戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 th chronic inflammation, including anemia of chronic kidney disease.
2 ibrosis in tissue samples from patients with chronic kidney disease.
3 ne and in human donors of kidney tissue with chronic kidney disease.
4 , increasing age, diabetes, hypertension and chronic kidney disease.
5 naemia and states of FGF23 excess, including chronic kidney disease.
6 n obesity and rheumatoid arthritis, and 2 on chronic kidney disease.
7 sed to diagnose and classify the severity of chronic kidney disease.
8 ith acute kidney injury or those at risk for chronic kidney disease.
9 associated with multiple diseases, including chronic kidney disease.
10 te levels are associated with progression of chronic kidney disease.
11 ce interval: 1.16, 1.74) among patients with chronic kidney disease.
12 ation is essential to prevent progression to chronic kidney disease.
13 erm profibrotic responses that could lead to chronic kidney disease.
14 isk of renal events than in patients without chronic kidney disease.
15  nephropathy has altered the epidemiology of chronic kidney disease.
16 in modulating pruritus in conditions such as chronic kidney disease.
17 ease, stroke, peripheral artery disease, and chronic kidney disease.
18  incomplete or maladaptive kidney repair and chronic kidney disease.
19 ular and total mortality, and progression of chronic kidney disease.
20 er renal IRI, thus preventing progression to chronic kidney disease.
21 nting for ~5% of monogenic disorders causing chronic kidney disease.
22 ed numbers of patients with high CV risk and chronic kidney disease.
23  or follow AKI in a continuum with acute and chronic kidney disease.
24 ment for metabolic acidosis in patients with chronic kidney disease.
25 ndrial energy metabolism may be causative to chronic kidney disease.
26  with type 2 diabetes and moderate-to-severe chronic kidney disease.
27 ut prior heart failure or moderate to severe chronic kidney disease.
28 t baseline was a better predictor of time to chronic kidney disease.
29  glomerular filtration rate in patients with chronic kidney disease.
30 ll-known clinical biomarker for the onset of chronic kidney disease.
31 d predicts accelerated functional decline in chronic kidney disease.
32  hypertension, type 2 diabetes mellitus, and chronic kidney disease.
33 s in two cohorts totaling 3315 patients with chronic kidney disease.
34 tage kidney disease, even at early stages of chronic kidney disease.
35 mediated by the known APOL1 association with chronic kidney disease.
36 which serves as a critical factor leading to chronic kidney disease.
37 on, treatment with ferric carboxymaltose and chronic kidney disease.
38 ncreased risk of developing hypertension and chronic kidney disease.
39  have routinely excluded those with advanced chronic kidney disease.
40 key biomarker for cardiovascular disease and chronic kidney disease.
41 population with type 2 diabetes and advanced chronic kidney disease.
42 ve therapies for the management of acute and chronic kidney disease.
43  diagnosis and prognostication for acute and chronic kidney diseases.
44 ns, sepsis, and ischemia/reperfusion, and in chronic kidney diseases.
45 eir damage contributes to the progression of chronic kidney diseases.
46 ase (1.3 [1.3-1.4]), stroke (2.2 [2.1-2.2]), chronic kidney disease (1.7 [1.7-1.8]), and peripheral a
47 emia (72.1%), diabetes mellitus (31.6%), and chronic kidney disease (28.2%); 20.2% received warfarin
48 disease, 12.8% (n=59), cancer, 11.7% (n=54), chronic kidney disease, 3.9% (n=18) and inflammatory bow
49 disease 1.6 (1.5-1.7), stroke 6.4 (6.3-6.5), chronic kidney disease 4.4 (4.3-4.6), and peripheral art
50 le on-switches in gene therapy for anemia of chronic kidney disease(6), we demonstrated regulated exp
51                                              Chronic kidney disease (89% vs 57% P = .0007), diabetes
52                                              Chronic kidney disease affects >15% of the U.S. populati
53                                              Chronic kidney disease affects 10% of the population wit
54  = 0.004), hypertension, hyperlipidemia, and chronic kidney disease (all p < 0.001).
55 e, moderate or severe ischemia, and advanced chronic kidney disease (an estimated glomerular filtrati
56                          Among patients with chronic kidney disease, an untargeted serum metabolomics
57                             In patients with chronic kidney disease and a high risk of progression, u
58 ture mortality from substance use disorders, chronic kidney disease and acute glomerulonephritis, and
59  Albuminuria acts as a marker of progressive chronic kidney disease and as an indicator for initiatio
60  metabolic acidosis including progression of chronic kidney disease and bone health.
