#spinalmuscularatrophy search results

This is a landmark judgement on #RareDisease therapies , and a boon for many patients with #SpinalMuscularAtrophy @curesmaindia

vinodscaria's tweet image. This is a landmark judgement on #RareDisease therapies , and a boon for many patients with #SpinalMuscularAtrophy @curesmaindia

11 महीने की बच्ची की SC से गुहार, जान बचाने के लिए चाहिए 14 करोड़ का इंजेक्शन, SC ने सरकार से मांगा जवाब #SupremeCourt #Injection #SpinalMuscularAtrophy स्पाइनल मस्क्युलर एट्रोफी (SMA) टाइप 1 नाम की दुर्लभ बीमारी से जूझ रही 11  महीने की बच्ची का जीवन बचाने के लिए सुप्रीम कोर्ट…

ZeeNews's tweet image. 11 महीने की बच्ची की SC से गुहार, जान बचाने के लिए चाहिए 14 करोड़ का इंजेक्शन, SC ने सरकार से मांगा जवाब

#SupremeCourt #Injection #SpinalMuscularAtrophy 

स्पाइनल मस्क्युलर एट्रोफी (SMA) टाइप 1 नाम की दुर्लभ बीमारी से जूझ रही 11  महीने की बच्ची का जीवन बचाने के लिए सुप्रीम कोर्ट…

The main reasons for my interest in reporting on rare diseases is my friendship with @abhi_bioinfo a bioinformatician and professor in Chennai, who is affected by Type 3 #SpinalMuscularAtrophy Was deeply moved by his latest post on FB, which I am sharing with his permission.

nandita_j's tweet image. The main reasons for my interest in reporting on rare diseases is my friendship with @abhi_bioinfo a bioinformatician and professor in Chennai, who is affected by Type 3 #SpinalMuscularAtrophy  
Was deeply moved by his latest post on FB, which I am sharing with his permission.
nandita_j's tweet image. The main reasons for my interest in reporting on rare diseases is my friendship with @abhi_bioinfo a bioinformatician and professor in Chennai, who is affected by Type 3 #SpinalMuscularAtrophy  
Was deeply moved by his latest post on FB, which I am sharing with his permission.
nandita_j's tweet image. The main reasons for my interest in reporting on rare diseases is my friendship with @abhi_bioinfo a bioinformatician and professor in Chennai, who is affected by Type 3 #SpinalMuscularAtrophy  
Was deeply moved by his latest post on FB, which I am sharing with his permission.

NORD and our Member organization @CureSMA honor the memory of Diane Coleman, a dedicated advocate for #SpinalMuscularAtrophy and #DisabilityRights whose work shaped critical conversations about dignity and equity in health care, leaving an enduring legacy in the fight against…

RareDiseases's tweet image. NORD and our Member organization @CureSMA honor the memory of Diane Coleman, a dedicated advocate for #SpinalMuscularAtrophy and #DisabilityRights whose work shaped critical conversations about dignity and equity in health care, leaving an enduring legacy in the fight against…

इंडियन एयरफ़ोर्स के जवान की नन्हीं बच्ची 'SMA' की शिकार #SpinalMuscularAtrophy #BreakingNews #SalaamTV


#SpinalMuscularAtrophy is caused by mutations in SMN1 (encoding survival motor neuron protein). The disease manifests as progressive muscle atrophy and weakness of limb, bulbar, trunk and respiratory muscles. go.nature.com/3Jsg7BM #SMA

DiseasePrimers's tweet image. #SpinalMuscularAtrophy is caused by mutations in SMN1 (encoding survival motor neuron protein). The disease manifests as progressive muscle atrophy and weakness of limb, bulbar, trunk and respiratory muscles.  

go.nature.com/3Jsg7BM 
#SMA

August is #SpinalMuscularAtrophy (SMA) Awareness Month. It's a rare genetic neuromuscular condition that causes progressive muscle weakness and atrophy from the degeneration of nerve cells in the spinal cord. There is a wide and varying spectrum of how severely #SMA affects…

