Prenatal diagnosis of genetic microcephaly

Acute infantile encephalopathy predominantly affecting the frontal lobe (AIEF): a European case.

European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society·2010

[Urology].

Revue medicale suisse·2010

The role of epilepsy in early language development in a child with a congenital lesion in the right hemisphere.

Developmental medicine and child neurology·2008

Deficit in memory consolidation (abnormal forgetting rate) in childhood temporal lobe epilepsy. Pre and postoperative long-term observation.

Neuropediatrics·2007

Maternal serum levels of placental proteins after in vitro fertilisation and their implications for prenatal screening.

Prenatal diagnosis·2004

Speech delay due to a prelinguistic regression of epileptic origin.

Neuropediatrics·2004

Multicentric Longitudinal Performance Monitoring of Different Prenatal Cell-Free DNA Screening Technologies in Belgium.

Prenatal diagnosis·2026

Maternal Sirolimus Therapy for Fetal Extensive Lymphatic Cystic Malformation: Selection Criteria, Management, and Outcomes in a Series of Six Cases.

Prenatal diagnosis·2026

When Fetal Anomalies Lead to Prognostic Clarification: An Underrecognized Application of Exome Sequencing.

Prenatal diagnosis·2026

Prenatal Phenotypic Features of Five Fetal Cases With RNU4ATAC-Associated Microcephalic Osteodysplastic Primordial Dwarfism Type I.

Prenatal diagnosis·2026

Trio-Exome-Based Mendelian Inheritance Error Analysis Helps Identify Uniparental Disomies and Resolve Discordant NIPT Findings.

Prenatal diagnosis·2026

Comparison of Medium-Coverage Whole-Genome Sequencing and Chromosomal Microarray in Prenatal Testing of Absence of Heterozygosity.

Prenatal diagnosis·2026

Linking Metabolic Subgroups and Adverse Pregnancy Outcomes in GDM: A Complementary Analytic Approach of Logistic Regressions and Machine Learning.

Diabetes, obesity & metabolism·2026

Donor human milk for maternal milk shortfall in preterm infants: a feasibility randomised controlled trial.

Archives of disease in childhood. Fetal and neonatal edition·2026

NHS healthcare worker experiences of moral injury: a follow-up qualitative study in England using reflexive thematic analysis.

BMJ open·2026

Assessing Skills in Managing Breastfeeding Challenges Among Community Health Care Providers: Development and Validation of the LactManage OSCE-Based Questionnaire.

Journal of human lactation : official journal of International Lactation Consultant Association·2026

Effectiveness of the BabyBreathe intervention for maintaining postpartum smoking cessation: multicentre pragmatic randomised controlled trial.

BMJ (Clinical research ed.)·2026

Acute exposure to cell-free mitochondrial DNA induces pregnancy-specific aortic endothelial dysfunction and organ-selective inflammation in rats.

American journal of physiology. Heart and circulatory physiology·2026

Related Experiment Videos

Prenatal diagnosis of genetic microcephaly

Related Concept Videos

Acute infantile encephalopathy predominantly affecting the frontal lobe (AIEF): a European case.

[Urology].

The role of epilepsy in early language development in a child with a congenital lesion in the right hemisphere.

Deficit in memory consolidation (abnormal forgetting rate) in childhood temporal lobe epilepsy. Pre and postoperative long-term observation.

Maternal serum levels of placental proteins after in vitro fertilisation and their implications for prenatal screening.

Speech delay due to a prelinguistic regression of epileptic origin.

Multicentric Longitudinal Performance Monitoring of Different Prenatal Cell-Free DNA Screening Technologies in Belgium.

Maternal Sirolimus Therapy for Fetal Extensive Lymphatic Cystic Malformation: Selection Criteria, Management, and Outcomes in a Series of Six Cases.

When Fetal Anomalies Lead to Prognostic Clarification: An Underrecognized Application of Exome Sequencing.

Prenatal Phenotypic Features of Five Fetal Cases With RNU4ATAC-Associated Microcephalic Osteodysplastic Primordial Dwarfism Type I.

Trio-Exome-Based Mendelian Inheritance Error Analysis Helps Identify Uniparental Disomies and Resolve Discordant NIPT Findings.

Comparison of Medium-Coverage Whole-Genome Sequencing and Chromosomal Microarray in Prenatal Testing of Absence of Heterozygosity.

Linking Metabolic Subgroups and Adverse Pregnancy Outcomes in GDM: A Complementary Analytic Approach of Logistic Regressions and Machine Learning.

Donor human milk for maternal milk shortfall in preterm infants: a feasibility randomised controlled trial.

NHS healthcare worker experiences of moral injury: a follow-up qualitative study in England using reflexive thematic analysis.

Assessing Skills in Managing Breastfeeding Challenges Among Community Health Care Providers: Development and Validation of the LactManage OSCE-Based Questionnaire.

Effectiveness of the BabyBreathe intervention for maintaining postpartum smoking cessation: multicentre pragmatic randomised controlled trial.

Acute exposure to cell-free mitochondrial DNA induces pregnancy-specific aortic endothelial dysfunction and organ-selective inflammation in rats.

Related Experiment Videos

Prenatal diagnosis of genetic microcephaly

Abstract:

Related Concept Videos

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