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1 nts were imaged with approximately 74 MBq of intraventricular (124)I-omburtamab via an Ommaya reservo
2 eurologic effects, such as ventriculomegaly, intraventricular adhesions, subependymal cysts, intracer
3             The aim is to review the role of intraventricular administration of antimicrobial agents
4                                              Intraventricular administration of antimicrobials may be
5 e to seizure-induced hippocampal damage, and intraventricular administration of leptin protects neuro
6                Consistent with this finding, intraventricular administration of melanotan-2, an analo
7                                              Intraventricular administration of MSCs in ICH rat model
8                                      In vivo intraventricular administration of the Lck-I using an or
9                                 In addition, intraventricular administration of VEGFB restored neurog
10  day-30 mortality and partially mitigated by intraventricular alteplase.
11 dymal denudation, and damage and scarring of intraventricular and parenchymal (glia-lymphatic) CSF pa
12                                              Intraventricular anti-miR-155 treatment derepressed micr
13       This article discusses indications for intraventricular antimicrobial agents, choice of antibio
14                                              Intraventricular baclofen pretreatment in rats subjected
15         Separate studies undertaken using an intraventricular balloon revealed no detrimental effects
16               Contractility was monitored by intraventricular balloon, energetics by (31)P nuclear MR
17 tfeeding < 3 months, artificial ventilation, intraventricular bleeding, and other perinatal adverse e
18 oid (Hijdra Sum Score 17 vs 14, p<0.001) and intraventricular blood (median IVH sum score 2 vs 1, p<0
19 h poor clinical grade, more subarachnoid and intraventricular blood seen on admission computed tomogr
20 hniques to remove clot, techniques to remove intraventricular blood, and management of intracranial p
21 cerebral ventricular drainage, 2) meticulous intraventricular catheter handling, 3) cerebrospinal flu
22                               No evidence of intraventricular clot was found.
23               In patients without AVB and no intraventricular conduction abnormalities, ventricular p
24 in 27 patients (left bundle branch block 17, intraventricular conduction defect 5, and right ventricu
25   Compared with women with no BBB, LBBB, and intraventricular conduction defect were strong predictor
26 io, 3.53; confidence interval, 2.14-5.81 for intraventricular conduction defect).
27                                        LBBB, intraventricular conduction defect, and RBBB combined wi
28  and indetermined-type BBBs (LBBB, RBBB, and intraventricular conduction defect, respectively).
29 proved cardiac contractility and ameliorated intraventricular conduction defects in LmnaH222P/H222P m
30 ubule cytoskeleton using Paclitaxel improved intraventricular conduction defects.
31  bundle branch block (HR=1.01, P=0.975), and intraventricular conduction delay (HR=1.31, P=0.172).
32 block (RBBB) in 48 patients, and nonspecific intraventricular conduction delay (IVCD) was present in
33 ure patients with narrow QRS and nonspecific intraventricular conduction delay (NICD) display a relat
34 mong Medicare-aged patients with nonspecific intraventricular conduction delay (NICD) versus right bu
35  of death in these patients who also have an intraventricular conduction delay and are treated with C
36                                   Left-sided intraventricular conduction delay is associated with mor
37 c imaging could be a more specific marker of intraventricular conduction delay rather than the surrog
38 of patients with left bundle branch block or intraventricular conduction delay treated with cardiac r
39 with advanced chronic heart failure (HF) and intraventricular conduction delay treated with optimal p
40  (LBBB; including right bundle branch block, intraventricular conduction delay) did not have clinical
41 h block, 18 left bundle branch block, and 12 intraventricular conduction delay).
42    Over half the affected cohort (28/52) had intraventricular conduction delay, or incomplete right b
43 ents with poor left ventricular function and intraventricular conduction delay.
