Clinical trials for orphan diseases are critical for developing effective therapies. One such condition, fibrodysplasia ossificans progressiva (FOP; MIM#135100), is characterized by progressive heterotopic ossification (HO) that leads to severe disability. Individuals with FOP are extremely sensitive to even minor traumatic events. There has been substantial recent interest in clinical trials for novel and urgently-needed treatments for FOP. The International Clinical Council on FOP (ICC) was established in 2016 to provide consolidated and coordinated advice on the best practices for clinical care and clinical research for individuals who suffer from FOP. The Clinical Trials Committee of the ICC developed a focused list of key consideration...
Fibrodysplasia ossificans progressiva (FOP) is an extremely rare autosomal dominant disorder having ...
Fibrodysplasia ossificans progressiva, (FOP), the most disabling condition of extra skeletal ossific...
Purpose: We report the first prospective, international, natural history study of the ultra-rare gen...
Clinical trials for orphan diseases are critical for developing effective therapies. One such condit...
Fibrodysplasia ossificans progressiva (FOP) is a rare and devastating genetic disease, in which soft...
A case of a patient with fibrodysplasia ossificans progressiva (FOP) is presented. Based on the know...
Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare progressive genetic disease effecting o...
Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare progressive genetic disease effecting o...
Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disease that is characterized by the f...
Fibrodysplasia ossificans progressiva (FOP) is a rare genetic condition characterized by progressive...
Abstract Fibrodysplasia ossificans progressiva (FOP), a disabling disorder of progressive heterotopi...
The Fibrodysplasia Ossificans Progressiva (FOP) Connection Registry is an international, voluntary, ...
Heterotopic ossification (HO) is a disorder characterised by the formation of ectopic bone in soft t...
Background Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare, disabling ...
Fibrodysplasia ossificans progressiva (FOP), a disabling disorder of progressive heterotopic ossific...
Fibrodysplasia ossificans progressiva (FOP) is an extremely rare autosomal dominant disorder having ...
Fibrodysplasia ossificans progressiva, (FOP), the most disabling condition of extra skeletal ossific...
Purpose: We report the first prospective, international, natural history study of the ultra-rare gen...
Clinical trials for orphan diseases are critical for developing effective therapies. One such condit...
Fibrodysplasia ossificans progressiva (FOP) is a rare and devastating genetic disease, in which soft...
A case of a patient with fibrodysplasia ossificans progressiva (FOP) is presented. Based on the know...
Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare progressive genetic disease effecting o...
Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare progressive genetic disease effecting o...
Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disease that is characterized by the f...
Fibrodysplasia ossificans progressiva (FOP) is a rare genetic condition characterized by progressive...
Abstract Fibrodysplasia ossificans progressiva (FOP), a disabling disorder of progressive heterotopi...
The Fibrodysplasia Ossificans Progressiva (FOP) Connection Registry is an international, voluntary, ...
Heterotopic ossification (HO) is a disorder characterised by the formation of ectopic bone in soft t...
Background Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare, disabling ...
Fibrodysplasia ossificans progressiva (FOP), a disabling disorder of progressive heterotopic ossific...
Fibrodysplasia ossificans progressiva (FOP) is an extremely rare autosomal dominant disorder having ...
Fibrodysplasia ossificans progressiva, (FOP), the most disabling condition of extra skeletal ossific...
Purpose: We report the first prospective, international, natural history study of the ultra-rare gen...