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Iron Deficiency and Incident Heart Failure in Older Community-Dwelling Individuals.
ESC Heart Fail
June 2024
Division of Nephrology-Hypertension, Department of Medicine, University of California San Diego, San Diego, CA, USA.
Aims: Among persons with prevalent heart failure (HF), iron deficiency has been linked to HF admissions, and intravenous iron replacement improves HF outcomes. Recent studies in persons with chronic kidney disease (CKD) demonstrate that iron deficiency is associated with incident HF. This study aimed to determine the relationship of iron status with incident HF in community-dwelling older adults irrespective of their kidney function.
View Article and Find Full Text PDFEvidence for converging pathophysiology in complex regional pain-syndrome and primary headache disorders: results from a case-control study.
J Neurol
April 2024
Department of Neurology, University Medicine Greifswald, Greifswald, Germany.
Background: Neuroinflammation and maladaptive neuroplasticity play pivotal roles in migraine (MIG), trigeminal autonomic cephalalgias (TAC), and complex regional pain syndrome (CRPS). Notably, CRPS shares connections with calcitonin gene-related peptide (CGRP) in its pathophysiology. This study aims to assess if the documented links between CRPS and MIG/TAC in literature align with clinical phenotypes and disease progressions.
View Article and Find Full Text PDFFunctional regeneration of dilated cardiomyopathy by transcatheter bilateral pulmonary artery banding: first-in-human case series.
Eur Heart J Case Rep
February 2023
Department of Pediatric Cardiology, Georg-August-University Medical Center, Göttingen, Germany.
Background: Dilated cardiomyopathy (DCM) is a leading cause of heart transplantation (HTx) in children. Surgical pulmonary artery banding (PAB) is used worldwide to achieve functional heart regeneration and remodelling.
Case Summary: We report for the first-time successful bilateral transcatheter implantation of bilateral pulmonary artery flow restrictors in a case series of three infants with severe DCM based on left-ventricular non-compaction morphology associated with Barth syndrome in one and a non-classified syndrome in another.
Rate of publication in predatory journals by orthopedic surgeons members of the French orthopedic and traumatology society (SOFCOT): A follow-up note.
Orthop Traumatol Surg Res
December 2020
Service d'orthopédie, CHU de Lille, Hôpital Roger-Salengro, 59000 Lille, France; University of Lille, CHU of Lille, ULR 2694-METRICS: évaluation des technologies de santé et des pratiques médicales, 59000 Lille, France.
Background: France ranks 9th worldwide for scientific publication in orthopedics and the increase in both the quantity and the quality of its scientific production has been described in detail. On the other hand, publishing by French orthopedic surgeons in predatory journals is more obscure. The journals in question are difficult to identify but are based on an open-access model with article processing charges (APC), except in rare cases that are difficult to specify, as they are not stated at the time of submission.
View Article and Find Full Text PDFReproductive alternatives for patients with dystrophic epidermolysis bullosa.
Einstein (Sao Paulo)
June 2019
Departamento de Saúde da Coletividade, Faculdade de Medicina do ABC, Santo André, SP, Brazil.
Epidermolysis bullosa describes a group of skin conditions caused by mutations in genes encoding proteins related to dermal-epidermal adhesion. In the United States, 50 cases of epidermolysis bullosa per 1 million live births are estimated, 92% of which classified as simplex, 5% dystrophic, 1% junctional and 2% non-classified. Dystrophic epidermolysis bullosa is associated with autosomal, dominant and recessive inheritance.
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