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1 r, and easier to administer than intravenous immune globulin.
2 y) without the adjunctive use of hepatitis B immune globulin.
3 of early clinical trials with intravenous Rh immune globulin.
4 ids, intravenous immunoglobulin G, or anti-D immune globulin.
5 f the 72 children were receiving intravenous immune globulin.
6 tient received variable doses of hepatitis B immune globulin.
7 ng the recommended number of doses of rabies immune globulin.
8 l consisting of rituximab and/or intravenous immune globulin.
9 n develop despite treatment with intravenous immune globulin.
10 th entecavir monotherapy without hepatitis B immune globulin.
11 eceived hepatitis A vaccine and 522 received immune globulin.
12 olated rat anti-B5 mAb (19C2) or by vaccinia immune globulin.
13 nses to conventional therapy and intravenous immune globulin.
14 s, immunosuppressive agents, and intravenous immune globulin.
15 ed, we evaluated the efficacy of intravenous immune globulin.
16 therapy with ganciclovir and cytomegalovirus immune globulin.
17 ensing TLR7 and TLR9 proliferate and secrete immune globulins.
18 more potent and broadly reactive hepatitis C immune globulins.
19 ence compromised the safety of the resulting immune globulins.
20 smapheresis every other day with intravenous immune globulin 100 mg/kg starting 1 week before the sch
21 rea) once weekly for 3 weeks and intravenous immune globulin (2 g per kilogram of body weight) in the
22 rtum cardiomyopathy treated with intravenous immune globulin (2 g/kg) with those of 11 recent histori
23 ceived conventional therapy with intravenous immune globulin, 2 g per kilogram, as well as aspirin, 8
24  vaccine (4.4%) and in 17 contacts receiving immune globulin (3.3%) (relative risk, 1.35; 95% confide
25 of 3 treated) and immunotherapy (intravenous immune globulin, 3 of 4 treated and plasmapheresis, 3 of
26 most promising dose range for intravenous Rh immune globulin (50-75 microg/kg).
27  it is possible to predict the reactivity of immune globulin against divergent lyssaviruses.
28 t of acute Kawasaki disease with intravenous immune globulin and aspirin reduces the risk of coronary
29 screening, including benefits of hepatitis B immune globulin and hepatitis B vaccine prophylaxis of n
30                  The efficacy of hepatitis B immune globulin and lamivudine to prevent de novo HBV in
31 3 despite empiric treatment with intravenous immune globulin and methylprednisolone, splenectomy was
32 =0.01 and P<0.001, respectively) between the immune globulin and placebo groups, and immune globulin
33        Postexposure prophylaxis using rabies immune globulin and rabies vaccine is effective in preve
34  in the U.S. study also received intravenous immune globulin and rituximab after transplantation to p
35  suggest that the combination of intravenous immune globulin and rituximab may prove effective as a d
36 lled and received treatment with intravenous immune globulin and rituximab.
37                   In addition to hepatitis B immune globulin and vaccination, oral antiviral therapie
38 with PV who required treatment with vaccinia immune globulin and who received 2 investigational agent
39 cury from thimerosal-containing vaccines and immune globulins and deficits in neuropsychological func
40 fever, rates of retreatment with intravenous immune globulin, and numbers of adverse events.
41                 The role of corticosteroids, immune globulin, and plasmapheresis is uncertain.
42 tients do not respond to initial intravenous immune globulin, and recommendations for additional ther
43  Hepatitis A vaccine has similar efficacy to immune globulin as postexposure prophylaxis.
44 that the inclusion of antihuman T-lymphocyte immune globulin (ATG) in a myeloablative conditioning re
45                 Eleven patients who received immune globulin became able to walk more easily or witho
46 mide pulse therapy together with intravenous immune globulin before transplant and as part of a cyclo
47        The D+R- patients were also given CMV immune globulin biweekly for 16 weeks.
48                        The human hepatitis C immune globulin Civacir is an investigational drug that
49 he association between cytomegalovirus (CMV) immune globulin (CMVIG) and clinical outcomes in pediatr
50                    After controlling for CMV immune globulin (CMVIG) prophylaxis, the association bet
51 ults (n = 20) 7 days after administration of immune globulin contained similar antibody levels by imm
52                                 No effect of immune globulin could be demonstrated in the direct inoc
53 diagnosis vary, and the doses of replacement immune globulin differ.
54                                 Using equine immune globulin (equine Ig) as a model Ag, we examined t
55                  Among patients who received immune globulin first, stiffness scores decreased signif
56 onthly infusion of rituximab and intravenous immune globulin for 4 consecutive months.
57  antiviral therapy alone without hepatitis B immune globulin for chronic hepatitis B patients with pr
58  hemolysis after infusions of intravenous Rh immune globulin for immune thrombocytopenic purpura has
59 n, and it may be a reasonable alternative to immune globulin for postexposure prophylaxis in many sit
60 ry other day plasmapheresis with intravenous immune globulin for the initial week.
