Results 21 to 30 of about 108,266 (269)

Retrospective Analysis of the Congenital Malformations in the Tertiary Center in Şanlıurfa

open access: yesVan Tıp Dergisi, 2019
INTRODUCTION: The aim of this study is to determine the incidence, type and distribution of congenital anomalies that were diagnosed prenatally in a tertiary center of Sanliurfa which is the city that has the highest birth rate of Turkey.
Sibel Sak   +4 more
doaj   +1 more source

Vertebral and Intraspinal Anomalies in Indian Population with Congenital Scoliosis: A Study of 119 Consecutive Patients [PDF]

open access: yesAsian Spine Journal, 2016
Study DesignRetrospective case study by clinical and radiological data analysis.PurposeTo analyze different types of vertebral anomalies and the incidence of associated intraspinal anomalies in the Indian population.Overview of LiteratureThis is the ...
Neeraj Gupta   +3 more
doaj   +1 more source

Congenital laryngeal anomalies

open access: yesBrazilian Journal of Otorhinolaryngology, 2014
It is essential for clinicians to understand issues relevant to the airway management of infants and to be cognizant of the fact that infants with congenital laryngeal anomalies are at particular risk for an unstable airway.To familiarize clinicians with issues relevant to the airway management of infants and to present a succinct description of the ...
openaire   +5 more sources

Real‐World Trends in Prenatal Antirheumatic Drug Utilization in Ontario, Canada: A Cross‐Sectional Time‐Series Analysis

open access: yesArthritis Care &Research, EarlyView.
Objective This study aimed to describe real‐world trends in preconception and prenatal use of antirheumatic drugs among pregnant individuals with rheumatic diseases in Ontario, Canada. Methods We conducted a time‐series analysis using repeated cross‐sectional data to examine annual patterns of disease‐modifying antirheumatic drug (DMARD) use among ...
Shenthuraan Tharmarajah   +6 more
wiley   +1 more source

Postlicensure safety surveillance of congenital anomaly and miscarriage among pregnancies exposed to quadrivalent human papillomavirus vaccine

open access: yesHuman Vaccines & Immunotherapeutics, 2018
Limited safety data are available on inadvertent exposure to quadrivalent human papillomavirus vaccine (4vHPV) during pregnancy. We conducted a descriptive observational postlicensure safety surveillance study in Kaiser Permanente Southern California and
Lina S. Sy   +12 more
doaj   +1 more source

Congenital Anomalies of the Breast [PDF]

open access: yesSeminars in Plastic Surgery, 2013
Poland syndrome is a combination of chest wall deformity and absent or hypoplastic pectoralis muscle and breast associated with shortening and brachysyndactyly of the upper limb. Clinical presentation varies widely; therefore, reconstructive procedures have to be adapted to the deformity, ranging from chest wall stabilization or augmentation, dynamic ...
Louise, Caouette-Laberge, Daniel, Borsuk
openaire   +2 more sources

MIS12 Is Required for Kinetochore‐Microtubule Attachment in Oocyte Meiosis

open access: yesAdvanced Science, EarlyView.
A model depicting the role of MIS12 in K‐MT attachment during oocyte meiosis. The presence of MIS12 stabilizes bipolar K‐MT attachments by maintaining the function of NDC80 and its interaction with TUBB. This, in turn, promotes KNL1 assembly and subsequent SAC protein recruitment to kinetochores.
Jian Li   +9 more
wiley   +1 more source

An Unusual First Presentation of Ebstein′s Anomaly in a 70-year-old Patient

open access: yesHeart India, 2015
Ebstein′s anomaly is a congenital heart defect. The septal and posterior leaflets of the tricuspid valve are displaced toward the apex of the right ventricle called as atrailazation of right ventricle. Most of them have interatrial communication. Ebstein′
Amit Achliya, Hitesh H Gulhane
doaj   +1 more source

Large‐scale Whole‐Exome Sequencing Defines the Protein‐Coding Architecture of Retinal Structure, Visual Function, and Major Blinding Diseases

open access: yesAdvanced Science, EarlyView.
Large‐scale whole‐exome sequencing in 356,982 UK Biobank participants defines the protein‐coding architecture of retinal structure, visual function, and major blinding diseases. Pleiotropic genes, including CFI, C3, and RIOX1, bridge multiple retinal phenotypes, while experimental validation of FYB2 implicates RPE barrier dysfunction, providing ...
Jianqing Li   +23 more
wiley   +1 more source

Diagnosis of Rare Association of Orthotopic Multicystic Dysplasia with Crossed Fused Renal Ectopia

open access: yesCase Reports in Urology, 2014
Orthotopic multicystic dysplastic kidney with crossed fused ectopia is a rare congenital anomaly. This congenital anomaly may give an appearance of a solitary kidney morphology during the initial imaging evaluation.
Linnan Tang   +4 more
doaj   +1 more source

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