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A Moosa

Showing results (131-140 of 138) with videos related to

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Human Mutation|October 23, 2001
Congenital insensitivity to pain with anhidrosis (CIPA): novel mutations of the TRKA (NTRK1) gene, a putative uniparental disomy, and a linkage of the mutant TRKA and PKLR genes in a family with CIPA and pyruvate kinase deficiencyY Indo, S Mardy, Y Miura, et al.
Saudi Medical Journal|April 16, 2002
Proinflammatory cytokines in open versus laparoscopic cholecystectomySaeed A Abu-Eshy, Riyad A Moosa, Abdalla A Al-Rofaidi, et al.
Plos One|February 22, 2022
Proportion and seasonality of blood parasites in animals in Mosul using the Veterinary Teaching Hospital Lab dataHussam M S Alimam, Dhiyaa A Moosa, Eva A Ajaj, et al.
Saudi Medical Journal|July 1, 2020
Prevalence of toxoplasmosis, rubella, cytomegalovirus, and herpes (TORCH) infections among women attending the antenatal care clinic, maternity hospital in Abha, Southwestern Saudi ArabiaAhmed M Al-Hakami, Esther Paul, Faten Al-Abed, et al.
Ecohealth|May 20, 2021
Toxocara Awareness Among Medical Practitioners in Saudi ArabiaFakhreldin M Omer, Nabil J Awadalla, Safar Abadi Alsaleem, et al.
American Journal of Human Genetics|May 20, 1999
Congenital insensitivity to pain with anhidrosis: novel mutations in the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factorS Mardy, Y Miura, F Endo, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|March 6, 2012
Concentration of free vascular endothelial growth factor and its soluble receptor, sFlt-1 in the maternal and fetal circulations of normal term pregnancies at high and low altitudesKamal Z M Ali, Graham J Burton, Ali M Al-Binali, et al.
Pediatrics|April 1, 1997
The clinical phenotype of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria): case reports of 23 new patientsK M Gibson, E Christensen, C Jakobs, et al.
Pageof 14

Showing results (131-140 of 138) with videos related to

Sort By:
Pageof 14
You have reached the last page of results.This site can display upto 138 results.
Human Mutation|October 23, 2001
Congenital insensitivity to pain with anhidrosis (CIPA): novel mutations of the TRKA (NTRK1) gene, a putative uniparental disomy, and a linkage of the mutant TRKA and PKLR genes in a family with CIPA and pyruvate kinase deficiencyY Indo, S Mardy, Y Miura, et al.
Saudi Medical Journal|April 16, 2002
Proinflammatory cytokines in open versus laparoscopic cholecystectomySaeed A Abu-Eshy, Riyad A Moosa, Abdalla A Al-Rofaidi, et al.
Plos One|February 22, 2022
Proportion and seasonality of blood parasites in animals in Mosul using the Veterinary Teaching Hospital Lab dataHussam M S Alimam, Dhiyaa A Moosa, Eva A Ajaj, et al.
Saudi Medical Journal|July 1, 2020
Prevalence of toxoplasmosis, rubella, cytomegalovirus, and herpes (TORCH) infections among women attending the antenatal care clinic, maternity hospital in Abha, Southwestern Saudi ArabiaAhmed M Al-Hakami, Esther Paul, Faten Al-Abed, et al.
Ecohealth|May 20, 2021
Toxocara Awareness Among Medical Practitioners in Saudi ArabiaFakhreldin M Omer, Nabil J Awadalla, Safar Abadi Alsaleem, et al.
American Journal of Human Genetics|May 20, 1999
Congenital insensitivity to pain with anhidrosis: novel mutations in the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factorS Mardy, Y Miura, F Endo, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|March 6, 2012
Concentration of free vascular endothelial growth factor and its soluble receptor, sFlt-1 in the maternal and fetal circulations of normal term pregnancies at high and low altitudesKamal Z M Ali, Graham J Burton, Ali M Al-Binali, et al.
Pediatrics|April 1, 1997
The clinical phenotype of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria): case reports of 23 new patientsK M Gibson, E Christensen, C Jakobs, et al.
Pageof 14