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Yshia Langer

Showing results (1-10 of 5) with videos related to

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Acta Paediatrica (Oslo, Norway : 1992)|June 12, 2018
Questionnaire-based study showed that neonatal chest radiographs could be reliably interpreted using the WhatsApp messaging applicationItai Gross, Yshia Langer, Yehonatan Pasternak, et al.
American Journal of Perinatology|August 4, 2025
Line Insertion through a Long Umbilical Stump: A Concept Generating Laboratory StudyItamar Nitzan, Yshia Langer, Yair Kasirer, et al.
CJEM|February 26, 2026
Point-of-care ultrasound for the evaluation of dental abscesses in the pediatric emergency departmentItai Gross, Maria Nassar, Noa Guzner, et al.
World Journal for Pediatric & Congenital Heart Surgery|March 13, 2025
The Association Between Platelet Transfusion and Acute Kidney Injury Following Fontan SurgeryMarianne E Nellis, Asaf Mandel, Yshia Langer, et al.
European Journal of Human Genetics : EJHG|November 13, 2014
A syndrome of congenital microcephaly, intellectual disability and dysmorphism with a homozygous mutation in FRMD4ADina Fine, Hagit Flusser, Barak Markus, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Acta Paediatrica (Oslo, Norway : 1992)|June 12, 2018
Questionnaire-based study showed that neonatal chest radiographs could be reliably interpreted using the WhatsApp messaging applicationItai Gross, Yshia Langer, Yehonatan Pasternak, et al.
American Journal of Perinatology|August 4, 2025
Line Insertion through a Long Umbilical Stump: A Concept Generating Laboratory StudyItamar Nitzan, Yshia Langer, Yair Kasirer, et al.
CJEM|February 26, 2026
Point-of-care ultrasound for the evaluation of dental abscesses in the pediatric emergency departmentItai Gross, Maria Nassar, Noa Guzner, et al.
World Journal for Pediatric & Congenital Heart Surgery|March 13, 2025
The Association Between Platelet Transfusion and Acute Kidney Injury Following Fontan SurgeryMarianne E Nellis, Asaf Mandel, Yshia Langer, et al.
European Journal of Human Genetics : EJHG|November 13, 2014
A syndrome of congenital microcephaly, intellectual disability and dysmorphism with a homozygous mutation in FRMD4ADina Fine, Hagit Flusser, Barak Markus, et al.
Pageof 1