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37 results on '"Haratz, K.K."'

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4. VP25.20: Molar tooth dysplasias in the fetus: differential diagnosis with vermian anomalies from distinct origin

8. P18.08: Prenatal diagnosis of a new association of middle interhemispheric variant of holoprosencephaly with di‐mes‐rhombencephalosynapsis

10. OC03.07: Prenatal diagnosis of malformations of cortical development associated to midbrain‐hindbrain anomalies

11. OC03.01: Prenatal diagnosis of rhombencephalosynapsis: beyond the fusion of the cerebellar hemispheres

14. OC07.02: Differential diagnosis of irregular lateral ventricle walls: correlation between prenatal imaging and fetal neuropathological studies

16. OC21.02: Brainstem malformations in severe fetal ventriculomegaly

20. EP03.07: Prenatal diagnosis of 22q11.2 microdeletion: minor cardiac finding detected in mid-trimester scan associated with severe bilateral perisylvian polymicrogyria in late gestation

22. OC06.02: Prenatal diagnosis of brainstem anomalies: phenotypic spectrum and neuroimaging features

23. OP14.11: Prenatal diagnosis of medullary tegmental cap dysplasia: a rare disorder of axonal guidance

24. OP14.08: Prenatal diagnosis of a new cobblestone malformation complex disorder: Walker-Warburg syndrome associated with tectocerebellar dysraphia

27. P30.07: Sonographic diagnosis of fetal developmental venous anomaly: persistent echogenic brain lesion drained by a prominent collecting vein

29. OC12.05: Early second trimester diagnosis of fetal midbrain–hindbrain malformations: a transvaginal neurosonographic study.

36. OP05.01: The fourth ventricle index as a screening tool for Joubert syndrome and related disorders.

37. <scp>ISUOG</scp> Practice Guidelines (updated): sonographic examination of the fetal central nervous system. Part 1: performance of screening examination and indications for targeted neurosonography

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