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The requirements of a specialist breast centre

Breast (Edinburgh), 2020-06, Vol.51, p.65-84

2020

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An update on male breast cancer and future directions for research and treatment

European journal of pharmacology, 2013-10, Vol.717 (1-3), p.71-83

2013

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Can mindfulness facilitate posttraumatic growth in breast cancer patients? The mediating role of illness perceptions and positive emotions

Journal of health psychology, 2024-04, Vol.29 (5), p.438-451

2024

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Face-sparing Congenital Generalized Lipodystrophy Type 1 Associated With Nonclassical Congenital Adrenal Hyperplasia

The journal of clinical endocrinology and metabolism, 2022-09, Vol.107 (9), p.2433-2438

2022

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AutoMap is a high performance homozygosity mapping tool using next-generation sequencing data

Nature communications, 2021-01, Vol.12 (1), p.518-518, Article 518

2021

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Long term outcome data from the EORTC 75111-10114 ETF/BCG randomized phase II study: Pertuzumab and trastuzumab with or without metronomic chemotherapy for older patients with HER2-positive metastatic breast cancer, followed by T-DM1 after progression

Breast (Edinburgh), 2022-08, Vol.64, p.100-111

2022

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Digital Self‐Management Intervention Paths for Early Breast Cancer Patients: Results of a Pilot Study

The breast journal, 2024-01, Vol.2024 (1)

2024

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NGLY1 deficiency—A rare congenital disorder of deglycosylation

JIMD reports, 2020-05, Vol.53 (1), p.2-9

2020

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Cross-Cultural Adaptation and Psychometric Evaluation of the Perceived Ability to Cope With Trauma Scale in Portuguese Patients With Breast Cancer

Frontiers in psychology, 2022-02, Vol.13, p.800285-800285

2022

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Personalized Risk Analysis to Improve the Psychological Resilience of Women Undergoing Treatment for Breast Cancer: Development of a Machine Learning-Driven Clinical Decision Support Tool

Journal of medical Internet research, 2023-06, Vol.25 (1), p.e43838-e43838

2023

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Personalized prediction of one-year mental health deterioration using adaptive learning algorithms: a multicenter breast cancer prospective study

Scientific reports, 2023-04, Vol.13 (1), p.7059-7059, Article 7059

2023

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New clinical and molecular evidence linking mutations in ARSG to Usher syndrome type IV

Human mutation, 2021-03, Vol.42 (3), p.261-271

2021

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Cross-cultural adaptation and psychometric evaluation of the Portuguese version of the family resilience questionnaire - short form (FaRE-SF-P) in women with breast cancer

Frontiers in psychology, 2023-01, Vol.13, p.1022399-1022399

2023

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PSMB8 Encoding the β5i Proteasome Subunit Is Mutated in Joint Contractures, Muscle Atrophy, Microcytic Anemia, and Panniculitis-Induced Lipodystrophy Syndrome

American journal of human genetics, 2010-12, Vol.87 (6), p.866-872

2010

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Protective Factors against Fear of Cancer Recurrence in Breast Cancer Patients: A Latent Growth Model

Cancers, 2023-09, Vol.15 (18), p.4590

2023

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New clinical and molecular evidence linking mutations in ARSG to Usher syndrome type IV

Human mutation, 2022-12, Vol.43 (12), p.2326-2327

2022

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Associations between Physical Exercise, Quality of Life, Psychological Symptoms and Treatment Side Effects in Early Breast Cancer

The breast journal, 2022, Vol.2022, p.9921575-8

2022

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Trajectories of Quality of Life among an International Sample of Women during the First Year after the Diagnosis of Early Breast Cancer: A Latent Growth Curve Analysis

Cancers, 2023-03, Vol.15 (7), p.1961

2023

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Low social and family well-being is associated with greater RAGE ligand s100A8/A9 and interleukin-1 beta levels in metastatic breast cancer patients

Brain, behavior, & immunity. Health, 2022-05, Vol.21, p.100433-100433, Article 100433

2022

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Defective Proteolytic Processing of Fibrillar Procollagens and Prodecorin Due to Biallelic BMP1 Mutations Results in a Severe, Progressive Form of Osteogenesis Imperfecta

Journal of bone and mineral research, 2015-08, Vol.30 (8), p.1445-1456

2015

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Adding evidence to the role of NEUROG1 in congenital cranial dysinnervation disorders

