"Rare diseases" trang 1 - tải miễn phí từ tailieuXANH
Ebook Tropical diseases - A practical guide for medical practitioners and students: Part 2

Ebook Tropical diseases - A practical guide for medical practitioners and students: Part 2
182    109    0
EURO-WABB: An EU rare diseases registry for Wolfram syndrome, Alström syndrome and Bardet-Biedl syndrome

EURO-WABB: An EU rare diseases registry for Wolfram syndrome, Alström syndrome and Bardet-Biedl syndrome
7    30    0
Malignant mesothelioma of the tunica vaginalis testis: A rare case and review of literature

Malignant mesothelioma of the tunica vaginalis testis: A rare case and review of literature
6    48    0
GenIO: A phenotype-genotype analysis web server for clinical genomics of rare diseases

GenIO: A phenotype-genotype analysis web server for clinical genomics of rare diseases
6    49    0
NCBoost classifies pathogenic non-coding variants in Mendelian diseases through supervised learning on purifying selection signals in humans

NCBoost classifies pathogenic non-coding variants in Mendelian diseases through supervised learning on purifying selection signals in humans
22    16    1
Functioning and equality according to International Classification of Functioning, Disability and Health (ICF) in people with skeletal dysplasia compared to matched control subjects – a crosssectional survey study

Functioning and equality according to International Classification of Functioning, Disability and Health (ICF) in people with skeletal dysplasia compared to matched control subjects – a crosssectional survey study
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Báo cáo khoa học:

Báo cáo khoa học: "Sampling to Detect Rare Diseases"
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báo cáo khoa học:

báo cáo khoa học: " Shared communication processes within healthcare teams for rare diseases and their influence on healthcare professionals’ innovative behavior and patient satisfaction"
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Clinical profile of comorbidity of rare diseases in a Tunisian patient: A case report associating incontinentia pigmenti and Noonan syndrome

Clinical profile of comorbidity of rare diseases in a Tunisian patient: A case report associating incontinentia pigmenti and Noonan syndrome
7    40    0
Comparison of genotype clustering tools with rare variants

Comparison of genotype clustering tools with rare variants
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Diagnostic delay is common among patients with hypophosphatasia: Initial findings from a longitudinal, prospective, global registry

Diagnostic delay is common among patients with hypophosphatasia: Initial findings from a longitudinal, prospective, global registry
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Socioeconomic costs and health-related quality of life in juvenile idiopathic arthritis: A cost-of-illness study in the United Kingdom

Socioeconomic costs and health-related quality of life in juvenile idiopathic arthritis: A cost-of-illness study in the United Kingdom
9    71    1
Extensive eye-oral-bronchial mucosal nodules with eosinopgillia: A rare case report and literature review

Extensive eye-oral-bronchial mucosal nodules with eosinopgillia: A rare case report and literature review
9    37    1
A tricky and rare cause of pulmonary eosinophilia: Myeloid/lymphoid neoplasm with eosinophilia and rearrangement of PDGFRA

A tricky and rare cause of pulmonary eosinophilia: Myeloid/lymphoid neoplasm with eosinophilia and rearrangement of PDGFRA
4    63    1
Coexistence of pulmonary lymphangioleiomyomatosis and pulmonary angiomyolipoma

Coexistence of pulmonary lymphangioleiomyomatosis and pulmonary angiomyolipoma
5    42    1
Understanding rare and common diseases in the context of human evolution

Understanding rare and common diseases in the context of human evolution
14    34    2
Clinical and radiologic diagnosis of a patient with Maroteaux-Lamy syndrome

Clinical and radiologic diagnosis of a patient with Maroteaux-Lamy syndrome
5    20    1
Scoping review of patient- and family-oriented outcomes and measures for chronic pediatric disease

Scoping review of patient- and family-oriented outcomes and measures for chronic pediatric disease
9    56    0
Transient hyponatremia of prematurity caused by mild Bartter syndrome type II: A case report

Transient hyponatremia of prematurity caused by mild Bartter syndrome type II: A case report
6    63    0
Malignant mesothelioma of the pleura with desmoplastic histology: A case series and literature review

Malignant mesothelioma of the pleura with desmoplastic histology: A case series and literature review
6    43    0
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