Persistent idiopathic hyperphosphatasemia from bone alkaline phosphatase in a healthy boy
Whyte, Michael P., Ma, Nina S., Mumm, Steven, Gottesman, Gary S., McAlister, William H., Nenninger, Angela R., Bijanki, Vinieth N., Ericson, Karen L., Magnusson, Per
Published in Bone (New York, N.Y.) (01.09.2020)
Published in Bone (New York, N.Y.) (01.09.2020)
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Journal Article
Lenz‐Majewski Hyperostotic Dwarfism with Hyperphosphoserinuria from a Novel Mutation in PTDSS1 Encoding Phosphatidylserine Synthase 1
Whyte, Michael P, Blythe, Amanda, McAlister, William H, Nenninger, Angela R, Bijanki, Vinieth N, Mumm, Steven
Published in Journal of bone and mineral research (01.04.2015)
Published in Journal of bone and mineral research (01.04.2015)
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Journal Article
Multicentric carpotarsal osteolysis syndrome is caused by only a few domain-specific mutations in MAFB, a negative regulator of RANKL-induced osteoclastogenesis
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.
Published in American journal of medical genetics. Part A (01.09.2014)
Published in American journal of medical genetics. Part A (01.09.2014)
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Journal Article
Auricular ossification: A newly recognized feature of osteoprotegerin-deficiency juvenile Paget disease
Gottesman, Gary S., Madson, Katherine L., McAlister, William H., Nenninger, Angela, Wenkert, Deborah, Mumm, Steven, Whyte, Michael P.
Published in American journal of medical genetics. Part A (01.04.2016)
Published in American journal of medical genetics. Part A (01.04.2016)
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Journal Article
New explanation for autosomal dominant high bone mass: Mutation of low-density lipoprotein receptor-related protein 6
Whyte, Michael P., McAlister, William H., Zhang, Fan, Bijanki, Vinieth N., Nenninger, Angela, Gottesman, Gary S., Lin, Elizabeth L., Huskey, Margaret, Duan, Shenghui, Dahir, Kathryn, Mumm, Steven
Published in Bone (New York, N.Y.) (01.10.2019)
Published in Bone (New York, N.Y.) (01.10.2019)
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Journal Article
Bruck syndrome 2 variant lacking congenital contractures and involving a novel compound heterozygous PLOD2 mutation
Mumm, Steven, Gottesman, Gary S., Wenkert, Deborah, Campeau, Philippe M., Nenninger, Angela, Huskey, Margaret, Bijanki, Vinieth N., Veis, Deborah J., Barnes, Aileen M., Marini, Joan C., Stolina, Marina, Zhang, Fan, McAlister, William H., Whyte, Michael P.
Published in Bone (New York, N.Y.) (01.01.2020)
Published in Bone (New York, N.Y.) (01.01.2020)
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Journal Article
Melorheostosis: Exome sequencing of an associated dermatosis implicates postzygotic mosaicism of mutated KRAS
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
Published in Bone (New York, N.Y.) (01.08.2017)
Published in Bone (New York, N.Y.) (01.08.2017)
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Journal Article
Unique Variant of NOD2 Pediatric Granulomatous Arthritis With Severe 1,25‐Dihydroxyvitamin D‐Mediated Hypercalcemia and Generalized Osteosclerosis
Whyte, Michael P, Lim, Emilina, McAlister, William H, Gottesman, Gary S, Trinh, Lien, Veis, Deborah J, Bijanki, Vinieth N, Boden, Matthew G, Nenninger, Angela, Mumm, Steven, Buchbinder, David
Published in Journal of bone and mineral research (01.11.2018)
Published in Journal of bone and mineral research (01.11.2018)
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Journal Article
Juvenile Paget's Disease From Heterozygous Mutation of SP7 Encoding Osterix (Specificity Protein 7, Transcription Factor SP7)
Whyte, Michael P., Campeau, Philippe M., McAlister, William H., Roodman, G. David, Kurihara, Nori, Nenninger, Angela, Duan, Shenghui, Gottesman, Gary S., Bijanki, Vinieth N., Sedighi, Homer, Veis, Deborah J., Mumm, Steven
Published in Bone (New York, N.Y.) (01.08.2020)
Published in Bone (New York, N.Y.) (01.08.2020)
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Journal Article