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Galina Ling

Showing results (31-40 of 39) with videos related to

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Antibiotics (Basel, Switzerland)|September 28, 2024
The Effectiveness of Taurolidine Antimicrobial Locks in Preventing Catheter-Related Bloodstream Infections (CRBSIs) in Children Receiving Parenteral Nutrition: A Case SeriesGalina Ling, Shalom Ben-Shimol, Siham Elamour, et al.
European Journal of Human Genetics : EJHG|January 4, 2023
X-linked C1GALT1C1 mutation causes atypical hemolytic uremic syndromeNoam Hadar, Ruth Schreiber, Marina Eskin-Schwartz, et al.
Clinical Genetics|July 4, 2020
Pituitary stalk interruption syndrome broadens the clinical spectrum of the TTC26 ciliopathyOdeya David, Marina Eskin-Schwartz, Galina Ling, et al.
Clinical Genetics|October 10, 2023
CLDN1 Arg81His founder variant causes ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis (ILVASC) syndrome in Moroccan JewsMarina Eskin-Schwartz, Vadim Dolgin, Elena Didkovsky, et al.
Frontiers in Immunology|March 3, 2020
Alterations in T and B Cell Receptor Repertoires Patterns in Patients With IL10 Signaling Defects and History of Infantile-Onset IBDLael Werner, Yu Nee Lee, Erez Rechavi, et al.
Frontiers in Pediatrics|August 8, 2022
Hypoparathyroidism-retardation-dysmorphism syndrome-Clinical insights from a large longitudinal cohort in a single medical centerOdeya David, Rotem Agur, Rosa Novoa, et al.
Orphanet Journal of Rare Diseases|September 9, 2021
The effects of the COVID-19 pandemic on patients with lysosomal storage disorders in IsraelEyal Kristal, Ben Pode-Shakked, Guy Hazan, et al.
Journal of Pediatric Gastroenterology and Nutrition|September 14, 2020
Predictive Prenatal Diagnosis for Infantile-onset Inflammatory Bowel Disease Because of Interleukin-10 Signalling DefectsZiqing Ye, Wenhui Hu, Bingbing Wu, et al.
Blood|September 22, 2023
Loss of function of ENT3 drives histiocytosis and inflammation through TLR-MAPK signalingRuth Shiloh, Ruth Lubin, Odeya David, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Antibiotics (Basel, Switzerland)|September 28, 2024
The Effectiveness of Taurolidine Antimicrobial Locks in Preventing Catheter-Related Bloodstream Infections (CRBSIs) in Children Receiving Parenteral Nutrition: A Case SeriesGalina Ling, Shalom Ben-Shimol, Siham Elamour, et al.
European Journal of Human Genetics : EJHG|January 4, 2023
X-linked C1GALT1C1 mutation causes atypical hemolytic uremic syndromeNoam Hadar, Ruth Schreiber, Marina Eskin-Schwartz, et al.
Clinical Genetics|July 4, 2020
Pituitary stalk interruption syndrome broadens the clinical spectrum of the TTC26 ciliopathyOdeya David, Marina Eskin-Schwartz, Galina Ling, et al.
Clinical Genetics|October 10, 2023
CLDN1 Arg81His founder variant causes ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis (ILVASC) syndrome in Moroccan JewsMarina Eskin-Schwartz, Vadim Dolgin, Elena Didkovsky, et al.
Frontiers in Immunology|March 3, 2020
Alterations in T and B Cell Receptor Repertoires Patterns in Patients With IL10 Signaling Defects and History of Infantile-Onset IBDLael Werner, Yu Nee Lee, Erez Rechavi, et al.
Frontiers in Pediatrics|August 8, 2022
Hypoparathyroidism-retardation-dysmorphism syndrome-Clinical insights from a large longitudinal cohort in a single medical centerOdeya David, Rotem Agur, Rosa Novoa, et al.
Orphanet Journal of Rare Diseases|September 9, 2021
The effects of the COVID-19 pandemic on patients with lysosomal storage disorders in IsraelEyal Kristal, Ben Pode-Shakked, Guy Hazan, et al.
Journal of Pediatric Gastroenterology and Nutrition|September 14, 2020
Predictive Prenatal Diagnosis for Infantile-onset Inflammatory Bowel Disease Because of Interleukin-10 Signalling DefectsZiqing Ye, Wenhui Hu, Bingbing Wu, et al.
Blood|September 22, 2023
Loss of function of ENT3 drives histiocytosis and inflammation through TLR-MAPK signalingRuth Shiloh, Ruth Lubin, Odeya David, et al.
Pageof 4