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Correction: Estimating mortality in rare diseases using a population-based registry, 2002 through 2019

Orphanet journal of rare diseases, 2024-02, Vol.19 (1), p.43-43, Article 43

2024

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Estimating mortality in rare diseases using a population-based registry, 2002 through 2019

Orphanet journal of rare diseases, 2023-11, Vol.18 (1), p.362-362, Article 362

2023

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Coding undiagnosed rare disease patients in health information systems: recommendations from the RD-CODE project

Orphanet journal of rare diseases, 2024-01, Vol.19 (1), p.28-28, Article 28

2024

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ORPHAcodes use for the coding of rare diseases: comparison of the accuracy and cross country comparability

Orphanet journal of rare diseases, 2023-09, Vol.18 (1), p.1-267, Article 267

2023

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Real-world use of orphan medicinal products (OMPs) in rare disease (RD) patients: A population-based registry study

Frontiers in pharmacology, 2022-09, Vol.13, p.940010-940010

2022

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Sharing Augmented Reality between a Patient and a Clinician for Assessment and Rehabilitation in Daily Living Activities

Information (Basel), 2023-03, Vol.14 (4), p.204

2023

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Hospitalization of children with sickle cell disease in a region with increasing immigration rates

Haematologica (Roma), 2008-03, Vol.93 (3), p.463-464

2008

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Diagnosis of pervasive developmental disorders: when and how? An area-based study about health care providers

World journal of pediatrics : WJP, 2015-02, Vol.11 (1), p.48-53

2015

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Exposure to PFAS and small for gestational age new-borns: A birth records study in Veneto Region (Italy)

Environmental research, 2020-05, Vol.184, p.109282-109282, Article 109282

2020

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Did changes in conception rates alone account for the decline in preterm births during the first year of the COVID‐19 pandemic?

BJOG : an international journal of obstetrics and gynaecology, 2023-09

2023

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Pregnancy outcomes in Italy during COVID‐19 pandemic: A population‐based cohort study

BJOG : an international journal of obstetrics and gynaecology, 2023-02, Vol.130 (3), p.276-284

2023

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The importance of helplines in National Plans

Orphanet journal of rare diseases, 2014-11, Vol.9 (9042), p.O12-O12

2014

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A population-based registry as a source of health indicators for rare diseases: the ten-year experience of the Veneto Region's rare diseases registry

Orphanet journal of rare diseases, 2014-03, Vol.9 (1), p.37-37, Article 37

2014

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The Epidemiology of Transition into Adulthood of Rare Diseases Patients: Results from a Population-Based Registry

International journal of environmental research and public health, 2018-10, Vol.15 (10), p.2212

2018

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Organ donation from patients with a rare disease is often safe: the italian guidelines

Clinical transplantation, 2022-09, Vol.36 (9), p.e14769-n/a

2022

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A European network of email and telephone help lines providing information and support on rare diseases: results from a 1-month activity survey

Interactive journal of medical research, 2014-05, Vol.3 (2), p.e9-e9

2014

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The Italian National Rare Diseases Registry: a model of comparison and integration with Hospital Discharge Data

Journal of public health (Oxford, England), 2019-03, Vol.41 (1), p.46-54

2019

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The Italian National Rare Diseases Registry

Blood transfusion = Trasfusione del sangue, 2014-04, Vol.12 Suppl 3 (Suppl 3), p.s606-s613

2014

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Hospitalization of children with sickle cell disease in a region with increasing immigration rates. Authors' Reply

Haematologica (Roma), 2008, Vol.93 (3), p.463-464

2008

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Impedance biosensor for real-time monitoring and prediction of thrombotic individual profile in flowing blood

PloS one, 2017-09, Vol.12 (9), p.e0184941-e0184941

2017

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Standardization of platelet releasate products for clinical applications in cell therapy: a mathematical approach

Journal of translational medicine, 2017-05, Vol.15 (1), p.107-107, Article 107

2017

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Improved GMP compliant approach to manipulate lipoaspirates, to cryopreserve stromal vascular fraction, and to expand adipose stem cells in xeno-free media

Stem cell research & therapy, 2018-05, Vol.9 (1), p.130-130, Article 130

2018

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Is Congenital Muscular Mitral-Aortic Discontinuity Another Feature of Obstructive Hypertrophic Cardiomyopathy? A Pathology Validation Study

Laboratory investigation, 2023-09, Vol.103 (9), p.100196-100196, Article 100196

2023

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Minor Changes in Expression of the Mismatch Repair Protein MSH2 Exert a Major Impact on Glioblastoma Response to Temozolomide

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15), p.3127-3138

2015

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1H-NMR and MALDI-TOF MS as metabolomic quality control tests to classify platelet derived medium additives for GMP compliant cell expansion procedures

PloS one, 2018, Vol.13 (9), p.e0203048-e0203048

2018

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Correction: Estimating mortality in rare diseases using a population-based registry, 2002 through 2019

Estimating mortality in rare diseases using a population-based registry, 2002 through 2019

Coding undiagnosed rare disease patients in health information systems: recommendations from the RD-CODE project

ORPHAcodes use for the coding of rare diseases: comparison of the accuracy and cross country comparability

Real-world use of orphan medicinal products (OMPs) in rare disease (RD) patients: A population-based registry study

Sharing Augmented Reality between a Patient and a Clinician for Assessment and Rehabilitation in Daily Living Activities

Hospitalization of children with sickle cell disease in a region with increasing immigration rates

Diagnosis of pervasive developmental disorders: when and how? An area-based study about health care providers

Exposure to PFAS and small for gestational age new-borns: A birth records study in Veneto Region (Italy)

Did changes in conception rates alone account for the decline in preterm births during the first year of the COVID‐19 pandemic?

Pregnancy outcomes in Italy during COVID‐19 pandemic: A population‐based cohort study

The importance of helplines in National Plans

A population-based registry as a source of health indicators for rare diseases: the ten-year experience of the Veneto Region's rare diseases registry

The Epidemiology of Transition into Adulthood of Rare Diseases Patients: Results from a Population-Based Registry

Organ donation from patients with a rare disease is often safe: the italian guidelines

A European network of email and telephone help lines providing information and support on rare diseases: results from a 1-month activity survey

The Italian National Rare Diseases Registry: a model of comparison and integration with Hospital Discharge Data

The Italian National Rare Diseases Registry

Hospitalization of children with sickle cell disease in a region with increasing immigration rates. Authors' Reply

Impedance biosensor for real-time monitoring and prediction of thrombotic individual profile in flowing blood

Standardization of platelet releasate products for clinical applications in cell therapy: a mathematical approach

Improved GMP compliant approach to manipulate lipoaspirates, to cryopreserve stromal vascular fraction, and to expand adipose stem cells in xeno-free media

Is Congenital Muscular Mitral-Aortic Discontinuity Another Feature of Obstructive Hypertrophic Cardiomyopathy? A Pathology Validation Study

Minor Changes in Expression of the Mismatch Repair Protein MSH2 Exert a Major Impact on Glioblastoma Response to Temozolomide

1H-NMR and MALDI-TOF MS as metabolomic quality control tests to classify platelet derived medium additives for GMP compliant cell expansion procedures

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