Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Raida Khalil"'
Autor:
Islam Oguz Tuncay, Nancy L. Parmalee, Raida Khalil, Kiran Kaur, Ashwani Kumar, Mohamed Jimale, Jennifer L. Howe, Kimberly Goodspeed, Patricia Evans, Loai Alzghoul, Chao Xing, Stephen W. Scherer, Maria H. Chahrour
Publikováno v:
npj Genomic Medicine, Vol 7, Iss 1, Pp 1-13 (2022)
Abstract Autism spectrum disorder (ASD) is a collection of neurodevelopmental disorders characterized by deficits in social communication and restricted, repetitive patterns of behavior or interests. ASD is highly heritable, but genetically and pheno
Externí odkaz:
https://doaj.org/article/d6d434712fd840fda9626e03757e5a1f
Autor:
Mahmoud N. Abo-Shehada, Raida Khalil, Marwan Abu-Halaweh, Kanar Sweis, Zuhair Amr, Lena Billeh
Publikováno v:
Revista Brasileira de Parasitologia Veterinária, Vol 30, Iss 3 (2021)
Abstract This cross-sectional study investigates Toxoplasma gondii and Neospora caninum among 445 recently spontaneously aborted (RSA) Jordanian women using ELISA and indirect fluorescent antibody (at a cut-off value of 1/200) tests, respectively. Th
Externí odkaz:
https://doaj.org/article/22db76e9f4c94002a477263cab01b393
Publikováno v:
Nanomaterials, Vol 12, Iss 8, p 1381 (2022)
Prosthetic joint infections (PJIs) ensued from total joint replacement (TJR) pose a severe threat to patients that involve poor health outcomes, severe pain, death (in severe cases), and negative influence patients’ quality of life. Antibiotic-load
Externí odkaz:
https://doaj.org/article/8264b8c273a64f59b5590bd7a55cd64e
Publikováno v:
Revista Brasileira de Parasitologia Veterinária, Vol 29, Iss 2 (2020)
Abstract A cross-sectional study was carried out on a sample of 379 horses to determine the seroprevalence of Neospora spp. in Jordan using the indirect fluorescent antibody test. Five variables, namely locality (n=10), climatic zone (n=4), age group
Externí odkaz:
https://doaj.org/article/79be0b2ff3594b4dbbae0bb48b54bfe8
Publikováno v:
Journal Of Advanced Pharmacy Education And Research. 12:46-55
Publikováno v:
AIMS Molecular Science. 8:60-75
Alkaptonuria (AKU) is a rare metabolic disease which is inherited as an autosomal recessive trait. It is characterized by the accumulation of homogentisic acid over time in various tissues of the body particularly connective tissues. This genetic dis
Autor:
Marwan Abu-Halaweh, Mahmoud N. Abo-Shehada, Lena Billeh, Raida Khalil, Zuhair S. Amr, Kanar Sweis
Publikováno v:
Revista Brasileira de Parasitologia Veterinária, Vol 30, Iss 3 (2021)
Revista Brasileira de Parasitologia Veterinária v.30 n.3 2021
Revista Brasileira de Parasitologia Veterinária
Colégio Brasileiro de Parasitologia Veterinária (CBPV)
instacron:CBPV
Revista Brasileira de Parasitologia Veterinária v.30 n.3 2021
Revista Brasileira de Parasitologia Veterinária
Colégio Brasileiro de Parasitologia Veterinária (CBPV)
instacron:CBPV
This cross-sectional study investigates Toxoplasma gondii and Neospora caninum among 445 recently spontaneously aborted (RSA) Jordanian women using ELISA and indirect fluorescent antibody (at a cut-off value of 1/200) tests, respectively. The type of
In the middle of 2020 coronavirus had becoming spread around the world with a high number of people infected with covid-19, which makes covid-19 international pandemic that leads the governments around the world to decided strict roles to prevent the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5cbac4abfdc912eae93a7c9c1e94813
Autor:
Amer Imraish, Wajdy Al-Awaida, Omar Al bawareed, Hamzeh J Al-Ameer, Hadeel Al‐Turk, Ghizal Fatima, Akram Al Deek, Moh'd Mohanad Al-Dabet, Raida Khalil, Muhanad Akash
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f807a2a3e2ef45c336a9410b90ace52
https://doi.org/10.1111/imig.12847/v4/response1
https://doi.org/10.1111/imig.12847/v4/response1
Autor:
Raida Khalil, Eman Albsoul, Nesrin Mwafi, Arwa Alsaraireh, Ibrahim Al Sbou, Dema Ali, Loiy Obeidat
Publikováno v:
BioMed Research International
BioMed Research International, Vol 2021 (2021)
BioMed Research International, Vol 2021 (2021)
Background. Metabolic disorder alkaptonuria is an autosomal recessive disorder caused by mutations in the HGD gene, and a deficiency HGD enzyme activity results in an accumulation of homogentisic acid (HGA), ochronosis, and destruction of connective