Zoekresultaten - Petryk, Anna

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  1. 1
    Holoprosencephaly: signalling interactions between the brain and the face, the environment and the genes, and the phenotypic variability in animal models and humans

    Holoprosencephaly: signalling interactions between the brain and the face, the environment and the genes, and the phenotypic variability in animal models and humans door Petryk, Anna, Graf, Daniel, Marcucio, Ralph

    Gepubliceerd in 2014
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  2. 2
    Burden of disease in pediatric patients with hypophosphatasia: results from the HPP Impact Patient Survey and the HPP Outcomes Study Telephone interview

    Burden of disease in pediatric patients with hypophosphatasia: results from the HPP Impact Patient Survey and the HPP Outcomes Study Telephone interview door Rush, Eric T., Moseley, Scott, Petryk, Anna

    Gepubliceerd in 2019
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  3. 3
    Self-renewal of neural stem cells: implications for future therapies

    Self-renewal of neural stem cells: implications for future therapies door Raitano, Susanna, Verfaillie, Catherine M., Petryk, Anna

    Gepubliceerd in 2013
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  4. 4
    Physical Function and Health‐Related Quality of Life in Adults Treated With Asfotase Alfa for Pediatric‐Onset Hypophosphatasia

    Physical Function and Health‐Related Quality of Life in Adults Treated With Asfotase Alfa for Pediatric‐Onset Hypophosphatasia door Genest, Franca, Rak, Dominik, Petryk, Anna, Seefried, Lothar

    Gepubliceerd in 2020
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  5. 5
    Iron Deficiency Alters Expression of Genes Implicated in Alzheimer Disease Pathogenesis

    Iron Deficiency Alters Expression of Genes Implicated in Alzheimer Disease Pathogenesis door Carlson, Erik S., Magid, Rhamy, Petryk, Anna, Georgieff, Michael K.

    Gepubliceerd in 2008
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  6. 6
    AN ADJUNCTIVE USE OF ASFOTASE ALFA AND ZOLEDRONIC ACID AFTER SPINAL SURGERY IN NEUROFIBROMATOSIS TYPE 1 RELATED DYSTROPHIC SCOLIOSIS

    AN ADJUNCTIVE USE OF ASFOTASE ALFA AND ZOLEDRONIC ACID AFTER SPINAL SURGERY IN NEUROFIBROMATOSIS TYPE 1 RELATED DYSTROPHIC SCOLIOSIS door Harindhanavudhi, Tasma, Takahashi, Takashi, Petryk, Anna, Polly, David W

    Gepubliceerd in 2020
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  7. 7
    Autosomal dominant mesomandibular fibro-osseous dysplasia: a self-resolving inherited fibro-osseous lesion of the jaws

    Autosomal dominant mesomandibular fibro-osseous dysplasia: a self-resolving inherited fibro-osseous lesion of the jaws door Koutlas, Ioannis G., Forsman, Cynthia L., Kyrkanides, Stephanos, Oetting, William S., Petryk, Anna

    Gepubliceerd in 2012
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  8. 8
    “English Disease”: Historical Notes on Rickets, the Bone–Lung Link and Child Neglect Issues

    “English Disease”: Historical Notes on Rickets, the Bone–Lung Link and Child Neglect Issues door Zhang, Mingyong, Shen, Fan, Petryk, Anna, Tang, Jingfeng, Chen, Xingzhen, Sergi, Consolato

    Gepubliceerd in 2016
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  9. 9
    Embryonic salivary gland dysmorphogenesis in Twisted gastrulation deficient mice

    Embryonic salivary gland dysmorphogenesis in Twisted gastrulation deficient mice door Melnick, Michael, Petryk, Anna, Abichaker, George, Witcher, Dan, Person, Anthony D., Jaskoll, Tina

    Gepubliceerd in 2005
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  10. 10
    Impact of retinoic acid exposure on midfacial shape variation and manifestation of holoprosencephaly in Twsg1 mutant mice

    Impact of retinoic acid exposure on midfacial shape variation and manifestation of holoprosencephaly in Twsg1 mutant mice door Billington, Charles J., Schmidt, Brian, Marcucio, Ralph S., Hallgrimsson, Benedikt, Gopalakrishnan, Rajaram, Petryk, Anna

    Gepubliceerd in 2015
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  11. 11
    The expression of Twisted gastrulation in postnatal mouse brain and functional implications

    The expression of Twisted gastrulation in postnatal mouse brain and functional implications door Sun, Mu, Forsman, Cynthia, Sergi, Consolato, Gopalakrishnan, Rajaram, O’Connor, Michael B., Petryk, Anna

    Gepubliceerd in 2010
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  12. 12
    WT1 regulates epicardial epithelial to mesenchymal transition through β-catenin and retinoic acid signaling pathways

    WT1 regulates epicardial epithelial to mesenchymal transition through β-catenin and retinoic acid signaling pathways door von Gise, Alexander, Zhou, Bin, Honor, Leah B., Ma, Qing, Petryk, Anna, Pu, William T.

