ライフサイエンスコーパス: soft tissue

1 lts in chronic functional impairments of the soft tissue.

2 Median SUV(max) was 20.6 in bone and 16.8 in soft tissue.

3 ase mutant, were highly attenuated in murine soft tissue.

4 of lipomas, the most common benign tumor of soft tissue.

5 hows localization in mCRPC sites in bone and soft tissue.

6 n result in pathological fibrosis of healthy soft tissue.

7 apply the method to in vivo imaging of human soft tissues.

8 mummification materials, and even desiccated soft tissues.

9 results in heterotopic ossification (HO) of soft tissues.

10 and stretchability comparable with those of soft tissues.

11 inflammatory responses originating deeply in soft tissues.

12 potential of breast cancer to metastasize to soft tissues.

13 lution and high sensitivity in depicting the soft tissues.

14 as a result of high contrast resolution for soft tissues.

15 49.6%), unknown origin (20.0%), and skin and soft tissue (17.0%).

16 included intra-abdominal (23%) and skin and soft tissue (28%) infections.

17 most prevalent infection sites were skin and soft tissue (39%), urinary tract (23%), bone and joint (

18 sity cholesterol; and total body weight) and soft tissues (abdominal subcutaneous fat [SAT], adipose

19 Natural soft tissue achieves a rich variety of functionality thr

20 and molecular healing response of overlying soft tissues after implant placement surgery.

21 The soft tissue anatomy includes key attributes of living ha

22 chronic inflammation, causing destruction of soft tissue and alveolar bone supporting the teeth.

23 t the utility of REE profiles as proxies for soft tissue and biomolecular preservation in fossil bone

24 s a common feature in subsets of sarcomas of soft tissue and bone and provide evidence of YAP1/TAZ-TE

25 such as muscle atrophy, oedema in peripheric soft tissue and bone marrow, joint effusion, or synoviti

26 Tumors of soft tissue and bone represent a heterogeneous group of

27 nt of YAP1/TAZ-mediated signals in tumors of soft tissue and bone.

28 We collected gingivitis and periodontitis soft tissue and characterized ILC subsets including RANK

29 fitness during competitive growth in murine soft tissue and in nutrient-limiting chemically defined

30 able needle delivery systems deform and move soft tissue and organs, leading to a non-diagnostic biop

31 nmar provide unprecedented insights into the soft tissue and skeletal anatomy of minute fauna, which

32 gressively delta(15)N-enriched during decay, soft tissues and bone were collected from beaver carcass

33 ited similar microstructures to the skin and soft tissues and contained rhPDGF-BB and rhIGF-I, while

34 hanics. However, the mechanical responses of soft tissues and semiflexible polymer gels differ in man

35 nasal cavity houses a bony system supporting soft tissues and sensory organs implicated in either olf

36 ensitivity of (18)F-DOPA PET/CT in detecting soft-tissue and bone or bone-marrow metastases was 77% a

37 ensitivity of (18)F-DOPA PET/CT in detecting soft-tissue and bone or bone-marrow metastases was 86% a

38 ave shown activity in patients with advanced soft-tissue and the median overall survival is only 18 m

39 id fibrils in abdominothoracic organs, skin, soft tissue, and peripheral nerves.

40 iation between the opioid epidemic and skin, soft-tissue, and venous infections (SSTVIs), endocarditi

41 (PMMDs) are alterations of the peri-implant soft tissue architecture characterized by an apical disc

42 classification of the inflamed peri-implant soft tissue around ceramic implants (CI) in comparison w

43 The thickness of the soft tissues around dental implants is crucial for both

44 Soft tissue arthritic changes associated with knee pain

45 We aimed at evaluating the soft tissue arthritic changes associated with pain in he

46 The frequencies of soft tissue arthritic changes found, which included redu

47 idisciplinary management to replace bone and soft tissues, as well as restore esthetics and physiolog

48 volving hard tissue augmentation (PhMT-b) or soft tissue augmentation (PhMT-s) has clinical benefits

49 tatus of autogenous soft tissue grafting for soft tissue augmentation and recession coverage at teeth

50 This manuscript reviews soft tissue augmentation and root coverage procedures us

51 d to identify clinical studies that involved soft tissue augmentation around dental implants and repo

52 alyze the evidence regarding the efficacy of soft tissue augmentation procedures aimed at modifying t

53 , however recent evidence support the use of soft tissue augmentation procedures around dental implan

54 thodontic treatment with or without hard and soft tissue augmentation procedures.

