Results 211 to 220 of about 12,421 (264)

Orthostatic proteinuria [PDF]

, 2014
Sonderman, David
core   +1 more source

High adherence to angiotensin-converting enzyme inhibitor in children and adolescents with Alport syndrome: objective verification using liquid chromatography-mass spectrometry. [PDF]

Pediatr Nephrol
Boeckhaus J, Tönshoff B, Weber LT, Haffner D, Pape L, Latta K, Fehrenbach H, Lange-Sperandio B, Kettwig M, König S, John-Kroegel U, Gellermann J, Galiano M, Hafke A, Streit F, Gross O.   +15 more
europepmc   +1 more source

Molecular Review of Suspected Alport Syndrome Patients-A Single-Centre Experience. [PDF]

Genes (Basel)
Halat-Wolska P, Ciara E, Pac M, Obrycki Ł, Wicher D, Iwanicka-Pronicka K, Bielska E, Chałupczyńska B, Siestrzykowska D, Kostrzewa G, Stawiński P, Płoski R, Litwin M, Chrzanowska K.   +13 more
europepmc   +1 more source

Whole-genome sequencing revealed a novel structural variant in COL4A4 causing autosomal dominant Alport syndrome: A case report

Clément Delage, Marine Andreani, Nihad Boukrout, Naoual Sabaouni, Michaël Perrais, Bruno Lefebvre, Christelle Cauffiez, Nicolas Pottier, Romain Larrue   +8 more
openalex   +1 more source

A retrospective study of kidney disease in Alport syndrome during and after pregnancy. [PDF]

J Nephrol
Kong X, Boeckhaus J, Wang F, Shi C, Zhang H, Gross O, Ding J, Zhang Y.   +7 more
europepmc   +1 more source

Severe Clinical Phenotype in Alport Syndrome Due to 2 <i>COL4A4</i> Exon-Skipping Events. [PDF]

Kidney Med
Pleško J, Kojc N, Kert Š, Petrin S, Matjašič A, Meglič A, Zupan A.   +6 more
europepmc   +1 more source

Diagnosis, management and treatment of the Alport syndrome - 2024 guideline on behalf of ERKNet, ERA and ESPN. [PDF]

Nephrol Dial Transplant
Torra R, Lipska-Zietkiewicz B, Acke F, Antignac C, Becker JU, Cornec-Le Gall E, van Eerde AM, Feltgen N, Ferrari R, Gale DP, Gear S, Gross O, Haeberle S, Heidet L, Lennon R, Massella L, Pfau K, Pizarro MDPV, Topaloglu R, Wlodkowski T, Zealey H, ERKNet, ERA Genes&Kidney and ESPN Inherited renal disorders working group .   +22 more
europepmc   +1 more source

Carrier screening for Alport syndrome: The clinical importance of heterozygosity for pathogenic or likely pathogenetic variants. [PDF]

J Genet Couns
Souter V, Johnson L, Becraft E, Cantu-Weinstein A, Tabriziani H, Benn P, Kashtan CE.   +6 more
europepmc   +1 more source

The impact on long-term kidney function of the renal resistive index in the immediate postoperative period after kidney transplantation : a cohort analysis

, 2017
Bogaert, Stijn, Decruyenaere, Alexander, Decruyenaere, Philippe, Hoste, Eric, PEETERS, PATRICK   +4 more
core  

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ALPORT'S SYNDROME

The Lancet, 1962
openaire   +3 more sources