• <em>SLCO2A1</em> gene is the causal gene for both primary hypertrophic osteoarthropathy and hereditary chronic enteropathy
• A 2-Year-Old Boy With Hypoxemia, Pulmonary Hypertension, and Digital Clubbing
• A case of complete form of pachydermoperiostosis with SLCO2A1 mutations
• A Case of Lung Adenocarcinoma with Pulmonary Hypertrophic Osteoarthropathy
• A Case of Progressive Thickening and Furrowing of Facial Skin and Scalp with Scarring Alopecia
• A case of secondary hypertrophic osteoarthropathy from medieval Tuscany (central Italy, 10th-12th centuries CE)
• A case report of an extremely rare association of ankylosing spondylitis with pachydermoperiostosis
• A Complete Form of Pachydermoperiostosis Accompanied by a Pituitary Microadenoma
• A novel compound mutation of SLCO2A1 in a Chinese patient with Primary hypertrophic osteoarthropathy
• A novel variant in the SLCO2A1 gene in a Chinese patient with chronic gastroenteropathy and primary hypertrophic osteoarthropathy
• A patient with pachydermoperiostosis harboring <em>SLCO2A1</em> variants with a history of differentiating from acromegaly
• A patient with pachydermoperiostosis harboring SLCO2A1 variants with a history of differentiating from acromegaly
• A rare helicobacter pylori infection-negative early gastric cancer in a young man with primary hypertrophic osteoarthropathy
• Ankle arthritis - an important signpost in rheumatologic practice
• Approach to the Patient With Pseudoacromegaly
• Bone Geometry, Density, Microstructure, and Biomechanical Properties in the Distal Tibia in Patients With Primary Hypertrophic Osteoarthropathy Assessed by Second-Generation High-Resolution Peripheral Quantitative Computed Tomography
• Case report: Novel homozygous HPGD variant leads to primary hypertrophic osteoarthropathy with intussusception and acro-osteolysis in a Chinese family
• Characterization of Mineral and Bone Metabolism Biomarkers in a Chinese Consanguineous Twin Family with Primary Hypertrophic Osteoarthropathy
• Chronic enteropathy associated with SLCO2A1 gene and hereditary fructose intolerance: A coincidence of two rare diseases
• Chronic Enteropathy Associated with SLCO2A1 with Pachydermoperiostosis
• Chronic enteropathy associated with SLCO2A1-associated primary hypertrophic osteoarthropathy in a female patient
• Clinical and biochemical characteristics of 12 Chinese primary hypertrophic osteoarthropathy patients with HPGD mutations
• Clinical and genetic characteristics of Chinese patients diagnosed with chronic enteropathy associated with SLCO2A1 gene
• Clinical and Genetic Characteristics of Korean Patients Diagnosed with Chronic Enteropathy Associated with <em>SLCO2A1</em> Gene: A KASID Multicenter Study
• Clinical and genetic characteristics of patients with chronic enteropathy associated with SLCO2A1 gene
• Clinical Outcomes of Utilizing a "W"-shaped Incision in the Management of Forehead Skin Thickening Induced by Hypertrophic Osteoarthropathy
• Coincidence of pachydermoperiostosis and synovitis, acne, pustulosis, hyperostosis, osteitis syndrome, a causal or casual association?
• Comparison of bone microstructure and strength in the distal radius and tibia between the different types of primary hypertrophic osteoarthropathy: an HR-pQCT study
• Complete form of pachydermoperiostosis with good initial response to etoricoxib: A case report
• Complete primary pachydermoperiostosis
• Comprehensive Treatment of a Rare Case of Complete Primary Pachydermoperiostosis with Large Facial Keloid Scars: A Case Report and Literature Review
• Differential Diagnosis of Acromegaly: Pachydermoperiostosis Two New Cases from Turkey
• Digital clubbing, joint pain, and skin changes in a young man: primary hypertrophic osteoarthropathy
• Eicosanoid profiling in patients with complete form of pachydermoperiostosis carrying SLCO2A1 mutations
• Establishment of a novel human iPSC line (SDQLCHi032-A) derived from a patient with primary hypertrophic osteoarthropathy caused by HPGD homozygous mutation
• Etoricoxib as a treatment of choice for patients with <em>SLCO2A1</em> mutation exhibiting autosomal recessive primary hypertrophic osteoarthropathy: A case report
• Etoricoxib as a treatment of choice for patients with SLCO2A1 mutation exhibiting autosomal recessive primary hypertrophic osteoarthropathy: A case report
• Familial Touraine-Solente-Gole syndrome
• Frontal lifting using a tissue expander in pachydermoperiostosis: A case report
• Gastrointestinal Multiple Adenomas in Primary Hypertrophic Osteoarthropathy
• Genotype and phenotype characterization of primary hypertrophic osteoarthropathy type 2 and chronic enteropathy associated with SLCO2A1: Report of two cases and literature review
• Homozygous Missense Variant in the Solute Carrier Organic Anion Transporter 2A1 (<em>SLCO2A1</em>) Gene Underlies Isolated Nail Clubbing
• Hypertrophic Osteoarthropathy
• Hypertrophic Osteoarthropathy
• Hypertrophic Osteoarthropathy Associated With Pancoast Tumor: Do Not Miss Secondary Hypertrophic Osteoarthropathy!
