Alkaline Phosphatase and Hypophosphatasia

Por Millán, José Luis, Whyte, Michael P.
Publicado no Calcif Tissue Int (2015)

MON-516 Skeletal Fluorosis from Fluorocarbon Inhalation

Por Seagrove-Guffey, Maighan, Whyte, Michael, Mumm, Steven, Cook, Fiona
Publicado no J Endocr Soc (2019)

Genetic approaches to metabolic bone diseases

Por Hannan, Fadil M., Newey, Paul J., Whyte, Michael P., Thakker, Rajesh V.
Publicado no Br J Clin Pharmacol (2018)

Camurati-Engelmann Disease: Unique Variant Featuring a Novel Mutation in TGFβ1 Encoding Transforming Growth Factor Beta 1 and a Missense Change in TNFSF11 Encoding RANK Ligand

Por Whyte, Michael P, Totty, William G, Novack, Deborah V, Zhang, Xiafang, Wenkert, Deborah, Mumm, Steven
Publicado em 2011

Juvenile Paget’s Disease In An Iranian Kindred With Vitamin D Deficiency And Novel Homozygous TNFRSF11B Mutation

Por Saki, Forough, Karamizadeh, Zohreh, Nasirabadi, Shiva, Mumm, Steven, McAlister, William H., Whyte, Michael P.
Publicado em 2013

Acute Severe Hypercalcemia After Traumatic Fractures and Immobilization in Hypophosphatasia Complicated by Chronic Renal Failure

Por Whyte, Michael P., Leelawattana, Rattana, Reinus, William R., Yang, Chang, Mumm, Steven, Novack, Deborah V.
Publicado no J Clin Endocrinol Metab (2013)

Outcome of Perinatal Hypophosphatasia in Manitoba Mennonites: A Retrospective Cohort Analysis

Por Leung, Edward C. W., Mhanni, Aizeddin A., Reed, Martin, Whyte, Michael P., Landy, Hal, Greenberg, Cheryl R.
Publicado em 2013

Congenital Insensitivity To Pain: Fracturing Without Apparent Skeletal Pathobiology Caused By An Autosomal Dominant, Second Mutation in SCN11A Encoding Voltage-Gated Sodium Channel...

Por Phatarakijnirund, Voraluck, Mumm, Steven, McAlister, William H., Novack, Deborah, Wenkert, Deborah, Clements, Karen L., Whyte, Michael P.
Publicado no Bone (2015)

Auricular Ossification: A Newly Recognized Feature of Osteoprotegerin-Deficiency Juvenile Paget Disease

Por Gottesman, Gary S., Madson, Katherine L., McAlister, William H., Nenninger, Angela, Wenkert, Deborah, Mumm, Steven, Whyte, Michael P.
Publicado no Am J Med Genet A (2016)

SAT-LB085 First Report of Burosumab (Anti-FGF23 Monoclonal Antibody) for Rickets Complicating HRAS-Associated Cutaneous Skeletal Hypophosphatemia Syndrome

Por Smith, Pamela, Bayliss, Susan, Shinawi, Marwan, Gottesman, Gary, McAlister, William, Sugarman, Jeffrey, Whyte, Michael, Arbelaez, Ana Maria
Publicado no J Endocr Soc (2019)

OR13-4 Safety Profile of Asfotase Alfa Treatment of Patients with Hypophosphatasia: A Pooled Analysis

Por Whyte, Michael, Bishop, Nick, Hasan, Jawad, Hofmann, Christine, Högler, Wolfgang, Rockman-Greenberg, Cheryl, Sena, Veruska, Zhou, Shanggen, Kishnani, Priya
Publicado no J Endocr Soc (2019)

Idiopathic Acquired Osteosclerosis In A Middle-aged Woman With Systemic Lupus Erythematosus

Por Guañabens, Núria, Mumm, Steven, Gifre, Laia, Gaspà, Silvia Ruiz, Demertzis, Jennifer L., Stolina, Marina, Novack, Deborah V., Whyte, Michael P
Publicado no J Bone Miner Res (2016)

Skeletal Fluorosis Due To Inhalation Abuse Of A Difluoroethane-Containing Computer Cleaner

Por Tucci, Joseph R., Whitford, Gary M., McAlister, William H., Novack, Deborah, Mumm, Steven, Keaveny, Tony M., Whyte, Michael P.
Publicado no J Bone Miner Res (2016)

Autosomal Recessive Hypophosphatasia Manifesting in Utero with Long Bone Deformity but Showing Spontaneous Postnatal Improvement

Por Stevenson, David A., Carey, John C., Coburn, Stephen P., Ericson, Karen L., Byrne, Janice L. B., Mumm, Steven, Whyte, Michael P.
Publicado em 2008

Dysosteosclerosis Presents as an “Osteoclast-Poor” Form of Osteopetrosis: Comprehensive Investigation of a 3-Year-Old Girl and Literature Review

Por Whyte, Michael P, Wenkert, Deborah, McAlister, William H, Novack, Deborah V, Nenninger, Angie R, Zhang, Xiafang, Huskey, Margaret, Mumm, Steven
Publicado em 2010

Juvenile Paget’s Disease With Heterozygous Duplication In TNFRSF11A Encoding RANK

Por Whyte, Michael P., Tau, Cristina, McAlister, William H., Zhang, Xiafang, Novack, Deborah V., Preliasco, Virginia, Santini-Araujo, Eduardo, Mumm, Steven
Publicado em 2014

Asfotase Alfa Treatment Improves Survival for Perinatal and Infantile Hypophosphatasia

Por Whyte, Michael P., Rockman-Greenberg, Cheryl, Ozono, Keiichi, Riese, Richard, Moseley, Scott, Melian, Agustin, Thompson, David D., Bishop, Nicholas, Hofmann, Christine
Publicado no J Clin Endocrinol Metab (2016)

Upregulation of Elastase Activity in Aorta in Mucopolysaccharidosis I and VII Dogs May be Due to Increased Cytokine Expression

Por Metcalf, Jason A., Linders, Bruce, Wu, Susan, Bigg, Paul, O’Donnell, Patricia, Sleeper, Meg M., Whyte, Michael P., Haskins, Mark, Ponder, Katherine P.
Publicado em 2009

Pathogenesis of lumbar spine disease in mucopolysaccharidosis VII

Por Smith, Lachlan J, Baldo, Guilherme, Wu, Susan, Liu, Yuli, Whyte, Michael P, Giugliani, Roberto, Elliott, Dawn M, Haskins, Mark E, Ponder, Katherine P
Publicado em 2012

Comparison of human chromosome 19q13 and syntenic region on mouse chromosome 7 reveals absence, in man, of 11.6 Mb containing four mouse calcium-sensing receptor-related sequences:...

Por Hannan, Fadil M, Nesbit, M Andrew, Turner, Jeremy J O, Stacey, Joanna M, Cianferotti, Luisella, Christie, Paul T, Conigrave, Arthur D, Whyte, Michael P, Thakker, Rajesh V
Publicado em 2010