• A Severe Case of Infantile Systemic Hyalinosis in an Asian Child: A Product of Consanguinity
• 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
• Autosomal Recessive Infantile Hyaline Fibromatosis Identified Using Artificial Intelligence-Assisted Rapid Whole Genome Sequencing: A Rare, Multisystemic, Hereditary Disorder
• Clinical and histopathological characteristics of biopsy-proven renal diseases in Croatia
• Clinical varieties of mastocytoses
• Cytological features of hyaline fibromatosis syndrome: A case report with summary of prior published cases
• 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
• Hereditary gingival fibromatosis in a family with the Zimmermann-Laband syndrome
• Histological Manifestations of Diabetic Kidney Disease and its Relationship with Insulin Resistance
• Hyaline Fibromatosis Syndrome
• 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 rare case of multifocal intra-articular involvement
• Hyaline fibromatosis syndrome: a rare, yet recognizable syndrome
• 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
• Impact of graft loss among kidney diseases with a high risk of post-transplant recurrence in the paediatric population
• Infantile Systemic Hyalinosis Presenting as Pseudo-Paralysis in Infancy: Study of Six Cases
• Infantile Systemic Hyalinosis: A Case Report and Literature Review
• Infantile systemic hyalinosis: report of four cases of a disease, fatal in infancy, apparently different from juvenile systemic hyalinosis
• 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 (Murray-Puretic-Drescher syndrome): oral and systemic findings in siblings
• Juvenile Hyaline Fibromatosis- A Rare Autosomal Recessive Disease
• Juvenile hyaline fibromatosis: A clinicopathological study of five cases
• Juvenile Hyaline Fibromatosis: Report of a Case with a Novel ANTXR2 Gene Mutation
• Lipoid proteinosis: A systematic presentation of an unusual disease
• Long-term monitoring of children with focal segmental glomerulosclerosis and a transplanted kidney
• Mechanism of cystogenesis in nephrotic kidneys: a histopathological study
• Multisystemic Manifestations of Hyaline Fibromatosis Syndrome: Implications for Diagnosis and Management
• Mycetismus in children--report of an epidemic of poisoning
• Overlapping Hyaline Fibromatosis Syndrome: A Rare Case of Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis
• Puretić syndrome--gingival fibromatosis with hyaline fibromas
• Self-limited autosomal recessive syndrome of skin ulceration, arthroosteolysis with pseudoacromegaly, keratitis, and oligodontia in a Kirghizian family
• The nail-patella syndrome
• The role of plasma exchange in the treatment of severe forms of hemolytic-uremic syndrome in childhood
• The spectrum of glomerular and vascular kidney pathology associated with myeloproliferative neoplasms
• 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