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Predicting pubertal development by infantile and childhood height, BMI, and adiposity rebound

Pediatric research, 2015-10, Vol.78 (4), p.445-450

2015

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Sexual Dimorphism of Size Ontogeny and Life History

Frontiers in pediatrics, 2020-07, Vol.8, p.387-387

2020

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People Are Taller in Countries With Better Environmental Conditions

Frontiers in endocrinology (Lausanne), 2020-03, Vol.11, p.106

2020

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Combined Gestational Age- and Birth Weight–Adjusted Cutoffs for Newborn Screening of Congenital Adrenal Hyperplasia

The journal of clinical endocrinology and metabolism, 2019-08, Vol.104 (8), p.3172-3180

2019

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Family Size and the Age at Infancy-Childhood Transition Determine a Child's Compromised Growth in Large Families

Frontiers in pediatrics, 2022-04, Vol.10, p.821048-821048

2022

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Environmental Rather than Genetic Factors Determine the Variation in the Age of the Infancy to Childhood Transition: A Twins Study

The Journal of pediatrics, 2015-03, Vol.166 (3), p.731-735

2015

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Energy Trade-off and 4 Extreme Human Body Types

The journal of clinical endocrinology and metabolism, 2023-05, Vol.108 (5), p.e89-e97

2023

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Human Type 1 Iodothyronine Deiodinase ( DIO1 ) Mutations Cause Abnormal Thyroid Hormone Metabolism

Thyroid (New York, N.Y.), 2021-02, Vol.31 (2), p.202

2021

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Validation of a Novel Assay to Distinguish Bacterial and Viral Infections

Pediatrics (Evanston), 2017-10, Vol.140 (4)

2017

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Periorbital inflammation associated with craniofacial fibrous dysplasia: Report of three cases and review of the literature

Bone (New York, N.Y.), 2021-12, Vol.153, p.116157-116157, Article 116157

2021

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Prediction of Adult Height by Machine Learning Technique

The journal of clinical endocrinology and metabolism, 2021-07, Vol.106 (7), p.e2700-e2710

2021

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Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathy

Human molecular genetics, 2020-07, Vol.29 (11), p.1772-1783

2020

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A novel truncating variant in the FGD1 gene associated with Aarskog–Scott syndrome in a family previously diagnosed with Tel Hashomer camptodactyly

American journal of medical genetics. Part A, 2021-10, Vol.185 (10), p.3161-3166

2021

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Control of Childhood Congenital Adrenal Hyperplasia and Sleep Activity and Quality with Morning or Evening Glucocorticoid Therapy

The journal of clinical endocrinology and metabolism, 2008-12, Vol.93 (12), p.4707-4710

2008

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OR01-01 Human Type 1 Iodothyronine Deiodinase (DIO1) Mutations Cause Abnormal Thyroid Hormone Metabolism

Journal of the Endocrine Society, 2020-05, Vol.4 (Supplement_1)

2020

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Clinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex developmentResearch in context

EBioMedicine, 2024-01, Vol.99, p.104941

2024

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Consecutive mutational events in a TSHR allele of Arab families with resistance to thyroid stimulating hormone

Thyroid (New York, N.Y.), 2012-03, Vol.22 (3), p.252

2012

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Trends in the incidence of type 1 diabetes among Jews and Arabs in Israel

Pediatric diabetes, 2014-09, Vol.15 (6), p.422-427

2014

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Clinical and genetic characteristics of congenital hypothyroidism due to mutations in the thyroid peroxidase (TPO) gene in Israelis

Clinical endocrinology (Oxford), 2007-05, Vol.66 (5), p.695-702

2007

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Increase in the incidence of type 1 diabetes in Israeli children following the Second Lebanon War

Pediatric diabetes, 2012-06, Vol.13 (4), p.326-333

2012

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A novel truncating variant in the FGD1 gene associated with Aarskog-Scott syndrome in a family previously diagnosed with Tel Hashomer camptodactyly

American journal of medical genetics. Part A, 2021, Vol.185 (10), p.3161-3166

2021

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Vexierbilder: Autor:inneninszenierung vom 19. Jahrhundert bis zur Gegenwart

1, 2021

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Predicting pubertal development by infantile and childhood height, BMI, and adiposity rebound

Sexual Dimorphism of Size Ontogeny and Life History

People Are Taller in Countries With Better Environmental Conditions

Combined Gestational Age- and Birth Weight–Adjusted Cutoffs for Newborn Screening of Congenital Adrenal Hyperplasia

Family Size and the Age at Infancy-Childhood Transition Determine a Child's Compromised Growth in Large Families

Environmental Rather than Genetic Factors Determine the Variation in the Age of the Infancy to Childhood Transition: A Twins Study

Energy Trade-off and 4 Extreme Human Body Types

Human Type 1 Iodothyronine Deiodinase ( DIO1 ) Mutations Cause Abnormal Thyroid Hormone Metabolism

Validation of a Novel Assay to Distinguish Bacterial and Viral Infections

Periorbital inflammation associated with craniofacial fibrous dysplasia: Report of three cases and review of the literature

Prediction of Adult Height by Machine Learning Technique

Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathy

A novel truncating variant in the FGD1 gene associated with Aarskog–Scott syndrome in a family previously diagnosed with Tel Hashomer camptodactyly

Alarming increase in ketoacidosis in children and adolescents with newly diagnosed type 1 diabetes during the first wave of the COVID‐19 pandemic in Israel

Primary Ovarian Insufficiency Nationwide Incidence Rate and Etiology Among Israeli Adolescents

Control of Childhood Congenital Adrenal Hyperplasia and Sleep Activity and Quality with Morning or Evening Glucocorticoid Therapy

OR01-01 Human Type 1 Iodothyronine Deiodinase (DIO1) Mutations Cause Abnormal Thyroid Hormone Metabolism

Clinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex developmentResearch in context

Consecutive mutational events in a TSHR allele of Arab families with resistance to thyroid stimulating hormone

Global Application of the Assessment of Communication Skills of Paediatric Endocrinology Fellows in the Management of Differences in Sex Development Using the ESPE E-Learning.Org Portal

Trends in the incidence of type 1 diabetes among Jews and Arabs in Israel

Clinical and genetic characteristics of congenital hypothyroidism due to mutations in the thyroid peroxidase (TPO) gene in Israelis

Increase in the incidence of type 1 diabetes in Israeli children following the Second Lebanon War

A novel truncating variant in the FGD1 gene associated with Aarskog-Scott syndrome in a family previously diagnosed with Tel Hashomer camptodactyly

Vexierbilder: Autor:inneninszenierung vom 19. Jahrhundert bis zur Gegenwart

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