RareRevolutionM's tweet image. August is #SpinalMuscularAtrophy (SMA) Awareness Month. It's a rare genetic neuromuscular condition that causes progressive muscle weakness and atrophy from the degeneration of nerve cells in the spinal cord. There is a wide and varying spectrum of how severely #SMA affects…

As family after family watches their children die awaiting treatment of #RareDisease -a sordid tale of how the govt made a policy that is stuck since 2021, 10 children died, not one got funds be it #spinalmuscularatrophy or #huntersyndrome #hurlersyndrome An exposé @IndiaToday


#SMAMyWay Champion, Martyn, discusses the challenges of transitioning to adulthood with #SpinalMuscularAtrophy. Beyond finding new care assistance, it’s about adapting to new responsibilities and shifting dynamics. Watch and hear Martyn’s experience.🔍 #SMA


The Khyber Pakhtunkhwa (KP) government to providing free treatment for patients with Spinal Muscular Atrophy (SMA), a rare and challenging genetic disorder. #KhyberPakhtunkhwa #SpinalMuscularAtrophy #HealthcareInitiative #DisabilityAwarenes

PakStartup's tweet image. The Khyber Pakhtunkhwa (KP) government to providing free treatment for patients with Spinal Muscular Atrophy (SMA), a rare and challenging genetic disorder. 

#KhyberPakhtunkhwa #SpinalMuscularAtrophy #HealthcareInitiative #DisabilityAwarenes

Special thanks to our wonderful contributors for providing their impactful perspectives on spinal muscular atrophy (SMA) and to Roche for sponsoring this Digital Spotlight. You can read all articles here: rarerevolutionmagazine.com/digital_spotli… #SpinalMuscularAtrophy #SMA

RareRevolutionM's tweet image. Special thanks to our wonderful contributors for providing their impactful perspectives on spinal muscular atrophy (SMA) and to Roche for sponsoring this Digital Spotlight. You can read all articles here: rarerevolutionmagazine.com/digital_spotli… 
#SpinalMuscularAtrophy #SMA

August is #SpinalMuscularAtrophy (SMA) Awareness Month 👶 Every newborn in Ontario is offered screening for SMA & other rare but treatable diseases through Newborn Screening Ontario. Early detection is key to giving babies the best start. Learn more: ontario.ca/page/newborn-s….

ONThealth's tweet image. August is #SpinalMuscularAtrophy (SMA) Awareness Month  👶

Every newborn in Ontario is offered screening for SMA & other rare but treatable diseases through Newborn Screening Ontario.

Early detection is key to giving babies the best start.

Learn more: ontario.ca/page/newborn-s….

🎧 The journey with #SpinalMuscularAtrophy (SMA) is unique for everyone, and the SMA My Way podcast is here to recognise and celebrate that. Join us to listen to the powerful stories of our SMA My Way Champions: spkl.io/60124N6Mr

Roche's tweet image. 🎧 The journey with #SpinalMuscularAtrophy (SMA) is unique for everyone, and the SMA My Way podcast is here to recognise and celebrate that. 

Join us to listen to the powerful stories of our SMA My Way Champions: spkl.io/60124N6Mr
Roche's tweet image. 🎧 The journey with #SpinalMuscularAtrophy (SMA) is unique for everyone, and the SMA My Way podcast is here to recognise and celebrate that. 

Join us to listen to the powerful stories of our SMA My Way Champions: spkl.io/60124N6Mr
Roche's tweet image. 🎧 The journey with #SpinalMuscularAtrophy (SMA) is unique for everyone, and the SMA My Way podcast is here to recognise and celebrate that. 

Join us to listen to the powerful stories of our SMA My Way Champions: spkl.io/60124N6Mr

August is #SpinalMuscularAtrophy (SMA) Awareness Month. Help your baby get the best start with a screening for numerous rare, but treatable diseases, including SMA, through screening available to every newborn in Ontario. Learn more: ontario.ca/page/newborn-s…

ONThealth's tweet image. August is #SpinalMuscularAtrophy (SMA) Awareness Month.

Help your baby get the best start with a screening for numerous rare, but treatable diseases, including SMA, through screening available to every newborn in Ontario.

