99 results on '"Raux, G"'
Search Results
2. Bilateral hypoglossal nerve stimulation for treatment of adult obstructive sleep apnoea
3. Hyperprolinemia is a risk factor for schizoaffective disorder
4. The −2 bp deletion in exon 6 of the ‘alpha 7-like’ nicotinic receptor subunit gene is a risk factor for the P50 sensory gating deficit
5. Bilateral hypoglossal nerve stimulation for treatment of obstructive sleep apnea
6. The promoter −194 C polymorphism of the nicotinic alpha 7 receptor gene has a protective effect against the P50 sensory gating deficit
7. Molecular diagnosis of autosomal dominant early onset Alzheimer’s disease: an update
8. Pemphigus is not associated with allotypic markers of immunoglobulin kappa
9. A polymorphic variant of the gene coding desmoglein 1, the target autoantigen of pemphigus foliaceus, is associated with the disease
10. The severe form of type I hyperprolinaemia results from homozygous inactivation of the PRODH gene
11. DETERMINATION OF SUSCEPTIBILITY FACTORS IN PEMPHIGUS AND BULLOUS PEMPHIGOID: GENETIC POLYMORPHISM OF IMMUNOGLOBULIN HEAVY AND LIGHT CHAIN GENES.
12. Analysis of the involvement of the 2 bp deletion polymorphism of the alpha7 nicotinic acetylcholine receptor gene in P50 sensory gating deficit associated to schizophrenia
13. Variations in the APP gene promoter region and risk of Alzheimer disease
14. Hyperprolinemia is a risk factor for schizoaffective disorder
15. Very early onset AD with a de novo mutation in the presenilin 1 gene (Met 233 Leu)
16. The promoter −194 C polymorphism of the nicotinic alpha 7 receptor gene has a protective effect against the P50 sensory gating deficit
17. Robustness Measure Using 6 Dimensional Model with Empirical Distribution Approach.
18. Empirical Distribution Approach to the Robustness Measure for Non-stationary Data.
19. Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation
20. A novel presenilin 1 missense mutation (L153V) segregating with early-onset autosomal dominant Alzheimer's disease Communicated by: Mark H. Paalman Online Citation: Human Mutation, Mutation and Polymorphism Report #134 (2000) Online http://journals.wiley.com/1059-7794/pdf/mutation/mpr134.pdf
21. Intracellular and extracellular epidermal antigens are recognized by different IgG subclass in autoimmune bullous skin diseases
22. Determination of susceptibility factors in bullous pemphigoid: Genetic polymorphisms of immunoglobulin light-chain genes
23. Comparison of Structural Characteristics of Antisubnucleosome and Anti-DNA Monoclonal Antibodies Derived from Lupus Mice
24. Immunoglobin Variable-Region mRNA Direct Sequencing: A Method to Bypass Aberrant Myeloma Light-Chain Transcripts
25. The -2 bp deletion in exon 6 of the 'alpha 7-like' nicotinic receptor subunit gene is a risk factor for the P50 sensory gating deficit.
26. Comparison of Structural Characteristics of Antisubnucleosome and Anti-DNA Monoclonal Antibodies Derived from Lupus Micea.
27. Variations in the APPgene promoter region and risk of Alzheimer disease
28. The promoter -194 C polymorphism of the nicotinic alpha 7 receptor gene has a protective effect against the P50 sensory gating deficit.
29. Detection of exon deletions and duplications of the mismatch repair genes in hereditary nonpolyposis colorectal cancer families using multiplex polymerase chain reaction of short fluorescent fragments
30. P50 sensory gating deficit in schizophrenics and controls: The 2-bp deletion in exon 6 of the alpha 7-like gene is a risk factor for the endophenotype
31. Le décor architectural figuré
32. Notices 18-26 du catalogue
33. Control of OSA in a patient with CCC of soft palate using bilateral hypoglossal nerve stimulation.
34. Bilateral hypoglossal nerve stimulation for treatment of adult obstructive sleep apnoea.
35. Implantation of the nyxoah bilateral hypoglossal nerve stimulator for obstructive sleep apnea.
36. A simple method for the routine detection of somatic quantitative genetic alterations in colorectal cancer.
37. Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.
38. Deleterious mutations in exon 1 of MECP2 in Rett syndrome.
39. Distribution of ENG and ACVRL1 (ALK1) mutations in French HHT patients.
40. APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy.
41. Acd, a peptidoglycan hydrolase of Clostridium difficile with N-acetylglucosaminidase activity.
42. A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24.
43. Analysis of the allele-specific expression of the mismatch repair gene MLH1 using a simple DHPLC-Based Method.
44. Severe myoclonus-dystonia syndrome associated with a novel epsilon-sarcoglycan gene truncating mutation.
45. Screening for TP53 rearrangements in families with the Li-Fraumeni syndrome reveals a complete deletion of the TP53 gene.
46. PRODH mutations and hyperprolinemia in a subset of schizophrenic patients.
47. IGHV3-associated restriction fragment length polymorphisms confer susceptibility to bullous pemphigoid.
48. APOE promoter polymorphisms do not confer independent risk for Alzheimer's disease in a French population.
49. Detection of exon deletions and duplications of the mismatch repair genes in hereditary nonpolyposis colorectal cancer families using multiplex polymerase chain reaction of short fluorescent fragments.
50. Association of KM genotype with bullous pemphigoid.
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