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「"Ferraris A "[Author]」の検索結果

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Answer to Letter to the Editor regarding the article "Striking phenotypic overlap between Nicolaides-Baraitser and Coffin-Siris syndromes in monozygotic twins with ARID1B intragenic deletion".

Left ventricular dysfunction in COVID-19: A diagnostic issue.

Bevacizumab for treating Hereditary Hemorrhagic Telangiectasia patients with severe hepatic involvement or refractory anemia.

Macrocyclic MR contrast agents: evaluation of multiple-organ gadolinium retention in healthy rats.

SYMPTOMATIC BILIARY DISORDERS DURING LENVATINIB TREATMENT FOR THYROID CANCER: AN UNDERESTIMATED PROBLEM?

COL1-related overlap disorder: a novel connective tissue disorder incorporating the osteogenesis imperfecta/Ehlers-Danlos syndrome overlap.

The Effect of Antipsychotic Treatment on Recurrent Venous Thromboembolic Disease: A Cohort Study.

Striking phenotypic overlap between Nicolaides-Baraitser and Coffin-Siris syndromes in monozygotic twins with ARID1B intragenic deletion.

Characterization of Two Novel Intronic Variants Affecting in -Related Disorders.

The facial dysmorphology analysis technology in intellectual disability syndromes related to defects in the histones modifiers.

Impact of the Supra-Aortic Trunks And Circle of Willis Patency on the Neurological Compensation During Carotid Endarterectomy.

From Design to Manufacture of a Carbon Fiber Monocoque for a Three-Wheeler Vehicle Prototype.

[Risk factors for in-hospital mortality among adult patients infected with colistin-resistant carbapenemase producing Klebsiella pneumoniae: a retrospective cohort study].

Ehlers-Danlos syndromes: state of the art on clinical practice guidelines.

Mottling score and skin temperature in septic shock: Relation and impact on prognosis in ICU.

Computer-based self-training for CT colonography with and without CAD.

All-cause mortality in older adults with affective disorders and dementia under treatment with antipsychotic drugs: A matched-cohort study.

Erratum to: Tubulin-related cerebellar dysplasia: definition of a distinct pattern of cerebellar malformation.

Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome.

Tubulin-related cerebellar dysplasia: definition of a distinct pattern of cerebellar malformation.

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