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Anjum Saeed

Showing results (41-50 of 49) with videos related to

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Saudi Medical Journal|May 20, 2015
Assessment of knowledge of celiac disease among health care professionalsAsaad M Assiri, Anjum Saeed, Elshazaly Saeed, et al.
Journal of Crohn'S & Colitis|November 5, 2016
Fungal Microbiota Profile in Newly Diagnosed Treatment-naïve Children with Crohn's DiseaseMohammad El Mouzan, Feng Wang, Mohammad Al Mofarreh, et al.
Annals of Saudi Medicine|June 5, 2014
Clinical, neuroimaging, and genetic features of L-2-hydroxyglutaric aciduria in Arab kindredsMuhammad Faiyaz-Ul-Haque, Moeenaldeen D Al-Sayed, Eissa Faqeih, et al.
NPJ Genomic Medicine|October 21, 2020
Genomic testing in 1019 individuals from 349 Pakistani families results in high diagnostic yield and clinical utilityHuma Cheema, Aida M Bertoli-Avella, Volha Skrahina, et al.
Molecular Diagnosis & Therapy|August 13, 2015
High frequency and poor prognosis of late childhood BCR-ABL-positive and MLL-AF4-positive ALL define the need for advanced molecular diagnostics and improved therapeutic strategies in pediatric B-ALL in PakistanZafar Iqbal, Tanveer Akhtar, Tashfin Awan, 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.
Journal of Medical Genetics|December 25, 2021
A disorder clinically resembling cystic fibrosis caused by biallelic variants in the <i>AGR2</i> geneAida Bertoli-Avella, Ronja Hotakainen, Maryam Al Shehhi, et al.
American Journal of Human Genetics|August 31, 2022
Bi-allelic loss-of-function variants in TMEM147 cause moderate to profound intellectual disability with facial dysmorphism and pseudo-Pelger-Huët anomalyQuentin Thomas, Marialetizia Motta, Thierry Gautier, et al.
Nature Communications|April 15, 2026
Variants in the proteasome regulator PSMF1 cause a phenotypic spectrum from parkinsonism to perinatal lethalityFrancesca Magrinelli, Christelle Tesson, Plamena R Angelova, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
Saudi Medical Journal|May 20, 2015
Assessment of knowledge of celiac disease among health care professionalsAsaad M Assiri, Anjum Saeed, Elshazaly Saeed, et al.
Journal of Crohn'S & Colitis|November 5, 2016
Fungal Microbiota Profile in Newly Diagnosed Treatment-naïve Children with Crohn's DiseaseMohammad El Mouzan, Feng Wang, Mohammad Al Mofarreh, et al.
Annals of Saudi Medicine|June 5, 2014
Clinical, neuroimaging, and genetic features of L-2-hydroxyglutaric aciduria in Arab kindredsMuhammad Faiyaz-Ul-Haque, Moeenaldeen D Al-Sayed, Eissa Faqeih, et al.
NPJ Genomic Medicine|October 21, 2020
Genomic testing in 1019 individuals from 349 Pakistani families results in high diagnostic yield and clinical utilityHuma Cheema, Aida M Bertoli-Avella, Volha Skrahina, et al.
Molecular Diagnosis & Therapy|August 13, 2015
High frequency and poor prognosis of late childhood BCR-ABL-positive and MLL-AF4-positive ALL define the need for advanced molecular diagnostics and improved therapeutic strategies in pediatric B-ALL in PakistanZafar Iqbal, Tanveer Akhtar, Tashfin Awan, 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.
Journal of Medical Genetics|December 25, 2021
A disorder clinically resembling cystic fibrosis caused by biallelic variants in the <i>AGR2</i> geneAida Bertoli-Avella, Ronja Hotakainen, Maryam Al Shehhi, et al.
American Journal of Human Genetics|August 31, 2022
Bi-allelic loss-of-function variants in TMEM147 cause moderate to profound intellectual disability with facial dysmorphism and pseudo-Pelger-Huët anomalyQuentin Thomas, Marialetizia Motta, Thierry Gautier, et al.
Nature Communications|April 15, 2026
Variants in the proteasome regulator PSMF1 cause a phenotypic spectrum from parkinsonism to perinatal lethalityFrancesca Magrinelli, Christelle Tesson, Plamena R Angelova, et al.
Pageof 5