ライフサイエンスコーパス: granulomatous

1 was initially neutrophilic, and later became granulomatous.

2 of the eye and the almost universally fatal granulomatous amoebic encephalitis.

3 Granulomatous and lymphocytic interstitial lung disease

4 occur in lymphomas, whereas others, such as granulomatous angiitis, are only described in HL.

5 The presence of VZV antigen in granulomatous aortitis was highly significant (P = .0001

6 rizes the pathology of giant cell arteritis, granulomatous aortitis, and intracerebral varicella zost

7 y produces stroke, giant cell arteritis, and granulomatous aortitis, and it develops after virus reac

8 tes with the significant detection of VZV in granulomatous aortitis.

9 Granulomatous arteritis characterizes the pathology of g

10 11 of 11 aortas with pathologically verified granulomatous arteritis, in 1 of 1 cases of nongranuloma

11 ing from mutations in the NOD2 gene, wherein granulomatous arthritis, uveitis, and dermatitis develop

12 delayed-onset combined immune deficiency and granulomatous/autoimmune manifestations (CID-G/AI), prod

13 The granulomatous character of Blau syndrome provides an opp

14 f an infant with severe IBD characterized by granulomatous colitis and severe perianal disease, we id

15 to identify genetic factors that might cause granulomatous colitis and severe perianal disease, with

16 patients develop other complications such as granulomatous colitis and/or fatal pulmonary fibrosis.

17 and in some patients, pulmonary fibrosis and granulomatous colitis.

18 hic epilepsy, lymphoma, mast cell tumour and granulomatous colitis; for morphological traits, we repo

19 unocompromising condition, including chronic granulomatous disease (CGD) (n=4), diabetes mellitus (DM

20 The rarer PID patients without chronic granulomatous disease (CGD) achieved an OS at 3 years of

21 s involved in the pathophysiology of chronic granulomatous disease (CGD) and sepsis.

22 circulating B cells in patients with chronic granulomatous disease (CGD) and those with HIV infection

23 Liver abscesses in chronic granulomatous disease (CGD) are typically difficult to t

24 Chronic granulomatous disease (CGD) can be cured by allogeneic h

25 fective neutrophils in patients with chronic granulomatous disease (CGD) cause susceptibility to extr

26 Patients with chronic granulomatous disease (CGD) experience immunodeficiency

27 leukocytes (PMN) from patients with chronic granulomatous disease (CGD) fail to produce microbicidal

28 educed in the blood of patients with chronic granulomatous disease (CGD) for reasons and consequences

29 Although prognosis of Chronic Granulomatous Disease (CGD) has greatly improved, few st

30 Patients with chronic granulomatous disease (CGD) have a mutated NADPH complex

31 t described the clinical features of chronic granulomatous disease (CGD) in 1959.

32 ears of age) often resembles that of chronic granulomatous disease (CGD) in extent and features of co

33 Chronic granulomatous disease (CGD) is a primary immune deficien

34 Chronic granulomatous disease (CGD) is a primary immunodeficienc

35 Chronic granulomatous disease (CGD) is a primary immunodeficienc

36 Chronic granulomatous disease (CGD) is a primary immunodeficienc

37 Chronic granulomatous disease (CGD) is a rare inherited disorder

38 Chronic granulomatous disease (CGD) is a rare phagocytic disorde

39 Chronic granulomatous disease (CGD) is a rare primary immunodefi

40 Chronic granulomatous disease (CGD) is an inherited disorder cha

41 aspergillosis (IA) in patients with chronic granulomatous disease (CGD) is Aspergillus fumigatus fol

42 Chronic granulomatous disease (CGD) is characterized by recurren

43 Chronic granulomatous disease (CGD) is due to defective nicotina

44 NADPH oxidase 2 (Nox2)-deficient chronic granulomatous disease (CGD) mice that lack the gp91(phox

45 Chronic granulomatous disease (CGD) patients have recurrent life

46 ide (NADPH) oxidase in patients with chronic granulomatous disease (CGD) results in susceptibility to

47 m-negative pathogen in patients with chronic granulomatous disease (CGD), a deficiency in the phagocy

48 hate oxidase 2 (NOX2) function cause chronic granulomatous disease (CGD), a primary immunodeficiency

49 r threat for patients suffering from chronic granulomatous disease (CGD), a primary immunodeficiency

50 bacterium that infects patients with chronic granulomatous disease (CGD), a primary immunodeficiency

51 stem cell transplants, patients with chronic granulomatous disease (CGD), and others.