44 icular ejection fraction of 35% or less, and intraventricular conduction delays (QRS > 120 ms), altho
45 for patients with advanced heart failure and intraventricular conduction delays and ventricular dyssy
46 ong patients with advanced heart failure and intraventricular conduction delays, but the cost effecti
47  block (LBBB), and in 15, it was nonspecific intraventricular conduction disturbance (NICD).
48 BB QRS pattern (right bundle-branch block or intraventricular conduction disturbances).
49 branch block, and 308 (17%) with nonspecific intraventricular conduction disturbances.
50 ction fraction of 30% or less, and prolonged intraventricular conduction with a QRS duration of 130 m
51       ECG QRS duration, a measure of cardiac intraventricular conduction, varies approximately 2-fold
52 raction order, and entropy (E), a measure of intraventricular contraction disorder, and interventricu
53 novel indices of synchrony (S), a measure of intraventricular contraction order, and entropy (E), a m
54 y awake rats to follow the redistribution of intraventricular contrast agent entrained to the light-d
55                                              Intraventricular corticosterone attenuated cocaine self-
56 te contraction, postsystolic shortening, and intraventricular delay were analyzed using 2-dimensional
57                                              Intraventricular delivery of EVP4593 in YAC128 mice resc
58 ded target cytotoxic concentrations after an intraventricular dose, but lumbar CSF concentrations 2 h
59  be easily achieved in ventricular CSF after intraventricular dosing.
60 ariety of schedules either by intralumbar or intraventricular drug delivery.
61 ariety of schedules either by intralumbar or intraventricular drug delivery.
62 ariety of schedules either by intralumbar or intraventricular drug delivery.
63                                Patients with intraventricular dyssynchrony on echocardiography were r
64  is characteristic for LBBB and results from intraventricular dyssynchrony.
65 re at the scene (p = .045), greater rates of intraventricular extension (p < .0001), and radiologic s
66 Scale (NIHSS) score, larger ICH, presence of intraventricular extension and use of proxy responders.
67 oedema with increased intracranial pressure, intraventricular extension of haemorrhage with hydroceph
68                               BACKGROUND AND Intraventricular extension of intracerebral haemorrhage
69                                              Intraventricular extension of intracerebral haemorrhage
70                                              Intraventricular extension of intracerebral hemorrhage (
71  (modified Rankin Scale score, 3-6), any new intraventricular extension or an increase in the modifie
72 igher diastolic blood pressure at the scene, intraventricular extension, and radiologically evident h
73                             IVH treatment by intraventricular fibrinolysis (IVF) was recently linked
74 , hypertrophy-related fetal gene expression, intraventricular fibrosis, cardiac apoptosis, and oxidat
75 his study sought to understand the impact of intraventricular flow patterns on filling and to assess
76                                              Intraventricular fluid dynamics can be assessed clinical
77                                        Thus, intraventricular fluid mechanics are an important determ
78 atients, designated PRE based on a decreased intraventricular gradient during exercise.
79 ients had no obstruction and 38 exhibited an intraventricular gradient, 9 of whom exhibited a decreas
80  paradoxical situations in which significant intraventricular gradients (>50 mm Hg) at rest occur in
81 t common underlying diagnoses were perinatal intraventricular haemorrhage (35.3%) and malformations (
82 oor outcome, but the significance of delayed intraventricular haemorrhage (dIVH) is less well defined
83 oor outcome, but the significance of delayed intraventricular haemorrhage (dIVH) is less well defined
84 eline and 24 h CTs, with dIVH defined as new intraventricular haemorrhage (IVH) on the latter scan.
