Results 91 to 100 of about 2,067 (196)

Molecular Analysis of Twist1 and FGF Receptors in a Rabbit Model of Craniosynostosis: Likely Exclusion as the Loci of Origin [PDF]

, 2013
Craniosynostosis is the premature fusion of the cranial vault sutures. We have previously described a colony of rabbits with a heritable pattern of nonsyndromic, coronal suture synostosis; however, the underlying genetic defect remains unknown.
Cooper, Gregory M., Cray, James J., Durham, Emily L., Gallo, Phillip H., Kathju, Sandeep, Mooney, Mark P.   +5 more
core   +3 more sources

ISUOG Practice Guidelines: performance of third‐trimester obstetric ultrasound scan

Ultrasound in Obstetrics &Gynecology, Volume 63, Issue 1, Page 131-147, January 2024.
A. Khalil, A. Sotiriadis, F. D'Antonio, F. Da Silva Costa, A. Odibo, F. Prefumo, A. T. Papageorghiou, L. J. Salomon   +7 more
wiley   +1 more source

Specific inhibition of fibroblast growth factor receptor 1 signaling by a DNA aptamer

Molecular Therapy: Nucleic Acids
Impaired fibroblast growth factor receptor (FGFR) signaling is associated with many human conditions, including growth disorders, degenerative diseases, and cancer.
Vladimira Zlinska, Zuzana Feketova, Aleksandra Czyrek, Julia Chudzian, Martina Lenarcic Zivkovic, Vlad-Constantin Ursachi, Pooja Dudeja, Bohumil Fafilek, Jan Rynes, Gustavo Rico-Llanos, Adolf Koudelka, Tanaya Roy, Martyna Biadun, Vendula Raskova, Katerina Svozilova, Michaela Stroblova, Mateusz Krzyscik, Kalina Hristova, Daniel Krowarsch, Silvie Foldynova-Trantirkova, Malgorzata Zakrzewska, Lukas Trantirek, Pavel Krejci   +22 more
doaj   +1 more source

Abnormal mandibular growth and the condylar cartilage [PDF]

, 2017
Deviations in the growth of the mandibular condyle can affect both the functional occlusion and the aesthetic appearance of the face. The reasons for these growth deviations are numerous and often entail complex sequences of malfunction at the cellular ...
Luder, Hans. U., Müller, Lukas, Peltomäki, Timo, Pirttiniemi, Pertti   +3 more
core  

Staged dissection reduces blood loss in surgery for metopic synostosis

Journal of Plastic Surgery and Hand Surgery
INTRODUCTION: Fronto-orbital remodelling for metopic synostosis is an extensive operation with substantial blood loss, particularly from emissary veins in the glabellar region.
Anna Sundelin, Madiha Bhatti-Søfteland, Ingrid Stubelius, Tobias Hallén, Robert Olsson, Giovanni Maltese, Peter Tarnow, Karin Säljö, Lars Kölby   +8 more
doaj   +1 more source

Genetic alterations in craniosynostosis, genotype-phenotype correlations [PDF]

, 2015
A koponyavarratok idő előtti fúziójának következtében kialakuló craniosynostosis klinikailag és etiológiailag heterogén betegségcsoport. A betegek többségére jellemző izolált (nem-szindrómás) forma kialakulásában a környezeti és a genetikai faktorok ...
Bessenyei, Beáta
core  

Correction of maxillofacial deformities in a patient with unilateral coronal craniosynostosis (plagiocephaly): a case report and a review of literatures.

Frontiers in Dentistry, 2013
Plagiocephaly (oblique skull) is premature fusion of one of the coronal sutures. Frontal plagiocephaly is a rare congenital deformity in the skull that is the most complicated form of craniosynostosis to treat. Examination of all sutures is necessary for
Mansour Khorasani, Mohsen Hasani Barzi, Bahman Derakhshan   +2 more
doaj  

Long-term treatment results of craniosynostosis [PDF]

Craniosynostosis patients experience multiple problems due to improper growth of the skull. The purpose of this study was to evaluate the long-term treatment results of patients operated on for sagittal or metopic synostosis in a single centre study.
Svalina, Anja
core   +1 more source

Advances in Craniofacial Surgery [PDF]

, 2016
Calvaria development initiates by growth from primary ossification centers meeting each other to form suture sites. The term craniosynostosis describes premature fusion of one or more of the calvarial sutures.
Hashemi, Hamid Mahmoud, Kahnamouii, Shiva Solahaye, Mohammadi, Farnoosh   +2 more
core   +1 more source

AI-based diagnosis and phenotype – Genotype correlations in syndromic craniosynostoses [PDF]

Apert (AS), Crouzon (CS), Muenke (MS), Pfeiffer (PS), and Saethre Chotzen (SCS) are among the most frequently diagnosed syndromic craniosynostoses. The aims of this study were (1) to train an innovative model using artificial intelligence (AI)–based ...
Amiel, Jeanne, Arnaud, Eric, Bongibault, Thomas, Bouygues, Thomas, Collet, Corinne, Cormier-Daire, Valérie, Douillet, Maxime, Dunaway, David J., Garcelon, Nicolas, Hennocq, Quentin, Jeelani, Nu Owase, Khonsari, Roman H., Lyonnet, Stanislas, Ong, Juling, Paternoster, Giovanna, Picard, Arnaud, Rickart, Alexander J., Rio, Marlène, Schievano, Silvia, van de Lande, Lara S.   +19 more
core   +3 more sources