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Microlissencephaly
Book Review
Prevalence and Incidence of Rare Diseases: Bibliographic Data
Supratentorial Brain Malformations
Congenital Microcephaly a Diagnostic Challenge During Zika Epidemics
Neuro-Anatomical Study of a Rare Brain Malformation: Lissencephaly, a Report of Eleven Patients
Ajnr.A4552.Full.Pdf
Blueprint Genetics Neuronal Migration Disorder Panel
Prenatal Contributions to Epilepsy: Lessons from the Bedside
TUBB2B Gene Tubulin Beta 2B Class Iib
Emerging Role of the Kinesin Family Member Genes in Birth Defects Silvia Kalantari ,1 Isabel Filges 1,2
International Consensus Recommendations on the Diagnostic Work-Up for Malformations of Cortical Development
Genetics of CNS Abnormalities the Prenatal Diagnosis Perspective Ignatia B
1 Overview of the Development of the Human Brain and Spinal Cord 1 Hans J
Lissencephaly, Generic Term
Molecular Genetic Approaches to Disease of Neural Development Mohamad Bydon Yale University
Prenatal Diagnosis of Fetal Microhydranencephaly: a Case Report and Literature Review Takahiro Omoto1,2, Toshifumi Takahashi3* , Keiya Fujimori2 and Shogo Kin1
The Role of Magnetic Resonance Imaging in the Diagnosis of Fetal Malformations
Bilateral, Posterior Parietal Polymicrogyria As Part of Speech Therapy Work-Up
Top View
Mutations in Tubulin Genes Are Frequent Causes of Various Foetal
ORPHA Number Disease Or Group of Diseases 300305 11P15.4
18Neuroimaging in the Evaluation of Pattern and Timing of Fetal and Neonatal Brain Abnormalities
Molecular Testing for Lissencephaly
Malformations of Cortical Development’ in the Pediatric Age Group
RECURRENT MICROLISSENCEPHALY: a CASE REPORT Garcia-Manau P.1, Esteve E
Clinical, Genetic and Imaging Findings Identify New Causes for Corpus
Central Nervous System Malformations 1D’Addario Vincenzo, 2Capuano Pasquale
Oup Jmcbio Mjy087 200..211 ++
Microcephalia Vera and Microcephaly with Simplified Gyral Pattern
Disorders of Cortical Formation: MR Imaging REVIEW ARTICLE Features
Comprehensive Genotype-Phenotype Correlation in Lissencephaly
Baraitser–Winter Cerebrofrontofacial Syndrome
Orphanet Report Series 180 160 Collection 140 Rare Diseases
Description Treatment Prognosis
Clinical Neuroembryology Development and Developmental Disorders of the Human Central Nervous System Hans J
Extreme Microcephaly, Diffuse Agyria, Agenesis of Corpus Callosum
Genetics and Mechanisms Leading to Human Cortical Malformations Delfina Romero, Nadia Bahi-Buisson, Fiona Francis
Prevalence and Incidence of Rare Diseases
MR Imaging of the Fetus in Utero I: a Practical Guide to Systematic Analysis - Central Nervous System
Congenital Microcephaly with a Simplified Gyral Pattern: Associated Findings and Their ORIGINAL RESEARCH Significance
De Novo TUBB2B Mutation Causes Fetal Akinesia
Extreme Microcephaly, Diffuse Agyria, Agenesis Of
Microcephaly (MIC)
Tubulinopathies Continued: Refining the Phenotypic Spectrum Associated with Variants in TUBG1
Orphanet Rep Rt Series