85 icular haemorrhage volume (IVH) with/without intraventricular haemorrhage (IVH) over 24 h were estima
86 ntracerebral haemorrhage of 10-100 mL and no intraventricular haemorrhage admitted within 48 h of ict
87             INTERPRETATION: In patients with intraventricular haemorrhage and a routine extraventricu
88                                              Intraventricular haemorrhage is a major complication of
89                                              Intraventricular haemorrhage is a subtype of intracerebr
90                                           As intraventricular haemorrhage leads to an inflammatory re
91 cerebral haemorrhage volume less than 30 mL, intraventricular haemorrhage obstructing the 3rd or 4th
92 stently higher in the forebrain of pups with intraventricular haemorrhage relative to pups without in
93 mine whether a greater frequency of complete intraventricular haemorrhage removal via alteplase produ
94 29], p=0.420) was found after adjustment for intraventricular haemorrhage size and thalamic intracere
95 age size, age, Glasgow Coma Scale, stability intraventricular haemorrhage size, and clot location).
96 5% CI 1.2 to 3.5; p=0.01) and higher SAH and intraventricular haemorrhage sum scores (OR 1.05, 95% CI
97 c regression, and (2) of increased haematoma+intraventricular haemorrhage volume (IVH) with/without i
98                                              Intraventricular haemorrhage was diagnosed by head ultra
99 atic measurement methods; shape, density and intraventricular haemorrhage were also assessed.
100                                The pups with intraventricular haemorrhage were treated with inhibitor
101     To this end, we used our rabbit model of intraventricular haemorrhage where premature pups, deliv
102 e aimed to test whether attempting to remove intraventricular haemorrhage with alteplase versus salin
103 ase-2 in the inflammatory cascade induced by intraventricular haemorrhage, and cyclooxygenase-2-inhib
104 le score, increasing ICH volume, presence of intraventricular haemorrhage, and deep/infratentorial IC
105 rtality, bronchopulmonary dysplasia, sepsis, intraventricular haemorrhage, periventricular leukomalac
106 uperficial intracerebral haemorrhage without intraventricular haemorrhage.
107 ricular haemorrhage relative to pups without intraventricular haemorrhage.
108 brain damage initiated by the development of intraventricular haemorrhage.
109 izing brain damage in premature infants with intraventricular haemorrhage.
110 els were comparable in pups with and without intraventricular haemorrhage.
111 d gliosis around the ventricles of pups with intraventricular haemorrhage.
112  CNS due to repeated chronic subarachnoid or intraventricular haemorrhage.
113                 Exclusion criteria were pure intraventricular haemorrhage; intracerebral haemorrhage
114  pro-inflammatory cytokines were elevated in intraventricular haemorrhage; whether their suppression
115  (10.7 [23.1] vs 9.2 [20.7]; p = 0.900), and intraventricular hematoma expansion (14.5 [63.2] vs 6.1
116 eath, chronic lung disease, neonatal sepsis, intraventricular hemorrhage >grade 2, periventricular le
117 8.3%), respiratory distress syndrome (8.3%), intraventricular hemorrhage (1.4%), intrauterine fetal d
118 al, 76.3; medical, 6.17), sepsis (2.66), and intraventricular hemorrhage (1.97) (P < 0.005).
119 8%] vs 13 of 103 12.6%]; P = .04) and severe intraventricular hemorrhage (11 infants [10.3%] vs 23 [2
120 5.3% [95% CI, 14.4%-16.3%]), death or severe intraventricular hemorrhage (17.5% [95% CI, 16.5%-18.6%]
121   Less platelet activity was associated with intraventricular hemorrhage (516.5 [interquartile range
122 ce of necrotizing enterocolitis, sepsis, and intraventricular hemorrhage (all grades).
123 fants of women receiving ANS included severe intraventricular hemorrhage (aRR = 0.68; 95% CI, 0.58-0.
