Results 171 to 180 of about 2,905 (217)

Reversal of elevatedGli3in Autosomal Recessive Polycystic Kidney Disease does not alter cystogenesis

Russell LG, Kolatsi-Joannou M, Wilson L, Chandler JC, Tejedor NP, Stagg G, Price KL, Rowan CJ, Crompton T, Rosenblum ND, Winyard PJ, Long DA.   +11 more
europepmc   +1 more source

Phenotypic Discordance among Siblings with Autosomal Recessive Polycystic Kidney Disease: Case Report and Review of the Literature.

Nephron
Henein M, Russo F, Sentell ZT, Goupil R, Kitzler TM.   +4 more
europepmc   +1 more source

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A Single-Center Experience of ARPKD in Adults

Journal of the American Society of Nephrology, 2021
. Background: Autosomal recessive polycystic kidney disease (ARPKD) is an inherited ciliopathy with 50% presenting with enlarged kidneys in utero or early infancy.
Meenakshi Sambharia, Sonali Gupta, Christie P. Thomas   +2 more
semanticscholar   +2 more sources

Autosomal-rezessive polyzystische Nierenerkrankung (ARPKD)

Der Nephrologe, 2022
K. Burgmaier, M. Liebau
semanticscholar   +2 more sources

Cyst Fluid From a Rat Model of ARPKD Has a Unique Electrolyte Composition and Sexually Dimorphic Metabolite Profile

Physiology, 2023
Polycystic kidney disease (PKD) is characterized by large fluid-filled cysts that lead to end-stage renal disease. Autosomal recessive polycystic kidney disease (ARPKD) is a rare genetic disorder characterized by the formation of fluid-filled cysts in ...
C. Klemens, Marharyta Semenikhina, Mykhailo Fedoriuk, Lashodya V. Dissanayake, O. Palygin, A. Staruschenko   +5 more
semanticscholar   +1 more source

Optimizing outcomes for neonatal ARPKD

Pediatric Transplantation, 2007
Abstract:  A retrospective analysis was conducted on 10 consecutive cases of neonatal ARPKD, 9 of whom received kidney transplants (KT). All were diagnosed antenatally (n = 6) or at birth. In the first month of life 70% required ventilatory support. Pre‐emptive bilateral nephrectomy and peritoneal dialysis (PD) catheter placement were performed in 9 at
Mona, Beaunoyer, Mohile, Snehal, Li, Li, Waldo, Concepcion, Oscar, Salvatierra, Minnie, Sarwal   +5 more
openaire   +2 more sources

Unusual sonographic features of ARPKD

Prenatal Diagnosis, 2006
AbstractThe classic sonographic appearance of the kidneys in fetuses with autosomal recessive polycystic kidney disease (ARPKD) has been well described. We report a case of enlarged kidneys with pyramidal hyperechogenicity quite similar to medullary nephrocalcinosis found in a fetus at 34 weeks' gestation.
Maria, Okumura, Victor, Bunduki, Christina, Shiang, Regina, Schultz, Marcelo, Zugaib   +4 more
openaire   +2 more sources

ARPKD Diagnosed in an Adult Without Kidney Manifestations

Journal of the American Society of Nephrology, 2022
B. R. Wagner
semanticscholar   +2 more sources