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

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)

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

Multicentric Carpotarsal Osteolysis Syndrome is Caused by Only a Few Domain-Specific Mutations in MAFB, a Negative Regulator of RANKL-Induced Osteoclastogenesis

Por Mumm, Steven, Huskey, Margaret, Duan, Shenghui, Wenkert, Deborah, Madson, Katherine L., Gottesman, Gary S., Nenninger, Angela R., Laxer, Ronald M., McAlister, William H., Whyte, Michael P.
Publicado no Am J Med Genet A (2014)

Rapid Skeletal Turnover In A Radiographic Mimic Of Osteopetrosis

Por Whyte, Michael P., Madson, Katherine L., Mumm, Steven, McAlister, William H., Novack, Deborah V., Blair, Jo C., Helliwell, Timothy R., Stolina, Marina, Abernethy, Laurence J., Shaw, Nicholas J.
Publicado no J Bone Miner Res (2014)

Panostotic Expansile Bone Disease With Massive Jaw Tumor Formation and a Novel Mutation in the Signal Peptide of RANK

Por Schafer, Anne L, Mumm, Steven, El-Sayed, Ivan, McAlister, William H, Horvai, Andrew E, Tom, Andrea M, Hsiao, Edward C, Schaefer, Frederick V, Collins, Michael T, Anderson, Mark S, Whyte, Michael P, Shoback, Dolores M
Publicado no J Bone Miner Res (2014)

Neonatal High Bone Mass With First Mutation Of The NF-κB Complex: Heterozygous De Novo Missense (p.Asp512Ser) RELA (Rela/p65)

Por Frederiksen, Anja L., Larsen, Martin J., Brusgaard, Klaus, Novack, Deborah V., Knudsen, Peter Juel Thiis, Schrøder, Henrik Daa, Qiu, Weimin, Eckhardt, Christina, McAlister, William H., Kassem, Moustapha, Mumm, Steven, Frost, Morten, Whyte, Michael P.
Publicado no J Bone Miner Res (2015)

Asfotase alfa therapy for children with hypophosphatasia

Por Whyte, Michael P., Madson, Katherine L., Phillips, Dawn, Reeves, Amy L., McAlister, William H., Yakimoski, Amy, Mack, Karen E., Hamilton, Kim, Kagan, Kori, Fujita, Kenji P., Thompson, David D., Moseley, Scott, Odrljin, Tatjana, Rockman-Greenberg, Cheryl
Publicado no JCI Insight (2016)

Melorheostosis: Exome Sequencing Of An Associated Dermatosis Implicates Postzygotic Mosaicism Of Mutated KRAS

Por Whyte, Michael P., Griffith, Malachi, Trani, Lee, Mumm, Steven, Gottesman, Gary S., McAlister, William H., Krysiak, Kilannin, Lesurf, Robert, Skidmore, Zachary L., Campbell, Katie M, Rosman, Ilana S., Bayliss, Susan, Bijanki, Vinieth N., Nenninger, Angela, Van Tine, Brian A., Griffith, Obi L., Mardis, Elaine R.
Publicado no Bone (2017)

COL1 C-propeptide Cleavage Site Mutations Cause High Bone Mass Osteogenesis Imperfecta

Por Lindahl, Katarina, Barnes, Aileen M., Fratzl-Zelman, Nadja, Whyte, Michael P., Hefferan, Theresa E., Makareeva, Elena, Brusel, Marina, Yaszemski, Michael J., Rubin, Carl-Johan, Kindmark, Andreas, Roschger, Paul, Klaushofer, Klaus, McAlister, William H., Mumm, Steven, Leikin, Sergey, Kessler, Efrat, Boskey, Adele L., Ljunggren, Östen, Marini, Joan C.
Publicado em 2011