55 stibular aspect of 19 implants who underwent soft tissue augmentation using FGG at second stage surge

56 sess the three-dimensional changes following soft tissue augmentation using free gingival grafts (FGG

57 Soft tissue augmentation was performed at second-stage s

58 technologies in periodontal and peri-implant soft tissue augmentation when used as alternatives to au

59 the combined prosthetic-surgical approach or soft tissue augmentation with a submerged healing) was a

60 e amount of shrinkage during healing of free soft tissue autografts (FSTAs) using different surgical

61 unstained formalin-fixed, paraffin-embedded soft tissue biopsy specimens because of a lack of image

62 tion and is the method of choice to evaluate soft tissue, bone marrow and preradiographic signs of os

63 m salicylic acid to inhibit lung, brain, and soft-tissue cancer cells.

64 of adults are diverse, rare, and aggressive soft tissue cancers.

65 perglycemia, compared with controls, without soft tissue changes.

66 examine the significance of the peri-implant soft tissue characteristics in relationship to the onset

67 Soft tissue closure was slower in GG (P < 0.01).

68 te determinants of hip fracture by assessing soft-tissue composition of the upper thigh at CT.

69 Eighty-seven descriptors of the soft-tissue composition were determined.

70 ement (TKR) positioning and patient-specific soft tissue conditions still causes a considerable numbe

71 biopsy showed involvement of the surrounding soft tissue, consistent with a satellite lesion.

72 ngly, no significant differences in terms of soft tissue contour change were observed between groups.

73 h BBT is proposed to be a key factor for the soft-tissue contour.

74 ble to rebuild stable facial hard-tissue and soft-tissue contours that were esthetically pleasing.

75 aging modality that is characterized by poor soft tissue contrast, low signal-to-noise using current

76 temporal resolution, spatial resolution, and soft-tissue contrast in a moving structure.

77 tabolic-functional information with the high soft-tissue contrast of MRI.

78 cro-CT of Thiel-embalmed samples resulted in soft-tissue contrast within the vertebral canal, despite

79 uided RT, has been motivated by the superior soft-tissue contrast, organ motion visualization, and ab

80 refraction properties to improve spatial and soft-tissue contrast.

81 osurgical reconstructions of lower extremity soft-tissue defects.

82 ciated with with reduction of probing depth, soft tissue dehiscence and plaque index compared to non-

83 th a significant reduction in probing depth, soft tissue dehiscence and plaque index, regardless of t

84 The incidence of a peri-implant soft tissue dehiscence/deficiency (PSTD) is not a rare f

85 ctors associated with the presence of buccal soft tissue dehiscences (BSTD).

86 y lead to less risk of infection of skin and soft tissues deveroping serious infections due to an und

87 Of 27 patients with measurable soft tissue disease, 15 (56%) achieved an objective resp

88 Of 27 patients with measurable soft-tissue disease, 15 (56%) achieved an objective resp

89 Excellent uptake was observed in bone and soft-tissue disease.

90 l roles of ENPP1 in mineralization and these soft tissue disorders.

91 stribute phosphorus and calcium from hard to soft tissues during its sexual development.

92 e depletion of internal stores from hard and soft tissues during maturation-induced body reorganizati

93 form of the neurocranium and its associated soft tissues during the evolution of sarcopterygian fish

94 ridge augmentation is a procedure to reduce soft tissue exposure and to improve bone graft density a

95 Primary rat skin fibroblasts, soft tissue fibroblasts, and osteoblasts were then cultu

96 iate analysis, patients reconstructed with a soft tissue flap and bridging plate (odds ratio (OR) 3.9

97 fibula flap reconstruction whereas 41 had a soft tissue flap and plate reconstruction.

98 r prolonged tube dependence compared to free soft tissue flap reconstructions.

