229 results on '"Pennec, Pierre-Yves"'
Search Results
2. Proof of principle for transfusion of in vitro–generated red blood cells
3. Noninvasive Diagnosis of Pulmonary Embolism
4. Nomenclature of Blood Group Antigens
5. Cardiac multislice spiral computed tomography as an alternative to coronary angiography in the preoperative assessment of coronary artery disease before aortic valve surgery: A management outcome study
6. Door-to-balloon delays before primary angioplasty in the Regional Acute Myocardial Infarction Registry of Brittany. An analysis of the Observatoire Régional Breton sur l’Infarctus du myocarde (ORBI)
7. CPAP for acute cardiogenic pulmonary oedema from out-of-hospital to cardiac intensive care unit: a randomised multicentre study
8. Molecular background of novel silent RHCE alleles
9. Identification of novel silent KEL alleles causing KEL:−5 (Ko) phenotype or discordance between KEL:1,−2 phenotype/KEL*01/02 genotype
10. Blood Group Genotyping by High-Throughput DNA-Analysis: Application to the Panel National de Référence du CNRGS
11. RHD*DOL1 and RHD*DOL2 encode a partial D antigen and are in cis with the rare RHCE*ceBI allele in people of African descent
12. In reply
13. Antibodies to co-trimoxazole (trimethoprim and/or sulfamethoxazole) related to the presence of the drug in a commercial low-ionic-strength solution
14. Anti-D investigations in individuals expressing weak D Type 1 or weak D Type 2: allo- or autoantibodies?
15. Analysis of RhCE variants among 806 individuals in France: considerations for transfusion safety, with emphasis on patients with sickle cell disease
16. Blood group genotyping by high-throughput DNA analysis applied to 356 reagent red blood cell samples
17. A functional AQP1 allele producing a Co(a–b–) phenotype revises and extends the Colton blood group system
18. Analysis of complement receptor Type 1 expression on red blood cells in negative phenotypes of the Knops blood group system, according to CR1 gene allotype polymorphisms
19. Anti-HrB and anti-hrB revisited
20. Alloanti-c/ce in a c+ ceAR/Ce patient suggests that the rare RHCE*ceAR allele (ceAR) encodes a partial c antigen
21. Alloanti-c (RH4) revealing that the (C)ces haplotype encodes a partial c antigen
22. Heterogeneous molecular background of the weak C, VS+, hrB–, HrB– phenotype in black persons
23. Identification and characterization of a novel XK splice site mutation in a patient with McLeod syndrome
24. Fatal hemolytic disease of the fetus and newborn associated with anti-Jra
25. Cardiac Tamponade in Medical Patients: A 10-Year Follow-Up Survey
26. Midterm Prognosis of Patients With Suspected Coronary Artery Disease and Normal Multislice Computed Tomographic Findings: A Prospective Management Outcome Study
27. Cardiac lymphangioma: a benign cardiac tumour
28. Relative immunogenicity of Fya and K antigens in a Caucasian population, based on HLA class II restriction analysis
29. RhD variants in Caucasians: consequences for checking clinically relevant alleles
30. Molecular background of D(C)(e) haplotypes within the white population
31. Two new alleles of the RHCE gene in Black individuals: the RHce allele ceMO and the RHcE allele cEMI
32. Nomenclature of Blood Group Antigens
33. Heterogeneity of blood group RhE variants revealed by serological analysis and molecular alteration of the RHCE gene and transcript
34. Rare RHCE phenotypes in black individuals of Afro-Caribbean origin: identification and transfusion safety
35. AQP3 Deficiency in Humans and the Molecular Basis of a Novel Blood Group System, GIL
36. Systematic RH genotyping and variant identification in French donors of African origin
37. The human porphyrin transporter ABCB6 is dispensable for erythropoiesis but responsible for the new blood group system Langereis
38. Takotsubo syndrome associated with seizures: An underestimated cause of sudden death in epilepsy?
39. Identification of novel silentKELalleles causing KEL:−5 (Ko) phenotype or discordance between KEL:1,−2 phenotype/KEL*01/02genotype
40. Molecular background of novel silentRHCEalleles
41. RHD*DOL1andRHD*DOL2encode a partial D antigen and are in cis with the rareRHCE*ceBIallele in people of African descent
42. ABCB6 is dispensable for erythropoiesis and specifies the new blood group system Langereis
43. Null alleles of ABCG2 encoding the breast cancer resistance protein define the new blood group system Junior
44. Antibodies to co‐trimoxazole (trimethoprim and/or sulfamethoxazole) related to the presence of the drug in a commercial low‐ionic‐strength solution
45. Takotsubo syndrome associated with seizures: The visible part of the iceberg?
46. 330 Immediate prognosis of STEMI complicated by cardiogenic shock requiring circulatory assist device. About 2700 patients in the Regional Acute Myocardial Infarction Registry of Brittany (ORBI)
47. Analysis of RhCE variants among 806 individuals in France: considerations for transfusion safety, with emphasis on patients with sickle cell disease
48. Blood group genotyping by high-throughput DNA analysis applied to 356 reagent red blood cell samples
49. Anti-HrBand anti-hrBrevisited
50. Alloanti-c/ce in a c+ceAR/Cepatient suggests that the rareRHCE*ceARallele (ceAR) encodes a partial c antigen
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