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1 induced by aging, UV-exposure, fibrosis, and connective tissue disorder.
2 r cases across the 2 cohorts had a diagnosed connective tissue disorder.
3 me (BCS), an autosomal-recessive generalized connective tissue disorder.
4 ormed in the donor to rule out a subclinical connective tissue disorder.
5 tment of the varied systems affected by this connective tissue disorder.
6 inantly inherited, genetically heterogeneous connective-tissue disorder.
7  may also cause similar, albeit less severe, connective tissue disorders.
8 apparatus, whose dysfunction causes numerous connective tissue disorders.
9 h implications for ILD associated with other connective tissue disorders.
10 sia, parturition, renal failure and multiple connective tissue disorders.
11  B-cell lineage hematologic malignancies and connective tissue disorders.
12 , with consequent implications for inherited connective tissue disorders.
13 cur in diseases such as cancer, fibrosis and connective tissue disorders.
14 etardation, thromboembolic complications and connective tissue disorders.
15  and cardiovascular outcomes in LDS or other connective tissue disorders.
16 rral centers that have expertise in managing connective tissue disorders.
17 marker of adverse cardiovascular outcomes in connective tissue disorders.
18  tertiary centers with expertise in managing connective tissue disorders.
19 genetic analysis in patients with idiopathic connective tissue disorders.
20 ce documents thyroid disease coexisting with connective tissue disorders.
21 in types of Ehlers-Danlos syndrome and other connective tissue disorders.
22  use of livers from donors with a history of connective tissue disorders.
23  cause the Marfan syndrome (MFS) and related connective tissue disorders.
24  from certain patients with undifferentiated connective-tissue disorders.
25 28, 0.18-0.43, p<0.0001), musculoskeletal or connective tissue disorder (0.46, 0.30-0.71, p=0.0004),
26 s, with the exception of musculoskeletal and connective tissue disorders (992 [8.69% per annum] vs 83
27                                    Inherited connective tissue disorders, among them Ehlers-Danlos sy
28 or undiagnosed individuals presenting with a connective tissue disorder and myopathy.
29 diovascular system development and function, connective tissue disorders and dermatological condition
30 h immune-related diseases (including asthma, connective tissue disorders and inflammatory bowel disea
31 myocarditis, and myocarditis associated with connective tissue disorders and may be beneficial in chr
32 nditions, especially with scleritis, are the connective tissue disorders and systemic vasculitis, but
33 inophilic esophagitis show a relationship to connective tissue disorders and that dietary management
34 isease, aortopathy, coarctation, dissection, connective tissue disorders, and age-related changes.
35 , including diabetes mellitus, hypertension, connective tissue disorders, and congenital heart diseas
36 ed with MCVD (cardiomyopathies, arrhythmias, connective tissue disorders, and familial hypercholester
37 gthen the overlap between SCAD and renal and connective tissue disorders, and we highlight several ne
38 ase (aOR, 9.92; 95% CI, 8.36-11.8), systemic connective tissue disorders (aOR, 3.01; 95% CI, 2.23-4.0
39  These results indicate that self-reports of connective tissue disorders are influenced by reporting
40 s of Weill-Marchesani syndrome, an inherited connective tissue disorder, are caused by mutations in A
41    BCS is an autosomal recessive generalized connective tissue disorder associated with extreme corne
42  syndrome (MFS) is the most common inherited connective tissue disorder associated with TAAD.
43 temic sclerosis is a systemic autoimmune and connective tissue disorder associated with the human leu
44 interstitial lung diseases (ILDs), including connective tissue disorders associated with ILD.
