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Transfusion Science|December 2, 2000

Transfusional iron overload and chelation therapy with deferoxamine and deferiprone (L1)G J Kontoghiorghes, K Pattichi, M Hadjigavriel, et al.

Hippokratia|January 29, 2014

X-linked, COL4A5 hypomorphic Alport mutations such as G624D and P628L may only exhibit thin basement membrane nephropathy with microhematuria and late onset kidney failureA Pierides, K Voskarides, M Kkolou, et al.

Scandinavian Journal of Gastroenterology|August 1, 1996

Serum/ascites albumin gradient: its value as a rational approach to the differential diagnosis of ascitesE A Akriviadis, D Kapnias, M Hadjigavriel, et al.

Zeitschrift Fur Kardiologie|January 1, 1985

Short-term, high-dose muzolimine treatment in patients with chronic renal failure and acute fluid retentionG Orsoni, A Di Felice, M Hadjigavriel, et al.

Human Genetics|January 28, 1999

Loss of heterozygosity in polycystic kidney disease with a missense mutation in the repeated region of PKD1M Koptides, R Constantinides, G Kyriakides, et al.

Clinical Genetics|February 22, 2011

X-linked Alport syndrome in Hellenic families: phenotypic heterogeneity and mutations near interruptions of the collagen domain in COL4A5P Demosthenous, K Voskarides, K Stylianou, et al.

Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:

Pageof 1

Transfusion Science|December 2, 2000

Transfusional iron overload and chelation therapy with deferoxamine and deferiprone (L1)G J Kontoghiorghes, K Pattichi, M Hadjigavriel, et al.

Hippokratia|January 29, 2014

X-linked, COL4A5 hypomorphic Alport mutations such as G624D and P628L may only exhibit thin basement membrane nephropathy with microhematuria and late onset kidney failureA Pierides, K Voskarides, M Kkolou, et al.

Scandinavian Journal of Gastroenterology|August 1, 1996

Serum/ascites albumin gradient: its value as a rational approach to the differential diagnosis of ascitesE A Akriviadis, D Kapnias, M Hadjigavriel, et al.

Zeitschrift Fur Kardiologie|January 1, 1985

Short-term, high-dose muzolimine treatment in patients with chronic renal failure and acute fluid retentionG Orsoni, A Di Felice, M Hadjigavriel, et al.

Human Genetics|January 28, 1999

Loss of heterozygosity in polycystic kidney disease with a missense mutation in the repeated region of PKD1M Koptides, R Constantinides, G Kyriakides, et al.

Clinical Genetics|February 22, 2011

X-linked Alport syndrome in Hellenic families: phenotypic heterogeneity and mutations near interruptions of the collagen domain in COL4A5P Demosthenous, K Voskarides, K Stylianou, et al.

Pageof 1