61 ract (CAKUTs) represent the leading cause of chronic kidney disease and end-stage kidney disease in c
62 requently reported in patients with advanced chronic kidney disease and is associated with early allo
63 ments are determined in patients with stable chronic kidney disease and may not translate to patients
64 hypertension, obesity, diabetes mellitus and chronic kidney disease and might contribute to disease b
65 e randomly assigned adults with stage 3 or 4 chronic kidney disease and no history of gout who had a
66  accumulate during aging, diabetes mellitus, chronic kidney disease and other chronic diseases.
67                 Conclusion For patients with chronic kidney disease and small renal tumors, personali
68 and cardiovascular outcomes in patients with chronic kidney disease and type 2 diabetes with optimize
69                          Among patients with chronic kidney disease and type 2 diabetes, finerenone r
70  weight, the risk of developing or worsening chronic kidney disease and/or atherosclerotic cardiovasc
71 ardiovascular disease (CVD) in patients with chronic kidney diseases and rheumatologic disorders.
72 athies, obesity, hypertension, diabetes, and chronic kidney disease) and yielded additional insights
73 stolic hypertension, -10.1 +/- 20.3 mm Hg in chronic kidney disease, and -10.0 +/- 19.1 mm Hg in atri
74  = 1.2-2.1 for >80 g/day), as were diabetes, chronic kidney disease, and end-stage liver disease (HR
75 ion such as in those with diabetes mellitus, chronic kidney disease, and high risk of future atherosc
76                                  Higher age, chronic kidney disease, and higher Charlson score increa
77 ients with stable coronary disease, advanced chronic kidney disease, and moderate or severe ischemia,
78 ion in the general population, patients with chronic kidney disease, and patients with heart failure.
79               Diabetes is a leading cause of chronic kidney disease, and the high prevalence of sympa
80 th peptic ulcer disease, depression, asthma, chronic kidney disease, and venous thromboembolism.
81 ociated with PH among patients with advanced chronic kidney disease appears to differ by etiology.
82 rbid conditions, including heart failure and chronic kidney disease, are increasingly prevalent in pa
83 athogenesis of acute kidney injury (AKI) and chronic kidney disease, as well as in abnormal kidney re
84      In a subgroup of patients with advanced chronic kidney disease at baseline (estimated glomerular
85                                              Chronic kidney disease at baseline was noted in 29% of p
86   Identification of people with diabetes and chronic kidney disease at high-risk of early mortality i
87 ngth (per mm; beta = -1.54), and presence of chronic kidney disease (beta = -1.49) were significantly
88         We found differences in incidence of chronic kidney disease between clusters; however, estima
89 y as a surrogate endpoint for progression of chronic kidney disease, but empirical evidence to suppor
90 Th17 cells play a role in the progression of chronic kidney disease, but the endogenous pathways that
91 relationship between periodontal disease and chronic kidney disease, but there is little evidence to
92 , the use of spironolactone in patients with chronic kidney disease can be restricted by hyperkalaemi
93 te risk equations for outcomes and develop a chronic kidney disease-cardiovascular disease (CKD-CVD)
94        Metabolic acidosis, a complication of chronic kidney disease, causes protein catabolism and bo
95  heart failure, peripheral vascular disease, chronic kidney disease, chronic obstructive pulmonary di
96 disease (OR 3.43, 95% CI 1.17 to 10.00), and chronic kidney disease (CKD) (OR 2.81, 95% CI 1.97 to 4.
97                      Our primary outcome was chronic kidney disease (CKD) - defined as confirmed decr
98                                              Chronic kidney disease (CKD) affects ~10% of the global
99                                Transition to chronic kidney disease (CKD) after an episode of acute k
100        A high proportion of patients develop chronic kidney disease (CKD) after liver transplantation
101                                              Chronic kidney disease (CKD) and aortic stenosis (AS) sh
102                                Patients with chronic kidney disease (CKD) and coincident heart failur
103 M(2.5)) is associated with increased risk of chronic kidney disease (CKD) and diabetes, a causal driv
104                         Associations between chronic kidney disease (CKD) and the gut microbiota have
105 in short-term trials involving patients with chronic kidney disease (CKD) and type 2 diabetes.
