Objective Titin gene ( TTN ) mutations have been described in eight families with hereditary myopathy with early respiratory failure (HMERF). Some of the original patients had features resembling ...

Myofibrillar Myopathy. Obituaries 1 Man, 3 Hearts: NJ Survivor Whose Story Touched Thousands Dies At 41 Christophe Lafontant, a New Jersey man who inspired thousands through his fight against rare ...

Myofibrillar Myopathy. Obituaries 1 Man, 3 Hearts: NJ Survivor Whose Story Touched Thousands Dies At 41 Christophe Lafontant, a New Jersey man who inspired thousands through his fight against rare ...

New Chinese medicine drug developed by HKBU for myofibrillar myopathy granted orphan drug designation by FDA. New Chinese medicine drug developed by HKBU for myofibrillar myopathy granted orphan drug ...

Success in obtaining orphan drug (a drug used for treating rare disease) designation will accelerate the approval process of the new drug, including speeding up of the review process, waiver of the ...

HONG KONG, Jan. 10, 2024 /PRNewswire/ -- The Centre for Chinese Herbal Medicine Drug Development of Hong Kong Baptist University (HKBU) has de ...

Focusing on myofibrillar myopathy caused by BAG3 gene mutation (Bag3opathy), the Centre for Chinese Herbal Medicine Drug Development made reference to clinical cases, integrated Chinese medicine ...

/PRNewswire/ -- The Centre for Chinese Herbal Medicine Drug Development of Hong Kong Baptist University (HKBU) has developed a new drug using effective ...

HONG KONG, Jan. 10, 2024 /PRNewswire/ -- The Centre for Chinese Herbal Medicine Drug Development of Hong Kong Baptist University (HKBU) has developed a new drug using effective components of a ...

HONG KONG, Jan. 10, 2024 /PRNewswire/ -- The Centre for Chinese Herbal Medicine Drug Development of Hong Kong Baptist University (HKBU) has developed a new drug using effective components of a Chinese ...

Introduction. Fatal infantile hypertonic myofibrillar myopathy (FIHMM) is an autosomal recessive hereditary disease caused by mutations in the CRYAB gene. Symptoms such as weak crying, sleep apnea, ...