Bradley S. Miller MD PhD

PubMed

• Letter to the editor from Miller et al: "long-acting growth hormone for treating growth hormone deficiency in children: a meta-analysis of randomized controlled trials...
  Bradley S Miller, Lars Sävendahl, Michael Højby, Michel Polak
  The Journal of Clinical Endocrinology and Metabolism. 2026-06-17
• A progeria syndrome links DNA hypermethylation to age-related pathology.
  Dan Sarni, Gráinne Neary, Paula L Carroll, Chris S Vink, Caroline V Billard
  Nature Genetics. 2026-06-12
• Disease-specific growth charts capture characteristic growth patterns in children with PMM2 - CDG.
  Kyriakie Sarafoglou, Christina Lam, Andrew C Edmondson, Andrea Miller, Rodrigo T Starosta
  Molecular Genetics and Metabolism. 2026-06-01

Journal Articles

• Adrenoleukodystrophy: Guidance for Adrenal Surveillance in Males Identified by Newborn Screen  
  Takara L Stanley, Kyriakie Sarafoglou, Rose Marino, Manmohan Kamboj, Bradley S Miller, The Journal of Clinical Endocrinology and Metabolism
• Neonatal Diabetes Mellitus in a Full-Term Male Infant  
  Barthell, J.E., Schwartz, B.L., Miller, B.S., and I. Agarwal., Journal of Neonatal-Perinatal Medicine, 1/1/2008

Books/Book Chapters

• Pediatric Endocrinology and Inborn Errors of Metabolism 
  Chapter: Endocrine Assays 
  Saenger, A.K., Ranke, M.B. and B.S. Miller.Editors: K. Sarafoglou, G.F. Hoffmann and K.S. Roth.McGraw HillEdition 2nd,2017
• Pediatric Endocrinology and Inborn Errors of Metabolism 
  Chapter: Developmental Disorders of the Anterior Pituitary. 
  Frohnert, B., Miller, B.S. and M. Dattani.Editors: K. Sarafoglou, G.F. Hoffmann and K.S. Roth.McGraw HillEdition 2nd,2017
• Advances in Pediatrics 
  Chapter: rhGH Safety and Efficacy Update. 
  Miller, B.S.Editors: M. Geffner and M. Kappy.Elsevier2011

Abstracts/Posters

• IGF-1 and IGFBP-3 at Hospital Discharge Predict Early Catch-up Growth in Preterm Infants.
  Ramel, S.E., Haapala, J., Miller, N.C., Miller, B.S. and E.W. Demerath., Pediatric Academic Societies, Toronto, Ontario, Canada, 1/1/2018
• Autosomal Dominant Growth Hormone Deficiency Due To A Novel c.178G>A Mutation in the gh1 Gene Causing Instability Of The Mutant GH Protein (p.Ala60Thr).
  Miller, B.S., Tan, J.W.L., Parween, S., Eble, A., Ternand, C., Gregory, L.C., Dattani, M.T., and A.V. Pandey., ENDO, Chicago, IL, 1/1/2018
• Pediatric ESAP 2017-2018: Pediatric Endocrine Self-Assessment Program.
  Gafni, R.I., Bauer, A.J., DeBoer, M., Boyce, A.M., Habiby, R.L., Lekarev, O., Miller, B.S., Palma Sisto, P.A., Pesce, L.M., Silverman, L. and P.S. Thornton., Endocrine Society, Washington, DC, 1/1/2017

Lectures

• Year In Review: Emergency Management of Adrenal Insufficiency in Children: A Clinical Practice Guideline 
  Toronto, Ontario, Canada - 1/1/2018
• Why Does Growth Matter? 
  Minneapolis, MN - 1/1/2018
• Controversies in the Management of Short Stature: Treatment Options 
  Rio de Janeiro, Brazil - 1/1/2018

Other

• The Role of cJun Kinases in Insulin-like Growth Factor 1 Receptor Signal Transduction, Doctoral Thesis. 
  Miller, B.S.,
  1/1/1997
• Use of Automated Bone Age for Critical Growth Assessment. 
  Khan, K.M., Gonzalez-Bolanos, M.T., Holm, T., Miller, B.S., and K. Sarafoglou., Clinical Pediatrics
  1/10/2015
• Improved growth and bone mineral density in siblings with type I trichorhinophalangeal syndrome in response to growth hormone therapy. 
  Sarafoglou, K., Moassesfar, S. and B.S. Miller., Clinical Genetics
  1/2./2010