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σφιχτός ζωτικότητα Σημεία στίξης hydrocephalus gene panel άλμα διατρυπώ Γιατρός της Φιλοσοφίας

Prenatal genetic considerations in congenital ventriculomegaly and  hydrocephalus | SpringerLink
Prenatal genetic considerations in congenital ventriculomegaly and hydrocephalus | SpringerLink

Metabolic Disorders | NGS Panels: centogene.com
Metabolic Disorders | NGS Panels: centogene.com

Neonatal hydrocephalus is a result of a block in folate handling and  metabolism involving 10‐formyltetrahydrofolate dehydrogenase - Naz - 2016 -  Journal of Neurochemistry - Wiley Online Library
Neonatal hydrocephalus is a result of a block in folate handling and metabolism involving 10‐formyltetrahydrofolate dehydrogenase - Naz - 2016 - Journal of Neurochemistry - Wiley Online Library

Characterization of Rfx4 +/-mice with hydrocephalus. (A) H&E staining.... |  Download Scientific Diagram
Characterization of Rfx4 +/-mice with hydrocephalus. (A) H&E staining.... | Download Scientific Diagram

Genetic etiologies associated with infantile hydrocephalus in a Chinese  infantile cohort | SpringerLink
Genetic etiologies associated with infantile hydrocephalus in a Chinese infantile cohort | SpringerLink

NTM meningitis, presenting as hydrocephalus, in a 30-year-old male.... |  Download Scientific Diagram
NTM meningitis, presenting as hydrocephalus, in a 30-year-old male.... | Download Scientific Diagram

Genes causing congenital hydrocephalus: Their chromosomal characteristics  of telomere proximity and DNA compositions - ScienceDirect
Genes causing congenital hydrocephalus: Their chromosomal characteristics of telomere proximity and DNA compositions - ScienceDirect

Navigating the ventricles: Novel insights into the pathogenesis of  hydrocephalus - ScienceDirect
Navigating the ventricles: Novel insights into the pathogenesis of hydrocephalus - ScienceDirect

Frontiers | Ependymal Cilia: Physiology and Role in Hydrocephalus
Frontiers | Ependymal Cilia: Physiology and Role in Hydrocephalus

Congenital hydrocephalus: new Mendelian mutations and evidence for  oligogenic inheritance | Human Genomics | Full Text
Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritance | Human Genomics | Full Text

Deletions in CWH43 cause idiopathic normal pressure hydrocephalus | EMBO  Molecular Medicine
Deletions in CWH43 cause idiopathic normal pressure hydrocephalus | EMBO Molecular Medicine

Genetic Deletion of Afadin Causes Hydrocephalus by Destruction of Adherens  Junctions in Radial Glial and Ependymal Cells in the Midbrain | PLOS ONE
Genetic Deletion of Afadin Causes Hydrocephalus by Destruction of Adherens Junctions in Radial Glial and Ependymal Cells in the Midbrain | PLOS ONE

Exome sequencing implicates genetic disruption of prenatal  neuro-gliogenesis in sporadic congenital hydrocephalus | Nature Medicine
Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus | Nature Medicine

Infantile hydrocephalus: a review of epidemiology, classification and  causes. | Semantic Scholar
Infantile hydrocephalus: a review of epidemiology, classification and causes. | Semantic Scholar

Multi-omic analysis elucidates the genetic basis of hydrocephalus
Multi-omic analysis elucidates the genetic basis of hydrocephalus

JCM | Free Full-Text | Reappraisal of Pediatric Normal-Pressure  Hydrocephalus
JCM | Free Full-Text | Reappraisal of Pediatric Normal-Pressure Hydrocephalus

Figure 2 from Congenital hydrocephalus in clinical practice: a genetic  diagnostic approach. | Semantic Scholar
Figure 2 from Congenital hydrocephalus in clinical practice: a genetic diagnostic approach. | Semantic Scholar

The genetic landscape of familial congenital hydrocephalus - Shaheen - 2017  - Annals of Neurology - Wiley Online Library
The genetic landscape of familial congenital hydrocephalus - Shaheen - 2017 - Annals of Neurology - Wiley Online Library

Primary Ciliary Dyskinesia and Hydrocephalus With Aqueductal Stenosis -  José Pedro Vieira, Patricia Lopes, Rita Silva, 2012
Primary Ciliary Dyskinesia and Hydrocephalus With Aqueductal Stenosis - José Pedro Vieira, Patricia Lopes, Rita Silva, 2012

Visualizing flow in an intact CSF network using optical coherence  tomography: implications for human congenital hydrocephalus
Visualizing flow in an intact CSF network using optical coherence tomography: implications for human congenital hydrocephalus

Unlocking the genetic complexity of congenital hydrocephalus | Nature  Medicine
Unlocking the genetic complexity of congenital hydrocephalus | Nature Medicine

Impaired neurogenesis alters brain biomechanics in a neuroprogenitor-based  genetic subtype of congenital hydrocephalus | Nature Neuroscience
Impaired neurogenesis alters brain biomechanics in a neuroprogenitor-based genetic subtype of congenital hydrocephalus | Nature Neuroscience

Frontiers | Diagnostic Approach to Macrocephaly in Children
Frontiers | Diagnostic Approach to Macrocephaly in Children

Visualizing flow in an intact CSF network using optical coherence  tomography: implications for human congenital hydrocephalus | Scientific  Reports
Visualizing flow in an intact CSF network using optical coherence tomography: implications for human congenital hydrocephalus | Scientific Reports

Hydrocephalus due to multiple ependymal malformations is caused by  mutations in the MPDZ gene | Acta Neuropathologica Communications | Full  Text
Hydrocephalus due to multiple ependymal malformations is caused by mutations in the MPDZ gene | Acta Neuropathologica Communications | Full Text