Genethon's First Lgmd Biotech  -  Afm-Telethon - October 28th 2020

Chris Calabrese on His Journey to Become a Filmmaker Despite His Disease – Los Angeles Wire – October 23th 2020

Chris Calabrese Defies Disease and Produces Quality Films – New York Weekly – October 22nd 2020

Sarepta Therapeutics investigational gene therapy SRP-9003 treatment of Limb Girdle Muscular Dystrophy type 2E - September 28th 2020

SRP-9003 Gene Therapy for LGMD2E  Shows Benefit after 1 year - Muscular Dystrophy News Today - June 9th 2020

New data gives hope for Limb Girdle Muscular Dystrophy gene therapy - Patient Worthy  - June 17th   2020

Owen Steckler – CsiNewsNow - Sunday June 28, 2020

First Duchenne Patient Dosed in Microdystrophin Gene Therapy! - January 10th 2018

Young Boy Becomes First DMD Patient to Receive Investigational Systemic Microdystrophin Gene Therapy  - January 19th 2018

MDA Clinical Conference Keynote Adress by Dr. Jerry Mendell - March 2018

 How Myonexus Therapeutics is developing the first treatment for Limb Girdle Muscular Dystrophies - March 29th 2018

Myonexus Therapeutics receives FDA orphan drug designation for LGMD type 2E treatment

Pioneering, corrective gene therapies have potential to transform quality of life  April 2018

Limb Girdle Muscular Dystrophy Type 2E Recruitment Study - Pubmed.gov -  April 10th 2018

Clinical Research Forum Top Ten Clinical Research Achivement Awards  - April 17th 2018 

Sarepta Therapeutics Announces Partnership with Myonexus Therapeutics for the Advancement of Multiple Gene Therapy Programs Aimed at Treating Distinct Forms of Limb-Girdle Muscular Dystrophies May 3th 2018

Myonexus  Therapeutics receives  FDA  Rare Pediatric Disease Designation  May 2018

 Gene Delivery for Limb-Girdle Muscular Dystrophy Type 2D  (LGMD2D) – PubMed.gov - June 2018

Positive preliminary results from the first three children dosed in phase 1/2A gene Therapy micro-dystrophin trial – Parent Project - June 19th 2018 

MDA Funds Creation of Limb-Girdle Muscular Dystrophy Clinical Research Network to Speed Therapy Development  -  July 27th 2018

Myonexus Therapeutics announced the initiation of a trial for the first-ever Gene Therapy for  Beta-Sarcoglycanopathy -   2018

Atrofia Muscolare Spinale: a luglio avvio in Italia sperimentazione di terapia genica. 

Our vision for the future of Precision Genetic Medicine - Sarepta Therapeutics 2018 R&D Day

Clinical Update: Micro-dystrophin Study-101 – Sarepta  - 2018

Myonexus Therapeutics recieves orphan drug designation for Myo-102 - Myonexus January 2nd 2019

Myonexus Therapeutics announces accelerated acquisition by Sarepta Therapeutics. - 2019

Clinical Update: Myo-101 For LGMD Type 2E Business update: Myonexus Acquisition - Sarepta - february 27 2019

Distrofia dei cingoli, Sarepta decide di acquisire Myonexus - Osservatorio Malattie Rare - march 12 2019

Distrofia dei cingoli 2E, primi risultati clinici favorevoli per la terapia genica - Osservatorio Malattie Rare OMAR -  April 12 2019

How an Ohio Kids hospital Quitly Became Groung Zero for Gene Therapy - Xconomy  -  april 15  2019

Gene Delivery for Limb Girdle Muscular Dystrophy Type 2D (LGMD2D)  by Isolated Limb Infusion - PubMed.gov - July 2019

La terapia genica  SRP-9003 mostra risultati molto incoraggianti a 9 mesi nella distrofia dei cingoli - Sarepta Reports - October 9 2019

Distrofia dei cingoli 2E, nuovi risultati positivi per la terapia genica SRP-9003 - Osservatorio Malattie Rare OMAR - October 22 2019

Myonexus Therapeutics Secures $ 2,5 Million Seed Financing to Clinically Advance Limb-Girdle Muscular Dystrophy (LGMD) Gene Theraphies -  December 13th 2017

Clinical Trials Bring Hope to Kids with Spinal Muscular Atrophy  - November 21th  2017

FDA Clears IND Application for Micro-dystrophin Gene Therapy Program to Treat Duchenne  - November 8th 2017

Sarepta & Nationwide Announce FDA Clearance of IND for Micro-Dystrophin Gene Therapy Program for the Treatment of Duchenne – November 6th 2017

Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy – November 2nd 2017

Gene Therapy Continues to Show Promise for Limb-Girdle Muscular Dystrophy – June 13th  2017 

Myonexus Therapeutics, Inc. Launches to Develop Pioneering, Clinical-Stage Gene Therapies Targeting Limb-Girdle Muscular Dystrophies  - June 7th 2017

Myonexus Launches Development of Gene Therapies Targeting Limb-Girdle MD - June 8th 2017

Promising Preclinical results for LGMD gene therapy – Muscular Dystrophy UK - February 8th 2017