PTEN hamartoma tumour syndrome: case report based on data from the Iranian hereditary colorectal cancer registry and literature review
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource, 1 online resource.
- Language
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Englisch
- Bibliographic citation
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PTEN hamartoma tumour syndrome: case report based on data from the Iranian hereditary colorectal cancer registry and literature review ; volume:18 ; number:1 ; day:4 ; month:4 ; year:2023 ; pages:1-31 ; date:12.2023
Diagnostic pathology ; 18, Heft 1 (4.4.2023), 1-31, 12.2023
- Creator
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Rahmatinejad, Zahra
Goshayeshi, Ladan
Bergquist, Robert
Goshayeshi, Lena
Golabpour, Amin
Hoseini, Benyamin
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s13000-023-01331-x
- URN
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urn:nbn:de:101:1-2023081909185700186891
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 11:03 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Rahmatinejad, Zahra
- Goshayeshi, Ladan
- Bergquist, Robert
- Goshayeshi, Lena
- Golabpour, Amin
- Hoseini, Benyamin
- SpringerLink (Online service)
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Differential expression of PTEN gene correlates with phenotypic heterogeneity in three cases of patients showing clinical manifestations of PTEN hamartoma tumour syndrome
Dysregulated PTEN/PI3K signaling in lipoma cells of children with PTEN Hamartoma Tumor Syndrome
PTEN hamartoma tumor syndrome: Clinical and genetic characterization in pediatric patients
“Thyroid nodular disease and PTEN mutation in a multicentre series of children with PTEN hamartoma tumor syndrome (PHTS)”
A rare pulmonary hamartoma: fibroleiomyomatous hamartoma
Recommendations on Surveillance for Differentiated Thyroid Carcinoma in Children with PTEN Hamartoma Tumor Syndrome
Sirolimus treatment of severe PTEN hamartoma tumor syndrome: case report and in vitro studies
Endosonographic Appearances of a Rare Duodenal Tumour, Brunner’s Gland Hamartoma
Immune dysregulation in patients with PTEN hamartoma tumor syndrome: analysis of FOXP3 regulatory T cells
Beta catenin and cytokine pathway dysregulation in patients with manifestations of the "PTEN hamartoma tumor syndrome"
Giant pulmonary hamartoma
PTEN hamartoma tumor syndrome in childhood and adolescence—a comprehensive review and presentation of the German pediatric guideline
Differential expression of PTEN gene correlates with phenotypic heterogeneity in three cases of patients showing clinical manifestations of PTEN hamartoma tumour syndrome
Dysregulated PTEN/PI3K signaling in lipoma cells of children with PTEN Hamartoma Tumor Syndrome
PTEN hamartoma tumor syndrome: Clinical and genetic characterization in pediatric patients
“Thyroid nodular disease and PTEN mutation in a multicentre series of children with PTEN hamartoma tumor syndrome (PHTS)”
A rare pulmonary hamartoma: fibroleiomyomatous hamartoma
Recommendations on Surveillance for Differentiated Thyroid Carcinoma in Children with PTEN Hamartoma Tumor Syndrome
Sirolimus treatment of severe PTEN hamartoma tumor syndrome: case report and in vitro studies
Endosonographic Appearances of a Rare Duodenal Tumour, Brunner’s Gland Hamartoma
Immune dysregulation in patients with PTEN hamartoma tumor syndrome: analysis of FOXP3 regulatory T cells
Beta catenin and cytokine pathway dysregulation in patients with manifestations of the "PTEN hamartoma tumor syndrome"
Giant pulmonary hamartoma