106                                 Persons with chronic kidney disease (CKD) are at high risk of infecti
107                                  Adults with chronic kidney disease (CKD) are hospitalized more frequ
108 rtality (ACM), but data at earlier stages of chronic kidney disease (CKD) are inconclusive.
109 ic features implicated in the progression of chronic kidney disease (CKD) are interstitial fibrosis a
110                                Patients with chronic kidney disease (CKD) are often 25(OH)D(3) and 1,
111 nd C-reactive protein (CRP) in patients with chronic kidney disease (CKD) are presented.
112 y protease inhibitors pose a similar risk of chronic kidney disease (CKD) as use of older protease in
113 re categorized by the presence or absence of chronic kidney disease (CKD) at baseline (estimated glom
114 d subnetworks that potentially differentiate chronic kidney disease (CKD) by severity or progression.
115   Although often considered a single-entity, chronic kidney disease (CKD) comprises many pathophysiol
116                                    The Japan Chronic Kidney Disease (CKD) Database (J-CKD-DB) is a la
117                                Patients with chronic kidney disease (CKD) exhibit reduced exercise ca
118                                              Chronic kidney disease (CKD) has a rapidly rising global
119 lance and whether their activities change in chronic kidney disease (CKD) has not yet been elucidated
120                                Patients with chronic kidney disease (CKD) have inability to maintain
121                                              Chronic kidney disease (CKD) in low-resource settings po
122 lar disease (ASCVD), heart failure (HF), and chronic kidney disease (CKD) in the ARIC Study.
123                      It is hypothesized that chronic kidney disease (CKD) induces oxidant stress whic
124                                              Chronic kidney disease (CKD) is a common complication of
125                                              Chronic kidney disease (CKD) is a global health epidemic
126                                              Chronic kidney disease (CKD) is a growing health burden
127                                              Chronic kidney disease (CKD) is a major risk factor for
128 Rac promotes tubulointerstitial fibrosis and chronic kidney disease (CKD) is currently unknown.
129                                              Chronic kidney disease (CKD) is deemed to be a worldwide
130                  Data on PCSK9 inhibition in chronic kidney disease (CKD) is limited.
131                                              Chronic kidney disease (CKD) is responsible for a public
132                                              Chronic kidney disease (CKD) is the 16th leading cause o
133 linical risk factors, and antiretrovirals to chronic kidney disease (CKD) is unknown.
134 ed with increased mortality and morbidity in chronic kidney disease (CKD) patients, especially in the
135 ophan has been associated with lower risk of chronic kidney disease (CKD) progression, implicating me
136 ssed in the kidney, but its possible role in chronic kidney disease (CKD) remains largely unknown.
137 e (SIHD) who have type 2 diabetes (T2DM) and chronic kidney disease (CKD) remains unclear.
138                 The increasing prevalence of chronic kidney disease (CKD) seriously is threatening hu
139 roke), and safety were analyzed according to chronic kidney disease (CKD) stage estimated from CKD-ep
140 urpose of this study was to assess change in chronic kidney disease (CKD) stage following TAVR, ident
141  exemplify this data integration issue for a chronic kidney disease (CKD) study, comprising complex c
142                                              Chronic kidney disease (CKD) substantially increases the
143 r filtration rate (eGFR) in individuals with chronic kidney disease (CKD) to predict the risk of end
144  rare, hereditary cause of kidney stones and chronic kidney disease (CKD) which is characterized by 2
145                                              Chronic kidney disease (CKD) with type 2 diabetes (T2D)
146 y injury (AKI) within 3 months and new-onset chronic kidney disease (CKD) within 1 year following hos
147 atients with heart failure (HF) and advanced chronic kidney disease (CKD), a population underrepresen
148 diabetes duration, retinopathy, nephropathy, chronic kidney disease (CKD), and anaemia as predictors
149 Hyperuricaemia is common among patients with chronic kidney disease (CKD), and increases in severity
150 eous ablation for risk factors for worsening chronic kidney disease (CKD), and otherwise PN; biopsy,
151  in conditions such as diabetes mellitus and chronic kidney disease (CKD), and they may be involved i
152  rare, hereditary cause of kidney stones and chronic kidney disease (CKD), characterized by 2,8-dihyd
153                                              Chronic kidney disease (CKD), commonly fostering nonrena
154                    Women with a diagnosis of chronic kidney disease (CKD), CVD, hypertension, or diab
155 y virus (HIV) infection have higher risk for chronic kidney disease (CKD), defined by a reduced estim
156                                              Chronic kidney disease (CKD), defined by low estimated g
157 gest new treatments for more common forms of chronic kidney disease (CKD), demonstrating the importan
158 lied to a range of human diseases, including chronic kidney disease (CKD), epilepsy, and amyotrophic
159              Felids have a high incidence of chronic kidney disease (CKD), for which the most common
160 he aetiology of cardiometabolic diseases and chronic kidney disease (CKD), in part via metabolism of
161 ally relevant to metabolic diseases, such as chronic kidney disease (CKD), in which dietary approache
162       Diabetes is the most frequent cause of chronic kidney disease (CKD), leading to nearly half of
163 ted retinopathy and modestly associated with chronic kidney disease (CKD), peripheral artery disease
164                          In animal models of chronic kidney disease (CKD), re-activation of BMP signa
165                             In patients with chronic kidney disease (CKD), reverse left ventricular (
166 and creatinine is an important biomarker for chronic kidney disease (CKD), we tested the FOLP probe f
167   An estimated glomerular filtration rate by chronic kidney disease (CKD)-EPI-CysC-creatinine <60 mL/
168 perphosphatemia as in tumoral calcinosis and chronic kidney disease (CKD).
