Search Results - "Geva, T"

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    Investigation and treatment of repeated implantation failure following IVF-ET by Margalioth, E.J., Ben-Chetrit, A., Gal, M., Eldar-Geva, T.

    Published in Human reproduction (Oxford) (01-12-2006)
    “…Pregnancy rate following one cycle of IVF and ET can be as high as 60%. But even in the very successful units, some couples fail repeatedly. The causes for…”
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    Ventricular size and function assessed by cardiac MRI predict major adverse clinical outcomes late after tetralogy of Fallot repair by Knauth, A L, Gauvreau, K, Powell, A J, Landzberg, M J, Walsh, E P, Lock, J E, del Nido, P J, Geva, T

    Published in Heart (British Cardiac Society) (01-02-2008)
    “…Factors associated with impaired clinical status in a cross-sectional study of patients with repaired tetralogy of Fallot (TOF) have been reported previously…”
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    Sexual dichotomy of gonadal function in Prader–Willi syndrome from early infancy through the fourth decade by Hirsch, H.J., Eldar-Geva, T., Bennaroch, F., Pollak, Y., Gross-Tsur, V.

    Published in Human reproduction (Oxford) (01-11-2015)
    “…STUDY QUESTION At what age does the type of hypogonadism, namely hypothalamic or primary gonadal defect, become established in men and women with Prader–Willi…”
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    ‘Why have women not returned to use their frozen oocytes?’: a 5-year follow-up of women after planned oocyte cryopreservation by Tsafrir, A., Holzer, H., Miron-Shatz, T., Eldar-Geva, T., Gal, M., Ben-ami, I., Dekel, N., Weintruab, A., Goldberg, D., Schonberger, O., Srebnik, N., Hyman, J.

    Published in Reproductive biomedicine online (01-12-2021)
    “…What are the reproductive choices and retrospective reflections of women at least 4 years after planned oocyte cryopreservation (POC)? This was an internet…”
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    Preimplantation Genetic Diagnosis for Fetal Neonatal Alloimmune Thrombocytopenia Due to Antihuman Platelet Antigen Maternal Antibodies by Altarescu, Gheona, Geva, T Eldar, Grisaru-Granovsky, Sorina, Bonstein, Lilach, Miskin, Hagit, Varshver, Irit, Margalioth, Ehud J, Levy-Lahad, Ephrat, Renbaum, Paul

    Published in Obstetrics and gynecology (New York. 1953) (01-02-2012)
    “…OBJECTIVE:To develop a reliable preimplantation genetic diagnosis protocol for antihuman platelet antigen-1 incompatibility for a family in whom antenatal…”
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    Anthropometric adjustments are helpful in the interpretation of BMD and BMC Z-scores of pediatric patients with Prader-Willi syndrome by Hangartner, T. N., Short, D. F., Eldar-Geva, T., Hirsch, H. J., Tiomkin, M., Zimran, A., Gross-Tsur, V.

    Published in Osteoporosis international (01-12-2016)
    “…Summary Anthropometric adjustments of bone measurements are necessary in Prader-Willi syndrome patients to correctly assess the bone status of these patients…”
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    Ovarian reserve and PGD treatment outcome in women with myotonic dystrophy by Srebnik, N, Margalioth, E.J, Rabinowitz, R, Varshaver, I, Altarescu, G, Renbaum, P, Levi-Lahad, E, Weintraub, A, Eldar-Geva, T

    Published in Reproductive biomedicine online (01-07-2014)
    “…Abstract Myotonic dystrophy (DM) is the most common form of muscular dystrophy in adults. There are conflicting reports about its effect on female fertility…”
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    Use of tissue velocity imaging in the diagnosis of fetal cardiac arrhythmias by REIN, A. J. J. T, O'DONNELL, C, GEVA, T, NIR, A, PERLES, Z, HASHIMOTO, I, LI, X.-K, SAHN, D. J

    Published in Circulation (New York, N.Y.) (01-10-2002)
    “…Precise diagnosis of cardiac arrhythmias in the fetus is crucial for a managed therapeutic approach. However, many technical, positional, and gestational…”
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    Familial haplotyping and embryo analysis for Preimplantation Genetic Diagnosis (PGD) using DNA microarrays: a proof of principle study by Altarescu, G., Zeevi, D. A., Zeligson, S., Perlberg, S., Eldar-Geva, T., Margalioth, E. J., Levy-Lahad, E., Renbaum, P.

    “…Purpose Development of PGD assays for molecular disorders is based on analysis of a familial mutation together with linked polymorphic STR markers; a process…”
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    Lidocaine–Prilocaine (EMLA) cream as analgesia for hysterosalpingography: a prospective, randomized, controlled, double blinded study by Liberty, G., Gal, M., Halevy-Shalem, T., Michaelson-Cohen, R., Galoyan, N., Hyman, J., Eldar-Geva, T., Vatashsky, E., Margalioth, E.

    Published in Human reproduction (Oxford) (01-05-2007)
    “…BACKGROUND The aim of our study is to evaluate the efficacy of applying lidocaine 25 mg–prilocaine-25 mg/G cream (EMLA 5%) on the uterine cervix for pain…”
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    Safety and Efficacy of Carvedilol Therapy for Patients with Dilated Cardiomyopathy Secondary to Muscular Dystrophy by Rhodes, J., Margossian, R., Darras, B. T., Colan, S. D., Jenkins, K. J., Geva, T., Powell, A. J.

    Published in Pediatric cardiology (01-03-2008)
    “…Background By the age of 20 years, almost all patients with Duchenne’s or Becker’s muscular dystrophy have experienced dilated cardiomyopathy (DCM), a…”
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    Phase-velocity cine magnetic resonance imaging measurement of pulsatile blood flow in children and young adults: in vitro and in vivo validation by Powell, A J, Maier, S E, Chung, T, Geva, T

    Published in Pediatric cardiology (01-03-2000)
    “…Quantification of blood flow in vessels provides valuable information that aids management decisions in a variety of cardiac conditions. Current flow…”
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    Blood flow measurement by magnetic resonance imaging in congenital heart disease by Powell, A J, Geva, T

    Published in Pediatric cardiology (01-01-2000)
    “…Investigation of blood flow in the heart and vessels may provide insight into the function of the cardiovascular system and aid patient management decisions…”
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    Anaesthesia considerations for cardiac MRI in infants and small children by Odegard, Kirsten C., DiNardo, James A., Tsai-Goodman, Beverly, Powell, Andrew J., Geva, Tal, Laussen, Peter C.

    Published in Pediatric anesthesia (01-06-2004)
    “…Summary Background : General anaesthesia is frequently necessary in infants and small children undergoing cardiac magnetic resonance imaging (MRI), because of…”
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    Single-sperm analysis for haplotype construction of de-novo paternal mutations: application to PGD for neurofibromatosis type 1 by Altarescu, G., Brooks, B., Kaplan, Y., Eldar-Geva, T., Margalioth, E.J., Levy-Lahad, E., Renbaum, P.

    Published in Human reproduction (Oxford) (01-08-2006)
    “…Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder caused by mutations in the neurofibromin gene. Approximately, 50% of cases are caused by…”
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