52 ing mutations in this enzyme lead to chronic granulomatous disease (CGD), associated with increased s

53 (HSCT) is a successful treatment for chronic granulomatous disease (CGD), but the safety and efficacy

54 c defects in NADPH oxidase result in chronic granulomatous disease (CGD), characterized by recurrent

55 ) and lungs of A. fumigatus-infected chronic granulomatous disease (CGD), hydrocortisone-treated, and

56 atients with cystic fibrosis (CF) or chronic granulomatous disease (CGD).

57 s is a major threat to patients with chronic granulomatous disease (CGD).

58 has been isolated from patients with chronic granulomatous disease (CGD).

59 n emerging pathogen in patients with chronic granulomatous disease (CGD).

60 people with cystic fibrosis (CF) and chronic granulomatous disease (CGD).

61 ls with the primary immunodeficiency chronic granulomatous disease (CGD).

62 basis for the human immunodeficiency chronic granulomatous disease (CGD).

63 Wiskott-Aldrich syndrome (WAS), and chronic granulomatous disease (CGD).

64 model, because in mice with X-linked chronic granulomatous disease (X-CGD) that lack oxidase subunits

65 (iPSCs) from a patient with X-linked chronic granulomatous disease (X-CGD), a defect of neutrophil mi

66 In HSPCs from patients with X-linked chronic granulomatous disease (X-CGD), caused by mutations in th

67 t in patients and mice with X-linked chronic granulomatous disease (X-CGD).

68 Genetic defects in NADPH oxidase (chronic granulomatous disease [CGD]) and corticosteroid-induced

69 In chronic granulomatous disease allogeneic haemopoietic stem-cell

70 leotide phosphate oxidase defects in chronic granulomatous disease and beta2 integrin defects in leuk

71 this complex have been implicated in chronic granulomatous disease and Crohn's disease, highlighting

72 ases of rhinosporidiosis, which is a chronic granulomatous disease and is endemic in India and Sri La

73 articularly beneficial in areas with endemic granulomatous disease and may improve clinical managemen

74 ted for other forms of PID including chronic granulomatous disease and Wiskott-Aldrich syndrome.

75 acoronavirus, resulting in a lethal systemic granulomatous disease called feline infectious peritonit

76 ways of host immune cells in tuberculosis, a granulomatous disease caused by the intracellular pathog

77 Destructive midline granulomatous disease characterized by necrotizing granu

78 A 28-year-old man with chronic granulomatous disease developed worsening respiratory st

79 G mutations associated with autoimmunity and granulomatous disease did not have altered overall diver

80 Sarcoidosis is a chronic granulomatous disease for which there are limited therap

81 Chest imaging was consistent with granulomatous disease in 46.7%.

82 virus (FIPV), which leads to lethal systemic granulomatous disease in cats.

83 ximately 30 degrees C, so we sought to model granulomatous disease in the ectothermic zebrafish.

84 Sarcoidosis is a complex systemic granulomatous disease of unknown etiology characterized

85 Sarcoidosis is a multisystemic granulomatous disease of unknown etiology that predomina

86 Sarcoidosis is a multisystem granulomatous disease of unknown etiology that primarily

87 Sarcoidosis is a systemic granulomatous disease of unknown etiology.

88 romised patients as well as in patients with granulomatous disease or cystic fibrosis.

89 h compromise p40(phox) function in a chronic granulomatous disease patient, also perturbed class II A

90 ed Mo-DC differentiation observed in chronic granulomatous disease patients lacking p22phox.

91 Additionally, neutrophils from chronic granulomatous disease patients, carrying mutations in th

92 promise antifungal immune control in chronic granulomatous disease patients.

93 While sarcoidosis is a chronic granulomatous disease presumably reflecting an exaggerat

94 y subjects, those from patients with chronic granulomatous disease produce larger swarms against Cand

95 ntal data and description of a novel chronic granulomatous disease subtype (p40(phox)-deficiency) imp

96 Sarcoidosis is a granulomatous disease that primarily affects the lungs a

97 SCID), Wiskott-Aldrich syndrome, and chronic granulomatous disease through retrospective, prospective

98 nd the susceptibility of humans with chronic granulomatous disease to mycobacterial infection.

