Zobrazeno 1 - 10
of 115
pro vyhledávání: '"A. Peykar"'
Publikováno v:
Grasas y Aceites, Vol 75, Iss 1 (2024)
In this study, sour cherry kernel oil was converted to biodiesel by microwave-assisted transesterification. Evaluations were made of several variables, namely, reaction time (1, 2, 3, 4, and 5 min), microwave power (100, 200, 300, 400, and 500 W), me
Externí odkaz:
https://doaj.org/article/cbcb6892c315494e822dfd2fafa5ab43
Autor:
Peykar, Sedigheh1 (AUTHOR), Vahedparast, Hakimeh2 (AUTHOR), Gharibi, Tayebeh3 (AUTHOR), Bagherzadeh, Razieh3 (AUTHOR) r.bagherzadeh@bpums.ac.ir
Publikováno v:
BMC Nursing. 12/8/2023, Vol. 22 Issue 1, p1-15. 15p.
Akademický článek
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Publikováno v:
International Journal of Nutrition Sciences; Sep2023, Vol. 8 Issue 3, p184-192, 9p
Autor:
Reza Ebrahimzadeh-Vesal, Seyed kianush Hosseini, Fereshteh Rezakhanlu, Pupak Derakhshandeh-Peykar
Publikováno v:
Reports of Biochemistry and Molecular Biology, Vol 2, Iss 1, Pp 52-55 (2013)
Holt-Oram syndrome (HOS) is a developmental disorder inherited in an autosomal-dominant pattern. Affected organs are the heart and forelimbs with upper extremity skeletal defects and congenital heart malformation. In this study we present three cases
Externí odkaz:
https://doaj.org/article/0edd24bbbeea482689b3480d920a4944
Autor:
Aliakbar Rahbarimanesh, Pupak Derakhshandeh-Peykar, Amirhassan Barkhordari, Reza Ebrahimzadeh-Vesal, Soja Shamizadeh Kalkhoran
Publikováno v:
Reports of Biochemistry and Molecular Biology, Vol 1, Iss 2, Pp 87-90 (2013)
Background: Here we describe a new case of partial distal 10q trisomy in a 6-year-old Iranian girl from healthy parents with mental, growth, and psychomotor retardations. Methods: Additional clinical features include dysmorphic craniofacial features
Externí odkaz:
https://doaj.org/article/d1e67c92f2834d64bf195dc821d1d0df
Autor:
Vahideh Moin-Vaziri, Mohammad Ali Oshaghi, Mohammad Reza Yaghoobi-Ershadi, Pupak Derakhshandeh-Peykar, Mohammad Reza Abaei, Fatemeh Mohtarami, Ali Reza Zahraei-Ramezani, Aboulhassan Nadim
Publikováno v:
Journal of Arthropod-Borne Diseases, Vol 10, Iss 4 (2016)
Background: Phlebotomus sergenti s.l. is considered the most likely vector of Leishmania tropica in Iran. Although two morphotypes- P. sergenti sergenti (A) and P. sergenti similis (B)-have been formally described, further morphological and a molec
Externí odkaz:
https://doaj.org/article/4af09d76b1c0416cb6ce6ec7c7454082
Autor:
Akhavan-Niaki, Haleh, Derakhshandeh-Peykar, Poupak, Banihashemi, Ali, Mostafazadeh, Amrollah, Asghari, Beheshteh, Ahmadifard, Mohammad-Reza, Azizi, Mandana, Youssefi, Ali, Elmi, Maryam Mitra
Publikováno v:
In Blood Cells, Molecules and Diseases 2011 47(1):29-32
Publikováno v:
Tehran University Medical Journal, Vol 67, Iss 1, Pp 42-48 (2009)
"nBackground: Leukemia is one of the most common pediatric malignancies. T-cell Acute Lymphoblastic Leukemia (T-ALL) accounts for 15% of hematopoetic cancers. It has been well understood that identification of genetic alterations associated with leuk
Externí odkaz:
https://doaj.org/article/7e68c54bbf36418f990b5b5a305bc8ed
Publikováno v:
Iranian Journal of Public Health, Vol 37, Iss 2, Pp 106-111 (2008)
Background: β -thalassemia is a common autosomal recessive disorder resulting from over 200 different mutations of beta globin genes. The aim of the present study was to identify the distribution and frequency of the most common β -thalassemia muta
Externí odkaz:
https://doaj.org/article/1b1408bd257b4fe6a13ee7ee2243d642