45                      Exclusion criteria were connective tissue disorders, bicuspid aortic valves, and
46 nt a series of genetic evaluations for known connective-tissue disorders, but the evaluations were un
47 enesis imperfecta (Col1a2(oim)), a heritable connective tissue disorder caused by abnormalities in th
48                         Marfan syndrome is a connective tissue disorder caused by FBN1 mutations, lea
49 los syndrome (vEDS) is an autosomal-dominant connective tissue disorder caused by heterozygous mutati
50         Marfan syndrome (MFS) is a heritable connective tissue disorder caused by mutations in FBN1,
51                   Marfan syndrome (MFS) is a connective tissue disorder caused by mutations in fibril
52 Marfan syndrome (MFS), an autosomal-dominant connective tissue disorder caused by mutations in fibril
53  syndrome (MFS) is a highly variable genetic connective tissue disorder caused by mutations in the ca
54                   Marfan syndrome (MFS) is a connective tissue disorder caused by mutations in the FB
55         Marfan syndrome (MFS) is a heritable connective tissue disorder caused by mutations in the ge
56                         Marfan syndrome is a connective tissue disorder caused by mutations in the ge
57 ies in actions of otherwise normal EOMs, and connective tissue disorders causing these instabilities
58 1, result in Marfan syndrome (MFS), a common connective tissue disorder characterised by tall stature
59                     Bruck syndrome (BS) is a connective tissue disorder characterized at the molecula
60  pathogenesis of systemic sclerosis (SSc), a connective tissue disorder characterized by autoimmunity
61  Osteogenesis imperfecta (OI) is a heritable connective tissue disorder characterized by bone fragili
62                      Systemic sclerosis is a connective tissue disorder characterized by excessive fi
63                Systemic sclerosis (SSc) is a connective tissue disorder characterized by fibrosis of
64 erma (systemic sclerosis [SSc]) is a complex connective tissue disorder characterized by hardening an
65                    Inherited cutis laxa is a connective tissue disorder characterized by loose skin a
66 ations cause osteogenesis imperfecta (OI), a connective tissue disorder characterized by severe bone
67 hat Marfan syndrome - a dominantly inherited connective tissue disorder characterized by tall stature
68                                      All are connective tissue disorders characterized by defects of
69 s crucial for elucidating pathomechanisms of connective tissue disorders characterized by ECM deficie
70   Ehlers-Danlos syndrome (EDS) is a group of connective tissue disorders characterized by joint hyper
71 me (EDS) designates a heterogeneous group of connective tissue disorders characterized by skin elasti
72 s syndrome (EDS) is a heterogeneous group of connective-tissue disorders characterized by skin fragil
73  V collagen alpha1(V) chain can underlie the connective tissue disorder classic Ehlers-Danlos syndrom
74 t results in 21-hydroxylase deficiency and a connective-tissue disorder consisting of skin and joint
75      Its pathophysiology remains unclear but connective tissue disorders (CTD) and other vasculopathi
76 absence of clinical features associated with connective tissue disorders (CTDs) since CMI and CTDs fr
77 o holds potential for automated diagnosis of connective tissue disorders (CTDs), contributing to both
78 bnormal fibrillinogenesis is associated with connective tissue disorders (CTDs), including Marfan syn
79 perfect predictor of aortic complications in connective tissue disorders (CTDs).
80 prevalence of EoE in patients with inherited connective tissue disorders (CTDs).
81 e alter mitochondrial function and cause the connective tissue disorder cutis laxa.
82 ene (FBN1) cause Marfan syndrome and related connective tissue disorders (fibrillinopathies) that sho
83 atherosclerosis, other vasculitic processes, connective tissue disorders, fistulas, mycotic aneurysms
84 MTSL2 mutations cause an autosomal recessive connective tissue disorder, geleophysic dysplasia 1 (GPH
85   Occipital horn syndrome (OHS), an X-linked connective tissue disorder, has recently been shown to r
86 ons in type I collagen associated with human connective tissue disorders have been described.
87 ants in several genes, such as those causing connective tissue disorders, have been implicated; howev
88 vation was achieved by analysis of inherited connective tissue disorders having TGF-beta dysregulatio
89 ibromuscular dysplasia was present in 62.7%, connective tissue disorder in 4.9%, and systemic inflamm
90                            With a history of connective tissue disorder in an immediate family member
91 Importance: Eosinophilic fasciitis (EF) is a connective tissue disorder in which conventional treatme
92 ies presenting with features of a congenital connective tissue disorder including osteopenia, blue sc
93 with respiratory, musculoskeletal system and connective tissue disorders is more prevalent in Whites.
