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Prevalence and reasons for non‐nursing tasks as perceived by nurses: Findings from a large cross‐sectional study

Journal of nursing management, 2021-11, Vol.29 (8), p.2658-2673

2021

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Non-nursing tasks as experienced by nursing students: Findings from a phenomenological interpretative study

Nurse education today, 2019-05, Vol.76, p.234-241

2019

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MAX Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma

Clinical cancer research, 2012-05, Vol.18 (10), p.2828-2837

2012

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New pathogenic variants in ARMC5 gene in a series of Italian patients affected by primary bilateral macronodular adrenocortical hyperplasia (PBMAH)

Molecular genetics & genomic medicine, 2023-04, Vol.11 (4), p.e2126-n/a

2023

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When the diagnosis is written in the DNA: a case of erythropoietic protoporphyria in a patient with a chromosome 18 deletion

Dermatology reports, 2023-09, Vol.16 (2)

2023

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Reduced thymic output, increased spontaneous apoptosis and oligoclonal B cells in polyethylene glycol‐adenosine deaminase‐treated patients

European Journal of Immunology, 2005-11, Vol.35 (11), p.3376-3386

2005

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Relationship between different subpopulations of circulating CD4+ T lymphocytes and microvascular or systemic oxidative stress in humans

Blood pressure, 2017-07, Vol.26 (4), p.237-245

2017

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Clinically Guided Genetic Screening in a Large Cohort of Italian Patients with Pheochromocytomas and/or Functional or Nonfunctional Paragangliomas

The journal of clinical endocrinology and metabolism, 2009-05, Vol.94 (5), p.1541-1547

2009

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ENIGMA CHEK2 gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk

Clinical cancer research, 2023-08, Vol.29 (16), p.3037-3050

2023

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ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk

Clinical cancer research, 2023-08, Vol.29 (16), p.OF1-3050

2023

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p.Ser891Ala RET gene mutations in medullary thyroid cancer: Phenotypical and genealogical characterization of 28 apparently unrelated kindreds and founder effect uncovering in Northern Italy

Human mutation, 2019-07, Vol.40 (7), p.926-937, Article humu.23754

2019

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Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas

JAMA : the journal of the American Medical Association, 2010-12, Vol.304 (23), p.2611

2010

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Identical TP53 mutations in pelvic carcinosarcomas and associated serous tubal intraepithelial carcinomas provide evidence of their clonal relationship

Virchows Archiv : an international journal of pathology, 2016-07, Vol.469 (1), p.61-69

2016

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Relationship Between Different Subpopulations of Circulating CD4+ T-lymphocytes and Microvascular Structural Alterations in Humans

American journal of hypertension, 2017-01, Vol.30 (1), p.51-60

2017

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Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome

Human molecular genetics, 2013-02, Vol.22 (4), p.804-815

2013

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Combined decrease of defined B and T cell subsets in a group of common variable immunodeficiency patients

Clinical Immunology, 2006-11, Vol.121 (2), p.203-214

2006

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Halting the pandemic outside ‘CORTINA2021’ alpine world ski championships: a challenge for sport and public health in times of COVID-19

Journal of public health (Oxford, England), 2022-06, Vol.44 (2), p.e203-e210

2022

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GB virus C infection in patients with type II mixed cryoglobulinemia

Annals of internal medicine, 1997-11, Vol.127 (10), p.891

1997

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Cardiac rehabilitation and mid-term follow-up after transcatheter aortic valve implantation

Journal of geriatric cardiology : JGC, 2014-12, Vol.11 (4), p.279-285

2014

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HTLV-II infection in Italian drug abusers

The Lancet (British edition), 1990-09, Vol.336 (8714), p.575-576

1990

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Detection of HIV-1 in Epidermal Langerhans Cells of HIV-Infected Patients Using the Polymerase Chain Reaction

Journal of investigative dermatology, 1991-06, Vol.96 (6), p.979-982

1991

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Clock recovery and reconstruction of PAL pictures for MPEG coded streams transported over ATM networks

IEEE transactions on circuits and systems for video technology, 1995-12, Vol.5 (6), p.508-514

1995

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"Let's share a story": Socially-enhanced multimedia storytelling

IEEE multimedia, 2015, p.1-1

2015

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"Let's Share a Story"': Socially Enhanced Multimedia Storytelling

IEEE multimedia, 2015-07, Vol.22 (3), p.54-65

2015

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Physics of phonon-polaritons in amorphous materials

The Journal of chemical physics, 2021-01, Vol.154 (1), p.014501-014501

2021

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Prevalence and reasons for non‐nursing tasks as perceived by nurses: Findings from a large cross‐sectional study

Non-nursing tasks as experienced by nursing students: Findings from a phenomenological interpretative study

MAX Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma

New pathogenic variants in ARMC5 gene in a series of Italian patients affected by primary bilateral macronodular adrenocortical hyperplasia (PBMAH)

When the diagnosis is written in the DNA: a case of erythropoietic protoporphyria in a patient with a chromosome 18 deletion

Reduced thymic output, increased spontaneous apoptosis and oligoclonal B cells in polyethylene glycol‐adenosine deaminase‐treated patients

Relationship between different subpopulations of circulating CD4+ T lymphocytes and microvascular or systemic oxidative stress in humans

Clinically Guided Genetic Screening in a Large Cohort of Italian Patients with Pheochromocytomas and/or Functional or Nonfunctional Paragangliomas

ENIGMA CHEK2 gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk

ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk

p.Ser891Ala RET gene mutations in medullary thyroid cancer: Phenotypical and genealogical characterization of 28 apparently unrelated kindreds and founder effect uncovering in Northern Italy

Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas

Identical TP53 mutations in pelvic carcinosarcomas and associated serous tubal intraepithelial carcinomas provide evidence of their clonal relationship

Relationship Between Different Subpopulations of Circulating CD4+ T-lymphocytes and Microvascular Structural Alterations in Humans

Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome

Combined decrease of defined B and T cell subsets in a group of common variable immunodeficiency patients

Halting the pandemic outside ‘CORTINA2021’ alpine world ski championships: a challenge for sport and public health in times of COVID-19

GB virus C infection in patients with type II mixed cryoglobulinemia

Cardiac rehabilitation and mid-term follow-up after transcatheter aortic valve implantation

HTLV-II infection in Italian drug abusers

Detection of HIV-1 in Epidermal Langerhans Cells of HIV-Infected Patients Using the Polymerase Chain Reaction

Clock recovery and reconstruction of PAL pictures for MPEG coded streams transported over ATM networks

"Let's share a story": Socially-enhanced multimedia storytelling

"Let's Share a Story"': Socially Enhanced Multimedia Storytelling

Physics of phonon-polaritons in amorphous materials

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