as integrity and perseverance are the best example to the next generation of scientists pursuing a career in our field! Thanks Clara for all you have done!

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Università Vita-Salute San Raffaele @MyUniSR

2 years ago

A study by #UniSR and @SanRaffaeleMI unveils a mechanism of FKBP12 in modulating the BMP-SMAD pathway activation. The research, published in @AjHematology, may offer tools for treating diseases such as hemochromatosis and beta-thalassemia. Read more: hubs.ly/Q01QQRl00

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AmericanJournalofHematology @AjHematology

3 years ago

✨Congratulations to our 2022 Young Investigator Award winner, @simonadimodica ✨

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AmericanJournalofHematology @AjHematology

3 years ago

Genetic Tfr2 deletion in the bone marrow improves anemia and abolishes blood transfusion requirement in transfusion-dependent β-thalassemia mice. onlinelibrary.wiley.com/doi/epdf/10.10…

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Kevin Kuo @CaptainAV

3 years ago

Bone marrow Tfr2 deletion and RAP-536 synergistically improves anemia, ineffective erythropoiesis and splenomegaly in Hbbth3/- mice #EHA2022 Nai A, et al., HemaSphere, 2022;6:(S3):S271

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Università Vita-Salute San Raffaele @MyUniSR

4 years ago

Dr. @simonadimodica, researcher @MyUniSR, has won the Under40 in #Hematology Best Poster Award. Her project is supported by @FondCariplo funding received by her supervisor, @AntonellaNai83: ➡️ hubs.ly/H0_WFsv0

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Karra Jones, MD, PhD @BrainIsThePath

7 years ago

Central core myopathy. Central cores seen on H&E, phosphotungstic acid-hematoxylin (PTAH), and COX-SDH. The most common mutations leading to central core disease occur in the RYR1 gene or less commonly the SEPN1 gene. #neuropath #musclepath