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48 results on '"Susan, Price"'

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1. Adults with impaired gastrointestinal function show improvements in gastrointestinal symptoms and protein intake with a high-protein, peptide-based oral nutritional supplement

2. AMANA CALICO AND AMANA QUILTS

3. An adaptive, probabilistic, cognitive agent architecture for modelling sugarcane growers’ operational decision-making

4. Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

5. CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

6. Corrigendum: Paradoxical CD4 Lymphopenia in Autoimmune Lymphoproliferative Syndrome (ALPS)

7. Paradoxical CD4 Lymphopenia in Autoimmune Lymphoproliferative Syndrome (ALPS)

8. The contribution of rare copy number variants in FAS toward pathogenesis of autoimmune lymphoproliferative syndrome

9. Fas/CD95 prevents autoimmunity independently of lipid raft localization and efficient apoptosis induction

10. Analysis of In Vivo Skin Anisotropy Using Elastic Wave Measurements and Bayesian Modelling

11. A Double-Blind, Placebo-Controlled, Crossover Study of Magnesium Supplementation in Patients with XMEN Disease

12. Bone marrow findings in autoimmune lymphoproliferative syndrome with germline FAS mutation

13. TCF12 haploinsufficiency causes autosomal dominant Kallmann syndrome and reveals network-level interactions between causal loci

14. Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease

15. A Double-Blind, Placebo-Controlled, Crossover Study of Magnesium Supplementation in Patients with XMEN Disease

16. Ghost Drum

17. HEM1 deficiency disrupts mTORC2 and F-actin control in inherited immunodysregulatory disease

18. 18F-FDG PET Imaging Features of Patients With Autoimmune Lymphoproliferative Syndrome

19. Genetic immunodeficiency and autoimmune disease reveal distinct roles of Hem1 in the WAVE2 and mTORC2 complexes

20. Corrigendum: Paradoxical CD4 Lymphopenia in Autoimmune Lymphoproliferative Syndrome (ALPS)

21. Paradoxical CD4 Lymphopenia in Autoimmune Lymphoproliferative Syndrome (ALPS)

22. SAT-LB071 Loss of Function (LoF) mutations in TCF12 Cause Autosomal Dominant Kallmann Syndrome and Reveal Network-level Interactions Between Causal Loci

23. Reading Planet KS2 - Game-Changers: Super Scientists - Level 8: Supernova (Red+ Band)

24. Complex Enterally Tube-Fed Community Patients Display Stable Tolerance, Improved Compliance and Better Achieve Energy and Protein Targets with a High-Energy, High-Protein Peptide-Based Enteral Tube Feed: Results from a Multi-Centre Pilot Study

25. Genetic bone and joint disease

26. Hwabyung Experiences Among Korean Immigrant Women in the United States

27. Patients with LRBA deficiency show CTLA4 loss and immune dysregulation responsive to abatacept therapy

28. FAS Inactivation Releases Unconventional Germinal Center B Cells that Escape Antigen Control and Drive IgE and Autoantibody Production

29. JMML and RALD (Ras-associated autoimmune leukoproliferative disorder): common genetic etiology yet clinically distinct entities

30. A Sterkarm Tryst

31. Abstract 145: Thrombus Composition is Associated With Endothelial Injury and Stroke Etiology in Patients Undergoing Mechanical Thrombectomy for Emergent Large Vessel Occlusion

32. RELA haploinsufficiency in CD4 lymphoproliferative disease with autoimmune cytopenias

33. Diversity policies meet the competency movement: towards reshaping law firm partnership models for the future

34. A Study of the Clinical and Radiological Features in a Cohort of 93 Patients with a COL2A1 Mutation Causing Spondyloepiphyseal Dysplasia Congenita or a Related Phenotype

35. The Sterkarm Handshake

36. A Sterkarm Kiss

37. A collaborative care skills workshop for carers: Can it be delivered in 1 day?

41. Molecular and clinical delineation of the 17q22 microdeletion phenotype

42. Pulmonary Manifestations of the Autoimmune Lymphoproliferative Syndrome. A Retrospective Study of a Unique Patient Cohort

43. Spare the Spleen in ALPS: It Is Not an Expendable Vestigial Organ

44. Spectrum of PEX1 and PEX6 variants in Heimler syndrome

45. AUTOIMMUNE DISEASE. Patients with LRBA deficiency show CTLA4 loss and immune dysregulation responsive to abatacept therapy

46. A double-blind, placebo-controlled, crossover study of magnesium supplementation in patients with XMEN syndrome: preliminary results

47. Clinical Spectrum of Autoimmune Lymphoproliferative Syndrome Associated with Caspase10 Mutations (ALPS-CASP10)

48. Utility of Fluorodeoxyglucose Positron Emission Tomography(FDG-PET) and Biomarkers, Serum Vitamin B12 and HDL for Assessing Lymphoproliferation in Children and Adults with Autoimmune Lymphoproliferative Syndrome Due to FAS Mutations (ALPS-FAS)

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