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The Cochrane Database of Systematic Reviews|November 2, 2016
Bisphosphonate therapy for osteogenesis imperfectaKerry Dwan, Carrie A Phillipi, Robert D Steiner, et al.
Pediatric Dermatology|September 29, 2012
Association of Piebaldism, multiple café-au-lait macules, and intertriginous freckling: clinical evidence of a common pathway between KIT and sprouty-related, ena/vasodilator-stimulated phosphoprotein homology-1 domain containing protein 1 (SPRED1)Yvonne E Chiu, Stefanie Dugan, Donald Basel, et al.
The Cochrane Database of Systematic Reviews|July 24, 2014
Bisphosphonate therapy for osteogenesis imperfectaKerry Dwan, Carrie A Phillipi, Robert D Steiner, et al.
Molecular Syndromology|January 28, 2021
A Deep Intronic Variant Activates a Pseudoexon in the <i>MTM1</i> Gene in a Family with X-Linked Myotubular MyopathyJamie Fitzgerald, Cori Feist, Paula Dietz, et al.
Photobiomodulation, Photomedicine, and Laser Surgery|January 20, 2021
Photodynamic Therapy for Benign Cutaneous Neurofibromas Using Aminolevulinic Acid Topical Application and 633 nm Red Light IlluminationBrendan Quirk, Edit Olasz, Suresh Kumar, et al.
The Medical Clinics of North America|November 11, 2023
Attaining Diagnostic Excellence: How the Structure and Function of a Rare Disease Service Contribute to Ending the Diagnostic OdysseyBrett J Bordini, Ryan D Walsh, Donald Basel, et al.
Clinics in Perinatology|February 1, 2020
Undiagnosed and Rare Diseases in Perinatal Medicine: Lessons in Context and Cognitive Diagnostic ErrorBrett J Bordini, Robert M Kliegman, Donald Basel, et al.
Pediatric Clinics of North America|November 30, 2016
How Doctors Think: Common Diagnostic Errors in Clinical Judgment-Lessons from an Undiagnosed and Rare Disease ProgramRobert M Kliegman, Brett J Bordini, Donald Basel, et al.
Pediatric Dermatology|January 3, 2013
A review of next-generation genetic testing for the dermatologistEun-Kyung M Kwon, Donald Basel, Dawn Siegel, et al.
Pediatric Cardiology|July 21, 2017
Genetic Testing Protocol Reduces Costs and Increases Rate of Genetic Diagnosis in Infants with Congenital Heart DiseaseGabrielle C Geddes, Donald Basel, Peter Frommelt, et al.
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