124                    Low-grade germinal matrix-intraventricular hemorrhage (GM-IVH) is the most common
125 s were categorized into three classes: 1) no intraventricular hemorrhage (grade 0); 2) mild-moderate
126 cular hemorrhage (grade 0); 2) mild-moderate intraventricular hemorrhage (grades 1-2, i.e., germinal
127 lar dilatation, respectively); and 3) severe intraventricular hemorrhage (grades 3-4, i.e., intravent
128                         Thrombocytopenia and intraventricular hemorrhage (IVH) are common among very-
129                                              Intraventricular hemorrhage (IVH) in premature infants r
130                                              Intraventricular hemorrhage (IVH) in preterm infants lea
131                                              Intraventricular hemorrhage (IVH) is a major complicatio
132                                              Intraventricular hemorrhage (IVH) is a negative prognost
133                                              Intraventricular hemorrhage (IVH) remains a major cause
134                                              Intraventricular hemorrhage (IVH) results in neural cell
135 ventricles due to CSF accumulation following intraventricular hemorrhage (IVH), is a common disease u
136                      ICH volume (p = 0.025), intraventricular hemorrhage (p = 0.019), presence of mic
137 rophylactic indomethacin may decrease Severe Intraventricular Hemorrhage (SIVH).
138 et function on admission are associated with intraventricular hemorrhage and death after ICH.
139                  The risk of death or severe intraventricular hemorrhage and death or necrotizing ent
140 es is uniquely associated with both neonatal intraventricular hemorrhage and death.
141 th or chronic lung disease as well as severe intraventricular hemorrhage and periventricular leukomal
142                          Perinatal asphyxia, intraventricular hemorrhage and stroke are common causes
143            Acute intracranial hemorrhage and intraventricular hemorrhage are devastating disorders.
144 l-age infants with low-grade periventricular-intraventricular hemorrhage are not significantly differ
145 arly-onset sepsis and severe periventricular-intraventricular hemorrhage as compared with unexposed n
146 ed to preempt the occurrence and severity of intraventricular hemorrhage as detected by ultrasound.
147  mortality, nosocomial infection, and severe intraventricular hemorrhage but not of 28-day mortality
148  cord milking group died or developed severe intraventricular hemorrhage compared with 8% (20/238) of
149       Thrombocytopenia was a risk factor for intraventricular hemorrhage during the first 7 days of l
150                                 Detection of intraventricular hemorrhage during the first postnatal d
151 prising an imbalance in the number of severe intraventricular hemorrhage events by study group was ob
152 or neonatal morbidity (specifically, without intraventricular hemorrhage grade 3-4, cystic periventri
153  severe neonatal brain injury, defined as an intraventricular hemorrhage grade of 3 or greater or cys
154  or severe neonatal morbidity, defined as an intraventricular hemorrhage grade of 3 or greater, cysti
155                   Early bedside detection of intraventricular hemorrhage holds promise for advancing
156  Lysis: Evaluating Accelerated Resolution of Intraventricular Hemorrhage III trial and the Minimally
157 njection of thrombin (20U) was used to model intraventricular hemorrhage in adult rats.
158 rain activity that preempt the occurrence of intraventricular hemorrhage in extremely preterm infants
159 premature ovine fetuses and the incidence of intraventricular hemorrhage in premature infants.
160                              The etiology of intraventricular hemorrhage in preterm infants is multif
161 ns between sodium intake, hypernatremia, and intraventricular hemorrhage in preterm infants.
162 roencephalography preempts the occurrence of intraventricular hemorrhage in the extremely preterm.
163 stically significantly higher rate of severe intraventricular hemorrhage in the umbilical cord milkin
164 m appears to be a modifiable risk factor for intraventricular hemorrhage in very low birth weight inf
165 ompared with no abnormality, germinal matrix/intraventricular hemorrhage increased risk for current m
166                 Diagnostic discrimination of intraventricular hemorrhage infants using measures of bu
167 f electroencephalography bursts found in the intraventricular hemorrhage infants were significantly s
168                                              Intraventricular hemorrhage is a common neurologic compl
169                    Low-grade periventricular-intraventricular hemorrhage is a common neurologic morbi
170 he management of intracranial hemorrhage and intraventricular hemorrhage is complex.