99 Patients aged 0-40 years with chronic granulomatous disease were assessed and enrolled at the

100 n age 12.7 years; IQR 6.8-17.3) with chronic granulomatous disease were enrolled from June 15, 2003,

101 age quiescence and prevents mTORC1-dependent granulomatous disease with clinical implications for sar

102 efects in oxidase function result in chronic granulomatous disease with hallmark recurrent microbial

103 6PD deficiency can be a phenocopy of chronic granulomatous disease with regard to the cellular and cl

104 the phagocyte NADPH oxidase complex (chronic granulomatous disease), severe congenital neutropenia (S

105 mmatory disease, 15.4%; malabsorption, 5.9%; granulomatous disease, 9.7%; liver diseases and hepatiti

106 Chronic granulomatous disease, an inherited disorder of the NADP

107 ed severe combined immunodeficiency, chronic granulomatous disease, and other diseases.

108 tations in the NADPH oxidase lead to chronic granulomatous disease, characterized by severe infection

109 ncies in the oxidative burst seen in chronic granulomatous disease, could lead to pathologic inflamma

110 such as Wiskott-Aldrich syndrome and chronic granulomatous disease, offering curative engraftment wit

111 bronchiectasis, autoimmunity, other cancers, granulomatous disease, or previous splenectomy.

112 in persons with cystic fibrosis and chronic granulomatous disease, represents one such group where n

113 Treatment of tuberculosis, a complex granulomatous disease, requires long-term multidrug ther

114 gene therapy for immunodeficiencies, chronic granulomatous disease, suicide gene therapy for graft-ve

115 ranswells and cells of patients with chronic granulomatous disease, we show that this downregulation

116 OS) because cells from patients with chronic granulomatous disease, which are defective in ROS produc

117 as also observed in individuals with chronic granulomatous disease, who lack NADPH oxidase activity b

118 ts with the NADPH oxidase deficiency chronic granulomatous disease, who require antibiotic and antimy

119 hagocyte functional defects, such as chronic granulomatous disease.

120 ive ROS production machinery develop chronic granulomatous disease.

121 sed by a Phellinus sp. in a boy with chronic granulomatous disease.

122 ficacious in high-risk patients with chronic granulomatous disease.

123 n-1 deficiency, CARD9 deficiency, or chronic granulomatous disease.

124 ctions, such as the genetic disorder chronic granulomatous disease.

125 es, including splenomegaly, hepatomegaly, or granulomatous disease.

126 EROS mutations are a novel cause of chronic granulomatous disease.

127 the oxidative burst in patients with chronic granulomatous disease.

128 iency, Wiskott-Aldrich syndrome, and chronic granulomatous disease.

129 , and the exclusion of alternative causes of granulomatous disease.

130 ity, lymphoid proliferation, malignancy, and granulomatous disease.

131 tage of ABC-like cells in patients with lung granulomatous diseases and decrease in treated patients

132 arthritis and uveitis in general as well as granulomatous diseases in particular.

133 osus, Sjogren syndrome or Behcet disease and granulomatous diseases such as sarcoidosis.

134 neumonitis (occupational burden, 19%); other granulomatous diseases, including sarcoidosis (occupatio

135 hic macrophages constitutes the basis of all granulomatous diseases, such as tuberculosis or sarcoido

136 and questions about macrophage function and granulomatous diseases.

137 -like cell percentages in patients with lung granulomatous diseases.Methods: Peripheral blood and BAL

138 Sarcoidosis is an inflammatory granulomatous disorder characterized by accumulation of

139 Chronic beryllium disease (CBD) is a granulomatous disorder characterized by an influx of ber

140 Sarcoidosis is a complex systemic granulomatous disorder of unknown etiology.

141 Sarcoidosis is a multisystem granulomatous disorder that most often affects the lungs

142 Similar abnormalities may extend to other granulomatous disorders, but not diseases such as ulcera

143 f PBC even in the absence of characteristic, granulomatous, duct destructive lesions.

144 e decline and death were explained by active granulomatous encephalitis, with widespread involvement

145 erculosis (MAP), occurs worldwide as chronic granulomatous enteritis of domestic and wild ruminants.

146 murafenib treatment, the patient developed a granulomatous eruption, which resolved 3 weeks after ces

147 o patients with melanoma developed cutaneous granulomatous eruptions during targeted BRAF inhibitor t

148 Granulomatous eruptions have not been previously reporte

149 We report 2 cases of cutaneous granulomatous eruptions on treatment with targeted BRAF

150 In our previous studies, resolution of granulomatous experimental autoimmune thyroiditis (G-EAT

151 in 30 nongranulomatous and 12 granulomatous eyes, the OCT cell counts correlated well

152 nongranulomatous eyes and 2.0 cells/grade in granulomatous eyes.

