Rare Disease trang 1 tải miễn phí từ TAILIEUCHUNG

"Rare Disease" trang 1 - tải miễn phí từ Tailieuchung

Thyroid acropachy: A rare manifestation of graves disease in joints

Thyroid acropachy: A rare manifestation of graves disease in joints

3 42 0

Rare genital malformations in women’s health research: Sociodemographic, regional, and disease-related characteristics of patients with Mayer-Rokitansky-KüsterHauser syndrome

Rare genital malformations in women’s health research: Sociodemographic, regional, and disease-related characteristics of patients with Mayer-Rokitansky-KüsterHauser syndrome

10 40 1

Cutaneous botryomycosis: A rare case report

Cutaneous botryomycosis: A rare case report

4 45 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 1

Identification of p.HIS119LEU mutation in the G6PC gene of a Vietnamese patient with glycogen storage disease type Ia

Identification of p.HIS119LEU mutation in the G6PC gene of a Vietnamese patient with glycogen storage disease type Ia

8 38 1

Prognostic factors for disease-specific survival in 108 patients with Hürthle cell thyroid carcinoma: A single-institution experience

Prognostic factors for disease-specific survival in 108 patients with Hürthle cell thyroid carcinoma: A single-institution experience

9 47 1

Integrating 400 million variants from 80,000 human samples with extensive annotations: Towards a knowledge base to analyze disease cohorts

Integrating 400 million variants from 80,000 human samples with extensive annotations: Towards a knowledge base to analyze disease cohorts

13 35 1

Gorham-Stout disease of the malleolus: A rare case report

Gorham-Stout disease of the malleolus: A rare case report

6 34 1

Molecular Basis of Pulmonary Disease Insights from Rare Lung Disorders

Molecular Basis of Pulmonary Disease Insights from Rare Lung Disorders

443 49 0

Impulse control disorder and response-inhibition alterations in Parkinson’s disease. A rare case of totally absent functionality of the medial-prefrontal cortex and review of literature

Impulse control disorder and response-inhibition alterations in Parkinson’s disease. A rare case of totally absent functionality of the medial-prefrontal cortex and review of literature

4 50 0

Kawasaki shock syndrome in an Arab female: Case report of a rare manifestation and review of literature

Kawasaki shock syndrome in an Arab female: Case report of a rare manifestation and review of literature

3 62 0

MiR-155, a potential serum marker of extramammary Paget’s disease

MiR-155, a potential serum marker of extramammary Paget’s disease

8 26 1

Anti-synthetase syndrome: A rare and challenging diagnosis for bilateral ground-glass opacities-a case report with literature review

Anti-synthetase syndrome: A rare and challenging diagnosis for bilateral ground-glass opacities-a case report with literature review

6 15 1

Sarcoidosis as a rare cause for symmetrical giant bullous disease

Sarcoidosis as a rare cause for symmetrical giant bullous disease

3 30 1

Anaesthesia and orphan disease: Management of a case of NicolaidesBaraitser syndrome undergoing cleft palate surgery

Anaesthesia and orphan disease: Management of a case of NicolaidesBaraitser syndrome undergoing cleft palate surgery

3 21 1

Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing

Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing

26 18 3

Sclerosteosis: A rare, sclerosing bone dysplasia in a Bangladeshi male

Sclerosteosis: A rare, sclerosing bone dysplasia in a Bangladeshi male

6 4 1

báo cáo hóa học:

báo cáo hóa học: " Measuring disease-specific quality of life in rare populations: a practical approach to cross-cultural translation"

8 37 0

báo cáo hóa học:

báo cáo hóa học:" Measuring disease-specific quality of life in rare populations: a practical approach to cross-cultural translation"

8 71 0

Báo cáo khoa học:

Báo cáo khoa học: "A rare disease"

2 54 0

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