"rare diseases" trang 2 - tải miễn phí từ tailieunhanh
Real-time clinical note monitoring to detect conditions for rapid follow-up: A case study of clinical trial enrollment in drug-induced torsades de pointes and Stevens-Johnson syndrome

Real-time clinical note monitoring to detect conditions for rapid follow-up: A case study of clinical trial enrollment in drug-induced torsades de pointes and Stevens-Johnson syndrome
6    1    1
Improving a full-text search engine: The importance of negation detection and family history context to identify cases in a biomedical data warehouse

Improving a full-text search engine: The importance of negation detection and family history context to identify cases in a biomedical data warehouse
7    1    1
An effective treatment in Erdheim Chester disease: Vemurafenib: A case report

An effective treatment in Erdheim Chester disease: Vemurafenib: A case report
3    27    1
Using multi-scale genomics to associate poorly annotated genes with rare diseases

Using multi-scale genomics to associate poorly annotated genes with rare diseases
22    11    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    85    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
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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    54    1
The first case of multiple pulmonary granulomas with amyloid deposition in a dental technician; a rare manifestation as an occupational lung disease

The first case of multiple pulmonary granulomas with amyloid deposition in a dental technician; a rare manifestation as an occupational lung disease
5    29    1
Pulmonary alveolar proteinosis in Korea: Analysis of prevalence and incidence via a nationwide population-based study

Pulmonary alveolar proteinosis in Korea: Analysis of prevalence and incidence via a nationwide population-based study
8    41    1
A de novo missense mutation of FGFR2 causes facial dysplasia syndrome in Holstein cattle

A de novo missense mutation of FGFR2 causes facial dysplasia syndrome in Holstein cattle
9    9    1
Rare copy-number variants as modulators of common disease susceptibility

Rare copy-number variants as modulators of common disease susceptibility
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