169 M1A and PTEN emerged as novel suppressors of chronic kidney disease (CKD).
170 equisite for effective therapy in preventing chronic kidney disease (CKD).
171  kidney failure or death in individuals with chronic kidney disease (CKD).
172 ertrophy, and fibrosis, is a complication of chronic kidney disease (CKD).
173  a modifiable risk factor for progression of chronic kidney disease (CKD).
174  material for MR angiography for safe use in chronic kidney disease (CKD).
175 is activity in acute kidney injury (AKI) and chronic kidney disease (CKD).
176 on (MAC) is a common outcome in diabetes and chronic kidney disease (CKD).
177 in the United States-37 million persons-have chronic kidney disease (CKD).
178 troke (ST), cardiovascular disease (CVD) and chronic kidney disease (CKD).
179 etiology of secondary hyperparathyroidism in chronic kidney disease (CKD).
180 in skin is a common symptom in patients with chronic kidney disease (CKD).
181 ery disease, cancer, liver-, rheumatic-, and chronic kidney disease (CKD).
182 f drug-induced acute kidney injury (AKI) and chronic kidney disease (CKD).
183  baclofen to encephalopathy in patients with chronic kidney disease (CKD).
184 on absorption, and amelioration of anemia in chronic kidney disease (CKD).
185 ith atherosclerotic disease in patients with chronic kidney disease (CKD).
186 es a phenotype strikingly similar to that of chronic kidney disease (CKD).
187 ility and is commonly found in patients with chronic kidney disease (CKD).
188 ed number of older LT recipients with pre-LT chronic kidney disease (CKD).
189 te kidney injury [AKI] and atrophy-fibrosis [chronic kidney disease (CKD)] and rejection.
190 ssion models and stratified for diabetes and chronic kidney disease (CKD, defined as estimated glomer
191  intervals: 0.07% overall, 0.2% for stage 5D chronic kidney disease [CKD], 0.5% for stage 5 CKD and n
192                                              Chronic kidney diseases (CKDs) are currently classified
193          Clearance of 25-hydroxyvitamin D in Chronic Kidney Disease (CLEAR), NCT02937350; Clearance o
194 betes in coronary artery disease, stroke and chronic kidney disease, complemented by a systematic rev
195 e aimed to investigate the relations between chronic kidney disease, coronary microvascular dysfuncti
196                                Most forms of chronic kidney disease culminate in renal fibrosis that
197 y: Diet or Diuretics for Salt-sensitivity in Chronic Kidney Disease (DD), NCT02875886.