99 The autogenous soft tissue graft (CTG/FGG) proved to be superior in all

100 advantages and disadvantages of harvesting a soft tissue graft from the tuberosity and to compare it

101 logical, and molecular evidence shows that a soft tissue graft obtained from the maxillary tuberosity

102 Subjects that received an autogenous soft tissue graft over 10 years ago were screened and in

103 APF with any evaluated soft tissue graft was associated with with reduction of

104 A soft tissue graft was harvested from each side for histo

105 ation, crown lengthening, implant placement, soft tissue graft, open flap debridement or surgical rem

106 vidence and the current status of autogenous soft tissue grafting for soft tissue augmentation and re

107 Patient experience of previous autogenous soft tissue grafting has an influence on their decision

108 hiscence and plaque index, regardless of the soft tissue grafting material employed, whereas bilamina

109 of this study was to evaluate the impact of soft tissue grafting procedures conducted over a decade

110 hat bilaminar techniques in combination with soft tissue grafts (connective tissue graft [CTG], colla

111 The clinical benefits of autogenous soft tissue grafts are countered by donor site morbidity

112 ) technologies as alternatives to autogenous soft tissue grafts for periodontal and peri-implant plas

113 Soft tissue grafts from the maxillary tuberosity are ric

114 loped and used as alternatives to autogenous soft tissue grafts in keratinized tissue augmentation an

115 tion when used as alternatives to autogenous soft tissue grafts.

116 e-owners undergoing surgery for breast, skin-soft-tissue, head-and-neck, or abdominal cancer (July 20

117 ally characterize the melanin content of the soft tissue headcrest of the pterosaur Tupandactylus imp

118 ed to investigate its effect on peri-implant soft tissue healing after implant uncovery.

119 However, the soft tissue healing is technically sensitive to the surg

120 However, the influence on peri-implant soft tissue healing is unclear.

121 This study aimed to determine and compare soft tissue healing outcomes following implant placement

122 Soft tissue healing was uneventful in all patients.

123 yed extensively in clinical applications for soft tissue imaging, the acoustic beams can also be used

124 loss reduced volumes of several upper airway soft tissues in subjects with obesity and OSA.

125 atively the solid-fluid tissue properties of soft tissues in vivo.

126 These specimens preserve skeletal and soft tissues, including an elongated median hyoid elemen

127 All soft tissues, including muscle, were significantly delta

128 CrI 1.96-8.20), and report interval skin and soft tissue infection (OR 1.32, CrI 1.07-1.64).

129 pproach to decolonization decreases skin and soft tissue infection (SSTI) incidence, though this is b

130 fense against Staphylococcus aureus skin and soft tissue infection (SSTI) is dependent on both estrog

131 dia databases for suggestion of AIT skin and soft tissue infection (SSTI) risk and compare this risk

132 Soft tissue infection (STI) was based on negative bone c

133 Using an established mouse model of skin and soft tissue infection and a newly developed histopatholo

134 Osteomyelitis and distant soft tissue infection may occur less frequently when BCG

135 Skin and soft tissue infection was present in 50%, sepsis/bactere

136 ced dermonecrosis, a key feature of skin and soft tissue infection.

137 teomyelitis or septic arthritis, and skin or soft tissue infection.

138 thogenesis of Staphylococcus aureus skin and soft tissue infection.

139 ntially influence GAS pathophysiology during soft tissue infection.

140 ing fasciitis (NF) is a destructive skin and soft tissue infection.

141 view was conducted for estimates of skin and soft-tissue infection and endocarditis disease burden wi

142 Soft-tissue infection and osteomyelitis were the most co

143 that are critical for fitness during murine soft-tissue infection at both 24 h and 48 h postinfectio

144 osteitis/osteomyelitis (27.9%), and distant soft tissue infections (3.0%).

145 commendations regarding complicated skin and soft tissue infections (cSSTIs).

146 Necrotizing soft tissue infections (NSTIs) caused by group A Strepto

147 Skin and soft tissue infections (SSTIs) disproportionately impact

148 is an opportunistic pathogen that can cause soft tissue infections but is also a frequent cause of f

149 ients with group A Streptococcus necrotizing soft tissue infections demonstrated a negative correlati

150 er respiratory tract infections and skin and soft tissue infections with local pharmacists.

151 4.4 to 32.9 per 100 000 persons for skin and soft tissue infections.

152 ged as a frequent cause of purulent skin and soft tissue infections.

153 ureus is the most frequent cause of skin and soft tissue infections.

154 ed for the traditional treatment of skin and soft tissue infections.

155 cci are frequently implicated in necrotizing soft-tissue infections (NSTIs).

156 The incidence of skin and soft-tissue infections (SSTIs), for which human immunode

157 ersons who inject drugs (PWID) with skin and soft-tissue infections annually in the United States.

