Search

Your search keyword '"Raynaud Disease genetics"' showing total 76 results

Search Constraints

Start Over You searched for: Descriptor "Raynaud Disease genetics" Remove constraint Descriptor: "Raynaud Disease genetics"
76 results on '"Raynaud Disease genetics"'

Search Results

1. Genetic and functional analysis of Raynaud's syndrome implicates loci in vasculature and immunity.

2. Comparison of serum exosome miRNA from patients with Raynaud's phenomenon with positive and negative serum antinuclear antibodies.

4. ADRA2A and IRX1 are putative risk genes for Raynaud's phenomenon.

5. Hereditary Angiopathy With Nephropathy, Aneurysm, and Muscle Cramps (HANAC) Syndrome Presenting to Neuro-Ophthalmology With Metamorphopsia.

6. Genomic Analysis to Avoid Misdiagnosis of Adults With Bilateral Renal Cysts.

7. Association of Raynaud's phenomenon with a polymorphism in the NOS1 gene.

8. Col4a1 mutation generates vascular abnormalities correlated with neuronal damage in a mouse model of HANAC syndrome.

9. HANAC Col4a1 Mutation in Mice Leads to Skeletal Muscle Alterations due to a Primary Vascular Defect.

10. HTR1B gene variants associate with the susceptibility of Raynauds' phenomenon in workers exposed hand-arm vibration.

11. HANAC Syndrome Col4a1 Mutation Causes Neonate Glomerular Hyperpermeability and Adult Glomerulocystic Kidney Disease.

12. Case of H syndrome with massive skin involvement, retroperitoneal fibrosis and Raynaud's phenomenon with a novel mutation in the SLC29A3 gene.

13. Understanding Raynaud phenomenon.

14. Porencephaly in a fetus and HANAC in her father: variable expression of COL4A1 mutation.

15. Prothrombotic polymorphisms in patients with Raynaud's phenomenon and migraine.

16. Primary biliary cirrhosis in a genetically homogeneous population: disease associations and familial occurrence rates.

17. Polymorphism of clotting factors in Hungarian patients with Raynaud's phenomenon.

18. Novel COL4A1 mutations associated with HANAC syndrome: a role for the triple helical CB3[IV] domain.

19. Heritability of vasculopathy, autoimmune disease, and fibrosis in systemic sclerosis: a population-based study.

20. Association study of serotonin transporter gene (SLC6A4) in systemic sclerosis in European Caucasian populations.

21. Transcriptional activity of genes coding transforming growth factor beta-1 and its receptors in patients with systemic sclerosis and Raynaud phenomenon.

22. Manganese superoxide dismutase Ala-9Val mitochondrial targeting sequence polymorphism in systemic lupus erythematosus in Poland.

23. Angiotensin-converting enzyme gene polymorphism in Kuwaiti patients with systemic lupus erythematosus.

24. Heritability of Raynaud's phenomenon and vascular responsiveness to cold: a study of adult female twins.

25. [Heredity and genetic aspects of Raynaud's disease].

26. Glutathione S-transferase M1 and GST T1 genetic polymorphisms and Raynaud's phenomenon in French vinyl chloride monomer-exposed workers.

27. The 3p21.1-p21.3 hereditary vascular retinopathy locus increases the risk for Raynaud's phenomenon and migraine.

28. Raynaud phenomena and migraine in two children: inclusion within a family of related disorders.

29. Familial clustering of Leiomyomatosis peritonealis disseminata: an unknown genetic syndrome?

30. A common genetic factor underlies hypertension and other cardiovascular disorders.

31. Chromosome aberrations in Raynaud's phenomenon.

32. Platelet GPIIb/IIIa (P1A 1/2) polymorphism in SLE: clinical and laboratory association.

33. Spontaneous chromosome damage (micronuclei) in systemic sclerosis and Raynaud's phenomenon.

34. [Chromosome aberrations, valued as frequency of spontaneous micronuclei, in subjects with suspected presclerodermic Raynaud's phenomenon].

35. Association of novel polymorphisms with the expression of SPARC in normal fibroblasts and with susceptibility to scleroderma.

37. Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3.

38. Homocysteine concentration in primary and systemic sclerosis associated Raynaud's phenomenon.

40. Genetic factors in the etiology of systemic sclerosis and Raynaud phenomenon.

41. A two-stage, genome-wide screen for susceptibility loci in primary Raynaud's phenomenon.

42. A case-control study of candidate vasoactive mediator genes in primary Raynaud's phenomenon.

43. HLA associations in a family with autoimmune phenomena.

44. Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenon.

45. Familial aggregation of primary Raynaud's disease.

47. Familial scleroderma-like deformity of the fingers.

48. Primary Raynaud's phenomenon. Age of onset and pathogenesis in a prospective study of 424 patients.

49. Two sisters producing anti-U1RNP exhibit serological concordance and clinical discordance.

50. CENP-C, an autoantigen in scleroderma, is a component of the human inner kinetochore plate.

Catalog

Books, media, physical & digital resources