ライフサイエンスコーパス: connective tissue disorder

1 me (BCS), an autosomal-recessive generalized connective tissue disorder.

2 ormed in the donor to rule out a subclinical connective tissue disorder.

3 tment of the varied systems affected by this connective tissue disorder.

4 inantly inherited, genetically heterogeneous connective-tissue disorder.

5 B-cell lineage hematologic malignancies and connective tissue disorders.

6 , with consequent implications for inherited connective tissue disorders.

7 cur in diseases such as cancer, fibrosis and connective tissue disorders.

8 etardation, thromboembolic complications and connective tissue disorders.

9 and cardiovascular outcomes in LDS or other connective tissue disorders.

10 rral centers that have expertise in managing connective tissue disorders.

11 marker of adverse cardiovascular outcomes in connective tissue disorders.

12 tertiary centers with expertise in managing connective tissue disorders.

13 genetic analysis in patients with idiopathic connective tissue disorders.

14 ce documents thyroid disease coexisting with connective tissue disorders.

15 in types of Ehlers-Danlos syndrome and other connective tissue disorders.

16 use of livers from donors with a history of connective tissue disorders.

17 cause the Marfan syndrome (MFS) and related connective tissue disorders.

18 from certain patients with undifferentiated connective-tissue disorders.

19 28, 0.18-0.43, p<0.0001), musculoskeletal or connective tissue disorder (0.46, 0.30-0.71, p=0.0004),

20 s, with the exception of musculoskeletal and connective tissue disorders (992 [8.69% per annum] vs 83

21 Inherited connective tissue disorders, among them Ehlers-Danlos sy

22 h immune-related diseases (including asthma, connective tissue disorders and inflammatory bowel disea

23 myocarditis, and myocarditis associated with connective tissue disorders and may be beneficial in chr

24 nditions, especially with scleritis, are the connective tissue disorders and systemic vasculitis, but

25 inophilic esophagitis show a relationship to connective tissue disorders and that dietary management

26 , including diabetes mellitus, hypertension, connective tissue disorders, and congenital heart diseas

27 ase (aOR, 9.92; 95% CI, 8.36-11.8), systemic connective tissue disorders (aOR, 3.01; 95% CI, 2.23-4.0

28 These results indicate that self-reports of connective tissue disorders are influenced by reporting

29 s of Weill-Marchesani syndrome, an inherited connective tissue disorder, are caused by mutations in A

30 BCS is an autosomal recessive generalized connective tissue disorder associated with extreme corne

31 temic sclerosis is a systemic autoimmune and connective tissue disorder associated with the human leu

32 enesis imperfecta (Col1a2(oim)), a heritable connective tissue disorder caused by abnormalities in th

33 Marfan syndrome (MFS) is a heritable connective tissue disorder caused by mutations in FBN1,

34 Marfan syndrome (MFS), an autosomal-dominant connective tissue disorder caused by mutations in fibril

35 Marfan syndrome (MFS) is a heritable connective tissue disorder caused by mutations in the ge

36 Marfan syndrome is a connective tissue disorder caused by mutations in the ge

37 ies in actions of otherwise normal EOMs, and connective tissue disorders causing these instabilities

38 1, result in Marfan syndrome (MFS), a common connective tissue disorder characterised by tall stature

39 Bruck syndrome (BS) is a connective tissue disorder characterized at the molecula

40 pathogenesis of systemic sclerosis (SSc), a connective tissue disorder characterized by autoimmunity

41 Osteogenesis imperfecta (OI) is a heritable connective tissue disorder characterized by bone fragili

42 Systemic sclerosis (SSc) is a connective tissue disorder characterized by fibrosis of

43 erma (systemic sclerosis [SSc]) is a complex connective tissue disorder characterized by hardening an

44 Inherited cutis laxa is a connective tissue disorder characterized by loose skin a

45 hat Marfan syndrome - a dominantly inherited connective tissue disorder characterized by tall stature

46 All are connective tissue disorders characterized by defects of

47 s crucial for elucidating pathomechanisms of connective tissue disorders characterized by ECM deficie

48 me (EDS) designates a heterogeneous group of connective tissue disorders characterized by skin elasti

49 s syndrome (EDS) is a heterogeneous group of connective-tissue disorders characterized by skin fragil

50 V collagen alpha1(V) chain can underlie the connective tissue disorder classic Ehlers-Danlos syndrom

51 t results in 21-hydroxylase deficiency and a connective-tissue disorder consisting of skin and joint

52 absence of clinical features associated with connective tissue disorders (CTDs) since CMI and CTDs fr

53 bnormal fibrillinogenesis is associated with connective tissue disorders (CTDs), including Marfan syn

54 perfect predictor of aortic complications in connective tissue disorders (CTDs).