158 for infective endocarditis (IE) and skin and soft-tissue infections related to IDU in the United Stat

159 and emergency department visits for skin and soft-tissue infections related to IDU yielded a crude es

160 itides, infective endocarditis, and skin and soft-tissue infections.

161 It is hypothesized that peri-implant soft tissue inflammation and crestal bone loss (CBL) are

162 the rate of healing associated with reduced soft tissue inflammation and osteoclast activation.

163 Conclusion Soft-tissue injuries and osseous findings other than mor

164 features, femoral distal cam, and associated soft-tissue injuries.

165 versus other oral analgesic agents for acute soft tissue injury.

166 Infiltrative tumor growth into adjacent soft tissues is a major cause of the frequent recurrence

167 nd elastic bioink for 3D printing of complex soft tissues is demonstrated.

168 r-wave elastography can increase accuracy of soft-tissue lesion diagnosis in conjunction with US.

169 vasive tool for the diagnosis of superficial soft tissue lesions and may negate the need for unnecess

170 Multiple superficial soft tissue lesions were studied, the majority of which

171 based threshold are used to segment bone and soft-tissue lesions, respectively.

172 peri-implant probing depth, and peri-implant soft tissue level (secondary outcome variables).

173 Specifically, how biofilms form on soft, tissue-like materials remains unknown.

174 Patients with bulky or deep-seated soft-tissue malignancies not amenable to resection parti

175 onstrated encouraging antitumour activity in soft-tissue malignancies; a single course of treatment p

176 88 years), who were referred for biopsy of a soft-tissue mass were prospectively recruited from Decem

177 hy (SWE) improves the accuracy of diagnosing soft-tissue masses as benign or malignant compared with

178 differentiating between benign and malignant soft-tissue masses depicted on US images, with performan

179 Traditional thermoplastics cannot match soft tissue mechanics, while gels leach into the body an

180 the sensitivity in detecting primary tumors, soft-tissue metastases, and bone or bone-marrow metastas

181 is, sensitivity in detecting primary tumors, soft-tissue metastases, and bone or bone-marrow metastas

182 tocol, except for the surgical management of soft tissue (MIST versus NIPSA).

183 eal reactive bone formation, bone marrow and soft tissue oedema, presence of synovial effusion, muscu

184 indicated the potential to accumulate in the soft tissue of freshwater mussels following exposure to

185 tituted Keggin polyoxometalate (Zr-POM), the soft tissue of the placenta (i.e., different layers and

186 Soft tissues of extinct organisms are rarely preserved a

187 To successfully integrate with the soft tissues of the body (eg.

188 ry to mm-scale devices implanted deep within soft tissues of the body.

189 and surgical modification of the pharyngeal soft tissues or facial skeleton to enlarge the upper air

190 urgical techniques for ridge preservation on soft tissue parameters has seldom been investigated.

191 Results of soft-tissue parameters were compared with bone mineral d

192 The peri-implant soft tissue phenotype (PSP) encompasses the keratinized

193 o warrant the clinical benefits of modifying soft tissue phenotype around tooth-supported restoration

194 articles reporting on the outcomes of buccal soft tissue phenotype modification around implants were

195 view endeavored to investigate the effect of soft tissue phenotype modification therapy (PhMT-s) at s

196 Surgical modification of peri-implant soft tissue phenotype via PhMT-s may decrease the amount

197 gen depleted waters explains the exceptional soft tissue preservation.

198 NIPSA showed significant soft tissue preservation.

199 also be because of deposition of calcium in soft tissues producing reduced vision /cataract or calci

200 permafrost Pleistocene mammal carcasses with soft tissue remains are subject to intensive study and h

201 ating biomaterial scaffold (bioscaffold) for soft tissue repair is presented.

202 However, the current standard of care soft tissue repair meshes for hernia repair is highly in

203 nflammation modulating polymer scaffolds for soft tissue repair with minimal postsurgical complicatio

204 Linear changes of facial soft-tissue resorption at immediately placed implants we

205 te-specific antigen responses (0% to 11%) or soft tissue responses (0% to 6%).

206 o observed, reflecting the elasticity of the soft-tissue restraints.

207 ge of the healing region differentiated into soft tissue resulting in smaller volume of bone tissue a

208 The peri-implant soft tissue samples were retrieved from the sites during

209 f care in patients with advanced, inoperable soft tissue sarcoma (STS).

