Comprehensive Oral Diagnosis and Management for Women with Turner Syndrome

Autor: Victoria Tallón-Walton, Meritxell Sánchez-Molins, Wenwen Hu, Neus Martínez-Abadías, Aroa Casado, María Cristina Manzanares-Céspedes

Publikováno v: Diagnostics, Vol 14, Iss 7, p 769 (2024)

Turner Syndrome (TS) is a rare genetic disorder that affects females when one of the X chromosomes is partially or completely missing. Due to high genetic and phenotypic variability, TS diagnosis is challenging and is often delayed until adolescence,

Externí odkaz: https://doaj.org/article/7f7259fa920e496ab6b49c01717f92e2

Frameshift mutations in dentin phosphoprotein and dependence of dentin disease phenotype on mutation location

Autor: Janna Waltimo-Sirén, Sirpa Arte, Satu Alaluusua, Eduard Chimenos Küstner, Victoria Tallón Walton, Heidi Holappa, Jaap Veerkamp, Pekka Nieminen, Sára Karjalainen, Lisa Papagiannoulis-Lascarides, Tarja Siltanen, Pirjo-Liisa Lukinmaa, Päivi Ollila

Publikováno v: Nieminen, P, Papagiannoulis-Lascarides, L, Waltimo-Siren, J, Ollila, P, Karjalainen, S, Arte, S, Veerkamp, J, Tallon Walton, V, Chimenos Küstner, E, Siltanen, T, Holappa, H, Lukinmaa, P L & Alaluusua, S 2011, ' Frameshift mutations in dentin phosphoprotein and dependence of dentin disease phenotype on mutation location ', Journal of Bone and Mineral Research, vol. 26, no. 4, pp. 873-880 . https://doi.org/10.1002/jbmr.276
Journal of Bone and Mineral Research, 26(4), 873-880. Wiley-Blackwell
Journal of Bone and Mineral Research, 26(4), 873-880. American Society for Bone and Mineral Research

We describe results from a mutational analysis of the region of the dentin sialophosphoprotein (DSPP) gene encoding dentin phosphoprotein (DPP) in 12 families with dominantly inherited dentin diseases. In eight families (five mutations in the N-termi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e92dfb999beec60501adfad659759919
https://pubmed.ncbi.nlm.nih.gov/20949630

Mandible measurements and dental midline deviation after alveolar nerve transection in growing rabbits

Autor: Vicente Lozano de Luaces, Victoria Tallón Walton, María Cristina Manzanares Céspedes, Iván Valdivia Gandur, Patricia Carvalho Lobato

Publikováno v: Recercat. Dipósit de la Recerca de Catalunya
instname
Dipòsit Digital de la UB
Universidad de Barcelona
International Journal of Morphology v.29 n.1 2011
SciELO Chile
CONICYT Chile
instacron:CONICYT

Summary: the relationship between sensitive innervation and normal mandibular bone development has been described in the literature. Therefore, neural damage is a potential cause of osseous deformities, particularly in growing subjects. The aim of th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46f1b8574fa2ef2080a103b1d24f81d0
http://hdl.handle.net/2445/106803