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Viscoelastic behavior of hydrogel‐based xanthan gum/aluminum lactate with potential applicability for conformance control

Journal of applied polymer science, 2021-07, Vol.138 (27), p.n/a

2021

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Identification of Protective Actions to Reduce the Vulnerability of Safety‐Critical Systems to Malevolent Intentional Acts: An Optimization‐Based Decision‐Making Approach

Risk analysis, 2020-03, Vol.40 (3), p.565-587

2020

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Angiosarcoma of the heart: Report of a case in a 9-year-old boy

Medical and pediatric oncology, 1983, Vol.11 (5), p.336-338

1983

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Facial seborrheic keratosis with unusual dermoscopic patterns can be differentiated from other skin malignancies by in vivo reflectance confocal microscopy

Journal of the European Academy of Dermatology and Venereology, 2021-11, Vol.35 (11), p.e784-e787

2021

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Conversion from forests to pastures in the Colombian Amazon leads to contrasting soil carbon dynamics depending on land management practices

Global change biology, 2016-10, Vol.22 (10), p.3503-3517

2016

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Is a five-category reporting scheme for thyroid fine needle aspiration cytology accurate? Experience of over 18 000 FNAs reported at the same institution during 1998-2007

Cytopathology (Oxford), 2011-06, Vol.22 (3), p.164-173

2011

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Application of a niched Pareto genetic algorithm for selecting features for nuclear transients classification

International journal of intelligent systems, 2009-02, Vol.24 (2), p.118-151

2009

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Identification of Muir-Torre syndrome among patients with sebaceous tumors and keratoacanthomas: Role of clinical features, microsatellite instability, and immunohistochemistry

Cancer, 2005-03, Vol.103 (5), p.1018-1025

2005

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Attenuated familial adenomatous polyposis and Muir-Torre syndrome linked to compound biallelic constitutional MYH gene mutations

Clinical genetics, 2005-11, Vol.68 (5), p.442-447

2005

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Microsatellite instability in multiple colorectal tumors

International journal of cancer, 1999-03, Vol.81 (1), p.1-5

1999

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Different phenotypes in Muir–Torre syndrome: clinical and biomolecular characterization in two Italian families

British journal of dermatology (1951), 2005-06, Vol.152 (6), p.1335-1338

2005

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Frequency of constitutional MSH6 mutations in a consecutive series of families with clinical suspicion of HNPCC

Clinical genetics, 2007-09, Vol.72 (3), p.230-237

2007

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Is a five-category reporting scheme for thyroid fine needle aspiration cytology accurate? Experience of over 18 000 FNAs reported at the same institution during 1998-2007: Cytological classification of thyroid FNA

Cytopathology (Oxford), 2011-06, Vol.22 (3), p.164-173

2011

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Methylation pattern of different regions of the MLH1 promoter and silencing of gene expression in hereditary and sporadic colorectal cancer

Genes chromosomes & cancer, 2001-08, Vol.31 (4), p.357-361

2001

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UV Spectrophotometry: Improvements in the Study of the Degree of Acetylation of Chitosan

Macromolecular bioscience, 2003-10, Vol.3 (10), p.531-534

2003

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Histology of aberrant crypt foci in the human colon

Histopathology, 1997-04, Vol.30 (4), p.328-334

1997

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K‐ras and p53 mutations in hereditary non‐polyposis colorectal cancers

International journal of cancer, 1997-02, Vol.74 (1), p.94-96

1997

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Clinical and biologic heterogeneity of hereditary nonpolyposis colorectal cancer

International journal of cancer, 2001-09, Vol.95 (5), p.323-328

2001

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Genomic instability and target gene mutations in colon cancers with different degrees of allelic shifts

Genes chromosomes & cancer, 2000-04, Vol.27 (4), p.424-429

2000

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Short Report: Frequency of constitutional MSH6 mutations in a consecutive series of families with clinical suspicion of HNPCC

Clinical genetics, 2007-09, Vol.72 (3), p.230

2007

Volltextzugriff (PDF)

