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Showing results (31-40 of 37) with videos related to

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Archives of Disease in Childhood|March 26, 2010
Mitochondrial encephalocardio-myopathy with early neonatal onset due to TMEM70 mutationTomás Honzík, Markéta Tesarová, Johannes A Mayr, et al.
Social Science & Medicine (1982)|December 3, 2014
Experiences of stigma and discrimination of people with schizophrenia in IndiaMirja Koschorke, R Padmavati, Shuba Kumar, et al.
Journal of Inherited Metabolic Disease|October 22, 2020
Clinical and molecular characterization of adult patients with late-onset MTHFR deficiencyCecilia Marelli, Christian Lavigne, Karolina M Stepien, et al.
Trials|April 3, 2014
The effectiveness and cost-effectiveness of lay counsellor-delivered psychological treatments for harmful and dependent drinking and moderate to severe depression in primary care in India: PREMIUM study protocol for randomized controlled trialsVikram Patel, Benedict Weobong, Abhijit Nadkarni, et al.
Blood|April 11, 2020
A homozygous deletion in the SLC19A1 gene as a cause of folate-dependent recurrent megaloblastic anemiaMichael Svaton, Karolina Skvarova Kramarzova, Veronika Kanderova, et al.
Diabetes Technology & Therapeutics|May 30, 2025
Hybrid Closed-Loop Therapy in Adults with Type 1 Diabetes in England: Long-Term Outcomes from a Real-World Observational StudyAlexandros L Liarakos, Thomas S J Crabtree, Tomás P Griffin, et al.
Journal of Inherited Metabolic Disease|February 19, 2019
Phenotype, treatment practice and outcome in the cobalamin-dependent remethylation disorders and MTHFR deficiency: Data from the E-HOD registryMartina Huemer, Daria Diodato, Diego Martinelli, et al.
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Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Archives of Disease in Childhood|March 26, 2010
Mitochondrial encephalocardio-myopathy with early neonatal onset due to TMEM70 mutationTomás Honzík, Markéta Tesarová, Johannes A Mayr, et al.
Social Science & Medicine (1982)|December 3, 2014
Experiences of stigma and discrimination of people with schizophrenia in IndiaMirja Koschorke, R Padmavati, Shuba Kumar, et al.
Journal of Inherited Metabolic Disease|October 22, 2020
Clinical and molecular characterization of adult patients with late-onset MTHFR deficiencyCecilia Marelli, Christian Lavigne, Karolina M Stepien, et al.
Trials|April 3, 2014
The effectiveness and cost-effectiveness of lay counsellor-delivered psychological treatments for harmful and dependent drinking and moderate to severe depression in primary care in India: PREMIUM study protocol for randomized controlled trialsVikram Patel, Benedict Weobong, Abhijit Nadkarni, et al.
Blood|April 11, 2020
A homozygous deletion in the SLC19A1 gene as a cause of folate-dependent recurrent megaloblastic anemiaMichael Svaton, Karolina Skvarova Kramarzova, Veronika Kanderova, et al.
Diabetes Technology & Therapeutics|May 30, 2025
Hybrid Closed-Loop Therapy in Adults with Type 1 Diabetes in England: Long-Term Outcomes from a Real-World Observational StudyAlexandros L Liarakos, Thomas S J Crabtree, Tomás P Griffin, et al.
Journal of Inherited Metabolic Disease|February 19, 2019
Phenotype, treatment practice and outcome in the cobalamin-dependent remethylation disorders and MTHFR deficiency: Data from the E-HOD registryMartina Huemer, Daria Diodato, Diego Martinelli, et al.
Pageof 4