171                   Early bedside detection of intraventricular hemorrhage is crucial to enabling timel
172  RD, -0.14 [95% CI, -0.25 to -0.04]) and for intraventricular hemorrhage of all grades (RR, 0.62 [95%
173 d treatment group was significant for severe intraventricular hemorrhage only (P = .003); among infan
174 gorized as either (1) germinal matrix and/or intraventricular hemorrhage or (2) parenchymal lesions a
175 ecrotizing enterocolitis or death and severe intraventricular hemorrhage or death.
176        Secondary outcomes included secondary intraventricular hemorrhage or hydrocephalus upon follow
177 r absence of chronic lung disease and severe intraventricular hemorrhage or periventricular leukomala
178              Chronic lung disease and severe intraventricular hemorrhage or periventricular leukomala
179 cance of intracranial hypertension in severe intraventricular hemorrhage requiring extraventricular d
180 w cerebral perfusion pressure in obstructive intraventricular hemorrhage requiring extraventricular d
181    Patients with intracranial hemorrhage and intraventricular hemorrhage should be cared for in an in
182 y outcome was a composite of death or severe intraventricular hemorrhage to determine noninferiority
183 rainage placement ipsilateral to the largest intraventricular hemorrhage volume (p=.001), but not wit
184 mained significantly associated with initial intraventricular hemorrhage volume (p=.002) and extraven
185 20 mm Hg), both intracerebral hemorrhage and intraventricular hemorrhage volume, and pulse pressure.
186  Hg and initial intracerebral hemorrhage and intraventricular hemorrhage volumes were independent pre
187                                       Severe intraventricular hemorrhage was 7.2% in RNE hospitals an
188                               Grade II to IV intraventricular hemorrhage was associated with increase
189                             New or increased intraventricular hemorrhage was observed in 18% (8 of 45
190   The association of high sodium intake with intraventricular hemorrhage was of similar magnitude to
191 ally significant difference in death, severe intraventricular hemorrhage was statistically significan
192 ts born at 23 to 27 weeks' gestation, severe intraventricular hemorrhage was statistically significan
193 ys or younger and participants with isolated intraventricular hemorrhage were excluded.
194 traventricular hemorrhage (grades 3-4, i.e., intraventricular hemorrhage with ventricular dilatation
195 es 1-2, i.e., germinal matrix hemorrhages or intraventricular hemorrhage without ventricular dilatati
196 rhage; 4, thick subarachnoid hemorrhage with intraventricular hemorrhage).
197  stay mortality, 12.9% (9278/71,936); severe intraventricular hemorrhage, 7.6% (4842/63,525); and inf
198 ventricular drainage in patients with severe intraventricular hemorrhage, although intracranial press
199 severe retinopathy of prematurity and severe intraventricular hemorrhage, and 8 years to achieve the
200 nimally invasive interventions, clearance of intraventricular hemorrhage, and adequate blood pressure
201 ibutor to the risk of death, death or severe intraventricular hemorrhage, and death or necrotizing en
202  during extraventricular drainage for severe intraventricular hemorrhage, and level and duration pred
203                    Intracerebral hemorrhage, intraventricular hemorrhage, and perihematomal edema vol
204                          Hematoma expansion, intraventricular hemorrhage, and reversal of anticoagula
205 prematurity, bronchopulmonary dysplasia, and intraventricular hemorrhage, as well as death.