Tumour spectrum in hereditary non‐polyposis colorectal cancer (HNPCC) and in families with “suspected hnpcc”. A population‐based study in northern Italy

International journal of cancer, 1993-05, Vol.54 (3), p.371-377

1993

Volltextzugriff (PDF)

Short Report: Attenuated familial adenomatous polyposis and Muir-Torre syndrome linked to compound biallelic constitutional MYH gene mutations

Clinical genetics, 2005-11, Vol.68 (5), p.442-447

2005

Volltextzugriff (PDF)

Risk of cancer revealed by follow‐up of families with hereditary non‐polyposis colorectal cancer: A population‐based study

International journal of cancer, 1993-09, Vol.55 (2), p.202-207

1993

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Cell kinetics evaluation of colorectal tumors after in vivo administration of bromodeoxyuridine

International journal of cancer, 1992-12, Vol.52 (6), p.856-861

1992

Volltextzugriff (PDF)

Cloning of a novel pilin‐like gene from Bordetella pertussis: homology to the fim2 gene

Molecular microbiology, 1988-07, Vol.2 (4), p.539-543

1988

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Viscoelastic behavior of hydrogel‐based xanthan gum/aluminum lactate with potential applicability for conformance control

Identification of Protective Actions to Reduce the Vulnerability of Safety‐Critical Systems to Malevolent Intentional Acts: An Optimization‐Based Decision‐Making Approach

Angiosarcoma of the heart: Report of a case in a 9-year-old boy

Facial seborrheic keratosis with unusual dermoscopic patterns can be differentiated from other skin malignancies by in vivo reflectance confocal microscopy

Conversion from forests to pastures in the Colombian Amazon leads to contrasting soil carbon dynamics depending on land management practices

Is a five-category reporting scheme for thyroid fine needle aspiration cytology accurate? Experience of over 18 000 FNAs reported at the same institution during 1998-2007

Application of a niched Pareto genetic algorithm for selecting features for nuclear transients classification

Identification of Muir-Torre syndrome among patients with sebaceous tumors and keratoacanthomas: Role of clinical features, microsatellite instability, and immunohistochemistry

Attenuated familial adenomatous polyposis and Muir-Torre syndrome linked to compound biallelic constitutional MYH gene mutations

Microsatellite instability in multiple colorectal tumors

Different phenotypes in Muir–Torre syndrome: clinical and biomolecular characterization in two Italian families

Frequency of constitutional MSH6 mutations in a consecutive series of families with clinical suspicion of HNPCC

Is a five-category reporting scheme for thyroid fine needle aspiration cytology accurate? Experience of over 18 000 FNAs reported at the same institution during 1998-2007: Cytological classification of thyroid FNA

Methylation pattern of different regions of the MLH1 promoter and silencing of gene expression in hereditary and sporadic colorectal cancer

UV Spectrophotometry: Improvements in the Study of the Degree of Acetylation of Chitosan

Histology of aberrant crypt foci in the human colon

K‐ras and p53 mutations in hereditary non‐polyposis colorectal cancers

Clinical and biologic heterogeneity of hereditary nonpolyposis colorectal cancer

Genomic instability and target gene mutations in colon cancers with different degrees of allelic shifts

Short Report: Frequency of constitutional MSH6 mutations in a consecutive series of families with clinical suspicion of HNPCC

Tumour spectrum in hereditary non‐polyposis colorectal cancer (HNPCC) and in families with “suspected hnpcc”. A population‐based study in northern Italy

Short Report: Attenuated familial adenomatous polyposis and Muir-Torre syndrome linked to compound biallelic constitutional MYH gene mutations

Risk of cancer revealed by follow‐up of families with hereditary non‐polyposis colorectal cancer: A population‐based study

Cell kinetics evaluation of colorectal tumors after in vivo administration of bromodeoxyuridine

Cloning of a novel pilin‐like gene from Bordetella pertussis: homology to the fim2 gene

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