• A Case of Hyaline Fibromatosis Syndrome with a New Variant of Genetic Mutation in <em>ANTXR2</em> Gene
• A Case of Hyaline Fibromatosis Syndrome with a New Variant of Genetic Mutation in ANTXR2 Gene
• A mild case of hyaline fibromatosis syndrome, presenting in an adult
• A molecular biopsy test based on arteriolar under-hyalinosis reflects increased probability of rejection related to under-immunosuppression
• A Severe Case of Infantile Systemic Hyalinosis in an Asian Child: A Product of Consanguinity
• Analysis of pathogenic variants in a Chinese pedigree affected with hyaline fibromatosis syndrome
• Anesthetic Management of a Juvenile Hyaline Fibromatosis Patient With Trismus and Cervical Movement Limitation
• Anesthetic Management of a Patient With Juvenile Hyaline Fibromatosis: A Case Report Written With the Assistance of the Large Language Model ChatGPT
• Anesthetic Management of an Adult Patient With Hyaline Fibromatosis Syndrome Undergoing Laparoscopic Colectomy: A Case Report
• Anti-proliferative impact of resveratrol on gingival fibroblasts from juvenile hyaline fibromatosis
• Ascending haemorrhagic myelomalacia associated with systemic hypertension in a hyperthyroid cat
• Atypical Presentation of Juvenile Hyaline Fibromatosis of Hands
• Atypical Presentation of Lip Nodules in Clinically Diagnosed Juvenile Hyaline Fibromatosis
• Autosomal Recessive Infantile Hyaline Fibromatosis Identified Using Artificial Intelligence-Assisted Rapid Whole Genome Sequencing: A Rare, Multisystemic, Hereditary Disorder
• Beyond Skin Deep: A Case Report of Infantile Systemic Hyalinosis in a Six-Month-Old Infant
• Clinical aspects of Hyaline Fibromatosis Syndrome and identification of a novel mutation
• Clinical Significance of Serum Soluble TNF Receptor I/II Ratio for the Differential Diagnosis of Tumor Necrosis Factor Receptor-Associated Periodic Syndrome From Other Autoinflammatory Diseases
• CMG2/ANTXR2 regulates extracellular collagen VI which accumulates in hyaline fibromatosis syndrome
• Comment on "Treatment of Massive Labial and Gingival Hypertrophy in a Patient With Infantile Systemic Hyalinosis--A Case Report"
• Converging physiological roles of the anthrax toxin receptors
• Cytological features of hyaline fibromatosis syndrome: A case report with summary of prior published cases
• Diagnosis implications of the whole genome sequencing in a large Lebanese family with hyaline fibromatosis syndrome
• Differential dependence on N-glycosylation of anthrax toxin receptors CMG2 and TEM8
• Enhanced Collagen Deposition in the Duodenum of Patients with Hyaline Fibromatosis Syndrome and Protein Losing Enteropathy
• Erratum to: Diagnosis implications of the whole genome sequencing in a large Lebanese family with hyaline fibromatosis syndrome
• Fatal cerebrovascular accident in a captive red panda (Ailurus fulgens fulgens) with concurrent amdoparvovirus infection
• Femur fracture in a paediatric patient with hereditary hyaline fibromatosis syndrome
• Genetic, clinical and biochemical characterization of a large cohort of patients with hyaline fibromatosis syndrome
• Gingival Hypertrophy in a Child with Hyaline Fibromatosis Syndrome
• Histological Manifestations of Diabetic Kidney Disease and its Relationship with Insulin Resistance
• Hyaline Fibromatosis Syndrome
• Hyaline fibromatosis syndrome (juvenile hyaline fibromatosis): whole-body MR findings in two siblings with different subcutaneous nodules distribution
• Hyaline Fibromatosis Syndrome Diagnosed by Whole Genome Sequencing
• Hyaline Fibromatosis Syndrome Presenting with Nasal Mass: A Case Report
• Hyaline fibromatosis syndrome with a novel 4.41-kb deletion in ANTXR2 gene: A case report and literature review
• Hyaline fibromatosis syndrome: a case presenting with gingival enlargement as the only clinical manifestation and a report of two new mutations in the ANTXR2 gene
• Hyaline fibromatosis syndrome: A case report
• Hyaline Fibromatosis Syndrome: A Novel Mutation and Recurrent Founder Mutation in the CMG2/ANTXR2 Gene
• Hyaline fibromatosis syndrome: A rare case of multifocal intra-articular involvement
• Hyaline Fibromatosis Syndrome: A Rare Inherited Disorder
• Hyaline fibromatosis syndrome: a rare, yet recognizable syndrome
• Hyaline fibromatosis syndrome: case report of two siblings
• Hyaline fibromatosis syndrome: Clinical update and phenotype-genotype correlations
• Hyaline fibromatosis syndrome: cutaneous manifestations
• Hyaline Fibromatosis Syndrome: Early Outcomes Following Major Craniofacial Mass Excision
• Hyaline juvenile fibromatosis: clinic, diagnostics, treatment
• Hypercalcemia as a rare presentation of hyaline fibromatosis syndrome from different Sudanese families: two case reports
