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Johanna Norderyd

Showing results (1-10 of 13) with videos related to

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International Journal of Paediatric Dentistry|July 26, 2011
Hypoplastic root cementum and premature loss of primary teeth in Coffin-Lowry syndrome: a case reportJohanna Norderyd, Johan Aronsson
Disability and Rehabilitation|November 23, 2016
Specialised dental care for children with complex disabilities focusing on child's functioning and need for general anaesthesiaJohanna Norderyd, Gunilla Klingberg, Denise Faulks, et al.
International Journal of Paediatric Dentistry|May 18, 2017
Which factors most influence referral for restorative dental treatment under sedation and general anaesthesia in children with complex disabilities: caries severity, child functioning, or dental service organisation?Johanna Norderyd, Denise Faulks, Gustavo Molina, et al.
BMC Medical Genetics|November 25, 2016
Abnormal primary and permanent dentitions with ectodermal symptoms predict WNT10A deficiencyBirgitta Bergendal, Johanna Norderyd, Xiaolei Zhou, et al.
Disability and Rehabilitation|September 25, 2014
Oral health, medical diagnoses, and functioning profiles in children with disabilities receiving paediatric specialist dental care - a study using the ICF-CYJohanna Norderyd, Anne Lillvist, Gunilla Klingberg, et al.
American Journal of Medical Genetics. Part A|June 1, 2011
Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genesBirgitta Bergendal, Joakim Klar, Christina Stecksén-Blicks, et al.
European Journal of Oral Sciences|February 26, 2022
Dental health care for children with Down syndrome: Parents' description of their children's needs in dental health care settingsMalin Stensson, Johanna Norderyd, Marcia Van Riper, et al.
American Journal of Medical Genetics. Part A|January 23, 2014
WNT10A mutations account for ¼ of population-based isolated oligodontia and show phenotypic correlationsPakeeza Shaiq Arzoo, Joakim Klar, Birgitta Bergendal, et al.
Plos One|April 25, 2013
Using the International Classification of Functioning, Disability and Health (ICF) to describe children referred to special care or paediatric dental servicesDenise Faulks, Johanna Norderyd, Gustavo Molina, et al.
American Journal of Medical Genetics. Part A|March 21, 2017
Further evidence for specific IFIH1 mutation as a cause of Singleton-Merten syndrome with phenotypic heterogeneityMaria Pettersson, Birgitta Bergendal, Johanna Norderyd, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
International Journal of Paediatric Dentistry|July 26, 2011
Hypoplastic root cementum and premature loss of primary teeth in Coffin-Lowry syndrome: a case reportJohanna Norderyd, Johan Aronsson
Disability and Rehabilitation|November 23, 2016
Specialised dental care for children with complex disabilities focusing on child's functioning and need for general anaesthesiaJohanna Norderyd, Gunilla Klingberg, Denise Faulks, et al.
International Journal of Paediatric Dentistry|May 18, 2017
Which factors most influence referral for restorative dental treatment under sedation and general anaesthesia in children with complex disabilities: caries severity, child functioning, or dental service organisation?Johanna Norderyd, Denise Faulks, Gustavo Molina, et al.
BMC Medical Genetics|November 25, 2016
Abnormal primary and permanent dentitions with ectodermal symptoms predict WNT10A deficiencyBirgitta Bergendal, Johanna Norderyd, Xiaolei Zhou, et al.
Disability and Rehabilitation|September 25, 2014
Oral health, medical diagnoses, and functioning profiles in children with disabilities receiving paediatric specialist dental care - a study using the ICF-CYJohanna Norderyd, Anne Lillvist, Gunilla Klingberg, et al.
American Journal of Medical Genetics. Part A|June 1, 2011
Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genesBirgitta Bergendal, Joakim Klar, Christina Stecksén-Blicks, et al.
European Journal of Oral Sciences|February 26, 2022
Dental health care for children with Down syndrome: Parents' description of their children's needs in dental health care settingsMalin Stensson, Johanna Norderyd, Marcia Van Riper, et al.
American Journal of Medical Genetics. Part A|January 23, 2014
WNT10A mutations account for ¼ of population-based isolated oligodontia and show phenotypic correlationsPakeeza Shaiq Arzoo, Joakim Klar, Birgitta Bergendal, et al.
Plos One|April 25, 2013
Using the International Classification of Functioning, Disability and Health (ICF) to describe children referred to special care or paediatric dental servicesDenise Faulks, Johanna Norderyd, Gustavo Molina, et al.
American Journal of Medical Genetics. Part A|March 21, 2017
Further evidence for specific IFIH1 mutation as a cause of Singleton-Merten syndrome with phenotypic heterogeneityMaria Pettersson, Birgitta Bergendal, Johanna Norderyd, et al.
Pageof 2