Zobrazeno 1 - 10
of 255
pro vyhledávání: '"A. Rachmel"'
Autor:
Aviner, Shraga, Garty, Ben-Zion, Rachmel, Avinoam, Baris, Hagit N., Sidransky, Ellen, Shuffer, Avinoam, Attias, Joseph, Yaniv, Yisaac, Cohen, Ian J.
Publikováno v:
In Blood Cells, Molecules and Diseases 2009 43(3):294-297
Publikováno v:
In Annals of Emergency Medicine February 2003 41(2):223-226
Autor:
Gilmor I. Keshet-Maor, Shlomit Rachmel
Publikováno v:
Policy and Practice in Science Education for the Gifted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc9b5d3f83be475c04acc6db5441c0d6
https://doi.org/10.4324/9781315814155-5
https://doi.org/10.4324/9781315814155-5
Autor:
Ian J. Cohen, Yisaac Yaniv, Joseph Attias, Avinoam Rachmel, Ben-Zion Garty, Hagit N. Baris, Avinoam Shuffer, Ellen Sidransky, Shraga Aviner
Publikováno v:
Blood Cells, Molecules, and Diseases. 43:294-297
Patients with Gaucher disease (GD) are divided into three types based on the presence and rate of progression of the neurologic manifestations. While type 1 GD has a strong predilection in the Jewish Ashkenazi population, both other types lack such a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5b58fcfae283604fe985f8cb12d01a0
https://doi.org/10.1016/j.bcmd.2009.08.004
https://doi.org/10.1016/j.bcmd.2009.08.004
Autor:
Shlomit Rachmel
Publikováno v:
Gifted Education International. 20:123-128
• Three major dilemmas: Is there a need for special education for gifted and talented children? What is the best kind of program for gifted and talented students? Which approach should be used to identify gifted students, quantitative or qualitativ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::124d6f7f06a7d0dc69a550e55a74558e
https://doi.org/10.1177/026142940502000204
https://doi.org/10.1177/026142940502000204
Autor:
Ran Steinberg, Yehuda Nofech-Mozes, M Schwarz, Tommy Schonfeld, Avinoam Rachmel, Shai Ashkenazi
Publikováno v:
Journal of Paediatrics and Child Health. 40:716-719
This study highlights the less common presentations of Hirschsprung disease (HD) and HD-associated enterocolitis (HAE) in neonates and infants. We present three infants whose diagnosis was delayed because of atypical presenting features, especially w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad0398a0137dc4cfbefbeb27dd6e43da
https://doi.org/10.1111/j.1440-1754.2004.00519.x
https://doi.org/10.1111/j.1440-1754.2004.00519.x
Autor:
Liat Ben Sira, Avinoam Rachmel, Arye Blachar, Mark Weinberg, Ada Kessler, Elka Miller, Sergei Keidar
Publikováno v:
Journal of Ultrasound in Medicine. 22:527-530
Wandering spleen is an extremely rare condition in which the spleen is lacking its normal ligamentous attachments and therefore can move to an ectopic position in the abdomen or pelvis. Wandering spleen predisposes the patient to life-threatening com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b7ca3535abbc9acb7aa19dd0d8ecf1a
https://doi.org/10.7863/jum.2003.22.5.527
https://doi.org/10.7863/jum.2003.22.5.527
Autor:
Shlomit Rachmel, Rachel Zorman
Publikováno v:
Gifted and Talented International. 18:36-43
Path-breaking leaders produce new knowledge that changes conceptualizations in an area that is valued by society, enabling the field to progress in leaps and bounds. Gifted children are usually excellent consumers of knowledge, a necessary but not su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea0a5cafb37ee9b15f63ed9e25134461
https://doi.org/10.1080/15332276.2003.11673006
https://doi.org/10.1080/15332276.2003.11673006
Publikováno v:
Annals of Emergency Medicine. 41:223-226
We present the case of a 12-year-old boy admitted with a complaint of recurrent syncopal episodes. A careful history taking revealed the cause of the syncopal episodes to be a dangerous game played by adolescents called "suffocation roulette." We bel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7c7abde92c76bfbaf7f7fea1ba78cf4
https://doi.org/10.1067/mem.2003.49
https://doi.org/10.1067/mem.2003.49
Publikováno v:
Clinical Chemistry. 47:1710-1713
Hereditary neuroporphyrias [aminolevulinate dehydratase deficiency porphyria, acute intermittent porphyria, hereditary coproporphyria, or variegate porphyria (VP)], and lead poisoning (LP), which is thought to be an acquired form of neuroporphyria, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2758be8a5119ec9bdcb402d1045dd984
https://doi.org/10.1093/clinchem/47.9.1710
https://doi.org/10.1093/clinchem/47.9.1710