• 18q21.1q21.32 Deletion in a Patient With Juvenile Cerebral Infarction
• A case of early gastric cancer in a patient with gastric juvenile polyposis diagnosed by magnifying endoscopy and resected by endoscopic submucosal dissection
• A case of juvenile gastric polyposis with gastric cancer successfully treated by laparoscopic total gastrectomy -review of 36 reported cases in Japan
• A Case of Juvenile Polyposis Syndrome in a 13-year-old: A Case Report
• A Case of Laparoscopic Total Gastrectomy for Juvenile Polyposis of Stomach with Synchronous Multiple Intramucosal Carcinomas
• A case report of adult juvenile polyposis syndrome with SMAD4 pathogenic variant
• A New <em>SMAD4</em> Splice Site Variant in a Three-Generation Italian Family with Juvenile Polyposis Syndrome
• A New SMAD4 Splice Site Variant in a Three-Generation Italian Family with Juvenile Polyposis Syndrome
• A novel BMPR1A mutation affects mRNA splicing in juvenile polyposis syndrome
• A novel germline SMAD4 variant detected in a Japanese family with juvenile polyposis syndrome and hereditary hemorrhagic telangiectasia
• A Rare Case of Juvenile Polyposis Syndrome Mimicking Menetrier's Disease
• Acquired Juvenile-Type Polyposis Syndrome Presenting After Age 70 Years: Cap Polyposis Syndrome
• Adenomatous Polyposis Phenotype in BMPR1A and SMAD4 Variant Carriers
• An additional patient with SMAD4-Juvenile Polyposis-Hereditary hemorrhagic telangiectasia and connective tissue abnormalities: SMAD4 loss-of-function and gain-of-function pathogenic variants result in contrasting phenotypes
• An Unexpected Anemia Hiding a Rare Syndrome With Overlapping Phenotypes
• Cancer risk and mortality in patients with solitary juvenile polyps-A nationwide cohort study with matched controls
• Clinical and functional characterisation of the SMAD4 germline variant c.1035C &gt; A in a family with juvenile polyposis syndrome by whole-exome sequencing
• Clinical and functional characterisation of the SMAD4 germline variant c.1035C > A in a family with juvenile polyposis syndrome by whole-exome sequencing
• Clinical and Molecular Characterization of SMAD4 Splicing Variants in Patients with Juvenile Polyposis Syndrome
• Clinical Guidelines for Diagnosis and Management of Juvenile Polyposis Syndrome in Children and Adults-Secondary Publication
• Clinical Spectrum and Science Behind the Hamartomatous Polyposis Syndromes
• Cold snare polypectomy for juvenile polyposis syndrome in a child
• De novo brain vascular malformation in an adult with hereditary hemorrhagic telangiectasia and juvenile polyposis overlap syndrome
• Deciphering the clinical spectrum of gastric disease in patients with Juvenile Polyposis Syndrome
• Detection of Colonic Polyps During Colonoscopy in a Tertiary Care Center of Nepal
• Diagnosis and management of cancer risk in the gastrointestinal hamartomatous polyposis syndromes: recommendations from the U.S. Multi-Society Task Force on Colorectal Cancer
• Diagnosis and Management of Cancer Risk in the Gastrointestinal Hamartomatous Polyposis Syndromes: Recommendations From the US Multi-Society Task Force on Colorectal Cancer
• Diagnosis and Management of Cancer Risk in the Gastrointestinal Hamartomatous Polyposis Syndromes: Recommendations From the US Multi-Society Task Force on Colorectal Cancer
• Distinct gastric phenotype in patients with pathogenic variants in <em>SMAD4:</em> A nationwide cross-sectional study
• Dual primary gastric and colorectal cancer: The known hereditary causes and underlying mechanisms
• Effect of genetic profiling on surgical decisions at hereditary colorectal cancer syndromes
• Endoscopic and Pathological Characteristics of Cronkhite- Canada Syndrome: A Retrospective Analysis of 76 Cases
• Endoscopic Surveillance in Patients with the Highest Risk of Gastric Cancer: Challenges and Solutions
• Failed 2-Stage Revision Knee Arthroplasty for Periprosthetic Joint Infection-Patient Characteristics and Outcomes
• Familial and hereditary gastric cancer, an overview
• Familial intestinal polyposis and device assisted enteroscopy: where do we stand?
• FOCAD Indel in a Family With Juvenile Polyposis Syndrome
• Gastric juvenile polyposis syndrome with inflammatory changes in the intervening mucosa
• Gastric Juvenile Polyposis with Intramucosal Cancer Diagnosed by Magnifying Endoscopy with Narrow-band Imaging
• Gastrointestinal Bleeding in the Setting of Juvenile Polyposis Syndrome Due to SMAD4 Mutation
• Genetic Predisposition to Colorectal Cancer: How Many and Which Genes to Test?
