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「"Picard C "[Author]」の検索結果

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A 1-Year Prospective French Nationwide Study of Emergency Hospital Admissions in Children and Adults with Primary Immunodeficiency.

Monogenic lupus: Dissecting heterogeneity.

Association of PPP2R1A with Alzheimer's disease and specific cognitive domains.

A deep intronic splice mutation of underlies hyper IgE syndrome by negative dominance.

Large slippage and depletion layer at the polyelectrolyte/solid interface.

Perspectives on Scedosporium species and Lomentospora prolificans in lung transplantation: results of an international practice survey from ESCMID Fungal Infection Study Group and Study Group for Infections in Compromised Hosts, and European Confederation of Medical Mycology.

FCGR3A and FCGR2A Genotypes Differentially Impact Allograft Rejection and Patients' Survival After Lung Transplant.

Kinetics of -induced gene silencing can be predicted from combinations of epigenetic and genomic features.

Association of TLR4 with Alzheimer's disease risk and presymptomatic biomarkers of inflammation.

Analyzing the Influence of Landscape Aggregation on Disease Spread to Improve Management Strategies.

The bipartite TAD organization of the X-inactivation center ensures opposing developmental regulation of Tsix and Xist.

Skin characterization and immediate effects of different dermocosmetic treatments in French and Brazilian skin.

Hematopoietic stem cell transplant effectively rescues lymphocyte differentiation and function in DOCK8-deficient patients.

Rechallenge of immune checkpoint inhibitor after pembrolizumab-induced myasthenia gravis.

Life-threatening pulmonary interstitial lung disease complicating pediatric non-humoral immunodeficiencies.

Clinical and economic aspects of newborn screening for severe combined immunodeficiency: DEPISTREC study results.

Fulminant arterial vasculitis as an unusual complication of disseminated staphylococcal disease due to the emerging CC1 methicillin-susceptible Staphylococcus aureus clone: a case report.

Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genes.

Spectrum of pulmonary aspergillosis in Hyper IgE syndrome with autosomal dominant STAT3 deficiency.

Haploidentical HSCT with post-transplant CY for primary immunodeficiencies and inherited disorders in children.

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