153 se includes indolent chronic rhinosinusitis, granulomatous fungal sinusitis, and acute fulminant fung

154 stinal histoplasmosis manifesting with acute granulomatous hepatitis and cholestasis in a 48-year-old

155 Similarly, cholestatic granulomatous hepatitis in liver histoplasmosis is rarel

156 Herein, a case of severe vemurafenib-induced granulomatous hepatitis leading to chronic cholestasis i

157 Treg cells to modulate the beryllium-induced granulomatous immune response.

158 elopment of the egg-induced T-helper 2 (Th2) granulomatous immune response.

159 that PTHrP expression is part of the normal granulomatous immune response.

160 correlates, high lung bacterial burden, and granulomatous immunopathology.

161 Ocular rhinosporidiosis is a chronic granulomatous infection caused by a newly classified org

162 By using a model of chronic granulomatous infection, we also show that lymphatic rem

163 is an uncommon complication of disseminated granulomatous infections.

164 on of PTHrP is the cause of hypercalcemia in granulomatous infections.

165 small vessel disease and other inflammatory, granulomatous, infective, metabolic, and genetic causes

166 ells and macrophages form tissue-destructive granulomatous infiltrates, and the artery responds with

167 ) T cells and macrophages to form prototypic granulomatous infiltrates.

168 the predominant finding (42.2%), followed by granulomatous inflammation (29%), steatosis/steatohepati

169 i develop severe CD4 T cell-mediated hepatic granulomatous inflammation against parasite eggs associa

170 nonhematopoietic cells may partly facilitate granulomatous inflammation and bacterial dissemination.

171 humans is attributed to parasite egg-induced granulomatous inflammation and fibrosis in the host live

172 Crohn disease (CD) are both characterized by granulomatous inflammation and related to nucleotide oli

173 occupational lung disorder characterized by granulomatous inflammation and the accumulation of beryl

174 crotizing vasculitis that is associated with granulomatous inflammation and the presence of anti-neut

175 nsure that any further complications such as granulomatous inflammation are managed and documented.

176 CBA/J (CBA) mice develop severe hepatic granulomatous inflammation associated with prominent Th1

177 Exserohilum provokes robust neutrophilic and granulomatous inflammation capable of thwarting fungal g

178 understanding of the pathways underlying the granulomatous inflammation characteristic of sarcoidosis

179 ysis of all 3 cases revealed elastolysis and granulomatous inflammation characterized by multinucleat

180 -->TLR2KO) exhibited a marked attenuation in granulomatous inflammation compared with WT mice.

181 Granulomatous inflammation consistent with Crohn's disea

182 linical presentation, finding nonnecrotizing granulomatous inflammation in one or more tissue samples

183 The granulomatous inflammation in the bowel of patients with

184 ritical for the development of Th17-mediated granulomatous inflammation in the lung in response to S.

185 dritic cell-mediated development of a type 1 granulomatous inflammation in the lung in response to SC

186 responses are required for the generation of granulomatous inflammation induced by inhaled S. chartar

187 responses are required for the generation of granulomatous inflammation induced by inhaled SC.

188 Granulomatous inflammation is characteristic of many aut

189 Extravascular granulomatous inflammation may be initiated by ANCA-indu

190 lated mainly to the egg stage, which induces granulomatous inflammation of affected tissues.

191 se resulting from lymphocytic and frequently granulomatous inflammation of the peripheral airways, al

192 is (GPA; or Wegener's granulomatosis) is the granulomatous inflammation of the upper respiratory trac

193 Sarcoidosis is a disorder characterized by granulomatous inflammation of unclear etiology.

194 is syndrome had chronic active colitis, with granulomatous inflammation present in 7 of 11 patients (

195 SC-mediated granulomatous inflammation required IFN-gamma and was TL

196 S. chartarum-mediated granulomatous inflammation required intact IL-23 or IL-1

197 in 2 patients and demonstrated noncaseating granulomatous inflammation surrounding tattoo ink in the

198 ith schistosome helminths is associated with granulomatous inflammation that forms around parasite eg

199 While a non-degradable UPS polymer induces granulomatous inflammation that persists over months at

200 by biopsy identification of suppurative and granulomatous inflammation with fungal elements.

