• An Updated Classification of Primary Lymphedema Based on Age of Onset, Lymphatic Anomalies, and Genetics
• Case report: Noonan syndrome with protein-losing enteropathy
• Clinical insights from an unusual Turner syndrome manifestation: Congenital cutis verticis gyrata
• Clinical situations for which 3D Printing is considered an appropriate representation or extension of data contained in a medical imaging examination: vascular conditions
• Combination of conservative and surgical methods in the treatment of giant lymphedema of the scrotum: A case report
• Congenital lymphatic dysplasia and severe bone disease in a term neonate with a novel homozygous PIEZO1 variant
• Critical care management of patients with lymphatic conduction disorders
• Current Concepts in the Management of Primary Lymphedema
• Endothoracic lymphatic plexus‑hemiazygos vein anastomosis for chylothorax complicated with hepatocellular carcinoma: A case report
• Erythematous capillary-lymphatic malformations mimicking blood vascular anomalies
• Fibrodysplasia Ossificans Progressiva
• FLT4 causes developmental disorders of the cardiovascular and lymphovascular systems via pleiotropic molecular mechanisms
• Genetic association analysis of 77,539 genomes reveals rare disease etiologies
• Genetic variant in the <em>BRAF</em> gene compatible with Noonan spectrum disorders in an adult Fontan patient with refractory protein losing enteropathy: a follow-up report
• Genetics, diagnostics and clinical presentation of primary lymphoedema
• Giant Scrotal Lymphoedema: A Case Series
• Late management of amniotic bands syndrome with incomplete syndactyly: A case report of 4-year-old child
• Lymphatic disorders caused by mosaic, activating KRAS variants respond to MEK inhibition
• Lymphatic failure and lymphatic interventions: Knowledge gaps and future directions for a new frontier in congenital heart disease
• Lymphatic Vascular Permeability Determined from Direct Measurements of Solute Flux
• Lymphedema in Turner syndrome: correlations with phenotype and karyotype
• MR Lymphangiography: Congenital Lymphatic Flow Disorders
• Multiple vascular anomalies and refractory pericardial effusion in a young patient with Cantu syndrome: a case report and review of the literature
• Neonatal perspective on central lymphatic disorders
• Patient with composite haemangioendothelioma containing angiosarcoma-like areas in the setting of congenital lymphoedema mimicking Stewart-Treves syndrome: a case report
• Persistent chylothorax associated with lymphatic malformation type 6 due to biallelic pathogenic variants in PIEZO1
• Plasmacytoid urothelial carcinoma: a rare cause of localized lymphedema
• Possible biallelic inheritance in TIE1 in a family with congenital lymphedema, intestinal lymphangiectasia and cutis aplasia
• Primary lymphedema of childhood: Treatment results from a tertiary center
• Respiratory distress syndrome due to pulmonary hypoplasia and neonatal congenital lymphedema
• Rictor induces AKT signaling to regulate lymphatic valve formation
• Rictor, an mTORC2 Protein, Regulates Murine Lymphatic Valve Formation Through the AKT-FOXO1 Signaling
• Secondary Lymphedema: Clinical Interdisciplinary Tricks to Overcome an Intriguing Disease
• Surgical Treatment for Primary Lymphedema: A Systematic Review of the Literature
• The Possible Role of Lymphaticovenous and Lymph Node to Vein Anastomosis for Improvement of Milroy Disease Related Congenital Chylothorax and Lower Extremity Lymphedema
• Update on nevi and nevoid skin disorders