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searching for Autosomal recessive polycystic kidney disease 14 found (23 total)

alternate case: autosomal recessive polycystic kidney disease

Cystic kidney disease (1,144 words) [view diff] exact match in snippet view article find links to article

autosomal recessive and more prevalent autosomal dominant. Autosomal recessive polycystic kidney disease (ARPKD) is primarily diagnosed in infants and young

Congenital hepatic fibrosis (266 words) [view diff] exact match in snippet view article find links to article

associated with other congenital defects, commonly with autosomal recessive polycystic kidney disease, the most severe form of PKD. Some suggest that these

Polycystic liver disease (377 words) [view diff] exact match in snippet view article find links to article

autosomal dominant polycystic kidney disease (ADPKD), or autosomal recessive polycystic kidney disease (ARPKD). Many patients are asymptomatic and thus are

Vanishing bile duct syndrome (272 words) [view diff] exact match in snippet view article find links to article

and ALGS1 MIM:118450) Extrahepatic bile duct atresia Autosomal recessive polycystic kidney disease Congential hepatic fibrosis Caroli's disease Von Meyenburg

IFT88 (850 words) [view diff] exact match in snippet view article find links to article

hTg737 gene and its polymorphic sites in patients with autosomal recessive polycystic kidney disease". Mamm. Genome. 6 (11): 805–8. doi:10.1007/BF00539009

MCM3 (1,553 words) [view diff] exact match in snippet view article find links to article

protein (MCM3) and its exclusion as a candidate for autosomal recessive polycystic kidney disease". Eur. J. Hum. Genet. 8 (3): 163–6. doi:10.1038/sj.ejhg

Caroli disease (1,288 words) [view diff] exact match in snippet view article find links to article

usually occurs in the presence of other diseases, such as autosomal recessive polycystic kidney disease, cholangitis, gallstones, biliary abscess, sepsis, liver

Intraflagellar transport (2,108 words) [view diff] no match in snippet view article find links to article

the loss of this protein has been found to cause an autosomal-recessive polycystic kidney disease model phenotype in mice. Further, the mislocalization

Polycystin cation channel family (1,385 words) [view diff] exact match in snippet view article find links to article

cytoskeleton and up-regulates its channel function. Autosomal recessive polycystic kidney disease is caused by mutations in PKHD1, which encodes the membrane-associated

Martin Barratt (1,467 words) [view diff] exact match in snippet view article find links to article

Trompeter, Richard S.; Barratt, T. Martin (26 May 1997). "Autosomal recessive polycystic kidney disease: long-term outcome of neonatal survivors". Pediatric

Glutathione S-transferase A1 (1,164 words) [view diff] exact match in snippet view article find links to article

Guay-Woodford L, Zerres K (Apr 1998). "Fine mapping of the autosomal recessive polycystic kidney disease locus (PKHD1) and the genes MUT, RDS, CSNK2 beta, and

Tesevatinib (381 words) [view diff] exact match in snippet view article find links to article

progression of polycystic kidney disease in rodent models of autosomal recessive polycystic kidney disease". World Journal of Nephrology. 6 (4): 188–200. doi:10

Potter sequence (2,364 words) [view diff] exact match in snippet view article find links to article

and not another form. Type I 263200 Type I is due to autosomal recessive polycystic kidney disease (ARPKD), which occurs at a frequency of approximately

CSNK2B (2,258 words) [view diff] exact match in snippet view article find links to article

Guay-Woodford L, Zerres K (April 1998). "Fine mapping of the autosomal recessive polycystic kidney disease locus (PKHD1) and the genes MUT, RDS, CSNK2 beta, and