• "Laminopathies": a wide spectrum of human diseases
• A new case of Greenberg dysplasia and literature review suggest that Greenberg dysplasia, dappled diaphyseal dysplasia, and Astley-Kendall dysplasia are allelic disorders
• A novel case of Greenberg dysplasia and genotype-phenotype correlation analysis for LBR pathogenic variants: An instructive example of one gene-multiple phenotypes
• Autosomal recessive HEM/Greenberg skeletal dysplasia is caused by 3 beta-hydroxysterol delta 14-reductase deficiency due to mutations in the lamin B receptor gene
• Components of the nuclear envelope and their role in human disease
• Congenital abnormalities reported in Pelger-Huet homozygosity as compared to Greenberg/HEM dysplasia: highly variable expression of allelic phenotypes
• Correlation of Fecal Immunochemical Testing Levels With Pathology Results in a National Colorectal Cancer Screening Program
• Detailed ultrasonographic findings in Greenberg dysplasia
• Disorders of cholesterol metabolism and their unanticipated convergent mechanisms of disease
• Fetal transabdominal biometry at 11-14 weeks of gestation
• Greenberg dysplasia (HEM) and lethal X linked dominant Conradi-Hünermann chondrodysplasia punctata (CDPX2): presentation of two cases with overlapping phenotype
• Greenberg Skeletal Dysplasia: first reported case in the Democratic Republic of Congo
• HEM dysplasia and ichthyosis are likely laminopathies and not due to 3beta-hydroxysterol Delta14-reductase deficiency
• Human malformation syndromes due to inborn errors of cholesterol synthesis
• Hydrops-ectopic calcification-moth-eaten skeletal dysplasia (Greenberg dysplasia): prenatal diagnosis and further delineation of a rare genetic disorder
• Immunomodulatory Effects of <em>Momordica charantia</em> Extract in the Prevention of Oral Cancer
• Malformation syndromes caused by disorders of cholesterol synthesis
• Mutations causing Greenberg dysplasia but not Pelger anomaly uncouple enzymatic from structural functions of a nuclear membrane protein
• Nephroptosis and hypertension
• Pathologic, radiographic and molecular findings in three fetuses diagnosed with HEM/Greenberg skeletal dysplasia
• Pelger-huet anomaly and a mild skeletal phenotype secondary to mutations in LBR
• Pregnancy-Related Complications in Patients With Fibromuscular Dysplasia: A Report From the European/International Fibromuscular Dysplasia Registry
• Psychological and clinical characteristics of female patients with spontaneous coronary artery dissection
• Restenosis of the renal artery after percutaneous transluminal renal angioplasty: an inevitable outcome?
• Restenosis prevalence and long-term effects on renal function after percutaneous transluminal renal angioplasty
• Short-term effects of percutaneous transluminal renal angioplasty on renal function in unilateral renal artery stenosis
• Special considerations for clinical trials in fibrodysplasia ossificans progressiva (FOP)
• Spontaneous coronary artery dissections and associated predisposing factors: a narrative review
• The danger of "multi-tasking": LBR out of control
• The Lamin B receptor is essential for cholesterol synthesis and perturbed by disease-causing mutations
• The lamin B receptor under transcriptional control of C/EBPepsilon is required for morphological but not functional maturation of neutrophils
• Use of Hem-o-lok Clips for Vascular Control During Retroperitoneoscopic Nephrectomy in Children