Zobrazeno 1 - 10
of 56
pro vyhledávání: '"I Peltekova"'
Publikováno v:
Trakia Journal of Sciences, Vol 19, Iss Suppl. 1, Pp 399-404 (2021)
The article analyzes the problems of sports injuries, the main focus is on ankle injuries received during training and basketball competition. Given the growing incidence of ankle pain complaints not only from pupils and students- game lovers, but
Externí odkaz:
https://doaj.org/article/38ae88022516483a86197863b0aadbba
Publikováno v:
Trakia Journal of Sciences, Vol 19, Iss Suppl. 1, Pp 405-410 (2021)
The article covers matters related to traumatic injuries of the knee in basketball players, emphasizing on diagnostic imaging as a non-invasive test that allows evaluation of the player’s condition. Precise and prompt diagnosis of the trauma can
Externí odkaz:
https://doaj.org/article/8e02ee3cfa0f431c80a157fafd571337
Autor:
I. Peltekova
Publikováno v:
Trakia Journal of Sciences, Vol 18, Iss Suppl. 1, Pp 813-817 (2020)
This report is provoked by the concrete work with students from Sofia University “St. Kliment Ohridski "in Physical Education and Sports. The study contingent is 147 students (men and women) who are future teachers of physical education and sports.
Externí odkaz:
https://doaj.org/article/40df92e7275044a6864b629c70516a19
Autor:
I. Peltekova
Publikováno v:
Trakia Journal of Sciences, Vol 17, Iss Suppl. 1, Pp 736-741 (2019)
This report is provoked by the specific work with students from Sofia University “St. Kliment Ohridski”. The contingent of the study was 77 students (men and women) who chose to practice basketball in group-educated groups at the University. The
Externí odkaz:
https://doaj.org/article/1d11d0431f2149dca93a9a8212acd504
Autor:
I. Peltekova
Publikováno v:
Trakia Journal of Sciences, Vol 17, Iss Suppl. 1, Pp 742-746 (2019)
The article presents the results of the measurements made on the physical development of students who have chosen basketball as a compulsory discipline. The measurements include height, weight, and body mass index (BMI). All participants in the study
Externí odkaz:
https://doaj.org/article/b5fd562a32be417f833ed30d0f91c17b
Akademický článek
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Autor:
I Peltekova, Namik Kaya, Ahmed Al-Abdullatif, Mohammed Al-Owain, Eissa Faqeih, Anjum Saeed, Mohamed S. Rashed, Mohamed Saleh Amoudi, Syed H.E. Zaidi, Muhammad Faiyaz-Ul-Haque, Masood Jamil, Halah Abalkhail, Moeenaldeen Al-Sayed
Publikováno v:
Annals of Saudi Medicine, Vol 34, Iss 2, Pp 107-114 (2014)
BACKGROUND AND OBJECTIVES: L-2-hydroxyglutaric aciduria is a neurometabolic disorder with autosomal recessive mode of inheritance in which patients exhibit elevated L-2-hydroxyglutaric acid in body fluids, central nervous system manifestations, and i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8031d0e8fcc44370b7d70fc5091ea3e6
https://doi.org/10.5144/0256-4947.2014.107
https://doi.org/10.5144/0256-4947.2014.107
Autor:
H A Abalkhail, Muhammad Faiyaz-Ul-Haque, I Peltekova, Zuhair Rahbeeni, Taghreed Shuaib, Zuhair N. Al-Hassnan, S H E Zaidi, A Balobaid, Mohammed Al-Owain, A Al-Abdullatif
Publikováno v:
Clinical Genetics. 81:563-570
Zaidi SHE, Faiyaz-Ul-Haque M, Shuaib T, Balobaid A, Rahbeeni Z, Abalkhail H, Al-Abdullatif A, Al-Hassnan Z, Peltekova I and Al-Owain M. Clinical and molecular findings of 13 families from Saudi Arabia and a family from Sudan with homocystinuria. Homo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cc514da4f1743fd8e2e05363c063105
https://doi.org/10.1111/j.1399-0004.2011.01690.x
https://doi.org/10.1111/j.1399-0004.2011.01690.x
Autor:
Abdullah Al-Jefri, Monogaran S. Pulicat, Ameera Gaafar, I Peltekova, Hala Abalkhail, Syed H.E. Zaidi, Muhammad Faiyaz-Ul-Haque, Randa Al-Nounou, Ayodele Alaiya, Ahmed Al-Abdullatif, Jalaluddin A. K. M. Bhuiyan, Fouad Al-Dayel
Publikováno v:
European Journal of Pediatrics. 169:661-666
Autosomal recessive severe congenital neutropenia (SCN) results from a maturation arrest of granulopoiesis at the level of promyelocytes and apoptosis of myeloid cells. In SCN patients, mutations have been described in the HAX1 gene. Most of the SCN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41c656e624944df9a74f763eb4ea9de1
https://doi.org/10.1007/s00431-010-1150-6
https://doi.org/10.1007/s00431-010-1150-6
Akademický článek
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