210 tcomes for children and adults with advanced soft tissue sarcoma are poor with traditional therapy.

211 Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in children and represents a high-gr

212 In this presumed first prospective trial of soft tissue sarcoma spanning nearly the entire age spect

213 therlands, who were enrolled in the European Soft Tissue Sarcoma Study Group (E pSSG) RMS 2005 study.

214 The European paediatric Soft tissue sarcoma Study Group (EpSSG) aimed to investi

215 (TILs) in leiomyosarcoma (LMS), a subtype of soft tissue sarcoma that exhibits histological heterogen

216 ed trunk or extremity chemotherapy-sensitive soft tissue sarcoma, which were larger than 5 cm in diam

217 ination in children and adults with advanced soft tissue sarcoma.

218 utrophils in an autochthonous mouse model of soft tissue sarcoma.

219 Liposarcoma is the most common soft tissue sarcoma.

220 ochthonous mouse model of Kras(G12D) -driven soft tissue sarcoma.

221 7), breast cancer (4.6; 95% CI, 3.5 to 6.0), soft-tissue sarcoma (3.4; 95% CI, 1.9 to 5.7), thyroid c

222 t outcome in paediatric non-rhabdomyosarcoma soft-tissue sarcoma (NRSTS), but no risk stratification

223 r predicting the histopathologic response of soft-tissue sarcoma (STS) to neoadjuvant isolated limb p

224 [standard deviation], 45 men) with recurrent soft-tissue sarcoma and 63 age-, sex-, and tumor-matched

225 rapy is beneficial in pre-clinical models of soft-tissue sarcoma and deserves further exploration in

226 ns a large field of clinical applications in soft-tissue sarcoma and possibly other cancers.

227 ancer, and in a mouse model of autochthonous soft-tissue sarcoma driven by a G12D mutation in KRAS an

228 I, 2.3% to 4.8%), whereas body and extremity soft-tissue sarcoma incidence was rare until age 30, whe

229 ults (aged >=18 years) with locally advanced soft-tissue sarcoma of the extremity or trunk wall, of a

230 Strikingly elevated bone and soft-tissue sarcoma risks differ by age, location, and s

231 Epithelioid sarcoma is a rare and aggressive soft-tissue sarcoma subtype.

232 , and T1-weighted MRI) from 51 patients with soft-tissue sarcoma was used to prospectively assess rep

233 onfirms the immune subtypes in patients with soft-tissue sarcoma, and unravels the potential of B-cel

234 habdomyosarcoma is the most common childhood soft-tissue sarcoma, yet patients with metastatic or rec

235 n profiles in 608 tumours across subtypes of soft-tissue sarcoma.

236 coma of the liver, or unclassified malignant soft-tissue sarcoma.

237 arcoma (RMS) is the most prevalent pediatric soft-tissue sarcoma.

238 nostic performance in detection of recurrent soft-tissue sarcoma.

239 ; colorectal; non-Hodgkin lymphoma; thyroid; soft-tissue sarcoma; ovarian; bladder; other female geni

240 ere Ewing sarcoma family tumors (54%), other soft tissue sarcomas (21%), osteosarcoma (11%), rhabdomy

241 e pre-clinical activity of ATR inhibition in soft tissue sarcomas (STS).

242 Soft tissue sarcomas (STSs) are mesenchymal tumours wher

243 t malignant neoplasms, particularly bone and soft tissue sarcomas, uterine leiomyosarcoma, melanomas,

244 rential diagnosis of liposarcomas from other soft tissue sarcomas, whereas perilipin 2 correlates neg

245 neuroblastoma, Wilms' tumours, and bone and soft tissue sarcomas.

246 sarcoma (UPS) are highly genetically complex soft tissue sarcomas.

247 to 2,873 v SIR, 169; 95% CI, 115 to 239) and soft-tissue sarcomas (SIR, 542; 95% CI, 418 to 692 v SIR

248 olated limb perfusion (ILP) in patients with soft-tissue sarcomas (STS).

