Latest papers

Atypical Alport syndrome associated with a novel COL4A5 mutation.

Expression of macrophage metalloelastase (MMP-12) in podocytes of hereditary nephrotic mice (ICGN strain).

Alport syndrome and thin glomerular basement membrane nephropathy: a practical approach to diagnosis.

Alport syndrome: significance of gingival biopsy in the initial diagnosis and periodontal evaluation after renal transplantation.

[Esophageal leiomyomatosis revealing an Alport syndrome].

MLPA and cDNA analysis improves COL4A5 mutation detection in X-linked Alport syndrome.

[Alport's syndrome and benign familial haematuria: light and electron microscopic studies of the kidney]

Spectrum of collagen type IV nephropathies: from thin basement membrane nephropathy to Alport syndrome.

[A novel COL4A5 splicing mutation causing Alport syndrome in a Chinese family]

[The significance of Goodpasture antigen in hereditary nephritis].

[Clinical and pathological study of 47 cases with Alport syndrome].

Antigen retrieval with protease digestion applied in immunohistochemical diagnosis of Alport syndrome.

X inactivation, female mosaicism, and sex differences in renal diseases.

Gene symbol: COl4A5. Disease: Alport Syndrome.

Gene symbol: COL4A5. Disease: Alport Syndrome.

Gene symbol: COl4A5. Disease: Alport Syndrome.

Stem cell-based therapy for glomerular diseases: an evolving concept.

Two cases of calcineurin inhibitor-associated reversible posterior leukoencephalopathy syndrome in renal transplant recipients.

Somatic mosaicism for a mutation of the COL4A5 gene is a cause of mild phenotype male Alport syndrome.

The dialysis diary: what 40 years on dialysis has taught me.