201 The pathology of human coccidioidomycosis is granulomatous inflammation with many neutrophils surroun

202 nge with 10(6) S. chartarum spores developed granulomatous inflammation with multinucleate giant cell

203 and challenged with 10(6) SC spores develop granulomatous inflammation with multinucleate giant cell

204 With granulomatous inflammation, 52% met the criteria for tub

205 exclude infectious and autoimmune causes of granulomatous inflammation, followed by dermatologic wor

206 Since both responses usually correlate with granulomatous inflammation, we tested six prominently ex

207 but these may include carcinogenic change or granulomatous inflammation.

208 intravenously into eight mice bearing local granulomatous inflammation.

209 nocytes, and macrophages and produce typical granulomatous inflammation.

210 necrotizing vasculitis, and eosinophil-rich granulomatous inflammation.

211 d by degradation of interstitial crystals by granulomatous inflammation.

212 attenuated P. acnes-induced ear swelling and granulomatous inflammation.

213 of HPS and CD, 2 entities characterized by a granulomatous inflammatory reaction pattern but with uni

214 BeS with evidence of a granulomatous inflammatory response in the lung is diagn

215 two models, with CFA causing a nonresolving granulomatous inflammatory response whereas tissue incis

216 s, but not JAK/STAT signaling, can attenuate granulomatous interstitial nephritis.

217 controlling Johne's disease (JD), a chronic granulomatous intestinal inflammatory disease caused by

218 amination revealed the presence of bilateral granulomatous keratic precipitates, anterior chamber cel

219 activated endothelium into the valve to form granulomatous lesions and Aschoff bodies.

220 ve to conditions likely to be present within granulomatous lesions and mediate aspects of M. tubercul

221 lammatory myeloid neoplasia characterized by granulomatous lesions containing pathological CD207(+) d

222 there are no good models that replicate the granulomatous lesions found in granulomatosis with polya

223 f Crohn disease (CD); however, mucocutaneous granulomatous lesions have not been considered among the

224 This bacterium persists within granulomatous lesions in a poorly characterized, nonrepl

225 his study, we show that Wnt6 is expressed in granulomatous lesions in the lung of Mycobacterium tuber

226 hich were observed in close proximity within granulomatous lesions in the lungs of GPA patients.

227 D4(+) T cells and macrophages form organized granulomatous lesions in the walls of affected arteries,

228 induced in the lungs and particularly in the granulomatous lesions of macaques experimentally infecte

229 ammoma body calcifications indicative of the granulomatous lesions that occur during Leishmania infec

230 Tuberculous pneumonia, necrotic granulomatous lesions, and bacterial dissemination chara

231 olytic enzymes in macrophages and T cells in granulomatous lesions.

232 r accumulating only in peripheral regions of granulomatous lesions.

233 We present a case of symptomatic granulomatous liver disease secondary to sarcoidosis, mi

234 Chronic beryllium disease (CBD) is a granulomatous lung disease characterized by the accumula

235 sensitivity pneumonitis; other noninfectious granulomatous lung diseases, including sarcoidosis; and

236 Chronic beryllium disease (CBD) is a granulomatous lung disorder caused by a hypersensitivity

237 Sarcoidosis is a granulomatous lung disorder of unknown cause.

238 Chronic beryllium (Be) disease is a granulomatous lung disorder that results from Be exposur

239 n exposure, these mice developed more robust granulomatous lung fibrosis than wild-type counterparts.

240 -4Ralpha were associated with development of granulomatous lung inflammation triggered by silica.

241 -negative bacillus initially isolated from a granulomatous lung lesion.

242 In situ hybridization of sarcoidosis granulomatous lung tissues showed abundance of HIF-1alph

243 Patient 2 developed inguinal granulomatous lymphadenitis about 40 days after onset of

244 necrotizing vasculitis, glomerulonephritis, granulomatous lymphadenitis, and bronchointerstitial pne

245 , HP is characterized by a bronchiolocentric granulomatous lymphocytic alveolitis, which evolves to f

246 a chronic and destructive, small bile duct, granulomatous lymphocytic cholangitis, with typical sero

247 d manifestations (notably the development of granulomatous-lymphocytic interstitial lung disease in C

248 sy of 2 eyes of 1 patient revealed prominent granulomatous lymphohistiocytic choroiditis with giant c

249 anent vision loss, 30 (94%) had a subretinal granulomatous mass/scar, peripheral granuloma with tract

250 Subretinal granulomatous mass/scar, vitritis, and scotoma were the

251 ssociated with inflammatory breast diseases (granulomatous mastitis and acute suppurative mastitis) a

252 s of false positive benign lesions, such as: granulomatous mastitis, sclerosing adenosis, chronic inf

253 Fatal cases had necrosuppurative to granulomatous meningitis and vasculitis, with thrombi an

254 1-like macrophages with adenosine attenuated granulomatous nephritis and the progressive decline in G

255 emia and chronic UA crystal nephropathy with granulomatous nephritis.

