Results 21 to 30 of about 166,333 (293)

Surgical treatment of retrosternal extraosseous Ewing Sarcoma in a 6-years old female: a clamshell approach with hemysternectomy and application of a non-crosslinked extracellular matrix [PDF]

open access: yes, 2017
Background Ewing Sarcoma (ES) and Neuroblastoma (NB) belong to a family of tumours of primitive neuroectodermal origin (PNET) that occurs in both bone and soft tissue. Notwithstanding ES and NB are two distinct malignant tumours, sometimes there could be
Angotti, Rossella   +9 more
core   +3 more sources

Assessment of diaphragmatic thickness by ultrasonography in Duchenne muscular dystrophy (DMD) patients. [PDF]

open access: yesPLoS ONE, 2018
INTRODUCTION:In Duchenne muscular dystrophy (DMD) the assessment of diaphragmatic function is crucial because respiratory muscle weakness can cause respiratory failure.
Marianna Laviola   +3 more
doaj   +1 more source

X-ray signs of congenital diaphragmatic hernias in term newborns

open access: yesDigital Diagnostics, 2023
BACKGROUND: Imaging plays a major role in the initial diagnosis, treatment, and subsequent assessment of congenital diaphragmatic hernias. Chest X-ray is still of great importance in newborns due to the availability and relative ease of use.
Nargiz F. Khanaliyeva   +1 more
doaj   +1 more source

Morphology of the Esophageal Hiatus: Is It Different in 3 Types of Hiatus Hernias? [PDF]

open access: yes, 2020
Background/aimsThe esophageal hiatus is formed by the right crus of the diaphragm in the majority of subjects. Contraction of the hiatus exerts a sphincter-like action on the lower esophageal sphincter (LES). The aim is to study the hiatal anatomy (using
Ghahremani, Gary   +5 more
core   +1 more source

Treatment responses to antiangiogenetic therapy and chemotherapy in nonsecreting paraganglioma (PGL4) of urinary bladder with SDHB mutation: a case report [PDF]

open access: yes, 2018
Paraganglioma (PGL) is a rare neuroendocrine tumor. Currently, the malignancy is defined as the presence of metastatic spread at presentation or during follow-up.
Aschelter, Am   +10 more
core   +1 more source

A Retrospective Surgical Experience Regarding Open and Laparoscopic Procedures of the Hepatic Hydatid Cyst with an up to Date Complete Review of the Literature And a Focus On Original Romanian Techniques [PDF]

open access: yes, 2016
Introduction: Even though the development of the recent anti-parasitic drugs has led to a high degree of efficiency, surgical treatment still remains the gold standard for a number of conditions. Material and method.
Moldovan, Cosmin Alec   +3 more
core   +3 more sources

Duodenal Stenosis with Diaphragmatic Hernia—A Rare Combination—Delayed Diagnoses with Barium Study

open access: yesJournal of Gastrointestinal and Abdominal Radiology, 2019
Duodenal stenosis is part of a spectrum of disorders due to non-cannulization of the fetal gut lumen occurring in 11 to 13 weeks of fetal life. The diagnosis is often made in the neonatal period owing to bilious vomiting.
Rupa Ananthasivan   +4 more
doaj   +1 more source

Reparação da traquéia de cã o com segmaneto muscular homólogo de diafragma conservado em glicerina a 98% Canine tracheal repair with homologous diaphragmatic muscle fragment preserved in 98% glycerin

open access: yesCiência Rural, 2000
A viabilidade de segmento muscular de diafragma homólogo conservado em solução de glicerina a 98% foi estudada na reparação da traquéia cervical de cães.
Alexandre Mazzanti   +8 more
doaj   +1 more source

Iatrogenic diaphragmatic hernia and intestinal obstruction following laparoscopic hepatectomy: A case report [PDF]

open access: yesJournal of Clinical and Investigative Surgery, 2019
Diaphragmatic hernias may be either congenital or acquired. Acquired diaphragmatic hernias generally develop in association with blunt or penetrating thoraco-abdominal injuries. Iatrogenic diaphragmatic hernias are rare in the literature.
Ercan KORKUT   +2 more
doaj   +1 more source

Further supporting evidence for REEP1 phenotypic and allelic heterogeneity. [PDF]

open access: yes, 2019
Heterozygous mutations in REEP1 (MIM #609139) encoding the receptor expression-enhancing protein 1 (REEP1) are a well-recognized and relatively frequent cause of autosomal dominant hereditary spastic paraplegia (HSP), SPG31.1 REEP1 localizes in the ...
Behnam, M   +5 more
core   +3 more sources

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