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Case Series | Open Access
Published on : 17 Jan 2026
Is Epilepsy a Complication of Type 1 Diabetes? A Series of Four Cases and Review of the Literature
Introduction: The association between type 1 diabetes (T1D) and epilepsy has been reported more frequently than in the general population. However, the exact pathophysiological link remains poorly understood.
Objective: To describe the clinical characteristics of patients presenting with an association of T1D and epilepsy and to discuss the possible pathophysiological mechanisms in light of data from the…
DOI: 10.5281/zenodo.18392743 »
Research Article | Open Access
Published on : 15 Jan 2026
Efficacy of Integrated Neuromechanical Rehabilitation on Symptom Resolution and Recurrence Rates in Medial Tibial Stress Syndrome: A Randomized Controlled Trial
Background: Medial tibial stress syndrome (MTSS) affects 4-35% of runners with substantial recurrence rates ranging from 25-57% following standard care protocols. While individual interventions (load management, gait retraining, strengthening) demonstrate independent efficacy, high-quality randomized controlled trial evidence evaluating integrated models combining all three components remains limited in the current literature.
Objective: To…
DOI: 10.5281/zenodo.18367039 »
Research Article | Open Access
Published on : 15 Jan 2026
Mechanistic Effects of Gait Retraining Combined with Neuromuscular Strengthening on Lower Limb Biomechanics and Tissue Stress in Participants with Medial Tibial Stress Syndrome: A Three-Dimensional Motion Capture and Electromyographic Analysis
Background: While gait retraining and neuromuscular strengthening demonstrate individual clinical efficacy in medial tibial stress syndrome (MTSS) management, the integrated biomechanical mechanisms through which combined intervention modifies lower limb loading parameters and tissue stress remains inadequately characterized in contemporary literature. High-resolution biomechanical quantification integrating three-dimensional motion capture, ground reaction force analysis,…
DOI: 10.5281/zenodo.18367229 »
Case Series | Open Access
Published on : 15 Jan 2026
Complications of Primary Hyperparathyroidism: A Retrospective Study of 83 Cases
Introduction: Primary hyperparathyroidism (PHPT) is one of the most common endocrine disorders, characterized by inappropriate secretion of parathyroid hormone (PTH), leading to disturbances in calcium–phosphate metabolism and multisystem complications.
Objective: To determine the prevalence and profile of clinical, biological, and radiological complications of PHPT in a Moroccan hospital-based cohort.
Materials and…
DOI: 10.5281/zenodo.18367963 »
Case Presentation | Open Access
Published on : 15 Jan 2026
Celiac Disease in Patients with Type 1 Diabetes and Negative Serology: About Two Cases and Literature Review
Introduction: Celiac disease (CD) is an autoimmune enteropathy triggered by gluten ingestion in genetically predisposed individuals. It is frequently associated with type 1 diabetes (T1D), with a prevalence significantly higher than that observed in the general population. Diagnosis usually relies on positivity of specific autoantibodies and histological confirmation. However, seronegative forms can be observed, notably in T1D patients, making diagnosis more…
DOI: 10.5281/zenodo.18368161 »
Case Series | Open Access
Published on : 15 Jan 2026
Differentiated Thyroid Carcinoma Associated with Graves’ Disease: A Series of Six Cases and Review of the Literature
Introduction: Graves’ disease is an autoimmune disorder characterized by hyperthyroidism related to the presence of thyroid-stimulating hormone receptor antibodies. Long considered protective against thyroid cancer, it is now recognized as potentially associated with differentiated thyroid carcinomas, mainly papillary carcinoma.
Objective: To describe the clinical, histological, therapeutic, and outcome characteristics of thyroid carcinomas…
DOI: 10.5281/zenodo.18369068 »
Systematic Review | Open Access
Published on : 13 Jan 2026
The Role of Artificial Intelligence–Based Systems in Early Detection of Patient–Ventilator Asynchrony: Implications for Physical Therapy Practice – A Systematic Review
Background: Patient–ventilator asynchrony (PVA) is a common complication in mechanically ventilated patients, leading to increased morbidity, prolonged ventilation, and respiratory muscle fatigue. Early detection is critical. Artificial intelligence (AI) systems, including convolutional neural networks (CNNs) and machine learning algorithms, have been applied to automate detection.
Objective: To systematically review current evidence on AI-based…
DOI: 10.5281/zenodo.18307632 »
Review Article | Open Access
Published on : 13 Jan 2026
Infantile Hypertrophic Pyloric Stenosis: A Multidimensional Systems‑Biology Perspective Integrating Early‑Life Determinants, PNEI Interactions, and Functional Gastrointestinal Mechanisms
Objectives: To re‑examine infantile hypertrophic pyloric stenosis (IHPS) through a contemporary, multidimensional framework that integrates structural, functional, and psycho‑neuro‑endocrine‑immune (PNEI) mechanisms. This review synthesises current evidence on IHPS epidemiology, pathophysiology, and clinical presentation, and evaluates minimally invasive diagnostic and therapeutic approaches. It further explores how emerging insights into gut–brain and neuroimmune regulation…
DOI: 10.5281/zenodo.18307787 »
Case Report | Open Access
Published on : 13 Jan 2026
Retroperitoneal Dumbbell Neurofibroma Presenting as Wilms’ Tumour with Postoperative Spinal Cord Compression
A six‑year‑old girl presented with a left‑sided abdominal mass and a non‑functioning left kidney, initially diagnosed radiologically as Wilms’ tumor. Intraoperatively, the kidney was found to be compressed—not invaded—by a massive, benign‑appearing retroperitoneal tumor. The mass was excised with preservation of the kidney. Unrecognised extension of the tumor through the lumbar intervertebral foramen resulted in a postoperative spinal epidural hematoma, causing acute paraparesis. Emergency…
DOI: 10.5281/zenodo.18307948 »
Case Series | Open Access
Published on : 10 Jan 2026
Turner Syndrome and the SRY Gene: Report of Two Cases
Turner syndrome (TS) is a rare chromosomal disorder characterized by partial or complete monosomy X. The presence of Y chromosome material, particularly the sex-determining region Y(SRY) gene, has important clinical implications due to the increased risk of gonadoblastoma. We report two cases of young women with Turner syndrome harboring Y chromosome material detected by fluorescence in situ hybridization (FISH), illustrating the phenotypic variability, diagnostic challenges, and therapeutic…
DOI: 10.5281/zenodo.18287818 »