Results 181 to 190 of about 300,155 (312)

Easily missed?: femoral hernias [PDF]

, 2011
Kidd, G.A., O'Dwyer, P.J., Whalen, H.R.
core   +1 more source

The Importance of Newborn Genetic Screening for Early Identification of GJB2 and SLC26A4 Related Hearing Loss

Otolaryngology–Head and Neck Surgery, EarlyView.
Abstract Objective To assess the added benefit of newborn genetic screening for GJB2 and SLC26A4 variants in conjunction with newborn hearing screening. Study Design Retrospective cohort study. Methods Children with known variants of GJB2 and SLC26A4 were identified from 485 children with hearing loss who underwent testing with Next Generation ...
Emily R Wener, Sharon L Cushing, Blake C Papsin, Dimitrios J. Stavropoulos, Roberto Mendoza‐Londono, Nada Quercia, Karen A. Gordon   +6 more
wiley   +1 more source

PREVASCULAR FEMORAL HERNIA

, 1912
Alexis V. Moschcowitz
openalex   +2 more sources

REPORT OF A CASE OF DIAPHRAGMATIC HERNIA [PDF]

, 1917
George F. Koehler
openalex   +1 more source

Three and Four Courses of Radiation for Children with Recurrent Diffuse Intrinsic Pontine Glioma

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Purpose Re‐irradiation (RT2) for children with diffuse intrinsic pontine glioma (DIPG) is increasingly used upon recurrence; however, limited data are available for evaluating additional courses of radiotherapy (RT) for DIPG. The purpose of this case series was to report our institutional experience in treating patients with recurrent DIPG ...
Nisha Shariff, Anthony Lausch, Eric Bouffet, Derek S. Tsang   +3 more
wiley   +1 more source

HERNIA OF URINARY BLADDER: [PDF]

, 1918
H. Blakeway
openalex   +1 more source

Genetic Diagnosis and Clinical Features of Fetuses With Congenital Diaphragmatic Hernia

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective Congenital diaphragmatic hernia (CDH) is a rare abnormality with highly heterogeneous genetic causes. This study investigated chromosomal and monogenic abnormalities in fetal CDH patients and evaluated the efficacy of chromosomal microarray analysis (CMA) and whole‐exome sequencing (WES) for genetic diagnosis.
Yan Lü, Yi Yu, Jiazhen Chang, Mengmeng Li, Xueting Yang, Xiya Zhou, Na Hao, Hua Meng, Zhenghong Li, Lishuang Ma, Hui You, Shan Jian, Ying Wang, Shengjie Li, Yiqing Yu, Kaili Yin, Mingming Wang, Yulin Jiang, Qingwei Qi   +18 more
wiley   +1 more source

Strangulated Hernia of the Left Ovary in the Femoral Region [PDF]

, 1892
A Ernest Maylard
openalex   +1 more source

Effectiveness of pre-operative chemical component separation with computed tomography-guided intramuscular injection of OnabotulinumtoxinA in outcomes of large complex incisional ventral abdominal hernia repair: a propensity score-weighted comparative analysis. [PDF]

Hernia
Jahangiri Y, Goldsmith D, Banks-Venegoni A, Fritz G, Zambito G, Jiao A, King L, Castle J, Quasem K, Morrison J.   +9 more
europepmc   +1 more source

Whole Genome Sequencing in Prenatal Diagnostics: The Danish Approach to Guideline Formation and Implementation Within Public Healthcare

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective To describe the implementation of whole genome sequencing (WGS) in prenatal diagnostics and outline the national guideline system facilitating this. Methods Clinical guidelines for WGS in prenatal diagnostics were developed and implemented by the Danish Fetal Medicine Society.
Ida Vogel, Lotte Andreasen, Marie Balslev‐Harder, Naja Becher, Anja Ernst, Kasper Gadsbøll, Tina Duelund Hjortshøj, Marie Skov Hvidbjerg, Martin Larsen, Stina Lou, Ida Charlotte Bay Lund, Lars Henning Pedersen, Laura Kirstine Sønderberg Roos, Lene Sperling, Lone Sunde, Pernille Mathiesen Tørring, Cathrine Vedel, Olav Bjørn Petersen   +17 more
wiley   +1 more source