198  and analyze the association between AKI and chronic kidney disease (defined as at least mildly decre
199 tients with atrial fibrillation and advanced chronic kidney disease (defined as creatinine clearance
200 e/incidence of cardiovascular disease (CVD), chronic kidney disease, depression, diabetes, high total
201 specific expression of genes associated with chronic kidney disease, diabetes and hypertension, provi
202 ailure, peripheral arterial disease, asthma, chronic kidney disease, diabetes or COPD in the 12 month
203 and atherosclerosis), comorbidities (anemia, chronic kidney disease, diabetes, and so on), and diseas
204 isk were most sensitive to the prevalence of chronic kidney disease, diabetes, cardiovascular disease
205 ailure, peripheral arterial disease, asthma, chronic kidney disease, diabetes, or COPD in the 12 mont
206 and/or myocardial infarction, heart failure, chronic kidney disease, dialysis, stroke, inpatient admi
207 e, moderate or severe ischemia, and advanced chronic kidney disease did not have substantial or susta
208 ary artery disease among individuals without chronic kidney disease during the 12.5-year follow-up pe
209                                    Acute and chronic kidney disease encompasses a complex set of dise
210 ons between PPI use and acute kidney injury, chronic kidney disease, end-stage renal disease, and ele
211                  GRAIL was compared with the Chronic Kidney Disease Epidemiology Collaboration (CKD-E
212                   Individuals with 2 or more Chronic Kidney Disease Epidemiology Collaboration (CKD-E
213 d glomerular filtration rate (eGFR) with the Chronic Kidney Disease Epidemiology Collaboration (CKD-E
214 n Study (CKiD) equation for children and the Chronic Kidney Disease Epidemiology Collaboration (CKD-E
215 ndomization to week 104, calculated with the Chronic Kidney Disease Epidemiology Collaboration creati
216 st error were observed with cystatin C-based chronic kidney disease epidemiology collaboration equati
217  glomerular filtration rate (eGFR) using the Chronic Kidney Disease Epidemiology Collaboration equati
218 al contribution to the future development of chronic kidney disease, ESKD, and mortality.
219  mellitus (glycated hemoglobin level, >=7%), chronic kidney disease (estimated glomerular filtration
220 aged 18-85 years with non-dialysis-dependent chronic kidney disease (estimated glomerular filtration
221            Eligible patients were those with chronic kidney disease (estimated glomerular filtration
222 t time of LTBI testing (e.g., HIV, diabetes, chronic kidney disease, etc.) were identified from physi
223 tudied in the treatment of heart failure and chronic kidney disease, even in patients without diabete
224 e (ESKD) in 4,843 participants of the German Chronic Kidney Disease (GCKD) study.
225 replication in 765,289 participants from the Chronic Kidney Disease Genetics (CKDGen) Consortium.
226 lomerular filtration rate and lowest rate of chronic kidney disease (&gt;=stage 3) from year 1 onwards u
227                                Patients with chronic kidney disease had elevated serum levels of IL-2
228 hoice of optimal chemotherapy and prognosis, chronic kidney disease has drawn attention in the treatm
229 e on patients with chronic heart failure and chronic kidney disease has identified hypochloremia as a
230 e general population, patients with advanced chronic kidney disease have a >10-fold higher burden of
231                                              Chronic kidney diseases have become a major issue worldw
232 tension, coronary artery disease, arthritis, chronic kidney disease, heart failure, stroke, asthma, c
233 h diabetes (HR, 1.95; 95% CI, 1.06-3.58) and chronic kidney disease (HR, 1.97; 95% CI, 1.05-3.67) eme
234 rrhythmias (HR: 1.62; 95% CI: 1.28 to 2.05), chronic kidney disease (HR: 2.41; 95% CI: 1.54 to 3.78),
235 es and established cardiovascular disease or chronic kidney disease, if kidney function is adequate.
236 d simple method of screening for the risk of chronic kidney disease in adults.
237                          Using data from the Chronic Kidney Disease in Children (CKiD) study, we exam
238                                          The Chronic Kidney Disease in Children Study (CKiD) equation
239                                          The Chronic Kidney Disease in Children Study, a prospective
240 618 children and adolescents enrolled in the Chronic Kidney Disease in Children study, an observation
241                                              Chronic kidney disease in combination with anemia was th
242 fects and represent the most common cause of chronic kidney disease in the first three decades of lif
243 y tract (CAKUT) are the most common cause of chronic kidney disease in the first three decades of lif
244 disease in clinical trials of progression of chronic kidney disease in the setting of increased album
245 increased risk of cardiovascular disease and chronic kidney disease in those with gout, novel associa
246 ase III clinical trials for the treatment of chronic kidney disease in type 2 diabetes.
