WilliamMcalisterMD

PubMed

• 4 citations
  Drug-induced osteopetrosis.
  Michael P Whyte, William H McAlister, Vandana Dhiman, Nirmal Raj Gopinathan, Sanjay K Bhadada> ;Bone. 2023 Aug 1
• Periarticular calcifications containing giant pseudo-crystals of francolite in skeletal fluorosis from 1,1-difluoroethane "huffing".
  Nilton Salles Rosa Neto, Daniel Englert, William H McAlister, Steven Mumm, David Mills, Deborah J Veis, Alan Burshell, Alan Boyde, Michael P Whyte> ;Bone. 2022 Jul 1
• 6 citations
  Vitamin B6 deficiency with normal plasma levels of pyridoxal 5'-phosphate in perinatal hypophosphatasia.
  Michael P. Whyte, Jennifer D. May, William H. McAlister, Katherine Burgener, Samuel R. Cortez, Raymond Kreienkamp, Olivia Castro, Rachel Verzola, Ana Solis Zavala, Chr...> ;Bone. 2021 May 14
• 5 citations
  Coalescing expansile skeletal disease: Delineation of an extraordinary osteopathy involving the IFITM5 mutation of osteogenesis imperfecta type V.
  Michael P. Whyte, James Aronson, William H. McAlister, Robert S. Weinstein, Deborah Wenkert, Karen L. Clements, Gary S. Gottesman, Katherine L Madson, Marina Stolina, ...> ;Bone. 2021 Apr 1
• 12 citations
  Non-endemic skeletal fluorosis: Causes and associated secondary hyperparathyroidism (case report and literature review).
  Fiona J. Cook, Maighan Seagrove-Guffey, Steven Mumm, Deborah J. Veis, William H. McAlister, Vinieth N. Bijanki, Deborah Wenkert, Michael P. Whyte> ;Bone. 2021 Apr 1
• 3 citations
  Persistent idiopathic hyperphosphatasemia from bone alkaline phosphatase in a healthy boy.
  Michael P. Whyte, Nina S. Ma, Steven Mumm, Gary S. Gottesman, William H. McAlister, Angela Nenninger, Vinieth N. Bijanki, Karen L. Ericson, Per Magnusson> ;Bone. 2020 May 28
• 11 citations
  Juvenile Paget's disease from heterozygous mutation of SP7 encoding osterix (specificity protein 7, transcription factor SP7)
  Michael P. Whyte, Philippe M. Campeau, William H. McAlister, G. David Roodman, Nori Kurihara, Angela Nenninger, Shenghui Duan, Gary S. Gottesman, Vinieth N. Bijanki, H...> ;Bone. 2020 Aug 1
• 9 citations
  Healing of vitamin D deficiency rickets complicating hypophosphatasia suggests a role beyond circulating mineral sufficiency for vitamin D in musculoskeletal health.
  Elizabeth L. Lin, Gary S. Gottesman, William H. McAlister, Vinieth N. Bijanki, Karen E. Mack, Donna Griffin, Steven Mumm, Michael P. Whyte> ;Bone. 2020 Jul 1
• 13 citations
  Bruck syndrome 2 variant lacking congenital contractures and involving a novel compound heterozygous PLOD2 mutation.
  Steven Mumm, Gary S. Gottesman, Deborah Wenkert, Philippe M. Campeau, Angela Nenninger, Margaret Huskey, Vinieth N. Bijanki, Deborah J. Veis, Aileen M. Barnes, Joan C....> ;Bone. 2020 Jan 1
• 9 citations
  Hypophosphatemic osteosclerosis, hyperostosis, and enthesopathy associated with novel homozygous mutations of DMP1 encoding dentin matrix protein 1 and SPP1 encoding o...
  Michael P. Whyte, S. Deepak Amalnath, William H. McAlister, Marc D. McKee, Deborah J. Veis, Margaret Huskey, Shenghui Duan, Vinieth N. Bijanki, Suhas Alur, Steven Mumm> ;Bone. 2020 Mar 1
• 35 citations
  New explanation for autosomal dominant high bone mass: Mutation of low-density lipoprotein receptor-related protein 6.
  Michael P. Whyte, William H. McAlister, Fan Zhang, Vinieth N. Bijanki, Angela Nenninger, Gary S. Gottesman, Elizabeth L. Lin, Margaret Huskey, Shenghui Duan, Kathryn D...> ;Bone. 2019 May 11
• 7 citations
  Phenotype and response to growth hormone therapy in siblings with B4GALT7 deficiency.
  Carla Sandler-Wilson, Jennifer A. Wambach, Bess A. Marshall, Daniel J. Wegner, William H. McAlister, F. Sessions Cole, Marwan Shinawi> ;Bone. 2019 Mar 23
• 11 citations
  No vascular calcification on cardiac computed tomography spanning asfotase alfa treatment for an elderly woman with hypophosphatasia
  Michael P. Whyte, William H. McAlister, Steven Mumm, Andrew J. Bierhals> ;Bone. 2019 May 1
• 4 citations
  Absence of an osteopetrosis phenotype in IKBKG (NEMO) mutation-positive women: A case-control study.
