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| http://dx.doi.org/10.1038/s41467-024-49020-7 | DOI Listing |
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View Article and Find Full Text PDFObjective: To describe the anatomical and functional outcome of autologous internal limiting membrane (ILM) transplant with 27-gauge plus (27G+) three ports pars plana vitrectomy (PPV) in failed and recurrent full-thickness macular holes (MH) in a spectrum of pathologies.
Study Design: Observational cohort study Methods: Seven eyes of seven patients who had failed or recurrent MH were included from January 2017 to January 2022. A single vitreoretinal surgeon performed all surgeries using a 27G+ PPV system in a tertiary care hospital.
Husband's Contributions to Stimulate Wife's Confidence Experiencing Role Transition: Cross-Sectional Study.
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Introduction: Pregnancy can cause various physical and physiological changes. It affects confidence, resulting in depression and disturbing health not only for a mother but also for her fetus. These will also determine the ability of the mother to take care of her baby after delivery.
View Article and Find Full Text PDFDiagonalizing Bose Gases in the Gross-Pitaevskii Regime and Beyond.
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We present a novel approach to the Bogoliubov theory of dilute Bose gases, allowing for an elementary derivation of the celebrated Lee-Huang-Yang formula in the Gross-Pitaevskii regime. Furthermore, we identify the low lying excitation spectrum beyond the Gross-Pitaevskii scaling, extending a recent result (Brennecke et al. in Rev Math Phys 34, 2022) to significantly more singular scaling regimes.
View Article and Find Full Text PDFPulmonary arterial hypertension with left to right shunts: When to treat and/or close?
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Pulmonary arterial hypertension (PAH) is defined as increase in mean pulmonary arterial pressure and pulmonary vascular resistance (PVR). It can be associated with congenital heart disease (CHD) with the following subtypes: 1) uncorrected left-to-right (L-R) intracardiac shunt leading to overload of the pulmonary circulation and a progressive increase of PVR; 2) Eisenmenger syndrome, appearing when a large post-tricuspid shunt is left uncorrected and pulmonary vascular disease (PVD) is severe, so the shunt becomes bidirectional or right-to-left, causing cyanosis; 3) PAH after shunt closure, when PVR arises after a defect correction; and 4) PAH associated with small or coincidental defects. While the treatment of patients with Eisenmenger syndrome is well established, the treatment of patients with PAH in whom there is a L-R shunt (with no cyanosis) remains unclear and requires expertise.
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