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Clinical trials with retinoids for breast cancer chemoprevention

Endocrine-related cancer, 2006-03, Vol.13 (1), p.51-68

2006

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Plasma levels of amyloid beta-protein 42 are increased in women with mild cognitive impairment

Neurology, 2004-09, Vol.63 (5), p.828

2004

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Development and Validation of a Self-Administered Multidimensional Prognostic Index to Predict Negative Health Outcomes in Community-Dwelling Persons

Rejuvenation research, 2019-08, Vol.22 (4), p.299

2019

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EFFICHRONIC study protocol: a non-controlled, multicentre European prospective study to measure the efficiency of a chronic disease self-management programme in socioeconomically vulnerable populations

BMJ open, 2019-12, Vol.9 (12), p.e032073-e032073

2019

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SERMs in chemoprevention of breast cancer

European journal of cancer (1990), 2005-09, Vol.41 (13), p.1980-1989

2005

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Phase I-II trial of weekly bicalutamide in men with high PSA and negative biopsy

Journal of clinical oncology, 2007-06, Vol.25 (18_suppl), p.1500-1500

2007

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G6PD Kalyan and G6PD Kerala; two deficient variants in India caused by the same 317 Glu↑Lys mutation

Human molecular genetics, 1992-06, Vol.1 (3), p.209-210

1992

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Strategies to optimize tamoxifen use

European journal of cancer supplements, 2006-03, Vol.4 (2), p.47-47

2006

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Cytogenetic and molecular study of 32 Down syndrome families: potential leukaemia predisposing role of the most proximal segment of chromosome 21q

British journal of haematology, 1998-10, Vol.103 (1), p.213-216

1998

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Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients

American journal of medical genetics, 1999-07, Vol.85 (3), p.311-316

1999

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Molecular and cytogenetic analysis of the fragile X syndrome in a series of 453 mentally retarded subjects: A study of 87 families

American journal of medical genetics, 1996-07, Vol.64 (1), p.176-180

1996

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Prenatal diagnosis of 30 fetuses at risk for fragile X syndrome

American journal of medical genetics, 1996-07, Vol.64 (1), p.187-190

1996

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G6PD Kalyan and G6PD Kerala; two deficient variants in India caused by the same 317 Glu arrow right Lys mutation

Human molecular genetics, 1992-01, Vol.1 (3), p.209-210

1992

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Ph-positive CML in blastic phase with monosomy 7 in a down syndrome patient: Monitoring by interphase cytogenetics and demonstration of maternal allelic loss

Cancer genetics and cytogenetics, 1997-11, Vol.99 (1), p.77-80

1997

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Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in theFMR1 gene in eight fragile X patients

American journal of medical genetics, 1999-07, Vol.85 (3), p.311-316

1999

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Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients: X-Linked Mental Retardation. Part III

American journal of medical genetics, 1999, Vol.85 (3), p.311-316

1999

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Prenatal diagnosis of 30 fetuses at risk for fragile X syndrome: X-Linked mental retardation. Part I

American journal of medical genetics, 1996, Vol.64 (1), p.187-190

1996

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Molecular and cytogenetic analysis of the fragile X syndrome in a series of 453 mentally retarded subjects : A study of 87 families: X-Linked mental retardation. Part I

American journal of medical genetics, 1996, Vol.64 (1), p.176-180

1996

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The PRO‐HOME Project. A multicomponent intervention for the protected discharge from the hospital of multimorbid and polytreated older individuals by using innovative technologies: A pilot study

Health expectations : an international journal of public participation in health care and health policy, 2024-02, Vol.27 (1), p.n/a

2024

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Frailty and anticoagulants in older subjects with atrial fibrillation: the EUROSAF study

Age and ageing, 2023-11, Vol.52 (11)

2023

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Evaluation Design of EFFICHRONIC: The Chronic Disease Self-Management Programme (CDSMP) Intervention for Citizens with a Low Socioeconomic Position

International journal of environmental research and public health, 2019-05, Vol.16 (11), p.1883

2019

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A Phase I-II Preoperative Biomarker Trial of Fenretinide in Ascitic Ovarian Cancer

Cancer epidemiology, biomarkers & prevention, 2006-10, Vol.15 (10), p.1914-1919

2006

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A Randomized, Placebo-Controlled, Preoperative Trial of Allopurinol in Subjects with Colorectal Adenoma

Cancer prevention research (Philadelphia, Pa.), 2013-02, Vol.6 (2), p.74-81

2013

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Evaluating the effectiveness and risks of oral anticoagulant treatments in multimorbid frail older subjects with atrial fibrillation using the multidimensional prognostic index: the EURopean study of older subjects with atrial fibrillation—EUROSAF

European geriatric medicine, 2018-04, Vol.9 (2), p.149-154

2018

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Clinical trials with retinoids for breast cancer chemoprevention

Plasma levels of amyloid beta-protein 42 are increased in women with mild cognitive impairment

Development and Validation of a Self-Administered Multidimensional Prognostic Index to Predict Negative Health Outcomes in Community-Dwelling Persons

EFFICHRONIC study protocol: a non-controlled, multicentre European prospective study to measure the efficiency of a chronic disease self-management programme in socioeconomically vulnerable populations

SERMs in chemoprevention of breast cancer

Phase I-II trial of weekly bicalutamide in men with high PSA and negative biopsy

G6PD Kalyan and G6PD Kerala; two deficient variants in India caused by the same 317 Glu↑Lys mutation

Strategies to optimize tamoxifen use

Cytogenetic and molecular study of 32 Down syndrome families: potential leukaemia predisposing role of the most proximal segment of chromosome 21q

Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients

Molecular and cytogenetic analysis of the fragile X syndrome in a series of 453 mentally retarded subjects: A study of 87 families

Prenatal diagnosis of 30 fetuses at risk for fragile X syndrome

G6PD Kalyan and G6PD Kerala; two deficient variants in India caused by the same 317 Glu arrow right Lys mutation

Ph-positive CML in blastic phase with monosomy 7 in a down syndrome patient: Monitoring by interphase cytogenetics and demonstration of maternal allelic loss

Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in theFMR1 gene in eight fragile X patients

Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients: X-Linked Mental Retardation. Part III

Prenatal diagnosis of 30 fetuses at risk for fragile X syndrome: X-Linked mental retardation. Part I

Molecular and cytogenetic analysis of the fragile X syndrome in a series of 453 mentally retarded subjects : A study of 87 families: X-Linked mental retardation. Part I

The PRO‐HOME Project. A multicomponent intervention for the protected discharge from the hospital of multimorbid and polytreated older individuals by using innovative technologies: A pilot study

Frailty and anticoagulants in older subjects with atrial fibrillation: the EUROSAF study

ERANET JTC 2011: Submission and Activation of an International Academic Translational Project in Advanced Breast Cancer. Experience From the ET-FES Study

Evaluation Design of EFFICHRONIC: The Chronic Disease Self-Management Programme (CDSMP) Intervention for Citizens with a Low Socioeconomic Position

A Phase I-II Preoperative Biomarker Trial of Fenretinide in Ascitic Ovarian Cancer

A Randomized, Placebo-Controlled, Preoperative Trial of Allopurinol in Subjects with Colorectal Adenoma

Evaluating the effectiveness and risks of oral anticoagulant treatments in multimorbid frail older subjects with atrial fibrillation using the multidimensional prognostic index: the EURopean study of older subjects with atrial fibrillation—EUROSAF

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