  Morten Frost, Michaela Tencerova, Christina Møller Andreasen, Thomas Levin Andersen, Charlotte Ejersted, Dea Svaneby, Weimin Qui, Moustapha Kassem, Allahdad Zarei, Wil...> ;Bone. 2019 Apr 1
• 9 citations
  Lamin B receptor-related disorder is associated with a spectrum of skeletal dysplasia phenotypes.
  Eliza R Thompson, Ebtesam M. Abdalla, Andrea Superti-Furga, William H. McAlister, Lisa E. Kratz, Sheila Unger, Beryl Royer-Bertrand, Belinda Campos-Xavier, Lauréane Mi...> ;Bone. 2019 Mar 1
• 64 citations
  Asfotase alfa for infants and young children with hypophosphatasia: 7 year outcomes of a single-arm, open-label, phase 2 extension trial.
  Michael P. Whyte, Jill H. Simmons, Scott Moseley, Kenji P Fujita, Nick Bishop, Nada J. Salman, John W. Taylor, Dawn Phillips, Mairead McGinn, William H. McAlister> ;The Lancet. Diabetes & Endocrinology. 2019 Feb 1
• 15 citations
  Sclerosteosis: Report of type 1 or 2 in three Indian Tamil families and literature review.
  Michael P. Whyte, S. Deepak Amalnath, William H. McAlister, Radhakrishna Pedapati, Vivekanandan Muthupillai, Shenghui Duan, Margaret Huskey, Vinieth N. Bijanki, Steven...> ;Bone. 2018 Nov 1
• 5 citations
  Unique Variant of NOD2 Pediatric Granulomatous Arthritis With Severe 1,25-Dihydroxyvitamin D-Mediated Hypercalcemia and Generalized Osteosclerosis.
  Michael P. Whyte, Emilina Lim, William H. McAlister, Gary S. Gottesman, Lien Trinh, Deborah J. Veis, Vinieth N. Bijanki, Matthew G Boden, Angela Nenninger, Steven Mumm...> ;Journal of Bone and Mineral Research. 2018 Nov 1
• 23 citations
  Validation of a Novel Scoring System for Changes in Skeletal Manifestations of Hypophosphatasia in Newborns, Infants, and Children: The Radiographic Global Impression ...
  Michael P. Whyte, Kenji P Fujita, Scott Moseley, David D. Thompson, William H. McAlister> ;Journal of Bone and Mineral Research. 2018 May 1
• 19 citations
  Gnathodiaphyseal Dysplasia: Severe Atypical Presentation with Novel Heterozygous Mutation of the Anoctamin Gene(ANO5)
  Ghada A. Otaify, Michael P. Whyte, Gary S. Gottesman, William H. McAlister, J. Eric Gordon, Abby S. Hollander, Marisa V. Andrews, Samir K. El-Mofty, Wei-Shen Chen, Deb...> ;Bone. 2018 Feb 1
• 30 citations
  Melorheostosis: Exome sequencing of an associated dermatosis implicates postzygotic mosaicism of mutated KRAS.
  Michael P. Whyte, Malachi Griffith, Lee Trani, Steven Mumm, Gary S. Gottesman, William H. McAlister, Kilannin Krysiak, Robert Lesurf, Zachary L. Skidmore, Katie M. Cam...> ;Bone. 2017 Aug 1
• 32 citations
  Raine Syndrome (OMIM #259775), Caused By FAM20C Mutation, Is Congenital Sclerosing Osteomalacia With Cerebral Calcification (OMIM 259660).
  Michael P. Whyte, William H. McAlister, M. Fallon, Mary Ella M Pierpont, Vinieth N. Bijanki, Shenghui Duan, Ghada A. Otaify, William S. Sly, Steven Mumm> ;Journal of Bone and Mineral Research. 2017 Apr 1
• 20 citations
  Skeletal Fluorosis Due To Inhalation Abuse of a Difluoroethane-Containing Computer Cleaner.
  Joseph R. Tucci, Gary M. Whitford, William H. McAlister, Deborah V. Novack, Steven Mumm, Tony M. Keaveny, Michael P. Whyte> ;Journal of Bone and Mineral Research. 2017 Jan 1
• 92 citations
  Asfotase alfa therapy for children with hypophosphatasia.
  Michael P. Whyte, Katherine L Madson, Dawn Phillips, Amy Reeves, William H. McAlister, Amy Yakimoski, Karen E. Mack, Kim Hamilton, Kori Kagan, Kenji P Fujita, David D....> ;JCI Insight. 2016 Jun 16
• 40 citations
  Congenital insensitivity to pain: Fracturing without apparent skeletal pathobiology caused by an autosomal dominant, second mutation in SCN11A encoding voltage-gated s...
  Voraluck Phatarakijnirund, Steven Mumm, William H. McAlister, Deborah V. Novack, Deborah Wenkert, Karen L. Clements, Michael P. Whyte> ;Bone. 2016 Mar 1
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Journal Articles

• Unique Variant of NOD2 Pediatric Granulomatous Arthritis with Severe 1,25‐Dihydroxyvitamin D‐Mediated Hypercalcemia and Generalized Osteosclerosis*  
  William H McAlister, Michael P Whyte, Gary S Gottesman, Journal of Bone and Mineral Research