55 prevalence of EoE in patients with inherited connective tissue disorders (CTDs).

56 e alter mitochondrial function and cause the connective tissue disorder cutis laxa.

57 ene (FBN1) cause Marfan syndrome and related connective tissue disorders (fibrillinopathies) that sho

58 Occipital horn syndrome (OHS), an X-linked connective tissue disorder, has recently been shown to r

59 ons in type I collagen associated with human connective tissue disorders have been described.

60 vation was achieved by analysis of inherited connective tissue disorders having TGF-beta dysregulatio

61 ibromuscular dysplasia was present in 62.7%, connective tissue disorder in 4.9%, and systemic inflamm

62 With a history of connective tissue disorder in an immediate family member

63 Importance: Eosinophilic fasciitis (EF) is a connective tissue disorder in which conventional treatme

64 Marfan syndrome (MFS), a heritable connective tissue disorder, is caused by mutations in th

65 ead to the awareness of important underlying connective tissue disorders like the Marfan syndrome.

66 It supports the hypothesis that a variety of connective tissue disorders may confer increased suscept

67 id lupus erythematosus; and four had 4 mixed connective tissue disorders (MCTD).

68 medical evacuation were: musculoskeletal and connective tissue disorders (n=8104 service members, 24%

69 Marfan syndrome (MFS) is a systemic connective tissue disorder notable for the development o

70 h systemic inflammation (NUSI) without known connective tissue disorder or malignancy.

71 The quantitative metric is shown for the connective tissue disorder Osteogenesis Imperfecta (char

72 ations at these loci result primarily in the connective tissue disorders osteogenesis imperfecta and

73 d with Ehlers-Danlos syndrome, a generalized connective tissue disorder resulting from altered metabo

74 ic science show great promise in eliminating connective tissue disorders such as Marfan syndrome in t

75 racellular microfibrils, are associated with connective tissue disorders such as Marfan's syndrome or

76 Connective tissue disorders, such as some forms of Ehler

77 eatment of several major systemic autoimmune connective tissue disorders: systemic lupus erythematosu

78 Pelvic organ prolapse is a common connective tissue disorder that affects women.

79 found in Marfan syndrome (MFS), a heritable connective tissue disorder that is caused by reduced lev

80 Loeys-Dietz syndrome (LDS) is a connective tissue disorder that is characterized by a hi

81 Loeys-Dietz syndrome (LDS) is a connective tissue disorder that is characterized by skel

82 ssociated with the Ehlers-Danlos syndrome, a connective tissue disorder that leads to a defect in typ

83 Systemic connective tissue disorders that present as DG at initia

84 molecularly heterogeneous group of inherited connective tissue disorders that share similar skeletal

85 he Ehlers-Danlos syndrome (EDS), a heritable connective-tissue disorder that severely alters the coll

86 hlers-Danlos syndrome (SCD-EDS), a heritable connective tissue disorder.Those previous studies sugges

87 echanical factors combine with an underlying connective tissue disorder to cause the CSF leaks.

88 achnodactyly (CCA), a usually mild heritable connective-tissue disorder, to FBN2, the fibrillin gene

89 us vasculitis, giant cell arteritis, diverse connective tissue disorders; viral, spirochete, fungal,

90 No underlying connective tissue disorder was diagnosed in any patient.

91 cent of those found in many human autoimmune connective tissue disorders, which suggests that defects

92 LDS, Ehlers-Danlos syndrome, or nonspecific connective tissue disorder who underwent thoracic contra

93 omatous degeneration appears to consist of a connective tissue disorder with altered extracellular ma

94 cular Ehlers-Danlos syndrome (EDS) is a rare connective tissue disorder with serious hemorrhagic cons

95 xanthoma elasticum, a multi-system heritable connective tissue disorder with variable phenotypic expr

96 ystemic lupus erythematosus is an autoimmune connective-tissue disorder with a wide range of clinical

97 suggested by its association with hereditary connective tissue disorders, youthful onset in some pati