Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Lucia Zalman"'
Autor:
Joseph M. Tilghman, Lucia Zalman, Morad Khayat, Aravinda Chakravarti, Ilana Chervinsky, Stavit A. Shalev
Publikováno v:
American Journal of Medical Genetics Part A. 170:176-182
Mutations in the PIGN gene involved in the glycosylphoshatidylinositol (GPI) anchor biosynthesis pathway cause Multiple Congenital Anomalies–Hypotonia–Seizures syndrome 1 (MCAHS1). The syndrome manifests developmental delay, hypotonia, and epilep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f58aeca495cc6aafdfc0df67af184a2a
https://doi.org/10.1002/ajmg.a.37375
https://doi.org/10.1002/ajmg.a.37375
Autor:
Lucia Zalman, Morad Khayat, Ariel Koren, Stavit Allon Shalev, Ihsan Salama, Hagit Hauschner, Nurit Rosenberg, Boris Shenkman, Carina Levin, Etheresia Pretorius, Orly Elpeleg
Publikováno v:
Journal of Thrombosis and Haemostasis. 13:1285-1292
SummaryBackground The FYB gene encodes adhesion and degranulation-promoting adaptor protein (ADAP), a hematopoietic-specific protein involved in platelet activation, cell motility and proliferation, and integrin-mediated cell adhesion. No ADAP-relate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30d25c807614b2177b60668d86267803
https://doi.org/10.1111/jth.12966
https://doi.org/10.1111/jth.12966
Autor:
Tanya Krasnov, Morad Khayat, Hannah Tamary, Carina Levin, Ariel Koren, Lucia Zalman, Ihsan Salama, Stavit A. Shalev
Publikováno v:
Pediatric Blood & Cancer. 60:E128-E130
We describe the clinical and laboratory features of a family of Arab ancestry and consanguinity. Five affected individuals were diagnosed in two sibships. All affected members have small platelets, severe to moderate thrombocytopenia of neonatal onse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::027b4e12e09e3a2df58849073f509e88
https://doi.org/10.1002/pbc.24581
https://doi.org/10.1002/pbc.24581
Publikováno v:
Pediatric Hematology and Oncology. 16:469-472
Vaso-occlusive crisis is the most common cause of morbidity in patients with sickle cell anemia (SCA). Central nervous system involvement that leads to hemiplegia is the most frequent neurological complication in those patients. Peripheral deep venou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b4fafe264e4bc46f65169094206ba68
https://doi.org/10.1080/088800199277047
https://doi.org/10.1080/088800199277047
Autor:
Dina Attias, Carina Levin, D Segal-Kupershmit, Haya Palmor, Lucia Zalman, Ariel Koren, M Abu Hana, A Luder
Publikováno v:
Pediatric Hematology and Oncology. 16:221-232
This study evaluated the efficacy of hydroxyurea treatment in the prevention of vaso-occlusive crises among children and teenagers with severe sickle cell anemia and sickle cell beta-thalassemia. Nineteen children and young adults with severe sickle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::412007fe1696f9080f15037a0d08bc55
https://doi.org/10.1080/088800199277272
https://doi.org/10.1080/088800199277272
Autor:
Carina, Levin, Lucia, Zalman, Hannah, Tamary, Tanya, Krasnov, Morad, Khayat, Stavit, Shalev, Ihsan, Salama, Ariel, Koren
Publikováno v:
Pediatric bloodcancer. 60(10)
We describe the clinical and laboratory features of a family of Arab ancestry and consanguinity. Five affected individuals were diagnosed in two sibships. All affected members have small platelets, severe to moderate thrombocytopenia of neonatal onse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::98dbc375b4d2f4f1564ca225c80fe513
https://pubmed.ncbi.nlm.nih.gov/23650215
https://pubmed.ncbi.nlm.nih.gov/23650215
Autor:
Ariel, Koren, Lucia, Zalman, Haya, Palmor, Ronit Bril, Zamir, Carina, Levin, Ariella, Openheim, Etty, Daniel-Spiegel, Stavit, Shalev, Dvora, Filon
Publikováno v:
The Israel Medical Association journal : IMAJ. 11(4)
Sickle cell anemia is a hemolytic anemia caused by a single mutation in position 6 of the beta globin molecule. About 80 patients with SCA in northern Israel are currently receiving treatment.To assess a screening program in northern Israel aimed at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e2f2fc6f745a3971d85f29162357f79b
https://pubmed.ncbi.nlm.nih.gov/19603597
https://pubmed.ncbi.nlm.nih.gov/19603597
Autor:
Carina Levin, Ariel Koren, Orly Dgany, Lucia Zalman, Tatyan Kransnov, Hannah Tamary, Ronit Elhasid, Haya Palmor
Publikováno v:
American journal of hematology. 83(5)
Although a relatively small number of previous studies suggest a modest response to hydroxyurea (HU) therapy in beta-thalassemia, more recent investigations have revealed that some transfusion-dependent patients can become transfusion-independent fol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24088e938f37330a28854989b1c9d99b
https://pubmed.ncbi.nlm.nih.gov/18181203
https://pubmed.ncbi.nlm.nih.gov/18181203
Autor:
Eli Schwartz, Lucia Zalman, Abed Nasereddin, Moshe Ephros, Charles L. Jaffe, Stephanie Kamil, Michal Ramon, Dganit Rozenman, Ayelet Shani-Adir
Publikováno v:
Journal of the American Academy of Dermatology. 53(5)
Background In Israel, most cutaneous leishmaniasis (CL) is caused by Leishmania major . Recently a new focus of CL caused by Leishmania tropica has been described in Tiberias and the surrounding area of northern Israel. Objective The aim of this stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::892d3527f4ff5f58647aa6740183e35a
https://pubmed.ncbi.nlm.nih.gov/16243129
https://pubmed.ncbi.nlm.nih.gov/16243129
Autor:
Ariel, Koren, Lucia, Zalman, Haia, Palmor, Edna, Ekstein, Yona, Schneour, Amir, Schneour, Stavit, Shalev, Eliezer A, Rachmilewitz, Dvora, Filon, Ariela, Openhaim
Publikováno v:
Harefuah. 141(11)
beta thalassemia is an hereditary disease caused by mutations in the beta globin gene. The clinical course is characterized by chronic hemolytic anemia that required regular blood transfusions. Secondary to the blood transfusions, patients developed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::44d2bf83d0def262ee46e3132293d963
https://pubmed.ncbi.nlm.nih.gov/12476624
https://pubmed.ncbi.nlm.nih.gov/12476624