247                  Biopsies from patients with chronic kidney disease, including AS were compared with
248 re urgently needed in patients with advanced chronic kidney disease, including those receiving dialys
249 d frequently occurs in patients with cancer, chronic kidney disease, infection, and many other illnes
250 ron deficiency, which include heart failure, chronic kidney disease, inflammatory bowel disease, pati
251                                              Chronic kidney disease is a common comorbid condition am
252                                              Chronic Kidney Disease is a growing problem across the w
253                                              Chronic kidney disease is a public health burden and it
254                                              Chronic kidney disease is associated with an increased r
255                                     Advanced chronic kidney disease is associated with further cortic
256                                     Although chronic kidney disease is associated with reduced graft
257              In patients with heart failure, chronic kidney disease is common and associated with a h
258                                              Chronic kidney disease is divided into 5 groups, ranging
259 sodium reabsorption during the initiation of chronic kidney disease is not established.
260 cal treatments for kidney disease - by 2040, chronic kidney disease is projected to be the fifth lead
261                                              Chronic kidney disease, lactate, ferritin, and fibrinoge
262 idney injury and those with risk factors for chronic kidney disease limit conclusions about safety in
263                       Patients with advanced chronic kidney disease lose the capacity to fully excret
264                 Prediction of development of chronic kidney disease (mGFR < 20 mL/min/1.73 m(2) , ini
265 displays multiple key features of late stage chronic kidney disease-mineral bone disorder (CKD-MBD),
266 therosclerosis, hypertension, heart failure, chronic kidney disease, obesity, and type 2 diabetes mel
267 idities, the most common being hypertension, chronic kidney disease, obstructive sleep apnoea, and me
268 dney repair after acute kidney injury and to chronic kidney disease of varied aetiologies, including
269 scular dysfunction may mediate the effect of chronic kidney disease on abnormal cardiac function and
270 dministrations in patients with stage 4 or 5 chronic kidney disease or undergoing dialysis, the upper
271                                  Conversely, chronic kidney disease (OR, 0.53) and invasive mechanica
272 aturation (OR, 0.94 [95% CI 0.93-0.96]), and chronic kidney disease (OR, 1.53 [95% CI 1.20-1.95]) wer
273 core of >=8 (p < 0.0001), anemia (p = 0.02), chronic kidney disease (p = 0.003), and higher N-termina
274 ic obstructive pulmonary disease (P = 0.73), chronic kidney disease (P = 0.09), and hearing loss (P =
275                                              Chronic kidney disease (P=0.02), prior cancer treatment
276 are effective for the treatment of anemia in chronic kidney disease patients and may also be benefici
277  In patients with resistant hypertension and chronic kidney disease, patiromer enabled more patients
278 s of 1-year mortality were old age, anaemia, chronic kidney disease, presence of valvular heart disea
279 CKD to kidney failure was assessed using the Chronic Kidney Disease Prognosis Consortium (CKD-PC) equ
280 dual-level data from eligible cohorts in the Chronic Kidney Disease Prognosis Consortium (CKD-PC) wit
281           Kidney fibrosis is the hallmark of chronic kidney disease progression; however, at present
282 c susceptibility of complex diseases such as chronic kidney disease remains challenging.
283 delivery approaches for acute kidney injury, chronic kidney disease, renal fibrosis, renovascular hyp
284 ellitus, hypertension, hypercholesterolemia, chronic kidney disease, smoking, and exercise.
285  cohort of patients with type 2 diabetes and chronic kidney disease, sTNFR1 predicted short-to-medium
286 dary Care Partnership to Improve Outcomes in Chronic Kidney Disease study.
287  daily for patients with or without advanced chronic kidney disease, supporting conventional dosing i
288 nces of obesity, diabetes, hypertension, and chronic kidney disease than white patients.
289 tion in patients over 60 years with advanced chronic kidney disease: the BiCARB RCT.
290 tcontrast acute kidney injury in adults with chronic kidney disease: the Kompas randomized clinical t
291 atients with type 2 diabetes and albuminuric chronic kidney disease to receive canagliflozin, an oral
292 nt diabetes, hypertension, dyslipidemia, and chronic kidney disease were investigated using survival
293 t males, hypertension, diabetes, obesity and chronic kidney disease were most frequent in the COVID-1
294 onstitutional disorders in adults, including chronic kidney disease, which affects more than 1 in 10
295 ular filtration rate (eGFR) in patients with chronic kidney disease who are at risk for progression i
296  testing in an African American patient with chronic kidney disease who is being evaluated for a kidn
297 f renal events in patients with diabetes and chronic kidney disease who were selected to optimise eff
298 scular events in patients with diabetes with chronic kidney disease with or without albuminuria have
299                In patients with diabetes and chronic kidney disease, with or without albuminuria, sot
300 lar events are prevalent among patients with chronic kidney disease without overt obstructive coronar

 
Page Top