Facial angiofibromas, composed of fibrous tissue and blood vessels appearing on the face, are closely associated with tuberous sclerosis complex. Historically, oral rapamycin, a mammalian target of the rapamycin inhibitor of cell proliferation, has been used to treat visceral tuberous sclerosis–related tumors; however, the side effect profile of this medicine generally precludes its use in patients lacking significant internal involvement. The authors developed a novel topical formulation of rapamycin cream to treat the facial angiofibroma without exposing patients to possible systemic side effects. We followed 11 patients in a long-term, open-label, prospective study to evaluate the safety and effectiveness of rapamycin cream when used chr...
Birt-Hogg-Dubé syndrome (BHD) is a rare autosomal dominant disorder characterised by the occurrence ...
Birt-Hogg-Dubé syndrome (BHD) is a rare autosomal dominant disorder characterised by the occurrence ...
Background: Birt-Hogg-Dube ́ syndrome (BHD) is a rare autosomal dominant disorder characterised by t...
Abstract Background and Objectives: Facial angiofibromas are disfiguring facial lesions, present in ...
Tuberous sclerosis complex (TSC) is a neurocutaneus disease that causes various other tumors includi...
Aim: Topical rapamycin for angiofibromas has been reported to be a new promising treatment. This stu...
Facial angiofibromas are dermatological manifestations of tuberous sclerosis complex, a neurocutaneo...
BACKGROUND: Tuberous sclerosis complex (TSC) is an autosomal dominant neurocutaneous syndrome causi...
The use of topical rapamycin or rapalog, an mTOR inhibitor, has shown promising results in treating ...
Background and Objectives: Facial angiofibromas are disfiguring facial lesions, present in up to 80%...
Background: The skin is one of the most affected organs in tuberous sclerosis complex and angiofibro...
International audienceObjectives: In recent years, various formulations containing rapamycin, mainly...
Medicines for the treatment of rare diseases frequently do not attract the interest of the pharmaceu...
<p><b>Article full text</b></p> <p><br></p> <p>The full text of this article can be found here<b>....
International audienceWe report here the effect of topical rapamycin 1%, an efficient topical treatm...
Birt-Hogg-Dubé syndrome (BHD) is a rare autosomal dominant disorder characterised by the occurrence ...
Birt-Hogg-Dubé syndrome (BHD) is a rare autosomal dominant disorder characterised by the occurrence ...
Background: Birt-Hogg-Dube ́ syndrome (BHD) is a rare autosomal dominant disorder characterised by t...
Abstract Background and Objectives: Facial angiofibromas are disfiguring facial lesions, present in ...
Tuberous sclerosis complex (TSC) is a neurocutaneus disease that causes various other tumors includi...
Aim: Topical rapamycin for angiofibromas has been reported to be a new promising treatment. This stu...
Facial angiofibromas are dermatological manifestations of tuberous sclerosis complex, a neurocutaneo...
BACKGROUND: Tuberous sclerosis complex (TSC) is an autosomal dominant neurocutaneous syndrome causi...
The use of topical rapamycin or rapalog, an mTOR inhibitor, has shown promising results in treating ...
Background and Objectives: Facial angiofibromas are disfiguring facial lesions, present in up to 80%...
Background: The skin is one of the most affected organs in tuberous sclerosis complex and angiofibro...
International audienceObjectives: In recent years, various formulations containing rapamycin, mainly...
Medicines for the treatment of rare diseases frequently do not attract the interest of the pharmaceu...
<p><b>Article full text</b></p> <p><br></p> <p>The full text of this article can be found here<b>....
International audienceWe report here the effect of topical rapamycin 1%, an efficient topical treatm...
Birt-Hogg-Dubé syndrome (BHD) is a rare autosomal dominant disorder characterised by the occurrence ...
Birt-Hogg-Dubé syndrome (BHD) is a rare autosomal dominant disorder characterised by the occurrence ...
Background: Birt-Hogg-Dube ́ syndrome (BHD) is a rare autosomal dominant disorder characterised by t...