Zobrazeno 1 - 10
of 83
pro vyhledávání: '"Houcher, A."'
Publikováno v:
In Journal of Magnetism and Magnetic Materials 15 October 2020 512
Publikováno v:
In Egyptian Journal of Medical Human Genetics July 2018 19(3):225-229
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 19, Iss 3, Pp 225-229 (2018)
Background: Neural tube defects (NTDs) are severe birth defects, with genetic and/or environmental risk factors. Aim: The objective of this study was to analyze data on NTDs cases at the Batna Maternity Hospital and to investigate some environmental
Externí odkaz:
https://doaj.org/article/0e82842bf37e40279dc181eb6c8c4ff3
Autor:
Amrane Mounira, Begag Samia, Houcher Zahira, Houcher Bakhouche, Touabti Abderrezak, Nasri Ramdane, Boussouf Kheira, Khattabi Soumia
Publikováno v:
Pteridines, Vol 25, Iss 3-4, Pp 69-74 (2014)
We studied total plasma homocysteine levels (tHcy) in Algerian patients with a deep venous thrombosis (DVT). We measured tHcy levels in a total of 99 subjects enrolled in this study, including 40 patients with DVT and 59 healthy controls. The mean tH
Externí odkaz:
https://doaj.org/article/303967776e3449c796e3b377871961ee
Publikováno v:
Pteridines, Vol 24, Iss 3-4, Pp 251-255 (2013)
α-Thalassemia (α-thal) is one of the most common genetic disorders in the world. It is characterized by the absence or reduced expression of α-globin genes. This study was carried out to evaluate the allelic frequency of α-thal defects in a patie
Externí odkaz:
https://doaj.org/article/5bcc46fbe35c4f188a22c61711ddd569
Autor:
Amrane Mounira, Houcher Zahira, Begag Samia, Houcher Bakhouche, Benlatreche Cherifa, Touabti Abderrezak, Laouamri Slimane, Malek Rachid
Publikováno v:
Pteridines, Vol 23, Iss 1, Pp 96-103 (2012)
Homocysteine (HCY) has been identified as a risk factor for vascular disease in the general population. Diabetic retinopathy (DR) itself rather than hyperhomocysteinemia is the leading cause of blindness among patients with type 2 diabetes mellitus (
Externí odkaz:
https://doaj.org/article/a57e198143644e258febf41b90c4faa1
Publikováno v:
Pteridines, Vol 23, Iss 1, Pp 14-21 (2012)
The C677T variant of methylenetetrahydrofolate reductase (MTHFR), a key enzyme in the remethylation of homocysteine (HCY) to methionine, is a frequent genetic cause of moderate hyperhomocysteinemia (HHCY) among individuals with cardiovascular disease
Externí odkaz:
https://doaj.org/article/e32b584e8907494b93521dcd6aab5660
Autor:
Houcher Zahira, Houcher Bakhouche, Touabti Abderezak, Begag Samia, Öztürk Ayşenur, Egin Yonca, Akar Nejat, Djabi Farida
Publikováno v:
Pteridines, Vol 21, Iss 1, Pp 103-109 (2010)
The aim of the present study was to explore the influence of age and gender, on the association between the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and plasma total homocysteine (tHcy) concentrations in patients with cardiovasc
Externí odkaz:
https://doaj.org/article/fe08ff39c87b4f10832a4262fbc3fcdf
Publikováno v:
Pteridines, Vol 19, Iss 1, Pp 12-18 (2008)
Neural tube defects (NTDs) including spina bifida, anencephaly and encephalocele are among the most common birth defects, with high associated mortality and morbidity. There are no data concerning the incidence, associated anomalies, treatment and ou
Externí odkaz:
https://doaj.org/article/fc6bc43d2caf46cbb477546c6360cdf8
Publikováno v:
Pteridines, Vol 18, Iss 1, Pp 8-18 (2007)
Nigella sativa is a medicinal plant widely used in the Arabic and Islamic world against a number of human pathologies. In this present study the methanol extraction (85 % then 50 %) of plant seeds gave an important yield of 27 % of dry substance. The
Externí odkaz:
https://doaj.org/article/65dd80e4ca81448799f1399931bc3e26