• Hypertrophic pulmonary osteoarthropathy with esophageal sarcomatoid carcinoma: a case report
• Identification of three novel mutations in <em>SLCO2A1</em> in Asian-Indians with Pachydermoperiostosis
• Identification of three novel mutations in SLCO2A1 in Asian-Indians with Pachydermoperiostosis
• Inflammatory Granulomas, Accompanied by Mild Proliferation of Spinous Layer in Primary Hypertrophic Osteoarthropathy
• Juvenile Disease Processes Affecting the Forelimb in Canines
• Lack of cutis verticis gyrata is associated with c.1279_1290del12 of SLCO2A1 in 43 Japanese patients with pachydermoperiostosis
• Lost bones: differential diagnosis of acro-osteolysis seen by the pediatric rheumatologist
• Monoallelic mutations in SLCO2A1 cause autosomal dominant primary hypertrophic osteoarthropathy
• Multiple small intestinal ulcers with SLCO2A1 and PLA2G4A mutation in a Chinese patient
• Non-invasive visualization of epidermal hypertrophy of pachydermoperiostosis
• Novel pathogenic variants in SLCO2A1 causing autosomal dominant primary hypertrophic osteoarthropathy
• Pachydermoperiostosis
• Pachydermoperiostosis
• Pachydermoperiostosis and Work Restrictions: A Case Report
• Pachydermoperiostosis combined with pyloric gland adenoma with foveolar-type adenoma
• Pachydermoperiostosis complicated with psoriatic arthritis successfully treated with an anti-interleukin 17A antibody
• Pachydermoperiostosis Presenting With End-Stage Kidney Disease
• Pachydermoperiostosis Presenting With Vision Loss Secondary to Severe Phlyctenular Keratoconjunctivitis
• Pachydermoperiostosis with bilateral ptosis and its associated systemic comorbidities: a rare case report
• Pachydermoperiostosis with Chronic Venous Disease
• Pachydermoperiostosis with Hearing Loss
• Pachydermoperiostosis: a case report of initial improvement with etoricoxib
• Pachydermoperiostosis: Cosmetic implications in a multi-system genetic condition
• Palmoplantar keratoderma and digital clubbing in 2 sisters with hypertrophic osteoarthropathy
• Paraneoplastic Syndromes in Lung Cancers: Manifestations of Ectopic Endocrinological Syndromes and Neurologic Syndromes
• Pierre-Marie Bamberger Syndrome Leading to the Diagnosis and Surgical Treatment of a Localized Lung Cancer
• Primary Hypertrophic Osteoarthropathy
• Primary hypertrophic osteoarthropathy - a rare cause of pain and arthritis in children. Description of 5 cases
• Primary hypertrophic osteoarthropathy and bilateral transient lateral patellar dislocation in an adolescent
• Primary Hypertrophic Osteoarthropathy With Myelofibrosis
• Primary hypertrophic osteoarthropathy with severe arthralgia identified by gene mutation of <em>SLCO2A1</em>
• Primary hypertrophic osteoarthropathy with severe arthralgia identified by gene mutation of SLCO2A1
• Primary hypertrophic osteoarthropathy: genetics, clinical features and management
• Primary pachydermoperiostosis associated with pigmented villonodular synovitis: An unknown association?
• Primary pulmonary lymphoepithelioma-like carcinoma accompanied by hypertrophic pulmonary osteoarthropathy in a non-epidemic region: a case report and literature review
• Pseudoacromegaly-A challenging entity in the endocrine clinic: A systematic review
• Rare gastric manifestations in primary pachydermoperiostosis
• Recalcitrant psoriatic onycho-pachydermo-periostitis successfully treated with guselkumab
• Recent advances in studies of SLCO2A1 as a key regulator of the delivery of prostaglandins to their sites of action
• Reclassification of the <em>HPGD</em> p.Ala13Glu variant causing primary hypertrophic osteoarthropathy
• Reclassification of the HPGD p.Ala13Glu variant causing primary hypertrophic osteoarthropathy
• Rhytidectomy for pachydermoperiostosis
• Role of bisphosphonates in hypertrophic osteoarthropathy: a systematic review
• Role of Prostaglandin E-Major Urinary Metabolite Levels in Identifying the Phenotype of Pachydermoperiostosis
• Rosai-Dorfman Disease Occurring in an Elderly Patient With Long-Standing Idiopathic Hypertrophic Osteoarthropathy
• Scalp "Petals" Sign in Touraine-Solente-Gole Syndrome
• Secondary Hypertrophic Osteoarthropathy
• Secondary Hypertrophic Osteoarthropathy
• Secondary Hypertrophic Osteoarthropathy
• Secondary hypertrophic osteoarthropathy revealing a metastatic melanoma
• Skin anomalies in acromegalic patients (Review of the practical aspects)
• SLCO2A1 gene is the causal gene for both primary hypertrophic osteoarthropathy and hereditary chronic enteropathy
• Touraine-Solente-Gole syndrome: pathogenic variant in SLCO2A1 presented with polyarthralgia and digital clubbing
• Touraine-Solente-Gole syndrome: The elephant skin disease
• Whole body diffusion weighted imaging with background suppression in pachydermoperiostosis: a case report