61 partum cardiomyopathy, patients treated with immune globulin had a greater improvement in ejection fr
62                                  Intravenous immune globulin has been reported to improve left ventri
63  were anti-HBs-, HbsAg- received hepatitis B immune globulin (HBIG) 10,000 IU i.v. daily for 7 days a
64 long-term antiviral and low-dose hepatitis B Immune globulin (HBIG) can effectively prevent HBV recur
65                                  Hepatitis B immune globulin (HBIG) dosing regimens have been poorly
66                                  Hepatitis B immune globulin (HBIG) has been an integral component of
67                        Long-term hepatitis B immune globulin (HBIG) has been shown to reduce hepatiti
68 of antiviral therapy with either hepatitis B immune globulin (HBIg) or lamivudine; however, HBV recur
69 e received high-dose intravenous hepatitis B immune globulin (HBIG) treatment with continued lamivudi
70  been passive immunotherapy with hepatitis B immune globulin (HBIG).
71 venous immune globulin (IGIV) or hepatitis C immune globulin (HCIG), and a third animal was not treat
72 G (IgG) subclasses from polyclonal human HIV immune globulin (HIVIG) in the neutralization of HIV-1 s
73 y by antibody combinations, we evaluated HIV immune globulin (HIVIG), and human monoclonal antibodies
74 IgG, including pharmacologic formulations of immune globulin i.v. (IGIV), contain Abs that specifical
75  the effects of commercial intravenous human immune globulin (i.v.IG) preparations and found that i.v
76 ated against hepatitis A and should be given immune globulin if they used methamphetamine with a case
77 Measles, mumps, and rubella vaccine (MMR) or immune globulin (IG) are routinely used for measles post
78  h later with anti-HCV--negative intravenous immune globulin (IGIV) or hepatitis C immune globulin (H
79  treatment of the initial episode with human immune globulin in addition to ganciclovir.
80 with hepatitis B vaccination and hepatitis B immune globulin in certain endemic regions as well as fa
81         Since the institution of intravenous immune globulin in the treatment of the disease, outcome
82 ents were treated with high-dose intravenous immune globulin infusions (2 g/kg).
83  Drug Administration (FDA) licensed Rh(o)(D) immune globulin intravenous (anti-D IGIV) on March 24, 1
84                                     Rh(o)(D) immune globulin intravenous (anti-D IGIV) was licensed b
85    We created the orphan drug Human Botulism Immune Globulin Intravenous (Human) (BIG-IV), which neut
86  affects mnAb levels in contemporary lots of Immune Globulin Intravenous (Human) (IGIV).
87 hether 10% caprylate-chromatography purified immune globulin intravenous (IGIV-C) has short-term and
88                           The use of passive immune globulin is a crucial component of rabies postexp
89 ow platelet counts and confirmed that anti-D immune globulin is a front-line treatment option.
90                                  Intravenous immune globulin is a well-tolerated and effective, albei
91               Immune modulatory therapy with immune globulin is an effective therapy for Kawasaki dis
92 accumulating to indicate that intravenous Rh immune globulin is as effective, probably safer, and eas
93 The combination of rituximab and intravenous immune globulin is effective in patients with refractory
94  antiviral therapy alone without hepatitis B immune globulin is highly effective in preventing HBV re
95                         Although intravenous immune globulin is the mainstay of initial treatment, th
96             Desensitization with intravenous immune globulin (IVIG) and rituximab improves transplant
97             Desensitization with intravenous immune globulin (IVIG) and rituximab improves transplant
98               We now report that intravenous immune globulin (IVIG) derived from pools of human plasm
99                        High-dose intravenous immune globulin (IVIg) has emerged as an important thera
100 ppressive mechanism of action of intravenous immune globulin (IVIG) has remained enigmatic despite th
101 as designed to determine whether intravenous immune globulin (IVIG) improves left ventricular ejectio
102  (CLL) or multiple myeloma (MM), intravenous immune globulin (IVIg) may be administered to reduce the
103                                  Intravenous immune globulin (IVIG) suppresses autoantibody-mediated
104      All 3 patients responded to intravenous immune globulin (IVIG) treatment.
105      In living-donor recipients, intravenous immune globulin (IVIG) was added to the CMX evaluation t
106 gen (SLA) class I antibodies or pooled human immune globulin (IVIg) were used to reverse the effects
107 D.: We have shown that high-dose intravenous immune globulin (IVIG; 2 g/kg x2 doses)+rituximab (1 g x
108 ng human immunoglobulin G (IgG) (intravenous immune globulin [IVIG]), AAV-Go.1 had higher resistance
109 iciency characterized by low levels of serum immune globulins, lack of Ab, and reduced numbers of CD2
110   Pretreatment with bacterial polysaccharide immune globulin led to a significant reduction in coloni
111 h CVID who have mutations in TACI but normal immune globulin levels still have detectable in vitro B-
112 ilated cardiomyopathy treated with high-dose immune globulin, LVEF improved 17 EF units.