94           Marfan syndrome (MFS), a heritable connective tissue disorder, is caused by mutations in th
95 ead to the awareness of important underlying connective tissue disorders like the Marfan syndrome.
96 It supports the hypothesis that a variety of connective tissue disorders may confer increased suscept
97 id lupus erythematosus; and four had 4 mixed connective tissue disorders (MCTD).
98 medical evacuation were: musculoskeletal and connective tissue disorders (n=8104 service members, 24%
99 gion (exon 23-34) of FBN2 cause a hereditary connective tissue disorder named congenital contractural
100          Marfan syndrome (MFS) is a systemic connective tissue disorder notable for the development o
101 h systemic inflammation (NUSI) without known connective tissue disorder or malignancy.
102 tory and infectious disorders, autoimmune or connective tissue disorders, or malignancies).
103     The quantitative metric is shown for the connective tissue disorder Osteogenesis Imperfecta (char
104 ations at these loci result primarily in the connective tissue disorders osteogenesis imperfecta and
105 d with Ehlers-Danlos syndrome, a generalized connective tissue disorder resulting from altered metabo
106 ers-Danlos syndrome (vEDS) is a rare genetic connective tissue disorder secondary to pathogenic varia
107                         Pathogeneses include connective tissue disorders, smooth muscle contraction d
108 ic science show great promise in eliminating connective tissue disorders such as Marfan syndrome in t
109 racellular microfibrils, are associated with connective tissue disorders such as Marfan's syndrome or
110                                              Connective tissue disorders, such as some forms of Ehler
111 eatment of several major systemic autoimmune connective tissue disorders: systemic lupus erythematosu
112            Pelvic organ prolapse is a common connective tissue disorder that affects women.
113  found in Marfan syndrome (MFS), a heritable connective tissue disorder that is caused by reduced lev
114              Loeys-Dietz syndrome (LDS) is a connective tissue disorder that is characterized by a hi
115              Loeys-Dietz syndrome (LDS) is a connective tissue disorder that is characterized by skel
116 ssociated with the Ehlers-Danlos syndrome, a connective tissue disorder that leads to a defect in typ
117                   Marfan syndrome (MFS) is a connective tissue disorder that results in aortic root w
118                                     Systemic connective tissue disorders that present as DG at initia
119 molecularly heterogeneous group of inherited connective tissue disorders that share similar skeletal
120 he Ehlers-Danlos syndrome (EDS), a heritable connective-tissue disorder that severely alters the coll
121 hlers-Danlos syndrome (SCD-EDS), a heritable connective tissue disorder.Those previous studies sugges
122 echanical factors combine with an underlying connective tissue disorder to cause the CSF leaks.
123 achnodactyly (CCA), a usually mild heritable connective-tissue disorder, to FBN2, the fibrillin gene
124 us vasculitis, giant cell arteritis, diverse connective tissue disorders; viral, spirochete, fungal,
125                                No underlying connective tissue disorder was diagnosed in any patient.
126 cent of those found in many human autoimmune connective tissue disorders, which suggests that defects
127  LDS, Ehlers-Danlos syndrome, or nonspecific connective tissue disorder who underwent thoracic contra
128 ular Ehlers-Danlos syndrome (vEDS) is a rare connective tissue disorder with a high risk for arterial
129 omatous degeneration appears to consist of a connective tissue disorder with altered extracellular ma
130        Marfan syndrome (MFS) is a hereditary connective tissue disorder with an estimated prevalence
131     Exfoliation syndrome (XFS) is a systemic connective tissue disorder with elusive pathophysiology.
132 cular Ehlers-Danlos syndrome (EDS) is a rare connective tissue disorder with serious hemorrhagic cons
133            Stickler syndrome is an inherited connective tissue disorder with severe ocular manifestat
134 xanthoma elasticum, a multi-system heritable connective tissue disorder with variable phenotypic expr
135 ystemic lupus erythematosus is an autoimmune connective-tissue disorder with a wide range of clinical
136 n-Goldberg syndrome (SGS) is a multisystemic connective tissue disorder, with considerable clinical o
137 suggested by its association with hereditary connective tissue disorders, youthful onset in some pati

 
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