Learn more:
ontario.ca/page/newborn-s…

एक डेढ़ साल के बच्चे के जानलेवा बीमारी के बीच में अरविंद केजरीवाल और उनकी पार्टी अपना प्रचार और विज्ञापन चला रही है लज्जाजनक 👎🏻 वास्तविकता ये है की लगभग 1.5 लाख लोगों ने मिलकर “crowdfunding” से बच्चे के इंजेक्शन के पैसे जमा किए हैं #ArvindKejriwal #SMA #SpinalMuscularAtrophy

PrakashShriRSS's tweet image. एक डेढ़ साल के बच्चे के जानलेवा बीमारी के बीच में अरविंद केजरीवाल और उनकी पार्टी अपना प्रचार और विज्ञापन चला रही है

लज्जाजनक 👎🏻

वास्तविकता ये है की लगभग 1.5 लाख लोगों ने मिलकर “crowdfunding” से बच्चे के इंजेक्शन के पैसे जमा किए हैं

#ArvindKejriwal #SMA #SpinalMuscularAtrophy
PrakashShriRSS's tweet image. एक डेढ़ साल के बच्चे के जानलेवा बीमारी के बीच में अरविंद केजरीवाल और उनकी पार्टी अपना प्रचार और विज्ञापन चला रही है

लज्जाजनक 👎🏻

वास्तविकता ये है की लगभग 1.5 लाख लोगों ने मिलकर “crowdfunding” से बच्चे के इंजेक्शन के पैसे जमा किए हैं

#ArvindKejriwal #SMA #SpinalMuscularAtrophy
PrakashShriRSS's tweet image. एक डेढ़ साल के बच्चे के जानलेवा बीमारी के बीच में अरविंद केजरीवाल और उनकी पार्टी अपना प्रचार और विज्ञापन चला रही है

लज्जाजनक 👎🏻

वास्तविकता ये है की लगभग 1.5 लाख लोगों ने मिलकर “crowdfunding” से बच्चे के इंजेक्शन के पैसे जमा किए हैं

#ArvindKejriwal #SMA #SpinalMuscularAtrophy

Sidra Medicine, a member of Qatar Foundation, successfully administered a life-saving medication for Malkha Rouhi, a baby diagnosed with Spinal Muscular Atrophy (SMA), a statement said Wednesday. #MalkhaRouhi #SpinalMuscularAtrophy @SidraMedicine gulf-times.com/article/691342…

GulfTimes_QATAR's tweet image. Sidra Medicine, a member of Qatar Foundation, successfully administered a life-saving medication for Malkha Rouhi, a baby diagnosed with Spinal Muscular Atrophy (SMA), a statement said Wednesday.
#MalkhaRouhi #SpinalMuscularAtrophy @SidraMedicine 
gulf-times.com/article/691342…
GulfTimes_QATAR's tweet image. Sidra Medicine, a member of Qatar Foundation, successfully administered a life-saving medication for Malkha Rouhi, a baby diagnosed with Spinal Muscular Atrophy (SMA), a statement said Wednesday.
#MalkhaRouhi #SpinalMuscularAtrophy @SidraMedicine 
gulf-times.com/article/691342…

We are honoured to welcome Manasa Varanasi,Femina Miss India 2020,as the Brand Ambassador of #CureSMAIndia! She joins us in raising awareness for #SpinalMuscularAtrophy (SMA) and supporting thousands of families across India in our #BattleAgainstSMA Welcome to the family, Manasa!


As six-month-old baby girl Ibaadat Kaur suffers from rare Spinal Muscular Atrophy (SMA Type-1), the treatment cost, which is in crores, has left the family shocked and in tears #ReporterDiary #SpinalMuscularAtrophy (@AseemBassi)


For columnist Alyssa Silva, control has always been her safety net. But in reality, it doesn't protect her; it exhausts her. buff.ly/kmofZFo #SpinalMuscularAtrophy #SMAResearch #SMANewsToday #SMANews #SMATreatment #Bionews


Most children SMA type 1 can survive an episode of pARDS, a life-threatening respiratory failure, under standard protocols, per a case series. buff.ly/FdxJro2 #SpinalMuscularAtrophy #SMAResearch #SMANewsToday #SMANews #SMATreatment #Bionews


