Reena Kartha(@rvkartha) 's Twitter Profileg
Reena Kartha

@rvkartha

#RareDisease Translational Pharmacology Researcher @UMN_Pharmacy, Center for Orphan Drug Research, views my own

ID:875444659522224128

linkhttps://www.pharmacy.umn.edu/centers-and-institutes/center-orphan-drug-research calendar_today15-06-2017 20:07:26

467 Tweets

214 Followers

321 Following

Reena Kartha(@rvkartha) 's Twitter Profile Photo

I am pleased to be Faculty at the Annual Meeting, Sept 8 – 10, 2024 as part of Hot Topics: Advancements in Antisense Oligonucleotide Development: Challenges, Strategies & Novel Approaches on 9/10/2024. Hope you can attend UMN Pharmacy UMN Experimental and Clinical Pharmacology Mila's Miracle IndoUSrare

I am pleased to be Faculty at the #2024ACCP Annual Meeting, Sept 8 – 10, 2024 as part of Hot Topics: Advancements in Antisense Oligonucleotide Development: Challenges, Strategies & Novel Approaches on 9/10/2024. Hope you can attend @UMN_Pharmacy @UMN_ECP @stopbatten @indousrare
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IndoUSrare(@indousrare) 's Twitter Profile Photo

Apply to be a speaker - bit.ly/bridge4rarespe…
🌐 Connecting the Global Rare Disease Community
🗓️ October 29-30, 2023
📍 George Mason University, Arlington, VA, USA
More event information at - indousrare.org/summit

Apply to be a speaker - bit.ly/bridge4rarespe… 🌐 Connecting the Global Rare Disease Community 🗓️ October 29-30, 2023 📍 George Mason University, Arlington, VA, USA More event information at - indousrare.org/summit #speaker #invitation #bridge4rare #bridgingrare
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Harsha K Rajasimha(@Harsharajasimha) 's Twitter Profile Photo

👉 Join us for Rare Disease Day with Abbey Meyers Listen live to the legend who started the revolution with the US Orphan Drug Act of 1983
- mailchi.mp/indousrare/rar…

👉 Join us for Rare Disease Day with Abbey Meyers Listen live to the legend who started the #RARE revolution with the US Orphan Drug Act of 1983 #indousrare #rarediseaseday #OrphanDrugAct #rarediseaselegend #art4rare #science4rare - mailchi.mp/indousrare/rar…
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M Health Fairview Pediatrics(@mhfvpediatrics) 's Twitter Profile Photo

On Rare Disease Day, join UMN Pharmacy's event to learn from a panel of experts who serve underrepresented communities living with , and listen to keynote speaker and genetic counselor Amy Gaviglio, MS, CGC. Register here. ➡️ bit.ly/3jsCBKu

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IndoUSrare(@indousrare) 's Twitter Profile Photo

Experience the power of art and the beauty of through children's eyes!
Last year, by IndoUSrare brought together art submissions from all around the world.
These amazing works have inspired us to keep fighting for a better world.
bit.ly/art4rare2023

Experience the power of art and the beauty of #rarediseases through children's eyes! Last year, #Art4Rare by @indousrare brought together art submissions from all around the world. These amazing works have inspired us to keep fighting for a better world. bit.ly/art4rare2023
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IndoUSrare(@indousrare) 's Twitter Profile Photo

IndoUSrare is partnering with Ginkgo Leaf Rare Disease Family Care Center and Engage Health Inc. to better understand the motivators and deterrents for rare disease patients and their caregivers when considering participation in a clinical trial.

Click👉tinyurl.com/indousrare

@indousrare is partnering with Ginkgo Leaf Rare Disease Family Care Center and @EngageHealthInc to better understand the motivators and deterrents for rare disease patients and their caregivers when considering participation in a clinical trial. Click👉tinyurl.com/indousrare
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UMN Experimental and Clinical Pharmacology(@UMN_ECP) 's Twitter Profile Photo

📌Get your FREE tickets 🎟 here to see this production in collaboration with the UMN Experimental and Clinical Pharmacology Center for Orphan Drug Research 💊!

📌Upcoming Twin cities shows on October 8 and 10! Reena Kartha UMN Pharmacy

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IndoUSrare(@indousrare) 's Twitter Profile Photo

Register for the Motor Neuron Disease Day event cohosted by Indousrare, @NIMHANS and Tust.

Best Practices for Patient Registries in the Indian Context

Free registration for all
bit.ly/mndday-indousr…
Spread the word

Register for the Motor Neuron Disease Day event cohosted by Indousrare, @NIMHANS and #MND Tust. #ALS #MOTORNEURONDISEASE Best Practices for Patient Registries in the Indian Context Free registration for all bit.ly/mndday-indousr… Spread the word
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Rare Disease and Orphan Drugs Journal(@OAE_RDODJ) 's Twitter Profile Photo

🔔🔔🔔Call for papers! A new special issue 'Neutrophil Serine Proteases in Rare Diseases' edited by Dr. Brice Korkmaz Brice Korkmaz CEPR_Pathophysiology_Respiratory_Infections @UnivTours Inserm is CALLING FOR PAPERS!
👇👇👇
rdodjournal.com/journal/specia…

🔔🔔🔔Call for papers! A new special issue 'Neutrophil Serine Proteases in Rare Diseases' edited by Dr. Brice Korkmaz @bricekorkmaz @CEPR_Inf_Immun @UnivTours @Inserm is CALLING FOR PAPERS! 👇👇👇 rdodjournal.com/journal/specia…
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