Hamartomatous polyposis

Known as: Hamartomatous Polyp, Hamartomatous polyps 
A polyp characterized by an overgrowth of mature cells and tissues that normally occur in the affected area.
National Institutes of Health

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Hamartoma Syndrome, MultiplePeutz-Jeghers Polyp

Papers overview

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2013
2013
Hamartomatous polyposis syndromes
Hamartomas are tumour-like malformations, consisting of disorganized normal tissues, typical of the site of tumour manifestation… (More)
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Review
2007
Review
2007
Hamartomatous polyposis syndromes
The hamartomatous polyposis syndromes are a heterogeneous group of disorders that share an autosomal-dominant pattern of… (More)
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2002
2002
Advances in Brief Gastrointestinal Hamartomatous Polyposis in Lkb 1 Heterozygous Knockout Mice 1
Peutz-Jeghers syndrome (PJS) is a hereditary disorder characterized by gastrointestinal hamartomatous polyposis associated with… (More)
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Highly Cited
2000
Highly Cited
2000
LKB1, a novel serine/threonine protein kinase and potential tumour suppressor, is phosphorylated by cAMP-dependent protein kinase (PKA) and prenylated in vivo.
Peutz-Jeghers syndrome (PJS) is an autosomal dominant disease characterized by melanocytic macules, hamartomatous polyps and an… (More)
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Highly Cited
1998
Highly Cited
1998
Mutations in the SMAD4/DPC4 gene in juvenile polyposis.
Familial juvenile polyposis is an autosomal dominant disease characterized by a predisposition to hamartomatous polyps and… (More)
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Highly Cited
1998
Highly Cited
1998
Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase.
Peutz-Jeghers (PJ) syndrome is an autosomal-dominant disorder characterized by melanocytic macules of the lips, multiple… (More)
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Highly Cited
1998
Highly Cited
1998
Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity.
Peutz-Jeghers syndrome (PJS) is an autosomal dominant disease characterized by mucocutaneous pigmentation and hamartomatous… (More)
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Highly Cited
1997
Highly Cited
1997
Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis
Many human cancer susceptibility genes have been successfully mapped by genetic linkage studies1. One that has so far eluded… (More)
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Review
1995
Review
1995
The hamartomatous polyposis syndromes: clinical and radiologic features.
Most radiologists are familiar with the clinical and radiologic features of the familial adenomatous polyposis syndromes [1]. The… (More)
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1993
1993
Neoplastic transformation arising in Peutz-Jeghers polyposis.
PURPOSE AND METHODS To clarify the potential for malignancy of Peutz-Jeghers polyposis, we investigated 75 gastrointestinal… (More)
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