Results 281 to 290 of about 145,893 (342)

Genetic and Molecular Determinants of Familial Transmission of Skeletal Malocclusions

Orthodontics &Craniofacial Research, EarlyView.
ABSTRACT Families studies conducted in different ethnic populations worldwide have helped elucidate the molecular and genetic factors involved in the development of skeletal class III malocclusion. Therefore, the aim of this study is to provide an updated summary.
Alexandra Dehesa‐Santos, Lucia Carreño‐Gomez, Rosa Yañez‐Vico, Alejandro Iglesias‐Linares   +3 more
wiley   +1 more source

Pontine Tegmental Cap Dysplasia: A Rare Case in South Africa. [PDF]

Cureus
Nyila T, Mndebele G, Koranteng N, Peiser G.   +3 more
europepmc   +1 more source

Estrés nutricional, hipoplasia y explotación de recursos en el centro sur de Mendoza (Argentina) Nutritional stress, enamel hypoplasia, and resource exploitation in south-central Mendoza

, 2007
Paula Novellino, Adolfo Gil
openalex   +1 more source

3D Analysis of Mandibular and Glenoid Fossa Responses to Bone‐Anchored Maxillary Protraction in Patients With UCLP

Orthodontics &Craniofacial Research, EarlyView.
ABSTRACT Introduction Bone‐anchored maxillary protraction (BAMP) has been increasingly used to correct midface deficiency and Class III malocclusion in patients with unilateral cleft lip and palate (UCLP). However, its three‐dimensional (3D) effects on the mandible remain insufficiently explored.
Jeroen Wagemans, Ralph Steegman, Yijin Ren   +2 more
wiley   +1 more source

Congenital Cleft Earlobe: Classification and Surgical Techniques with a Scoping Review of the Literature. [PDF]

J Clin Med
Jun YJ, Park YJ, Kim MR, Baek MJ, Kim SH.   +4 more
europepmc   +1 more source

Periodontal Architecture in Ectodermal Dysplasia: An Observational Clinical and Histological Study

Oral Diseases, EarlyView.
ABSTRACT Objective To investigate gingival and periodontal characteristics in Ectodermal dysplasia (ED), focusing on soft‐tissue phenotype, anatomical variations, and periodontal architecture. Materials and Methods Observational clinical study of 11 individuals (16–30 years) with confirmed clinical or genetic ED diagnosis.
Marco Montevecchi, Margherita Giorgia Liguori, Ilaria Santini, Nicola Marco Sforza, Giulia Querzoli, Leoluca Valeriani   +5 more
wiley   +1 more source

Congenital Syngnathia With Holoprosencephaly: A Case Report of a Fatal Presentation in a Resource-Limited Setting. [PDF]

Clin Case Rep
Haile AM, Mengistie BT, Tamiru TY, Mengistie CT, Abebe DG, Haile BM.   +5 more
europepmc   +1 more source

A rare case of de novo 20p12.3 microdeletion syndrome in a nine-year-old female: case report and literature review. [PDF]

Front Genet
Aljedani H, Faden Y, Alghamdi M, Alzahrani A, Shawli A, Albakistani R.   +5 more
europepmc   +1 more source

Congenital Biliary Hypoplasia

Annals of Surgery, 1964
openaire   +3 more sources

Associations of Intraoperative Hypotension and Vasopressor Administration With Postoperative Acute Kidney Injury in Children Undergoing Liver Transplantation: A Retrospective Cohort Study

Pediatric Anesthesia, EarlyView.
ABSTRACT Background Both intraoperative hypotension (IOH) and vasopressor administration are independently associated with postoperative acute kidney injury (AKI) in adults undergoing major noncardiac surgery. Whether these associations extend to children undergoing major noncardiac surgery, such as liver transplantation, remains unknown.
Theodora Wingert, Kelly Feldman, Tiffany Williams, Amelie Delaporte, Matthew Lum, Tristan Grogan, Christine Nguyen‐Buckley, Alexandre Joosten   +7 more
wiley   +1 more source