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Mashup Score: 0
The Global Paroxysmal Nocturnal Hemoglobinuria (PNH) Patient Registry registry powered by NORD platform.
Source: pnh.iamrare.orgCategories: Latest Headlines, Rare DiseaseTweet
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Mashup Score: 0
The Global Paroxysmal Nocturnal Hemoglobinuria (PNH) Patient Registry registry powered by NORD platform.
Source: pnh.iamrare.orgCategories: Latest Headlines, Rare DiseaseTweet-
This year for #PNH Awareness Week, let's push #research forward! Join the Global PNH Patient Registry to help contribute to PNH research! https://t.co/j63ABXJern https://t.co/hmgfxjszvK
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Mashup Score: 0
The Global Paroxysmal Nocturnal Hemoglobinuria (PNH) Patient Registry registry powered by NORD platform.
Source: pnh.iamrare.orgCategories: Latest Headlines, Rare DiseaseTweet-
Have you been wondering how to get involved with PNH research but did not know where to start? Here’s your chance! Check out the Global PNH Patient Registry at https://t.co/ZHcXJ0yg6B
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Mashup Score: 3
The Global Paroxysmal Nocturnal Hemoglobinuria (PNH) Patient Registry registry powered by NORD platform.
Source: pnh.iamrare.orgCategories: Latest Headlines, Rare DiseaseTweet-
Make a mark on the future of research by enrolling in the Global PNH Patient Registry! Participation can be done at your own pace and is open to anyone with a paroxysmal nocturnal hemoglobinuria (PNH) diagnosis: https://t.co/Wo9cOrLtCh
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Mashup Score: 4
The Global Paroxysmal Nocturnal Hemoglobinuria (PNH) Patient Registry registry powered by NORD platform.
Source: pnh.iamrare.orgCategories: Latest Headlines, Rare DiseaseTweet-
For PNH awareness week October 10-17, we are encouraging anyone with PNH to join the Global PNH Patient Registry at https://t.co/ZHcXJ0yg6B
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Mashup Score: 2
The Global Paroxysmal Nocturnal Hemoglobinuria (PNH) Patient Registry registry powered by NORD platform.
Source: pnh.iamrare.orgCategories: Latest Headlines, Rare DiseaseTweet-
This year for PNH Awareness Week, we are excited to push research forward! Join the Global PNH Patient Registry to help contribute to PNH research! https://t.co/ZHcXJ0yg6B
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Mashup Score: 0
The Global Paroxysmal Nocturnal Hemoglobinuria (PNH) Patient Registry registry powered by NORD platform.
Source: pnh.iamrare.orgCategories: Latest Headlines, Rare DiseaseTweet-
PNH Awareness Week is coming up on Oct 10-17, 2021! Raise awareness and enhance research efforts by joining the Global PNH Patient Registry at https://t.co/ZHcXJ0yg6B
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Mashup Score: 2
The Global Paroxysmal Nocturnal Hemoglobinuria (PNH) Patient Registry registry powered by NORD platform.
Source: pnh.iamrare.orgCategories: Latest Headlines, Rare DiseaseTweet-
For PNH awareness week, we are encouraging anyone with PNH to join the Global PNH Patient Registry at https://t.co/ZHcXJ0yg6B
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-
Mashup Score: 2
The Global Paroxysmal Nocturnal Hemoglobinuria (PNH) Patient Registry registry powered by NORD platform.
Source: pnh.iamrare.orgCategories: Latest Headlines, Rare DiseaseTweet-
Drive paroxysmal nocturnal hemoglobinuria (PNH) research forward! Sign up for the Global PNH Patient Registry at https://t.co/ZHcXJ0yg6B
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-
Mashup Score: 0
The Global Paroxysmal Nocturnal Hemoglobinuria (PNH) Patient Registry registry powered by NORD platform.
Source: pnh.iamrare.orgCategories: Latest Headlines, Rare DiseaseTweet-
Have you been wondering how to get involved with PNH research but did not know where to start? Here’s your chance! Check out the Global PNH Patient Registry at https://t.co/ZHcXJ0yg6B
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Have you ever been diagnosed with #ParoxysmalNocturnalHemoglobinuria (#PNH)? Consider enrolling in our global registry today! Research moves forward when patients share their experience. https://t.co/EgBjcFvgTA https://t.co/0cC4LSfFk8