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Ali Asery

Showing results (11-20 of 20) with videos related to

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Frontiers in Pediatrics|December 3, 2021
Clinical, Biochemical, and Molecular Characterization of Neonatal-Onset Dubin-Johnson Syndrome in a Large Case Series From the ArabsAbdulrahman Al-Hussaini, Badr AlSaleem, Hamad AlHomaidani, et al.
The Journal of Pediatrics|April 29, 2021
ATP8B1, ABCB11, and ABCB4 Genes Defects: Novel Mutations Associated with Cholestasis with Different Phenotypes and OutcomesAbdulrahman Al-Hussaini, Khurram Lone, Muhammed Salman Bashir, et al.
Journal of Pediatric Gastroenterology and Nutrition|December 21, 2020
Deamidated Gliadin Antibodies: Do They Add to Tissue Transglutaminase-IgA Assay in Screening for Celiac Disease?Ashraf Abdulrahim, Mosa Fagih, Riccardo Troncone, et al.
Pediatric Emergency Care|July 27, 2019
What Do Saudi Children Ingest?: A 10-Year Retrospective Analysis of Ingested Foreign Bodies From a Tertiary Care CenterAhmed H Ibrahim, Abdurahman Andijani, Muhammed Abdulshakour, et al.
The Journal of Pediatrics|December 11, 2013
Clinical and molecular characteristics of mitochondrial DNA depletion syndrome associated with neonatal cholestasis and liver failureAbdulrahman Al-Hussaini, Eissa Faqeih, Ayman W El-Hattab, et al.
Inflammatory Bowel Diseases|May 3, 2014
Incidence of pediatric inflammatory bowel disease in Saudi Arabia: a multicenter national studyMohammad I El Mouzan, Omar Saadah, Khalid Al-Saleem, et al.
Frontiers in Pediatrics|August 4, 2022
The Epidemiology and Outcome of Biliary Atresia: Saudi Arabian National Study (2000-2018)Abdulrahman Al-Hussaini, Mohammed Abanemai, Homoud Alhebbi, et al.
European Journal of Human Genetics : EJHG|May 30, 2013
Clinical, biochemical, cellular and molecular characterization of mitochondrial DNA depletion syndrome due to novel mutations in the MPV17 geneJohanna Uusimaa, Julie Evans, Conrad Smith, et al.
Frontiers in Genetics|January 18, 2021
Exploiting the Autozygome to Support Previously Published Mendelian Gene-Disease Associations: An UpdateSateesh Maddirevula, Hanan E Shamseldin, Amy Sirr, et al.
Genome Medicine|June 18, 2019
Exome sequencing in routine diagnostics: a generic test for 254 patients with primary immunodeficienciesPeer Arts, Annet Simons, Mofareh S AlZahrani, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

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Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Frontiers in Pediatrics|December 3, 2021
Clinical, Biochemical, and Molecular Characterization of Neonatal-Onset Dubin-Johnson Syndrome in a Large Case Series From the ArabsAbdulrahman Al-Hussaini, Badr AlSaleem, Hamad AlHomaidani, et al.
The Journal of Pediatrics|April 29, 2021
ATP8B1, ABCB11, and ABCB4 Genes Defects: Novel Mutations Associated with Cholestasis with Different Phenotypes and OutcomesAbdulrahman Al-Hussaini, Khurram Lone, Muhammed Salman Bashir, et al.
Journal of Pediatric Gastroenterology and Nutrition|December 21, 2020
Deamidated Gliadin Antibodies: Do They Add to Tissue Transglutaminase-IgA Assay in Screening for Celiac Disease?Ashraf Abdulrahim, Mosa Fagih, Riccardo Troncone, et al.
Pediatric Emergency Care|July 27, 2019
What Do Saudi Children Ingest?: A 10-Year Retrospective Analysis of Ingested Foreign Bodies From a Tertiary Care CenterAhmed H Ibrahim, Abdurahman Andijani, Muhammed Abdulshakour, et al.
The Journal of Pediatrics|December 11, 2013
Clinical and molecular characteristics of mitochondrial DNA depletion syndrome associated with neonatal cholestasis and liver failureAbdulrahman Al-Hussaini, Eissa Faqeih, Ayman W El-Hattab, et al.
Inflammatory Bowel Diseases|May 3, 2014
Incidence of pediatric inflammatory bowel disease in Saudi Arabia: a multicenter national studyMohammad I El Mouzan, Omar Saadah, Khalid Al-Saleem, et al.
Frontiers in Pediatrics|August 4, 2022
The Epidemiology and Outcome of Biliary Atresia: Saudi Arabian National Study (2000-2018)Abdulrahman Al-Hussaini, Mohammed Abanemai, Homoud Alhebbi, et al.
European Journal of Human Genetics : EJHG|May 30, 2013
Clinical, biochemical, cellular and molecular characterization of mitochondrial DNA depletion syndrome due to novel mutations in the MPV17 geneJohanna Uusimaa, Julie Evans, Conrad Smith, et al.
Frontiers in Genetics|January 18, 2021
Exploiting the Autozygome to Support Previously Published Mendelian Gene-Disease Associations: An UpdateSateesh Maddirevula, Hanan E Shamseldin, Amy Sirr, et al.
Genome Medicine|June 18, 2019
Exome sequencing in routine diagnostics: a generic test for 254 patients with primary immunodeficienciesPeer Arts, Annet Simons, Mofareh S AlZahrani, et al.
Pageof 2