Gustavo Malinger
Overview
Explore the profile of Gustavo Malinger including associated specialties, affiliations and a list of published articles.
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92
Citations
892
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Recent Articles
1.
Malinger G, Singer A, Grinshpun-Cohen J, Sagi-Dain L, Mizrahi E
Harefuah
. 2024 Dec;
163(11):738-740.
PMID: 39692379
Letters to Editor: The risk for clinically significant copy number variants in pregnancies with two soft markers, Geriatriophobia - a new concept in the medical world in Israel.
2.
Birnbaum R, Malinger G, Ben Sira L, Goldenberg-Furmanov M, Miremberg H, Shohat M, et al.
Prenat Diagn
. 2024 Nov;
44(13):1659-1662.
PMID: 39487702
No abstract available.
3.
Hausman-Kedem M, Libzon S, Fattal Valevski A, Malinger G, Krajden Haratz N, Tokatly Latzer I, et al.
Arch Dis Child Fetal Neonatal Ed
. 2024 Oct;
PMID: 39477526
Objectives: To characterise perinatal, clinical and neuroimaging patterns and aetiology of perinatal intracranial haemorrhage (pICH), and to assess potential differences between cases diagnosed antenatally and postnatally. Methods: Prospective, observational, single-centre...
4.
Krajden Haratz K, Malinger G, Miremberg H, Hartoov J, Wolman I, Jaffa A, et al.
Fetal Diagn Ther
. 2024 Oct;
:1-11.
PMID: 39369703
Introduction: Among the fetal brain anomalies described in cases of congenital infection, callosal insults are rarely cited in medical literature. The aim of this study was to describe the rate...
5.
Prenatal Diagnosis of a KIDINS220 De Novo Heterozygous Variant in a Fetus With a Complex CNS Anomaly
Miremberg H, Birnbaum R, Trigubov D, Botvinik A, Yaron Y, Mory A, et al.
Prenat Diagn
. 2024 Oct;
44(12):1518-1521.
PMID: 39367534
Following termination of pregnancy due to multiple brain malformations, a non-consanguineous couple of Jewish descent sought genetic counseling. Brain malformations identified on neurosonogram included corpus callosum dysgenesis, abnormal brain stem...
6.
Krajden Haratz K, Malinger G, Erlik U, Goldstein R, Shohat M, Birnbaum R
Prenat Diagn
. 2024 Feb;
44(3):357-359.
PMID: 38366977
A 36 years old woman in her first pregnancy was referred at 24w3d for a dedicated neurosonographic examination due to a suspected short corpus callosum (CC). The examination depicted a...
7.
de Robertis V, Sen C, Timor-Tritsch I, Volpe P, Galindo A, Khalil A, et al.
Fetal Diagn Ther
. 2024 Feb;
51(3):203-215.
PMID: 38310852
These guidelines follow the mission of the World Association of Perinatal Medicine, in collaboration with the Perinatal Medicine Foundation, which brings together groups and individuals worldwide, with the aim to...
8.
Bornstein E, Reiss S, Malinger G
Prenat Diagn
. 2023 Dec;
44(3):360-363.
PMID: 38152001
Sotos syndrome is a rare genetic disorder that occurs in less than 1 in 10,000 births. It is characterized by rapid growth during childhood (tall stature and unusually large head),...
9.
Birnbaum R, Kuperberg M, Brusilov M, Wolman I, Malinger G, Krajden Haratz K
Prenat Diagn
. 2023 Nov;
43(12):1520-1526.
PMID: 37946665
Objective: To study the early second trimester development of brain hemispheres, lateral ventricles, choroid plexus, and ganglionic eminence/basal ganglia complex (GEBG). Methods: A retrospective analysis of TVUS 3D volumes of...
10.
Hourvitz N, Kurolap A, Mory A, Krajden Haratz K, Kidron D, Malinger G, et al.
Prenat Diagn
. 2023 Aug;
43(10):1374-1377.
PMID: 37639281
A Jewish couple of mixed origin was referred for genetic counseling following termination of pregnancy at 18 weeks of gestation due to severe ventriculomegaly with aqueduct stenosis. Trio exome sequencing...