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Archive for category: treatment

Duchenne and Becker, News2, treatment

In a long-term study, new data show that Givinostat continues to delay the progression of Duchenne disease.

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August 24, 2021/0 Comments/by admin
https://neuromuscular-iran.ir/wp-content/uploads/2021/02/logo_neuromuscular-300x138.png 0 0 admin https://neuromuscular-iran.ir/wp-content/uploads/2021/02/logo_neuromuscular-300x138.png admin2021-08-24 13:37:292022-07-02 10:31:53In a long-term study, new data show that Givinostat continues to delay the progression of Duchenne disease.
News2, treatment

RGX-202 for the treatment of Duchenne muscular dystrophy (DMD)

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August 16, 2021/0 Comments/by admin
https://neuromuscular-iran.ir/wp-content/uploads/2021/02/logo_neuromuscular-300x138.png 0 0 admin https://neuromuscular-iran.ir/wp-content/uploads/2021/02/logo_neuromuscular-300x138.png admin2021-08-16 08:56:582021-08-23 11:39:49RGX-202 for the treatment of Duchenne muscular dystrophy (DMD)
Muscular dystrophy, News2, treatment

Approval of accelerated treatment of voiltolarsen for Duchenne muscular dystrophy by the FDA

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August 16, 2021/0 Comments/by admin
https://neuromuscular-iran.ir/wp-content/uploads/2021/02/logo_neuromuscular-300x138.png 0 0 admin https://neuromuscular-iran.ir/wp-content/uploads/2021/02/logo_neuromuscular-300x138.png admin2021-08-16 08:31:292021-08-23 11:40:08Approval of accelerated treatment of voiltolarsen for Duchenne muscular dystrophy by the FDA
News2, treatment

Losmapimod for FSHD patients by Fulcrum

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August 16, 2021/0 Comments/by admin
https://neuromuscular-iran.ir/wp-content/uploads/2021/02/logo_neuromuscular-300x138.png 0 0 admin https://neuromuscular-iran.ir/wp-content/uploads/2021/02/logo_neuromuscular-300x138.png admin2021-08-16 08:11:222022-07-02 10:37:12Losmapimod for FSHD patients by Fulcrum
Muscular dystrophy, News2, treatment

Exondys 51 or eteplirsen for the treatment of patients with Duchenne Exon 51

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August 16, 2021/0 Comments/by admin
https://neuromuscular-iran.ir/wp-content/uploads/2021/02/logo_neuromuscular-300x138.png 0 0 admin https://neuromuscular-iran.ir/wp-content/uploads/2021/02/logo_neuromuscular-300x138.png admin2021-08-16 08:02:122021-08-23 11:40:40Exondys 51 or eteplirsen for the treatment of patients with Duchenne Exon 51
News2, treatment

FDA Accepts IND for Limb-Girdle Muscular Dystrophy Gene Therapy

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August 16, 2021/0 Comments/by admin
https://neuromuscular-iran.ir/wp-content/uploads/2021/02/logo_neuromuscular-300x138.png 0 0 admin https://neuromuscular-iran.ir/wp-content/uploads/2021/02/logo_neuromuscular-300x138.png admin2021-08-16 07:29:452021-08-23 11:40:50FDA Accepts IND for Limb-Girdle Muscular Dystrophy Gene Therapy
Muscular dystrophy, News2, treatment

Invest in cell therapy for muscular dystrophic diseases, especially LGMD2A

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August 15, 2021/0 Comments/by admin
https://neuromuscular-iran.ir/wp-content/uploads/2021/02/logo_neuromuscular-300x138.png 0 0 admin https://neuromuscular-iran.ir/wp-content/uploads/2021/02/logo_neuromuscular-300x138.png admin2021-08-15 14:16:152021-08-23 11:41:00Invest in cell therapy for muscular dystrophic diseases, especially LGMD2A
Muscular dystrophy, News2, treatment

Gene modification holds good promise for the treatment of Duchenne disease

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August 15, 2021/0 Comments/by admin
https://neuromuscular-iran.ir/wp-content/uploads/2021/02/logo_neuromuscular-300x138.png 0 0 admin https://neuromuscular-iran.ir/wp-content/uploads/2021/02/logo_neuromuscular-300x138.png admin2021-08-15 13:49:292021-08-23 11:41:10Gene modification holds good promise for the treatment of Duchenne disease
Muscular dystrophy, News2, treatment

Clinical trial findings show that vamorolone confidently improves muscle function in Duchenne boys

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August 15, 2021/0 Comments/by admin
https://neuromuscular-iran.ir/wp-content/uploads/2021/02/logo_neuromuscular-300x138.png 0 0 admin https://neuromuscular-iran.ir/wp-content/uploads/2021/02/logo_neuromuscular-300x138.png admin2021-08-15 10:31:582021-08-23 11:41:20Clinical trial findings show that vamorolone confidently improves muscle function in Duchenne boys

جستجو

نوشته‌های تازه

  • Low Bone Density Raises Risk of Fractures in DMD Boys With Scoliosis
  • از بین بردن میلین را در موش ها کاهش داد CMT1Aژن درمانی
  • In a long-term study, new data show that Givinostat continues to delay the progression of Duchenne disease.
  • Introduction of limb girdle disease (LGMD) 
  • Duchenne muscular dystrophy

اخبار جدید

  • Low Bone Density Raises Risk of Fractures in DMD Boys With ScoliosisJuly 5, 2022 - 1:06 pm
  • In a long-term study, new data show that Givinostat continues to delay the progression of Duchenne disease.August 24, 2021 - 1:37 pm
  • RGX-202 for the treatment of Duchenne muscular dystrophy (DMD)August 16, 2021 - 8:56 am
  • Approval of accelerated treatment of voiltolarsen for Duchenne muscular dystrophy by the FDAAugust 16, 2021 - 8:31 am
Popular
  • Clinical trial findings show that vamorolone confidently...August 15, 2021 - 10:31 am
  • Gene modification holds good promise for the treatment of...August 15, 2021 - 1:49 pm
  • Invest in cell therapy for muscular dystrophic diseases,...August 15, 2021 - 2:16 pm
  • FDA Accepts IND for Limb-Girdle Muscular Dystrophy Gene...August 16, 2021 - 7:29 am
Recent
  • Low Bone Density Raises Risk of Fractures in DMD Boys With...July 5, 2022 - 1:06 pm
  • از بین بردن میلین را در موش ها کاهش...September 15, 2021 - 8:06 am
  • In a long-term study, new data show that Givinostat continues...August 24, 2021 - 1:37 pm
  • Introduction of limb girdle disease (LGMD) August 24, 2021 - 12:27 pm
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