Hello Well Wishers, Kindly Donate Share Repost, Rudraunsh SMA Fundraiser #saverudraunsh #smaawareness #spinalmuscularatrophy #9crores #communityforacause

Rudraunsh_SMA2's tweet image. Hello Well Wishers,
Kindly Donate Share Repost, Rudraunsh SMA Fundraiser 
#saverudraunsh #smaawareness #spinalmuscularatrophy #9crores #communityforacause

#SpinalMuscularAtrophy (SMA) has long been defined as a neuromuscular disorder, caused by homozygous loss or mutation of the #SMN1Gene, leading to reduced survival motor neuron (#SMN) protein. Learn more: bit.ly/3WxZOe5 #RareDisease #SMA #Neurology


The change of seasons brings colder weather, meaning columnist Connie Chandler must seek to adapt to her changing physical needs. buff.ly/ecESSvg #SpinalMuscularAtrophy #SMAResearch #SMANewsToday #SMANews #SMATreatment #Bionews


This is a landmark judgement on #RareDisease therapies , and a boon for many patients with #SpinalMuscularAtrophy @curesmaindia

vinodscaria's tweet image. This is a landmark judgement on #RareDisease therapies , and a boon for many patients with #SpinalMuscularAtrophy @curesmaindia

My name is Nadja and I have lived with #SpinalMuscularAtrophy since birth. I embraced my near-death experience, turning my disability into a path of growth. Without this way of thinking, I would never be where I am today. #IamUnique #RareDisease #SMAAwareness

SMA_UK_'s tweet image. My name is Nadja and I have lived with #SpinalMuscularAtrophy since birth.

I embraced my near-death experience, turning my disability into a path of growth. Without this way of thinking, I would never be where I am today.

#IamUnique #RareDisease #SMAAwareness
SMA_UK_'s tweet image. My name is Nadja and I have lived with #SpinalMuscularAtrophy since birth.

I embraced my near-death experience, turning my disability into a path of growth. Without this way of thinking, I would never be where I am today.

#IamUnique #RareDisease #SMAAwareness

A research team led by #geneediting pioneer @davidrliu has published how it has applied the technology to develop a one-time treatment for #spinalmuscularatrophy that showed effectiveness in cell and mouse models. Learn more: ow.ly/37o950NwnsN

GENbio's tweet image. A research team led by #geneediting pioneer @davidrliu has published how it has applied the technology to develop a one-time treatment for #spinalmuscularatrophy that showed effectiveness in cell and mouse models. Learn more: ow.ly/37o950NwnsN

11 महीने की बच्ची की SC से गुहार, जान बचाने के लिए चाहिए 14 करोड़ का इंजेक्शन, SC ने सरकार से मांगा जवाब #SupremeCourt #Injection #SpinalMuscularAtrophy स्पाइनल मस्क्युलर एट्रोफी (SMA) टाइप 1 नाम की दुर्लभ बीमारी से जूझ रही 11  महीने की बच्ची का जीवन बचाने के लिए सुप्रीम कोर्ट…

ZeeNews's tweet image. 11 महीने की बच्ची की SC से गुहार, जान बचाने के लिए चाहिए 14 करोड़ का इंजेक्शन, SC ने सरकार से मांगा जवाब

#SupremeCourt #Injection #SpinalMuscularAtrophy 

स्पाइनल मस्क्युलर एट्रोफी (SMA) टाइप 1 नाम की दुर्लभ बीमारी से जूझ रही 11  महीने की बच्ची का जीवन बचाने के लिए सुप्रीम कोर्ट…

Patients with #SpinalMuscularAtrophy have deletions or point mutations in both copies of SMN1 (encoding survival motor neuron protein) go.nature.com/3vEwVQo

DiseasePrimers's tweet image. Patients with #SpinalMuscularAtrophy have deletions or point mutations in both copies of SMN1 (encoding survival motor neuron protein) go.nature.com/3vEwVQo

One-Time Treatment: Base Editing Shows Promise vs. SMA A team led by @davidrliu has published how it has applied #baseediting to develop a one-time treatment for #spinalmuscularatrophy that showed effectiveness in cell and mouse models. Read more: ow.ly/37o950NwnsN

