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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 application
Itai 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 Study
Itamar 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 department
Itai 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 Surgery
Marianne 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 FRMD4A
Dina Fine, Hagit Flusser, Barak Markus, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 5) with videos related to
Sort By:
Page
of 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 application
Itai 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 Study
Itamar 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 department
Itai 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 Surgery
Marianne 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 FRMD4A
Dina Fine, Hagit Flusser, Barak Markus, et al.
Page
of 1