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2 ensaios clínicos encontrados, 2 ativos.
Therapy for Myhre Syndrome: Goals, Misconceptions, and Current Agents.
Myhre Syndrome Presenting With Congenital Proximal Radioulnar Synostosis: A Case Report.
Review of Cutaneous Manifestations in Myhre Syndrome With Histopathological Analyses and Genotype-Phenotype Correlation.
Unraveling the Mechanistic Spectrum of Myhre Syndrome: SMAD4 Signaling Disruption, Skeletal Phenotypes, and Translational Innovation.
A Novel Gain-of-Function ITPR1 Variant Associated With a Movement Disorder Characterized by Tremor and Dystonia.