576 results on '"Pras, E"'
Search Results
2. Adjuvant chemoradiotherapy versus radiotherapy alone in women with high-risk endometrial cancer (PORTEC-3): patterns of recurrence and post-hoc survival analysis of a randomised phase 3 trial
3. Chromatic pupilloperimetry for objective diagnosis of Best vitelliform macular dystrophy
4. Vulva
5. Adjuvant chemoradiotherapy versus radiotherapy alone in women with high-risk endometrial cancer (PORTEC-3): patterns of recurrence and post-hoc survival analysis of a randomised phase 3 trial
6. Dermatofibrosarcoma protuberans: Recurrence is related to the adequacy of surgical margins
7. SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosum
8. Exome sequencing as a differential diagnosis tool: resolving mild trichohepatoenteric syndrome
9. Founder mutation for Huntington disease in Caucasus Jews
10. Decreased Expression of Thrombospondin-1 in Failing Hearts May Favor Ventricular Remodeling
11. Adjuvant chemoradiotherapy versus radiotherapy alone for women with high-risk endometrial cancer (PORTEC-3): final results of an international, open-label, multicentre, randomised, phase 3 trial
12. A new locus for autosomal dominant posterior polar cataract in Moroccan Jews maps to chromosome 14q22-23
13. Primary sarcoma of the heart: case report and literature review
14. A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC)
15. Correlation Between Mast Cell Density and Myocardial Fibrosis in Congestive Heart Failure Patients
16. Down-Regulation of Matrix Metalloproteinase-9 (MMP-9) Expression in the Myocardium of Congestive Heart Failure Patients
17. NOD2/CARD 15 gene mutations in patients with Familial Mediterranean Fever
18. Exome-sequencing identifies a mutation in the ASNS gene as a cause of progressive microcephaly and brain atrophy in Iranian Jews: C2–P1
19. Severe congenital lymphoedema not caused by mutations in known lymphoedema genes
20. Rapidly progressive Creutzfeldt–Jakob disease in patients with Familial Mediterranean Fever
21. Adjuvant chemoradiotherapy versus radiotherapy alone for women with high-risk endometrial cancer (PORTEC-3): final results of an international, open-label, multicentre, randomised, phase 3 trial
22. Presentations of endometrial activity after curative radiotherapy for cervical cancer
23. A novel GJB6 missense mutation in hidrotic ectodermal dysplasia 2 (Clouston syndrome) broadens its genotypic basis
24. Evidence for blood chimerism in dizygotic spontaneous twin pregnancy discordant for Down syndrome
25. IGNT (GCNT2) MUTATION ANALYSIS OF ADULT I PHENOTYPE IN ISRAEL: DETECTION OF A NOVEL MUTATION: P-274
26. Basic aspect of genetic in hair growth
27. A common ancestral haplotype in carrier chromosomes from different ethnic backgrounds in vacuolating megalencephalic leucoencephalopathy with subcortical cysts
28. Adjuvant chemoradiotherapy versus radiotherapy alone in women with high-risk endometrial cancer (PORTEC-3): patterns of recurrence and post-hoc survival analysis of a randomised phase 3 trial
29. Outcome of Nonsurgical Management of Extra-Abdominal, Trunk, and Abdominal Wall Desmoid-Type Fibromatosis: A Population-Based Study in the Netherlands
30. Fractures after multimodality treatment of soft tissue sarcomas with isolated limb perfusion and radiation; likely to occur and hard to heal
31. OP0087 Increased risk of ischaemic heart disease and mortality among fmf patients – perspective from a big database
32. Hepatic Iron Overload following Liver Transplantation from a C282Y/H63D Compound Heterozygous Donor
33. Ductular reaction cells promote angiogenesis via SLIT2/ROBO1 pathway in chronic liver disease
34. Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin
35. FIFTEEN-YEAR RADIOTHERAPY OUTCOMES OF THE RANDOMIZED PORTEC-1 TRIAL FOR ENDOMETRIAL CARCINOMA
36. Radiation-induced sarcoma: a challenge for the surgical oncologist
37. Hyperthermic isolated limb perfusion with TNF and Melphalan for primarily irresectable soft tissue sarcoma; three time periods at risk for amputation
38. Mutations in AIFM1 cause a potentially treatable X-linked childhood cerebellar ataxia
39. Vulva
40. Corynebacterium CDC Group A-4 native valve endocarditis
41. Treatment of cervical cancer
42. Behavior of biometric parameters during clinical hours
43. Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (bo,+AT) of rBAT
44. Autosomal dominant congenital cataract in a Libyan Jewish family: cosegregation with a reciprocal chromosomal translocation [t(3;5)(p22.3; p15.1)]
45. Chromosomal microarray analysis of miscarriage products in recurrent pregnancy loss
46. Very Early In-Utero Diagnosis of Walker-Warburg Phenotype: The Cutting Edge of Technology
47. A role forTENM1mutations in congenital general anosmia
48. PS-169 - Ductular reaction cells promote angiogenesis via SLIT2/ROBO1 pathway in chronic liver disease
49. Mutations in the sarcosine dehydrogenase gene in patients with sarcosinemia
50. Functional analysis of mutations in SLC7A9, and genotype/phenotype correlation in non-Type I cystinuria
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