256 emarkably, one celiac patient presented with granulomatous nodulae in the ileum, thus reflecting an i

257 t, metastatic disease, where ulcerations and granulomatous nodules can affect multiple secondary site

258 hils were detected, GPTD does not resemble a granulomatous or eosinophilic condition.

259 ing complaint for systemic disorders such as granulomatous or eosinophilic polyangiitis, and sarcoido

260 e remaining 2 patients had bilateral chronic granulomatous panuveitis.

261 antly diminished clinical manifestations and granulomatous pathology and characterized by the presenc

262 that a subset of severe "asthma" manifests a granulomatous pathology, which we term "asthmatic granul

263 NOD2) and is phenotypically characterized by granulomatous polyarthritis and uveitis.

264 It is a granulomatous process with the possibility of palisading

265 her, variable manifestations included atopy, granulomatous rash, autoimmune thyroiditis, the presence

266 ines from these CAR T cells in vivo drives a granulomatous reaction resulting in chronic toxicity.

267 ells in the mediastinal lymph nodes and lung granulomatous regions while concomitantly accelerating t

268 57BL6/J lacking SK1), to investigate how the granulomatous response and SK1-S1P pathway are interrela

269 For the host, the granulomatous response can be both protective and pathol

270 y showed that B cells can modulate the local granulomatous response in M. tuberculosis-infected macaq

271 perienced a maturation defect of the ex vivo granulomatous response involving monocytes as well as na

272 apped eggs induce a distinct immune-mediated granulomatous response that causes local and systemic pa

273 ant cells is a distinguishing feature of the granulomatous response to inflammation, infection, and f

274 rain injury patients to develop an effective granulomatous response to mycobacteria.

275 We used zebrafish larvae to visualize the granulomatous response to Schistosomamansoni eggs and in

276 rine proteases for antibacterial protection, granulomatous response, and survival.

277 en- (Ag-) Ag-coated beads to elicit a recall granulomatous response, CCR4(-/-) mice displayed abrogat

278 ular killing by phagocytes, and generating a granulomatous response.

279 ity to M. tuberculosis in the context of the granulomatous response.

280 s a significant decrease in the intensity of granulomatous responses to bladder-wall-injected S. haem

281 the phenotypes of recruited T cells, and the granulomatous responses were also similar between WT and

282 y pulmonary infections, chronic invasive and granulomatous rhinosinusitis, and aspergillus bronchitis

283 Inflammation from injections is granulomatous, seen only with intravitreal injections, a

284 -FDG PET/CT for detection of inflammation in granulomatous sites and management of patients with chro

285 Using an ovine model of granulomatous skin inflammation, we demonstrate that B c

286 Granulomatous skin lesions sparing warm regions (eg, fle

287 are found within the mycobacterially induced granulomatous structure in the livers of infected Rag2(-

288 eficient macrophages formed mTORC1-dependent granulomatous structures in vitro and showed constitutiv

289 e from long-term persistent infection within granulomatous structures.

290 The large B-cell infiltrates in granulomatous tissue and increased molecular signs of an

291 These data demonstrate that surveillance of granulomatous tissue by CD11c+ cells is continuous and t

292 phage differentiation program that regulates granulomatous tissue remodeling.

293 el sprouting and increased lymphatic area in granulomatous tissue.

294 Giant cell arteritis is a granulomatous vasculitis of the aorta and its branches t

295 based on findings of eosinophil-infiltrating granulomatous vasculitis of the skin accompanied by nota

296 mic antibodies (ANCA)-associated necrotizing granulomatous vasculitis that affects small to medium si

297 Vitreitis and granulomatous vasculitis were noted in 7 of 30 intravitr

298 Patients with a cytologic diagnosis of granulomatous vitritis seeking treatment from 2004 throu

299 three patients with a cytologic diagnosis of granulomatous vitritis were identified, 8 of whom demons

300 e patients were diagnosed cytologically with granulomatous vitritis.