Chronic liver disease and hepatic calcium-oxalate deposition in patients with primary hyperoxaluria type I.

Recker, Pia; Beck, Bodo Bernhard; Sikora, Przemyslaw; Göbel, Heike; Kemper, Markus Josef; Nazco, Angel; Martin-Higueras, Cristina; Hoppe, Bernd

Recker, Pia; Beck, Bodo Bernhard; Sikora, Przemyslaw; Göbel, Heike; Kemper, Markus Josef; Nazco, Angel; Martin-Higueras, Cristina; Hoppe, Bernd.

Afiliação

Recker P; Department of Pediatric and Adolescent Medicine, Division of Pediatric Nephrology, University Hospital Cologne, Cologne, Germany.
Beck BB; Department of Pediatric and Adolescent Medicine, HELIOS University Hospital Wuppertal, Wuppertal, Germany.
Sikora P; Institute of Human Genetics, University Hospital Cologne, Cologne, Germany.
Göbel H; Department of Pediatric Nephrology, Lublin Medical University, Lublin, Poland.
Kemper MJ; Department of Pathology, University Hospital Cologne, Cologne, Germany.
Nazco A; Department of Pediatric and Adolescent Medicine, Asklepios Klinik Hamburg, Hamburg, Germany.
Martin-Higueras C; Department of Pathology, Nuestra Señora de Candelaria University Hospital, Tenerife, Spain.
Hoppe B; Department of Basic Medical Sciences, Centre for Biomedical Research in Rare Diseases (CIBERER), Institute of Biomedical Technologies (ITB), University of La Laguna, Tenerife, Spain.

Sci Rep ; 12(1): 16725, 2022 10 06.

Article em En | MEDLINE | ID: mdl-36202824

Assuntos

Calcinose; Hiperoxalúria Primária; Hepatopatias; Cálcio; Oxalato de Cálcio; Fibrose; Humanos; Ferro; Rim; Oxalatos

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hiperoxalúria Primária / Calcinose / Hepatopatias Limite: Humans Idioma: En Revista: Sci Rep Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Alemanha

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