433 results on '"González-Sarmiento, R"'
Search Results
2. Genetic study in patients operated dentally and anesthetized with articaine-epinephrine
3. Analysis of the relationship between interleukin polymorphisms within miRNA-binding regions and alcoholic liver disease
4. Análisis de la relación entre polimorfismos en regiones diana de micro-ARN y la enfermedad hepática alcohólica
5. Gorlin Syndrome
6. Síndrome de Gorlin
7. Epidermal growth factor receptor (EGFR) pathway polymorphisms as predictive markers of cetuximab toxicity in locally advanced head and neck squamous cell carcinoma (HNSCC) in a Spanish population
8. Functional characterization of rs2229094 (T>C) polymorphism in the tumor necrosis factor locus and lymphotoxin alpha expression in human retina: the Retina 4 project
9. The presence of CFH, HTRA1, ARMS2, VEGF-A and VEGF-R and the appearance of age-related macular degeneration sub-types
10. Relación de la presencia de polimorfismos de CFH, HTRA1, ARMS2, VEGF-A y VEGF-R con la aparición de los subtipos de degeneración macular asociada a la edad
11. 701P Genomic alteration relationships with toxicity to TPF induction chemotherapy in head and neck squamous cell carcinoma patients participating in a clinical trial
12. 692P Copy number alterations and response to radiotherapy + cisplatin vs radiotherapy + cetuximab after docetaxel-cisplatin-fluorouracil induction chemotherapy in patients with locally advanced unresectable head and neck cancer
13. Estudio de las deleciones de los genes GSTM1 y GSTT1 y del polimorfismo Ile105Val del gen GSTP1 en pacientes con enfermedad ósea de Paget
14. 914P The landscape of somatic copy number alterations of head and neck squamous cell carcinoma across different anatomic sites
15. 913P Characterisation of genomic biomarkers of response to cetuximab versus cisplatin in concomitance with radiotherapy in locally advanced squamous head and neck cancer
16. First Symposium of Ichthyosis Experts
17. I Jornada de expertos en ictiosis
18. Association of IL1Β (-511 A/C) and IL6 (-174 G > C) polymorphisms with higher disease activity and clinical pattern of psoriatic arthritis
19. Hypotrichosis simplex of the scalp and peeling skin disease, two sides of the same coin
20. P-210 Germline testing in pancreatic adenocarcinoma
21. Influence of CFH, HTRA1 and ARMS2 haplotype polymorphisms in the development of age-related macular disease
22. Influencia de haplotipos de polimorfismos de CFH, HTRA1 y ARMS2 en la aparición de degeneración macular asociada a la edad
23. Novel mutations in FATP4 gene in two families with ichthyosis prematurity syndrome
24. Role of XRCC3, XRCC1 and XPD single-nucleotide polymorphisms in survival outcomes following adjuvant chemotherapy in early stage breast cancer patients
25. Acral peeling skin syndrome resulting from mutations in TGM5
26. Comment on: Clinicopathological features and oncological outcomes of patients with young-onset rectal cancer
27. Estudio genético del complejo enzimático succinato deshidrogenasa en los paragangliomas carotídeos. Implicaciones diagnósticas
28. Letter: PNPLA3 and alcoholic liver disease – an alert to methodological limitations. Authorsʼ reply
29. HOX11, a Homeobox-Containing T-Cell Oncogene on Human Chromosome 10q24
30. Early-onset acral basal cell carcinomas in Gorlin syndrome
31. Systematic review with meta-analysis: the I148M variant of patatin-like phospholipase domain-containing 3 gene (PNPLA3) is significantly associated with alcoholic liver cirrhosis
32. Molecular evidence of type 2 mosaicism in Gorlin syndrome
33. Growth hormone expression in ontogenic development in gilthead sea bream
34. Ectodermal dysplasia–skin fragility syndrome: a novel mutation in the PKP1 gene
35. Clinical, molecular and biochemical characterization of nine Spanish families with Conradi–Hünermann–Happle syndrome: new insights into X-linked dominant chondrodysplasia punctata with a comprehensive review of the literature
36. Meta-analysis: glutathione-S-transferase allelic variants are associated with alcoholic liver disease
37. Comment on: Clinicopathological features and oncological outcomes of patients with young-onset rectal cancer
38. Analysis of the STS gene in 40 patients with recessive X-linked ichthyosis: a high frequency of partial deletions in a Spanish population
39. A Haplotype Containing the p53 Polymorphisms Ins16bp and Arg72Pro Modifies Cancer Risk in BRCA2 Mutation Carriers
40. X-linked ichthyosis
41. Immunoglobulin lambda chain gene rearrangement in a case of acute nonlymphoblastic leukemia
42. X-linked ichthyosis: an update
43. 隐性 XLI: 神经系统疾病的高患病率
44. Recessive XLI: high prevalence of neurological disorders
45. Evidence of the high prevalence of neurological disorders in nonsyndromic X-linked recessive ichthyosis: a retrospective case series
46. Familial seborrhoeic keratosis associated with multiple ‘pure reticulated acanthomas’ and infundibulocystic basal cell carcinomas
47. 242P Reclassification of variants of unknown significance in BRCA 1/2 genes for the improvement of care quality in oncological genetic council units
48. Estudio de las deleciones de los genes GSTM1 y GSTT1 y del polimorfismo Ile105Val del gen GSTP1 en pacientes con enfermedad ósea de Paget
49. Cognitive outcome and gamma noise power unrelated to neuregulin 1 and 3 variation in schizophrenia
50. Limited family structure and triple-negative breast cancer (TNBC) subtype as predictors of BRCA mutations in a genetic counseling cohort of early-onset sporadic breast cancers
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