Zobrazeno 1 - 10
of 35
pro vyhledávání: '"C. A. Murdoch-Kinch"'
Autor:
Elo Andersen, Joel J. Napeñas, Michael T. Brennan, Siri Beier Jensen, Nilza Nelly Fontana Lopes, Salivary Gland Hypofunction, Xerostomia Section, Linda S. Elting, A. Nogueira-Rodrigues, Carlton G. Brown, A. L. S. Mello, Anne Marie Lynge Pedersen, Raj G. Nair, L. V. Muniz, J. Dutilh, Arjan Vissink, Fred K. L. Spijkervet, Deborah P. Saunders, C. A. Murdoch-Kinch, Andrew Davies, Ljiljana Janković, Dianna Weikel, I. von Bültzingslöwen, B. Stirling, Janet S. Fulton
Publikováno v:
Supportive Care in Cancer. 18(8):1061-1079
This systematic review aimed to assess the literature for management strategies and economic impact of salivary gland hypofunction and xerostomia induced by cancer therapies and to determine the quality of evidence-based management recommendations. T
Autor:
Le Guevelou, J.1 (AUTHOR) jennifer.leguevelou@gmail.com, Palard‐Novello, X.2 (AUTHOR), Kammerer, E.1 (AUTHOR), Baty, M.1 (AUTHOR), Perazzi, M.1 (AUTHOR), Larnaudie, A.3 (AUTHOR), De Crevoisier, R.1 (AUTHOR), Castelli, J.1 (AUTHOR)
Publikováno v:
Cancer Medicine. Dec2024, Vol. 13 Issue 24, p1-16. 16p.
Autor:
Frederik Spijkervet, L. V. Muniz, Raj G. Nair, Linda S. Elting, Elo Andersen, Deborah P. Saunders, C. A. Murdoch-Kinch, C. G. Brown, Arjan Vissink, Dianna Weikel, J. Dutilh, A. Nogueira-Rodrigues, Andrew Davies, I. von Bültzingslöwen, Ljiljana Janković, Anne Marie Lynge Pedersen, A. L. S. Mello, B. Stirling, Siri Beier Jensen, Nilza Nelly Fontana Lopes, Michael T. Brennan, Joel J. Napeñas, Janet S. Fulton
Publikováno v:
University of Copenhagen
This systematic review aimed to assess the literature for prevalence, severity, and impact on quality of life of salivary gland hypofunction and xerostomia induced by cancer therapies. The electronic databases of MEDLINE/PubMed and EMBASE were search
Publikováno v:
American journal of medical genetics. 77(5)
Crouzon syndrome (CS) is an autosomal dominant condition comprising orbital proptosis, midfacial hypoplasia, premature sutural synostosis, and altered proportions of bone lengths in the hands. In families the CS trait is highly variable. Several case
Autor:
C A, Murdoch-Kinch, R E, Ward
Publikováno v:
American journal of medical genetics. 73(1)
Crouzon syndrome (CS) is characterized by premature craniosynostosis, orbital proptosis, and midfacial hypoplasia and is related to the acrocephalosyndactylies (ACS) with limb abnormalities. In CS the hands are considered to be normal, but a previous
Autor:
C A, Murdoch-Kinch, J R, Geist
Publikováno v:
The Journal of the Michigan Dental Association. 78(3)
Publikováno v:
Oral surgery, oral medicine, and oral pathology. 75(3)
The ectodermal dysplasias are a clinically and genetically heterogeneous group of more than 120 syndromes involving ectodermally derived structures. The syndrome that is autosomal dominantly inherited and characterized by hypodontia, dysplastic nails
Publikováno v:
The International journal of oralmaxillofacial implants. 7(2)
A modified technique for presurgical evaluation of intraosseous implant placement using linear tomography has been developed. The simplified technique is applicable to tomographic systems equipped with a cephalometric head positioner (cephalostat) an
Autor:
Kerälä S; Oulu University of Applied Sciences, Oulu, Finland., Laurila K; Oulu University of Applied Sciences, Oulu, Finland., Kajula O; Oulu University of Applied Sciences, Oulu, Finland., Keinänen AL; Oulu University of Applied Sciences, Oulu, Finland.
Publikováno v:
International journal of dental hygiene [Int J Dent Hyg] 2024 Nov 17. Date of Electronic Publication: 2024 Nov 17.
Autor:
Preshaw PM; School of Dentistry, University of Dundee, Dundee, UK., Minnery H; Private Practice, Liverpool, UK., Dunn I; Private Practice, Liverpool, UK.; University of Central Lancashire, Preston, UK., Bissett SM; School of Dental Sciences, Newcastle University, Newcastle upon Tyne, UK.
Publikováno v:
International journal of dental hygiene [Int J Dent Hyg] 2024 Nov 04. Date of Electronic Publication: 2024 Nov 04.