[Congenital deficiency of thyroxine binding globulin (TBG). Study of 3 families]

Clinical utility of left atrial diameter normalized for body weight in healthy and cardiomyopathic cats.

Journal of veterinary cardiology : the official journal of the European Society of Veterinary Cardiology·2025

Congenital cytomegalovirus infection and audiological follow-up: electrophysiological auditory threshold before 3 months of age as a predictor of hearing outcome at 3 years of age.

Journal of perinatology : official journal of the California Perinatal Association·2020

Cardiorespiratory events in infants with gastroesophageal reflux symptoms: Is there any association?

Neurogastroenterology and motility·2017

Quality control of ultrasound for fetal biometry: results from the INTERGROWTH-21st Project.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology·2017

Fast glycorrhachia and cerebrospinal fluid protein as predictors of sensory block in anesthesia with subarachnoid Ropivacaine.

La Clinica terapeutica·2017

International estimated fetal weight standards of the INTERGROWTH-21st Project.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology·2016

Developmental and behavioral profile in a domestic adoptees sample: a new challenge for the pediatrician.

Minerva pediatrica·2020

A new approach to the diagnosis of short stature.

Minerva pediatrica·2020

Kounis Syndrome: a pediatric perspective.

Minerva pediatrica·2020

Human inborn errors of immunity caused by defects of receptor and proteins of cellular membrane.

Minerva pediatrica·2020

Tall stature in children and adolescents.

Minerva pediatrica·2020

Precocious puberty.

Minerva pediatrica·2020

Rare missense variants identified by whole-genome sequencing in men with oligoasthenoteratozoospermia: An experimental study.

International journal of reproductive biomedicine·2026

Whole-Exome Sequencing Reveals the Genetic Landscape and Genotype-Phenotype Spectrum of Dystonia in a Chinese Cohort.

CNS neuroscience & therapeutics·2026

Genome-wide analysis of 439 mass spectrometry-based proteomic profiles in a population of 15,035 Scottish individuals.

Nature communications·2026

Generation of a human induced pluripotent stem cell line (PNUYHi004-A) from a patient with hereditary spastic paraplegia type 46 (SPG46) carrying compound heterozygous GBA2 variants.

Stem cell research·2026

Polygenic Risk Scores for Islet Autoantibody Positive Early-Stage Type 1 Diabetes Pre-Screening.

Diabetes, obesity & metabolism·2026

Analysis of Genomic Testing of Congenital Heart Disease in a Cohort From a Consanguineous Population.

Clinical genetics·2026

Related Experiment Videos

[Congenital deficiency of thyroxine binding globulin (TBG). Study of 3 families]

Related Concept Videos

Clinical utility of left atrial diameter normalized for body weight in healthy and cardiomyopathic cats.

Congenital cytomegalovirus infection and audiological follow-up: electrophysiological auditory threshold before 3 months of age as a predictor of hearing outcome at 3 years of age.

Cardiorespiratory events in infants with gastroesophageal reflux symptoms: Is there any association?

Quality control of ultrasound for fetal biometry: results from the INTERGROWTH-21st Project.

Fast glycorrhachia and cerebrospinal fluid protein as predictors of sensory block in anesthesia with subarachnoid Ropivacaine.

International estimated fetal weight standards of the INTERGROWTH-21st Project.

Developmental and behavioral profile in a domestic adoptees sample: a new challenge for the pediatrician.

A new approach to the diagnosis of short stature.

Kounis Syndrome: a pediatric perspective.

Human inborn errors of immunity caused by defects of receptor and proteins of cellular membrane.

Tall stature in children and adolescents.

Precocious puberty.

Rare missense variants identified by whole-genome sequencing in men with oligoasthenoteratozoospermia: An experimental study.

Whole-Exome Sequencing Reveals the Genetic Landscape and Genotype-Phenotype Spectrum of Dystonia in a Chinese Cohort.

Genome-wide analysis of 439 mass spectrometry-based proteomic profiles in a population of 15,035 Scottish individuals.

Generation of a human induced pluripotent stem cell line (PNUYHi004-A) from a patient with hereditary spastic paraplegia type 46 (SPG46) carrying compound heterozygous GBA2 variants.

Polygenic Risk Scores for Islet Autoantibody Positive Early-Stage Type 1 Diabetes Pre-Screening.

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Related Experiment Videos

[Congenital deficiency of thyroxine binding globulin (TBG). Study of 3 families]

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