Search Results - "KAPELUSHNIK, J"

P1554: INCREASED PREVALENCE OF THROMBOEMBOLIC EVENTS IN PATIENTS WITH CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE I by Asleh, M., Khalaila, A., Eshel, Y., Miskin, H., Kapelushnik, J.

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Fertility preservation of pre-pubertal cancer patient boys before aggressive chemotherapy. peliminary results from in vitro cultue of fresh testicular tissue from three pre-pubertal patients by Huleihel, M, Azab, M, Kapelushnik, J, Lunenfeld, E

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P119. Metastatic neuroblastoma of the mandible – A cytogenetic and molecular genetic study by Manor, E, Kapelushnik, J, Joshua, B.Z, Bodner, L

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Long-term results of the Israeli National Studies in childhood acute lymphoblastic leukemia: INS 84, 89 and 98 by Stark, B, Nirel, R, Avrahami, G, Abramov, A, Attias, D, Ballin, A, Bielorai, B, Burstein, Y, Gavriel, H, Elhasid, R, Kapelushnik, J, Sthoeger, D, Toren, A, Wientraub, M, Yaniv, I, Izraeli, S

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Microbiological spectrum and susceptibility patterns of pathogens causing bacteraemia in paediatric febrile neutropenic oncology patients: comparison between two consecutive time periods with use of different antibiotic treatment protocols by Greenberg, D., Moser, A., Yagupsky, P., Peled, N., Hofman, Y., Kapelushnik, J., Leibovitz, E.

“…This study was devised to look at trends in the microbiological spectrum and susceptibility patterns of pathogens causing bacteraemia in paediatric febrile…”
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Familial factor VII deficiency with foetal and neonatal fatal cerebral haemorrhage associated with homozygosis to Gly180Arg mutation by LANDAU, D., ROSENBERG, N., ZIVELIN, A., STARETZ-CHACHAM, O., KAPELUSHNIK, J.

“…Inherited factor VII (FVII) deficiency is a rare autosomal recessive disorder with a wide heterogeneous clinical pattern. Intracranial haemorrhage in infants…”
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Can Fourier transform infrared spectroscopy at higher wavenumbers (mid IR) shed light on biomarkers for carcinogenesis in tissues? by Sahu, R K, Argov, S, Salman, A, Zelig, U, Huleihel, M, Grossman, N, Gopas, J, Kapelushnik, J, Mordechai, S

“…Fourier transform infrared microspectroscopy (FTIR-MSP) has shown promise as a technique for detection of abnormal cell proliferation and premalignant…”
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Post renal transplantation human herpesvirus 8‐associated lymphoproliferative disorder and Kaposi's sarcoma by Kapelushnik, Joseph, Ariad, Samuel, Benharroch, Daniel, Landau, Daniel, Moser, Asher, Delsol, Georges, Brousset, Pierre

“…Post‐transplantation lymphoproliferative disorders (PTLDs) and Kaposi's sarcoma (KS) are immunosuppression‐related tumours developing in solid organ transplant…”
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Allogeneic cell therapy for relapsed leukemia after bone marrow transplantation with donor peripheral blood lymphocytes by Slavin, S, Naparstek, E, Nagler, A, Ackerstein, A, Kapelushnik, J, Or, R

“…Allogeneic bone marrow transplantation (BMT) is the treatment of choice for hematologic malignancies resistant to conventional chemotherapy and for patients…”
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Indices of iron deficiency and anaemia in Bedouin and Jewish toddlers in southern Israel by Urkin, J, Adam, D, Weitzman, D, Gazala, E, Chamni, S, Kapelushnik, J

“…Aims: To estimate the prevalence of iron deficiency and iron deficiency anaemia using haematological indices. Methods: Prospective interventional study…”
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A fludarabine-based protocol for bone marrow transplantation in Fanconi's anemia by KAPELUSHNIK, J, OR, R, SLAVIN, S, NAGLER, A

“…Allogeneic bone marrow transplantation (BMT) is an effective therapy for Fanconi's anemia (FA). However, mortality and transplant-related complications are…”
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Characteristic Absorbance of Nucleic Acids in the Mid-IR Region as Possible Common Biomarkers for Diagnosis of Malignancy by Sahu, R. K., Argov, S., Salman, A., Huleihel, M., Grossman, N., Hammody, Z., Kapelushnik, J., Mordechai, S.

“…FTIR spectroscopy has been extensively used to understand the differences between normal and malignant cells and tissues. In the present study, FTIR…”
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Leukemoid Reaction in Children: Lymphocytes Flow Cytometry Characterization and Clinical Etiologies by Beigelman, A, Kapelushnik, J, Shubinsky, G, Haim, A, Moser, A.M

“…Clinical investigation included blood count and morphology; Mycoplasma pneumoniae (M. pneumoniae), Epstein-Barr Virus (EBV), and Cytomegalovirus serology;…”
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Infective Endocarditis Successfully Treated in Extremely Low Birth Weight Infants With Recombinant Tissue Plasminogen Activator by Marks, Kyla A, Zucker, Nili, Kapelushnik, Joseph, Karplus, Michael, Levitas, Aviva

“…Increased survival of extremely low birth weight infants depends on the use of indwelling catheters. These catheters expose the infant to the risk of thrombus…”
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Donor lymphocyte infusion post-non-myeloablative allogeneic peripheral blood stem cell transplantation for chronic granulomatous disease by NAGLER, A, ACKERSTEIN, A, KAPELUSHNIK, J, OR, R, NAPARSTEK, E, SLAVIN, S

“…Chronic granulomatous disease (CGD) is a primary immunodeficiency disease symptomized by failure to generate superoxide and recurrent bacterial and fungal…”
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Chronic graft-versus-host disease treated with UVB phototherapy by ENK, C. D, ELAD, S, VEXLER, A, KAPELUSHNIK, J, GORODETSKY, R, KIRSCHBAUM, M

“…Chronic graft-versus-host disease (cGVHD) is a major complication of allogeneic bone marrow transplantation. Immunosuppressive treatment regimens carry the…”
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Fanconi anaemia group A (FANCA) mutations in Israeli non-Ashkenazi Jewish patients by TAMARY, H, BAR-YAM, R, ZAIZOV, R, SHALMON, L, RACHAVI, G, KROSTICHEVSKY, M, ELHASID, R, BARAK, Y, KAPELUSHNIK, J, YANIV, I, AUERBACH, A. D

“…Fanconi anaemia (FA) is a genetically heterogeneous disease with at least eight complementation groups (A-H). In the present study, we investigated the…”
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Fludarabine-based protocol for haploidentical peripheral blood stem cell transplantation in Hurler syndrome by KAPELUSHNIK, J, MANDEL, H, VARADI, G, NAGLER, A

“…To assess the feasibility of performing a haploidentical peripheral blood stem cell transplantation (PBSCT) in a child with Hurler syndrome after a novel…”
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Bone marrow transplantation from a cadaveric donor by KAPELUSHNIK, J, AKER, M, PUGATSCH, T, SAMUEL, S, SLAVIN, S

“…A 2.5-year-old girl with neurogenic Gaucher's disease was transplanted with donor bone marrow from her HLA-compatible 12-year-old brother whose marrow was…”
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ANTI-D EXERTS A VERY EARLY RESPONSE IN CHILDHOOD ACUTE IDIOPATHIC THROMBOCYTOPENIC PURPURA by Moser, A. M., Shalev, H., Kapelushnik, J.

“…Acute idiopathic (immune) thrombocytopenic purpura (ITP) in the pediatric population is a disease in which autoimmune features are mainly self-limited, with a…”
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