Pages that link to "Q69426545"
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The following pages link to Polycystic kidney disease in the first year of life (Q69426545):
Displaying 46 items.
- The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein (Q24292750) (← links)
- Intraflagellar transport (Q28131775) (← links)
- Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella (Q28593253) (← links)
- IFT80 is essential for chondrocyte differentiation by regulating Hedgehog and Wnt signaling pathways (Q28593506) (← links)
- Magnetic Resonance Imaging of Fetal Autosomal Recessive Polycystic Kidney Disease (Q32066099) (← links)
- Renal asymmetry in children with autosomal dominant polycystic kidney disease (Q33749221) (← links)
- Autosomal recessive polycystic kidney disease: a hepatorenal fibrocystic disorder with pleiotropic effects (Q34086721) (← links)
- Polycystic kidney disease: inheritance, pathophysiology, prognosis, and treatment (Q34194508) (← links)
- Deletion of the TSC2 and PKD1 genes associated with severe infantile polycystic kidney disease--a contiguous gene syndrome (Q34321198) (← links)
- Sequence analysis of the human hTg737 gene and its polymorphic sites in patients with autosomal recessive polycystic kidney disease (Q34374806) (← links)
- Consensus expert recommendations for the diagnosis and management of autosomal recessive polycystic kidney disease: report of an international conference (Q34428848) (← links)
- Dysplastic and polycystic kidneys: diagnosis, associations and management (Q34464518) (← links)
- Genetic diseases pediatrics (Q35064244) (← links)
- The Spectrum of Polycystic Kidney Disease in Children (Q35201633) (← links)
- Molecular genetics of autosomal recessive polycystic kidney disease (Q35637400) (← links)
- Current diagnosis and management of fetal genitourinary abnormalities (Q36673395) (← links)
- Role of genetic modifiers in an orthologous rat model of ARPKD (Q37175838) (← links)
- Trials and tribulations of multicenter studies. Lessons learned from the experiences of the Southwest Pediatric Nephrology Study Group (SPNSG). (Q37235155) (← links)
- Diagnosis and management of childhood polycystic kidney disease (Q37806654) (← links)
- Autosomal dominant polycystic kidney disease--more than a renal disease (Q37991548) (← links)
- Polycystic kidney disease: neoplasia in disguise (Q38140599) (← links)
- Polycystic kidney diseases in childhood (Q38725128) (← links)
- Pathology of selected abdominal masses in children (Q39253649) (← links)
- Polycystic kidney disease: Etiology, pathogenesis, and treatment (Q40432138) (← links)
- Hereditary and acquired cystic disease of the kidney (Q40597028) (← links)
- Intrafamilial phenotypic expression of autosomal dominant polycystic kidney disease (Q41118554) (← links)
- Autosomal Recessive Polycystic Kidney Disease: The Clinical Experience in North America (Q44503166) (← links)
- Factors affecting the progression of renal disease in autosomal-dominant polycystic kidney disease (Q46452669) (← links)
- Autosomal recessive polycystic kidney disease: outcomes from a single-center experience (Q51686811) (← links)
- Renal cystic disease of infancy: results of histochemical studies. A report of the Southwest Pediatric Nephrology Study Group. (Q52848551) (← links)
- Prognosis of autosomal dominant polycystic kidney disease diagnosed in utero or at birth (Q63461247) (← links)
- Autosomal recessive polycystic kidney disease (Q67592828) (← links)
- Autosomal dominant polycystic kidney disease with liver and pancreatic involvement in early childhood (Q69584280) (← links)
- Chemical modification of cell proliferation and fluid secretion in renal cysts (Q69704303) (← links)
- Glomerulocystic disease: unilateral involvement of a horseshoe kidney and in trisomy 18 (Q70479539) (← links)
- Nephrocalcinosis in a child with autosomal dominant polycystic kidney disease and a prolapsing ectopic ureterocele (Q71567492) (← links)
- Functional correction of renal defects in a mouse model for ARPKD through expression of the cloned wild-type Tg737 cDNA (Q71717714) (← links)
- Aggressive respiratory support and unilateral nephrectomy for infants with severe perinatal autosomal recessive polycystic kidney disease (Q71962335) (← links)
- Autosomal recessive polycystic kidney disease in 15 Arab children (Q72326316) (← links)
- Does liver biopsy provide sufficient diagnostic information to differentiate autosomal recessive from autosomal dominant polycystic kidney disease? (Q72771739) (← links)
- Autosomal recessive polycystic kidney disease: improvement of renal function (Q73414109) (← links)
- Autosomal recessive polycystic disease with biliary dysgenesis (Q74460305) (← links)
- Morbidity from congenital hepatic fibrosis after renal transplantation for autosomal recessive polycystic kidney disease (Q74464434) (← links)
- Survival of childhood polycystic kidney disease following renal transplantation: the impact of advanced hepatobiliary disease (Q75316207) (← links)
- Recombinant human growth hormone therapy in autosomal recessive polycystic kidney disease (Q78681608) (← links)
- Severe neurological outcomes after very early bilateral nephrectomies in patients with autosomal recessive polycystic kidney disease (ARPKD) (Q100385921) (← links)