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Journal Abstract Search

275 related items for PubMed ID: 36657418

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  • 2. Genotype-phenotype of autosomal dominant polycystic kidney disease in Malta.
    Ciantar N, Zahra G, Delicata J, Sammut F, Calleja-Agius J, Farrugia E, Said E.
    Eur J Med Genet; 2024 Jun; 69():104934. PubMed ID: 38537868
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  • 3. Hypomagnesaemia is absent in children with autosomal dominant polycystic kidney disease.
    Seeman T, Fořtová M, Sopko B, Průša R, Pohl M, John U.
    Ann Clin Biochem; 2019 Jan; 56(1):90-94. PubMed ID: 29874928
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  • 9. Cilia and polycystic kidney disease.
    Ma M.
    Semin Cell Dev Biol; 2021 Feb; 110():139-148. PubMed ID: 32475690
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  • 11. The spectrum of polycystic kidney disease in children.
    Dell KM.
    Adv Chronic Kidney Dis; 2011 Sep; 18(5):339-47. PubMed ID: 21896375
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  • 16. PKD1 Truncating Mutations Accelerate eGFR Decline in Autosomal Dominant Polycystic Kidney Disease Patients.
    Ali H, Alahmad B, Senum SR, Warsame S, Bahbahani Y, Abu-Farha M, Abubaker J, Alqaddoumi M, Al-Mulla F, Harris PC.
    Am J Nephrol; 2024 Sep; 55(3):380-388. PubMed ID: 38194940
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  • 18. Hereditary polycystic kidney diseases in children: changing sonographic patterns through childhood.
    Avni FE, Guissard G, Hall M, Janssen F, DeMaertelaer V, Rypens F.
    Pediatr Radiol; 2002 Mar; 32(3):169-74. PubMed ID: 12164348
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  • 19. Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease.
    Audrézet MP, Corbiere C, Lebbah S, Morinière V, Broux F, Louillet F, Fischbach M, Zaloszyc A, Cloarec S, Merieau E, Baudouin V, Deschênes G, Roussey G, Maestri S, Visconti C, Boyer O, Abel C, Lahoche A, Randrianaivo H, Bessenay L, Mekahli D, Ouertani I, Decramer S, Ryckenwaert A, Cornec-Le Gall E, Salomon R, Ferec C, Heidet L.
    J Am Soc Nephrol; 2016 Mar; 27(3):722-9. PubMed ID: 26139440
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