GENbio's tweet image. One-Time Treatment: Base Editing Shows Promise vs. SMA

A team led by @davidrliu has published how it has applied #baseediting to develop a one-time treatment for #spinalmuscularatrophy that showed effectiveness in cell and mouse models. Read more: ow.ly/37o950NwnsN

Well worth watching/listening to (yes I'm biased ... But it's very interesting and informative) #podcasts #youtube #spinalmuscularatrophy #twins @Sammy_Bolts_05 @alexbolty05 @SMA_UK_

auntierarer's tweet image. Well worth watching/listening to (yes I'm biased ... But it's very interesting and informative) #podcasts #youtube #spinalmuscularatrophy #twins @Sammy_Bolts_05 @alexbolty05 @SMA_UK_

Actors with #SpinalMuscularAtrophy star in new musical, "Most Likely Not To...,” now streaming: bit.ly/3IYaMmd #BrainAndLife

BrainandLifeMag's tweet image. Actors with #SpinalMuscularAtrophy star in new musical, "Most Likely Not To...,” now streaming: bit.ly/3IYaMmd

#BrainAndLife

Medicare rebated genetic tests are now available to determine carrier status of #cysticfibrosis #spinalmuscularatrophy and #fragilex for anyone planning or in the early stages of pregnancy. Learn more about reproductive carrier screening here genetics.edu.au/SitePages/Repr… @ACRRM @RACGP

CGE_HETI's tweet image. Medicare rebated genetic tests are now available to determine carrier status of #cysticfibrosis #spinalmuscularatrophy and #fragilex for anyone planning or in the early stages of pregnancy. Learn more about reproductive carrier screening here genetics.edu.au/SitePages/Repr… @ACRRM @RACGP

Recent discovery from the lab of Yongchao C. Ma, PhD, offers a novel approach to developing a safer, more effective treatment for children with spinal muscular atrophy. luriechildrens.org/en/news-storie… @LurieChildrens @NUFeinbergMed #Neurology #pediatricresearch #spinalmuscularatrophy

ManneResearch's tweet image. Recent discovery from the lab of Yongchao C. Ma, PhD, offers a novel approach to developing a safer, more effective treatment for children with spinal muscular atrophy. luriechildrens.org/en/news-storie… @LurieChildrens @NUFeinbergMed #Neurology #pediatricresearch #spinalmuscularatrophy

NORD and our Member organization @CureSMA honor the memory of Diane Coleman, a dedicated advocate for #SpinalMuscularAtrophy and #DisabilityRights whose work shaped critical conversations about dignity and equity in health care, leaving an enduring legacy in the fight against…

RareDiseases's tweet image. NORD and our Member organization @CureSMA honor the memory of Diane Coleman, a dedicated advocate for #SpinalMuscularAtrophy and #DisabilityRights whose work shaped critical conversations about dignity and equity in health care, leaving an enduring legacy in the fight against…

Via @GreenJournal: Adding #NewbornScreening for #SpinalMuscularAtrophy to best practice recommendations for diagnosis of the condition is the first step to improving outcomes for patients: bit.ly/455KCbI #NeuroTwitter @AANMember

NeurologyToday's tweet image. Via @GreenJournal: Adding #NewbornScreening for #SpinalMuscularAtrophy to best practice recommendations for diagnosis of the condition is the first step to improving outcomes for patients: bit.ly/455KCbI

#NeuroTwitter @AANMember

#SpinalMuscularAtrophy is caused by mutations in SMN1 (encoding survival motor neuron protein). The disease manifests as progressive muscle atrophy and weakness of limb, bulbar, trunk and respiratory muscles. go.nature.com/3Jsg7BM #SMA

DiseasePrimers's tweet image. #SpinalMuscularAtrophy is caused by mutations in SMN1 (encoding survival motor neuron protein). The disease manifests as progressive muscle atrophy and weakness of limb, bulbar, trunk and respiratory muscles.  

go.nature.com/3Jsg7BM 
#SMA

Via @GreenJournal: Patients with #SpinalMuscularAtrophy will inevitably lose a high degree of motor function, and those with types 2 and 3 who go untreated risk losing motor milestones during late adulthood: bit.ly/46xFkog #NeuroTwitter @AANMember #SMAawareness

