Unexpectedly high prevalence of rare genetic disorders in kidney transplant recipients with an unknown causal nephropathy

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Uromodulin: from physiology to rare and complex kidney disorders.Inverted formins: A subfamily of atypical formins.Autosomal dominant tubulointerstitial kidney disease caused by uromodulin mutations: seek and you will find.

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Unexpectedly high prevalence of rare genetic disorders in kidney transplant recipients with an unknown causal nephropathy

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http://www.wikidata.org/entity/Q58620408

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im Juli 2014 veröffentlichter wissenschaftlicher Artikel

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wetenschappelijk artikel

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наукова стаття, опублікована в липні 2014

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Unexpectedly high prevalence o ...... an unknown causal nephropathy

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Unexpectedly high prevalence o ...... an unknown causal nephropathy

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Unexpectedly high prevalence o ...... an unknown causal nephropathy

@en

Unexpectedly high prevalence o ...... an unknown causal nephropathy

@nl

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Unexpectedly high prevalence o ...... an unknown causal nephropathy

@en

Unexpectedly high prevalence o ...... an unknown causal nephropathy

@nl

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Unexpectedly high prevalence o ...... an unknown causal nephropathy

@en

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Andrea Airoldi

http://www.w3.org/2001/XMLSchema#string

Claudio Musetti

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Cristina Izzo

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Elisa Lazzarich

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Fabio Settanni

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Gian Marco Ghiggeri

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Giovanni Battista Fogazzi

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Mara Giordano

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Marco Quaglia

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Piero Stratta

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Mechanisms of nephronophthisis and related ciliopathies

Adenine phosphoribosyltransferase deficiency

Female with Fabry Disease Unknowingly Donates Affected Kidney to Sister: A Call for Pre-transplant Genetic Testing.

Unexpected Fabry disease in a renal allograft kidney: an underrecognized cause of poor allograft function.

Two patients with history of STEC-HUS, posttransplant recurrence and complement gene mutations.

Hereditary causes of kidney stones and chronic kidney disease

Phenotype and outcome in hereditary tubulointerstitial nephritis secondary to UMOD mutations

Senior-Løken syndrome: a syndromic form of retinal dystrophy associated with nephronophthisis.

Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis.

The rediscovery of uromodulin (Tamm-Horsfall protein): from tubulointerstitial nephropathy to chronic kidney disease.

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995-1003

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scholarly article

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10.1111/CTR.12408

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http://www.w3.org/2001/XMLSchema#string

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http://www.w3.org/2001/XMLSchema#string

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2014-07-18T00:00:00Z

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Unexpectedly high prevalence of rare genetic disorders in kidney transplant recipients with an unknown causal nephropathy

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Unexpectedly high prevalence of rare genetic disorders in kidney transplant recipients with an unknown causal nephropathy

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