Hypophosphatasia: Nonlethal disease despite skeletal presentation in utero (17 new cases and literature review) von Wenkert, Deborah, McAlister, William H, Coburn, Stephen P, Zerega, Janice A, Ryan, Lawrence M, Ericson, Karen L, Hersh, Joseph H, Mumm, Steven, Whyte, Michael P

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Calcific Periarthritis as the Only Clinical Manifestation of Hypophosphatasia in Middle‐Aged Sisters von Guañabens, Núria, Mumm, Steven, Möller, Ingrid, González‐Roca, Eva, Peris, Pilar, Demertzis, Jennifer L, Whyte, Michael P

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Acute Severe Hypercalcemia After Traumatic Fractures and Immobilization in Hypophosphatasia Complicated by Chronic Renal Failure von Whyte, Michael P, Leelawattana, Rattana, Reinus, William R, Yang, Chang, Mumm, Steven, Novack, Deborah V

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Fibrodysplasia ossificans progressiva: Middle‐age onset of heterotopic ossification from a unique missense mutation (c.974G > C, p.G325A) in ACVR1 von Whyte, Michael P, Wenkert, Deborah, Demertzis, Jennifer L, DiCarlo, Edward F, Westenberg, Erica, Mumm, Steven

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Pyridoxine-responsive seizures as the first symptom of infantile hypophosphatasia caused by two novel missense mutations (c.677T > C, p.M226T; c.1112C > T, p.T371I) of the tissue-n... von Baumgartner-Sigl, Sara, Haberlandt, Edda, Mumm, Steven, Scholl-Bürgi, Sabine, Sergi, Consolato, Ryan, Lawrence, Ericson, Karen L, Whyte, Michael P, Högler, Wolfgang

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Infantile Hypophosphatasia: Transplantation Therapy Trial Using Bone Fragments and Cultured Osteoblasts von Cahill, Richard A., Wenkert, Deborah, Perlman, Sharon A., Steele, Ann, Coburn, Stephen P., McAlister, William H., Mumm, Steven, Whyte, Michael P.

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Osteoprotegerin deficiency and aneurysm formation: Case report of iliac artery aneurysms in Juvenile Paget's disease von Gaston, Brandon T., Chou, Elizabeth L., Patel, Aman B., Lindsay, Mark E., Mumm, Steven, Whyte, Michael P., Mohapatra, Abhisekh

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Dysosteosclerosis: Clinical and Radiological Evolution Reflecting Genetic Heterogeneity von Turan, Serap, Mumm, Steven, Alavanda, Ceren, Kaygusuz, Betul Sare, Gurpinar Tosun, Busra, Arman, Ahmet, Huskey, Margaret, Guran, Tulay, Duan, Shenghui, Bereket, Abdullah, Whyte, Michael P.

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X‐Linked Hypophosphatemia Caused by the Prevailing North American PHEX Variant c.231A>G; Exon 13–15 Duplication Is Often Misdiagnosed as Ankylosing Spondylitis and Manifests in Bot... von Dahir, Kathryn McCrystal, Black, Margo, Gottesman, Gary S, Imel, Erik A, Mumm, Steven, Nichols, Cindy M, Whyte, Michael P

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Marrow Cell Transplantation for Infantile Hypophosphatasia von Whyte, Michael P, Kurtzberg, Joanne, McALISTER, William H, Mumm, Steven, Podgornik, Michelle N, Coburn, Stephen P, Ryan, Lawrence M, Miller, Cindy R, Gottesman, Gary S, Smith, Alan K, Douville, Judy, Waters‐Pick, Barbara, Armstrong, R Douglas, Martin, Paul L

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Hypophosphatasia: Validation and expansion of the clinical nosology for children from 25years experience with 173 pediatric patients von Whyte, Michael P., Zhang, Fan, Wenkert, Deborah, McAlister, William H., Mack, Karen E., Benigno, Marci C., Coburn, Stephen P., Wagy, Susan, Griffin, Donna M., Ericson, Karen L., Mumm, Steven

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Hyperphosphatemia with low FGF7 and normal FGF23 and sFRP4 levels in the circulation characterizes pediatric hypophosphatasia von Whyte, Michael P., Zhang, Fan, Wenkert, Deborah, Mumm, Steven, Berndt, Theresa J., Kumar, Rajiv

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Adult Hypophosphatasia Treated with Teriparatide von Whyte, Michael P., Mumm, Steven, Deal, Chad

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High bone mass from mutation of low-density lipoprotein receptor-related protein 6 (LRP6) von Brance, María Lorena, Brun, Lucas R., Cóccaro, Nicolás M., Aravena, Andrés, Duan, Shenghui, Mumm, Steven, Whyte, Michael P.

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Non-endemic skeletal fluorosis: Causes and associated secondary hyperparathyroidism (case report and literature review) von Cook, Fiona J., Seagrove-Guffey, Maighan, Mumm, Steven, Veis, Deborah J., McAlister, William H., Bijanki, Vinieth N., Wenkert, Deborah, Whyte, Michael P.

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Early identification of a 12-bp tandem duplication in TNFRSF11A encoding receptor activator of nuclear factor-kappa B (RANK): Clinical characterization and response to bisphosphona... von Craven, Meghan, Vajravelu, Mary Ellen, Shekdar, Karuna V., Levine, Michael A., Mumm, Steven, Whyte, Michael P., Mancilla, Edna E.

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Transmembrane protein 53 craniotubular dysplasia (OMIM # 619727): The skeletal disease and consequent blindness of this new disorder von Whyte, Michael P., Weinstein, Robert S., Phillips, Paul H., McAlister, William H., Ramakrishnaiah, Raghuhr H., Schaefer, G. Bradley, Cai, Rongsheng, Hutchison, Michele R., Duan, Shenghui, Gottesman, Gary S., Mumm, Steven

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Periarticular calcifications containing giant pseudo-crystals of francolite in skeletal fluorosis from 1,1-difluoroethane "huffing" von Salles Rosa Neto, Nilton, Englert, Daniel, McAlister, William H., Mumm, Steven, Mills, David, Veis, Deborah J., Burshell, Alan, Boyde, Alan, Whyte, Michael P.

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X‐Linked Hypophosphatemia: Uniquely Mild Disease Associated With PHEX 3′‐UTR Mutation c.231A>G (A Retrospective Case–Control Study) von Smith, Pamela S, Gottesman, Gary S, Zhang, Fan, Cook, Fiona, Ramirez, Beatriz, Wenkert, Deborah, Wollberg, Valerie, Huskey, Margaret, Mumm, Steven, Whyte, Michael P

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Bisphosphonate-Induced Osteopetrosis von Whyte, Michael P, Wenkert, Deborah, Clements, Karen L, McAlister, William H, Mumm, Steven

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