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Last Updated: 10/31/2025
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Found 598 publications
Intestinal injury and repair: insights from hyaline fibromatosis syndrome.
Journal: EMBO molecular medicine
Published: July 10, 2025
Decoding the Mystery of Multiple Swellings and Joint Contractures: Hyaline Fibromatosis Syndrome.
Journal: Indian journal of dermatology
Published: June 09, 2025
Injury-induced intestinal stem cell renewal requires capillary morphogenesis gene 2.
Journal: EMBO molecular medicine
Published: May 27, 2025
Segmental and Focal Glomerulosclerosis Secondary to MELAS Syndrome and Long-Term Outcomes After Kidney Transplant: Case Report and Literature Review.
Journal: Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation
Published: March 17, 2025
Comprehending the Role of Metabolic and Hemodynamic Factors Alongside Different Signaling Pathways in the Pathogenesis of Diabetic Nephropathy.
Journal: International journal of molecular sciences
Published: February 07, 2025
Systemic inflammation accelerates the development of focal segmental glomerulosclerosis in a mouse model of adriamycin induced nephrosis.
Journal: Scientific reports
Published: February 05, 2025
Infantile systemic Hyalinosis in a 6-month-old male: identification of homozygous ANTXR2 gene mutation.
Journal: Oxford medical case reports
Published: January 12, 2025
Clinicopathological Challenge: Five Males Presenting With Progressive Skin Thickening and Hoarse Voices.
Journal: International journal of dermatology
Published: January 02, 2025
Unraveling Juvenile Hyaline Fibromatosis: A Case of Novel ANTXR2 Mutations Associated with Subcutaneous Masses and Hydronephrosis.
Journal: Pediatric blood & cancer
Published: December 01, 2024
Recurrent Giant Subcutaneous Tumor in Juvenile Hyaline Fibromatosis.
Journal: The Journal of craniofacial surgery
Published: November 25, 2024
Juvenile Hyaline Fibromatosis Syndrome: A Novel Variant in the ANTXR2 Gene Causing Severe Phenotype.
Juvenile Hyaline Fibromatosis Syndrome: A Novel Variant in the ANTXR2 Gene Causing Severe Phenotype.
Journal: Pediatric dermatology
Published: November 20, 2024
Genetic Insights Into Hyaline Fibromatosis Syndrome: A Case Report of an ANTXR2 Mutation Featuring a Rare Variant c.697+1G>A.
Journal: Clinical case reports
Published: November 15, 2024
Last Updated: 10/31/2025