Autosomal recessive polycystic kidney disease presenting in adulthood. Molecular diagnosis of the family (original) (raw)

Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD): kidney-related and non-kidney-related phenotypes

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A study of long-term morbidity associated with autosomal recessive polycystic kidney disease

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Characteristics of very early onset autosomal dominant polycystic kidney disease

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Autosomal recessive polycystic kidney disease (ARPKD) in a Nigerian newborn: a case report

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Autosomal recessive polycystic kidney disease in 115 children: clinical presentation, course and influence of gender

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Prognosis of autosomal dominant polycystic kidney disease diagnosed in utero or at birth

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Nephrectomy in an autosomal recessive polycystic kidney disease (ARPKD) patient with rapid kidney enlargement and increased expression of EGFR

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Genetic Diagnosis of a Lethal Form of Autosomal Recessive Polycystic Kidney Disease

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Genetic Diagnosis if a Lethal Form of Autosomal Recessive Polycystic Kidney Disease

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Autosomal recessive polycystic kidney disease: case report of a newborn with rare PKHD1 mutation, rapid renal enlargement and early fatal outcome

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Polycystic kidney disease in the first year of life

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Hepatorenal findings in obligate heterozygotes for autosomal recessive polycystic kidney disease

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Progression of autosomal-dominant polycystic kidney disease in children

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Autosomal recessive polycystic kidney disease: the importance of autopsy of suspected cases and genetic counselling

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Sonographic pattern of recessive polycystic kidney disease in young adults. Differences from the dominant form

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Clinical courses and complications of young adults with Autosomal Recessive Polycystic Kidney Disease (ARPKD)

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Autosomal recessive polycystic kidney disease (ARPKD) in fetus: Autopsy based approach

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Spectrum of Mutations in the Gene for Autosomal Recessive Polycystic Kidney Disease (ARPKD/PKHD1)

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A stable, nonsense mutation associated with a case of infantile onset polycystic kidney disease 1 (PKD1

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Polycystic kidney disease: Clues to pathogenesis

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Chapter 3 Rare Inherited Diseases Among Hemodialysis Patients

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Diagnosis of autosomal dominant polycystic kidney disease in utero and in the young infant

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Phenotypic heterogeneity in pediatric autosomal dominant polycystic kidney disease at first presentation: a single-center, 20-year review

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American Journal of Kidney Diseases, 2004

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An Integrated Genetic and Physical Map of the Autosomal Recessive Polycystic Kidney Disease Region

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Genomics, 1997

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Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD)

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Molecular genetic diagnosis of autosomal dominant polycystic kidney disease in a newborn with bilateral cystic kidneys detected prenatally and multiple skeletal malformations

Alberto Turco

Journal of Medical Genetics, 1993

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Bioinformatic tools to determine the pathogenicity of a missense mutation in PKHD1 in autosomal recessive polycystic kidney disease

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A Spectrum of Mutations in the Second Gene for Autosomal Dominant Polycystic Kidney Disease (PKD2)

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Genotype–phenotype correlations in fetuses and neonates with autosomal recessive polycystic kidney disease

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Newly Detected PKHD1 Gene Mutation in a Newborn with Fatal Autosomal Recessive Polycystic Kidney Disease

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Autosomal Recessive Polycystic Kidney Disease in a Child Complicated by Autoimmune Hemolytic Anemia: A Case Report

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Autosomal dominant polycystic kidney disease in a family with mosaicism and hypomorphic allele

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