206 ith substantial neonatal morbidities such as intraventricular hemorrhage, bronchopulmonary dysplasia,
207 te of a composite outcome of death or severe intraventricular hemorrhage, but there was a statistical
208  following adverse outcomes: grade III or IV intraventricular hemorrhage, cystic periventricular leuk
209                           Rates of secondary intraventricular hemorrhage, hydrocephalus, and thromboe
210 Coma Scale, intracerebral hemorrhage volume, intraventricular hemorrhage, infratentorial hemorrhage,
211  cTI elevation included poor clinical grade, intraventricular hemorrhage, loss of consciousness at ic
212  seizure, cardiomyopathy, periventricular or intraventricular hemorrhage, necrotizing enterocolitis,
213 h, severe retinopathy of prematurity, severe intraventricular hemorrhage, necrotizing enterocolitis,
214  CLD alone, death alone, air leakage, severe intraventricular hemorrhage, neurodevelopmental impairme
215 two points; infratentorial PICH, two points; intraventricular hemorrhage, one point; PICH volume grea
216 enterocolitis, sepsis, chronic lung disease, intraventricular hemorrhage, or cholestasis.
217 h by 18 to 22 months; hospital death; death, intraventricular hemorrhage, or periventricular leukomal
218  severe complications (defined as high-grade intraventricular hemorrhage, surgery for abdominal compl
219 activity prior to ultrasound confirmation of intraventricular hemorrhage.
220 ; p < 0.015) than in preterm infants without intraventricular hemorrhage.
221 itis, retinopathy of prematurity, and severe intraventricular hemorrhage.
222 ounts were not significantly associated with intraventricular hemorrhage.
223                    Low-grade periventricular-intraventricular hemorrhage.
224 ms leading to poor outcomes in patients with intraventricular hemorrhage.
225  days after birth; and severe (grade 3 or 4) intraventricular hemorrhage.
226 elial cell wall, thereby preventing neonatal intraventricular hemorrhage.
227  consequences of intracranial hemorrhage and intraventricular hemorrhage.
228 he acute care of intracranial hemorrhage and intraventricular hemorrhage.
229 ns between sodium intake, hypernatremia, and intraventricular hemorrhage.
230  contribute to poor outcomes in hypertensive intraventricular hemorrhage.
231 rrhage; 2, thin subarachnoid hemorrhage with intraventricular hemorrhage; 3, thick [>= 1 mm] subarach
232 on, necrotic foci, periventricular cysts and intraventricular hemorrhages were observed distal to sta
233 apy, we conducted the first phase 1 study of intraventricular immunochemotherapy in patients with rec
234  gadolinium imaging depicted parenchymal and intraventricular inflammation.
235                                              Intraventricular infusion of 5HT2C agonist or antagonist
236                                 In contrast, intraventricular infusion of a soluble form of the Nogo
237 ately followed by 3 or 14 days of continuous intraventricular infusion of either human recombinant de
238                               We report that intraventricular infusion of ganglioside GM1 induces pho
239                                              Intraventricular infusion of Shh and a Shh receptor inhi
240                                              Intraventricular infusion of sNgR for 1 month results in
241                                              Intraventricular infusion of ss-siRNA produced selective
242 d in R6/2 mice treated only with AdBDNF, and intraventricular infusion of the mitotic inhibitor Ara-C
243 phosphate-buffered saline placebo via direct intraventricular infusion.
244                                              Intraventricular injected AFSC that homed within the glo
245                                              Intraventricular injected EVs were taken up by CD11b/IBA
246 ide in the subventricular zone of the brain, intraventricular injection has been used as an administr
247                                              Intraventricular injection of 15d-Delta(12,14)-prostagla
248 re, by inhibiting SDF1 signaling in utero by intraventricular injection of a receptor antagonist, we
249 memory deficits in wild type mice induced by intraventricular injection of Abeta4-42.
250                                              Intraventricular injection of an MrgA1 ligand increased
251 y neurons in the mouse neocortex by in utero intraventricular injection of enhanced green fluorescent
252                                      Second, intraventricular injection of HA oligosaccharide reduced
253 sistant to the excitotoxic damage induced by intraventricular injection of kainic acid.
254 ic responses of rodents to the peripheral or intraventricular injection of many individual neurotrans
255                                              Intraventricular injection of tPA or active PDGF-CC, in
256                          We found that after intraventricular injection, a spread of CSF tracers occu
257                Within 15 to 30 min following intraventricular injection, there is only diffuse, non-s
258 dogenous choroid plexus epithelium following intraventricular injection.