    Gepubliceerd in 2011
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  13. 13
    Compartmentalization of bone morphogenetic proteins and their antagonists in lymphoid progenitors and supporting microenvironments and functional implications

    Compartmentalization of bone morphogenetic proteins and their antagonists in lymphoid progenitors and supporting microenvironments and functional implications door Passa, Ourania, Tsalavos, Sotiris, Belyaev, Nikolai N, Petryk, Anna, Potocnik, Alexandre J, Graf, Daniel

    Gepubliceerd in 2011
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  14. 14
    Short-Term PTH(1-34) Therapy in Children to Correct Severe Hypocalcemia and Hyperphosphatemia due to Hypoparathyroidism: Two Case Studies

    Short-Term PTH(1-34) Therapy in Children to Correct Severe Hypocalcemia and Hyperphosphatemia due to Hypoparathyroidism: Two Case Studies door Mishra, Pooja E., Schwartz, Betsy L., Sarafoglou, Kyriakie, Hook, Kristen, Kim, Youngki, Petryk, Anna

    Gepubliceerd in 2016
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  15. 15
    Feasibility and tolerability of whole‐body, low‐intensity vibration and its effects on muscle function and bone in patients with dystrophinopathies: a pilot study

    Feasibility and tolerability of whole‐body, low‐intensity vibration and its effects on muscle function and bone in patients with dystrophinopathies: a pilot study door Petryk, Anna, Polgreen, Lynda E., Grames, Molly, Lowe, Dawn A., Hodges, James S., Karachunski, Peter

    Gepubliceerd in 2017
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  16. 16
    Case Report: The Specter of Untreated Congenital Hypothyroidism in Immigrant Families

    Case Report: The Specter of Untreated Congenital Hypothyroidism in Immigrant Families door Hamdoun, Elwaseila, Karachunski, Peter, Nathan, Brandon, Fischer, Melissa, Torkelson, Jane L., Drilling, Amy, Petryk, Anna

    Gepubliceerd in 2016
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  17. 17
    First Phase Insulin Release and Glucose Tolerance in Children with Fanconi Anemia After Hematopoietic Cell Transplantation

    First Phase Insulin Release and Glucose Tolerance in Children with Fanconi Anemia After Hematopoietic Cell Transplantation door Polgreen, Lynda E, Thomas, William, MacMillan, Margaret L., Wagner, John E., Moran, Antoinette, Petryk, Anna

    Gepubliceerd in 2009
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  18. 18
    Distinct populations within Isl1 lineages contribute to appendicular and facial skeletogenesis through the β-catenin pathway

    Distinct populations within Isl1 lineages contribute to appendicular and facial skeletogenesis through the β-catenin pathway door Akiyama, Ryutaro, Kawakami, Hiroko, Taketo, M. Mark, Evans, Sylvia M., Wada, Naoyuki, Petryk, Anna, Kawakami, Yasuhiko

    Gepubliceerd in 2014
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  19. 19
    Severe Congenital Hypothyroidism Due to a Novel Deep Intronic Mutation in the TSH Receptor Gene Causing Intron Retention

    Severe Congenital Hypothyroidism Due to a Novel Deep Intronic Mutation in the TSH Receptor Gene Causing Intron Retention door Larrivée-Vanier, Stéphanie, Magne, Fabien, Hamdoun, Elwaseila, Petryk, Anna, Kibar, Zoha, Van Vliet, Guy, Deladoëy, Johnny

    Gepubliceerd in 2020
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  20. 20
    Wnt5 signaling in vertebrate pancreas development

    Wnt5 signaling in vertebrate pancreas development door Kim, Hyon J, Schleiffarth, Jack R, Jessurun, Jose, Sumanas, Saulius, Petryk, Anna, Lin, Shuo, Ekker, Stephen C

    Gepubliceerd in 2005
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