113                                              Immune globulins made from anti-HCV-positive plasma and
114                                  Using human immune globulins made from antihepatitis C virus (HCV)-p
115 luate the effect of therapy with intravenous immune globulin on recovery of left ventricular function
116 ies, in random order, to receive intravenous immune globulin or placebo for three months, followed by
117 30% after the second infusion of intravenous immune globulin (P<0.001 for the comparison with the pre
118 lovir, adefovir, respiratory syncytial virus immune globulin, palivizumab, and imiquimod are discusse
119 le-center study examined whether intravenous immune globulin plus rituximab could reduce anti-HLA ant
120  corticosteroids, cidofovir, and intravenous immune globulin, PML progressed rapidly, rendering the p
121 s 412 to 426, as it did with an HCV-specific immune globulin preparation, which was derived from the
122 ng and protective antibodies in experimental immune globulin preparations made from anti-HCV-positive
123 containing preservative used in vaccines and immune globulin preparations, is associated with neurops
124                                              Immune globulins prepared by ethanol fractionation of pl
125 long been considered safe until a commercial immune globulin product, Gammagard, prepared from plasma
126 ing in cytokine secretion, IgG class switch, immune globulin production, and potentially, the preserv
127  randomized, placebo-controlled trial of CMV immune globulin prophylaxis.
128 groups indicate that hepatitis A vaccine and immune globulin provided good protection after exposure.
129 nsplant patients, and valganciclovir and CMV immune globulin reduce rejection rates and cardiovascula
130 were given respiratory syncytial virus (RSV) immune globulin (RSVIG) at the time of transplantation a
131                              Titration of 62 immune globulin samples (prepared from 1957 to 1994) sho
132 munodeficiency who was receiving intravenous immune globulin suddenly had paralysis of all four limbs
133 bo-controlled trial of cytomegalovirus (CMV) immune globulin that included 146 patients who underwent
134 at immunity may be augmented by vaccines and immune globulins that include strong antibody responses
135 ong-term protection conferred by hepatitis A immune globulin, the efficacy of a single injection (20
136            Over the past decade, intravenous immune globulin therapy (IVIG) has gained widespread use
137 inistration but dropped significantly during immune globulin therapy (P=0.01).
138    Anti-GAD65 antibody titers declined after immune globulin therapy but not after placebo administra
139 tivity scores decreased substantially during immune globulin therapy but rebounded during placebo adm
140 thylprednisolone to conventional intravenous immune globulin therapy for the routine primary treatmen
141  the immune globulin and placebo groups, and immune globulin therapy had a significant direct treatme
142 remains unknown, but fortunately intravenous immune globulin therapy has proved to be effective at re
143                                  The role of immune globulin therapy in adults with this disorder has
144             The effectiveness of intravenous immune globulin therapy in this disorder should be evalu
145 or Kawasaki disease resistant to intravenous immune globulin therapy is an area of research and contr
146 stemic inflammation, but despite intravenous immune globulin therapy, coronary-artery abnormalities d
147 d the administration of low-dose intravenous immune globulin to desensitize 211 HLA-sensitized patien
148 we report a novel approach using intravenous immune globulin to modulate anti-HLA antibody and improv
149             Despite the widespread use of Rh immune globulin to prevent pregnancy associated anti-D a
150    The duration of the beneficial effects of immune globulin varied from six weeks to one year.
151     Penicillin, clindamycin, and intravenous immune globulin (Venoglobulin-S; IVIG) alone and in comb
152  neutralizing determinants and that vaccinia immune globulin (VIG) derived from Dryvax recipients con
153                                     Vaccinia immune globulin (VIG) has been used therapeutically to t
154 h improved safety profiles, and new vaccinia immune globulin (VIG) products, there is an immediate ne
155                   Intravenous Rh [corrected] immune globulin was licensed by the U.S. Food and Drug a
156 r ejection fraction in patients treated with immune globulin was significantly greater than in the co
157  9 months post-OLT, and prophylaxis with HBV immune globulin was then established.
158 IV-1-infected patients as well as pooled HIV immune globulin were selectively depleted of antibodies
159  monoclonal antibodies 2F5 and 2G12, and HIV immune globulin were tested.
160 lar damage in dermatomyositis by intravenous immune globulin which appears to intercept the assembly
161  A virus has not been compared directly with immune globulin, which is known to be highly effective i
162 tinfection passive treatment with polyclonal immune globulin with high neutralizing titers against SI
163  comparing conventional doses of intravenous immune globulin with the most promising dose range for i
164 e-appropriate dose of hepatitis A vaccine or immune globulin within 14 days after exposure to patient

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