259 ne transfer to the subventricular zone after intraventricular injection.
260 ctions of 5-bromo-2'-deoxyuridine (BrdU) and intraventricular injections of replication-deficient ret
261 toxicity, pharmacokinetics, and dosimetry of intraventricular iodine-131-labeled monoclonal antibody
262            Improgan (60, 100 and 140 microg, intraventricular [ivt]) elicited significant decreases i
263 atrioventricular, interventricular, and left intraventricular levels.
264 ow that there is a finite risk of forming an intraventricular mass, presumably from the cellular debr
265  significantly reduced LV volume indices and intraventricular mechanical delay, and improved LV eject
266 1 +/- 29 ms to 202 +/- 39 ms, p < 0.001) and intraventricular mechanical dyssynchrony (15 +/- 26 ms t
267 ntional systemic chemotherapy without serial intraventricular methotrexate injection failed to achiev
268                    Systemic chemotherapy and intraventricular methotrexate led to favorable survival
269 on a modified HIT SKK 2000 regimen excluding intraventricular methotrexate, aiming to achieve similar
270 ic medulloblastoma by systemic chemotherapy, intraventricular methotrexate, and risk-adapted local ra
271                                              Intraventricular NPQ/spexin and NPQ 53-70 also produced
272  tissue Doppler imaging techniques to assess intraventricular opposing wall delay or dispersion of ti
273 nd other adverse outcomes after placement of intraventricular or interventricular stents for this ind
274 f the ventricular system, presence of raised intraventricular pressure and topographic relationships
275 of systolic LV function such as the ejection intraventricular pressure difference (EIVPD) and the sys
276            The Doppler-derived peak ejection intraventricular pressure difference should be preferred
277 oninvasive indices tested, the peak ejection intraventricular pressure difference showed the best cor
278 ion analyses demonstrated that peak ejection intraventricular pressure difference was less sensitive
279 s color M-mode Doppler (CMM) can quantify LV intraventricular pressure gradients (IVPGs).
280                Favorable vortical effects on intraventricular pressure gradients were observed in the
281      In contrast, application of short-lived intraventricular pressure surges neither triggers PVEM n
282 d mild chamber remodelling with ageing while intraventricular pressure-volume loop analysis showed si
283 improvement in cardiac functions measured by intraventricular pressure-volume loops.
284                             We conclude that intraventricular rituximab in combination with MTX is fe
285                    Phase I study showed that intraventricular rituximab plus methotrexate is feasible
286        KEY POINTS: Phase I study showed that intraventricular rituximab plus methotrexate is feasible
287    Fourteen patients received 10 mg or 25 mg intraventricular rituximab twice weekly for 4 weeks, wit
288                        The safety profile of intraventricular rituximab was defined in 10 patients.
289 ed a first complete response of CNS NHL with intraventricular rituximab/MTX, including 1 with CNS lym
290 alternate dosing between the intralumbar and intraventricular routes was tested.
291 as administered, alternating intralumbar and intraventricular routes.
292 LVID), wall thicknesses (posterior [PWT] and intraventricular septum [IVST]), and relative wall thick
293 aminepentaacetic acid injection into the CSF intraventricular space followed by nuclear medicine imag
294  the five hemorrhage subtypes (subarachnoid, intraventricular, subdural, epidural, and intraparenchym
295 h central nervous system (CNS) tumors before intraventricular therapy has not been described.
296 idered when attempting to ensure appropriate intraventricular therapy in the pediatric population.
297 tion of a stable scar and protection against intraventricular thrombi after acute infarction.
298 s in significant shortening of the diastolic intraventricular time delay which is closely related to
299                                              Intraventricular UTP injection transiently decreased blo
300                             We used neonatal intraventricular viral injections to express VAPB or YFP

 
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