Clinical aspects of autosomal recessive polycystic kidney disease (2007)
- Authors:
- Autor USP: ONUCHIC, LUIZ FERNANDO - FM
- Unidade: FM
- Subjects: RIM (FISIOLOGIA); CISTOS (DIAGNÓSTICO); MORTALIDADE
- Language: Inglês
- Imprenta:
- Source:
- Título: Abstracts
- Volume/Número/Paginação/Ano: p. 20, res. FC08, 2007
- Conference titles: World Congress of Nephrology/WCN'07 Satellite Symposium on Pediatric Nephro-Urological Diseases
-
ABNT
DIAS, N. F. et al. Clinical aspects of autosomal recessive polycystic kidney disease. 2007, Anais.. São Paulo: Faculdade de Medicina, Universidade de São Paulo, 2007. p. 20. . Acesso em: 17 fev. 2026. -
APA
Dias, N. F., Lanzarini, V., Onuchic, L. F., & Koch, V. (2007). Clinical aspects of autosomal recessive polycystic kidney disease. In Abstracts (p. 20). São Paulo: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Dias NF, Lanzarini V, Onuchic LF, Koch V. Clinical aspects of autosomal recessive polycystic kidney disease. Abstracts. 2007 ; 20.[citado 2026 fev. 17 ] -
Vancouver
Dias NF, Lanzarini V, Onuchic LF, Koch V. Clinical aspects of autosomal recessive polycystic kidney disease. Abstracts. 2007 ; 20.[citado 2026 fev. 17 ] - Doenças císticas e tumores renais
- Refinement of the autosomal recessive polycystic kidney disease (PKHD1) interval and exclusion of an EF hand-containing gene as a PKHD1 candidate gene
- Regulation of CFTR Expression and Arginine Vasopressin Activity Are Dependent on Polycystin-1 in Kidney-Derived Cells
- Expression of Polyductin, the PKHD1 gene product, in Normal, Dysgenetic and Neoplastic Liver
- Genomic structure and exclusion of two candidate genes for the PKHD1 locus and three new polymorphic markers within the critical interval
- Direct association of full-lenght PKD1 and PKD2 proteins in mammalian cells
- Genomic structure of the gene for the human P1 protein (MCM3) and its exclusion as a candidate for atosomal recessive polycystic kidney disease
- Giant renal angiomyolipoma following ovarian stimulation therapy
- Hematúria em histórico de doença renal familiar
- KDIGO 2025 clinical practice guideline for the evaluation, management, and treatment of autosomal dominant polycystic kidney disease (ADPKD): executive summary
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