[Familial and hereditary microcephaly. Study of 10 cases in 4 families]

Empowering non-designers with tangible tools for divergent thinking.

Ergonomics·2025

Arterial Spin-Labeling in the Assessment of Pediatric Nontraumatic Orbital Lesions.

AJNR. American journal of neuroradiology·2023

Prenatal diagnosis of microcephaly with simplified gyral pattern: series of eight cases.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology·2023

Dexmedetomidine sedation vs. inhaled general anesthesia for pediatric MRI: A retrospective cohort study: Dexmedetomidine sedation vs. inhaled general anesthesia for MRI.

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2022

Enhanced light extraction efficiency of Eu-related emission from a nano-patterned GaN layer grown by MOCVD.

Scientific reports·2019

Pronase treatment improves flow cytometry crossmatching results.

HLA·2017

[Psychological aspects of bone marrow donation in donor brothers and sisters in bone marrow transplantation].

Pediatrie·1993

[Lethargy in the course of treatment with ranitidine in a newborn infant].

Pediatrie·1993

[Delayed detection of hip dislocation: is the physician to blame?].

Pediatrie·1993

[Renal tubular acidosis in children].

Pediatrie·1993

[CD23: structures, functions and practical perspectives in allergy reactions].

Pediatrie·1993

[Accessory thymus in cervical ectopy: apropos of a case].

Pediatrie·1993

Network analysis of the genetic relationships between twenty psychiatric and substance use disorders.

World psychiatry : official journal of the World Psychiatric Association (WPA)·2026

Clinical Utility of Trio Exome Sequencing in Rwandan Children With Autism Spectrum Disorder.

Molecular genetics & genomic medicine·2026

Heterogeneity of azithromycin resistance markers in Neisseria gonorrhoeae and challenges in implementing molecular assays for routine surveillance.

New microbes and new infections·2026

Large-Scale Neuroimaging and Genetic Analyses of the Human Thalamus in Loneliness.

Biological psychiatry global open science·2026

A recurrent CCDC82 frameshift variant associated with syndromic neurodevelopmental disorder in a consanguineous Pakistani family.

Biochemistry and biophysics reports·2026

Clinical and molecular characterization of giant axonal neuropathy due to a homozygous c.851 + 1G>A variant in GAN: A case report and literature review.

Global medical genetics·2026

Related Experiment Videos

[Familial and hereditary microcephaly. Study of 10 cases in 4 families]

Related Concept Videos

Empowering non-designers with tangible tools for divergent thinking.

Arterial Spin-Labeling in the Assessment of Pediatric Nontraumatic Orbital Lesions.

Prenatal diagnosis of microcephaly with simplified gyral pattern: series of eight cases.

Dexmedetomidine sedation vs. inhaled general anesthesia for pediatric MRI: A retrospective cohort study: Dexmedetomidine sedation vs. inhaled general anesthesia for MRI.

Enhanced light extraction efficiency of Eu-related emission from a nano-patterned GaN layer grown by MOCVD.

Pronase treatment improves flow cytometry crossmatching results.

[Psychological aspects of bone marrow donation in donor brothers and sisters in bone marrow transplantation].

[Lethargy in the course of treatment with ranitidine in a newborn infant].

[Delayed detection of hip dislocation: is the physician to blame?].

[Renal tubular acidosis in children].

[CD23: structures, functions and practical perspectives in allergy reactions].

[Accessory thymus in cervical ectopy: apropos of a case].

Network analysis of the genetic relationships between twenty psychiatric and substance use disorders.

Clinical Utility of Trio Exome Sequencing in Rwandan Children With Autism Spectrum Disorder.

Heterogeneity of azithromycin resistance markers in Neisseria gonorrhoeae and challenges in implementing molecular assays for routine surveillance.

Large-Scale Neuroimaging and Genetic Analyses of the Human Thalamus in Loneliness.

A recurrent CCDC82 frameshift variant associated with syndromic neurodevelopmental disorder in a consanguineous Pakistani family.

Clinical and molecular characterization of giant axonal neuropathy due to a homozygous c.851 + 1G>A variant in GAN: A case report and literature review.

Related Experiment Videos

[Familial and hereditary microcephaly. Study of 10 cases in 4 families]

Related Concept Videos

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