• Genetic Syndromes Associated with Gastric Cancer
• Genotype-phenotype correlation of BMPR1a disease causing variants in juvenile polyposis syndrome
• Giant Gastric Folds in Juvenile Polyposis
• Hamartomatous polyps: Diagnosis, surveillance, and management
• Hereditary haemorrhagic telangiectasia and SMAD4 mutation in a patient with complex single ventricle heart disease
• Hereditary haemorrhagic telangiectasia in Danish patients with pathogenic variants in <em>SMAD4:</em> a nationwide study
• Hereditary hemorrhagic telangiectasis with juvenile polyposis syndrome: a case report
• Hereditary polyposis syndromes remain a challenging disease entity: Old dilemmas and new insights
• Identification of a novel pathogenic deep intronic variant in PTEN resulting in pseudoexon inclusion in a patient with juvenile polyps
• Importance of Magnifying Endoscopy in the Diagnosis and Management of Gastric Juvenile Polyposis Syndrome
• Iron deficiency anemia as the first manifestation of juvenile polyposis syndrome
• Juvenile polyposis diagnosed with an integrated histological, immunohistochemical and molecular approach identifying new SMAD4 pathogenic variants
• Juvenile Polyposis of the Stomach
• Juvenile Polyposis Syndrome Complicated With Gastric Outlet Obstruction
• Juvenile polyposis syndrome in children: The impact of SMAD4 and BMPR1A mutations on clinical phenotype and polyp burden
• Juvenile polyposis syndrome with gastric and duodenal polyposis presenting with refractory anemia and protein-leakage gastroenteropathy in a patient with SMAD4 mutation: a case report
• Juvenile polyposis syndrome: A case report
• Juvenile polyposis syndrome: An overview
• Juvenile polyposis without a germline variant in <em>SMAD4/BMPR1A</em>: defining a clinically distinct polyposis syndrome
• Juvenile polyposis: Focus on less described manifestations
• Large- and medium-sized arterial aneurysms in two patients with SMAD4-related juvenile polyposis syndrome
• Loss of bone morphogenetic protein signaling in fibroblasts results in CXCL12-driven serrated polyp development
• Massive Gastric Juvenile Polyposis Associated With Intermittent Gastric Outlet Obstruction: A Case Report
• Meaningful relationships as a driving force in the experience of parents of a child living with polyposis conditions
• Multidisciplinary coordinated care of hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease)
• Non-Odontogenic Tumors of the Jaws
• Nonsense suppression induces read-through of a novel BMPR1A variant in a Chinese family with hereditary colorectal cancer
• Occurrence of gastric cancer in patients with juvenile polyposis syndrome: a systematic review and meta-analysis
• Outcomes of patients with Juvenile Polyposis-Hereditary Haemorrhagic Telangiectasia caused by pathogenic SMAD4 variants in a pan-Scotland cohort
• Periprosthetic hip infection in octogenarians : a single institution experience of 33 cases
• Phenotypic characterisation of <em>SMAD4</em> variant carriers
• Phenotypic diversity among juvenile polyposis syndrome patients from different ethnic background
• Polygenic Infantile Juvenile Polyposis Syndrome Managed With Sirolimus and Endoscopic Polypectomy
• Polyposis found on index colonoscopy in a 56-year-old female - <em>BMPR1A</em> variant in juvenile polyposis syndrome: A case report
• Polyposis found on index colonoscopy in a 56-year-old female - BMPR1A variant in juvenile polyposis syndrome: A case report
• Polyps and Polyposis Syndromes in Children: Novel Endoscopic Considerations
• Potential impact of sirolimus on gastric polyposis burden in juvenile polyposis syndrome
• Rare Isolated Duodenal Hamartomatous Polyp in an Elderly Patient
• Re-recognition of <em>BMPR1A</em>-related polyposis: beyond juvenile polyposis and hereditary mixed polyposis syndrome
• Rectal Polyposis in Mucosal Prolapse Syndrome
• Risk of cancer and mortality in Peutz-Jeghers syndrome and Juvenile Polyposis Syndrome - a nationwide cohort study with matched controls
• Risk of Cancer and Mortality in Peutz-Jeghers Syndrome and Juvenile Polyposis Syndrome-A Nationwide Cohort Study With Matched Control Individuals
• Risk of Cancer and Mortality in Peutz-Jeghers Syndrome and Juvenile Polyposis Syndrome-A Nationwide Cohort Study With Matched Controls
• Roth spots in a Rendu-Osler-Weber syndrome
• SMAD4 mosaicism in juvenile polyposis: Essential contribution of somatic analysis in diagnosis
• SMAD4 variants and its genotype-phenotype correlations to juvenile polyposis syndrome
• Sporadic gastric juvenile polyposis with a novel SMAD4 nonsense mutation in a mosaic pattern
• Strong Hereditary Predispositions to Colorectal Cancer
• Studying the Effect of the Host Genetic Background of Juvenile Polyposis Development Using Collaborative Cross and <em>Smad4</em> Knock-Out Mouse Models
• Successful treatment of juvenile polyposis of infancy with sirolimus: a case report
• The c.386A&gt;C p.(Asn129Thr) variant in SMAD4 is likely to be pathogenic, causing Juvenile Polyposis Syndrome. A case report of a mosaic variant
• The c.386A>C p.(Asn129Thr) variant in SMAD4 is likely to be pathogenic, causing Juvenile Polyposis Syndrome. A case report of a mosaic variant
• Transcriptomic Profiling Reveals Claudin 18.2 as a Diagnostic Biomarker of Ménétrier's Disease and the Role of Hedgehog Signaling in Pathogenesis
• Ulcerative Colitis or Not? A Case of Dysplasia, Gastrointestinal Bleeding, and Juvenile Polyposis in a 27-Year-Old Man
• Updates in the diagnosis and management of non-ampullary small-bowel polyposis
• Video technical notes for approaching a unique case of Juvenile Polyposis with massive gastric ingrowth
• Whole genome sequencing and disease pattern in patients with juvenile polyposis syndrome: a nationwide study
• Whole Genome Sequencing Applied in Familial Hamartomatous Polyposis Identifies Novel Structural Variations
• Will previous antimicrobial therapy reduce the positivity rate of metagenomic next-generation sequencing in periprosthetic joint infections? A clinical study