NeurologyToday's tweet image. Via @GreenJournal: Patients with #SpinalMuscularAtrophy will inevitably lose a high degree of motor function, and those with types 2 and 3 who go untreated risk losing motor milestones during late adulthood: bit.ly/46xFkog

#NeuroTwitter @AANMember #SMAawareness

Via @GreenJournal: Patients with later-onset types 2 and 3 #SpinalMuscularAtrophy saw their motor function improve after treatment with apitegromab: bit.ly/3OyLX3p #NeuroTwitter #SMAawareness @AANMember

NeurologyToday's tweet image. Via @GreenJournal: Patients with later-onset types 2 and 3 #SpinalMuscularAtrophy saw their motor function improve after treatment with apitegromab: bit.ly/3OyLX3p

#NeuroTwitter #SMAawareness @AANMember

My continued biological education The physiology of #AlternativeSplicing 🦇TRPV1 AS-infrared sensing😍 Antisense oligonucleotides control AS to treat #SpinalMuscularAtrophy #DuchenneMuscularDystrophy @unvivodito Alberto Kornblihtt @NatRevMCB 2023 nature.com/articles/s4158…

HaoYin20's tweet image. My continued biological education

The physiology of #AlternativeSplicing

🦇TRPV1 AS-infrared sensing😍

Antisense oligonucleotides control AS to treat #SpinalMuscularAtrophy
#DuchenneMuscularDystrophy

@unvivodito Alberto Kornblihtt @NatRevMCB 2023 
nature.com/articles/s4158…

MDC and @NMD4Canada are pleased to invite you to a webinar on newborn screening for neuromuscular conditions, with a focus on #SpinalMuscularAtrophy and #PompeDisease. Please join us on 🗓: Tuesday, April 2, 2024 🕐: 5:00 pm ET 🔗: muscle.ca/discover-md/we…

MD_Canada's tweet image. MDC and @NMD4Canada are pleased to invite you to a webinar on newborn screening for neuromuscular conditions, with a focus on #SpinalMuscularAtrophy and #PompeDisease.

Please join us on
🗓: Tuesday, April 2, 2024
🕐: 5:00 pm ET
🔗: muscle.ca/discover-md/we…

முதுகெலும்பு தசைநார் வலுவிழப்பு நோயால் பாதிக்கப்பட்டுள்ள 5 மாதக் குழந்தையை காப்பாற்ற உதவிக்கரம் கோரும் பெற்றோர்! #SpinalMuscularAtrophy | #SMA | #Thiruvarur | @CMOTamilnadu | @Subramanian_ma | @CollectorTVR

PttvNewsX's tweet image. முதுகெலும்பு தசைநார் வலுவிழப்பு நோயால் பாதிக்கப்பட்டுள்ள 5 மாதக் குழந்தையை காப்பாற்ற உதவிக்கரம் கோரும் பெற்றோர்!

#SpinalMuscularAtrophy | #SMA | #Thiruvarur | @CMOTamilnadu | @Subramanian_ma | @CollectorTVR

സ്‌പൈനൽ മസ്കുലാർ അട്രോഫി മരുന്നുകളുടെ വില കുറയ്ക്കാന്‍ അടിയന്തര നടപടി വേണമെന്ന് കേന്ദ്ര സര്‍ക്കാരിനോട് ഹൈക്കോടതി. #spinalmuscularatrophy #HighCourt #CentralGovernment #medicines #newsmalayalamtv #newsmalayalam24x7

newsmalayalamtv's tweet image. സ്‌പൈനൽ മസ്കുലാർ അട്രോഫി മരുന്നുകളുടെ വില കുറയ്ക്കാന്‍ അടിയന്തര നടപടി വേണമെന്ന് കേന്ദ്ര സര്‍ക്കാരിനോട് ഹൈക്കോടതി.

#spinalmuscularatrophy #HighCourt #CentralGovernment #medicines #newsmalayalamtv #newsmalayalam24x7

Loading...

Something went wrong.


Something went wrong.


United States Trends