• Hyperpigmentation over the metacarpophalangeal joints and the malleoli in a case of hyaline fibromatosis syndrome with ANTXR2 mutations
• Identical Twins with Infantile Systemic Hyalinosis: Case study and review of literature
• Identification of novel compound heterozygous mutations in the ANTXR2 gene in a Chinese patient with juvenile hyaline fibromatosis
• Imaging manifestations of juvenile hyaline fibromatosis: a case report and literature review
• Infantile Systemic Hyalinosis
• Infantile Systemic Hyalinosis Complicated with Right Atrial Thrombus and Pericardial Effusion in an Infant
• Infantile systemic hyalinosis in an Iranian family with a mutation in the CMG2/ANTXR2 gene
• Infantile Systemic Hyalinosis Presenting as Pseudo-Paralysis in Infancy: Study of Six Cases
• Infantile Systemic Hyalinosis with Mutation in ANTXR2
• Infantile systemic hyalinosis: a case report and literature review
• Infantile Systemic Hyalinosis: A Case Report and Literature Review
• Infantile systemic hyalinosis: a report of two new cases, one with prolonged survival
• Infantile Systemic Hyalinosis: Novel Founder Mutation in the Initiation Codon among "Malis (Farmers)" in Jodhpur
• Infantile systemic hyalinosis: Report of two severe cases from Saudi Arabia and review of the literature
• Infantile systemic hyalinosis: Variable grades of severity
• Investigating the Influence of <em>ANTXR2</em> Gene Mutations on Protective Antigen Binding for Heightened Anthrax Resistance
• Juvenile Hyaline Fibromatosis
• Juvenile Hyaline Fibromatosis
• Juvenile hyaline fibromatosis in siblings
• Juvenile Hyaline Fibromatosis Management With a Diode Laser: A Rare Case Report
• Juvenile Hyaline Fibromatosis- A Rare Autosomal Recessive Disease
• Juvenile Hyaline Fibromatosis: A 10-year Follow-up
• Juvenile hyaline fibromatosis: A clinicopathological study of five cases
• Juvenile hyaline fibromatosis: a rare oral disease case report and literature review
• Juvenile hyaline fibromatosis: an unusual clinical presentation
• Juvenile Hyaline Fibromatosis: Impact of Periodontal Care on Quality of Life and a Patient Perspective
• Juvenile Hyaline Fibromatosis: Literature Review and a Case Treated With Surgical Excision and Corticosteroid
• Juvenile Hyaline Fibromatosis: Report of a Case with a Novel ANTXR2 Gene Mutation
• Juvenile hyaline fibromatosis: report of a rare case at an advanced stage with osteosclerosis and scoliosis
• Ligand Binding to the Collagen VI Receptor Triggers a Talin-to-RhoA Switch that Regulates Receptor Endocytosis
• Lipoid proteinosis: A systematic presentation of an unusual disease
• Looking beyond the exome: a phenotype-first approach to molecular diagnostic resolution in rare and undiagnosed diseases
• Melorheostosis mimicking synovial osteochondromatosis
• Multicentric Castleman disease of hyaline vascular variant presenting with unusual systemic manifestations: a case report
• Multiple Scalp Tumors in Juvenile Hyaline Fibromatosis with Antxr-2 Mutation in a Family
• Multisystemic Manifestations of Hyaline Fibromatosis Syndrome: Implications for Diagnosis and Management
• Neuropathology of Spontaneous Hypertensive Encephalopathy in Cats
• Novel variation in ANTXR2 gene causing hyaline fibromatosis syndrome: A report from India
• Overlapping Hyaline Fibromatosis Syndrome: A Rare Case of Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis
• Prevalence and Management of Diabetic Nephropathy in Western Countries
• Protein-losing enteropathy and joint contractures caused by a novel homozygous ANTXR2 mutation
• Pulmonary hyalinosis in captive sugar gliders ( Petaurus breviceps)
• Systemic Hyalinosis With Heterozygous CMG2 Mutations: A Case Report and Review of Literature
• The diagnostic challenge of juvenile hyaline fibromatosis, a case report with literature reviews
• The genetic basis of hyaline fibromatosis syndrome in patients from a consanguineous background: a case series
• The physical education and the Infantile Systemic Hyalinosis: A case report
• The spectrum of glomerular and vascular kidney pathology associated with myeloproliferative neoplasms
• Treatment of Massive Labial and Gingival Hypertrophy in a Patient With Infantile Systemic Hyalinosis-A Case Report
• Two novel compound heterozygous anthrax toxin receptor 2 mutations in a Chinese patient with hyaline fibromatosis syndrome
• Two novel mutations in the ANTXR2 gene in a Chinese patient suffering from hyaline fibromatosis syndrome: A case report
• Unusual cause for gum hypertrophy and skin nodules in a child
• Vasa Vasorum Lumen Narrowing in Brain Vascular Hyalinosis in Systemic Hypertension Patients Who Died of Ischemic Stroke
• Zimmermann-Laband syndrome and infantile systemic hyalinosis: an enigma with two separate terms with overlapping features: a case report