Clinical genetics, 2021-04, Vol.99 (4), p.588-593

2021

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Predicting Effective Adaptation to Breast Cancer to Help Women BOUNCE Back: Protocol for a Multicenter Clinical Pilot Study

JMIR research protocols, 2022-10, Vol.11 (10), p.e34564-e34564

2022

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An Autosomal Recessive Syndrome of Joint Contractures, Muscular Atrophy, Microcytic Anemia, and Panniculitis-Associated Lipodystrophy

The journal of clinical endocrinology and metabolism, 2010-09, Vol.95 (9), p.E58-E63

2010

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Upper limb phocomelia: A prenatal case of thrombocytopenia-absent radius (TAR) syndrome illustrating the importance of chromosomal microarray in limb reduction defects

Taiwanese journal of obstetrics & gynecology, 2020-03, Vol.59 (2), p.318-322

2020

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Spondyloepiphyseal dysplasia type Stanescu: Expanding the clinical and molecular spectrum of a very rare type II collagenopathy

American journal of medical genetics. Part A, 2020-11, Vol.182 (11), p.2715-2721

2020

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The requirements of a specialist breast centre

An update on male breast cancer and future directions for research and treatment

Can mindfulness facilitate posttraumatic growth in breast cancer patients? The mediating role of illness perceptions and positive emotions

Face-sparing Congenital Generalized Lipodystrophy Type 1 Associated With Nonclassical Congenital Adrenal Hyperplasia

AutoMap is a high performance homozygosity mapping tool using next-generation sequencing data

Long term outcome data from the EORTC 75111-10114 ETF/BCG randomized phase II study: Pertuzumab and trastuzumab with or without metronomic chemotherapy for older patients with HER2-positive metastatic breast cancer, followed by T-DM1 after progression

Digital Self‐Management Intervention Paths for Early Breast Cancer Patients: Results of a Pilot Study

NGLY1 deficiency—A rare congenital disorder of deglycosylation

Cross-Cultural Adaptation and Psychometric Evaluation of the Perceived Ability to Cope With Trauma Scale in Portuguese Patients With Breast Cancer

Personalized Risk Analysis to Improve the Psychological Resilience of Women Undergoing Treatment for Breast Cancer: Development of a Machine Learning-Driven Clinical Decision Support Tool

Personalized prediction of one-year mental health deterioration using adaptive learning algorithms: a multicenter breast cancer prospective study

New clinical and molecular evidence linking mutations in ARSG to Usher syndrome type IV

Cross-cultural adaptation and psychometric evaluation of the Portuguese version of the family resilience questionnaire - short form (FaRE-SF-P) in women with breast cancer

PSMB8 Encoding the β5i Proteasome Subunit Is Mutated in Joint Contractures, Muscle Atrophy, Microcytic Anemia, and Panniculitis-Induced Lipodystrophy Syndrome

Protective Factors against Fear of Cancer Recurrence in Breast Cancer Patients: A Latent Growth Model

New clinical and molecular evidence linking mutations in ARSG to Usher syndrome type IV

Associations between Physical Exercise, Quality of Life, Psychological Symptoms and Treatment Side Effects in Early Breast Cancer

Trajectories of Quality of Life among an International Sample of Women during the First Year after the Diagnosis of Early Breast Cancer: A Latent Growth Curve Analysis

Low social and family well-being is associated with greater RAGE ligand s100A8/A9 and interleukin-1 beta levels in metastatic breast cancer patients

Defective Proteolytic Processing of Fibrillar Procollagens and Prodecorin Due to Biallelic BMP1 Mutations Results in a Severe, Progressive Form of Osteogenesis Imperfecta

Adding evidence to the role of NEUROG1 in congenital cranial dysinnervation disorders

Predicting Effective Adaptation to Breast Cancer to Help Women BOUNCE Back: Protocol for a Multicenter Clinical Pilot Study

An Autosomal Recessive Syndrome of Joint Contractures, Muscular Atrophy, Microcytic Anemia, and Panniculitis-Associated Lipodystrophy

Upper limb phocomelia: A prenatal case of thrombocytopenia-absent radius (TAR) syndrome illustrating the importance of chromosomal microarray in limb reduction defects

Spondyloepiphyseal dysplasia type Stanescu: Expanding the clinical and molecular spectrum of a very rare type II collagenopathy

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