249 nscriptomic marker that identifies high-risk soft-tissue sarcomas and is associated with high metasta

250 e conducted analyses separately for bone and soft-tissue sarcomas occurring in the head and neck (in/

251 hese three groups contained either recurrent soft-tissue sarcomas or positive postoperative findings

252 Soft-tissue sarcomas represent a heterogeneous group of

253 Head and neck bone and soft-tissue sarcomas were diagnosed beginning in early c

254 A retrospective study of patients with soft-tissue sarcomas who were imaged from January 2009 t

255 a, CNS tumours, neuroblastoma, Wilms tumour, soft-tissue sarcomas, and bone cancer) by comparing both

256 ially increased risks of subsequent bone and soft-tissue sarcomas, particularly after radiotherapy.

257 factor fusions (TFFs) are present in ~30% of soft-tissue sarcomas.

258 sed mussels showed accumulation of Ba in the soft tissue several hundred times above background water

259 nriched in skeletal sites of metastasis over soft tissue sites.

260 ficacy Studies, MR-Contrast Agent, Oncology, Soft Tissues/Skin(C) RSNA, 2020.

261 A perfectly preserved, fully grown soft-tissue specimen of the octobrachian coleoid Plesiot

262 inical study was to compare the peri-implant soft tissue status and CBL around adjacent implants plac

263 Peri-implant soft tissue status and crestal bone levels were comparab

264 ing the detection of micrometric spinal cord soft-tissue structure and vasculature.

265 Unlike the classic view, we identified a soft-tissue structure between the BM and OSL in humans,

266 ave provided insights into the morphology of soft-tissue structures in extinct animals [3-7], in part

267 Soft tissue substitutes have been proposed to replace au

268 digital image correlation for reconstructing soft-tissue surfaces under dynamic deformations as well

269 elements impede their conformal contact with soft-tissue surfaces, limit the scope of their uses, len

270 tary angioedema (HAE) experience episodes of soft tissue swelling as a consequence of unregulated kal

271 penetrant hydrocephalus, white spotting and soft tissue syndactyly.

272 head like-3 (GRHL3), and Grhl3(-/-)mice have soft-tissue syndactyly.

273 the geometries and mechanical properties of soft tissue systems and multimaterial assemblies for nex

274 Computed tomography (CT) noted ill-defined soft tissue thickening anterior to the right globe, pred

275 the root; connective tissue adaptation; and soft tissue thickness (STT).

276 The influence of CTGs on soft tissue thickness and keratinized tissue width are a

277 plant placement, implants were uncovered and soft tissue thickness measured again.

278 r than hard bones and shells, it is rare for soft tissues to fossilize, but occasionally they are wel

279 Airway sizes and soft tissue, tongue fat, and abdominal fat volumes were

280 ins as markers for differential diagnosis of soft tissue tumors has only been studied in a few cases.

281 gland and primary orbital and ocular adnexal soft tissue tumors; reappraisal of diagnostic, prognosti

282 radical ablative therapy in the treatment of soft-tissue tumors in the liver, kidney, prostate, and p

283 c, colorectal, esophago-gastric, and sarcoma/soft-tissue tumors.

284 rmediate (rarely metastasising) or malignant soft-tissue tumour (apart from tumour types eligible for

285 ) classification categorises musculoskeletal soft tissue tumours (STT) based on their similarity to n

286 Similarly to soft tissue tumours, the World Health Organisation (WHO)

287 led preservation of different intervertebral soft tissue types (cartilage, probable notochord) seen i

288 Numerous approaches to augment soft tissue volume around endosseous dental implants hav

289 hypothesized that weight loss would decrease soft tissue volumes and tongue fat, and that these chang

290 each sample, the hydrophilic extract of the soft tissue was analyzed by proton nuclear magnetic reso

291 Peri-implant soft tissue was evaluated using an ordinal mucosal index

292 Development of soft tissue was observed both in the coronal region due

293 Soft tissues were stable, with no statistically signific

294 Results: In total, 162 lesions (82 bone, 80 soft tissue) were assessed in patients with breast cance

295 embedded in the now phosphatised cephalopod soft tissue, which makes a chance association highly imp

296 ntrast-enhanced CT scan showed a big mass of soft tissue with diffuse infiltration of the gallbladder

297 da, USA), we report evidence of recognizable soft tissues within their external tubes.

298 smacytoma (EMP) is a plasma cell neoplasm of soft tissue without bone marrow involvement or other sys

299 c and histologic analysis revealed a reduced soft tissue wound opening and more rapid re-epithelializ

300 epidermidis and Streptococcus pyogenes in a soft-tissue wound biofilm model.