Results 41 to 50 of about 79,027 (268)
The study aimed to establish and evaluate anatomoradiological landmarks in trigeminal neuralgia patients using computed tomography (CT) and cone-beam CT.
Seçil Aksoy +4 more
doaj +1 more source
ABSTRACT WAGR spectrum disorder (WAGRSD) is an ultra‐rare congenital disorder caused by heterozygous deletion of chromosome 11p13. While classically associated with Wilms tumor, Aniridia, Genitourinary anomalies, and a Range of developmental delays, accurate delineation of the deletion is critical for prognosis because the phenotypic spectrum extends ...
Andrew M. George +11 more
wiley +1 more source
Background: This study investigated the shapes and dimensions of the foramen ovale (FO) and foramen spinosum (FS) in a specific population sample from Delta State, Nigeria, emphasizing their significance in various neurosurgical procedures. Materials and
Beryl Shitandi Ominde +4 more
doaj +1 more source
Echocardiographic guided, transatrial closure of a patent foramen ovale
Background The management of an incidental patent foramen ovale found during planned cardiac surgery remains a challenge, and current guidelines are not helpful.
Felix Fleissner +3 more
doaj +1 more source
Defining Features of Gabriele‐de Vries Syndrome in Adults: A Case Report and Literature Review
ABSTRACT Gabriele‐de Vries syndrome (GADEVS) is a neurodevelopmental disorder caused by heterozygous pathogenic variants in the YY1 gene. Like most rare genetic syndromes, the adult manifestations of GADEVS remain poorly defined. Here, we describe the oldest patient reported to date with GADEVS—a 63‐year‐old woman with a c.1177_1179del YY1 variant ...
Ethan W. Hollingsworth, Changrui Xiao
wiley +1 more source
The aim of this study was to evaluate apical transportation and apical root canal sealing after root canal filling in human teeth prepared with MTwo® Rotary System with and without apical foramen enlargement. Twenty mandibular premolars were divided into
Matheus Albino Souza +8 more
doaj +1 more source
A Case of Multiple Mitochondrial Dysfunctions Syndrome 1 and Review of the Literature
ABSTRACT Multiple mitochondrial dysfunctions syndrome 1 (MMDS1, MIM #605711) due to NFU1 gene defects is an ultra‐rare autosomal recessive inborn error of metabolism associated with reduced function of NFU1 iron–sulfur cluster (ISC) scaffold protein.
Charles R. DiFalco +6 more
wiley +1 more source
La columna vertebral del perro ha sido utilizada como modelo experimental en medicina humana, y es uno de los animales domésticos más estudiados en medicina veterinaria.
G. O. Alonso +2 more
doaj
Morphometric Study of Nutrient Foramen of Adult Human Tibia Bone [PDF]
Introduction: The position of nutrient foramen on the shaft of long bones is specific. It transmits nerve and vessels which help in maintaining nutrition of bone. Blood supply by nutrient artery is essential during early phases of ossification as well
Hiren S Chavda, Nishita K Jethva
doaj +1 more source
Structural-heart-disease specialists perform procedures that will correct anatomic abnormalities of the heart, such as patent foramen ovale (PFO): a congenital opening in the interatrial septum. In utero, the foramen ovale is an extremely important structure, because it enables oxygenated blood from the placenta to travel from the fetus's right atrium ...
openaire +2 more sources

