Results 51 to 60 of about 32,890 (270)

Case Report: 21 Cases of Umbilical Hernia Repair Using a Laparoscopic Cephalic Approach Plus a Posterior Sheath and Extraperitoneal Approach

Frontiers in Surgery, 2021
Purpose: In this study, a novel surgical technique was developed for umbilical hernias, in which a laparoscopic cephalic approach plus a posterior sheath and an extraperitoneal approach was employed.
Kunjie Zhang, Mingfang Qin, Guoqian Ding
doaj   +1 more source

A woman with recurrent umbilical bleeding: a case report

Journal of Medical Case Reports, 2022
Background Umbilical discharge in an adult is rare and generates broad diagnostic considerations. Umbilical anatomy is variable owing to congenital abnormalities and acquired pathology such as umbilical hernias.
Yong-hun Kim, Abigail K. Wegehaupt, Majken T. Wingo   +2 more
doaj   +1 more source

Genome-wide association study reveals a QTL and strong candidate genes for umbilical hernia in pigs on SSC14

BMC Genomics, 2018
Background Umbilical hernia is one of the most prevalent congenital defect in pigs, causing economic losses and substantial animal welfare problems. Identification and implementation of genomic regions controlling umbilical hernia in breeding is of great
Eli Grindflek, Marianne H. S. Hansen, Sigbjørn Lien, Maren van Son   +3 more
doaj   +1 more source

Update of Guidelines for laparoscopic treatment of ventral and incisional abdominal wall hernias (International Endohernia Society (IEHS)) : Part B [PDF]

, 2019
In 2014 the International Endohernia Society (IEHS) published the first international "Guidelines for laparoscopic treatment of ventral and incisional abdominal wall hernias".
Bain, K., Bansal, V. K., Berrevoet, Frederik, Bingener-Casey, J., Bittner, R., Chen, D., Chen, J., Chowbey, P., de Beaux, A., Dietz, U. A., Ferzli, G., Fortelny, R., Hoffmann, H., Iskander, M., Jorgensen, L. N., Khullar, R., Kirchhoff, P., Koeckerling, F., Kukleta, J., LeBlanc, K., Li, J., Li, Z., Lomanto, D., Mayer, F., Meytes, V, Misra, M., Morales-Conde, S., Niebuhr, H., Radvinsky, D., Ramshaw, B., Ranev, D., Reinpold, W., Schrittwieser, R., Sharma, A., Stechemesser, B., Sutedja, B., Tang, J., Warren, J., Weyhe, D., Wiegering, A., Woeste, G., Yao, Q.   +41 more
core   +4 more sources

3D (Bio) Printing Combined Fiber Fabrication Methods for Tissue Engineering Applications: Possibilities and Limitations

Advanced Functional Materials, EarlyView.
Biofabrication aims at providing innovative technologies and tools for the fabrication of tissue‐like constructs for tissue engineering and regenerative medicine applications. By integrating multiple biofabrication technologies, such as 3D (bio) printing with fiber fabrication methods, it would be more realistic to reconstruct native tissue's ...
Waseem Kitana, Indra Apsite, Leonid Ionov   +2 more
wiley   +1 more source

LIPECTOMY AND UMBILICAL HERNIA [PDF]

Journal of the American Medical Association, 1916
The fact that umbilical hernia is a dangerous abdominal condition, if allowed to exist without an attempt at relief, is sufficient reason for calling attention to this defect of anatomy. The radical treatment by the overlapping, or Mayo method, is so well known that it seems almost superfluous to mention it, but it is valuable enough to stand ...
openaire   +2 more sources

Stratification of surgical site infection by operative factors and comparison of infection rates after hernia repair [PDF]

, 2014
OBJECTIVE: The National Healthcare Safety Network does not risk adjust surgical site infection (SSI) rates after hernia repair by operative factors. We investigated whether operative factors are associated with risk of SSI after hernia repair.
Fraser, Victoria J, Mines, Daniel, Nickel, Katelin B, Olsen, Margaret A, Wallace, Anna E, Warren, David K   +5 more
core   +2 more sources

Trisomy 5p: Long Recognized, Rarely Published‐ Three New Cases and Review of the Literature

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Complete trisomy 5p is a rare chromosomal disorder caused by a duplication of the short arm of chromosome 5. Current data suggest that complete trisomy 5p presents as a distinct clinical syndrome including but not limited to seizures, developmental delays, facial dysmorphisms, failure to thrive, and recurrent respiratory infections.
Gabriela J. Kim, Kristen N. Lee, Amanda B. Pritchard   +2 more
wiley   +1 more source

Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy. [PDF]

, 2020
Developmental and epileptic encephalopathies are a heterogeneous group of early-onset epilepsy syndromes dramatically impairing neurodevelopment. Modern genomic technologies have revealed a number of monogenic origins and opened the door to therapeutic ...
Alix, E, Alkaya, DU, Ashrafzadeh, F, Becker, F, Bilguvar, K, Chatron, N, de Bellescize, J, EuroEpinomics-RES consortium AR working group, Gunes, N, Hardies, K, Hussien, H, Karimiani, EG, Kok, F, Labalme, A, Lerche, H, Lesca, G, Maroofian, R, May, P, Morsy, H, Moslemi, A-R, Nabil, A, Najafi, M, Omar, T, Poulat, A-L, Ramos, L, Roselli, S, Sanlaville, D, Schmidts, M, Tajsharghi, H, Tuysuz, B, Weckhuysen, S   +30 more
core   +2 more sources

De Novo Heterozygous ZFX Frameshift Variant in a Female With an X‐Linked Neurodevelopmental Disorder

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Germline ZFX variants are associated with an X‐linked neurodevelopmental disorder, with 14 males and 16 females reported to date. We describe a 20‐year‐old female with a heterozygous ZFX frameshift variant, p.(Met666Valfs*2), identified by genome sequencing, previously reported in an affected male.
Iftekhar A. Showpnil, Allison Daley, Emily R. Sites, Shayne M. Plourde, Jesse M. Hunter, Dennis W. Bartholomew, April N. Lehman, Daniel C. Koboldt, Rolf W. Stottmann   +8 more
wiley   +1 more source