Search Results - "MONAHAN, P."
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Gene therapy in an era of emerging treatment options for hemophilia B
Published in Journal of thrombosis and haemostasis (01-06-2015)“…Summary Factor IX deficiency (hemophilia B) is less common than factor VIII deficiency (hemophilia A), and innovations in therapy for hemophilia B have…”
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Psychosocial Impact of COVID-19 Nursing Home Restrictions on Visitors of Residents With Cognitive Impairment: A Cross-Sectional Study as Part of the Engaging Remotely in Care (ERiC) Project
Published in Frontiers in psychiatry (26-10-2020)“…Background: COVID-19 has disproportionately affected older people. Visiting restrictions introduced since the start of the pandemic in residential care…”
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3
Adeno-associated virus terminal repeat (TR) mutant generates self-complementary vectors to overcome the rate-limiting step to transduction in vivo
Published in Gene therapy (01-12-2003)“…An important limitation of recombinant adeno-associated virus (rAAV) vector efficiency is the requirement of hostcell-mediated synthesis of double-stranded DNA…”
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Neutralizing antibodies against adeno-associated virus examined prospectively in pediatric patients with hemophilia
Published in Gene therapy (01-03-2012)“…Recombinant adeno-associated virus (rAAV) is a promising gene delivery vector and has recently been used in patients with hemophilia. One limitation of AAV…”
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5
Self-complementary recombinant adeno-associated virus (scAAV) vectors promote efficient transduction independently of DNA synthesis
Published in Gene therapy (01-08-2001)“…Adeno-associated virus (AAV) vectors package single-stranded genomes and require host-cell synthesis of the complementary strand for transduction. However,…”
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6
AAV vectors : is clinical success on the horizon?
Published in Gene therapy (2000)“…Potential applications and impact of the adeno-associated virus (AAV) as a gene transfer vector have expanded rapidly in the last decade. Recent advances in…”
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7
IL‐6 receptor antagonist as adjunctive therapy with clotting factor replacement to protect against bleeding‐induced arthropathy in hemophilia
Published in Journal of thrombosis and haemostasis (01-05-2013)“…Summary Background The most common morbidity that results from hemophilia is bleeding‐induced hemophilic arthropathy (HA), which once established may not be…”
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Prevalent inhibitors in haemophilia B subjects enrolled in the Universal Data Collection database
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-01-2014)“…Summary Several risk factors for inhibitors have recently been described for haemophilia A. It has been assumed that similar risk factors are also relevant for…”
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Evaluation of risks related to the use of adeno-associated virus-based vectors
Published in Current gene therapy (01-12-2003)“…Recombinant AAV efficacy has been demonstrated in numerous gene therapy preclinical studies. As this vector is increasingly applied to human clinical trials,…”
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10
The effects of hypogonadism on quality of life in survivors of germ cell tumors treated with surgery alone versus surgery plus platinum-based chemotherapy
Published in Supportive care in cancer (01-07-2020)“…Background It is important to assess the prevalence of hypogonadism and to identify the correlation between hypogonadism and cancer treatment with quality of…”
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11
Inhibitor recurrence after immune tolerance induction: a multicenter retrospective cohort study
Published in Journal of thrombosis and haemostasis (01-11-2015)“…Summary Background Immune tolerance induction (ITI) in patients with congenital hemophilia A is successful in up to 70%. Although there is growing…”
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12
Long-term phenotypic correction in factor IX knockout mice by using phiC31 integrase-mediated gene therapy
Published in Gene therapy (01-08-2011)“…Hemophilia B, a hereditary bleeding disorder caused by a deficiency of coagulation factor IX (FIX), is an excellent candidate for gene therapy. However, to…”
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13
The expanding menagerie: animal models of hemophilia A
Published in Journal of thrombosis and haemostasis (01-11-2010)“…See also Booth CJ, Brooks MB, Rockwell S, Murphy JW, Rinder HM, Zelterman D, Paidas MJ, Compton SR, Marks PW. WAG‐F8m1Ycb rats harboring a factor VIII gene…”
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14
Ampiginous choroiditis following quadrivalent human papilloma virus vaccine
Published in British journal of ophthalmology (01-01-2010)Get more information
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15
Recombinant porcine factor VIII for high‐risk surgery in paediatric congenital haemophilia A with high‐titre inhibitor
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-03-2017)“…Introduction High‐titre factor VIII (FVIII) inhibitors complicate peri‐operative haemostasis. Recombinant porcine FVIII (r‐pFVIII) may provide an alternative…”
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16
Confirmatory test of two factors and four subtypes of bipolar disorder based on lifetime psychiatric co-morbidity
Published in Psychological medicine (01-07-2015)“…The first aim was to use confirmatory factor analysis (CFA) to test a hypothesis that two factors (internalizing and externalizing) account for lifetime…”
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17
Adaptation of family caregivers during the acute phase of adult BMT
Published in Bone marrow transplantation (Basingstoke) (01-06-2009)“…This study examined the course of adaptation as indicated by the level of emotional distress for family caregivers of adult BM recipients across the acute…”
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Joint bleeding in factor VIII deficient mice causes an acute loss of trabecular bone and calcification of joint soft tissues which is prevented with aggressive factor replacement
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-09-2014)“…Summary While chronic degenerative arthropathy is the main morbidity of haemophilia, a very high prevalence of low bone density is also seen in men and boys…”
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19
Familial deficiency of vitamin K-dependent clotting factors
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-11-2008)“…Combined deficiency of vitamin K‐dependent clotting factors II, VII, IX and X (and proteins C, S, and Z) is usually an acquired clinical problem, often…”
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Abnormal hemostasis in a knock‐in mouse carrying a variant of factor IX with impaired binding to collagen type IV
Published in Journal of thrombosis and haemostasis (01-11-2009)“…Background: Factor IX binds to collagen type IV, but this binding has no known consequence. Objectives: To determine the effect of reduced binding of FIX to…”
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