Associated Papers
Impact of Age-3 Urine Screening on Diagnosis and Treatment Timing in Alport Syndrome.
Kitakado H et al.
Kidney International Reports, 2025
41426028 (PubMed )
Supplement: mmc1.pdf
Importance of family history and health checkup for school-aged children for type IV collagen-associated nephropathy in hereditary kidney disease.
Kawamoto R et al.
Journal of Nephrology, 2025
40753325 (PubMed )
Supplement: 40620_2025_2355_MOESM1_ESM.docx
Prenatal diagnosis of Alport syndrome.
Nomura S et al.
Genetic Counseling (geneva, Switzerland), 1997
Relationship between COL4A5 gene mutation and distribution of type IV collagen in male X-linked Alport syndrome. Japanese Alport Network.
Naito I et al.
Kidney International, 1996
The COL4A5 gene in Japanese Alport syndrome patients: spectrum of mutations of all exons. The Japanese Alport Network.
Kawai S et al.
Kidney International, 1996
A single-base mutation in exon 31 converting glycine 852 to arginine in the collagenous domain in an Alport syndrome patient.
Kawai S et al.
Nephron, 1996
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