|1.||Zenker, Martin: 9 articles (05/2012 - 10/2004)|
|2.||Miner, Jeffrey H: 6 articles (08/2013 - 03/2006)|
|3.||Matejas, Verena: 6 articles (05/2012 - 02/2007)|
|4.||Jarad, George: 3 articles (09/2011 - 03/2006)|
|5.||Zurowska, Aleksandra: 3 articles (09/2010 - 01/2006)|
|6.||Wühl, Elke: 3 articles (09/2010 - 02/2007)|
|7.||Kogan, Jillene: 3 articles (09/2010 - 08/2006)|
|8.||Reis, André: 3 articles (02/2007 - 10/2004)|
|9.||Suh, Jung Hee: 2 articles (08/2013 - 09/2011)|
|10.||Kikkawa, Yamato: 2 articles (07/2013 - 05/2011)|
|1.||Hereditary Nephritis (Alport Syndrome)
08/01/2013 - "Together with findings from genetic studies in mice, the discoveries of four human mutations affecting GBM components in two inherited kidney disorders, Alport syndrome and Pierson syndrome, support essential roles for the GBM in glomerular permselectivity. "
01/01/2011 - "This review provides current information about glomerular disorders that arise directly from inherited abnormalities in extracellular matrix proteins intrinsic to the glomerular basement membrane (Alport syndrome, thin basement membrane nephropathy, HANAC syndrome and Pierson syndrome). "
07/01/2012 - "Genetic diseases affecting laminin and type IV collagen synthesis also are presented, with an emphasis on mutations to LAMB2 (Pierson syndrome) and COL4A3, COL4A4, and COL4A5 (Alport syndrome), and their experimental mouse models. "
01/01/2011 - "This chapter describes several well-characterized animal models of type IV collagen disorders (Alport syndrome, HANAC syndrome), a laminin disorder (Pierson syndrome), nail-patella syndrome and HERNS syndrome. "
01/01/2008 - "The importance of the GBM has been demonstrated by identification of hereditary glomerular diseases linked to structural anomalies of its components; for example, type IV collagen in Alport syndrome and familial benign hematuria, and laminin in Pierson syndrome. "
|2.||Lambert-Eaton Myasthenic Syndrome (Lambert-Eaton Syndrome)
12/01/2012 - "These molecular mechanisms are supported by studies in P/Q- and N-type VDCCs double-knockout mice, and they are consistent with the pathological conditions of Lambert-Eaton myasthenic syndrome and Pierson syndrome, which are caused by autoantibodies against VDCCs or by a laminin β2 mutation. "
|3.||Nephrotic Syndrome (Syndrome, Nephrotic)
12/01/2014 - "Pierson syndrome - a rare cause of congenital nephrotic syndrome."
09/01/2010 - "Mutations of LAMB2 typically cause autosomal recessive Pierson syndrome, a disorder characterized by congenital nephrotic syndrome, ocular and neurologic abnormalities, but may occasionally be associated with milder or oligosymptomatic disease variants. "
03/01/2010 - "Pierson syndrome is typically manifested with congenital nephrotic syndrome (CNS) and peculiar ocular changes. "
09/01/2006 - "These findings demonstrate that the spectrum of LAMB2-associated disorders is broader than previously anticipated and includes congenital nephrotic syndrome without eye anomalies or with minor ocular changes different from those observed in Pierson syndrome. "
08/01/2006 - "We conclude that Pierson syndrome should be included in the differential diagnosis for congenital nephrotic syndrome, especially in patients with ocular abnormalities."
03/01/2006 - "Prenatal findings in four consecutive pregnancies with fetal Pierson syndrome, a newly defined congenital nephrosis syndrome."
10/01/2011 - "Paternal isodisomy of chromosome 3 unmasked by autosomal recessive microcoria-congenital nephrosis syndrome (Pierson syndrome) in a child with no other phenotypic abnormalities."
09/01/2006 - "The LAMB2 gene, which was recently reported as mutated in Pierson syndrome (microcoria-congenital nephrosis syndrome; OMIM #609049), was located in the linkage interval. "
10/01/2004 - "We propose that this syndrome should be designated microcoria-congenital nephrosis syndrome or Pierson syndrome. "
|5.||Eye Abnormalities (Eye Abnormality)
01/01/2006 - "Mutations in the LAMB2 gene encoding laminin beta2, a component of the glomerular basement membrane and the neuro-muscular junction are responsible for the characteristic renal and eye abnormalities of Pierson syndrome. "
02/15/2007 - "Pierson syndrome is an autosomal recessive disorder comprising congenital nephrotic syndrome with diffuse mesangial sclerosis and distinct eye abnormalities with microcoria reported as the most prominent clinical feature. "
03/01/2006 - "To describe the prenatal findings in Pierson syndrome, a newly defined autosomal recessive entity, comprising congenital nephrotic syndrome (CNS) with diffuse mesangial sclerosis and distinct eye abnormalities due to LAMB2 mutations. "
|3.||diffuse Mesangial sclerosis
|4.||Collagen Type IV (Type IV Collagen)
|6.||laminin beta2 (S-laminin)
|8.||Extracellular Matrix Proteins
|9.||Galloway Mowat syndrome
|1.||Renal Replacement Therapy (Therapies, Renal Replacement)